Associate Director, GMP Quality—CGT & Personalized Medicine
Scorpion Therapeutics
Scorpion Therapeutics is seeking a senior Quality leader to design and execute robust quality systems across programs. You will align QMS strategy with cross-functional teams to drive improvements and ensure regulatory compliance. You will oversee APQR/QPQA, data integrity, change control, CAPA, and audits while guiding risk management and quality culture. Travel up to 15% may be required. #J-18808-Ljbffr Scorpion Therapeutics
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Associate Director, GMP Quality—CGT & Personalized Medicine in Boston, MA vacancy
$148k - $222k
...strategic design and tactical execution of quality systems, risk management, and quality... ...regulatory requirements, and monitor/support CGT quality risk management items; identify and... ...Knowledge/Skills Deep expertise in global GMP regulations/guidances and GxP QMS; strong...SuggestedLocal area- Vertex Inc. is seeking a Senior Director of CGT Quality Systems to provide strategic quality leadership for personalized medicine and advanced cell therapies across the patient journey. The role partners with Global Quality, Manufacturing, MS&T, Regulatory, Commercial,...Suggested
$156.6k - $234.8k
...Job DescriptionGeneral Summary:The Associate Director, GMP Operational Quality is responsible for oversight of team activities, development of personnel... ...expectations, planning, coaching, training and developing personal growth opportunities through IDPs.Accountable to...SuggestedFull timeWork experience placementSummer workRemote workFlexible hoursDay shift2 days per week$94.6k - $141.8k
Job DescriptionGeneral Summary:The Associate Director, GMP Operational Quality Assurance is a Quality leader and advanced technical resource responsible... ...employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age...SuggestedFull timeContract workSummer workRemote workFlexible hours2 days per week$180.8k - $271.2k
Job Description General/Position Summary The Senior Director, CGT Quality Systems, Personalized Medicine provides strategic Quality leadership for personalized... ...the end to end patient CGT treatment journey assuring GMP requests are assessed, governed, documented,...SuggestedSummer workRemote workFlexible hours2 days per week$172k - $202k
...establishing a new class of medicines that engage... ...resourceful, and enthusiastic quality control lead excited... ...also support CDMO on GMP commercial manufacturing... ...and developing associated limits/specifications.... ...otherwise process, your Personal Information. Please reference...Work at officeLocal areaRemote work1 day per week$160k - $180k
Associate Director, GMP Quality Batch disposition/release for Clinical Trial Materials and Commercial batches Technical review, quality oversight,... ...quality agreements (may include periodic CMO visits) Serve as Person in Plant (PIP) when critical processing occurs Support...$160k - $180k
Associate Director GMP Quality Reporting to the Head of GMP Quality, you will oversee GMP activities related to Olema’s clinical and commercial products... ...agreements, including periodic visits Represent Olema as Person in Plant (PIP) when critical processing occurs Support...Work experience placementWork at officeFlexible hours$180k - $195k
Associate Director, Quality Assurance - CMC Seaport Therapeutics is a clinical-stage... ...of novel neuropsychiatric medicines in areas of high unmet... ...Quality Assurance CMC to manage GMP quality assurance... ...Motivated by patient focus and personal commitment to high performance...$200k - $217k
Associate Director, GMP Quality Drug Product About Celea Therapeutics Celea Therapeutics is dedicated to advancing transformative treatments for people... ...product batches, working collaboratively with Qualified Persons and Manufacturing Quality teams as required. Provide...Contract workFor contractors$185k - $225k
...integrated platform for precision genetic medicines. To achieve this vision, Beam has... ...diseases.Position Overview:We are seeking an Associate Director, Quality Control to lead the Beam Massachusetts... ..., scientifically sound, and timely GMP testing while maintaining a continuous...Full time$142.5k - $256.5k
The RoleThe Associate Director, Quality Control Lab Automation Strategy & Digital... ...requires strong expertise in GMP laboratory automation,... ...infrastructure to reimagine how medicines are created and delivered,... ...have always believed an in-person culture is critical to our...Permanent employmentFull timeWork at officeWork from home- Olema Oncology is seeking an Associate Director, GMP Quality to oversee GMP activities for clinical and commercial products, including QA review of batch records and supplier compliance. This role partners with CMC, Regulatory and Supply Chain, and will be based in SF or...
- Vertex is seeking an Associate Director, GMP Operational Quality Assurance to lead day-to-day quality operations across multiple programs, ensuring decisions align with patient safety, product quality, regulatory expectations, and business continuity. This role partners...
$160k - $240k
...seeking an experienced Associate Director, Manufacturing Systems and Automation - CGT to lead the manufacturing... ...improvement of GMP manufacturing systems supporting... ...with enterprise IT and Quality Assurance to define... ...applicants without regard to a person's race, color, sex,...Full timeSummer workFlexible hours$190k - $230k
...Job Description Job Description Associate Director/Director, Technical Quality – Solid Biosciences Charlestown,... ...Biosciences is a precision genetic medicine company focused on advancing a... ...transfer of processes and analytics, CDMO GMP manufacture, CTL testing, and...Temporary workRemote workFlexible hoursSolid Biosciences
Charlestown, MA8 days ago- Vertex Pharmaceuticals is seeking an Associate Director, GMP Operational Quality in Boston to oversee team activities and ensure quality deliverables within department purview. The role requires comprehensive knowledge of quality assurance and compliance principles. You...
$161.5k - $202k
...may ultimately limit the number of new medicines that can reach patients, Formation Bio... .... About the Position The Digital Quality Associate Director/Director is a critical member of the Quality... ...(e.g., ALCOA+) and applicable GMP, GCP, and/or GLP regulations as they pertain...Work at officeLocal area3 days per week$160.6k - $240.8k
Job DescriptionGeneral Summary:The Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality assurance oversight of clinical... ...employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age,...Full timeWork experience placementSummer workWork at officeRemote workFlexible hours2 days per week$145.6k - $218.4k
...General Summary: As the Associate Director of Strategic... ...and Gene Therapy (CGT) Raw Materials, you... ...regulations, quality expectations, capacity... ...Manufacturing Practices (GMP) and ISO standards... ...regard to a person's race, color, sex... ...transformative medicines for people with serious...Long term contractContract workSummer workWork at officeRemote workFlexible hours2 days per week$160k - $200k
Kiniksa is seeking an experienced Associate Director, GMP Quality Assurance Operations to be a key leader within the Quality organization, responsible for providing hands-on-Quality Operations oversight for GMP manufacturing activities supporting clinical programs. This...Work at officeRemote work$148k - $222k
## Associate Director, Quality Systems - Cell and Gene Therapies (VCGT)Applylocations: Boston, MAtime type... ...management program items associated with CGT. Identify and implement continuous... ...*** Broad and deep expertise in global GMP regulations, guidances, and Quality Management...Summer workLocal areaRemote workFlexible hours2 days per week$155k - $214k
About This Role:As the Associate Director, Global Quality Risk Management, you will be... ...preferred.At least 10 years of GMP and Quality experience,... ...+ 3 paid days off for Personal Significance 80 hours of sick... ...to deliver life-changing medicines, with every role playing a...Full timeTemporary workLocal area- Xenon Pharmaceuticals invites an experienced Associate Director to lead Quality Control activities across DS/DP programs in line with ICH and cGMP. The role requires managing analytical testing, stability programs, investigations, and collaboration with QA and external...Remote work
- A leading global pharmaceutical company is seeking an Associate Director for Clinical & Quality Process Compliance. This role involves ensuring high-quality standards across processes and compliance with regulatory requirements. The ideal candidate will have significant...
$153.6k - $241.34k
Associate Director, Clinical & Quality Process Compliance Location: Cambridge, MA - Hybrid (not remote). Relocation benefit available. Job Description The Associate Director, Clinical & Quality Process Compliance is responsible for ensuring the quality of processes and...Temporary workLocal areaRelocation package- ...transformative gene-based medicines for serious human... ...Position Summary The Associate Director, Medical Safety is responsible... ...and gene therapy (CGT) / CRISPR-based... ...Biostatistics, and Manufacturing/Quality. Responsibilities Case... ...the benefits of in‑person interactions. Our...Work at officeRemote work
$175k - $201k
...establishing a new class of medicines that engage... ...formulation, development, and GMP manufacturing. If you... ....The OpportunityThe Associate Director, Drug Product Development... ...execution, ensure quality, and deliver timely technical... ...contributions each person brings. We believe...Work at office2 days per week3 days per week$160k - $240k
...Pharmaceuticals in Boston is looking for an Associate Director of Manufacturing Systems & Automation.... ...systems and automation team for CGT, ensuring compliance with FDA regulations... ...candidate will have a strong background in GMP manufacturing, digital transformations,...- Job DescriptionGeneral Summary:The Associate Director, CMC Quality Compliance and Inspection Readiness, is responsible for inspection readiness and... ...employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion...Full timeSummer workRemote workFlexible hours2 days per week
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Associate Director, GMP Quality—CGT & Personalized Medicine. Be the first to apply!
Related searches
- associate manager brand marketing Boston, MA
- associate creative director copy Boston, MA
- associate business manager Boston, MA
- associate creative manager Boston, MA
- associate clinical manager Boston, MA
- associate director marketing Boston, MA
- associate director contracts Boston, MA
- associate director communications Boston, MA
- associate medical director Boston, MA
- associate product manager web Boston, MA