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Manufacturing Admin Assistant
Bakersfield, California
Sep 25, 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.  
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
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
QA Lead (Food)
Pomona, California
Our client, a growing food and snack manufacturer, is looking for a skilled QA Lead to join their team in Chino, CA! Title: QA Lead (Food) Location: Chino, CA Schedule: 2nd shift- 1pm start time  Pay rate: $21- $23/ hr. Job type: Contract- hire Position Summary: The QA Lead is responsible for supporting and overseeing quality assurance activities on the production floor. This role involves supervising QA staff, ensuring compliance with food safety standards, and maintaining quality systems throughout production shifts. Key Responsibilities: Provide daily oversight and support to QA personnel on the production floor. Collaborate with management to ensure appropriate staffing and scheduling. Monitor quality control processes and escalate issues as necessary. Conduct quality inspections of raw materials, in-process, and finished products. Perform pre-operational inspections, allergen controls, and GMP audits. Document and manage non-conforming product holds and investigations. Collect and log production and processing samples. Support the investigation and resolution of customer complaints. Deliver training on policies, procedures, and quality programs. Ensure compliance with all applicable food safety and quality regulations (e.g., GMP, HACCP, FDA, USDA). Promote a culture of safety, quality, and continuous improvement. Perform additional duties as assigned by quality leadership. Qualifications: Bachelor’s degree in Food Science or a related field, or equivalent experience. Minimum 3 years of experience in a food manufacturing environment. At least 1 year of experience in a quality control leadership role. Strong working knowledge of food safety programs and regulatory requirements (FDA, USDA, HACCP, GMP, etc.). Familiarity with food labeling regulations and nutritional data systems (e.g., ESHA Genesis). Strong communication skills in English, both written and verbal. Note: 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  
Quality Systems Specialist
Florence, Kentucky
  Quality Systems Specialist Florence, KY Mon–Fri, 8am–5pm $25–$28/hr Join a global leader in the fragrance and flavor industry! We’re seeking a Quality Systems Specialist to help elevate food safety and quality programs at our Florence, KY location. Maintain and improve quality and food safety systems. Lead internal audits and monthly inspections. Manage customer complaints and implement corrective actions. Support certifications (Halal, Kosher, Organic) and regulatory audits. Train staff on quality and safety protocols. Conduct vendor audits and drive compliance. Requirements Bachelor’s in Chemistry, Food Science, Microbiology, or related field. 3+ years in Quality Assurance or Food Safety. Familiarity with ISO 9001/22000, FSSC 22000, FDA (PCQI preferred). SAP and Microsoft Office proficiency. Auditor experience is a plus. We encourage all confident candidates to apply, even if they don't meet every requirement. We look forward to learning more about you! INDBH            #LI-RL1  
Production Worker - 2nd shift
Rancho Dominguez, California
Our client, a global leader in bioprocessing, is looking for a skilled assembler to join their team in L.A County, CA! This is a great opportunity for a more entry-level candidate looking to gain assembly experience with a leading life science company. Pay rate: $20 - 21/hr. Job type: 6-month contract Schedule: 2nd shift Location: Los Angeles County, California Overview: This is a hands-on manufacturing role focused on assembling fiber and filtration components for medical or industrial devices. The assembler must follow detailed instructions to ensure high product quality and compliance with manufacturing standards. This role is entry-level and works under the guidance of more experienced assemblers and supervisors. Key Responsibilities: Assemble fiber, filtration, and plastic components manually and with tools. Follow work instructions, blueprints, and manufacturing procedures. Conduct visual inspections and routine testing for quality assurance. Operate and maintain small hand tools and some automated equipment. Clean workstations and follow Good Manufacturing and Documentation Practices (GMP/GDP). Package finished goods and kits per Bill of Materials (BOM). Work across multiple product lines as needed. Identify and report quality issues promptly. Qualifications: High school diploma or equivalent required. 0–1 year of manufacturing experience preferred (medical device industry is a plus). Ability to read blueprints and work instructions. Comfortable with repetitive tasks and working in a cleanroom environment. Physical & Work Environment Requirements: Regular standing, walking, reaching, bending, and lifting (up to 50 lbs occasionally). Good hand-eye coordination and visual acuity (depth perception and peripheral vision). Exposure to moving machinery, vibration, and occasionally chemicals or airborne particles. Work is done in a cleanroom environment with loud noise levels. Note: 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    
QC Lab Technician
Chino , CA
Our client, a leading personal care manufacturer, is looking to hire a QC Lab Technician to join their team in San Bernadino County, CA! Location: San Bernadino County, CA Pay rate: $20/hr. - $25/hr. Schedule: Monday-Friday 1pm-9:30pm, with possibility of Sat.  Job type: Contract - hire Job Summary The QC Lab Technician is responsible for performing routine laboratory testing of raw materials, in-process samples, and finished products to ensure compliance with company and regulatory standards. This position supports the QC department through data entry, documentation, and laboratory maintenance while adhering to Good Manufacturing Practices (GMP) and safety guidelines. Key Responsibilities Perform pH, viscosity, specific gravity, and other routine QC tests on samples. Assist with the approval of in-process and finished product samples. Prepare and transcribe analytical data for Certificates of Analysis (CoA) release. Accurately label and distribute specimens to appropriate departments. Maintain cleanliness of laboratory work areas, equipment, and supplies. Perform quality control duties as directed by the Laboratory Manager. Ensure compliance with all GMP and safety requirements. Assist with shipping and receiving of QC materials and samples as needed. Support other areas of Quality Control as required. Perform additional duties as assigned. Qualifications BS Degree or High School Diploma with 1–2 years of formal laboratory experience, preferably in a wet chemistry or QC environment. Strong attention to detail and organizational skills. Ability to follow complex instructions and established procedures. Effective verbal and written communication skills. Excellent computer and data entry skills. Ability to prioritize and complete tasks in a fast-paced environment with limited supervision. Strong teamwork and interpersonal skills to interface with all departments. Ability to lift up to 40 lbs and perform physical activities such as standing, walking, bending, and climbing stairs. Commitment to maintaining confidentiality regarding laboratory data and results. #INDBH #LI-DNP  
QA Inspector- Personal Care (3rd Shift)
Pomona , California
Our client, a growing personal care and nutraceutical manufacturer in the San Bernadino, CA area is seeking a  QA Inspector to join their team! We are looking for talented & hardworking individuals to join this dynamic organization. In order to be successful in this position, our ideal candidate will possess the following skill sets: 1. Ability to multi-task and inspect multiple production lines 2. Can thrive in a fast paced environment & learn/adapt quickly! 3. Detail oriented  Contract length: 1 year contract-to-hire Location: San Bernadino County, CA Shift: 3rd shift 10pm- 6am, with OT and  Saturdays on occasion  Pay rate range: $20-25/hr. Key Responsibilities: Conduct thorough visual and functional inspections of personal care products, including creams, lotions, shampoos, and other related items, to identify defects or discrepancies. Maintain accurate records of inspection results, including defect classification, quantities, and any other relevant data. Ensure that all personal care products comply with industry regulations and standards, such as FDA guidelines, and work towards continuous improvement in meeting these requirements. Collaborate with production and quality teams to identify areas for process improvement and implement corrective actions to prevent defects and non-conformities. Communicate with the production team to address and resolve quality issues, deviations, or non-conformities, and report to the Quality Manager. Qualifications: High school diploma or equivalent.  Proven experience as a QC Inspector in a GMP regulated environment.  Strong attention to detail and the ability to identify defects or deviations in product quality. Effective communication skills and the ability to work well in a team environment. Analytical and problem-solving skills to assist in process improvement and root cause analysis. Good computer skills for recording and reporting inspection data. Strong organizational skills and a commitment to maintaining a clean and organized inspection area. *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
Quality Assurance Technician - 2nd Shift
Pomona, California
Our client, a growing food manufacturer, is looking for a skilled QA Technician (2nd shift) to join their team in Pomona, CA! Pay: $18–$20 per hour Location: Pomona, CA Schedule: 2pm – 10:30pm with OT Job type: 6-month contract- hire Position Summary: The Quality Assurance Technician plays a vital role in supporting production processes and maintaining product quality in a food manufacturing environment. This position is responsible for conducting inspections, audits, and quality checks; collecting and analyzing samples; investigating product complaints; and ensuring compliance with company and regulatory standards. Key Responsibilities: Support production processes and remain accessible to production staff. Conduct quality checks, inspections, and audits to ensure compliance with specifications. Collect, log, and retain product samples for testing and traceability. Investigate customer complaints and perform product inspections as needed. Maintain accurate documentation and retain samples per company policy. Ensure compliance with company quality policies, food safety standards, and applicable regulations. Qualifications: Bachelor’s degree in a related field or equivalent relevant experience. Strong knowledge of food safety programs and quality assurance principles. Excellent verbal and written communication skills in English. Proficiency in Microsoft Office (Word, Excel, Outlook). Ability to work a flexible schedule, including potential weekends or off-shifts. Preferred Qualifications: Proficiency in an additional language. Experience in food manufacturing, metal detection systems, or laboratory testing. *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
Associate Food Technologist (Beverages)
Pacoima, California
We are seeking a motivated Associate R&D Food Technologist to join our team! This contract-to-hire role is ideal for someone who is passionate about product development, enjoys hands-on formulation work, and thrives in a fast-paced, collaborative environment. Title: Associate Food Technologist  Location: North Los Angeles, CA Job type: Contract - hire Pay Rate: $25/hr. –$30/hr. (DOE) Key Responsibilities Develop and improve new and existing products based on customer or internal requirements. Demonstrate creativity and innovation in formulation development. Taste, evaluate, and validate all developed products for quality and consistency. Work independently with minimal supervision to meet project objectives. Perform product costing calculations and maintain accurate cost data. Create and maintain master formulas within company databases. Draft product specifications for supervisor review and approval. Conduct shelf-life and stability testing on finished products. Establish and manage protocols for all outgoing product samples. Requirements Bachelor’s degree in Food Science, Food Technology, Chemistry, or a related scientific field. Minimum 1 year of experience in the food industry or relevant field. Strong mathematical skills, including working knowledge of algebra. Excellent verbal and written communication skills. Strong sensory acuity for taste and aroma evaluation. Ability to occasionally lift and carry up to 15 lbs. #INDBH #LI - DNP
Maintenance Mechanic/Technician
McDonough, GA
A premier food manufacturer is seeking a Maintenance Mechanic Technician to join their growing team and support innovative, health-focused product development. Pay: $23–$30/hr Schedule: 2nd shift (OT as needed) Type: Contract-to-Hire Essential Functions Troubleshoot and repair facility equipment and systems Maintain automated packaging machinery, pumps, pneumatics, and hydraulics Read and interpret electrical schematics Safely work with low/high voltage circuits and diagnose motor and control issues Requirements High School Diploma/GED 5+ years industrial mechanical/electrical experience Food processing/packaging equipment experience preferred   INDBH #LI-DNP  
Maintenance Mechanic (packaging)
Monroe, New Jersey
Pay Rate Low: 30.00 | Pay Rate High: 40.00Openings on 2nd and 3rd shift, will train on 1st shift!  Fantastic opportunity to join a stable and growing manufacturer with a nationwide footprint and a long-standing reputation for quality and innovation. This role is based in Monroe Township, NJ, which serves as a key hub for production, packaging, and quality operations. Position Summary The Industrial Maintenance Mechanic is responsible for troubleshooting, repairing, and maintaining manufacturing equipment to support safe, efficient, and reliable operations. This role plays a key part in minimizing downtime and ensuring equipment performs at optimal levels.  Key Responsibilities Troubleshoot and repair manufacturing equipment and machinery. Maintenance mechanic experience on packaging equipment a plus! Perform preventive maintenance on production equipment, conveyors, motors, pneumatic systems, and other mechanical equipment. Diagnose and repair pneumatic and hydraulic systems. Install, set up, and maintain injection molding equipment and related systems. Use hand tools, power tools, and testing equipment to complete repairs and maintenance tasks. Follow equipment manuals, schematics, and technical drawings to support repairs and installations. Service equipment through routine lubrication, greasing, and general upkeep. Identify and address potential safety hazards to maintain a safe work environment. Support facility maintenance projects and other duties as assigned. Qualifications 2+ years of industrial maintenance or mechanical maintenance experience preferred. Strong knowledge of pneumatics, hydraulics, and mechanical systems. Ability to read and interpret schematics, blueprints, and technical documentation. Experience troubleshooting manufacturing equipment in a production environment. Strong problem-solving and communication skills. Commitment to workplace safety and safe work practices. Ability to work overtime and flexible weekend schedules as needed. Ability to lift, push, pull, or move up to 50 pounds. 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
Senior Animal Research Technician
Birmingham, Alabama
Our client is a leader in the life sciences and biomedical research industry, driving innovation through advanced laboratory techniques and rigorous scientific methods. Title: Sr Animal Lab Tech Location: Jefferson County, Alabama Job type: Contract – hire Pay rate: $32/hr. - $36/hr. Summary: The Senior Laboratory Animal Resources Technician provides comprehensive research and technical support within Laboratory Animal Resources facilities. This role requires a strong understanding of scientific principles and research methodologies, proficiency in laboratory and animal-handling techniques, and the ability to work effectively in a collaborative team environment. The Senior Technician also serves as a mentor and trainer for junior staff and may act as a study lead, providing task direction and ensuring adherence to quality standards. Key Responsibilities: Study Conduct & Compliance Execute study activities in alignment with protocols, SOPs, laboratory methods, Good Laboratory Practices (GLP), and established safety requirements. Demonstrate working knowledge of study design and proper execution of research procedures. Administer test and control materials via multiple routes, including gavage, intravenous, intramuscular, intraperitoneal, subcutaneous, capsule, and diet/drinking water. Administer anesthesia across all species in the facility and monitor anesthetic recovery. Animal Care & Technical Procedures Collect and review in-life and husbandry data (e.g., body weights, clinical observations, food consumption) for various study types including toxicology, reproductive toxicity, oncology, and infectious disease studies. Perform specialized reproductive procedures such as mating, estrous stage identification, vaginal lavage, handling pregnant/nursing animals, and evaluating pubertal developmental indices. Safely handle and restrain multiple species including rodents, rabbits, ferrets, dogs, and non-human primates at ABSL-1, 2, and 3 levels. Conduct sample and specimen collection, animal identification procedures, necropsies, and tissue harvesting. Assist in surgeries, including equipment sterilization and preparation. Data Management & Documentation Set up, maintain, and review study files using the Provantis data collection system. Perform electronic randomization procedures within Provantis. Create and revise forms, SOPs, and documentation as needed. Leadership & Training Assist with onboarding and training new laboratory personnel in technical procedures. Act as study lead as assigned, managing supplies, ensuring paperwork accuracy, and cross-checking study protocols with ACUP and BPR requirements. Monitor junior team member work quality and provide coaching and mentoring. Minimum Qualifications: Bachelor’s degree in a science-related field and at least 4 years of relevant laboratory experience. Ability to read, understand, and follow SOPs, GLP regulations, and study protocols. Strong communication skills and the ability to collaborate effectively. Proficiency with Microsoft Office applications. Ability to wear PPE (including N95 or PAPR) for extended periods. Ability to work overtime and participate in rotating weekend/holiday schedules. Demonstrated ability to learn, apply, and teach scientific methods and laboratory techniques. Must meet all entry, medical, and vaccination requirements for ABSL-2 and ABSL-3 environments, with immunizations determined by the agents handled (e.g., Tetanus, Hepatitis B, Smallpox, Polio, Yellow Fever, Influenza).