Pharma Manufacturing QA
773 open positions
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Senior Quality Manager↗ TFS HealthScienceMadrid, Community of Madrid, Spain 1mo Ensures functional and project-level quality oversight for clinical research projects, ensuring compliance with GCP and GxP regulations.
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Manager, Manufacturing Product Quality (Small Molecule)↗ OtsukaRemote, US $108k–$108k1mo Ensuring GMP compliance in the manufacturing, packaging, labeling, and distribution of commercial and clinical trial materials across global operations.
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?QA Specialist-35619↗ Juncos, PR, US 1mo QA Specialist supporting site Quality Assurance program with minimal supervision in a highly regulated biopharmaceutical environment.
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Associate Director, Program Quality Management↗ FujifilmHolly Springs, NC, US 1mo Building and sustaining quality relationships with partners to ensure unprecedented delivery of biopharmaceutical programs from initial discussions through end-of-program review.
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QA Associate - Eurofins BioPharma Product Testing Toronto, Inc. EurofinsToronto, ON, ca 1mo Provide documentation and technical support for designated clients, ensuring product quality and GMP compliance.
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Quality Assurance Manager AbbVieCincinnati, OH, us 1mo Provide quality assurance support for pharmaceutical, medical device, and biologics manufacturing processes, ensuring compliance from raw material inspection to final shipment.
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Associate Director/Director, Technical Quality↗ Solid BiosciencesRemote $190k–$190k1mo Provide strategic and operational leadership over external parties to ensure outsourced manufacturing, testing, packaging, and distribution activities comply with global cGMP, GDP, and regulatory requirements for gene therapy candidates.
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Principal Auditor, QA *GCP Exp Required↗ Syneos HealthBuenos Aires, B, AR 1mo Conduct audits to assess compliance with GCP regulations, company policies, and SOPs for clinical trials; host/support customer audits and regulatory inspections.
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Associate Supervisor, Quality MenashaEdison, New Jersey 1mo Oversee compliance for material movement, storage, reconciliation, segregation, quarantine, destruction, and issuance to production while ensuring finished goods meet customer requirements and cGMP regulations.
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Dir, Project Management MsdCHN - Beijing - Beijing (Wangjing Park) 1mo Lead global project management for late-stage pipeline programs and commercial product lifecycle, specifically focusing on establishing and maintaining robust local testing programs for biologics and vaccines in China.
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QA Supervisor (1 Day Shift & 2 Night Shift Positions)↗ Thermo Fisher ScientificGreenville, NC, US 1mo Lead and develop a team of quality professionals while overseeing quality operations including batch record review, quality monitoring, and continuous improvement initiatives in a pharmaceutical manufacturing environment.
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Associate Director Clinical Quality Assurance and GxP Compliance↗ UltragenyxNovato, CA, US 1mo Strategic leadership for clinical quality assurance strategies, GxP compliance, and inspection readiness for rare disease medicine programs.
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Director Failure Investigation DanaherLodi, California, United States $160k–$160k1mo Leading failure investigation strategy, execution, and continuous improvement in a high-volume, regulated manufacturing environment to ensure compliant root cause analysis and product quality.
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Senior Manager, GxP Computerized Systems Auditing↗ Beone MedicinesRemote, US $137k–$137k1mo Manage and execute a risk-based audit program for GxP-regulated computerized systems, providing independent quality oversight across the system lifecycle.
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Quality Assurance Manager↗ Siegfried (usa), IncPennsville, NJ, US $105k–$135k1mo Manage all aspects of Quality Assurance, supervise QA specialists, and ensure GMP compliance for pharmaceutical product releases and regulatory inspections.
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QA Associate - Eurofins BioPharma Product Testing Toronto, Inc.↗ Eurofins Canada BiopharmaToronto, ON, CA 1mo Provide documentation and technical support for designated clients in a GMP environment, ensuring product quality and compliance.
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サPrincipal Auditor, QA *GCP Exp Required↗ サイネオス・ヘルスBuenos Aires, B, AR 1mo Conduct audits to assess compliance with GCP regulations, company policies, and SOPs for clinical trials; host customer audits and regulatory inspections.
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QA Compliance Specialist - LSA LonzaUS - Portsmouth, NH 1mo Ensures adherence to GMP regulations and internal quality standards by supporting Quality Systems and Compliance programs.
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QA Compliance Specialist↗ Bora PharmaceuticalsMississauga, ON, CA $68k–$85k1mo QA support for new project transfers into Bora, ensuring GMP compliance and client regulatory requirements for complex pharmaceutical products.
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QA Operations Supervisor↗ AbzenaSan Diego, CA, US 1mo Lead Quality oversight activities and foster a culture of quality across biologics manufacturing processes including cell culture, fermentation, harvest, purification, and bulk drug substance.
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Senior Specialist, Quality Training (Contract) 4dmoleculartherapeuticsRemote $0k–$0k1mo Manage GxP training governance, LMS administration, and compliance for a biotech company's quality training program.
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Specialist/Senior Specialist, Quality Assurance↗ Protagonist TherapeuticsNewark, CA, US $130k–$160k1mo Perform Quality Assurance activities to ensure GMP manufacturing compliance for biopharmaceutical peptide therapeutics.
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Senior Analyst, Quality Assurance (Analytical)↗ Insmed IncorporatedSan Diego, CA, US $100k–$127k1mo Provide Quality Assurance oversight of internal and external Quality Control laboratory operations for Gene Therapy programs to ensure compliance with cGMP regulations and global health authority guidelines.
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VP Quality↗ Atomvie Global Radiopharma Inc.Hamilton, ON, CA 1mo Ensuring product quality and safety for clinical and commercial radiopharmaceuticals while driving GMP compliance and operational culture.
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?QA and Auditing Lead↗ Remote, US 1mo Lead quality management systems, audits, investigations, and regulatory compliance for a fast-growing nutraceutical company.
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Healthcare QA/RA Specialist↗ UPSBurlington, ON, CA $55k–$55k1mo Manage Canadian regulatory reviews, licensing, transportation deviation programs, supplier qualifications, and documentation for healthcare logistics operations.
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Senior Manager/Associate Director, Quality Control↗ Xenon Pharmaceuticals Inc.Burnaby, BC, CA 1mo Lead Quality Control activities for clinical and commercial drug substance and drug product programs, ensuring compliance with ICH and cGMP requirements.
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Químico de Documentación y Liberación↗ Camber PharmaValle de Cuernavaca, MOR, MX $156k–$156k1mo Ensuring the integrity and compliance of finished product and API analytical files with Quality Management System requirements and applicable regulations prior to release.
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QA System Supervisor↗ ChemoLeón, Castilla and Leon, Spain 1mo Supervise quality systems and compliance for sterile injectable products, leading teams in managing deviations, CAPA, audits, and validation plans.
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QA Auditor (Sao Paulo)↗ TransPerfectSão Paulo, SP, BR 1mo Ensures adherence to international and local statutory/regulatory frameworks and quality standards (ISO 9001, ISO 17100, GxP) within TransPerfect's Global Quality Management System.
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Senior Manager, GMP Quality↗ Simulstat IncRemote 1mo Lead sponsor-side QA oversight of CMOs across pre-clinical, clinical, and commercial manufacturing for drug substance, drug product, and final product.
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Compliance Specialist III ThermofisherFlorence, South Carolina, USA 1mo Establishes and maintains quality systems for investigational new drugs, biologics, and medical devices to ensure regulatory and customer compliance.
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Assistant Manager, Quality Operation↗ Kiss ProductsEllabell, GA, US $31k–$98k1mo Support and maintain Quality Assurance (QA) and Quality Control (QC) systems to ensure products meet company standards, customer requirements, and regulatory requirements.
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?Associate Director, Quality Assurance and Compliance↗ Weston, FL, US 1mo Provides QA and compliance leadership to ensure adherence to cGLP/cGMP and regulatory requirements across R&D and manufacturing projects.
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Quality Specialist↗ CSL PlasmaNewark, DE, US 1mo Monitor plasma center processes to ensure compliance with operating procedures, local/state/federal regulations, and quality standards.
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Quality Assurance Line Auditor↗ Gh Manufacturing.ComBelleville, ON, CA $38k–$38k1mo Perform regular audits of production lines, finished products, and production components to verify conformance with quality and GMP standards.
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Quality Assurance Lead↗ Massco DentalRogers, AR, US $55k–$55k1mo Oversee quality systems and execution on the manufacturing production floor, ensuring compliance with GMP standards and maintaining audit-ready documentation.
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Sr Quality Specialist↗ Endo International PLCRaleigh, NC, US 1mo Ensures product release and maintains quality metrics for a pharmaceutical manufacturing site, supporting GMP compliance, audits, and customer inquiries.
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