Quality Control Specialist
MEDVACON Life Sciences
MEDVACON Life Sciences works with many leading pharmaceutical companies to hire FTE for projects & assignments in cGMP Quality, Compliance, Validation and CSV work. We currently have several W2 (FTE)Quality Control positions open with our gene therapy client in Lexington, MA. We cannot work with agencies on c/c on these opportunities. Job Description QC Analyst - Method Validation QC Analyst (2nd Shift) QC Sample Management Tech (2nd Shift) QC Supervisor/Manger (2nd Shift) QC LIMS Admin QC Planner Please apply if you think you would make a strong candidate for one of these positions. Qualifications MUST HAVE previous GMP experience!! MUST HAVE authorization to work in the US. No Visa sponsorships at this time. Additional Information 1099 CONTRACT CANDIDATES ONLY!!! NO C2C/CONSULTANTS!!! #J-18808-Ljbffr
- ...Doyon Technical Services (DTS), a subsidiary of Doyon Government Group, is seeking an early-career Quality Control Specialist to support the Quality Control Manager and Project Manager on federal construction projects. You will assist with implementing the project Quality...SuggestedContract work
- ..., and renovation/repair solutions at a wide variety of facilities for federal agencies. This position is an early-career Quality Control Specialist to support the Quality Control Manager and Project Manager in administering project-level quality control and project documentation...SuggestedContract work
$95k - $105k
...accommodation or an alternative application process. Senior Quality Systems Specialist 4 days ago Requisition ID: 1206 Salary Range: $95,000.00... ...reactive issue handling toward more consistent, scalable process control by building better structure, stronger records, and more...SuggestedWorldwide- ...Bicara Therapeutics, based in Boston, is seeking a Senior QA Specialist focused on GxP Document Control. The role includes leading the management and organization of the Quality Management System (QMS), ensuring quality documentation is maintained according to GxP requirements...Suggested
- ...Position Overview Bicara Therapeutics is seeking a Senior QA Specialist, GxP Document Control and Quality Systems to support the administration, organization, and continuous improvement of the Quality Management System (QMS). This role reports to the Sr. Director, GxP...SuggestedLocal areaRemote work3 days per week
- ...providing and communicating results, maintaining/operating specialized equipment, and initiating and/or implementing changes in controlled documents. Must learn and comply with safety guidelines, GLP, and cGMPs/CFRs which includes, but is not limited to, the maintenance...Work experience placementInternship
$76.44k
...Duties: • Develop, implement, and maintain the project-specific Quality Assurance Surveillance Plan (QASP) in compliance with Federal... ...standards. • Oversee construction contractor’s Quality Control meetings (Preparatory, Initial, and Follow-Up) with project stakeholders...Contract workFor contractorsWork experience placementFor subcontractorH1bImmediate startFlexible hours- ...biopharma industry with the high‑velocity, high‑quality, data‑driven development solutions... ...in an innovative way. Quality Assurance Specialist Dash Bio is seeking a detail‑oriented... ...Management System (QMS) activities: document control, logging and tracking CAPAs, deviations,...
$76.44k - $159.43k
...Description Develop, implement, and maintain the project‑specific Quality Assurance Surveillance Plan (QASP) in compliance with Federal... ...required standards. Oversee construction contractor’s Quality Control meetings (Preparatory, Initial, and Follow‑Up) with project stakeholders...Contract workFor contractorsFor subcontractorH1bFlexible hours$27 - $32 per hour
...Description Support all quality control efforts for raw materials for in‑process manufacturing. Follow SOP requirements. Release approved raw materials for testing. Perform OOS investigations for all rejected materials. Follow all documents and ensure to author and revise...Contract workTemporary workInternshipWork at office- ...Groe Advisors LLC is seeking a documentation specialist to manage Quality documentation within a medical device environment. The role focuses on filing, scanning, and ensuring immediate availability of critical records. Responsibilities include MasterControl and DocStar...Immediate start
- ...exemplify professional, respectful, and inclusive behavior in all interactions. Actively participates in and, at times, leads departmental quality initiatives. Assumes responsibility for designated tasks as assigned. Incumbent periodically works clinically as assigned and...Immediate start
- ...Seeking a detail-oriented Associate II, Analytical Development/Quality Control professional to support analytical testing, method development, and quality control activities within a regulated pharmaceutical or biotech environment. This role is responsible for executing...
$50 - $55 per hour
...Software Guidance & Assistance, Inc., (SGA), is searching for a Quality Assurance Specialist for a contract assignment with one of our premier BioTech... ..., original and above all, accurate. Review IT change control documents including risk analysis, IQ, OQ, URS and other software...Full timeContract workFor subcontractorCasual workShift work- ...We are seeking an experienced Quality Engineering & Validation Consultant to provide GMP Quality oversight in support of manufacturing... ...production. Review and approve quality documentation, including change controls, validation protocols, risk assessments, investigations, and...
$20.52 per hour
...Overview NYCOA seeks bright, detail-oriented, and highly organized Quality Assurance Lab Technicians for their team in Manchester, New Hampshire . The Lead Lab Technician will follow all quality control procedures for inspecting incoming raw materials and testing of finished...Hourly payMonday to FridayShift workNight shiftWeekend workDay shift$98.5k - $109.1k
...and experience as an auditor and compliance specialist. The QA/QI Specialist is responsible assisting in the monitoring for quality to ensure that systems are appropriate,... ...toxicities data Review manufacturing and quality control records. Document deviations / omissions...Flexible hoursShift workWeekend work$59.6k - $84k
...Duties & Responsibilities Responsible for activities involving quality assurance and compliance with applicable regulatory... ...duties on projects to meet necessary deadlines Ensures quality control procedures for operational processes are performed Validates...For contractorsWork experience placementH1bLocal area$77k - $86k
...Job Summary The Quality Assurance (QA) Specialist supports the effectiveness, compliance, and continual improvement of the Quality Management System... ...of findings and actions Initiate, revise, and review controlled documents including SOPs, work instructions, forms, and...Work at officeLocal area- ...BIOCYTOGEN seeks a detail‑oriented Quality Associate to support QA and facility compliance in a non‑GLP, research‑focused environment... ...quality deliverables for clients. The role emphasizes document control, data governance, and support for CAPAs, deviations, audits, and...
- ...of our volunteers. Each match is supported by clinical match specialists who ensure that the needs of the entire family are met. The Clinical... ...with strong interpersonal skills. A strong commitment to quality and results. Strong computer skills: proficiency in Microsoft...Full timeWork at officeRemote workFlexible hoursNight shiftWeekend workAfternoon shift
- ...Support Clinical Quality operations to ensure compliance of clinical studies, vendor management, and inspection readiness in accordance... ...requirements. Support the processing of audit reports, change controls, deviations, and audit plans. Support the Clinical Quality team...
- ...Environmental Monitoring, you will play a critical role in ensuring GMP compliance by performing environmental monitoring and quality control testing that supports the production of high-quality therapeutics. Working within a collaborative Quality Unit, you'll partner...Permanent employmentFull timeContract work
$28 - $29 per hour
...pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $28.00/hr - $29.00/hr Quality Control (QC) Analyst - Release Testing/Environmental Monitoring Overview Be a key part of a team that ensures safe, effective pharmaceutical...Full timeWork at office$80k - $90k
...About The Role We are seeking a detail-oriented and highly motivated QC Analyst II to join our growing Quality Control team. This role is responsible for supporting early-phase development through commercial manufacturing activities within a GMP-regulated environment....Contract workWorldwide$61.5k - $83.3k
...Overview The Quality Control Analyst I in support of QC Raw Materials/Sample Management (QC-RMSM) plays a crucial role in sample management operations for our internal and external GMP laboratories. This role ensures high standards of quality and compliance are met in...Full timeTemporary workLocal areaFlexible hoursShift work- ...Overview QC Analyst II to join the Quality Control team in a GMP-regulated environment. This role supports early-phase development through to commercial manufacturing activities. The QC Analyst II will perform a variety of analytical and microbiological testing activities...Contract work
- ...Vertex Pharmaceuticals Incorporated is seeking a GMP Quality Operations Manager to lead quality assurance efforts for Cell and Gene Therapy manufacturing operations. In this role, you will drive and support product disposition activities, ensure compliance, and implement...
$35 - $40 per hour
...Quality Control (QC) Microbiology Analyst About the Role We are seeking a Quality Control (QC) Microbiology Analyst to join a growing quality team supporting cGMP manufacturing operations. This role is responsible for performing routine microbiological and molecular...Contract workTemporary workMonday to FridayWeekend work- ...A leading staffing agency in New Hampshire seeks a Quality Control (QC) Analyst to support testing in a fast-paced pharmaceutical environment. You will perform critical quality checks and documentation to ensure compliance with GMP standards. Ideal candidates have a degree...Full time
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