Quality Control Analyst RD Partners San Francisco Contract
Overview
The Quality Control Analyst at RD Partners leads analytical testing of drug product intermediates under cGMP guidelines. This 12-month contract in Novato requires expertise in protein determination UV absorbance enzyme activity HPLC UPLC and method validation. Candidate will own in-process testing drive process improvements and mentor colleagues.
What You'll Do11
- 1Perform diverse analytical assays while maintaining sample throughput and managing lab supplies
- 2Prepare reagents and support process validation studies
- 3Execute in-process tests and report results promptly to meet customer timelines
- 4Evaluate assay validity and analyze data against specifications
- 5Contribute to trend analysis reports and method validation initiatives
- 6Collaborate on test method development and equipment validation
- 7Train staff on analytical techniques and SOP adherence
- 8Monitor inventory levels and coordinate supply chain logistics
- 9Identify operational efficiencies and implement process optimizations
- 10Attend team meetings and propose infrastructure enhancements
- 11Investigate compliance risks and document corrective actions
Requirements11
- 1Bachelor of Science degree with 0-3 years lab experience
- 2Proficiency in Spark Airflow and statistical analysis tools
- 3Familiarity with BINOCS scheduling systems and SAP platforms
- 4Certified Quality Assurance professional status
- 5Valid driver's license for onsite work in Novato
- 6Ability to pass drug substance and product testing audits
- 7Strong written and verbal communication skills
- 8Experience with GMP documentation and audit preparation
- 9Willingness to work flexible hours including weekends
- 10Basic computer literacy with Microsoft Office suite
- 11Previous supervisory experience preferred
Salary Insight
$52 - $62k per year
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
System One
VerifiedQC Analyst San Francisco Contract
Lead QC Analyst at biotech firm in Novato. Seeking candidate with bachelor's degree and 0-3 years lab experience. Responsibilities include managing sample receipt and reporting results while ensuring GMP compliance. Requires strong documentation skills and ability to train staff. This role offers competitive pay and flexible hours.
Aspect Biosystems
VerifiedScientist Quality Control Analytical Development Aspect Biosystems
Scientist leading end-to-end development of cell-based analytical methods for bioprinted tissue therapeutics in Fremont California. This role focuses on establishing robust analytical methods while partnering with QC Process Development and Research to achieve clinical readiness. The position requires expertise in precision scalable assays and regulatory compliance.
THRESHOLD ENTERPRISES LTD
VerifiedQC Laboratory Analyst II - San Jose CA
Seeking a seasoned Laboratory Analyst II to lead analytical work at Threshold Enterprises Ltd. This journey-level role requires proven expertise across multiple instruments and a track record of mentoring junior staff. The ideal candidate thrives in a collaborative environment while driving quality outcomes.
Nuclein
VerifiedQuality Control Scientist II Nuclein
Quality Control Scientist II at Nuclein leads development and maintenance of the quality management system. This role supports incoming material testing and finished product release while collaborating with Assay Development Operations and Engineering to ensure regulatory compliance. The position offers a unique opportunity to shape quality processes in a dynamic environment.
Rigel Pharmaceuticals, Inc.
VerifiedSenior Manager Quality Assurance Quality Operations
Senior Manager overseeing day-to-day GMP Quality Assurance activities across global contract manufacturers and laboratories. Responsible for operational Quality oversight throughout product lifecycle including manufacturing readiness and batch disposition. Partners with Technical Operations Supply Chain and regulatory affairs to ensure uninterrupted product supply. Compensation $175000 to $210000.
1010 Gilead Sciences, Inc.
VerifiedPrincipal Scientist Analytical Operations at Gilead
Lead Quality Control for small molecule clinical development programs. Drive QC strategy and lead cross-functional teams. Shape the future of healthcare through rigorous analytical oversight.