Onsite GMP Quality Records Specialist Release/Disposition
TechDigital Group
An established industry player is seeking an Associate Specialist for Quality Product Release-Disposition. This role is crucial for maintaining compliance with corporate policies and global cGMP standards. The successful candidate will manage quality records, support batch record processing, and ensure efficient documentation practices. This position offers a chance to work in a collaborative environment, where your contributions will enhance operational efficiency and support quality assurance efforts. If you have a strong foundation in GMP and are eager to take on responsibilities that make a difference, this opportunity is perfect for you. #J-18808-Ljbffr
- The Global Supplier Quality, External QC - Vector will process external deviation and change records from our Contract Test Laboratories (CTL). Other duties may include coordinating... ...shipping and testing of samples for lot release, PPQ, PSQ and compiling vendor documentation...SuggestedContract workWork at office
- 50% onsite PURPOSE AND SCOPE OF POSITION (Position... ...Summary): The Quality Assurance Specialist position plays a key... ..., completed batch records, material disposition, and manages implementation... ...directly supports release of vector timeline... ...guidance during GMP events and...Suggested
- ...biopharmaceutical company in New Jersey is seeking a Quality Assurance Specialist to support cGMP quality operations.... ...of controlled documents, batch records, and deviations. Candidates should... .... This position offers a blend of onsite and remote work. #J-18808-Ljbffr...SuggestedRemote work
- ...industry player is seeking a detail-oriented professional to manage external quality control processes. This role involves coordinating with Contract Test Laboratories and ensuring timely release of vector for various programs. The ideal candidate will have a strong...SuggestedContract work
$27.34 - $41.04 per hour
...or an alternative application process. Quality Specialist Full Time Hourly Professional New... ...clinical operations to assure tissue donor records meet established guidelines. Provides quality... ...lists giving the donors’ status. Onsite staff provides back-up for serology notification...SuggestedHourly payFull timeTemporary workH1bWork at officeLocal areaFlexible hours- ...NJ Sharing Network is seeking a Quality Specialist based in New Providence, NJ. This full-time hourly role involves reviewing tissue donor records and ensuring compliance with established guidelines. The ideal candidate will have at least one year of Quality Assurance...Hourly payFull timeWork at office
- 1 00% onsite Job Title: CTO QA Label Specialist Shift: This position is scheduled for Wed- Sat (1 pm to 11 pm). The Quality Assurance Document Control (QADC) Labeling Specialist supports the... ...management of production labels and records. To succeed in this role, you will have...Shift work
$77.05k - $143.09k
Quality Learning Systems Specialist The Quality Learning Systems Specialist ensures services, processes, and... ...quality audits, maintain inspection records, and support improvements via change... ...Work Location Hybrid role requiring onsite presence at the Parsippany, New Jersey...Temporary workWork at officeLocal areaRemote work1 day per week- ...Position Summary: The Global Product Quality Specialist will be responsible for managing (and owning as needed) documentation and change controls... ...business or technology initiatives. Minimum of 3 years working under GMP conditions. BA or BS degree. #J-18808-Ljbffr...Work at office
- ...the Client Pharma Corporate Quality Manual and Policies, and site... ...Coordinate and perform batch record issuance for internally manufactured... ...documents for raw material disposition, manufactured media. Perform... ...database system along with GMP, safety, and Ethics &...Immediate start
$77.05k - $143.09k
...world’s oldest enemy: disease. As the Quality Learning Systems Specialist you are responsible for ensuring... ...quality audit and documents inspection records. Requires understanding of external... ...classified as a hybrid role, requiring onsite work at the Parsippany office four...Full timeTemporary workWork at officeLocal areaRemote workWorldwideFlexible hours1 day per week- ...Join to apply for the Quality Control Analyst role at RYZE *Applications... ...and manage quarantine or release processes in collaboration with... ...and traceability of results. Record inspection data and deviations... ...environment. Solid understanding of GMP, FSMA, and HACCP standards....Immediate startFlexible hours
- Overview NOW HIRING - QUALITY ASSURANCE ASSOCIATE Kemin is seeking... ...Responsibilities Review batch records and bring variances forward, as... ..., as necessary. Facilitate GMP audits, as applicable. Trained... ...finished goods, and packaging release, with supervision, as applicable...Full timeSecond jobLocal areaImmediate start
- ...features. Job Title :QA Label Specialist Location : Summit, NJ Hours... ...: Contract Overview The Quality Assurance Label Control (QALC... ...management of production labels and records. Responsibilities Supports... ...Manager-Data Integrity/GMP/CSV Manhattan, NY $58,700.00-...Contract workAfternoon shift
- Wieland Group is seeking a Quality Coordinator in Parsippany, NJ. The role involves managing data entry for quality inspections, processing quality documentation, and supporting quality standards. Candidates should have at least 3 years of experience in a related field,...Work at office
$105k - $150k
Bastion Technologies, Inc. is looking for a Quality Assurance Specialist to support the Safety and Mission Assurance Services II contract in Springfield, NJ. The role includes inspection functions for space flight hardware, ensuring adherence to quality assurance plans...Contract work- ...The Quality Associate will perform independent examination (i.e., audit) of multiple trial‑related activities and documents to determine... ...trial‑related activities were conducted and the data were recorded, analyzed, and accurately reported according to the protocol, standard...Temporary workWork at officeLocal areaFlexible hours
$105k - $150k
...per year Location: Springfield, NJ Responsibilities Perform Quality Assurance Specialist (QAS) inspection functions for space flight hardware in... ...specification requirements. Work Location This position is located onsite; some travel may be required. Schedules are subject to...Full timeWork experience placementWork at officeFlexible hours- ...An established industry player is seeking a Project Management Specialist to support a cutting-edge cell therapy facility. This role... ...various departments, and ensuring projects are completed within quality metrics and timelines. The ideal candidate will have a strong...
- ...QA Specialist Reporting to the AAA Site Remediation Lead, the AAA Remediation QA Specialist is responsible for GMP quality assurance oversight of remediation activities and the on-time execution... ...equipment validation, compliance, record backlog elimination, and sterility...Local area
- ...A global ingredient manufacturer is seeking a Quality Assurance Associate for its Missouri campus, with the primary location in Sarcoxie. This role involves maintaining quality documentation, supporting audits, and ensuring compliance with food safety regulations. Candidates...
- ...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... ...to regulatory requirements, coordinating batch records, and approving documents for raw materials. A BS...
- Ferring Holding SA seeks a Quality Learning Systems Specialist located in Parsippany, New Jersey. The role ensures compliance with Quality Assurance... ...of Quality Management Systems. This hybrid role requires onsite presence four days a week and includes a comprehensive...
$100k - $125k
...Ferring Pharmaceuticals Inc. is hiring a Senior Technical Associate, Quality Assurance in Parsippany, NJ. This role ensures compliance with cGMP regulations and involves reviewing quality system documents, supporting audits, and mentoring QA staff. Candidates should have...- ...Responsible for assisting with laboratory analysis for clinical release and clinical stability testing. Conduct reference standards qualification analyses of developmental and commercial compounds, prototype formulations and finished products in support of clinical testing...
- 50% onsite Work Schedule: M-F (normal business hours) The primary responsibility of the Global QA Patients Operations Specialist is to support the Onboarding and Maintenance of Apheresis Centers... ...(English language required). Quality Operations and Systems Support including...Flexible hours
$97.8k - $133.46k
...their best health. For over 90 years , we have been New Jersey's health solutions leader driving innovations that improve health care quality, affordability, and member experience. Our members are our neighbors, our friends, and our families. It is this understanding that...Live inLocal area$500 per month
...Job Summary: The Quality Control Analyst is responsible for performing chemical, microbiological... ...products. This role ensures compliance with GMP, FDA, and radiation safety regulations, supporting the release of high-quality, sterile, and safe therapeutic products...Full timeWork at office$19 - $20.5 per hour
...expertly sourcing the highest quality foods and treating our customers... ...and review checklists to release production areas for daily use... ...questions. Actively support record-keeping programs (SafeFoods/EQMS... ...associate, visitor, and contractor GMP and Food Defense compliance....Hourly payFull timeFor contractorsSeasonal workImmediate startFlexible hoursShift work$34.92 - $42.32 per hour
Scorpion Therapeutics in Summit, NJ, is hiring for a role focused on supporting Label Operations. Responsibilities include issuing clinical and commercial labels, ensuring compliance, and training personnel. A B.S. degree and 2+ years of relevant experience are required...Hourly payAfternoon shift
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Onsite GMP Quality Records Specialist Release/Disposition. Be the first to apply!
- quality specialist Summit, NJ
- quality control associate Summit, NJ
- warehouse quality control associate Summit, NJ
- quality assurance auditor Summit, NJ
- quality auditor Summit, NJ
- quality management specialist Summit, NJ
- quality associate Summit, NJ
- quality equipment Summit, NJ
- quality manufacturing Summit, NJ
- water quality scientist Summit, NJ

