Quality Control Biochemistry Associate
Job Responsibilities:
- Associate II’s responsibilities include, but are not limited to testing pH, Appearance, Osmolality, Protein Concentration (UV, RI, and SoloVPE).
- The Associate II should possess a fundamental understanding of the Client Quality Systems and apply it in their daily support functions.
- Additional responsibilities include ensuring adherence to all GLP/GMP requirements, interfacing with Quality and manufacturing as applicable.
- Supporting investigations impacting the QC department.
- The Associate II should be able to work effectively within the group, within Quality and across site.
- This requires solid and robust written and verbal communication skills.
- Performs in-process, release testing, method transfer and validation support activities/testing. Supports investigational activities including testing. - 85%.
- Supports QC Biochemistry operations related to business and manufacturing schedules, support of process validation initiatives. - 10%.
- Supports maintenance of effective laboratory systems to ensure integrity of all laboratory results. - 5%.
Skills:
- Quality Control
- Biochemistry Testing
- In-Process Testing
- Release Testing
- Method Transfer
- Validation Testing
- GLP/GMP Compliance
- pH Testing
- Appearance Testing
- Osmolality Testing
- Protein Concentration Testing (UV, RI, SoloVPE)
- Quality Systems
- Investigation Support
- Laboratory Systems
- Written and Verbal Communication
Education/Experience:
- B.S. Degree (Science Preferred).
- 2+ years of relevant experience (M.S. degree) or 3+ years of relevant experience (B.S. degree).
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