In this role, you will be responsible for executing manufacturing activities in the drug product area in compliance with cGMP standards. Your tasks include performing visual inspections, supporting production processes, and ensuring documentation quality. 

Start Date: ASAP

Duration: 12 Months

Place of Work: Visp 

Key Responsibilities

  • Conduct manufacturing operations for drug products according to cGMP guidelines, ensuring proper batch execution and troubleshooting issues
  • Perform manual visual inspections of liquid and lyophilized vials to detect and remove defective units, ensuring final products are sterile and defect-free
  • Provide frontline technical and procedural support to the manufacturing team
  • Guarantee that each batch is produced safely, timely, and in accordance with instructions and quality standards
  • Prepare accurate and timely production documentation, including batch records and GMP-related logs
  • Assist in process investigations and contribute to decision-making on manufacturing issues
  • Support process changes and corrective actions within specified deadlines
  • Conduct training sessions for operators and support staff, including new hires
  • Operate, set up, and clean production equipment and facilities

Candidate Profile

  • Previous experience in a GMP environment, preferably in sterile drug product manufacturing
  • Knowledge of GMP requirements, SOPs, and quality procedures
  • Strong team player with excellent communication skills
  • Organized, detail-oriented, and able to manage multiple priorities
  • Highly motivated, proactive, and adaptable to flexible working hours

  • Languages: Fluent in English or German, with a preference for proficiency in both languages

     

Job ID 41181160