Join Our Team as a Manager Engineering (m/f/d)
We are a research-driven biopharmaceutical company dedicated to the belief that "following the science" leads to the development of groundbreaking medicines that can significantly impact global health. At our core, we are committed to innovation in medicine and vaccine development, striving to improve the lives of patients worldwide.
About Our Location
Our Schachen facility serves as a hub of creativity and collaboration, attracting individuals from diverse backgrounds who contribute to our mission. Employees feel a strong sense of belonging, knowing that their contributions shape the site and foster a vibrant work culture.
The state-of-the-art Biotech facility in Schachen empowers us to achieve excellence in our operations. By integrating advanced technology within a dynamic workspace, we facilitate seamless collaboration among teams, enhancing our capability to deliver exceptional Biologics Drug Substance manufacturing for Early Phase Clinical Supply and the implementation of Technology Innovations.
Role Overview
The Manager Engineering (m/f/d) will be a vital member of the extended Biotech Manufacturing Leadership Team, reporting to the Associate Director of Support Operations at the Schachen Site. This position requires a hands-on approach with a focus on leading the Solution Supply team, ensuring both team support and operational efficacy on-site.
Main Responsibilities
- Lead the Solution Supply team in day-to-day operations, including the weighing and dispensing of raw materials and preparation of cell culture media and buffers used in mAb manufacturing.
- Plan daily shop floor operations to align with the facility's schedule.
- Act as the first line of support for any floor issues, ensuring effective problem resolution.
- Maintain area compliance with Good Manufacturing Practice (GMP) standards.
- Support GMP Drug Substance Manufacturing by ensuring the seamless sharing of resources to maintain business continuity.
- Conduct investigations and root cause analysis, supporting deviations and change controls.
- Oversee and enhance departmental procedures to ensure operational efficiency and continuous improvement, including the management of GMP documentation.
- Implement innovative technologies to streamline manufacturing and administrative processes.
- Ensure the highest standards of Quality, Compliance, and Safety.
- Foster a culture of Diversity and Inclusion by building effective working relationships across cross-functional teams.
- Adhere to Safety, Health, and Environmental guidelines while striving toward corporate safety and environmental objectives.
- Collaborate across the company network to share best practices and leverage resources efficiently.
Required Education, Experience, and Skills
- Degree in science or engineering, complemented by experience in a people management role.
- A minimum of 5 years of experience in a GMP-regulated drug substance manufacturing environment, preferably with knowledge of single-use systems.
- Strong analytical skills, capable of addressing complex situations with practical solutions.
- Experience with quality management systems and excellent technical writing abilities.
- Proficiency in oral and written communication in both German and English.
Preferred Experience and Skills
- In-depth understanding of GMP manufacturing processes, with significant knowledge of upstream and downstream processing.
- Familiarity with Delta V and MES (Manufacturing Execution System) is a plus.
- Experience in Managing Staff and cross-functional project management.
- Knowledge of Problem, Deviation, and Change Management processes.
About Us
Established in Switzerland since 1963, our company has positioned its regional office and manufacturing capabilities in Lucerne, which serves as the operational hub for approximately 1,000 employees across four locations. We have recently expanded to Zurich to accelerate the development of our medicines and vaccines, further supporting our mission to save and enhance lives globally.
Proudly recognized as a “Top Employer Switzerland” and “Top Employer Europe,” we are committed to fostering a positive work environment for our employees and the communities we serve.
Our Werthenstein BioPharma site in Schachen is at the forefront of research and development for biological agents, producing innovative products and providing clinical trial supplies for global studies. This site also houses one of our global forensic laboratories, ensuring product security and patient safety throughout the supply chain.
Application Process
Apply online using the form below. Please note that only applications matching the job profile will be considered.
Relocation and Travel Requirements
- Relocation: None
- Visa Sponsorship: None
- Travel Requirements: 5%
- Flexible Working Arrangements: No
- Shift: No
- Valid Driver License: No
- Hazardous Materials: Yes