We are looking for a Deviation Manager to join a large-scale mammalian cell culture facility in Visp on a 6-month contract. This role offers the opportunity to work in a dynamic and regulated environment, ensuring compliance and quality in manufacturing processes.
Key Responsibilities:
- Own, author, and investigate deviations in manufacturing.
- Collaborate with Subject Matter Experts (SMEs) to determine root causes and assess impact.
- Use investigational tools like Fault Tree Analysis and Fishbone Diagrams to define root causes.
- Develop and implement Corrective and Preventive Actions (CAPAs) and Effectiveness Checks.
- Ensure cGMP compliance throughout the deviation management process.
- Drive timely closure of investigations and support process improvements.
Key Requirements:
- Bachelor's degree in Chemistry, Biotechnology, Life Sciences, or a related field.
- Experience with Deviation Management and cGMP in a pharmaceutical or API environment.
- Strong problem-solving, technical writing, and organizational skills.
- Ability to work independently and lead teams without formal authority.
- Fluent English (spoken & written); German is an advantage.
For further information about this position, please apply with your CV
*Please note, only those with the right to work in Switzerland can apply!
