Senior QC Analyst

Are you an experienced Senior QC Analyst with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced Senior QC Analyst to work at their company in Novato, CA. Position 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 procedures. The Senior Analyst works independently on assays they have mastered and performs advanced assays for multiple products. Work assignments will encompass performing and documenting activities and requires the ability to recognise deviations from approved procedures. Good record keeping, organizational, and written and verbal communication skills are essential. The Senior Analyst is expected to demonstrate strong cGMP and compliance acumen, become a subject matter expert for regulatory inspections, and provide training and educational development of other staff. Primary Responsibilities/Accountabilities: Performs, under minimal supervision, biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines 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 troubleshooting 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 Qualifications: 3+ years of experience in a cGMP/GLP laboratory 2+ years of 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 B.S./B.A. in Science (Major in Chemistry, Biology, Biochemistry). Preferred: 3-5 years of Quality Control laboratory experience 3-5 years of hands-on experience in separation sciences (HPLC, UPLC, CE)