What you will do:

• Execute manual visual inspection.
• Execute manufacturing activities in the area of Drug Product according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshooting manufacturing equipment, and making recommendations for resolution.
• Provide front‑line technical and procedural support while working with the manufacturing team.
• Secure that each batch is manufactured safely, on time, and in compliance with batch instructions and quality requirements.
• Establish timely and high‑quality production documentation (preparation, execution, and review of batch records) or other relevant GMP documents for the assigned production area.
• Support process‑related investigations and assist in decision‑making on production issues.
• Support process changes and CAPAs related to processes within required timelines.
• Perform training activities for relevant areas as ...