Quality Control Specialist
$40 - $48 per hourPiper Companies
Piper Companies is currently looking for an experienced Quality Control Specialist in Branchburg, New Jersey (NJ) to work for a pharmaceutical cell therapy company. Must have experience with Flow Cytometry experience. Responsibilities for the Quality Control Specialist include: Perform analytical testing (cell-based function, flow cytometry, and PCR-based assays) under cGMP in collaboration with QC Utilize knowledge of aseptic techniques using a BSC Track and trend analytical methods and assist in troubleshooting activities Maintain, calibrate, and operate analytical equipment Maintain laboratory material and reagent inventory Document testing in accordance with cGMP requirements Perform OOS/ Deviation investigations and carry out experiments in support of these investigations Qualifications for the Quality Control Specialist include: A minimum of 4+ years’ experience within quality control Hands-on experience conducting Flow Cytometry and PCR testing within a GMP laboratory environment Ability to conduct a deviation or OOS investigation Hands on experience within cell therapy or biologics manufacturing Technical writing experience preferred Bachelor’s degree in chemistry or related field Compensation for the Quality Control Specialist include: Compensation is $40.00/hr - $48.00/hr Comprehensive benefits package Keywords Pharmaceutical, quality control, Analytical Chemistry, Cell Therapy, Biologics, PCR, Flow Cytometry, Deviation, OOS, Investigations, Assay qualification, technical writing, FDA, manufacturing, Science, comprehensive benefits package, Health, Vision, Dental #LI-ONSITE #LI-DF1 #J-18808-Ljbffr
- ...ID33079379Reference26-01729Summary :We are seeking a Senior Quality Specialist with 10+ years of experience in Quality Assurance and Quality... ..., CAPA, deviation management, risk assessment, and change control. This role will provide Quality oversight of suppliers and third...SuggestedContract work
- We are seeking an experienced Quality Specialist to join a growing Regulatory Affairs & Quality Assurance team supporting medical device, pharmaceutical... ...excellence. Key Responsibilities Manage the Change Control process, including ECO documentation, SOP creation,...SuggestedContract work
- ...limited to Work with suppliers to complete required supplier surveys and maintain supplier survey files. Maintain and archive supplier quality paper records. Monitor supplier quality TW records to ensure timely closure Support supplier quality associates as needed....SuggestedPermanent employmentTemporary workWork at officeWorldwide
$69.5k - $102.35k
Johnson & Johnson, QA Specialist II (1 of 2) - Application via WayUp Join to apply for the... ...humanity. Learn more at Job Function: Quality Job Sub Function: Quality Assurance Job... ...management processes including formal change controls by evaluating the proposed changes,...SuggestedContract workTemporary workPart timeLocal areaImmediate startAfternoon shift- Legend Biotech is seeking a QC Analyst as part of the Quality Operations team based in Raritan, NJ. Role Overview The QC Analyst is... ...therapy products for clinical trials and commercial operations in a controlled GMP environment. Key Responsibilities Be responsible for the...SuggestedPermanent employmentFull timeFor contractorsWork experience placementLocal areaWorldwideShift workNight shiftAfternoon shift
- Legend Biotech is seeking a QC Analyst to join the Quality Operations team in Raritan, NJ. The role involves performing QC testing for... ...used in clinical trials and commercial operations within a controlled cGMP cleanroom. The candidate will ensure compliance with procedures...
- Legend Biotech, based in Bridgewater, NJ, is seeking a QC Analyst to join the Quality Operations team in Raritan. The role tests autologous CAR‑T products in a compliant cGMP environment, supporting clinical trials and commercial operations. Candidates should have a science...Shift workAfternoon shift
- ...Nestlé Health Science Quality And Food Safety By Design Role At Nestlé Health Science, we believe that nutrition, science, and wellness... ...worldwide. Key Responsibilities: Support Quality Specialists throughout the Idea-to-Launch (I2L) process by providing...Worldwide
$70.67k - $92.76k
QA Document Control Specialist I/II/III Legend Biotech is a global biotechnology company dedicated to treating life‑threatening diseases. Headquartered... ...Perform tasks in a manner consistent with safety policies, quality systems and cGMP requirements. Review and approve SOPs and...Work experience placementFlexible hours- ...owners. Collaborating to complete deliverables with global Quality Teams. Reviewing Quality System reports in Veeva QMS and... ...support of QMS processes as needed (Deviation, CAPA, Document Control, Change Control). Requirements: ~5+ Years experience in Quality...
$32 per hour
...Quality Specialist Guardian of Quality and Compliance by Design following the quality requirements and deliverables for Food Safety initiatives in raw material specifications (mainly RMPS and testing specifications) to full compliance to Quality, Food Safety and Regulatory...Hourly pay- The Quality Specialist is responsible for supporting and maintaining the Quality Management System (QMS) for medical device, pharma and combination... .... This role is responsible for managing the change control process, creating and updating standard operating procedures...Contract work
$80.14k - $112.85k
...patients and consumers. POSITION SUMMARY: The Quality Specialist-Certifications & Retail Testing ensures product and brand compliance... ...or equivalent tools) ~ Working knowledge of document control, label/specification review, compliance programs, and...Contract workWork at officeRemote 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...
- ...Quality Assurance Specialist-Junior Bridgewater, NJ (Hybrid) 6-12+ Months contract Summary: The primary responsibility of this position involves the daily management of commercial Product Quality Complaints. The daily management of complaints may...Contract workWork at office
$31 per hour
...Job Description Job Description Job Title: Quality Systems Training Associate Job Description The Quality Systems Training Associate supports the global Learning Management System (LMS), ComplianceWire, within the Quality Systems Services organization. This role...Contract workTemporary work$102.3k - $140.13k
...Nestle Health Science Position Summary: As a Sr. Quality by Design Specialist, you will play a key role in bringing innovative products... ...knowledge of hygienic design, zoning, statistical process control, and thermal processing. ~ Preventive Controls Qualified...
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