Quality Control Associate

Responsibilities

• Perform release and stability testing, including cell-based bioassays, ID ELISA, potency ELISA, and impurities ELISA
• Execute method qualification, validation, and transfer activities
• Conduct laboratory investigations regarding deviations, Out of Specification (OOS), and Out of Trend (OOT) results
• Manage standard operating procedures, work instructions, protocols, and reports
• Maintain a compliant, clean, and safe working environment in accordance with ICH, GMP, and safety regulations
• Participate in internal and external audits, inspections, and regulatory assessments

Requirements

• BS/MS in an applicable discipline (Biochemistry or Biology preferred)
• Minimum of 1 year of experience in the biopharmaceutical industry
• Hands-on experience with bioassays and potency assays
• Ability to lift 25 pounds

Preferred Qualifications

• 2–3 years of experience in the biopharmaceutical industry
• Proficiency with LIMS, Trackwise, or SoftMax Pro

Benefits

• Comprehensive Health Insurance (Medical, Dental, Vision, and Prescription) starting on day one
• 401(k) with employer match up to 6% and an annual 3.75% Defined Contribution
• Paid Time Off including vacation, sick/safe time, and holidays
• Company-paid Life and Disability insurance
• Additional perks including Employee Stock Purchase Plan, Tuition Assistance, and Paid Parental Leave

About the Company

Teva is a leading innovative biopharmaceutical company dedicated to addressing patients' needs through neuroscience, immunology, and high-quality generic medicines worldwide. We foster a high-performing, inclusive culture that values collaboration and fresh thinking.