Job Title: Manufacturing Operator – Drug Product
About the Role
We are seeking a motivated and detail-oriented Manufacturing Operator to join our Drug Product manufacturing team on a contingent basis. In this role, you will execute manufacturing activities in compliance with cGMP guidelines, ensuring safe, timely, and high-quality production of sterile drug products. You will be the first line of technical and procedural support, working closely with production teams to maintain operational excellence.
Key Responsibilities
- Execute manufacturing activities for Drug Product in line with cGMP, batch instructions, and quality requirements.
- Operate, set up, clean, and maintain production equipment for liquid and freeze-dried drug forms (e.g., compounding, parts washing, autoclaving, filter integrity testing, visual inspection).
- Evaluate test results, troubleshoot equipment issues, and recommend solutions.
- Prepare, execute, and review batch records and other GMP documentation accurately and on time.
- Support process-related investigations, process changes, and CAPA implementation within defined timelines.
- Provide training and on-the-job support to team members and new joiners.
- Collaborate effectively with cross-functional teams to resolve operational issues and drive improvements.
Requirements
- 2–4 years of experience in a GMP environment, preferably in sterile Drug Product manufacturing.
- Fluent in English or German (both preferred).
- Strong understanding of GMP requirements, quality procedures, and SOP execution.
- Team-oriented with excellent interpersonal and communication skills.
- Organized, structured, and detail-focused working style.
- Highly motivated and proactive.
- IT literacy; SAP and MES experience is a plus.
- Willingness to work in a 2-shift pattern.
Practical’s
- Location: Visp
- Duration: +4months
- Start Date: ASAP
- Work Model: Full-time, 2-shift pattern
Interested or know someone who might be?
Send your CV or inquiries to e.cabral@panda-int.com to apply or learn more.
Job Title: Manufacturing Operator – Drug Product
About the Role
We are seeking a motivated and detail-oriented Manufacturing Operator to join our Drug Product manufacturing team on a contingent basis. In this role, you will execute manufacturing activities in compliance with cGMP guidelines, ensuring safe, timely, and high-quality production of sterile drug products. You will be the first line of technical and procedural support, working closely with production teams to maintain operational excellence.
Key Responsibilities
- Execute manufacturing activities for Drug Product in line with cGMP, batch instructions, and quality requirements.
- Operate, set up, clean, and maintain production equipment for liquid and freeze-dried drug forms (e.g., compounding, parts washing, autoclaving, filter integrity testing, visual inspection).
- Evaluate test results, troubleshoot equipment issues, and recommend solutions.
- Prepare, execute, and review batch records and other GMP documentation accurately and on time.
- Support process-related investigations, process changes, and CAPA implementation within defined timelines.
- Provide training and on-the-job support to team members and new joiners.
- Collaborate effectively with cross-functional teams to resolve operational issues and drive improvements.
Requirements
- 2–4 years of experience in a GMP environment, preferably in sterile Drug Product manufacturing.
- Fluent in English or German (both preferred).
- Strong understanding of GMP requirements, quality procedures, and SOP execution.
- Team-oriented with excellent interpersonal and communication skills.
- Organized, structured, and detail-focused working style.
- Highly motivated and proactive.
- IT literacy; SAP and MES experience is a plus.
- Willingness to work in a 2-shift pattern.
Practical’s
- Location: Visp
- Duration: +4months
- Start Date: ASAP
- Work Model: Full-time, 2-shift pattern
Interested or know someone who might be?
Send your CV or inquiries to e.cabral@panda-int.com to apply or learn more.