We Are Teva

How You’ll Spend Your Day

• Review and approve/reject printed packaging materials in a timely manner according to the production plan.
• Prioritise packaging materials listed in the Exceptions Report and ensure same-day review when entered into SAP.
• Review and approve printed packaging material specifications, including Version 1 and non-Version 1 documents.
• Sample printed packaging materials upon request.
• Compile Certificates of Analysis (CoAs) for printed packaging materials as required.
• Prepare Batch Release Certificates (Commercial and Registration), including CoAs, BRCs, and CoCs, prior to Qualified Person (QP) review and within agreed timelines.
• Provide clients with commercial batch documentation, including approved certificates, starting material certificates, and manufacturing/packaging batch documentation as specified in Technical Agreements or product specifications.
• Coordinate the preparation and distribution of finished product samples, registration documentation, and supporting information required for product registration and business expansion activities.
• Act as the primary liaison between clients and internal departments for quality-related queries and requests, ensuring responses are provided within 48 hours.
• Perform training on new or updated Standard Operating Procedures (SOPs) and ensure compliance with authorised SOPs at all times.
• Maintain and update QA records, databases, and logbooks regularly to support efficient and reliable operations.
• Archive and retrieve QA batch documentation, logbooks, and packaging material samples as required.
• Participate actively in projects aimed at improving quality assurance processes and departmental performance.
• Compile assigned Product Quality Reviews (PQRs) on a monthly basis.
• Perform additional duties and responsibilities as required by the department.

Your Skills and Experience

How We’ll Take Care of You

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