Our client, a leading global player in the pharmaceutical industry with modern offices in the Lucerne area, is looking for a hands-on Senior Process Engineer (a) to support the growing Biotech Engineering Team. The candidate will play an important role within the team and contribute significantly to its overall success
Description
The selected candidate will be responsible for the primary following activities :
- Guide the team and facilitate collaboration with colleagues at the local site across the global network to shape and implement next-generation technologies with innovations for GMP Batch and Continuous Manufacturing in Drug Substance and Drug Product
- Serve as a subject matter expert in assessing innovative equipment to enhance manufacturing processes, including the development of user requirements and preparation of capital investment proposals
- Strive to align technologies across batch and continuous manufacturing to enable seamless flexibility in transitioning between both approaches
- Support the development of GMP Documentation such as: Risk Assessments, Batch Records, Sampling Plans, Qualification Documents, and SOPs
- Deliver QA and GMP compliance expertise while collaborating with global, cross-functional teams
Profile
To be considered for this position, the ideal candidate must have :
- A minimum of 5 years of work experience in the pharmaceutical or biotech industry
- Minimum of 3 years of experience with quality management and compliance systems, Working knowledge of quality auditing - preferred.
- Familiarity with Upstream and Downstream Unit Operations for biologics manufacturing.
- Experience as a Project Manager with cross-functional team members Competent in analyzing complex situations and showing practical problem-solving capabilities
- Excellent communication skills and fluency in English, German is a plus
Job Offer
This is a unique opportunity to immediately join a renowned international company and assume a key leadership role as an integral part of the team for the next 18 months.