Average salary: $62,915 /yearly
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- ...leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of QA Associate – Report Generation. The candidate will be responsible for review and approval of reports generated from laboratory data, such...Suggested
- ...Quality Assurance Document Control Associate Specialist Top skills: 2+ years of document control and reporting experience, Veeva experience preferred, technical troubleshooting, self-motivated, independent, great communication, experience working cross-functionally...Suggested
- ...Hauppauge, NY, operates as part of a global pharmaceutical network. Job Overview Join the Analytical Quality Assurance (AQA) team as a QA Associate II responsible for ensuring compliance across all analytical operations. This role requires strong analytical chemistry...SuggestedFull timeWork at officeRemote workRelocationMonday to FridayShift workSaturdayAfternoon shift
- ...QA Associate The QA Associate is responsible for the rigorous review, verification, and archival of batch records and associated documentation to ensure compliance with internal SOPs, cGMP, and FDA regulations. This role is primarily desk-based and involves close collaboration...SuggestedContract workTemporary workWork at officeMonday to FridayFlexible hoursDay shift
- ...Quality Associate Onsite Role Onsite role Devens, MA--Local Candidates Only Work Schedule: Mon - Fri, 8AM - 5PM EST *May need to adjust hours based on the needs of the business* This position will perform routing testing in support of the Biologics Manufacturing and...SuggestedLocal area
- ...QC Associate The purpose of Quality Control Associate is to update and coordinate the planning, implementation, and supervision of the quality control plan. This includes working with employees as well as outside agencies or consultants involved in inspections and testing...SuggestedFor contractorsFor subcontractorWork at office
- ...Job Title: QA Associate Specialist Document Control Location: Bothell, WA - ONSITE Part of the JUMP Project Initiative Top Skills: # EDMS Experience. Preferably 3-5 years. Systems include VIVA, Master Control, & Documentum etc. # Ability to manage...SuggestedShift work
- Job Opportunity Must Have List: 5+ years of experience with the following: Library Science, MS Office including Word, Adobe, Visio. Document scanning experience, FDA documentation & compliance like 21 CFR Part 11/CGMP. Ability to manage competing priorities, accuracy...SuggestedContract workWeekend work
- ...screen (subject to applicable law) and reading comprehension test. Responsibilities The Quality Assurance Incoming Associate (QAIA) will follow current Good Manufacturing Practices (cGMP) and current Good Documentation Practices (cGDP) to record all procedures...SuggestedWork at officeAfternoon shift
- ...Quality Assurance Document Control Job Title: QA Associate Specialist Document Control Location: Bothell, WA Onsite Apart of the JUMP Project Initiative Top Skills: EDMS Experience. Preferably 3-5 years. Systems include VIVA, Master Control, & Documentum...Suggested
- ...Quality Associate II Shift Schedule is 2100-0730, Wednesday-Saturday The Quality Associate II position plays a key role in supporting the cGMP quality operations for the Bothell Manufacturing Plant (Jump). Primary responsibilities include the review of cGMP controlled...SuggestedShift workSaturday
- ...Job Description Job Description JOB SUMMARY: The QA Associate personnel have the primary responsibility for performing line clearances and quality checks for manufacturing. They are also cross trained in raw material sampling, in-process sampling, finished goods...Suggested
$30 - $33 per hour
...packaged goods (CPG) manufacturer dedicated to delivering high-quality and safe food products. Their team is now looking for a Supplier QA Specialist (Food) . Salary/Hourly Rate: $30/hr - $33/hr Position Overview: The Supplier QA Specialist (Food) will oversee...SuggestedHourly pay- ...needed to contribute to continuous quality improvements. Submit monthly to the Director of Compliance and Accountability via the QA Manager Compliance reports detailing on-site observations and action taken. Prepare monthly narrative report outlining activities,...SuggestedFull timeTemporary workLocal areaMonday to Friday
- ...medical devices, is seeking a Quality Assurance Specialist to join their team. As a Quality Assurance Specialist, you will be part of the QA Department supporting batch release and compliance functions. The ideal candidate will demonstrate attention to detail, proactive...SuggestedPermanent employmentTemporary workWork experience placementWork at officeMonday to FridayShift workSaturday
- ...Microbiology, Environmental Monitoring, Assay validation/transfer, laboratory information and sample logistics and includes all personnel associated with the department i.e. FTE, interns and contractors Develops and executes the QC strategy for the site. Ensures quality...For contractors
- ...you prepared to become a part of a top-tier team and contribute significantly in the life sciences industry? Lonza AG is looking for a QA Manager - Raw Materials Compliance who demonstrates dedication to lead our hard-working team in New Hampshire, USA. This challenging...WorldwideMonday to FridayShift work
- ...record (up to the discretion of the Company; internal only) Preferred Qualifications Beef processing Experience QA or Supervisory Experience Test and hold or Lab experience Bi-lingual (English, Spanish) Please note that this...Seasonal workWork at officeRelocationVisa sponsorshipShift work
$27 - $42 per hour
...sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: At MilliporeSigma, the QA Product Release Specialist will perform a variety of functions according to established protocols to support quality review and...Hourly payWork at office- ...performance, reliability, and quality of complex, mission-critical software tools. The ideal candidate will bring hands-on experience with QA methodologies, automation frameworks, and enterprise web applications in an agile development environment, while also contributing to...Hourly payFull timeContract workTemporary workFor contractorsInterim role
- ...samples to sections, routing results for review, monitoring results and initiating corrective action. ~ Coordinates activities associated with point-of-care (POC) testing program throughout the hospital to include evaluation of equipment, policy development and...Work experience placementWork at office
- ...the world. If that mission has you hungry in more ways than one, you've found the right job posting. The Quality Assurance Associate performs activities associated with quality control of meals. You will be responsible for ensuring the safety of our meals in...
$55k - $65k
Shift: Monday through Friday 8:30am to 5:00pmAre you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and...Full timeWork at officeLocal areaImmediate startMonday to FridayFlexible hoursShift work- The Position Hillsboro Technical Operations (HTO) is a drug product & finished goods manufacturing organization responsible for the reliable delivery of Roche's commercial portfolio & pipeline products. The Quality organization at HTO comprises Quality Assurance, Quality...Local areaRelocation packageShift work
- ...Job Description Quality Assurance and Regulatory Compliance Associate Role Summary The QARC Associate oversees all Quality Assurance... ...regulatory requirements and are consistent with internal QA goals and initiatives. This role is Key Results Area...Local area
$91.1k - $169.1k
...equipment set up, etc.). Who you are: You hold a Bachelor's degree (preferably within the Life Sciences or Engineering) For a QA Specialist, you have at least 5 years of experience in the pharmaceutical industry. For a Senior QA Specialist, you have at least 8...Full timeLocal areaRemote workRelocation package- Position: Quality Assurance Specialist Location: Charleston, SC Shift: 2nd Shift | Monday – Friday | 3:00 PM – 11:00 PM Compensation: $65,000 – $85,000 Benefits: Full Benefits Package | Paid Time Off | 401(k) | Relocation Assistance Available Overview ...Full timeWork at officeRelocation packageMonday to FridayShift workAfternoon shift
- ...programs by ensuring adherence to global GCP standards and regulatory requirements. In this role, you will act as a key Quality Assurance (QA) representative across assigned clinical studies, partnering closely with cross-functional R&D teams. You will also engage with...Contract workRemote workShift work
- ...our website at eliquent.com. We at Eliquent are looking for a QA Calibration Specialist to immediately join our Eliquent... ...related field; or equivalent relevant experience. ~2+ years (Associate) / 5+ years (Specialist) experience in GMP calibration, metrology...Full timePart timeImmediate startFlexible hours
- ...Job Description Job Description QA Investigations Specialist II Job Description Join our quality team to oversee Investigations... ...requirements and storage conditions. Evaluate processes associated with sample management to identify gaps and implement improvements...Temporary work