About this Role

In this Small Scale Manufacturing (SSM) Manufacturing Specialist II role, you will be responsible for manufacturing support tasks including technical writing, project management, and process implementation. This position requires you to be highly detail oriented with excellent technical writing skills and a continuous improvement mindset.

What You’ll Do

• Author manufacturing documentation including procedures, work instructions, logbooks, changeover protocols, batch production records, solution lot records and deliver on key stakeholder requirements with a minor degree of supervision.
• Project management and project execution – lead or participate in projects, facilitating timely execution.
• Partner with cross functional groups (e.g. Manufacturing, Manufacturing Sciences, Engineering, Automation, Quality, Planning, and Materials Management) to identify continuous improvement opportunities and drive implementation
•  Support the technology transfer of products into manufacturing and communicate across functional teams to ensure production schedules are met.
• Initiate, own, and manage manufacturing focused change controls, CAPAs, and planned exceptions
• This site-based role supports MFG, primarily during core weekday business hours, but may require infrequent off-hours support.

Who You Are:

If you are a highly detailed and focused individual who demonstrates a moderate to advanced level of technical process knowledge, technical writing ability, and subject matter expertise with manufacturing processes and equipment, you would be a great fit for our Manufacturing Technical Operations Team!  This position will provide you the opportunity to collaborate and innovate with a group of individuals who are all passionate about transforming patient lives

Required Skills:

• Bachelor’s degree (Life Sciences or Engineering ) preferred, with 1 years of transferrable experience
• Associates Degree or Bioworks Certificate and 2 years of transferrable Experience
• High School Diploma (or Equivalent) 4 years of transferrable experience

Preferred Skills:

• Prior experience in manufacturing – drug substance biologics, downstream or upstream operations
• Understanding of business processes and roles of cross-functional groups supporting manufacturing operations
• Robust understanding of quality and cGMP principles
• Fundamental knowledge of change control in cGMP environment
• Intermediate to advanced skills in Microsoft Office and computer-based quality systems
• Intermediate to advanced level of technical writing skill
• Ability to interpret manufacturing process design documentation
• Excellent oral and written communication skills

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.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.