Quality Control Biochemistry Associate

• 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%.

Quality Control Biochemistry Testing In-Process Testing Release Testing Method Transfer Validation TestingGLP/GMP CompliancepH Testing Appearance Testing Osmolality Testing Protein Concentration Testing (UV, RI, SoloVPE)
Quality Systems Investigation Support Laboratory Systems Written and Verbal Communication

B.S. Degree (Science Preferred).2+ years of relevant experience (M.S. degree) or 3+ years of relevant experience (B.S. degree).