QC Laboratory Manager - GMP Peptide Analytics
Yowei Therapeutics
Yowei Therapeutics seeks a Quality Control Manager to lead a QC lab of 5–8 analysts, ensuring timely testing and compliant documentation for peptide programs. You will mentor analysts, troubleshoot instrument issues, and coordinate method transfers and investigations in a GMP setting. The role requires a strong background in analytical chemistry, leadership experience, and collaboration with QA, Manufacturing, and Validation teams to enable accurate batch disposition and continuous improvement. #J-18808-Ljbffr Yowei Therapeutics
- ...Quality Control Analyst to perform and review analytical testing supporting raw materials, in-... ..., release, and stability testing in a GMP-lab setting in Milpitas, CA. The role... ...help maintain compliance with regulated laboratory practices, documenting results and preparing...Suggested
$90k - $105k
...Therapeutics, Inc. in Newark, CA seeks a Quality Control Analyst II, Analytical to perform routine and non-routine testing for drug substances... ...a Master’s in Biotechnology or related field, experience in GMP QC labs, and familiarity with US/EU regulations. Salary range $90,...SuggestedRemote job$90k - $105k
...Quality Control Analyst II, Analytical ( Newark, CA) Revance Therapeutics, Inc... ...activities. Author/ revise SOPs. Review of laboratory records generated in support of QC testing including procedures,... ...with biological products in a GMP environment. # Working with US and...SuggestedContract workInternshipWork at officeRemote work$20k
...CSBio to advance peptide-based clinical programs... ...microbiology and laboratory capabilities.... ...as Quality Control Manager. Core duties and responsibilities... ...and develop a QC laboratory team of... .... Review analytical data, calculations... ..., API, or another GMP-regulated...SuggestedContract workWorldwide2 days per week$20k
...companies working closely with CSBio to advance peptide-based clinical programs. Their work... ..., and supporting microbiology and laboratory capabilities. Together, they are building... ...oriented Clinical Research Coordinator to manage day-to-day study coordination for early...SuggestedContract workImmediate startWorldwide2 days per week- ...envision and achieve Digital Laboratory Transformation through co-creation... ..., Internet of Things, analytics, and cloud, in combination with... ...our clients better capture, manage, integrate, and analyze complex... ..., within R&D and/or QC Manufacturing spaces ~ Bachelor...Live inWork at officeLocal area
- ...environment. The role focuses on inspection of incoming materials and finished products, ensuring adherence to ISO and GMP standards. The candidate will record QC data, participate in inventory counts, and collaborate with other departments to resolve inspection discrepancies...
$106k - $142k
Job Description SUMMARY The EMC Laboratory Manager oversees all Electromagnetic Compatibility (EMC) testing operations, ensuring the facility meets both global regulatory requirements and automotive industry standards. This leadership role is responsible for driving operational...Local areaImmediate start$191k - $202k
...ResponsibilitiesEstablish and maintain a phase-appropriate, GMP compliant Quality Management System (QMS) across all development... ....Provide support to the QC functions responsible for developing,... ..., and reliability for all GxP analytical and nonclinical data used in...$140k - $185k
...neuroscience-based therapeutics. Primary Role The Clinical Trial Manager owns the operational health of the investigator sites assigned... ...Experience with RBQM/KRI frameworks and centralized monitoring analytics. Prior participation in an FDA, EMA, or MHRA inspection or a...Interim roleImmediate startRemote work- Yowei Therapeutics seeks a detail-oriented Clinical Research Coordinator to manage day-to-day study coordination for early clinical and longevity programs. Core duties include coordinating startup, screening, visits, data entry, and vendor readiness to support investigators...
- BD (Becton, Dickinson and Company) is looking for a Senior CRA/Associate Clinical Project Manager in Milpitas, CA. The position entails managing clinical studies, supporting project plans and participant coordination. The ideal candidate should have a Bachelor's degree,...Remote job
$41 per hour
...Independently perform assays under GMP, maintaining data integrity... ...guidance, participate in laboratory investigations Independently... ...experience performing relevant analytical techniques (HPLC, GC, FTIR). Experience... ...validation requirements for QC methods and regulatory...Full time$60k
...matter experts (SMEs) and management system owners (MSOs) in... ...presence during GMP operations to provide in... ...day alignment across QA, QC, Operations, and MSAT;... ...checks, drug substance or laboratory areas, and sampling/... ...product Knowledge of analytical testing and quality control...Local area$210k - $250k
...the product lifecycle, from GMP starting materials and... ...effective, risk-based Quality Management System that ensures products... ...for manufacturing processes, analytical methods, laboratory operations, technical... ...Operations, Manufacturing, QC, Engineering, Regulatory Affairs...Temporary workLocal area- Protagonist Therapeutics is seeking an Associate Director, Quality Assurance to lead QA activities for GMP manufacturing and CMC programs. You will provide regulatory-focused QA leadership, review batch records, deviations, and CAPA, and guide cross-functional teams toward...
$22 - $24 per hour
...inspection processes and tools like SmartScope. Contractors will work onsite at the client’s facilities, ensuring adherence to good laboratory practices and safety protocols. Compensation is between $22 to $24 per hour, reflecting the role's technical demands. #J-18808-...Hourly payFor contractors$92.7k - $152.9k
Position Title Senior CRA/Associate Clinical Project Manager Location Milpitas, CA (Hybrid model or fully remote work from anywhere in the US for highly qualified candidates) Job Overview Associate Clinical Project Manager / Senior CRA collaborates with the core team, clinical...Remote work$175k - $225k
...de novo discovery of peptide therapeutics. Two novel... ...responsible for leading and managing QA activities,... ...Protagonist’s CMC team with GMP manufacturing. This... ...records, deviations, analytical data, stability data,... ...of external analytical laboratories, ensuring method lifecycle...Full timeTemporary workWork at officeFlexible hours- ...materials through finish goods and stability, including method transfers, deviations, and documentation. You will lead investigations on QC failures and drive process improvements in a fast-growing environment. The role requires a BS in molecular biology or related field...
$38 - $51 per hour
...Job Description Job Description Job Title: Senior QA/QC Inspector – Semiconductor Construction Job Description The Senior QA... ...with minimal training while collaborating closely with project management, construction supervision, and key stakeholders to deliver successful...Contract workTemporary workLocal area$240k - $280k
...Bionova Scientific's QC function. This role sets... ...oversight for sample management, stability, in-process... ...by developing robust analytical transfer and qualification... ...Scientific's QC laboratories and related operations... ...Control, or a related GMP laboratory environment...Full time- ...SUMMARY:Provides operational leadership and support for clinical laboratory services under the direction of the CLIA Laboratory Director.... ...with the CLIA Laboratory Director on the development and management of the laboratory budget, ensuring financial sustainability within...Work experience placementLocal area
$110k - $140k
...Services seeks a Histology Lab Manager for a client located in the... ...Role Reporting to senior laboratory leadership, the Laboratory... ...and support staff across pre-analytical, histology, and customer service... ...Ensure all QA/QC is completed per SOP Ensure...Permanent employmentWork at officeLocal areaShift workDay shift- ...Description We are seeking a highly motivated Technical Program Manager (TPM) to lead the planning, development, and deployment of... ...risk management, and stakeholder communication skills. Strong analytical, problem‑solving, and decision‑making abilities. Proven ability...Temporary workRemote workFlexible hoursShift work
- ...Job Title QE Lead / QA Manager (Embedded QE) Location Sunnyvale, California Job Description We are seeking a... ...for visual validation, accessibility testing (WCAG 2.1 AA), and analytics validation. Strong leadership, team management, and test strategy...
$28 - $34 per hour
...dimensional tolerances, craftsmanship and cosmetic defects Analyze parts against customer provided drawings and CAD files. Create and manage RMAs, SCARs, Templates, and Non-Conformances Interface with customers for all quality related issues Prepare quarterly...Hourly payFull timeWork at officeRelocationMonday to FridayShift workDay shift- ...Sr. Director of Quality Control in Fremont, CA. Lead the QC laboratories, set strategy, and ensure cGMP compliance across release... .... The role requires an advanced degree and 15+ years in Analytical Sciences or GMP labs, with strong regulatory interaction experience....
$86.25k - $100.16k
...progressively more complex projects/assignments. Independently manage significant and key aspects of a large study or all aspects of... ...addition to instruction on project work. Audit operations, including laboratory procedures, to ensure compliance with applicable regulations;...Hourly payContract workWork at office$140k - $180k
...products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology. Description: The Sr. Clinical Trial Manager (Sr. CTM) is a hands-on program owner responsible for the end-to-end execution of assigned clinical studies within a portfolio...Full timeContract workWork experience placementLocal area
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