Associate Director, GMP Quality & Regulatory Oversight
Beam Therapeutics Inc.
Beam Therapeutics Inc. seeks an Associate Director of Product Quality Assurance to lead phase-appropriate quality oversight of GMP operations, including internal testing and external manufacturing partners. The role drives risk management, investigations and release activities to support Beam’s transition from discovery to clinical development and commercial launch. The incumbent will oversee analytical method validation, vendor relationships, and ensure compliance with global cGMP standards #J-18808-Ljbffr Beam Therapeutics Inc.
$94.6k - $141.8k
Job DescriptionGeneral Summary:The Associate Director, GMP Operational Quality Assurance is a Quality leader and... ...strategic and operational Quality oversight across multiple complex programs.... ...patient safety, product quality, regulatory expectations, and business continuity...RegulatoryFull timeContract workSummer workRemote workFlexible hours2 days per week$156.6k - $234.8k
Job DescriptionGeneral Summary:The Associate Director, GMP Operational Quality is responsible for oversight of team activities, development of personnel and ensuring... ...with corporate goals and compliance with all regulatory requirements, refining goals and projects when...RegulatoryFull timeWork experience placementSummer workRemote workFlexible hours2 days per week$94.6k - $141.8k
...Vertex Pharmaceuticals seeks an Associate Director of GMP Operational Quality to lead quality oversight across biologics and device programs. The role manages complex... ...initiatives, deviation investigations, and regulatory compliance while partnering with cross-functional...RegulatoryContract work$156.6k - $234.8k
...Associate Director overseeing GMP operational quality for cell and genetic therapies at a rare disease-focused pharmaceutical... ...team, managing compliance with regulatory requirements, and developing... ...Lead quality team providing oversight and support to GMP business activities...RegulatoryWork experience placement$185k - $225k
...Overview:We are seeking an Associate Director, Quality Control to lead the Beam Massachusetts... ...sound, and timely GMP testing while maintaining a... ...ready for GMP use and regulatory inspection. Additionally, the... ...Provide direct leadership and oversight for QC staff performing...RegulatoryFull time$135.46k - $203.19k
Job Title: Associate Director, External QualityLocation: Boston... ...It is brand new and GMP compliant to meet the... ...Role:AD, External Quality - Radio Conjugates is... ...for end-to-end Quality oversight of external manufacturing... ...of effectiveness.Regulatory Readiness: Ensure partners...RegulatoryFull timeContract workTemporary work$185k - $225k
...diseases.Position Overview:The Associate Director of Product Quality Assurance (PQA) will be... ...appropriate quality oversight of internal and external... ...aspects of Quality support for GMP operations. Quality... ...Experience interacting with regulatory health authorities at pre...RegulatoryFull timeContract workWorldwide$172k - $202k
...resourceful, and enthusiastic quality control lead excited... ...will support CDMO to oversight the AD&QC aspect of... ..., and applicable regulatory guidelines. You will support... ...also support CDMO on GMP commercial... ...attributes and developing associated limits/specifications....RegulatoryWork at officeLocal areaRemote work1 day per week$158.8k - $238.2k
...DescriptionGeneral Summary:The Associate Director, QC Technical Services... ...group responsible for GMP release and stability... ...and operational oversight for QC activities,... ...operational oversight of quality event management, stability execution, regulatory support, and cross-...RegulatoryFull timeContract workSummer workRemote workFlexible hours2 days per week- ...Beam Therapeutics seeks an Associate Director to lead quality control operations at its... ...role involves overseeing GMP testing execution, laboratory... ...testing Provide direct oversight of QC staff and support... ...testing, method validation, and regulatory compliance standards...Regulatory
$171k - $192k
...The Opportunity The Quality Operations team is expanding... ...looking to hire an Associate Director of Quality Control... ...and CAPA oversight Provide oversight of... ...and coordination with Regulatory Affairs and external... ...supporting commercial GMP products is required....RegulatoryContract workLocal areaRemote work- ...Beam Therapeutics seeks an Associate Director of Product Quality Assurance to oversee... ...testing partners, ensures GMP compliance, and directs quality... ...Provide quality oversight for internal analytical testing... ...corrective actions, and regulatory compliance activities...RegulatoryContract work
$158.8k - $238.2k
...Associate Director leading technical services for GMP release and stability testing at external laboratories... ...compliance with quality standards, oversees... ...strategic and operational oversight of GMP release and stability... ..., supply management, regulatory affairs, and quality...RegulatoryContract work$210k - $290k
The Role: The Senior Director, GMP Quality will build/support and maintain fit... ...independent quality oversight of contract development and... ...processes meet applicable regulatory, GxP, and company requirements... ...uncertainty, time, and cost associated with developing protein-based...RegulatoryContract workFor contractorsShift work$190k - $230k
...Description Job Description Associate Director/Director, Technical Quality – Solid Biosciences... ...global cGMP, GDP, and regulatory requirements. This... ...Responsibilities CDMO/CTL Oversight Negotiate, execute,... ...and analytics, CDMO GMP manufacture, CTL testing...RegulatoryTemporary workRemote workFlexible hours- ...Senior Director of GMP Quality will establish and maintain quality systems, provide oversight of manufacturing partners and testing laboratories, and ensure regulatory compliance. This hands-on leadership role partners with cross-functional teams from development through...RegulatoryContract work
$155k - $225k
...Overview: The Senior Manager / Associate Director of Clinical Quality Assurance (CQA) will provide... ...qualification and ongoing quality oversight of CROs and other clinical service... ...investigator brochures, CSRs, and regulatory submission documents as requested....RegulatoryFull time$159.8k - $239.8k
Job DescriptionThe Associate Director of GMP Operational Quality Assurance is an advanced technical resource and... ...principles and application of quality and regulatory compliance. The individual adapts... ...Assurance is responsible for oversight of multiple Validation projects...RegulatoryFull timeContract workWork experience placementSummer work- ...targets.Reporting to the Director, Quality Operations, the Associate Director, Quality Operations will lead quality oversight of Viridian’s external manufacturing... ...readiness, and ongoing GMP readiness across EU and... ...readinessAssist with regulatory inspections and internal...RegulatoryWork at officeLocal areaImmediate startRemote work
- Role: Associate Director, Clinical QA, providing hands-on quality oversight of biopharma's clinical and nonclinical programs to ensure compliance with GCP, GLP, and... ...track audit findings and quality metrics assist in regulatory submissions and agency inspections Requirements...Regulatory
$155k - $214k
About This Role:As the Associate Director, Global Quality Risk Management, you will be at the forefront of... ...in aligning with ICH Q9 and global regulatory expectations. Reporting to the Director... ...PhD) preferred.At least 10 years of GMP and Quality experience, including 5+...RegulatoryFull timeTemporary workLocal area- ...Pharmaceuticals, Inc. is seeking an Associate Director of Quality Control to lead commercial QC operations... ...collaboration across Manufacturing, Regulatory Affairs, and QA to ensure timely... ...leadership experience, strong knowledge of GMP and regulatory expectations, and the...Regulatory
$116k - $174k
...This role will report to the Director of Quality and operate across... ...Quality Assurance, will provide GMP QA oversight for Tango’s CMC... ...with Technical Operations, Regulatory, and external manufacturing... ...strategic GMP QA activities associated with Tango CMC development...RegulatoryContract work- ...Description Job Description The Associate Director, Quality Systems leads the strategy, design and... ...appropriate, scalable and compliant with regulatory expectations. The Associate... ...years of Quality experience working in a GMP biotechnology manufacturing...RegulatoryWork at officeMonday to Friday3 days per week
- ...Beam Therapeutics seeks a Senior Manager/Associate Director of Clinical Quality Assurance to lead vendor qualification and oversight for clinical service providers, manage audit... ...assigned studies including protocol and regulatory document reviews Requirements ~...Regulatory
$190k - $220k
Position Summary: The Associate Director, Clinical QA will provide hands‑on quality oversight of Korro Bio's clinical and nonclinical programs, ensuring that studies... ...and nonclinical quality components of regulatory submissions and health authority interactions....RegulatoryContract work$160.6k - $240.8k
...DescriptionGeneral Summary:The Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality assurance oversight of clinical trial operations and... ...assigned disease areas to drive compliance with regulatory requirements to ensure the protection of...RegulatoryFull timeWork experience placementSummer workWork at officeRemote workFlexible hours2 days per week$160k - $195k
...LinkedIn and Facebook.Role Summary:The Associate Director, Quality Management Systems is a key member of... ...risk-based, and aligned with global regulatory expectations. The Associate Director... ...with exposure across GxPs (GCP, GLP, GMP, GVP preferred) Demonstrated experience...RegulatoryLocal area- ...Associate Director role overseeing clinical trial quality assurance and GCP compliance across assigned disease areas. The position involves... ...strategic GCP quality compliance oversight of assigned studies to ensure regulatory adherence and participant safety Develop...RegulatoryWork at office
$147.5k - $221.3k
Job DescriptionGeneral Summary:The Associate Director, CMC Quality Compliance and Inspection Readiness, is responsible for inspection readiness... ...and governance forumsKnowledge and Skills:Knowledge of regulatory requirements and inspection expectations globallyExperience...RegulatoryFull timeSummer workRemote workFlexible hours2 days per week
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