Quality Assurance & QMS Specialist II
Kashiv Biosciences LLC
Kashiv Biosciences LLC is seeking a Quality Assurance Specialist II in Piscataway, NJ. This full-time role involves supporting Quality Assurance management in reviewing and managing the quality system, ensuring compliance with cGMP requirements, and conducting quality audits. The ideal candidate should possess a 4-year degree in a science or engineering discipline, with 3–8 years of experience in quality or QMS roles. Strong communication skills and knowledge of eQMS tools are preferred. #J-18808-Ljbffr Kashiv Biosciences LLC
- ...SUMMARY The Quality Assurance Specialist II is a regular employee in a full-time exempt position at Kashiv BioSciences, LLC, in Piscataway NJ. This employee will be responsible for supporting Kashiv BioSciences Quality Assurance management in reviewing, implementing, and...SuggestedFull timeWork at officeFlexible hours
- ...Career Advancement Job Summary We are seeking an experienced Quality Assurance Specialist to join our team. In this role, you will be responsible for... ...and continuous improvement of Quality Management Systems (QMS) including Deviation Management, CAPA, Change Control,...SuggestedWorldwide
$69.5k - $102.35k
Johnson & Johnson, QA Specialist II (1 of 2) - Application via WayUp Join to apply for the Johnson & Johnson, QA Specialist... ...health for humanity. Learn more at Job Function: Quality Job Sub Function: Quality Assurance Job Category: Professional All Job Posting Locations:...SuggestedContract workTemporary workPart timeLocal areaImmediate startAfternoon shift$75.97k - $99.71k
...Role Overview Legend Biotech is seeking a QA Shop Floor Specialist II/III as part of the Quality Operations team based in Raritan, New Jersey . The QA... ...aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, technical...SuggestedWork experience placementImmediate startWorldwideFlexible hoursWeekend work- A leading healthcare company is looking for a Quality Assurance Incoming Specialist II based in Raritan, NJ. The role involves overseeing the quality and compliance of materials for CAR-T production in a regulated environment. Candidates should have a Bachelor's degree...Suggested
- A global biotechnology company in Raritan, New Jersey, is seeking a QA Shop Floor Specialist II/III to oversee floor quality in the production of CAR-T products. The ideal candidate will have a Bachelor’s degree in Life Sciences and relevant experience in an aseptic manufacturing...
$65k - $104.65k
...impact health for humanity. Learn more at Job Function Quality Job Sub Function Quality Assurance Job Category Professional All Job Posting Locations... ...currently seeking three Quality Assurance Incoming Specialist II. This position will be located in Raritan, NJ! At...Local areaImmediate startShift workDay shift$70.67k - $92.76k
QA Document Control Specialist I/II/III Legend Biotech is a global biotechnology company dedicated... ...consistent with safety policies, quality systems and cGMP requirements. Review... ...aseptic manufacturing facility, quality assurance, manufacturing compliance, clinical quality...Work experience placementFlexible hours- ...Quality Assurance Specialist Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline...Work at office
- ...Job Description Job Summary: Under minimal supervision, the Quality Assurance Specialist III will ensure systems and processes are in a state of... ...that identify whether there are uncontrolled risks within the QMS. Maintain the list of approved suppliers and subcontractors...Full timeContract workFor subcontractorMonday to Friday
- Job Title: Quality Assurance Specialist Duration: 12 Month Contract (Possible extension based on work performance) Location: Summit, NJ Hybrid Position Job Description The Quality Assurance Specialist position plays a key role in supporting the cGMP quality operations...Contract work
- Legend Biotech US is seeking a QA Shop Floor Specialist in Raritan, New Jersey, to provide quality oversight in the production of CAR-T products. This exempt-level position involves maintaining compliance in a cGMP cleanroom and supporting manufacturing activities. You...
- A biotechnology company seeks a QA Shop Floor Specialist responsible for overseeing quality in CAR-T cell therapy production in a cGMP cleanroom. Ideal candidates will have a Bachelor's degree in Life Sciences or Engineering and 0-2 years of relevant experience. Responsibilities...Afternoon shift
$96.27k - $126.35k
...multiple myeloma. Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New Jersey. Role... ...an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, technical...Permanent employmentFull timeTemporary workFor contractorsWork experience placementLocal areaImmediate startWorldwideFlexible hoursWeekend workDay shift- Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New Jersey. Role Overview The QA Shop... ...aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, technical operations...Permanent employmentFull timeFor contractorsLocal areaImmediate startFlexible hoursWeekend workDay shift
- ...Biotech in Raritan, New Jersey, is hiring a QA Shop Floor Specialist. This role involves quality oversight in the production of autologous CAR-T... ...experience in biotech or a related field, preferably in quality assurance. Key responsibilities include collaborating with site...
- JUPITER RESEARCH SERVICES INC is seeking a Quality Assurance Specialist to oversee the quality and compliance of our clinical trial materials. You will ensure that products meet regulatory standards throughout their lifecycle, from storage to distribution. Ideal candidates...
$57.5k - $83.4k
...Primary Purpose The Quality Assurance Specialist is responsible for ensuring consistent service quality by conducting comprehensive onsite quality assurance audits for all lines of business within the USS portfolio. This role exercises discretion and independent judgment...Full timeTemporary workPart timeSecond jobWork at officeLocal areaFlexible hours$31 - $35 per hour
...pharmaceutical manufacturing organization dedicated to producing high-quality products in a highly regulated environment. The company is... ...product excellence. They are currently seeking a Quality Assurance Specialist to join their Quality team. Salary/Hourly Rate: $31/hr - $35...Hourly payPermanent employmentTemporary workFor contractorsImmediate startMonday to Friday- The Quality Assurance Specialist will provide Quality oversight to the CMO with the ability to be on site up to support Quality Reviews and QA Shop Floor manufacturing support. You will manage CMO oversight for change management, deviation management, Annual Product Quality...
- Join a forward-thinking company as a Quality Assurance Specialist, where you will oversee critical quality processes in a dynamic environment. This role involves managing CMO oversight, ensuring compliance with GMP standards, and preparing for regulatory audits. You will...
- A leading clinical supply solutions firm in New Jersey is seeking an experienced Quality Assurance Specialist to oversee the quality of goods and services. The ideal candidate will ensure compliance with regulatory standards while performing regular inspections and implementing...
$81.27k - $106.67k
...treatment of multiple myeloma. Position QA Change Control Specialist II - Quality team, Raritan, NJ Role Overview The QA Specialist, Change... ...experience, preferably in a cGMP manufacturing facility, in quality assurance, manufacturing compliance, clinical quality, or cell...Permanent employmentContract workTemporary workWork experience placementWork at officeLocal areaWorldwideFlexible hoursShift work- A biotechnology company in New Jersey seeks a QA Change Control Specialist II responsible for quality oversight in a cell therapy manufacturing facility. Applicants should possess a Bachelor's degree in Science and a minimum of two years' experience within a cGMP environment...
- Sunrise Systems is seeking a Quality Assurance Specialist in Edison, NJ, to support cGMP quality operations. This hybrid role involves reviewing controlled documents, ensuring compliance with manufacturing practices, and supporting both clinical and commercial product...
- International Flavors & Fragrances Inc. seeks a Quality Product Safety Specialist in South Brunswick, NJ. This full-time role involves supporting quality and food safety operations on the plant floor, maintaining compliance with FDA regulations, and participating in food...Full time
$36 - $46 per hour
...structured environments, and enjoys ensuring that systems and processes perform exactly as intended. About the Role As a Quality Assurance Specialist, youll serve as the checkpoint for accuracy and consistency across our workflows. Youll verify execution against SOPs,...Hourly payContract workLocal areaRelocation$38 - $40 per hour
...Job Description Job Description Job Title: Quality Assurance Specialist Job Description We are seeking a motivated and detail-oriented Quality... ...a plus. Familiarity with TrackWise Digital electronic QMS, LabVantage and SAP. Work Environment The work...Contract workTemporary work$83.71k - $109.87k
...seeking a QA Laboratory Compliance Specialist III as part of the Quality team based in Raritan, NJ. Role Overview... .... Train and coach Level I/II QALC when performing newer day-to-day... ...a Subject Matter Expert on Quality Assurance topics within the group in support of...Permanent employmentFull timeTemporary workFor contractorsWork experience placementWork at officeLocal areaImmediate startWorldwideFlexible hours- Amneal Pharmaceuticals is seeking a QA Auditing Reviewer in Piscataway Township, New Jersey. The role focuses on auditing production records and making batch disposition decisions. Candidates should have a minimum of 2 years' experience in pharmaceutical QA, QC, or QM. ...
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