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Sr. Manufacturing Technician – Manufacturing Maintenance

Biogen · Research Triangle Park, NC

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Level
Technician
Team
Reliability
Experience asked
4+ years
Industry
Pharma & life sciences
Posted
2 days ago

The role in 30 seconds

An engineer-level reliability role at Biogen (pharma & life sciences) in Research Triangle Park, NC. You will play a critical role in supporting manufacturing and laboratory operations by ensuring equipment reliability and performance.

They ask for
4+ years
Tools it names
FDA / GMP, Validation (IQ/OQ/PQ)
Day to day
some off-shift / weekend coverage

Read from the posting. The full description is below.

How this role compares

Against 78 other live reliability postings in North Carolina.

Experience asked
More than usual (4+ vs 3+)

Similar roles usually ask 3+ years.

Skills these teams ask for most

  • Team leadership 47%
  • PLC 44%
  • Welding 32%
  • Tooling 24%
  • EHS / safety 24%

✓ = this posting asks for it too. % = share of similar postings that mention it.

Stands out: this posting asks for Validation (IQ/OQ/PQ), which few similar roles mention. If you have it, lead with it.

It asks for 4+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone on the team first.

At a glance

Off-shift / weekend coverageLifts up to 50 lbs

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Reliability team at Biogen

    Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • How does off-shift and weekend coverage work?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: Biogen in Research Triangle Park

3 other open roles at this site.

Full description from BiogenAs posted on their careers site.Show

Who you are

You’re a hands-on, solution-oriented technician who thrives in a fast-paced GMP manufacturing environment. You bring strong troubleshooting expertise, collaborate well across teams, and take pride in maintaining high standards of safety, compliance, and equipment performance.

Required skills

  • ✓High school diploma
  • ✓Minimum of 4 years of experience in a GMP-regulated manufacturing environment (biotech, pharma, or related industry)
  • ✓Hands-on experience with centrifuges, bioreactors, and/or CIP skids
  • ✓Experience working in a controlled cleanroom environment
  • ✓Demonstrated knowledge of industrial safety practices and system safety controls
  • ✓Ability to read and interpret engineering drawings
  • ✓Experience using CMMS systems
  • ✓Flexibility to support rotating shifts, extended hours, and weekends
  • ✓Physical

requirements

  • ✓Ability to climb ladders, work in tight spaces, and lift/move equipment up to 50 lbs
  • ✓Must be comfortable working in cleanroom environments with required gowning and able to stand for up to 3 hours at a time
Show full description ↓

Shift Details

  • •Schedule : Alternating schedule, Monday–Thursday one week; Tuesday–Friday the following week
  • •Hours : 10-hour shifts

About this role

As a Senior Manufacturing Technician, you will play a critical role in supporting manufacturing and laboratory operations by ensuring equipment reliability and performance. This role focuses on executing preventive and corrective maintenance, troubleshooting complex equipment issues, and partnering with engineering and validation teams to maintain a safe, compliant, and efficient GMP environment. You’ll be a key contributor to maintaining operational continuity and driving continuous improvement across site systems.

What you’ll do

  • •Perform preventive and corrective maintenance on manufacturing and laboratory equipment in alignment with site procedures
  • •Troubleshoot and resolve mechanical, electrical, and instrumentation issues to minimize downtime
  • •Create and execute work orders while ensuring adherence to safety and compliance standards
  • •Support validation and engineering activities as needed
  • •Author and update SOPs, job plans, and LOTO documentation
  • •Collaborate cross-functionally with Engineering, Facilities, Quality, and Manufacturing teams to resolve issues and improve workflows
  • •Identify opportunities for equipment improvements, spare parts optimization, and maintenance program enhancements
  • •Maintain accurate documentation within CMMS systems

Preferred skills

  • +Experience authoring SOPs and preventative maintenance procedures
  • +Strong understanding of GxP regulations
  • +Experience with validation and engineering support activities

Job Level: Professional

Additional Information

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.

  • +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.

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