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Sr. Principal Engineer - Bioprocess

Job in Richmond, Henrico County, Virginia, 23214, USA
Listing for: Eli Lilly and Company
Full Time position
Listed on 2026-08-29
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 172000 USD Yearly USD 80000.00 172000.00 YEAR
Job Description & How to Apply Below

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life‑changing medicines, strengthen how health is understood and managed, and support the communities we serve.

This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Lilly is currently constructing an advanced manufacturing facility for monoclonal antibodies, bioconjugates, and aseptic drug product manufacturing in Goochland County, Virginia. This facility is intended to provide capacity for current and future products. The successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.

Responsibilities

Some key responsibilities of the role include;

Facility Start-Up Phase;
  • Provide Process Engineering support to the Global Facility Delivery team (Lilly’s Global Large Scale Capital Delivery Team) with a strong focus on right first time and on schedule facility start-up (e.g. design reviews, process safety assessments, User Requirements, C&Q support, Unit Operation Shakedown, Facility Run Rate Readiness)
  • Define and own relevant aspects of the overall integrated Operational Readiness Plan (e.g. SOP development, maintenance strategy, automation optimization, run rate readiness, MES E  requirements, alarm requirements, Performance Qualification Study Requirements / Protocol Development etc.)
  • Own the Performance Qualification strategy and execution for area of responsibility
  • Support initial Operations Training requirements as the Equipment and Area SME
  • Lead/support the tech transfer of new processes into the facility
Post facility start-up phase;
  • Provide process engineering support through application of process engineering fundamentals
  • Identify and implement continuous improvement opportunities related to equipment and processes as core member of cross-functional process team.
  • Utilise root cause analysis techniques to investigate process and equipment issues and deliver robust and sustainable corrective and preventative actions
  • Monitor, assess and document equipment performance to maintain ongoing qualification.
  • Develop and maintain the basis of safety for process equipment
  • Develop and implement unit operation and equipment control strategy
Basic Qualifications
  • Bachelor's Degree in Process, Chemical, Biochemical Engineering or related applicable discipline
  • 7+ years of process team experience in pharmaceutical manufacturing, preferably monoclonal antibody manufacturing
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1
Additional Preferences
  • Deep technical interest and understanding in the field of monoclonal antibody manufacturing and Bioprocess Engineering.
  • Strong analytical and problem-solving skills.
  • Ability to work on own initiative and as part of a Process Team consisting of a diverse group of management, production, science, quality and engineering professionals.
  • Creativity to identify improvement opportunities and the tenacity/initiative to see them implemented.
  • Guidance/mentoring of others through processes.
  • Flexibility to meet business needs.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form () for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and…

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