QA Inspector II - GMP Packaging & Lab QC
Merck
Amneal is seeking a QA Inspector I to monitor and sample incoming raw materials, packaging components, and returned goods, ensuring compliance with established specifications throughout manufacturing and packaging operations. The role involves preparing samples for chemical and microbiological analysis, maintaining detailed records, verifying expiry and retest dates, and performing line checks and in-process tests to support GMP compliance and product quality. #J-18808-Ljbffr Merck & Co.
$20 - $26 per hour
...all incoming raw materials, packaging components and returned goods... ...Functions All Functions of QA Inspector I: Perform Inspection, sampling... ...analysis and delivering them to the QC lab. Inspection and test of... ...date and retest date for all GMP raw materials through vendor...SuggestedHourly payTemporary workFor contractorsLocal areaNight shift- Amneal is seeking a QA Inspector I to monitor and ensure all incoming raw materials, packaging components and returned goods are sampled, inspected and tested for compliance with specifications. The role also covers GMP compliance across all packaging stages and final QA...Suggested
$19.5 - $23.5 per hour
...Description The QA Inspector monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected... ...and delivering them to the QC lab. Inspection and test of... ...date and retest date for all the GMP raw materials through vendor COA...SuggestedHourly payTemporary workFlexible hoursWeekend work$70k - $75k
..., and/or review Out of Specification lab investigations, deviations, and corrective... ...Experience: Previous experience for QC I (0 to 2 years or more), QC II (2 to 5 years or more), and QC III (5... ...regulatory dossiers and data packages for interactions between Kashiv and regulatory...SuggestedWork at officeLocal areaFlexible hours- Legend Biotech USA is seeking a QC Analyst I (IPL) in the Quality Operations team, based in Raritan, NJ. The role focuses on performing... ...related to manufacturing cell therapy products in a controlled GMP environment. The position requires a Bachelor's degree in science...SuggestedDay shift
- Legend Biotech USA Inc. in Raritan, NJ seeks a QC Analyst I (IPL) to join the Quality Operations team. The role performs QC testing for cell therapy manufacturing in a controlled GMP environment, with a 1st shift from 7am-7pm and potential overtime. The position requires...Day shift
- Kashiv BioSciences, LLC is seeking a QC Analyst to support analytical testing for late-stage and commercial products in cGMP labs. A strong background in protein chemistry and techniques such as HPLC, SDS-PAGE, ELISA, and cell-based bioassays is essential. The role requires...
- ...We are placing QC Analysts with a leading biosimilars manufacturer in Piscataway, NJ. You will be performing analytical testing and... ...Collaborating cross‑functionally to advance projects and resolve lab investigations What you need: 2-3+ years of QC laboratory experience...
- ...Description Job Description Position Description: Position SummaryThe QA Inspector I is responsible for supporting Quality Assurance activities by ensuring products are manufactured, packaged, and released in compliance with current Good Manufacturing Practices (cGMP...Work at office
- ...innovative, cold chain & temperature-controlled packaging solutions manufacturer, for... ...Responsibilities): Our Quality Control (QC) Inspector performs incoming work in process and final... ...technical documentation such as SOP’s, GMP’s & Test Methods. Capable of working...Temporary workLocal areaFlexible hours
- Legend Biotech is seeking a QC Analyst (IPL) to perform QC testing related to the manufacturing of autologous CAR‑T products for clinical... ...Shift (7am-7pm). Bachelor’s degree in science required; 1 year of QA/QC experience preferred; knowledge of cGMP and aseptic technique...Shift workDay shift
- Kashiv BioSciences, LLC is seeking a Quality Control Analyst to support analytical testing and data verification for late-stage clinical and commercial products in cGMP laboratories. A strong background in protein chemistry is essential to perform and troubleshoot HPLC,...
- Legend Biotech in New Jersey is seeking a QC Analyst I (IPL) to perform QC testing for autologous CAR‑T products in a cGMP cleanroom. The role supports clinical trials and commercial operations, with shift work in a 1st shift schedule and potential travel as needed. Requirements...Shift workDay shift
- Global Life Science Hub is seeking a QC Analyst in Piscataway Township, NJ to perform analytical testing in a cGMP laboratory. You will handle HPLC and other methodologies, ensuring compliance and supporting late-stage clinical products. The ideal candidate has 2-3+ years...
- ...join their team in Edison, NJ. The ideal candidate will perform QC testing to assess the quality of pharmaceutical materials, ensuring... ...pharmaceutical industry, with opportunities to learn and grow in a dynamic lab environment. #J-18808-Ljbffr Integrated Resources Inc.
- ...Legend Biotech in Raritan, NJ is seeking a QC Analyst I (IPL) to perform QC testing related to manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. The role requires a Bachelor's degree in science or engineering...Weekend workAfternoon shift
- ...Kashiv Biosciences LLC is looking for a QC Analyst III in Piscataway Township, NJ. The ideal candidate will be responsible for analytical testing and data verification for clinical and commercial products. A Bachelor's degree in a related field with at least 10 years...
- ...best practices. Perform periodic audits to verify adherence to QA/QC Management Plan. Develop a comprehensive working knowledge of project... ...and eligible part time team members a comprehensive benefits package that’s among the best in our industry. Benefits include medical,...Full timeContract workTemporary workPart timeFor subcontractor
- ...Analyst to join our Quality Control (QC) team in Bridgewater, New Jersey. The... ...(CTOs) and internal satellite labs, including proper packaging, temperature monitoring, and regulatory... ...training records and complete all required GMP training in a timely manner; provide hands...Contract workFlexible hours
- Legend Biotech is seeking a QC Analyst I (IPL) in Raritan, NJ to perform QC testing related to manufacturing of autologous CAR‑T products in a GMP environment. The role is part of the Quality Operations team and requires 1 year of related experience, ASEPTIC technique,...Shift workDay shiftAfternoon shift
$83.71k - $109.87k
...an immunotherapy for multiple myeloma. Sr. QC Analyst - Quality team, Raritan, NJ Shift:... ...all applicable procedures, standards and GMP regulations. Conduct analytical testing of... ...speaking and interacting with regulatory inspectors. Occasional domestic travel to partner sites...Permanent employmentFull timeTemporary workFor contractorsWork experience placementLocal areaWorldwideFlexible hoursShift workNight shiftAfternoon shift$27 - $31 per hour
...Associate Quality Analyst – Histology Analyst II Job Description The Associate Quality... ...Proficiently perform histology testing for QC product release samples, clinical complaint... ...regulated laboratory environments such as GMP, GLP, and/or GCP settings. ~ Proficiency...Contract workTemporary workWork at office$25 - $35 per hour
...Quality Inspector Piscataway,NJ, US 6879756 2 days ago Job Description Experience: Mid Level Salary: $25 - $35 per hour Job Details My client is a leading manufacturing company and is looking to add multiple Quality Inspector's to their team. This position involves rigorous...Hourly payFlexible hours$70k - $83k
...Overview Quality Control Inspector — Full Time, Peapack, NJ, US Salary Range: $70,000.00 To $83,000.00 Annually About Komline As a pioneering... ...Engineering, Quality or related field 7+ years of QA/QC experience in a capital equipment manufacturing environment Minimum...Full time$51k - $66k
...Quality Control Inspector - Job Description The Quality Control Inspector performs detailed incoming inspection of vendor-supplied... ...Review and validate first article inspection (FAI) documentation packages, including material certifications, vendor-provided...Permanent employmentFlexible hours- Abbott seeks an detail-oriented Inspection Technician to join the Westfield, IN team in the Structural Heart division. You will receive materials, perform visual and dimensional inspections, and help ensure only compliant items move to production. In this role you’ll work...
- ...Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Mauser Packaging Solutions is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to...Work at officeShift work
$90k - $210k
.... This position will be responsible for routine and non-routine QC testing according to Standard Operating Procedures (SOPs). This... ...mindset $90,000 - $210,000 a year Cellares total compensation package contains competitive base salaries, highly subsidized Medical,...Flexible hours$26 per hour
Berjé Inc. is a third-generation, family-owned company with more than 70 years of excellence in the flavor and fragrance industry. Built on a foundation of innovation and resourcefulness, Berjé has grown into a trusted global supplier of high-quality aromatic ingredients...Work at officeWorldwide$90k - $115k
...known for innovation, high standards of product excellence, and a passionate consumer base. They are looking to add a Quality Control (QC) Manager to their team. Salary $90k - $115k annually. Position Overview The Quality Control (QC) Manager will lead product‑focused...Contract work
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