GMP QA Leader, Biologics & Cell Therapy
artivabio
Artiva Biotherapeutics is seeking anExecutive Director, GMP Quality Assurance to lead internal GMP quality operations and ensure compliance with FDA/EMA and global health authorities. The role includes governance, batch review, CAPAs, change control, and inspection readiness. Reporting to the VP of Quality, you will build and manage the GMP QA organization, establish policies, and foster a culture of quality and continuous improvement across the company, with on-site work in San Diego, CA. #J-18808-Ljbffr artivabio
$227.42k - $275.58k
...develop transformative radiopharmaceutical therapies that offer new hope for patients... ...are seeking an accomplished scientific leader to lead our biology organization. This individual will oversee... ...of robust biochemical and cell-based target engagement platforms, including...SuggestedHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaImmediate startRemote workFlexible hours- ...to serve as (i) subject‑matter expert and operational lead in GMP biologics production, responsible for upstream/downstream processes, training... ...troubleshooting, and adherence to cGMP while coordinating with QA/QC and MSAT teams. The role requires 3-4 years in purification...Suggested
- Mentor Technical Group seeks a Quality Compliance Lead to oversee QMS ensuring client GMP/GDP compliance. You will lead QA processes, audits, and training across departments in a regulated setting. The role requires a Bachelor's in Science/Engineering and 5+ years in compliance...Suggested
$130k - $145k
...Supply Chain Buyer/Planner to own end-to-end inventory and materials management for GMP-regulated manufacturing of biologics. You will collaborate with Manufacturing, Process Development, QA/QC, and suppliers to ensure compliant, cost-effective material flow and...Suggested$100k - $118k
...dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront... ...ensuring cGMP-compliant production of biologic products for clinical trials. You will... ...-based with required time in GMP spaces overseeing manufacturing operations...SuggestedFull time- Artiva is seeking a senior leader to head the cell potency analytical development team in San Diego. You will define strategy, oversee assay development... ...with R&D and Process Development to advance NK cell therapies. You will mentor scientists, author regulatory sections,...
- SRT Therapeutics Inc. is seeking an Associate Director, Biologics CMC, to support biologics development from upstream cell culture to regulatory submissions. The role offers a unique opportunity to influence large molecule programs. With responsibilities including technical...
- ...and improve GxP quality systems to support clinical and manufacturing operations. This hybrid role combines leadership with hands-on QA responsibilities. The ideal candidate will have over 8 years in the pharmaceutical industry with specific experience in compliance and...
- Artiva Biotherapeutics is seeking a Sr. Manager, Medical Writing to lead clinical and regulatory documentation across development programs. You will author and edit protocols, CSRs, IBs, and regulatory submissions, ensuring accuracy, consistency, and regulatory compliance...
- ...Quality Management System. The role suits a person with extensive QA experience and strong collaboration skills. The ideal candidate... ...processes, and contribute to continuous quality improvements in a GMP environment. #J-18808-Ljbffr PCI TRGR Penn Pharmaceutical Services...
- ...Biotechnology Life Science Therapeutics Specialties cell therapy autoimmune and lupus lupus multiple... .... This pivotal role demands a cross-functional leader with a proven track record in biologics and a deep understanding of the pharmaceutical...
- ...strategic leadership to guide large-scale ML projects that address real biological problems. Successful candidates will shape method choices, mentor a diverse team, and collaborate across functions to advance cell rejuvenation and resilience initiatives at scale. #J-18808-...
- ...hands-on in the technical trenches. You will partner with the IoC Leadership Team to define strategic ML priorities, mentor a team of ML scientists and engineers, and drive collaborations across Altos to advance cell rejuvenation and resilience. #J-18808-Ljbffr Altoslabs
$25 - $31 per hour
...Description Job Description Manufacturing Associate I / II – Cell Therapy BioPhase Solutions Location: San Diego, CA 92101... ...Associate (Level I or II) to support cell therapy production in a GMP-regulated environment. Level will be determined based on experience...Temporary work$258.68k - $313.46k
...uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work- ...Eurofins network of companies is the global leader in food, environment, pharmaceutical and... ..., origin, traceability and purity of biological substances and products. In 2021, Eurofins... ...the analysis of RNA therapeutics in a GMP-regulated environment. Proven ability...Full timeContract workLocal areaMonday to Friday
$85k - $100k
...extensive experience in developing biologics and bioconjugates, we offer a... ...and operational lead within GMP manufacturing operations supporting... ...activities, including cell culture expansion, bioreactor operations... ...work practices. Partner with QA, QC, MSAT, Engineering,...Local areaFlexible hoursShift workDay shift- ...materials operations in the biotech sector. This role involves managing inventory, sourcing strategies, and ensuring compliance with GMP regulations. The ideal candidate has over 7 years of experience in biotech or GMP environments and a strong background in materials management...
- ...strategic and operational regulatory leadership for global CMC activities across development and commercial programs, with a focus on biologics and rare diseases. You will partner with cross-functional teams to align CMC plans with regulatory requirements, lead global...Remote job
- ...development through lifecycle management. You will drive process validation, technology transfer, and lifecycle improvements, interfacing with QA, Regulatory, and Manufacturing to ensure compliant, scalable operations. Responsibilities include overseeing PPQ activities,...
$75k - $85k
Maximus is seeking a Quality Assurance Manager in San Diego to lead performance monitoring and manage the QA training team. This role involves establishing targets, performing trend analysis, and ensuring training excellence. The ideal candidate has a Bachelor's degree...Flexible hours- Syneos Health seeks a senior, client-facing leader to drive RPO partnerships in life sciences, shaping talent solutions that accelerate therapies. You will win complex engagements, manage executive relationships, and coordinate with delivery teams in a matrixed enterprise...
- Travere Therapeutics is seeking an Associate Director, Technical Operations, Biologics Drug Substance Manufacturing to lead technical oversight of biologics manufacturing from late‑stage development through commercialization at external CDMOs. Focus will be on downstream...Remote job
$19 - $30 per hour
A telecommunications company in California seeks small cell technicians across three tiers for various installation and maintenance responsibilities. Ideal candidates will have a willingness to learn, a high school diploma, and capabilities in lifting and working at heights...- ...will drive continuous improvement, coordinate with maintenance, and ensure documentation accuracy. The role requires strong leadership, GMP knowledge, and the ability to train team players, balance line capacity, and meet daily SLA goals while #J-18808-Ljbffr Argen...Afternoon shift
- ...develop personalized health optimization plans, and coordinate with a multidisciplinary team to deliver aging‑related and preventive therapies. The role requires NPLEX completion, CA ND licensure, and strong communication with patients and colleagues. #J-18808-Ljbffr NEXT...
$196.18k - $295k
...innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology,... ...of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives worldwide. Real-...Local areaWorldwideShift work- ...transportation, and travel expenses, enabling you to impact patient outcomes across communities. You will serve as a clinical resource, promote best practices, mentor therapy staff, and ensure regulatory compliance while adapting to new locations and #J-18808-Ljbffr Socket.devPermanent employmentFull time
- ...clinical programs, bringing IND‑enabling packages from discovery to first‑in‑human trials. You will lead in vivo pharmacology, efficacy, toxicology, ADME/PK, and collaborate across chemistry, biology, regulatory, and clinical teams, ensuring GLP/GMP #J-18808-Ljbffr Kelly
- Lead OT/PT at Scripps Mercy Hospital San Diego is a full-time role providing skilled therapy and serving as a clinical resource and mentor. Requires a Bachelor's in PT or OT, California licensure, and BLS certification. Strong communication and teamwork are essential for...Full time
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