Quality Control Analyst II
Genentech•Oceanside, CA
•Onsite
About The Position
As a QC Analyst II in our Quality department in Oceanside, you will play a critical role in ensuring the safety, quality, and compliance of our manufacturing environment and commercial products. You will collaborate closely with cross-functional teams using state-of-the-art techniques to implement innovative testing technologies. This role offers a unique opportunity to directly impact patient lives by maintaining the highest standards of good manufacturing and laboratory practices.
Requirements
- Bachelor's Degree in Biology, Microbiology, Biochemistry, Chemistry, or a related discipline with 1 year of relevant experience (or an AA with 4 years, or HS diploma with 6 years of related experience).
- Proficient in cGMP practices across all laboratory assignments and environments.
- Excel at teamwork, sharing responsibilities to accomplish required QC sample testing efficiently.
- Able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA) for warehouse access.
Nice To Haves
- Experience utilizing state-of-the-art laboratory techniques and driving new technology implementations.
- Strong communication skills and experience participating in routine cross-departmental projects and investigations.
Responsibilities
- Conduct routine and non-routine analysis of the manufacturing environment and in-process commercial products according to standard operating procedures.
- Perform microbiological and chemical assays, basic troubleshooting, and equipment calibration and maintenance.
- Represent QC and serve as a primary point of contact for manufacturing and other operational departments.
- Collect, process, and enter data into electronic systems to generate accurate analytical reports.
- Initiate, compile, and perform laboratory investigations, including document reviews, interviews, and tracking.
- Assist with data trending, data review, lab maintenance, and the onboarding and training of new personnel.
- Develop, optimize, revise, and update standard operating procedures and testing methods.
- Maintain compliance with cGMP, GLP, and environmental safety guidelines to foster a positive safety culture.
Benefits
- A discretionary annual bonus may be available based on individual and Company performance.
- Benefits detailed at the link provided below.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Upload and Match Resume
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
