Average salary: $46,292 /yearly
More statsGet new jobs by email
- A biopharmaceutical innovator in Boston seeks a Senior Manager/Associate Director, Clinical Quality Assurance. You will oversee quality assurance processes for clinical development, ensuring compliance with pharmacovigilance and good clinical practices. The ideal candidate...SuggestedFull time
- ...Job Description Job Title: Embedded QA Engineer Location: Westford, MA Job Type: Full-Time Overview: We are seeking an experienced Embedded QA Engineer to join our agile sprint team in Westford. The ideal candidate will be responsible for hands-on testing...SuggestedFull time
- ...written description as well as digital photographs as necessary Enter information into the ERP system to transfer materials from the QA Inspection area. Recommend and implement inspection and receiving related procedural improvement. Recommendations to improve...SuggestedHourly payFull timeRelocation
$110.18k - $119.21k
...and verify implementation of rework. You'll also perform audits, determine and manage the handling of "returned products", and author QA processing documentation. We'll rely on you to determine and evaluate root causes and corrective actions. What You'll Experience...SuggestedFlexible hours$70 - $75 per hour
...compliance with global GxP regulations (21 CFR, EU Annex 1, ISO 13485) Partner with Manufacturing, Supply Chain, Regulatory, and QA for launch execution Provide supplier and CMO quality oversight , including readiness and inspections Qualifications ~8+ years...SuggestedHourly payContract work$110.18k - $119.21k
..., and verify implementation of rework. Youll also perform audits, determine and manage the handling of returned products, and author QA processing documentation. Well rely on you to determine and evaluate root causes and corrective actions. What youll experience:...SuggestedFlexible hours$242.3k - $270k
...it the right way. What Youll Own Quality Operations Leadership: Manage the end-to-end lifecycle of GxP systems across QA, Clinical Ops, CMC, and Research, ensuring full compliance with 21 CFR Part 11 and modern industry standards. Vendor Oversight & Auditing...SuggestedRemote work3 days per week$105.33k - $127.64k
...readiness for regulatory inspections and interact with inspectors in response to requests as required. # Collaborate within the Supplier QA team, cross-functionally, and with Global Process Owners to continuously improve processes, innovate, and contribute to predictive...SuggestedHourly payFull timeTemporary workPart timeFor contractorsWork experience placementSummer workWork at officeLocal areaRemote workFlexible hoursShift work- ...individual will provide support to all functions reporting through the Quality Disposition organization, including incoming materials QA and disposition, systems, drug product disposition, and Material Review Board. This individual will provide oversight of projects...Suggested
$100.48k - $121.76k
...Manager, Shop Floor QA, Cell Therapy Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in...SuggestedWork experience placementInterim roleLocal areaRemote workMonday to FridayFlexible hoursShift work- ...standards, and support the lifecycle management of biologics and combination products. Candidates should possess substantial experience in QA leadership and analytical method development, along with strong communication skills for cross-functional collaboration. This...SuggestedContract work
$105k - $121.5k
...of the COO. Support corrective action plans and escalate findings to leadership for review and approval. Quality Coordinates QA/PI activities including patient experience surveys and reviews, clinical quality measure satisfaction (UDS measures, HEDIS measures,...SuggestedFull timePart timeLocal area2 days per week$146.96k - $219.65k
...Bachelor's degree in Chemistry, Biology or other Physical Sciences Ten years of combined and/or pharmaceutical manufacturing, QA or QC assurance roles managing and directing quality oversight of commercial and development controlled substances. Seven years of...SuggestedContract workTemporary workLocal areaFlexible hours- ...Quality Assurance systems both within company and external vendors. The Director will execute and/or ensure proper oversight of the GCP QA audit program management, clinical operations phase 1 to phase 4 study team support, regulatory inspections, and GCP QA...SuggestedFor contractorsLocal area
- Job Description As the Quality Lab Manager, you will be at the forefront of our commitment to excellence. You will lead a talented team of Quality Technicians and Mechanical Inspectors in ensuring that all products meet rigorous quality standards, and you will play...Suggested
- ...Kitting, the Franklin Distribution Center (GDC) and NPI (New Product Introduction), calibration activities within Milford and the Milford QA Laboratory. The role will also be responsible for critical Quality activity as it relates to new product transfers to Singapore. This...Contract workLocal area
- ...each expected to provide the foundation for expansion into additional opportunities. Prime Medicine is seeking a Quality Assurance (QA) Director to serve as the company's primary quality assurance expert across both clinical and nonclinical programs. This contractor...For contractors2 days per week3 days per week
$163k - $200k
...Cambridge, US; Gaithersburg, US; New Jersey, US | full time | Job ID: 9893 Responsibilities The Associate Director Clinical QA Compliance supports and oversees the proactive and risk-based Quality Strategy implementation in the clinical development activities,...Hourly payFull timeRemote workWorldwide$40 - $50 per hour
Job Description About Atrium: What you do matters . As a people-centric organization, we foster an environment of collaboration, high performance, and innovation where your talents are valued and your achievements are celebrated. Join us and become part of an inclusive...Hourly payWork at officeShift work$160k - $200k
...and applicable regulations governing clinical data Provide training and guidance to cross-functional teams on GCP/GVP regulations, QA procedures, and audit protocols Serve as a subject matter expert on GCP/GVP quality assurance matters Participate in the...Full timeLocal areaFlexible hours3 days per week$171.5k - $210k
...Collaborate with Clinical Operations, Technical Operations teams and CRO counterparts as needed, including participation in study team and QA meetings Support Quality Management in inspection readiness activities and collaborate with study and functional area teams as...Local area- Job Description A recognized pharma company is actively seeking a new Quality Control (QC) Analyst for a great entry-level position with their QC Bioassay group. In this role, the QC Analyst will be trained to perform cell-based bioassays, ELISAs, and other biological...Internship
- We are currently offering a $8,500 sign on bonus for new, full-time hires. Schedule: 11pm-7:30am Position Summary: The QA is responsible for reviewing assembled trays for accuracy of instrumentation according to the pick sheet as well as instrument placement,...Full timeImmediate startRelocation packageFlexible hoursNight shift
$170k - $206k
...compliance oversight utilizing proactive endtoend strategies for pre and postmarketing Pharmacovigilance activities and will provide QA GCP support to assigned clinical development programs. The incumbent may also be responsible for supporting relevant processes and programs...Full timeSummer holidayWork at officeHome office- ...regulated life sciences materials. Train large language models (LLMs) with Spanish linguistic data to enhance AI-driven translation, QA, and automation workflows. Translate, review, and edit Spanish content in active projects, ensuring accuracy, clarity, and...Full timeWork at officeRemote work
- A leading biopharmaceutical company in Boston, MA is seeking a Head of Global Research Quality (Sr Director) to oversee the strategic direction of Research Quality. The ideal candidate will possess at least 12 years of experience in the biopharma industry, with a strong...Full time
$137k - $246.6k
A leading research organization is seeking a Research Lead in Boston, MA, to direct significant AI cyber testing initiatives. This role involves managing technical research, overseeing complex projects, and leading a multidisciplinary team of experts. Candidates should...Full time- ...company is seeking a Vice President of Global Quality Assurance and Regulatory Affairs in Boston. The successful candidate will lead QA/RA efforts, ensuring compliance with FDA and international standards while collaborating with teams across the organization. Candidates...Full time
- A global healthcare company is seeking a Vice President of Global Quality Assurance and Regulatory Affairs. This critical leadership role involves shaping and executing quality and regulatory strategies, ensuring compliance with global standards, and driving continuous...Full time
$251.5k - $339.86k
...Overview We are seeking a dynamic and experienced Vice President of Global Quality Assurance and Regulatory Affairs to lead our global QA/RA organization. This executive will be responsible for shaping and executing the companys quality and regulatory strategy, ensuring...Full timeTemporary workSummer workLocal areaWorldwideFlexible hours








