2,120,498open jobs
134,160companies
239,710added this week
Browse all
Salary
$147k – $203k per year
Location
In office (Research Triangle Park)
Seniority
Staff · 10+ years exp
Visa
H-1B filings in 12 months: 79 · green card filings: 7
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 5, 2026. First seen by Alion on Nov 5, 2026. Biogen scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Biogen is an American biotechnology company headquartered in Cambridge, Massachusetts, that develops and sells therapies for neurological and neurodegenerative diseases. Founded in 1978, its products treat multiple sclerosis, spinal muscular atrophy, Alzheimer's disease and other rare and neuromuscular disorders. It is listed on Nasdaq and hires regulatory, manufacturing, medical science liaison and IT staff in Cambridge, Research Triangle Park, Baar and other sites.

About this role

The Manufacturing Engineering Lead manages a mission-critical function within Site Engineering and Facilities, overseeing the installation, validation, reliability, and optimization of manufacturing process equipment and cGxP warehouse technologies. This leader will guide a team of engineers, represent Site Engineering and Facilities in key operational decisions, and partner closely with Manufacturing, Quality, EHS, Maintenance, Automation, and global engineering teams. The role requires a strong technical foundation in biopharmaceutical manufacturing, validation, equipment performance, and regulated operations.

What you’ll do

  • Lead and develop the Manufacturing Engineering function, including a team of approximately 7-15 employees.
  • Ensure the ongoing reliability, performance, safety, and compliance of manufacturing process equipment and assigned systems.
  • Establish departmental goals, development plans, operating metrics, and tactical priorities aligned with manufacturing and site objectives.
  • Represent Site Engineering and Facilities in site and factory leadership discussions involving manufacturing strategy, technical risks, and operational direction.
  • Lead validation strategy, execution, and lifecycle management while ensuring alignment with the Quality Management System and global procedures.
  • Present and defend manufacturing engineering and validation programs during regulatory audits and inspections.
  • Develop operating and capital forecasts, manage departmental resources, and provide oversight of the site’s small-capital portfolio.
  • Prioritize continuous-improvement initiatives, equipment upgrades, and engineering solutions that improve reliability, efficiency, and manufacturing performance.
  • Provide technical direction during critical equipment issues and support uninterrupted manufacturing operations.
  • Collaborate with Quality and EHS to maintain equipment and systems in a safe, compliant, and validated state.
  • Support 24/7 manufacturing operations as business needs require.
  • Coach and develop engineering employees while promoting technical capability, accountability, and effective delegation.

Who you are

You are an experienced engineering leader who combines deep technical knowledge with sound operational judgment. You can lead through complex equipment and compliance challenges, develop engineering talent, influence senior stakeholders, and make timely decisions in a fast-paced manufacturing environment.

Required skills

  • Bachelor’s degree in engineering from an accredited college or university
  • At minimum, 10 years of relevant experience in biotechnology, pharmaceutical, or adjacent industry.
  • At minimum, 2 years of experience managing or leading engineering professionals, contractors, or cross-functional technical teams.
  • In-depth experience with GMP validation, manufacturing, engineering, or facilities.
  • Demonstrated knowledge of biopharmaceutical manufacturing operations, cGMP, GLP, EMEA, and ISO requirements.
  • Experience working with FDA or comparable regulatory investigators, preparing responses to observations, and implementing corrective measures.
  • Experience leading GMP validation activities and maintaining manufacturing systems in a compliant and validated state.
  • Experience with large operating and capital budgets and complex engineering projects.
  • Demonstrated ability to lead cross-site or cross-functional initiatives.

Preferred skills

  • Working knowledge of distributed control systems, programmable logic controllers, P&IDs, and standard operating procedures.
  • Experience with manufacturing process equipment and supporting utility or facility systems.
  • Lean Six Sigma, continuous-improvement, or operational-excellence experience.
  • Contract management and contractor safety-management experience.
  • Experience supporting large-scale, multi-use manufacturing facilities.
  • Strong business acumen, strategic planning, capital-investment analysis, and resource-management capabilities.
  • Ability to communicate engineering strategy and technical risk effectively to senior leaders, regulators, vendors, and cross-functional partners.
Job Level: Management

Additional Information

The base compensation range for this role is: $147,000.00-$202,500.00

Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.

In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:

  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation

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 Biogen.

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.

Free account
Stop reading job ads. Get the ones that fit.
One free account turns this page into a shortlist built around your stack, your level and your pay.
Match on every job. Stack, seniority, pay and location, scored against your profile.
2,120,498 open roles. Read straight off company career pages, refreshed every day.
Unlimited applications. Every one you send is tracked in one place, on-site or on a company board.
3 tailored CVs a month. Rewritten for the exact job you are applying to. Included free.
Create a free account Continue with Google
Free forever. No card. Under a minute.

Your match

How well do you fit this role?
Two answers are enough for a real match. No account needed.
Check my fit
Answers stay in this browser until you create an account.

Recommended for you based on this role

Industrial Engineering
Similar stack
Same company
Research Triangle Park
$93k – $140k per year · In office · Full-Time · 3+ years exp · Bachelor's Degree · Websterville
Apply
$40k – $52k per year · In office · Full-Time · Los Angeles
Apply
Hybrid · Full-Time · 3+ years exp · Bachelor's Degree · Jacksonville
Apply
$114k – $150k per year · Equity · In office · Nationals only · Full-Time · 8+ years exp · Bachelor's Degree · Round Rock
Apply
In office · Full-Time · 8+ years exp · Bachelor's Degree · United States
Apply
$120k – $174k per year · Equity · In office · Full-Time · 5+ years exp · Research Triangle Park
Python
Java
C++
DevOps
GCP
Azure
AWS
VLAN
BGP
OSPF
Apply
$120k – $174k per year · Equity · Hybrid · Full-Time · 5+ years exp · Research Triangle Park
DevOps
VLAN
Wi-Fi
BGP
OSPF
Apply
$120k – $174k per year · Equity · In office · Full-Time · 5+ years exp · Research Triangle Park
DevOps
VLAN
BGP
OSPF
Cybersecurity
Wireshark
Tcpdump
Web3
Layer 2
Apply
Consulting Engineer 3 days ago
$96k – $126k per year · Equity · Hybrid · Full-Time · 3+ years exp · Bachelor's Degree · Research Triangle Park
Python
DevOps
Ansible
Apply
$107k – $143k per year · Equity · In office · Full-Time · 6+ years exp · Bachelor's Degree · Research Triangle Park
Design
AutoCAD
Management
SharePoint
MedTech
CAPA
Apply
See all jobs
This is one of many
2,120,498 more open roles from verified company boards, updated every day.