Sr Engineer I, Manufacturing Sciences

Posted Yesterday
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Triangle Trailer Park, Township of Jacksonville, NC, USA
In-Office
98K-127K Annually
Senior level
Biotech
The Role
Serve as SME for single-use consumable raw materials across biopharma manufacturing. Lead material risk assessments, investigations, supplier audits, E/L studies, change control/CAPA processes, and support regulatory filings and inspections to ensure materials meet quality and regulatory expectations.
Summary Generated by Built In

About this role

The Senior Engineer I, Manufacturing Sciences is a key technical contributor providing subject matter expertise across end-to-end single-use consumable raw materials, from Drug Substance through Drug Product fill. This role supports the Process Optimization & Technology (PO&T) organization by assessing raw material changes, deviations, CAPAs, and regulatory documentation, while serving as the Subject Matter Expert (SME)  of extractables and leachables (E/L) program assessments.

The position partners closely with suppliers, manufacturing sites, and regulatory teams to ensure materials are fit for use, compliant with evolving global regulations, and capable of supporting both current and future manufacturing needs. This is a hybrid role with on-site presence required during inspections and vendor audits.

What you’ll do

  • Serve as a technical Subject Matter Expert (SME) for single-use consumable raw materials, supplier capabilities, control strategies, and manufacturing needs across the global manufacturing network
  • Support development and implementation of raw material control strategies and monitoring technologies to enable incoming material release
  • Lead continuous improvement initiatives related to raw materials, including technical support for new item requests and supplier audits
  • Conduct investigations by performing laboratory experiments, gathering supplier data, developing historical trends, and assessing lot usage
  • Troubleshoot single-use material failures (e.g., filter integrity test failures), perform root cause analyses, and evaluate potential process impacts
  • Perform technical risk assessments for Vendor Change Notifications (VCNs) and New Item Requests (NIRs), including chemical compatibility, stability, thermal properties, and extractables/leachables impact
  • Own and support global extractables/leachables studies, ensuring alignment with current global regulatory guidance
  • Participate in industry forums and external E/L collaborations to advance best practices
  • Support internal and agency inspections, vendor audits, and regulatory filings related to raw materials and single-use technologies

Who you are

You are a technically curious and analytical engineer who enjoys solving complex manufacturing challenges and collaborating across functions. You work independently, proactively identify improvements, and are comfortable serving as a technical leader within your area of expertise.

Required skills

  • Bachelor’s degree in relevant scientific or technical fields from an accredited college or university
  • At minimum 4 years of directly relevant industry or industry-adjacent experience
  • Proven scientific and analytical skills to evaluate suitability of plastics and single-use technologies across multiple manufacturing modalities
  • Knowledge of polymeric materials, chemistry, and single-use systems for biopharmaceutical manufacturing
  • Experience supporting deviations, change controls, CAPAs, and regulatory documentation
  • Previous experience performing root cause analysis and risk-based technical assessments
  • Willingness and ability to work on-site more frequently during training periods, critical projects, audits, etc.

Preferred skills

  • Bachelor’s degree in engineering, chemistry, materials science, or a related technical field from an accredited college or university
  • Hands-on experience with extractables and leachables studies and regulatory expectations
  • Familiarity with single-use systems, container closure systems, and supplier change management
  • Experience supporting regulatory inspections and vendor audits
  • Prior experience acting as a technical lead or SME within a manufacturing or engineering organization
  • Participation in industry forums, external collaborations, or technical working groups related to E/L or single-use technologies
  • Previous experience partnering with external contractors and vendors


 

Job Level: Professional


Additional Information

The base compensation range for this role is: $98,000.00-$127,000.00


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.



Skills Required

  • Bachelor's degree in a relevant scientific or technical field from an accredited college or university
  • Minimum 4 years of directly relevant industry or industry-adjacent experience
  • Proven scientific and analytical skills to evaluate suitability of plastics and single-use technologies
  • Knowledge of polymeric materials, chemistry, and single-use systems for biopharmaceutical manufacturing
  • Experience supporting deviations, change controls, CAPAs, and regulatory documentation
  • Previous experience performing root cause analysis and risk-based technical assessments
  • Willingness and ability to work on-site more frequently during training periods, critical projects, audits, etc.
  • Bachelor's degree in engineering, chemistry, materials science, or a related technical field
  • Hands-on experience with extractables and leachables studies and regulatory expectations
  • Familiarity with single-use systems, container closure systems, and supplier change management
  • Experience supporting regulatory inspections and vendor audits
  • Prior experience acting as a technical lead or SME within a manufacturing or engineering organization
  • Participation in industry forums, external collaborations, or technical working groups related to E/L or single-use technologies
  • Previous experience partnering with external contractors and vendors

Biogen Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Biogen and has not been reviewed or approved by Biogen.

  • Fair & Transparent Compensation Pay is generally positioned as competitive and often perceived as fair across roles, with total compensation framed as strong when bonus and equity are included. Compensation sentiment is described as above-average overall, though it varies by function and business cycle.
  • Equity Value & Accessibility Equity programs are repeatedly highlighted as a meaningful part of the total package, including stock programs and an employee stock purchase plan. Equity and bonus elements are portrayed as important contributors to feeling well rewarded beyond base pay.
  • Leave & Time Off Breadth Time-off benefits are described as distinctive, including a year-end shutdown and a paid sabbatical after extended tenure. Vacation, holidays, sick time, and personal-significance days are also presented as supportive of work-life needs.

Biogen Insights

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The Company
HQ: Cambridge, MA
9,575 Employees
Year Founded: 1978

What We Do

Through cutting-edge science and medicine, Biogen discovers, develops and delivers innovative therapies worldwide for people living with serious neurological and neurodegenerative diseases. Founded in 1978, Biogen is a pioneer in biotechnology and today the Company has the leading portfolio of medicines to treat multiple sclerosis, has introduced the first and only approved treatment for spinal muscular atrophy, and is at the forefront of neurology research for conditions including Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. Biogen also manufactures and commercializes biosimilars of advanced biologics. With approximately 7000 people worldwide, we are truly a global organization, headquartered in Cambridge, Massachusetts, which is also home to our research operations. Our international headquarters are based in Zug, Switzerland and we have world-class manufacturing facilities in North Carolina and Denmark. We offer therapies globally through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries. For more information, please visit www.biogen.com. Follow us on social media – Twitter, LinkedIn, Facebook, YouTube.

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