Manufacturing Associate III

Job Description

As a Manufacturing Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream or downstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP standards. If you thrive in a detail-oriented role with a strong grasp of automated systems and process controls, this position is tailor-made for you. Embrace the opportunity to maintain equipment and facilities while actively supporting various functions on site.

What You’ll Do 

• Execute manufacturing processing steps and support activities, ensuring alignment with the recipe and MFG documentation.
• Take the lead in troubleshooting equipment and process issues, showcasing your problem-solving skills.
• Demonstrate flexibility by revising documents as needed and facilitating equipment or process changes.
• Actively engage in training activities, managing your individual training plan, and providing guidance to fellow associates.
• Execute validation protocols with precision and attention to detail.
• Showcase leadership skills by taking charge of shifts in the absence of a supervisor, actively participating in exchanges, and coordinating activities across departments.
• Embrace additional duties that may be assigned, adding versatility to your skill set.

Qualifications

Want more jobs like this?

Get jobs in Solothurn, Switzerland delivered to your inbox every week.

Get Jobs

Send me The Muse newsletters for the best in career advice and job search tips.

By signing up, you agree to our Terms of Service & Privacy Policy.

Who You Are 

You are a detail-oriented Manufacturing Associate with a proven track record in cGMP environments. Your expertise lies in executing manufacturing processes, addressing equipment and process challenges, and contributing proactively to training initiatives. With many years of related industry experience and exposure to automated systems like Delta V or Syncade, you bring a wealth of knowledge to ensure the highest compliance standards are met.

Required Skills 

• Required Skills 

• High school diploma or equivalent experience with 5-7 years in Pharma/Biotech.
• Significant expertise in Manufacturing Upstream or Downstream process operations.
• Exposure to Delta V, Syncade, or similar automated systems.
• Language proficiency: English B1 is required; German and/or French is an asset.

Additional Information

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

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.