Biogen

Compensation

Full Description

## Key Role Overview As a Senior Process Engineer you will serve as a subject matter expert within the Drug Product Technical Authority supporting Finished Goods (FG) and Oral Solid Dosage (OSD) technologies. You will drive technical excellence across Biogen's global manufacturing network by optimizing equipment and system performance for device assembly, labeling, packaging, blistering and bottling operations, providing engineering guidance to site teams, supporting capital projects and tech transfers, and implementing continuous improvement and compliance activities. ## Key Responsibilities - Establish and update engineering standards and best practices for Finished Goods and Oral Solid Dosage operations across manufacturing sites. - Lead technical assessments, facility fit/feasibility studies and process improvement initiatives to inform senior leadership decision-making. - Integrate engineering considerations into new projects, participate in capital planning, and support execution of capital projects in line with modality requirements and capital project management processes. - Support technology transfers for OSD from an engineering and facilities perspective and provide direction to site engineering teams to ensure program adherence and technical excellence. - Implement continuous improvement strategies to improve equipment and system performance and investigate innovative technical, equipment and process solutions benchmarking against industry best practices. - Support development of business cases requiring capital investment and engage with external vendors and industry experts for new technologies relevant to FG and OSD manufacturing. - Employ a data-centric approach to engineering assets and ensure regulatory compliance, adherence to standards, and alignment with company policies for all engineering activities. ## Required Qualifications - BS in engineering (mechanical, chemical, electrical, industrial) or related discipline. - Minimum 4 years' experience in Engineering/Maintenance in Biotech, Pharmaceutical, Medical Device, or similar manufacturing industry. - Experience in either Finished Goods (device assembly, labeling, packaging) or Oral Solid Dosage environments; experience in both is highly preferred. - Strong communication, presentation, and technical skills with proven ability to influence at both site and enterprise levels. - Demonstrated expertise in core engineering principles and data-driven analysis. ## Preferred Qualifications - Master’s degree in Engineering. - Experience with engineering & architectural firms (A+E) in the study and design of processes for FG and/or OSD modalities. ## Compensation & Benefits - Base salary range: $91,000 - $118,000 per year. - Base salary determined using factors such as skills, experience, job location, and internal equity. - Eligible for short-term and long-term incentives, including cash bonus and equity incentive opportunities. - Medical, dental, vision, and life insurance coverage. - Fitness and wellness programs including fitness reimbursement. - Short- and long-term disability insurance. - Minimum of 15 days paid vacation plus an end-of-year shutdown (Dec 26-Dec 31). - Up to 12 company paid holidays plus 3 paid days off for personal significance. - 80 hours of sick time per calendar year. - Paid maternity and parental leave benefits. - 401(k) program with company matched contributions and employee stock purchase plan. - Tuition reimbursement up to $10,000 per calendar year. - Employee Resource Groups participation. ## Additional Information - Work arrangement: hybrid role based at Biogen offices in Research Triangle Park, NC. - Biogen emphasizes inclusion, belonging, and equal opportunity; all qualified applicants will receive consideration without regard to protected characteristics. - Biogen is an E - Verify Employer in the United States. - Job level: Professional.