Director, GMP QA & Quality Systems Biologics/Small Molecules (Phase 3)
Scorpion Therapeutics
IDEAYA Biosciences is seeking a Director of GMP Quality Assurance to lead quality operations for drug products and biologics from toxicology through Phase 3. The role oversees QA for CMC, manufacturing, and IT systems while driving continuous improvement and regulatory readiness. Responsibilities include leading QA support for clinical materials, vendor oversight, and support for regulatory submissions and inspections in a fast-paced, development-focused environment. #J-18808-Ljbffr Scorpion Therapeutics
$165k - $210k
...available, superior small molecule medicines that... ...limitations of biologic and peptide... ...Summary:The Associate Director, Global GCP QA is responsible... ...internally to ensure all systems; processes, and... ...Quality OversightIndependently... ...ongoing clinical phase and China clinical...QualityContract workRemote work- Role Director of GMP Quality Assurance at IDEAYA Biosciences, overseeing... ...drug products and biologics from toxicology through Phase 3. Responsibilities... ...manufacturing, and IT systems; lead QA support for clinical... ...environments supporting small molecules and biologics;...QualityContract work
$200k - $247k
...expertise in small-molecule drug discovery... ..., structural biology and... ...are seeking a Director of Good Manufacturing... ...Manufacturing Processes, Quality Assurance to... ...Director, GMP, Quality... ...lead GMP QA oversight for... ...toxicology through Phase 3. This role... ..., and IT Systems, while provided...QualityContract workTemporary workWork at officeLocal areaWork from home$273k - $290k
...causal human biology and accelerating... ...—whether small molecules, biologics, or... ...for a Senior Director of Quality Assurance to build... ...s approach to GMP and GCP quality... ...insitro’s Quality systems: standing up... ...through Phase 2 in partnership... ...progression into senior QA leadership....QualityHome officeFlexible hours3 days per week- ...Biosciences, Inc. is seeking a Director of Good Manufacturing Processes, Quality Assurance to lead GMP QA oversight for drug products and biologics. This onsite role drives phase-appropriate GMP compliance... ...CMC, development, and IT systems, shaping quality strategy and...Quality
$193.5k - $236.5k
...Associate Director, CMC Project ManagementJoin... ...with CMC, Quality, and key... ...Analytical, QA, CMC... ...industry.At least 3 years directly... ...manufacturing, quality systems, supply chain... ...with GMP/GxP-regulated... ...within small molecule modalities.Proficiency... ...to the biological pathways that...QualityWork at officeShift work- IDEAYA Biosciences Inc. is seeking a Director of Good Manufacturing Processes, Quality Assurance to lead GMP QA oversight across drug products and biologics programs from toxicology through Phase 3. The role drives phase-appropriate GMP compliance, risk management, and...Quality
$170k - $200k
...signaling pathways in the immune system. Reporting to the Director of Analytical Development and Quality Control, the Associate... ...with external vendors to drive phase-appropriate analytical method... ...of industrial experience in small molecule pharmaceutical development...QualityFull timeWork at officeImmediate start$200k - $220k
...of GPCR-targeted small molecule programs with potential... ...Associate Director of Process Chemistry... ...development, and GMP manufacture. Lead... ...safe, scalable, and phase-appropriate... ...delivery of high-quality products, and facilitate... ...development of the Quality system to ensure product...QualityFull timeContract work$186k - $220k
...available, superior small molecule medicines that... ...current limitations of biologic and peptide drugs... ...:The Associate Director of Clinical... ...studies across all phases, ensuring efficient... ..., budget, and quality; develop and implement... ...Authorities.Systems: Collaborate with...QualityContract workRemote work$198k - $257k
...The Associate Director, Clinical Pharmacology... ...for both small and large molecules. The role will develop... ...rigor, quality, and regulatory... ...Pharmaceutical Sciences, Systems Pharmacology,... ..., study design, phase transition, registration... ...Experience with biologics, ADCs,...QualityWorldwideRelocation package$250k - $290k
...Senior or Executive Director Quality Assurance GCP will... ...implementation of QA GCP operations in... ...programs (Phase 1, 2, 3), regulatory submissions... ...procedures to ensure systems align with... ...inspections Align with GMP Quality Assurance... ...degree in Biology, Chemistry, Physical...QualityTemporary workCasual workLocal areaWorldwideFlexible hours$205k - $218k
...Director, Quality Assurance insitro is a data... ...high-throughput biology to transform... ...clinical quality systems, manage global... ...implement a robust, phase-appropriate... ...GLP, GCP, and GMP work to ensure... ...: 10+ years of QA experience in biotech... ...of moving a small company through...QualityHome officeFlexible hours3 days per week- ...Senior Director, Quality As the Senior Director... ...Management System (QMS) and providing... ...(GCP, GMP, GLP). ·Lead... ...guidelines. ·Drive phase-appropriate quality... .... ·Develop 3 –5 year Quality... ...(Chemistry, Biology, Pharmacy, Biochemistry... ...spanning small molecules and/or biologics...Quality
$250k - $300k
...patients and is approaching Phase 3 development. Our... ...President, Biostatistics, the Director/Senior Director,... ...results to ensure high quality and compliant data handling... ...and implementation of systems and vendors Identify,... ...plans under pressure in a small, fast-paced environment...QualityFull timeLocal area3 days per week- ...opportunity to join a small team, work on... .... Position:Director/Senior Director of Quality Assurance -... ...Assurance (QA) team. Our ideal... ...developing quality systems, audit, and... ...Practices (GMP and ISO), safety... ...of all phases of project management... ...cell therapy, biologics is a plus)....QualityWorldwide
$186k - $235k
...orally available, superior small molecule medicines that... ...current limitations of biologic and peptide drugs. We... ...Summary:The Associate Director of Medical Writing will... ...while also performing quality control (QC) reviews,... ...Smartsheet, and related systems.Structure Therapeutics...QualityContract workRemote work$220k - $240k
...have fun, seriously.POSITION SUMMARYThe Director, GMP Quality Assurance is responsible for the... ...JOB FUNCTIONS/RESPONSIBILITIESProvide QA oversight of finished product (FP), from... ...validation, technology transfer, and small-molecule manufacturing operations.Experience supporting...QualityContract workLocal area- ...Associate Director, Quality Assurance ComplianceAt Gilead, we're... ...– including inspection system training, inspection support... ...:BS/BA degree in Biology, Sciences, or related discipline... ...3485 and Health Canada GMP/GDP guidance; as well... ...credible resource for QA compliance in other...QualityWork at officeLocal areaRemote work
$194.1k - $305.6k
...highly collaborative Senior Director to provide scientific,... ...strategies,- enabling high-quality, timely data packages that... ...activities across a portfolio of biologics, small molecules, conjugates, and novel... ...automation, digital tools, data systems, and continuous improvement...QualityFull timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$102.09k - $132.11k
...Responsibilities:Supports QA oversight of clinical small molecule drug substance and oral solid... ...risk-based and clinical phase appropriate approach.Reviews... ...complete, and timely (ALCOA) quality records in accordance with GMP and quality systems.Supports QA team members in...QualityFull timeFor contractorsWork at officeLocal area$67.7k - $80k
...determination to deliver quality and accuracy will... ...Support quality system activities •... ...applicable GDP and GMP requirements... ...Science, Immunology, Biology, Molecular Biology... ..., preferably in a small molecule environment o... ...paid parental leave (3 weeks for bonding...QualityFull timeTemporary workWork at office$220k - $233.5k
POSITION SUMMARY Position Title: Director, Medicinal Chemistry Reports... ...for co-leading a full-phase small molecule antiviral discovery program... ...computational chemistry and structural biology scientists Directing and... ...routes, safeguarding data quality and compound integrity, and...QualityFull time- ...Description Job Title: Associate Director, Bioanalysis Location:... ...Regulatory Affairs, and Quality teams to ensure delivery... ...supporting both small molecule and biologic drug development programs... ...Experience supporting Phase 1 through Phase 3 clinical studies. Experience...Quality
$142.5k - $199k
...powering the immune system to transform... ...Technical Operations Quality Control, is... ...CDMOs/CTLs) from Phase 1 through... ...expectation of 3 days per week in... ...execution of QC GMP processes (deviations... ...collaboration with QA. Coordinate QC... ...Biochemistry, Chemistry, Biology, Virology,...QualityFull timeContract workWork at officeWork visa3 days per week- ...Francisco, CA is seeking a Senior Manager, Quality Program Management to lead the integrated quality plan across QA and Quality Systems. This role partners with cross‑functional teams... ...state of control and compliance with GMP/ISO standards. The ideal candidate will have...Quality
- ...Amgen seeks a Director to lead pharmacokinetics/drug metabolism strategy and portfolio advancement for small molecule programs across discovery, development, and regulatory phases. The role combines scientific expertise with cross-functional project leadership to optimize...
$153k - $178k
...the most complex biologics ever attempted... ...with Quality Assurance (QA), to operationalize... ...operation as a Phase I/II early clinical... ...of laboratory GMP requirements who... ...report to the Director of Infrastructure... ...records, including systems such as... ...Hybrid (minimum of 3 days per week...QualityWork experience placement3 days per week$189.8k - $216.7k
...sites. The Associate Director, Chemical Engineering... ...optimize scalable routes for small‑molecule DS manufacturing,... ...with CDMOs and Nurix Quality Assurance, and Global... ...) of industrial, late-phase, small‑molecule drug substance... ...and experience in GMP drug substance...QualityContract work- ...opportunity to join a small team, work on... ...Position: Senior Manager, Quality Program Management... ...Quality Assurance (QA) team. Our ideal... ...Assurance and Quality Systems teams so those... ...Manufacturing Practices (GMP and ISO), safety... ...(cell therapy, biologics, or sterile pharmaceutical...Quality
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