Bayer Biochemistry Job Opening 2020 – Apply Online
Bayer Biochemistry Bayer biochemistry Job Bayer invites bachelors degree candidates in biochemistry for the post of an Analyst III QC Potency candidates can also apply for the post. Interested candidates check out all the details on the same below:
Country: United States
State: California
Location: Berkeley
Reference Code: 224612
Functional Area: Quality
Entry Level: Professional
Job Title: Analyst III QC Potency
Required Qualifications:
Bayer Biochemistry Job Opening
- Bachelor of Science in Biochemistry or related major with at least five years of experience in Biopharmaceutical or a related industry OR a Master of Science in a related field with at least two years of experience in automated potency/clinical/in vitro biological activity testing;
- Bayer Biochemistry Job Opening Experience with a cGMP and global regulatory compliance organization;
- Strong working knowledge of FVIII potency testing;
- Strong working knowledge automated liquid handling systems;
- Ability to troubleshoot automated potency testing;
- Ability to multi-task and good adaptability to changing business requirements in a dynamic corporate environment;
- Strong computer and communication skills;
- Experience with equipment and analytical and/or biological method validation laboratory execution.
Preferred qualifications:
Familiarity with Bayer products and manufacturing processes.
The primary responsibilities of this role, Analyst III QC Potency, are to:
Bayer Biochemistry Job Opening
- Perform potency testing of FVIII products in-process and drug product for release and stability;
- Perform reagent qualification testing and reporting for critical reagents, standards, and controls;
- Review and approve Quality Control data in LIMS and SAP;
- Provide training to colleagues on GMP or test method related subjects and train others on potency equipment use and maintenance and test methods;
- Bayer Biochemistry Job Opening Address questions during regulatory compliance audit and support inspection-related needs as required;
- Perform analytical equipment maintenance and laboratory cleaning activities per cGMP standards;
- Maintain lab to inspection-ready status at all times;
- Analyze and verify data in reports and process memos and reports through Valgenesis;
- Manage and host vendor PMs, renew service contracts with vendors, and ensure MSA ison file for business continuity.
