QA Associate: Elevate cGMP & Quality
Artech Information Systems LLC
A leading IT staffing company is seeking a candidate with 0-3 years of GMP manufacturing or QA experience for a role in compliance and quality assurance. Responsibilities include ensuring adherence to regulatory requirements, coordinating batch records, and approving documents for raw materials. A BS/BA in Biological Sciences or equivalent experience is required. This position is critical to maintaining product quality and compliance with site standards. #J-18808-Ljbffr Artech Information System LLC
- ...operational business comply with cGMP legal and regulatory... ...requirements, the Client Pharma Corporate Quality Manual and Policies, and site... ...maintenance of records between QA operations and Document Control Center; support cGMP and associated OJT training to QA and other departments...QualityImmediate start
- A biopharmaceutical company in New Jersey is seeking a Quality Assurance Specialist to support cGMP quality operations. The role focuses on ensuring compliance with regulatory standards through the review of controlled documents, batch records, and deviations. Candidates...QualityRemote work
$100k - $125k
...Pharmaceuticals Inc. is hiring a Senior Technical Associate, Quality Assurance in Parsippany, NJ. This role ensures compliance with cGMP regulations and involves reviewing quality... ...documents, supporting audits, and mentoring QA staff. Candidates should have a Bachelor’s...Quality- An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP Document Control operations. This role involves managing an electronic document system, ensuring compliance with policies and procedures, and supporting audits...Quality
- ...working cross-functionally Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client... ...Reports to: Jenna Walker - Associate Director, QA Training & Document Control Education: Bachelor...Quality
$100k - $125k
Ferring Pharmaceuticals is seeking a Senior Technical Associate in Quality Assurance located in Parsippany, NJ. This role focuses on ensuring compliance with cGMP regulations and internal quality standards, overseeing quality system document reviews, and supporting audits...Quality- Ferring Holding SA is seeking a Senior Technical Associate in Quality Assurance based in Parsippany, New Jersey. The role involves ensuring compliance with cGMP regulations, reviewing quality system documents, and mentoring QA staff. The ideal candidate will have extensive...Quality
- ...Description: Job Summary: The Quality Assurance Analyst supports organization with quality improvements efforts. Performs quality... ...Essential Duties and Responsibilities: • Performs SOX and QA audits and supports organization with internal and external audit...QualityWork experience placementRemote workShift workDay shift
- ...stability testing. Candidates must possess a BS/MS in analytical chemistry or a relevant discipline, along with 2 to 4 years of recent cGMP pharmaceutical laboratory experience. Proficiency in HPLC, UPLC, and other analytical techniques is essential. Strong communication...Quality
- ...including MELT-300, MELT-210, H-N08, and CR-01 Job Summary The Quality Assurance Complaints Specialist ensures manufacturing... ...Operating Procedures (SOPs), current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) standards and batch record...Quality
- ...POSITION (Position Summary): The Quality Assurance Specialist position... ...a key role in supporting the cGMP quality operations for the... ...environment. The primary focus of the QA Specialist role will be to... ...is preferred. Minimum of Associates degree Experience: • 3-5 years...Quality
$34.97 per hour
A leading staffing firm is seeking a QA CTO Label Specialist to join their team in Summit... ...year of relevant labeling experience in a cGMP/FDA regulated environment. Candidates... ...approximately $34.97/hour and is focused on quality assurance within the pharmaceutical manufacturing...QualityContract work- ...exclusive features. Job Title :QA Label Specialist Location :... ...Type: Contract Overview The Quality Assurance Label Control (QALC)... ...Labeling Specialist supports the cGMP Label Control operations for... ...Fine Jewelry Quality Assurance Associate New York, NY $50,000.00-$70,00...QualityContract workAfternoon shift
- An established industry player is seeking a meticulous Quality Assurance Label Specialist to support critical document control operations. This role involves ensuring compliance with cGMP regulations and managing the issuance of production labels. You will work collaboratively...Quality
$90k - $115k
...Livingston, NJ (on-site) Scope The Life Science Quality Assurance Specialist III is a senior‑... ...a four‑year college or university, or Associate’s degree (A.A.) with four to six years of... ...Medical Laboratories, AABB, FDA (HCT/P, cGMP, cGTP), 21 CFR 1271, FACT, and ISO 9001....QualityWork at office- Harrow, Inc. is seeking an In-Process Quality Assurance Inspector in Ledgewood, NJ, to ensure product quality and compliance with cGMP regulations. The role requires oversight of manufacturing and production areas, confirming adherence to cleaning and quality processes...QualityFull time
- 1 00% onsite Job Title: CTO QA Label Specialist Shift: This position... ...- Sat (1 pm to 11 pm). The Quality Assurance Document Control (... ...Specialist supports the cGMP Document Control operations for... ...Education: Bachelor's degree or Associate's Degree with 3+ Years of Experience...QualityShift work
$22 - $26 per hour
We are seeking a Quality Assurance Administrative Associate who will be responsible for supporting our quality assurance team onsite in our Parsippany, NJ... ..., team members, and taking meeting minutes, Support the QA team with deliverables and timelines, email responses, coordination...QualityHourly payFull timeWork experience placementWork at office- ...healthcare company in New Jersey is seeking a Warehouse Associate responsible for general warehouse functions including... ...processes. The role involves adhering to FDA CGMP guidelines and participating in quality control meetings. Candidates should have experience in...Quality
- Veritext is looking for a Quality Assurance Associate in Livingston, NJ to oversee quality management in legal transcription. This role requires effective collaboration and feedback processes to ensure the accuracy of transcripts in legal cases. Qualified candidates will...Quality
- SGS, located in Fairfield, NJ, is seeking a Quality Assurance Specialist II. This role involves the implementation and maintenance of quality systems, providing oversight to testing processes, and managing documentation control among other responsibilities. The ideal candidate...Quality
$27.34 - $41.04 per hour
NJ Sharing Network is looking for a Quality Specialist based in New Providence, New Jersey. The role involves collaborating with clinical operations to ensure tissue donor records meet standards while performing quality reviews and data entry. The ideal candidate should...QualityHourly pay- Veritext is seeking a Quality Assurance Associate to join our Digital Solutions Team in Livingston, NJ. The ideal candidate will have over 2 years of transcription experience, with at least 1 year in transcription quality assurance. Responsibilities include conducting quality...Quality
$25 - $28 per hour
...Duration: 3 Month Contract to Hire Pay Rate: $25-28/hr. Position Overview Insight Global is seeking an experienced and detail‑oriented Quality Assurance Specialist to establish, lead, and continuously improve our clients Quality Management System (QMS). This role is...QualityContract work- ...The primary responsibility of the Global QA Patients Operations Specialist is to support... ...in writing (English language required). Quality Operations and Systems Support including... ...-inclusive. Direct reporting line to the Associate Director of the Global Quality Patient...QualityFlexible hours
- Quality Assurance - Quality Assurance Associate Livingston, NJ, USA • Job Description Posted Thursday, May 14, 2026 at 7:00 AM At Veri text, we focus on the... ...years’ experience in legal field 1+ year transcription QA experience 1+ year Scopist experience Experience...QualityTemporary workFor contractorsSummer workLocal areaRemote work
- A leading testing, inspection, and certification company in Fairfield, NJ, is seeking a Specialist I in Quality Assurance. The role involves assisting management in maintaining Quality Systems, performing routine testing, and ensuring compliance with regulatory requirements...Quality
- Job Title: QA CTO Label Specialist Location: Summit, NJ 07901 Job Duration: 12+ Months Shift: 2nd Shift, This position is scheduled... ...on W2 Job Description: Purpose and product of position: The Quality Assurance Label Control Specialist at the S-12 Cell Therapy manufacturing...QualityWork experience placementWork at officeShift workAfternoon shift
$81.19k - $108.25k
...About the Role: The 3rd Party Operations (3PO) Food Safety & Quality (FSQ) Manager plays a critical role in safeguarding Ferrero’s commitment... ...warehousing sites in North America; follow up on findings and elevate critical non-conformities as needed. Drive the implementation...Quality- Join to apply for the Quality Control Analyst role at RYZE *Applications are reviewed on a rolling basis. We encourage interested candidates... ...Procedures (SOPs) and batch records. Ensure adherence to FDA, cGMP, FSMA, and HACCP requirements for dietary supplements and food...QualityImmediate startFlexible hours
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