About This Role

The main responsibilities for the Quality Control Associate I Microbiology includes execution of all the Microbiology related testing activities at Biogen’s large scale manufacturing facility in Solothurn, Switzerland. Microbiology related analysis at the site will include microbiological identification, bacterial endotoxin test (KCA and KTA), detection of microorganisms (BacT/Alert), growth promotion test and microbial enumeration test. In addition, the Quality Control Associate will contribute to the development and execution of QC Microbiology related supporting studies.

The Quality Control Associate I Microbiology must support all activities to ensure that the instrumentation in WIP labs is prepared for each corresponding unit operation to be performed in manufacturing.

The Quality Control Associate I Microbiology should have a background in microbiological analytical methodologies. The Associate must correctly work with cGMP regulated computerized systems which are necessary for the testing workflow as these systems will support the vision of establishing a paper-less lab and ensure the relevant data integrity. The Quality Control Associate I Microbiology supports the Microbiology Team with establishing analytical procedures and protocols related to microbiological analysis.

The Quality organization at the Solothurn site is envisioned to be supported by team members with diverse backgrounds that are capable of cross functional work to support the high throughput design of the facility. Quality staff is focused on incorporating a new operations strategy into the quality management systems, lab systems and business systems. The operational strategy strongly relies on the incorporation of online real-time monitoring, automation of routine testing wherever possible and integrated information technology systems to bring transparency to routine business operations.

What You'll Do

• Support the QC Microbiology team with day-to-day analytical operations including test execution and review activities of routine EM and UM samples, as well as MFG support samples (e.g. Cleaning samples) and in-process and drug-substance samples.
• Support administrative activities including archival of data, protocol/report and procedure drafting, analytical instrument maintenance activities, deviation management.

Who You Are

The ideal candidate should have a microbiological analytical background, familiarity with cGMP-regulated computerized systems, and the ability to work towards establishing a paperless lab. The role supports the Microbiology Team in protocol development and aligns with the site's focus on new operational strategies, real-time monitoring, and automation.

• Experience within Biological Quality Control, Microbiology and analytical function. Experience in pharmaceutical or biotech manufacturing environment is a plus.
• Apprenticeship degree (Laborant EFZ) in Biology or related Life Science or Technical discipline.
• Analytical skills in Microbiology.
• Must have a working understanding of modern analytical microbiological modalities to facilitate the execution of analytical quality strategies.
• Demonstrated problem solving skills.
• Demonstrated ability to work autonomously and cross-functionally.
• Strong presentation and organizational skills.
• Must have strong technical skills and be proficient with typical productivity software (Word, Excel, Power Point, Visio, etc.).
• Must have proficiencies with the Quality systems and business processes associated with Microbiology testing.
• English (minimum level B1).

Why Biogen?

Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine. Together, we pioneer. Together, we thrive.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts