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Registered Nurse - Occupational Health Lead

Irvine, California

Sep 24, 2026

CQC/Clinical Quality Assurance Exciting development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical and Vision Care Registered Nurse – Occupational Health Lead Benefits: Medical, Dental, Holiday, PTO 401K matching We are seeking an experienced Registered Nurse to provide onsite occupational health services in Houston, TX. The RN will deliver basic medical care, employee health screenings, emergency care, referrals, and wellness programs while maintaining confidential health records and supporting workplace safety initiatives. Active RN license Current CPR/AED/First Aid certification 2+ years of RN experience, including 1+ year in Occupational Health Proficiency with Microsoft Outlook, Teams, Excel, PowerPoint, and OneNote Strong communication and organizational skills Schedule: Approximately 3 days/week, 8-hour shifts, onsite Duration: 9 weeks + 5 days, starting in January This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Buyer - External Manufacturing

Trumbull, Connecticut

Sep 23, 2026

Laboratory Location: Trumbull, CT Pay Rate: $35–$40/hour Duration: Approximately 6 months Schedule: 1st shift (~8a-5p) Monday–Friday, 100% onsite Position Overview Our client is seeking a Buyer, External Manufacturing to support day-to-day procurement activities for external contract manufacturing operations and finished goods supply. This role will serve as the primary purchasing contact for assigned external manufacturing partners and suppliers, helping ensure material availability, continuity of supply, inventory optimization, and successful execution of production plans. This is an excellent opportunity for an experienced supply chain professional who is comfortable working in a fast-paced, evolving environment and can independently manage competing priorities with a strong sense of urgency and ownership. The role will support a global portfolio of suppliers and external manufacturing partners across multiple regions and time zones. Key Responsibilities Evaluate purchasing requirements and supplier commitments based on business needs, inventory objectives, customer demand, and external manufacturing production schedules. Manage the full purchasing lifecycle, including order placement, supplier follow-up, schedule changes, delivery management, and issue resolution. Monitor supplier commitments and proactively adjust purchasing activities based on changing forecasts, inventory requirements, and production priorities. Serve as the primary purchasing contact for assigned external manufacturing suppliers and manage day-to-day procurement activities. Ensure material availability and continuity of supply to support external manufacturing production requirements. Develop and maintain strong relationships with suppliers across multiple geographic regions and time zones. Identify potential supply risks and independently drive corrective actions to help prevent production or customer delivery disruptions. Coordinate material availability and supplier commitments to support external manufacturing production plans. Partner cross-functionally with Planning, Operations, Quality, Engineering, Finance, and External Manufacturing teams to resolve shortages and supply constraints. Maintain accurate supplier, purchasing, inventory, lead-time, and procurement data within Microsoft Dynamics 365 (D365) and related systems. Prepare purchasing, shortage, inventory, and supplier performance reports. Support new product introductions, product transfers, engineering changes, and supplier transitions. Escalate significant supply, delivery, and inventory issues while providing recommended corrective actions. Develop, prepare, review, and publish weekly and/or monthly reports as directed by management. Qualifications 5+ years of purchasing experience, preferably supporting external manufacturing, contract manufacturing organizations (CMOs), CDMOs, and/or finished goods suppliers. Experience managing a global portfolio of suppliers across multiple regions, cultures, and time zones. Experience within medical device, life sciences, pharmaceutical, or another regulated manufacturing environment. Strong ERP experience; Microsoft Dynamics 365 (D365) preferred. Advanced Microsoft Excel skills, including data analysis, reporting, and management of large datasets. Strong supplier management, communication, follow-up, and relationship-building skills. Ability to work independently and effectively in a fast-paced, evolving organization. Demonstrated ability to identify problems, assess priorities, and drive solutions with a strong sense of urgency. Strong ownership mentality, accountability, initiative, and commitment to execution. Ability to effectively communicate with and influence cross-functional stakeholders. Strong attention to detail and ability to manage multiple priorities while maintaining accuracy. Comfortable navigating ambiguity and driving results in a growing organization with evolving processes and systems. Work Environment This is a 100% onsite position based in Trumbull, Connecticut. The role is primarily office-based and requires prolonged sitting at a computer workstation.

Chemist I

Cincinnati, Ohio

Sep 23, 2026

Laboratory Chemist I – Finished Product Lab Location: Cincinnati, OH Pay: $25/hour Schedule: 3rd Shift | Sunday–Thursday | 10:00 PM–6:30 AM Department: Quality Services – Finished Product Lab Position Overview We are seeking a Chemist I to join the Quality Services (QS) team in the Finished Product Lab. This position will support product testing, quality documentation, raw material sampling, and timely release of products and components while ensuring compliance with GMP and safety requirements. This is a great opportunity for an entry-level Chemist or recent Science graduate with laboratory experience who is looking to build experience in a quality-focused manufacturing environment. What You Will Do Perform testing of bulk products, finished products, and packaging materials while maintaining GMP compliance. Accurately document and enter testing results into SAP. Report out-of-specification (OOS) results to the QS Leader or designee and Production, communicating with suppliers when necessary. Release bulk products in SAP when appropriate and within required timelines. Review production documentation to ensure compliance with established requirements. Support Quality and Manufacturing initiatives, including product testing for process improvements and other planned requests. Follow all GMP and safety requirements, including written procedures and applicable SDS guidelines. Maintain laboratory instruments in good working condition. Ensure the laboratory remains clean, organized, and inspection-ready. Maintain product retains as required. Provide coverage for other laboratory areas, including the Raw Materials Lab, as needed. Qualifications Bachelor's degree in Science, preferably Chemistry, Biology, Microbiology, Biochemistry, or a related field. Entry-level candidates are welcome; undergraduate laboratory experience is acceptable. 0–2 years of quality or laboratory experience preferred. Basic understanding of pH and viscosity testing. Familiarity with Gas Chromatography (GC) and wet chemistry/analytical techniques is a plus. Experience in an FDA-regulated environment, such as personal care, OTC pharmaceuticals, or contract testing, is preferred but not required. Strong verbal and written communication skills. Ability to multitask, organize, and prioritize responsibilities in a laboratory environment. Proficiency with Microsoft Office. Experience with SAP is a plus. Interview Process Virtual screening interview with the hiring manager Onsite interview Sensory Panel / Odor-Smell Test

R&D Analytical Chemist

Centerbrook, Connecticut

Sep 23, 2026

Laboratory Analytical R&D Chemist Location: Centerbrook, CT Employment Type: Full-Time, Exempt Compensation: $70,000–$140,000 annually Level: Mid–Senior Level Preferred; Associate-Level Candidates with Relevant Experience Will Be Considered Position Overview Our client is seeking an Analytical R&D Chemist to support research, development, and chemical manufacturing activities within a highly technical laboratory environment. This role will perform analytical testing on raw materials, intermediates, and finished products while providing critical data to support reaction monitoring, process development, optimization, and scale-up activities. The ideal candidate will have hands-on analytical laboratory experience and the ability to interpret data, troubleshoot analytical methods and instrumentation, and communicate results effectively in a collaborative, fast-paced environment. Key Responsibilities Perform routine and non-routine analytical testing using techniques including NMR, HPLC, GC, LC-MS, UV-Vis, and Karl Fischer. Support route scouting, process optimization, and scale-up activities through timely in-process control (IPC) testing and reaction profiling. Evaluate reaction conversion, selectivity, purity, and impurity profiles. Support identification and characterization of unknowns, degradants, intermediates, and isolated products. Generate accurate, reliable analytical data to support R&D and manufacturing projects. Support kinetic studies, Design of Experiments (DoE), and process safety evaluations through analytical characterization. Document and communicate analytical results clearly and within required timelines. Assist with troubleshooting analytical procedures, methods, and laboratory instrumentation. Maintain analytical laboratory equipment and help ensure instruments and methods are ready to support ongoing projects. Contribute to efficient day-to-day laboratory operations and provide support to project teams as needed. Collaborate with chemists, engineers, and other technical personnel to meet project objectives. Qualifications Bachelor’s degree or higher in Chemistry or a related scientific discipline with strong laboratory coursework. 3–5+ years of relevant analytical laboratory experience preferred; experienced Associate-level candidates may also be considered. Hands-on experience with chromatography, spectroscopy, and/or other analytical techniques. Experience working with Chromatography Data Systems (CDS) preferred. Strong computer skills and ability to learn new laboratory software and systems. Excellent attention to detail, organization, and ability to manage multiple priorities. Strong written and verbal communication skills. Ability to work effectively with technical staff across a collaborative, team-based environment. Strong problem-solving skills and ability to interpret analytical results. Comfortable working in a fast-paced environment where turnaround time and sound analytical judgment are important. Demonstrated ability and willingness to learn new techniques and skills. What This Opportunity Offers Opportunity to contribute to innovative chemical process development and manufacturing projects. Work alongside experienced chemists and engineers in a highly technical environment. Exposure to a variety of analytical techniques and challenging R&D projects. Opportunity for professional growth and increased technical responsibility. Competitive compensation and comprehensive benefits. Pre-Employment Requirements Background check Drug screening Academic transcript verification Authorization to work in the United States Work Environment This position involves working in a laboratory environment with chemicals and hazardous materials. Comprehensive training in chemical safety, hazardous materials handling, and emergency response will be provided.

Sr. Metal Additive Process Engineer

Irvine, California

Sep 22, 2026

Engineering Exciting development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical and Vision Care Sr. Metal Additive Process Engineer Location: Irvine, CA — 5 days onsite required Contract: 6 months, with likely extension Benefits: Medical, Dental, Holiday, PTO 401K matching We are seeking a Senior Metal Additive Process Engineer to lead the development, optimization, and scale-up of metal additive manufacturing processes. This role will focus on hands-on printer operation, process parameter development, DOE, data analysis, troubleshooting, and production qualification. Operate, maintain, and optimize metal additive manufacturing equipment. Develop and optimize print parameters to improve quality, productivity, and yield. Design and execute DOE studies and analyze process data. Troubleshoot printing, powder handling, and post-processing issues. Investigate root causes and implement process improvements. Support equipment/part qualification, process validation, and production scale-up. Required Qualifications 5+ years of experience in metal additive manufacturing process development; 7–10 years preferred. Hands-on experience with metal AM technologies and equipment. Strong knowledge of metal powders, melt pool dynamics, process parameters, and defect mechanisms. Experience with DOE, statistical analysis, and process optimization. Strong troubleshooting and root-cause analysis skills. BS/MS in Mechanical Engineering, Materials Science, Manufacturing Engineering, or related field. Preferred Qualifications Experience with machine learning, AI, or predictive modeling for process optimization. Knowledge of Design for Additive Manufacturing (DfAM). Experience with thermal modeling, FEA, or metal AM process simulation. This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Associate Quality Engineer

Duluth, Georgia

Sep 22, 2026

Manufacturing Exciting development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical and Vision Care Associate Quality Engineer – Johns Creek, GA Duration: 24 months Schedule: Night Shift, rotating 2-2-3 schedule Benefits: Medical, Dental, Holiday, PTO 401K matching Seeking an Associate Quality Engineer to support quality and manufacturing processes for medical devices in a regulated environment. Key Responsibilities: Lead root cause investigations for manufacturing issues and customer complaints. Develop and implement corrective/preventive actions and monitor effectiveness. Troubleshoot customer-returned devices and manufacturing nonconformities. Analyze product performance using statistical and risk-based approaches. Support quality projects and collaborate with cross-functional teams. Prepare technical documentation and communicate complex issues and solutions. Ensure compliance with FDA, ISO 13485, and Quality System requirements. Requirements: 0–2 years of experience in medical device/pharmaceutical regulated industries. Bachelor’s degree in Engineering or Physical Sciences required. Strong critical thinking, prioritization, communication, root cause analysis, and data analysis skills. Engineering degree and ASQ certification (CQA, CQE, CQM) preferred. This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Quality Control Analyst II

Fort Worth, Texas

Sep 22, 2026

Quality Control Exciting development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical and Vision Care Contract: 12 Months with extension and conversion potential Benefits: Medical, Dental, Holiday, PTO 401K matching Quality Control Analyst II Perform routine and non-routine analytical testing of raw materials, in-process materials, finished products, environmental, and stability samples while ensuring compliance with quality and regulatory requirements. Key Responsibilities: Perform analytical testing using HPLC, GC, and capillary electrophoresis. Develop, validate, transfer, and qualify analytical methods. Calibrate, maintain, troubleshoot, and qualify laboratory instruments and equipment. Review and interpret test data against specifications and control limits. Conduct OOS/failure investigations and recommend corrective actions. Prepare and revise SOPs, protocols, technical reports, deviations, and validation documentation. Support audits, regulatory submissions, and quality assessments. Train analysts on laboratory procedures and analytical methods. Coordinate testing with contract laboratories, vendors, and other departments. Identify quality issues and recommend improvements to analytical methods and processes. Maintain laboratory cleanliness, safety, documentation, and compliance standards. Preferred Experience: Capillary electrophoresis, HPLC/GC, and laboratory instrument qualification. INDBH #LI-RL1

Facilities and HSE Technician

Durham, North Carolina

Sep 22, 2026

Manufacturing Exciting Facilities HSE Technician development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical and Vision Care. Facilities Technician 2 – Durham, NC Schedule: Day Shift (7am–4pm or 8am–5pm) | Onsite: 5 days/week Benefits: Medical, Dental, Holiday, PTO 401K matching We are seeking a Facilities Technician 2 with strong hands-on HVAC/mechanical troubleshooting experience to support facility operations at a regulated manufacturing site. Key Responsibilities: Troubleshoot, maintain, and repair HVAC and mechanical systems, including AHUs, RTUs, VAVs, chillers, boilers, pumps, and exhaust fans. Perform preventive maintenance, filter/belt changes, coil cleaning, motor greasing, and sensor replacements. Monitor and troubleshoot BAS/Siemens Desigo CC systems and equipment alarms. Perform general building maintenance, including drywall repair, painting, lighting, and hardware repairs. Conduct safety inspections and assist with hazardous waste handling and spill response. Complete work orders, PM documentation, and CMMS records. Follow GxP/SOP requirements and support contractors/vendors. Requirements: High School Diploma or equivalent; technical/HVAC training preferred. 3–5 years of hands-on HVAC/facilities maintenance experience. EPA Section 608 Universal Certification required. HAZWOPER/hazardous waste training preferred or ability to obtain. Experience with BAS systems, preferably Siemens Desigo CC. Strong mechanical troubleshooting skills and ability to read basic electrical/mechanical diagrams. Ability to lift up to 50–80 lbs, climb ladders, and work in mechanical/utility areas. Must be available for occasional on-call facility emergencies. This is an urgent opening. Competitive pay is available for candidates who closely match the requirements. This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Sr. Reliability Engineer

Lake Forest, California

Sep 22, 2026

Manufacturing Exciting development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical and Vision Care Sr. Reliability Engineer Benefits: Medical, Dental, Holiday, PTO 401K matching Location: Lake Forest, CA – 100% onsite, 5 days/week Contract: 6 months to 1 year contract with extension/conversion potential Seeking a Sr. Reliability Engineer to support R&D and NPI through reliability, quality, and validation testing. Develop and execute reliability testing, including HALT, ALT, environmental, life, transportation, PCBA stress screening, and V&V. Review designs and test plans for reliability, quality, and compliance. Develop automated testing using LabVIEW, Python, and/or R. Perform statistical analysis, reliability assessments, and design reviews. Support validation, technical documentation, and resolution of design/manufacturing issues. Requirements: BS Engineering with 4+ years experience or MS with 2+ years. 4+ years R&D experience focused on reliability/quality engineering. Experience with reliability engineering, test automation, and statistical methods. Familiarity with GMP/QSR, lab testing, and equipment validation. Knowledge of mechanical, electrical, or optical design. Strong technical writing and communication skills. This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

SAP Project Manager

Waltham , Massachusetts

Sep 21, 2026

IT Our client is a leading life sciences company that develops and manufactures tools and materials used in the production of biologic drugs. They are looking for a skilled SAP Project Manager to join their team in Middlesex County, MA! Location: Middlesex County, MA (hybrid, 2 days a week on site) Pay rate: $100- $120/hr. Job type: 6-month contract with possibility of extension Job Summary A leading Life Science organization is seeking an experienced SAP Project Manager to lead SAP initiatives within complex, cross-functional technology programs. The role will oversee SAP projects from initiation through implementation, go-live, and stabilization, ensuring delivery aligns with business objectives, timelines, budgets, governance standards, and IT priorities. The ideal candidate will have strong SAP project management experience, including SAP GRC implementation experience, and the ability to coordinate business stakeholders, functional and technical teams, system integrators, vendors, and globally distributed resources. Responsibilities Lead SAP workstreams within large, cross-functional programs and ensure alignment with overall program objectives, timelines, dependencies, and business priorities. Manage SAP projects end-to-end, including implementations, enhancements, integrations, upgrades, remediation, and optimization initiatives. Develop and maintain project plans covering scope, schedule, budget, resources, risks, issues, dependencies, testing, cutover, go-live, and stabilization. Serve as the primary liaison between IT, business stakeholders, technical teams, vendors, and system integrators. Provide concise, proactive, and executive-ready communication on project status, risks, issues, decisions, milestones, and required actions. Drive project governance through working-team meetings, steering committees, RAID management, decision tracking, stage-gate reviews, and escalation processes. Coordinate requirements, solution design, configuration, development, integrations, data, testing, training, change management, cutover, and post-go-live activities. Proactively identify and manage project risks and issues related to resources, dependencies, data readiness, security, controls, testing, and business adoption. Lead and coordinate SAP GRC activities, including access governance, role design, controls, testing, remediation, and business readiness. Coordinate SAP functional consultants, technical resources, business process owners, system integrators, and globally distributed teams. Ensure SAP solutions align with business objectives, internal controls, compliance requirements, and measurable business value. Lead cutover, go-live, stabilization, and transition activities to ensure successful implementation and operational readiness. Qualifications Bachelor's degree in Information Technology, Computer Science, Business, or a related field with 8–10 years of project management experience, including significant SAP or ERP project leadership experience. Experience managing full lifecycle SAP projects from planning and requirements through design, build, testing, cutover, go-live, and stabilization. Successful SAP GRC implementation experience, including access governance, role design, controls, testing, remediation, and business readiness. Strong project management capabilities across scope, schedule, budget, resources, risks, issues, dependencies, vendors, and stakeholders. Working knowledge of SAP functional configuration, development, integrations, data, security, controls, testing, training, and change management. Experience coordinating SAP functional consultants, technical teams, business process owners, system integrators, and globally distributed teams. Excellent communication and stakeholder management skills, including the ability to communicate effectively with executive leadership. Preferred Experience with SAP security, internal controls, SOX, or regulated-system delivery. Familiarity with PMO frameworks, stage-gate governance, SDLC documentation, and enterprise application delivery models. Experience managing third-party vendors and system integrators. Experience working in global, complex, or highly regulated environments. Strong understanding of change management, organizational readiness, and business adoption. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Scientist III - Cell Biology

Ridgefield, Connecticut

Sep 21, 2026

Science & Research Our client, a leading pharmaceutical company, is looking for a skilled Scientist III - Cell Biology - to join their team in Ridgefield, CT! Pay rate: $49 - $53/hr. Location: Ridgefield, CT Job type: 1 year contract Job Summary The successful candidate will support discovery research programs in Cardiovascular-Renal-Metabolic (CRM) Diseases through hands-on execution of mammalian cell culture, cell-based assays, laboratory automation, functional genomics, and next-generation sequencing (NGS) workflows. The role will involve operating established automated workflows, supporting iPSC-derived kidney organoid processes, performing molecular biology and NGS experiments, maintaining accurate experimental records, and troubleshooting routine laboratory and platform issues. Responsibilities Design, execute, and analyze cell-based experiments supporting target validation and discovery research. Perform routine mammalian cell culture, cell-based assays, image-based analysis, and iPSC-derived cell workflows. Operate, monitor, and troubleshoot established laboratory automation platforms for cell-based and molecular assays. Perform tissue, cell, and nuclei dissociation for bulk RNA-seq, single-cell RNA-seq (scRNA-seq), and single-nucleus RNA-seq (snRNA-seq) workflows. Execute NGS workflows including library preparation, quality control, quantification, normalization, sequencing setup, and sequencer operation. Perform routine molecular biology techniques, including: DNA/RNA extraction PCR and qPCR Nucleic acid and protein quantification Western blotting Basic sample preparation Analyze and interpret experimental results, identify technical issues, troubleshoot routine problems, and recommend appropriate follow-up. Maintain accurate sample, reagent, consumable, experimental metadata, and electronic laboratory notebook (ELN) records. Follow established SOPs, laboratory safety requirements, data integrity standards, and organizational policies. Collaborate effectively with cross-functional teams including cell biology, automation, genomics, and bioinformatics. Escalate complex technical or platform issues appropriately and communicate experimental findings and recommendations clearly. Qualifications Master’s degree with 3+ years of relevant experience, or Bachelor’s degree with 7+ years of relevant experience, or an equivalent combination of education and experience in cell biology, molecular biology, genomics, or a related scientific discipline. Strong hands-on experience with mammalian cell culture, cell biology, and cell-based assay execution. Hands-on experience with NGS workflows, including tissue, cell, and/or nuclei dissociation, sequencing library preparation, quality control, and quantification. Experience with bulk RNA-seq, single-cell RNA-seq, single-nucleus RNA-seq, or related sequencing

Manufacturing Admin Assistant

Bakersfield, California

Sep 17, 2026

Manufacturing Our Client, a Fortune 500 leader, is hiring a Manufacturing Admin Assistant! Be part of a team setting science in motion across the biopharma, healthcare and advanced technologies industries. Are you ready to make a global impact? Join us now! Pay rate: $21/hr. Location: Bakersfield, CA Job type: 6-month contract Job Summary The Manufacturing Admin provides administrative and operational support to manufacturing activities, including production, receiving, shipping, inventory, quality documentation, and production scheduling. This position supports manufacturing teams and management by conducting research, preparing reports, maintaining accurate records, processing information, and coordinating requests across multiple departments. Responsibilities Provide administrative support for manufacturing, production, receiving, shipping, and inventory operations. Create, maintain, and track department employee records and other manufacturing documentation. Maintain established paper and electronic record-keeping systems and ensure information is accurate and up to date. Support and maintain materials labeling programs and related documentation. Assist with company inventory systems and maintain accurate inventory records. Support production scheduling by maintaining and updating production scheduling reports. Coordinate with manufacturing, MRP, QA, shipping, receiving, and other departments to meet production and product shipment requirements. Work closely with MRP and Quality Assurance teams to coordinate the manufacturing and testing of materials and related documentation. Ensure manufacturing and packaging paperwork is completed accurately, completely, and in accordance with established procedures. Review process reproducibility and production trends for applicable products and assist with identifying opportunities to improve processes and products. Prepare reports, spreadsheets, and other documentation to support manufacturing operations. Participate in special projects and provide administrative support to multiple departments as required. Use sound judgment and make well-grounded decisions when addressing routine operational issues. Perform other related duties as assigned to support manufacturing and business objectives. Qualifications One-year certificate from a college or technical school; or One to two years of related experience and/or training; or An equivalent combination of education, training, and experience. Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint. Strong data entry, record-keeping, organizational, and administrative skills. Excellent attention to detail and accuracy. Ability to manage multiple tasks and prioritize work effectively. Ability to make sound, well-grounded decisions and assessments. Ability to collaborate effectively with manufacturing, MRP, QA, and other departments. Experience in a chemical or mechanical manufacturing environment is preferred. Familiarity with inventory management, production scheduling, quality documentation, MRP systems, or document-control processes is preferred. Prior experience working at NuSil is preferred.

Assembly Associate (Biotech)

Somerset County, New Jersey

Sep 16, 2026

Manufacturing Pay Rate Low: 20 | Pay Rate High: 25 Our client is a leading life sciences company that develops and manufactures tools and materials used in the production of biologic drugs. They are looking for a skilled Assembly Associate to join their growing team in Somerset County, NJ! This is a great opportunity to contribute to an innovative life science organization! Pay rate: $20- $25/hr. DOE Job type: 6-month contract (possibility of extension) Location: Somerset County, NJ Job Summary The Assembler is responsible for performing manufacturing and assembly operations to produce high-quality products according to established procedures, technical drawings, and work instructions. This role involves assembling components, conducting in-process inspections, maintaining accurate production records, and ensuring products meet quality and performance standards. The Assembler will work independently and collaboratively while managing multiple tasks in a fast-paced manufacturing environment. Responsibilities Assemble components and sub-assemblies into completed products using assembly instructions, technical drawings, blueprints, and approved processes. Read and interpret assembly drawings, parts lists, work instructions, and visual aids. Use hand tools, measurement equipment, fixtures, and specialized tooling to complete assembly tasks accurately. Perform in-process quality inspections to identify defects and verify product accuracy. Complete manufacturing documentation, production records, and inspection reports accurately and legibly. Follow written and verbal instructions, standard operating procedures, and safety guidelines. Track production time, material usage, and waste accurately. Perform basic troubleshooting and identify opportunities for process improvements. Maintain and properly use tools, equipment, and work areas. Perform inventory checks and ensure required components and materials are available for production. Maintain a clean, organized, and safe workspace. Follow required safety procedures, including the proper use of personal protective equipment (PPE). Qualifications High school diploma or equivalent preferred. Previous experience in manufacturing, assembly, production, or a related field preferred. Ability to read and interpret technical drawings, work instructions, and assembly documentation. Strong attention to detail and commitment to producing quality work. Ability to use basic hand tools and measurement equipment such as calipers, scales, and other inspection devices. Good manual dexterity and ability to assemble small components accurately. Ability to perform basic math calculations and accurately measure components. Ability to work independently while also contributing effectively within a team environment. Strong organizational skills with the ability to manage multiple tasks and priorities.

Manufacturing Operator

Ridgefield, Connecticut

Sep 15, 2026

Manufacturing Pay Rate Low: 20 | Pay Rate High: 22Manufacturing Operator Contract @ $20-22/hour Job Summary The Manufacturing Operator is responsible for supporting pilot plant and bulk manufacturing operations in a regulated GMP environment. The Manufacturing Operator will operate manufacturing equipment, complete batch documentation, perform required calculations, and support troubleshooting of equipment and process-related challenges. Key Responsibilities Work collaboratively with Plant Technicians and Campaign Managers to identify and resolve process- and equipment-related challenges Develop and maintain proficiency in manufacturing equipment operation, batch record documentation, and manufacturing calculations. Follow all applicable GMP procedures, standard operating procedures (SOPs), work instructions, and safety requirements. Properly wear and use all required personal protective equipment (PPE). Maintain a clean, organized, and compliant manufacturing work area. Perform manufacturing operations accurately and efficiently while maintaining adherence to established processes and procedures. Support troubleshooting activities related to manufacturing equipment and processes Perform other duties and responsibilities as assigned. Required Skills and Qualifications Experience working in a GMP-regulated manufacturing environment. Experience with bulk manufacturing processes and established GMP procedures preferred. Technical understanding of manufacturing systems, methods, equipment, and procedures. High school diploma or equivalent required. INDBH #LIR- AR1

Animal Caretaker

Philadelphia, Pennsylvania

Sep 15, 2026

Laboratory Pay Rate Low: 20 | Pay Rate High: 22 Title: Animal Caretaker Location: Philadelphia, PA Contract to Hire The Vivarium Animal Facility is looking to hire a Animal Caretaker to take care of our animal colony. The team's responsibilities include clinical veterinary services, animal husbandry, animal procurement, animal enrichment, investigator support, training, and compliance oversight. Duties include: Performs daily animal health checks and reports any abnormal animal conditions to the veterinary technician and /or Area Supervisor. Disposes of dead animals following standard SOPs and policies. Changes animal caging, to include feed and water, according to SOPs and/or specific approved protocols and the schedule established by the Area Supervisor. Sexes and weans animals according the SOPs. Maintains daily animal census sheets, room equipment and status form sheets, and other forms requested by the Area Supervisor. Cleans and sanitizes animal facility, assigned rooms and cages according to SOPs. Maintains and repairs animal caging and support equipment. Receives, examines, transfers, identifies and properly houses incoming animal shipments according to SOPs. Assist with the restraint, handling and manipulation of various animal species as requested by the investigators. Perform routine cleaning, descaling, and preventative maintenance on the cage washers and autoclaves, including checking and cleaning filters and spray manifolds. Process clean caging and accessory equipment appropriately, including putting bedding into cages and autoclaving cages and supplies. Requirements: General background in animal care or research training preferred High School Diploma is required Must be self-motivated and able to work independently to perform required tasks and recognize operational problems Good communication skills and fluency in English Basic computer skills Ability to handle the physical requirements of the position (e.g., repetitive motions, lifting 6-liter (12 lb.) tanks of water, extended periods of standing, walking, and sitting) This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH #LI-AR1

Formulation Chemist

Columbus, Indiana

Sep 15, 2026

Laboratory Pay Rate Low: 25 | Pay Rate High: 30Formulations R&D Chemist Pay Rate: $25–$30/hour Schedule: Monday–Friday, 8:00 AM–5:00 PM Position Summary We are seeking an experienced Formulations Chemist to join our Research & Development team. This role focuses heavily on formulation development, method validation, product testing, and plant trials. The ideal candidate has strong formulation experience, is knowledgeable in developing, writing, and executing method validation protocols, and thrives in a hands-on manufacturing environment. The successful candidate will be detail-oriented, innovative, self-motivated, and possess a strong “can-do” attitude with excellent communication skills. Key Responsibilities Develop and formulate new products, converting concepts into physical products. Prepare laboratory solutions and conduct routine testing of products under development. Develop, write, and execute analytical method validation studies. Conduct plant, batching, and filling line trials. Assist with the development and implementation of cleaning procedures. Perform chromatography and other laboratory testing as needed. Clean and maintain R&D and production equipment following R&D use. Assist with formulation and cleaning of commercial pharmaceutical equipment. Coordinate and submit test samples to external laboratories. Compile and analyze R&D data, results, and observations. Maintain accurate laboratory notebooks and documentation. Follow GMP/cGMP requirements and established laboratory procedures. Perform other R&D duties as needed. Qualifications 3–5+ years of experience in an R&D or chemical laboratory environment. Strong hands-on formulation experience required. Experience writing and executing method validation studies. Experience with chromatography and laboratory testing. Experience working with chemical products, preferably in a manufacturing or pharmaceutical environment. Knowledge of GMP/cGMP regulations strongly preferred. Experience with commercial pharmaceutical equipment and cleaning procedures is a plus. Bachelor’s degree in Chemistry or a related field preferred. Strong attention to detail, organization, communication, and problem-solving skills. INDBH #LIR-AR1

Sterile Process Tech (2nd Shift)

Piscataway, NJ

Sep 15, 2026

Manufacturing Pay Rate Low: 23.50 | Pay Rate High: 25Our Client, a global nonprofit organization on the forefront of saving and healing lives through innovations in tissue and organ donation, transplantation, and research is seeking an Aseptic Technician to join their growing team. You will work in an aseptic environment for the processing of human cells and tissue products! Location: Middlesex County NJ Shift: M-F , 2pm-10pm Type: Contract, 6 Months Job Duties: Aseptically process in a regulated cleanroom environment. Follow ISO standards, SOPs, and safety protocols. Maintain aseptic techniques and ensure product quality. Conduct quality inspections and accurate documentation. Prepare tissue samples, chemicals, and transfer materials to storage. Clean and sanitize equipment and workspace. Assist in scheduled shutdown activities and collaborate with teams. Participate in training for skill development. Requirements: High School Diploma/GED Production experience in sterile environment Basic math and measurement skills for liquids and powders. INDBH #LIR-AR1

Equipment Engineer

Pasadena, California

Sep 12, 2026

Engineering Our private research university client is known for its strength in science and engineering, and is among a small group of institutes of technology in the United States which is primarily devoted to the instruction of pure and applied sciences Title: Laboratory Engineer Location: Pasadena, CA Pay: $40-50/hr The Laboratory Engineer will take an important role in maintaining performance of nanofabrication equipment. Follow established protocols to perform qualifying runs on equipment to ensure that equipment is operating at peak performance Maintain organized data records that can be us ed to verify peak performance and to indicate when maintenance and/ or alignments of equipment components are necessary. Preventative maintenance plans on equipment to keep performance at the established, high standard; this includes performing instrument alignments . Perform routine repairs of mechanical, electrical and vacuum systems Contribute to the lab culture and capabilities and strive to meet the high standards necessary to run a world-class research operation. Qualifications: Bachelor’s degree in engineering or sciences . 2+ years of semiconductor fabrication equipment OR other mechanical, vacuum, or scientific equipment operation, maintenance, repair, and installation. Proficiency with: Excel, Word, Outlook, and PowerPoint. Basic computer maintenance and troubles hooting skills , e.g. new hardware installs, networking, performing hard drive backup #INDBH

Junior Toxicologist

Fort Worth, Texas

Pay rate low: $22.00 | Pay rate high: $28.00 Exciting Junior Toxicologist/Research Scientist development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical and Vision Care. Junior Toxicologist Location: Fort Worth, TX (Onsite) Schedule: Monday–Friday, 8:00 AM – 5:00 PM CST Contract: 6 Months with extension/conversion potential Benefits: Medical, Dental, Holiday, PTO 401K matching Note: Only Local candidates will be considered Job Summary: Seeking a junior Toxicologist to support short-term projects by providing toxicology expertise, conducting risk assessments, and assisting with regulatory documentation. The role requires strong analytical thinking and the ability to work both independently and collaboratively with internal teams and external partners. Top 3 Required Skill Sets Ability to learn quickly and apply new toxicology concepts. Basic toxicology analysis skills – able to review reports and identify key toxicological findings (limited lab work required). Team and independent work capability – comfortable collaborating with cross-functional teams while managing individual tasks. Key Responsibilities Conduct toxicological risk assessments for chemicals, impurities, excipients, and extractables/leachables in alignment with ISO 10993 and ICH/FDA guidelines. Support nonclinical safety evaluations with internal teams and external CROs. Maintain documentation and assist with reports for regulatory submissions. Qualifications Bachelor’s degree in toxicology or a related field. 0–3 years of relevant experience. Onsite schedule: Monday–Friday, 8 AM–5 PM. Advanced degrees will not be considered Preferred Skills Experience with extractables/leachables studies and biological safety risk assessments. Strong collaboration and communication skills with internal stakeholders and vendor This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH #LI-RL1

Manufacturing Visual Inspection 1st shift

Fremont, California

Executes routine unit operations in Visual Inspection as assigned related to the manufacturing of drug product in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures. Executes independently with adequate training, complex fundamental operations as visual inspection, advance visual inspection, palletizing, cleaning, inspection hood prep for operations, BioMES Operations and Exceptions. Performs internal support duties including assisting drug product filling and packaging. Executes independently with adequate training fundamental operations: -Logistics Coordination -Batch record executions -Equipment use logs -Work order initiation and tracking -Support Projects -Support Creation/Maintain Training Kits Documents work according to cGMP and cGDP. -Adheres to established regulations and follows cGMP established by site. -Reports abnormalities and deviations in a timely and accurate manner. -Adheres to safety standards and identifies unsafe situations / habits and escalates appropriately. -Maintains production areas according to predefined standards (5s). -Maintains own training within compliance and trains other technicians and associates on operations upon completion of trainer qualification. -Contributes to Quality activities such as supporting investigations, corrective actions and area walk throughs. Skills: -1 or more years of experience in cGMP regulated industry. -Ability to concentrate on detail-oriented work in a complex technical setup with a Quality and “Right the first-time” mindset. -Strong written and verbal communication skills. -Ability to work with computer-based systems and manufacturing execution systems (MES). -Ability to read and understand SOPs and instructions and document work in a written format applying cGMP standards. -Ability to work as part of a high performing team and collaborate effectively with staff. -Must be able to read and see clearly. PHYSICAL DEMANDS: - Duties of this position may require the incumbent to exert some physical effort. -Lifting requirements may vary dependent on the drug product manufacturing visual inspection area activity. Weight is typically no more than 25 pounds. NOTE: Worker required to clear a Vision Test (including acuity & color blindness) prior to starting assignment. Education: High school degree + minimum 1 year work experience in GMP regulated industry Associates/Bachelor’s degree or biotechnology vocational training preferred

Principal Scientist

Elgin, IL

Principal Scientist Job Type: Direct Hire Employment Status: Exempt / Salaried Salary: $120,000 - $150,000 annually, depending on experience Schedule: Full-Time Department: Technical Services Reports To: Technical Services Manager Position Overview Our client is seeking an experienced Principal Scientist to join their Technical Services team. This is a highly hands-on R&D leadership role with approximately 75% of the position focused on laboratory research and bench-scale experimentation. The Principal Scientist will lead innovative product development initiatives, with a particular focus on enzyme applications within the food industry. This individual will identify new product opportunities, develop and optimize enzyme technologies and blends, support commercialization efforts, contribute to patent development, and serve as a technical resource for customers, Sales, and Marketing. The successful candidate will also oversee and mentor a multidisciplinary team of scientists while helping drive the strategic growth and technical capabilities of the department. Key Responsibilities Spend approximately 75% of the workday conducting hands-on laboratory research and bench-scale experimentation. Lead the development of at least three innovative product applications annually, from initial concept through commercialization. Identify new product application opportunities through industry research, conferences, market analysis, and customer engagement. Support and contribute technical data toward a minimum of two patent applications annually. Lead the design and conceptualization phase of new product development initiatives. Develop and optimize enzyme technologies and blends for food industry applications. Provide scientific data and technical content for promotional materials, webinars, customer presentations, and other business development initiatives. Deliver high-level scientific presentations to internal stakeholders, customers, and domestic/international industry conferences. Serve as a primary technical resource for Sales and Marketing teams. Lead joint R&D projects with key customers and external research partners. Establish and maintain relationships with food research institutes, universities, and other external technical organizations. Provide technical and analytical support to existing and prospective customers to support business retention and market expansion. Collaborate with global R&D teams to share technical knowledge and align research initiatives. Oversee laboratory operations, including equipment maintenance, laboratory safety, organization, and implementation of 5S principles. Ensure compliance with GMP, SQF, food safety requirements, and the company's quality management system. Maintain accurate laboratory notebooks, research documentation, data analysis, and visualizations. Identify and immediately escalate food safety concerns, quality issues, or deviations through appropriate channels. Assist with management of the annual Technical Services team budget. Prepare client call reports and monthly progress reports in accordance with departmental requirements. Recruit, train, mentor, and develop laboratory personnel. Conduct performance evaluations and provide ongoing coaching and professional development for direct reports. Help build and maintain a high-performing technical team. Perform other duties as assigned. Leadership Responsibilities This position will provide direct leadership and oversight to a multidisciplinary team of scientists, including assistant and senior-level research personnel. Responsibilities include: Recruiting and onboarding laboratory personnel. Training and mentoring team members. Setting performance expectations and providing ongoing feedback. Conducting performance evaluations. Supporting employee development and career growth. Managing personnel transitions and compensation-related activities. Optimizing departmental resources and overall team performance. Required Qualifications Ph.D. in Chemistry, Biochemistry, Biotechnology, Food Science, or another related scientific discipline. 3–5+ years of progressive R&D experience, preferably within the food, biotechnology, enzyme, or related industry. Demonstrated experience with industrial enzyme applications, particularly within food-related applications, is highly preferred. Proven experience with product development and commercialization. Experience contributing to or leading patent filings. Experience leading cross-functional R&D projects. Previous experience supervising, mentoring, or leading scientific personnel. Strong understanding of GMP, SQF, food safety, and quality systems. Hands-on laboratory experience with analytical instrumentation such as GC, HPLC, and spectrophotometry is highly preferred. Skills & Competencies Advanced scientific reasoning and analytical problem-solving abilities. Strong strategic thinking and ability to solve complex technical challenges. Excellent written and verbal communication skills. Ability to interpret complex scientific literature, regulatory standards, and technical reports. Ability to prepare compelling technical presentations, reports, and scientific materials. Strong presentation skills with the ability to communicate complex scientific concepts to both technical and non-technical audiences. Excellent organizational and time-management skills. Ability to balance significant hands-on laboratory responsibilities with strategic, administrative, and leadership duties. Strong attention to detail and commitment to accurate scientific documentation. Ability to work collaboratively with R&D, Sales, Marketing, customers, and external research partners. INDBH #LI-ES1

Manufacturing Associate I-Assembly & Packaging

Fremont, California

Our client, a leading organization in the pharmaceutical and biotechnology manufacturing sector, is seeking a detail-oriented Manufacturing Assembly & Packaging Associate to support drug product production in a cGMP-regulated, multi-product facility. In this role, you will perform routine unit operations for assembly, packaging, and support troubleshooting efforts—all in strict compliance with standard operating procedures (SOPs). Job Title: Manufacturing Assembly & Packaging Associate Location: Fremont, CA Terms: Contract-to-hire Shift: 1st Shift | Monday–Friday, 6:00 AM–2:30 PM Pay Rate: $22.15/hr Responsibilities: Assist in setting up automated and semi-automated equipment including autoinjector assembly, syringe assembly, and tabletop packaging systems. Retrieve and prepare components, tools, and documentation prior to equipment setup. Support equipment changeovers and minor equipment repairs or adjustments. Identify and resolve operational issues during assembly and packaging processes. Perform accurate documentation in controlled documents such as batch records, logbooks, and SOP attachments. Execute assembly and packaging tasks and assist with visual inspection/filling operations as needed. Ensure proper stocking of components, supplies, and materials before operations begin. Transfer products and materials within the Controlled Non-Classified (CNC) manufacturing area. Maintain cleanliness of production rooms, including waste disposal and sanitization in line with safety procedures. Follow all safety protocols and report unsafe conditions immediately. Participate in shift hand-off communications to ensure operational continuity. Maintain 5S standards and ensure equipment used is properly calibrated and documented. Complete required logbooks and maintain documentation compliance. Qualifications: High School Diploma or equivalent required; Associate or Bachelor's degree or biotechnology vocational training preferred. Minimum 1 year of experience in a GMP-regulated manufacturing environment (pharmaceutical or biotechnology industry strongly preferred). Basic computer skills (MS Office, Outlook, and other systems). Strong organizational skills and ability to work in small teams. Ability to read, comprehend, and follow written instructions. Demonstrated math proficiency, including basic arithmetic and conversions. Strong verbal and written communication skills. Ability to stand for extended periods and perform physical tasks including lifting, bending, twisting, and climbing. Must be fully vaccinated against COVID-19 or have an approved medical/religious exemption. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! #INDBH

Associate, Scientist, Method Development

Concord, Ohio

Our client is a contract research and development manufacturing service provider to chemical-based industries, and they’re looking for a Method Development Associate Scientist to join their growing team! Direct Hire Salary: $70-80K Shift: 1st shift 8a-5p M-F Position Summary We are seeking a detail-oriented and proactive Associate Scientist to join our cGMP Laboratory. This role involves supporting analytical stability studies in compliance with regulatory guidelines. The ideal candidate will have hands-on experience with small molecule drug substances and drug product batch release and stability testing, and experience working in a cGMP environment. We are seeking an Associate Scientist with at least 2 years of experience in a GMP analytical laboratory environment. The ideal candidate will have hands-on experience with HPLC, NMR, and Mass Spectrometry, supporting small molecule drug substance and product testing. Responsibilities include conducting stability studies, batch release testing, and generating analytical data using techniques such as FTIR, GC, KF, XRD, DSC, and TGA. Strong documentation practices, attention to detail, and ability to work cross-functionally are essential. Must have experience with HPLC, NMR and Mass Spec and coming from a GMP Lab environment and have 2 years of relevant analytical Lab environment experience. Minimum B.S. in chemistry with 2+ years related pharmaceutical analytical laboratory experience or equivalent combination of education and experience is required This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH #LI-DNP:

Materials Compliance Supervisor

Londonderry, New Hampshire

We are looking for a Materials Compliance Manager to lead our client's chemical compliance and international trade efforts. Salary: $80K - $90K Location: Rockingham County, NH (Hybrid) Type: Direct hire Summary: This role ensures their products and processes follow all relevant U.S. and global regulations - from chemical safety and labeling to import/export laws. You’ll oversee SDS documentation, labeling, SAP system updates, and hazardous material handling. You’ll also manage trade compliance across international markets, supporting global shipments and maintaining essential regulatory records. Key Responsibilities: Manage compliance with TSCA and global chemical regulations. Maintain accurate SDS/MSDS and labeling using SAP/GLM+. Oversee raw material screening for Kosher, Halal, NSF, and regulatory standards. Ensure products and materials meet EPA, DOT, OSHA, and TCEQ requirements. Supervise import/export operations and ensure compliance with Incoterms, export controls, and customs rules. Maintain trade documents such as invoices, certificates of origin, and bills of lading. Keep the Approved Products List updated in SAP. Monitor and report on compliance and trade KPIs. Support audits and improve compliance processes. Lead and mentor a small team, promoting a safe and compliant work environment. Required Qualifications: Bachelor’s degree in Chemistry, Biology, Environmental Engineering, International Trade, or a related field 3+ years of experience in international trade, preferably in chemicals or manufacturing Experience with SDS/MSDS creation and labeling (GLM+/SAP) Strong SAP experience in a manufacturing setting Knowledge of TSCA, chemical inventories, and regulatory restrictions Solid understanding of EPA, DOT, OSHA, and TCEQ regulations Familiarity with Incoterms, export controls, and customs compliance ***This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!***

Sr Staff Scientist - Medical Devices

Stafford, TX

Our client, a world-leading medical device company focused on improving lives through innovative, consumer-centered solutions is seeking a skilled Sr Staff Scientist. With a global presence spanning 30 countries, this is your chance to join an industry trailblazer making a difference every day. Location: onsite in Harris County, TX or Essex County, NJ Employment Type: Direct-Hire Salary: $128K- $184K DOE Travel Requirement: ~10% Position Overview: We are seeking a Sr. Staff Scientist to lead the technical strategy and execution of our IVF department, which plays a critical role in supporting embryo development during vitro fertilization. This high-impact, visible role is key to driving innovation, product improvements, and global expansion within the Life Sciences division. This individual will manage initiatives across product development, method validation, risk assessment, and regulatory compliance. Key Responsibilities: Lead the design and execution of product evaluations, analytical methods, and validation studies for IVF Media solutions. Provide biological risk assessments and technical support to manufacturing teams for process development and optimization. Manage R&D workstreams related to new product development, line extensions, and lifecycle improvements. Contribute to the creation of technical documentation to support regulatory submissions, global market entry, and ongoing compliance. Ensure scientific and technical rigor and enforce best practices across all research and development activities. Develop and refine design input requirements and oversee the verification and validation (V&V) strategy. Present key findings and project updates to senior leadership and executive stakeholders. Build and maintain relationships with external collaborators, vendors, and consultants. Ensure full compliance with design control standards, quality systems, and applicable regulatory requirements (e.g., ISO 10993, MDR/MDD). Qualifications: Bachelor’s degree in Life Sciences, Biochemistry, Analytical Chemistry, or a related field required. Advanced degree (Ph.D. or M.S. with 4–7 years of experience) strongly preferred. Minimum of 10 years’ relevant industry experience, ideally within medical devices, pharmaceuticals, or biotechnology. Direct experience with IVF Media or cell culture media development and manufacturing is highly advantageous. Strong working knowledge of medical device regulations, including MDR/MDD, ISO 10993, and classifications for Class II/III devices. Demonstrated hands-on proficiency in biochemical techniques, statistical methods, and experimental design. Proven ability to lead complex R&D projects and drive them to timely completion. Excellent problem-solving skills, with a structured and risk-based approach to decision-making. Strong communication and interpersonal skills, with experience engaging stakeholders at all levels—from engineers to executives. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! #INDBH #LI-DNP

Medical Science Liason

Boston, Massachusetts

At Astrix, we're expanding our team to support a diverse range of clients across various industries. We're seeking talented Medical Science Liaisons to join us! Our partners range from emerging biotech firms to established pharmaceutical companies, all seeking professionals who can bridge scientific insights with clinical application. Opportunities are available both remotely and on-site throughout the country! Key Responsibilities Scientific Engagement: Establish and maintain peer-to-peer relationships with key opinion leaders (KOLs), HCPs, and academic institutions to discuss scientific data, disease state education, and therapeutic insights. Medical Education: Deliver accurate and balanced scientific presentations to internal and external audiences, including at conferences, advisory boards, and educational events. Clinical Research Support: Collaborate with investigators on company-sponsored and investigator-initiated trials, providing medical and scientific support throughout the study lifecycle. Cross-Functional Collaboration: Work closely with internal teams such as Clinical Development, Regulatory Affairs, and Commercial to provide medical insights that inform strategic decisions. Compliance and Reporting: Ensure all activities comply with regulatory standards and company policies, and accurately document interactions and insights in the appropriate systems. Qualifications Education: Advanced degree (PharmD, PhD, MD, or equivalent) in a relevant scientific discipline. Experience: Minimum of 2 years in a field-based medical affairs role within the pharmaceutical, biotechnology, or medical device industry. Scientific Expertise: Deep understanding of therapeutic areas relevant to the company's portfolio, with the ability to interpret and communicate complex scientific data. Preferred Qualifications Familiarity with clinical trial processes and regulatory requirements. Proficiency in using CRM systems and digital communication tools. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

R&D Manager- Beverages

Pacoima, California

Our client, a growing innovative food & beverage manufacturer, is experiencing significant growth, and with that comes exciting opportunities. We’re seeking an R&D Manager to join their dynamic team! Job Title: R&D Product Development Manager Location: Los Angeles County , CA Job type: Contract-hire Pay rate: $45- $56/ hr. Position Summary: We are seeking a dynamic and experienced R&D Product Development Manager to lead our product development efforts from concept to commercialization. This role is ideal for a critical thinker with a strong background in food science and a passion for developing innovative flavor and beverage solutions. The ideal candidate will supervise a team of chemists and lab technicians while ensuring all products meet customer requirements, cost targets, and regulatory standards. Key Responsibilities: Oversee and manage all product development projects within the R&D department. Lead the formulation and development of products according to customer or internal specifications. Supervise, mentor, and provide technical guidance to R&D chemists and lab technicians. Collaborate with cross-functional teams including Quality Control, Analytical, Production, and Sales. Evaluate the technical feasibility of new products based on equipment, technology, and production capabilities. Conduct cost analysis and determine suggested selling prices for developed products. Ensure thorough documentation of master formulas and compounding instructions. Approve product specifications and ensure compliance with SQF (Safe Quality Food) standards. Communicate directly with customers to gather requirements, present prototypes, and provide technical support. Support scale-up processes and monitor initial production runs to ensure consistency and quality. Participate in special projects and other duties as assigned. Qualifications: Bachelor’s degree in Food Science, Nutrition, or a related field. Minimum of 4 years of supervisory or management experience in an R&D environment. Strong taste and aroma acuity for product evaluation and formulation. Proficient in Microsoft Office Suite; solid math skills (algebra level). Strong written and verbal communication skills in English. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Perfusion Scientist

Oklahoma City, Oklahoma

Our client is a biopharmaceutical CDMO that specializes in therapeutic proteins and antibodies. With over 20+ years of scientific experience and a solutions oriented approach, our client will offer you ingenuity from start to finish. Seeking a experienced Perfusion Scientist to join the team! Perfusion Scientist – Upstream Process Development Location: Must relocate to OKC Work Authorization: U.S. citizens, permanent residents (able to transfer H1B) Qualifications: Ph.D. in Bioprocess/Biochemical Engineering + 7+ years relevant experience (incl. 3+ years in industrial USP), or M.Sc. + 10+ years experience (incl. 2+ years industrial USP) Proven expertise in: High-throughput process optimization (DoE, QbD, statistics) Development and scale-up of perfusion and fed-batch systems Upstream scale-down/scale-up for commercialization High-throughput systems (Ambr15/250) Key Responsibilities: Lead multiple client-facing projects for biologics (mAbs, recombinant proteins) Develop and optimize scalable upstream processes (fed-batch, perfusion) Design and execute experiments using flasks, Ambr systems, and bench-scale bioreactors Support process transfer, troubleshooting, and cross-functional R&D collaboration Mentor junior scientists and contribute to strategic innovation Draft protocols, SOPs, batch records, and reports Preferred: Experience with CHO cell lines and SUB/SS bioreactors (up to 500L) Knowledge of GMP and regulatory guidelines (FDA, EMA, ICH) Prior CDMO experience in bioprocess development Soft Skills: Strong communication, leadership, and project management abilities Comfortable interpreting complex data and presenting to clients and leadership This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH #LI-DNP:

Manufacturing Process Technician

New Albany, Ohio

Our client, a renowned leader in biotechnology, is revolutionizing the use of living cells to create groundbreaking biologic medicines. As a guiding force in the biotech industry, they set the bar for innovation and advancement. We are excited to announce a fantastic opportunity to join their team as an Associate Manufacturing Process Technician! Let’s connect and get started—apply today! Type: 1 year contract with possible extension Pay: $18-$21/hr Requirements: High school/GED and 1 year of work or military experience OR? Associates degree? Responsibilities: Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipment. Perform basic, routine manufacturing process operations such as dispensing of raw materials, material reconciliation, line clearance, basic analytics, and record transactions Assist in the review of documentation for assigned areas (i.e. procedures, job plans, logs, area audits and batch records)Assist as training resource on manufacturing tasks and equipment use Use human machine interfaces (HMIs) to identify alarms and correct line stoppages. Ensures components and products are available for continuous operation. Carries out equipment inspections and generates emergency, corrective, or preventative work orders as needed in the Maximo system. Troubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processes. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH #LI-DNP

Senior Maintenance Technician

Thousand Oaks, California

Onsite: Thousand Oaks, CA PR: $38.00-$40.00/hr. Join a team that powers innovation in clinical manufacturing. We're seeking a skilled Senior Maintenance Technician to support our state-of-the-art manufacturing facility. You’ll play a key role in ensuring equipment reliability and enabling new technologies that drive the production of life-changing therapies. If you're a hands-on problem solver with a passion for continuous improvement and GMP excellence, we’d love to hear from you. Hands on maintenance tech experience Experience performing advanced installation, troubleshooting, maintenance, repair, testing, and documentation/logs of a wide variety of office utility and facility equipment used in manufacturing, utility plants, analytical labs, and office areas Develop, write, and complete a variety of technical and compliance documentation, including: Standard Operating Procedures (SOPs) Change Controls (CCMS) Non-Conformances (NCs) Work Orders (WOs) Job Plans (JPs) Hazard Risk Assessments (HRAs) Job Hazard Assessments (JHAs) Ensure all documentation meets applicable GMP, CFR, and internal Amgen standards. Support operations of building, utility, and production systems/equipment with a focus on quality and efficiency. Execute tasks safely and in accordance with applicable risk assessments (HRA, JHA), minimizing impact to production operations. Provide training to staff and stakeholders on documentation procedures, maintenance protocols, and safety practices. Participate in audits and inspections, offering documentation support and technical guidance as needed. Review and technically approve maintenance reports, forms, job plans, and records to ensure accuracy and compliance. Develop, revise, and review technical documentation related to equipment and maintenance processes. Qualifications: Strong working knowledge of GMP, CFR regulations, and quality systems in a pharmaceutical or life sciences environment. Proven experience with documentation systems such as SOPs, CCMS, NCs, and work orders. Technical expertise in utility, building, and production system maintenance. Ability to read and interpret technical drawings and schematics. Strong attention to detail and organizational skills. Proficient in using CMMS or other electronic documentation platforms. INDBH