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The QC Analytical Analyst is responsible for timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products under cGMP guidelines. · Performs biochemical/physical/chemical analyses of test samples. · Develops proficiency i ...
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The Senior Analyst works independently on assays they have mastered and performs advanced assays for multiple products. · The Senior Analyst is expected to demonstrate strong cGMP and compliance acumen, become a subject matter expert for regulatory inspections, and provide traini ...
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The QC Analytical Analyst is responsible for timely completion of lot release, stability, · and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines.Performs biochemical/physical/chemical analyses of test samples under cGMP to ...
Novato3 weeks ago
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The QC Analytical Senior Analyst works independently on assays they have mastered and performs advanced assays for multiple products. The Senior Analyst is expected to demonstrate strong cGMP and compliance acumen and provide training and educational development of other staff. · ...
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++ The QC Analytical Analyst is responsible for the timely execution of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products in accordance with cGMP guidelines. · +Perform biochemical, physical, and chemical analyses of test samples ...
Novato3 weeks ago
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The QC Analytical Analyst is responsible for the timely completion of lot release and stability testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures.Performs biochemical/physical/chemical analyses of test samples under cGMP ...
Novato, CA3 weeks ago
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The QC Analytical Analyst performs biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines. · Performs biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines. · Works independently on assays they have ma ...
Novato2 weeks ago
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The QC Analytical Analyst is responsible for the timely completion of lot release, · stability, · and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures. · Performs biochemical/physical/chemical analyses of tes ...
Novato, CA2 weeks ago
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The QC Analytical Analyst is responsible for the timely execution of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products in accordance with cGMP guidelines. · This role operates with minimal supervision and requires strong technica ...
Novato, CA2 weeks ago
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The QC Analytical Senior Analyst is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures. · Performs biochemical/physical/chemical analyses of ...
Novato2 weeks ago
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The QC Analytical Senior Analyst under minimal supervision responsible timely completion lot release stability non routine testing pharmaceutical drug substances drug products adhering cGMP guidelines procedures. · Performs biochemical physical chemical analyses test samples unde ...
Novato1 month ago
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The Senior Analyst, Quality Control Analytical is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures. · ...
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The Senior Quality Control (QC) Analytical Analyst is responsible for the timely execution of lot release, · stability, and non-routine testing of pharmaceutical drug substances and drug products in compliance with cGMP guidelines.Perform biochemical, physical, and chemical analy ...
Novato1 month ago
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The QC Analytical Senior Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures.The Senior Analyst works i ...
Novato1 month ago
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The Senior Analyst, Quality Control Analytical is responsible for the rigorous execution of lot release, · stability and non-routine testing of pharmaceutical drug substances · and products under strict cGMP guidelines. ...
Novato1 month ago
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The QC Analytical Senior Analyst is responsible for the timely completion of lot release and testing of pharmaceutical drug substances and drug products under cGMP guidelines. The job involves working independently on advanced assays for multiple products with minimal supervision ...
Novato1 month ago
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The QC Analytical Senior Analyst, under minimal supervision, is responsible for the timely completion of lot release, · stability,and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines · and procedures. · Performs biochemical ...
Novato1 month ago
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· Onsite: Novato · SUMMARY · The QC Analytical Senior Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedu ...
Novato, CA1 week ago
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TD Thornton · TD Thornton is a premier consulting firm specializing in project management and project controls solutions. We provide strong onboarding and ongoing support to help our people succeed. We welcome applicants from engineering, construction management, project manageme ...
Petaluma $115,000 - $140,000 (USD)1 day ago
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Position Overview: · InnoActive Group are leaders in providing project management and technology advisory primarily in public agencies and Fortune 500 entities. InnoActive Group has managed various construction and technology projects ranging in size from small projects to multi- ...
San Francisco1 week ago
Quality Control Analyst - Novato - GForce Life Sciences
Description
QC Analyst
12-month Contract
Onsite in Novato, CA
Must be able to work on a W2
SUMMARY
The QC Analytical Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures.
RESPONSIBILITIES
• Performs, under minimal supervision, biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines. General cGMP lab experience at the Analyst level.
• Works independently on assays they have mastered
• Develops and maintains proficiency in a broad range of test methods
• Develops a technical understanding of each assay and assists with trouble shooting and laboratory investigations
• Evaluates data against defined criteria/specifications
• Actively applies knowledge in non-routine situations using a thorough understanding of the work processes and practices
• Identifies key issues in complex situations, analyzes problems, and makes sound decisions
• Assists in the revision of written procedures, method/equipment validation, and/or method transfers as assigned
• Mentors and trains other analysts, including new hires and more junior analysts, in areas of expertise
• Holds self and others accountable for adherence to department and company policies and practices
• Maintains a safety and quality focused culture
EXPERIENCE
• B.S./B.A. in Science (Major in Chemistry, Biology, Biochemistry).
• 1-2 + years of experience in a cGMP/GLP laboratory
• 1-2+ years hands-on experience in separation sciences (HPLC, UPLC, CE)
• Ability to follow written instructions and to perform tasks with direct or minimal supervision
• Strong leadership skills demonstrated through past work history
• Use of a computer: e.g., Proficient in Windows, Microsoft Word, Excel
• Good written and verbal communication skills
• Attention to detail and strong documentation skills
• Ability to contribute effectively in team environments and independently
• 1-2+ years of Quality Control laboratory experience preferred
• 1-2+ years of hands-on experience in separation sciences (HPLC, UPLC, CE) preferred
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