About Us
We are a research-driven biopharmaceutical company dedicated to the belief that by "following the science," we can create great medicines that significantly impact the world. Our mission revolves around innovation in medicine and vaccine development, aimed at improving the lives of patients globally.
The Schachen Facility
Our Schachen site serves as a hub that attracts and integrates people from diverse backgrounds and perspectives. Employees feel a strong sense of belonging at Schachen, contributing to an environment shaped by their collective experiences.
The state-of-the-art Biotech facility in Schachen supports our best work by merging cutting-edge technology with a dynamic, activity-based workspace. It facilitates seamless connection and collaboration, offering Biologics Drug Substance manufacturing for early-phase clinical supplies and technology innovations.
Position Overview: Manager Engineering (m/f/d)
We are seeking a talented Manager Engineering, Solution Supply to join our extended Biotech Manufacturing Leadership Team. Reporting to the Associate Director of Support Operations at the Schachen Site, the successful candidate will lead the Solution Supply team and will be required to be physically present on-site to support team activities.
Main Responsibilities
- Lead the Solution Supply team in daily operations, including weighing and dispensing raw materials and preparing cell culture media:
- Plan daily shop floor operations in alignment with the facility schedule.
- Act as the first level of support for any operational issues on the shop floor.
- Maintain area compliance with Good Manufacturing Practice (GMP) standards.
- Provide full support to GMP Drug Substance Manufacturing to ensure business continuity.
- Conduct investigations, root cause analysis, and risk assessments related to deviations and change controls.
- Oversee and maintain departmental procedures and practices to ensure operational efficiency and continual improvement, including GMP documentation such as SOPs, Batch Records, Buffer Memo, and Qualification and Validation Protocols.
- Implement new technologies that streamline manufacturing and administrative processes.
- Ensure adherence to the highest standards of Quality, Compliance, and Safety.
- Encourage Diversity and Inclusion by building effective working relationships within a cross-functional team.
- Embody a "Safe by Choice" approach, adhering to Safety, Health, and Environment guidelines and working towards the company's safety and environmental goals.
- Collaborate across the network to share best practices and lessons learned, embodying an enterprise mindset to leverage resources effectively.
Required Education, Experience, and Skills
- Degree-level qualification in science or engineering, with experience in People Management.
- A minimum of 5 years' experience in a GMP-regulated drug substance manufacturing environment, preferably with experience in single-use systems.
- Proficient in analyzing complex situations with practical problem-solving capabilities.
- Experience with quality management and compliance systems along with strong technical writing skills.
- Fluency in both oral and written communication in German and English.
Preferred Experience and Skills
- Understanding of manufacturing/operational GMP environments, with significant knowledge of both upstream and downstream processes.
- Familiarity with Delta V and MES (Manufacturing Execution System) is advantageous.
- Experience in Problem, Deviation, and Change Management.
- Project management experience, specifically with cross-functional teams.
About Our Company
Established in Switzerland since 1963, our company has a regional office and manufacturing/packaging facility, with Lucerne serving as the operational center. Approximately 1,000 individuals collaborate across our four locations in Lucerne. A fifth location has been opened in Zurich to accelerate the development and commercialization of our medicines and vaccines, furthering our mission to save and enhance lives worldwide.
We take pride in being recognized as a "Top Employer Switzerland" and "Top Employer Europe," reflecting our commitment to our employees and the surrounding community.
Our Werthenstein BioPharma site in Schachen specializes in pioneering research, developing and analyzing biological agents, producing new products, and supplying clinical trial products for global studies. It also hosts one of our international forensic laboratories, monitoring product security and 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.
Additional Information
- Relocation: None
- Visa Sponsorship: None
- Travel Requirements: 5%
- Flexible Working Arrangements: No
- Shift: No
- Valid Driver License: No
- Hazardous Materials: Yes