Quality Analyst I

Responsibilities

• Evaluate and approve manufacturing and packaging documents, including physical copies and electronic batch records (eBR).
• Ensure all relevant information is gathered, assessed, and approved before product disposition.
• Assign QA statuses (Release/Reject/Quarantine/Impound) to work-in-process and finished products.
• Identify improvements, new procedures, or compliance gaps based on applicable regulations.
• Investigate and resolve routine issues arising during work assignments.
• Coordinate all necessary paperwork required for batch release.

Requirements

• 4-year Bachelor’s Degree in a Science-related field (preferred) or relevant GMP Quality experience.
• Minimum of one year of experience in a heavily regulated manufacturing environment, preferably in pharmaceuticals.
• Thorough understanding of current Good Manufacturing Practices (cGMPs).
• Ability to perform basic statistical analyses and comprehend AQL sampling plans.
• Proficiency in Veeva, eBR, MS Office, and other relevant software.
• Strong communication skills and the ability to collaborate with cross-functional teams.
• Ability to stand, walk throughout the facility, and lift up to 25 pounds.

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 Tuition Assistance, Employee Stock Purchase Plan, and Paid Parental Leave.

About the Company

Teva is a leading innovative biopharmaceutical company dedicated to addressing patients' needs through high-quality medicine and a world-class generics business. We foster a high-performing, inclusive culture that values collaboration and fresh thinking to improve health worldwide.