Job Description

WHAT YOU’LL DO

• Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the batch record and control system. May coordinate or lead process steps as requested.
• Documents/Records and Reviews cGMP data and information (including documentation of deviations) for processing steps and/or equipment activities, following standard operating procedures. Revises or creates documents as instructed. Key documentation includes batch records, SLRs, and equipment logbooks.
• Actively participates in training activities, managing their individual training plan. Trains other associates as required.
• Executes validation protocols with minimal supervision/direction of others.

WHO YOU ARE

• You enjoy being a part of a high performing team that is agile in its ability to meet its production schedule.  You also like being accountable in driving tasks and projects to completion while getting exposure to responsibilities supporting the manufacturing process

Qualifications

REQUIRED SKILLS:

• High School Diploma (or equivalent) in addition to 1.5 years of direct experience/3 years of related experience OR
• BioWork Certificate or Associate’s Degree in addition to 1 year of direct experience/2.5 years of related experience OR
• Bachelor’s Degree strongly preferred with 6 months of direct experience/2 years of related experience

PREFERRED SKILLS:

• Targeted biopharmaceutical training (Bioworks or equivalent) and/or related military training preferred
• Detailed oriented with excellent documentation skills
• Operates in a safe manner in order to avoid injury to self and others
• Adaptable to changing needs and demands, comfortable navigating in a changing environment
• Strong time-management skills 
• Mechanically inclined skillset 
• Ability to communicate clearly and effectively to all levels of the organization
• Capable of working 10+ hour-shifts with day and night flexibility preferred

Additional Information All your information will be kept confidential according to EEO guidelines.

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.