Average salary: $59,341 /yearly
More statsGet new jobs by email
$35 per hour
...across the U.S. and internationally. Job Description Sea Breeze is seeking a hardworking, self‑motivated, and detail‑oriented Quality Team Associate to join our Quality Assurance department. This position plays a key role in ensuring product safety, consistency, and...SuggestedHourly payMonday to Friday- 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
$58k - $60k
...Off (PTO) days 16 holidays that follow the NJ state calendar Generous sick leave 401k with employer match Reports to: NJSACC's Quality Team Director Position Summary NJSACC: New Jersey’s Afterschool and Out-of-School Time (OST) Professional Network works to build...SuggestedFull timeSummer workWork at officeHome officeMonday to FridayFlexible hoursNight shiftWeekday work- ...Global Supplier Quality, External Qc Quality Records Location: Summit, NJ Purpose And Scope Of Position: The Global Supplier Quality, External QC -Vector will process external deviation and change records from our Contract Test Laboratories (CTL). Other duties may...SuggestedContract work
- An established 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...SuggestedContract work
- ...This role involves executing project activities, collaborating with various departments, and ensuring projects are completed within quality metrics and timelines. The ideal candidate will have a strong background in project management, excellent communication skills, and...Suggested
- 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...SuggestedRemote work
- ...departments both orally and in writing (English language required). Quality Operations and Systems Support including deviation management,... ...be considered as all-inclusive. Direct reporting line to the Associate Director of the Global Quality Patient Operations and Apheresis...SuggestedFlexible hours
- ...Self motivated, independent, great communication Experience working cross-functionally Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization,...Suggested
- ...Saturday; 2nd Shift (4p - 2am) Type: Contract Overview The Quality Assurance Label Control (QALC) Labeling Specialist supports the... ...Markets Experience - NYC (Hybrid) Fine Jewelry Quality Assurance Associate New York, NY $50,000.00-$70,000.00 1 week ago New York, NY $90,...SuggestedContract workAfternoon shift
- ...onsite PURPOSE AND SCOPE OF POSITION (Position Summary): The Quality Assurance Specialist position plays a key role in supporting the... ...science or engineering discipline is preferred. Minimum of Associates degree Experience: • 3-5 years of relevant cGMP experience. Experience...Suggested
- Position Summary: The Global Product Quality Specialist will be responsible for managing (and owning as needed) documentation and change controls associated with key deliverables to clinical and commercial documentation across multiple programs. Functional responsibilities...SuggestedWork at office
$34.97 per hour
...possess strong communication and customer service skills, along with experience in the Biopharma industry. The role offers a pay rate of approximately $34.97/hour and is focused on quality assurance within the pharmaceutical manufacturing sector. #J-18808-Ljbffr BCforwardSuggestedContract work- ...Global Product Quality Specialist The Global Product Quality Specialist will be responsible for managing and owning as needed documentation and change controls associated with key deliverables to clinical and commercial documentation across multiple programs. Functional...Suggested
- ...Quality Assurance Specialist The Quality Assurance Specialist position plays a key role in supporting the cGMP quality operations for the Vector External Manufacturing. Primary responsibilities include the review of cGMP controlled documents such as SOPs, specifications...Suggested
- ...interpersonal and organizational skills Understands Regulatory, Quality and Supply Chain aspects of labeling and impact of non-... ...Manufacturing Execution System Participate in change projects and associated deliverables for launches, site transfers, country/area specific...Work at officeLocal areaWeekend work
- ...the writing, review, approval and maintenance of metrics, and associated training Standard Operating Procedures (SOPs) or Work Procedures... ..., with good documentation practices and in compliance with Quality Systems and retention programs. Work independently and perform...Full timeTraineeshipWork experience placementLocal areaRemote work
- ...This position is scheduled for Wed- Sat (1 pm to 11 pm). The Quality Assurance Document Control (QADC) Labeling Specialist supports... ...mindset. REQUIRED COMPETENCIES: Education: Bachelor's degree or Associate's Degree with 3+ Years of Experience in a cGMP/FDA Regulated...Shift work
$70k - $75k
...coordinate product labeling projects and maintain compliance documentation. The ideal candidate will have an associate degree and at least 3 years of experience in quality assurance within a food manufacturing environment. This full-time role offers a base salary between $70...Full time- ...solutions. ECLARO is looking for a QA CTO Label Specialist for our client in Summit, NJ. ECLARO's client is a leader in the biopharmaceutical industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all. ECLARO
- 100% onsite Education: • BA or BS degree; preferred. System experience desired: • Create, execute and/or approve UAT test scripts for system upgrade, bug fixes and enhancements. • Support the creation, review and approval of validation documents. • Contribute to training...Work at office
- ...facilitating governance meetings, and ensuring compliance with cGMP standards. The ideal candidate will have a strong background in quality processes and excellent communication skills, enabling them to effectively report findings and recommendations to management. Join...
- ...of deviation data and summarize information for Annual Product Quality Review and other required reports. Notification to management of... .... Able to effectively multi-task. Education and Experience: Associate degree or higher required, minimum of three years of experience...Work at office
- At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies. As specialists in recognising...Local areaImmediate start
- A leading talent management firm is seeking candidates for a laboratory role in Summit, New Jersey. The responsibilities include assisting with laboratory analysis for clinical release and routine stability testing, conducting analytical experiments and documenting lab ...
- An educational organization located in Westfield, NJ is seeking an OST Program Quality Specialist to enhance the quality and sustainability of out-of-school time programs across New Jersey. This full-time role involves providing technical assistance, conducting training...Full timeFlexible hours
- ...Conference Quality Administrator APN Consulting, Inc. is a progressive IT staffing and services company offering innovative business solutions to improve client business outcomes. We focus on high impact technology solutions in ServiceNow, Fullstack, Cloud & Data, and...Temporary work
APN Consulting
Piscataway, NJ1 day ago - Job Title Education: BA or BS degree; preferred. System experience desired: Create, execute and/or approve UAT test scripts for system upgrade, bug fixes and enhancements. Support the creation, review and approval of validation documents. Contribute to training...
$90.75k
...Quality Improvement Specialist Our team members are the heart of what makes us better. At Hackensack Meridian Health we help our... ...and Grant Funding: Departmental budgets and any grant funding associated with the job position may impact the pay that can be offered....Hourly payFull timePart timeApprenticeshipWork experience placementLocal areaShift workNight shiftWeekend workDay shiftAfternoon shift$25 - $35 per hour
A leading aerospace company is seeking a Quality Specialist to focus on activities within the Material Review Board and corrective action. The role involves assisting with MRB activities, reviewing materials, and supporting audits and investigations. Ideal candidates will...Hourly pay
