Associate Director, GMP Quality - Small Molecules
Olema Oncology
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 Boston with travel. The ideal candidate has 8+ years in FDA-regulated pharma GMP QA, experience with NDA/BLA submissions, and strong leadership and communication skills. #J-18808-Ljbffr Olema Oncology
$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, with a focus on the manufacture of small molecule drug substances (Active Pharmaceutical Ingredients). Responsibilities...SuggestedWork experience placementWork at officeFlexible hours- Olema Oncology seeks an Associate Director GMP Quality to oversee GMP activities for clinical and commercial products, focusing on small molecule drug substances. You will review analytical development and QC results, COAs, batch disposition, and support supplier compliance...Suggested
$159k - $219k
...highly motivated and creative Chemical Engineer to join our Small Molecule Chemical Development team. This position provides an... ...wide range of Small Molecules across various modalities. This Associate Director of Engineering position provides experiences in early phase...SuggestedFull timeContract workTemporary workLocal area- ...automated foundry for designing and building new organisms. Associate Director, Sales, Datapoints Small Molecule Business | Ginkgo Datapoints | Boston, MAAbout... ...Bioworks, built to meet the growing demand for high-quality, large-scale biological datasets for AI-driven drug...SuggestedContract work
$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 quality of deliverables within department purview. The incumbent has comprehensive knowledge of principles...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 for strategic and operational Quality oversight across multiple complex programs. This role leads day-to-day quality...Full timeContract workSummer workRemote workFlexible hours2 days per week- Ginkgo Datapoints in Boston, MA seeks an Associate Director of Sales for the Small Molecule Services portfolio. You will drive revenue growth by building pharma, biotech, and tech accounts and by leading end-to-end deal negotiations. The role requires scientific fluency...
- Ginkgo Datapoints seeks an Associate Director of Sales to drive revenue for the Small Molecule Services portfolio, partnering with science and commercial teams to close deals. The role reports to the Head of BD and requires scientific fluency and a track record of closing...
- 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...
- Amylyx Pharmaceuticals, Inc. is seeking an Associate Director, Quality Operations to provide end-to-end quality oversight of clinical and development... ...for non-commercial programs, ensuring compliance with GMP/GDP standards. The role involves authoring and reviewing IND...Remote job
$154.4k - $242.55k
...Sciences, Synthetic Molecule Process Development (... ...timedelivery of high-quality synthetic molecule drug... ...is searching for an Associate Scientific Director, Synthetic Molecule DS... ...in synthetic small molecule drug substance... ...organizations(internal GMP facilities and/or external...Minimum wageLocal area$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$185k - $225k
...suffering from serious diseases.Position Overview:We are seeking an Associate Director, Quality Control to lead the Beam Massachusetts Quality Control team in delivering compliant, scientifically sound, and timely GMP testing while maintaining a continuous state of laboratory...Full time$172k - $202k
...motivated, resourceful, and enthusiastic quality control lead excited to be a key contributor... ...requests. You will also support CDMO on GMP commercial manufacturing readiness.At... ...critical quality attributes and developing associated limits/specifications.Excellent communication...Work at officeLocal areaRemote work1 day per week$143k - $203k
...plan formulation / drug product R&D and GMP stability studies in collaboration with... ...chemical entities under cGMP.Knowledge of CMC quality guidelines (particularly US, EU, JP and... ..., with an initial focus on enhancing small molecule therapeutic discovery in targeted...$148k - $222k
## Associate Director, Quality Systems - Cell and Gene Therapies (VCGT)Applylocations: Boston, MAtime type: Full timeposted on: Posted Todayjob requisition... ...Knowledge/Skills*** Broad and deep expertise in global GMP regulations, guidances, and Quality Management Systems, as...Summer workLocal areaRemote workFlexible hours2 days per week$155k - $214k
About This Role:As the Associate Director, Global Quality Risk Management, you will be at the forefront of Biogen’s commitment to quality excellence.... ...advanced degree (MS/PhD) preferred.At least 10 years of GMP and Quality experience, including 5+ years leading QRM and...Full timeTemporary workLocal area$160k - $240k
...an industry-leading pipeline of oral small molecule degraders to provide a new generation... ...heard.How you’ll make an impact:As the Associate Director, Analytical Development, you will contribute... ...and QA to prepare and review GMP documentation, analytical data and technical...Contract work$172k - $194k
...position is responsible for providing CMC quality oversight of drug substance, drug... ...in various development stages. As the GMP quality expert, this role is accountable... ...contracted partners. We anticipate hiring the Associate Director, Quality Operations in September 2026....Contract workLocal areaRemote work$161.5k - $202k
...faster and more efficiently. About the Position The Digital Quality Associate Director/Director is a critical member of the Quality Governance... ...of data integrity principles (e.g., ALCOA+) and applicable GMP, GCP, and/or GLP regulations as they pertain to data, records...Work at officeLocal area3 days per week$142.5k - $256.5k
The RoleThe Associate Director, Quality Control Lab Automation Strategy & Digital Integration is responsible for leading the strategy, implementation... ...value. Success in this role requires strong expertise in GMP laboratory automation, digital systems integration,...Permanent employmentFull timeWork at officeWork from home$160k - $195k
...and follow us on X, LinkedIn and Facebook.Role Summary:The Associate Director, Quality Management Systems is a key member of the quality team responsible... ...environments, with exposure across GxPs (GCP, GLP, GMP, GVP preferred) Demonstrated experience with direct ownership...Local area$210k - $300k
...Opportunity OverviewAs the Senior Director, Analytical Development and Quality Control, you will provide strategic... ...programs.Quality Control & GMP OversightAct as Head of Quality Control... ...development and QC organizations supporting small molecule and/or peptide drug development...Contract workWork at office- Job DescriptionGeneral Summary:The Associate Director, CMC Quality Compliance and Inspection Readiness, is responsible for inspection readiness and compliance of external sites including evaluating, improving, and monitoring commercial level quality compliance and quality...Full timeSummer workRemote workFlexible hours2 days per week
$160k - $275k
...first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in...$154.4k - $242.55k
...DescriptionObjective / Purpose: The Associate Scientific Director, DNA-Encoded Library (DEL) Selection... ...DEL selection campaigns supporting small-molecule drug discovery. This individual will... ...meaningful hit series.Establish data-quality, hit-triage, and prioritization criteria...Minimum wageTemporary workLocal areaRemote work$156.9k - $247k
...welcome a curious, collaborative, and scientifically driven Associate Director to help support our growing cardiometabolic pipelines.In... .... You will contribute to the discovery and development of small molecules, biologics, and non-traditional therapeutics, including peptides...Full timeFor contractorsLocal areaFlexible hours$185k - $200k
...other presentations here. About the Role Associate Director, Clinical Supply Chain As the... ...knowledge of Good Manufacturing Practices (GMP) Experience 10+ years of... ...Prior experience in oncology trials using small molecules is preferred Excellent project management...Work at officeFlexible hours- ...Pharmaceuticals Incorporated is seeking an Associate Director, GxP Operations Support Manufacturing... .... You will partner with Manufacturing, Quality, IT, and Engineering to ensure... ...cybersecurity, and KPI tracking in a fast-paced GMP environment. #J-18808-Ljbffr Vertex...
$145k - $240k
...is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly... ...impact:We are seeking a highly motivated Senior Manager or Associate Director, Feasibility Analytics & Insights to serve as the...
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