Average salary: $54,216 /yearly
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- ...Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the... ...principles. Position Reports to: Jenna Walker - Associate Director, QA Training & Document Control Education: Bachelor's degree or...Suggested
- ...normal business hours) The primary responsibility of the Global QA Patients Operations Specialist is to support the Onboarding and... ...not be considered as all-inclusive. Direct reporting line to the Associate Director of the Global Quality Patient Operations and Apheresis...SuggestedFlexible hours
- ...perspective within a regulated cGMP environment. The primary focus of the QA Specialist role will be to support routine clinical and... ...science or engineering discipline is preferred. Minimum of Associates degree Experience: • 3-5 years of relevant cGMP experience. Experience...Suggested
- A reputable staffing agency is seeking a QA Associate in the Florham Park area (Hybrid). The role involves supporting Quality and Regulatory functions through technical documentation management and product sampling coordination. Ideal for candidates with 1-3 years of QA...SuggestedWork at office
- 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
- 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...Suggested
$30 - $34.96 per hour
We are seeking a QA Label Control Specialist- Pharma (Onsite- Summit, NJ) for a global pharmaceutical client. You will be responsible for supporting site Label Control activities at S-12 in accordance with client’s policies, standards, procedures and Global cGMPs. Functional...SuggestedContract workAfternoon shift- Summary The Specialist QA (CMO) position is an individual contributor role responsible for supporting Supplier Qualification activities... ...industry standards. Knowledge, Skills, and Abilities Education Associate degree or Bachelor's degree in biochemistry, cell biology,...SuggestedFor contractorsWork experience placement
- ...manufactured media. Perform administrative functions for filing and maintenance of records between QA operations and Document Control Center; support cGMP and associated OJT training to QA and other departments to improve "Right the First Time" (RTFT) and high quality...SuggestedImmediate start
- ...powered advice on this job and more exclusive features. Job Title :QA Label Specialist Location : Summit, NJ Hours/Schedule :... ...Markets Experience - NYC (Hybrid) Fine Jewelry Quality Assurance Associate New York, NY $50,000.00-$70,000.00 1 week ago New York, NY $90,0...SuggestedContract workAfternoon shift
- Job Title : QA Associate Location : Florham Park area (Hybrid) Hours / Schedule : 9am - 5pm Type : Direct Hire The QA Associate will support Quality and Regulatory functions by coordinating technical documentation and managing sampling activities (NON-LAB). This associate...SuggestedWork at office
$34.97 per hour
A leading staffing firm is seeking a QA CTO Label Specialist to join their team in Summit, NJ. This contract position demands a Bachelor's degree in Science and a minimum of 1 year of relevant labeling experience in a cGMP/FDA regulated environment. Candidates should possess...SuggestedContract work- A leading biotechnology firm in New Jersey is seeking a Specialist QA (CMO) to support Supplier Qualification activities and Quality Assurance for viral vector manufacturing. The role requires 5+ years of related experience, including quality assurance and compliance,...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
$70k - $75k
...Compliance Specialist to 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...SuggestedFull time- 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... .... REQUIRED COMPETENCIES: Education: Bachelor's degree or Associate's Degree with 3+ Years of Experience in a cGMP/FDA Regulated Environment...Shift work
- A leading technology firm is seeking a Quality Assurance Administrative Associate to support its QA team in Parsippany, NJ. The role requires strong organizational skills, multitasking abilities, and proficiency in regulatory processes. Candidates should have an associate...Hourly payFull timeWork experience placement
- 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...
- An established industry player is seeking a Global QA Patients Operations Specialist to enhance the onboarding and maintenance of Apheresis Centers. This role involves supporting systems and tools, ensuring compliance, and facilitating effective communication with technical...
$55.27 - $68.39 per hour
...Mammography /Xray Tech, Registered QA Specialist Req #: 0000215596 Category: Radiology / Imaging / Radiation Status... ...national patient safety goals and risk reduction procedures and associated policies as applicable to scope of practice Follows through on...Hourly payDaily paidWork experience placementLocal areaFlexible hoursShift workWeekend workWeekday workRWJBarnabas Health
Jersey City, NJ4 days ago- A biotechnology company based in Raritan, New Jersey, is seeking a QA Shop Floor Specialist to join its Quality Operations team. This role involves ensuring quality compliance in the production of CAR-T products for clinical trials and collaboration with manufacturing...Day shift
$75.97k - $99.71k
...immunotherapy in the treatment of multiple myeloma. Role Overview The QA Shop Floor Specialist is an exempt level position responsible... .... Ability to deal with complexity across the drug product, the associated manufacturing process, and the end-to-end supply chain process....Permanent employmentFull timeContract workTemporary workWork experience placementLocal areaImmediate startWorldwideFlexible hoursWeekend workAfternoon shift$70k - $90k
A leading hearing aid company seeks a Quality Assurance Specialist for their Designated Complaint Unit. This hybrid role involves managing and resolving customer complaints, requiring proficiency in complaint handling processes and Microsoft Office tools. Ideal candidates...Work at office- ...with the ability to be on site up to support Quality Reviews and QA Shop Floor manufacturing support. You will manage CMO oversight... ...functions. Coordinates and assists in timely review of documentation associated with manufacturing at CMO site. Assists with preparation for FDA...
- A leading staffing firm is seeking a QA Specialist based in Ridgefield, NJ. This full-time position offers $45/hr for a 12-month contract, with potential for extension. Candidates must have a Bachelor's degree and at least 2 years of experience in the pharmaceutical, biotechnology...Full timeContract work
- A leading medical device company is seeking a Quality Assurance Specialist on a 1-Year Contract in Vierpolders. This full-time position involves maintaining the Quality Management System in compliance with international standards, supporting product and process changes,...Full timeContract work
- A global research organization is seeking a Quality Assurance professional for oversight of its Global Research and Development Department. The role involves planning and conducting facility inspections, issuing audit reports, and ensuring compliance with regulatory guidelines...3 days per week
- A leading biotechnology firm is seeking a Specialist, QA Process Excellence based in Raritan, NJ. This role will provide quality oversight in a cell therapy manufacturing plant, guiding technical operations and ensuring compliance with GMP regulations. The ideal candidate...
- ...this role, you will oversee the quality of goods and services the company provides. You will perform routine inspections, implement QA policies and procedures, and identify workflow issues. The ideal candidate is an excellent verbal and written communicator with strong...Full timeWorldwide
- ...early morning calls with global Team 1-2x per month. Requirements Experience or knowledge with Complaint Handling processes and associated standards and regulations (FDA, ISO 13485, CFR, GMP, etc.) preferred Proficient with Microsoft Office tools (Excel, PowerPoint,...Work at officeLocal areaEarly shift
