Lead Process Engineer: Drug Substance Manufacturing

Bavarian Nordic

Rom By

On-site

DKK 900,000 - 1,200,000

Full time

3 days ago
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Job summary

Bavarian Nordic is seeking an Engineering Specialist to strengthen our Drug Substance manufacturing processes in Denmark. The role combines hands-on problem solving with technical leadership to ensure reliable performance, quality, and GMP compliance.

You will lead process design and optimization, oversee CIP/SIP strategies, support equipment introduction and validation, and contribute to technology transfer and investigations.

Qualifications

  • Master's degree in Chemical, Bioprocess, Process, or Mechanical Engineering or related field.
  • At least 10 years of industrial process engineering experience in GMP/pharma/biotech settings.

Responsibilities

  • Lead process design and optimization to improve efficiency, reliability and quality.
  • Act as SME for CIP/SIP design, operation and optimization.
  • Guide equipment introduction, vendor reviews, qualification, validation and site acceptance testing.
  • Support validation strategies, PPQ and technology transfer between sites.
  • Lead deviations, root cause investigations, CAPAs, change controls, and risk assessments; support audits and inspections.
  • Coach colleagues and share engineering knowledge to strengthen process understanding across teams.

Skills

Process design
CIP/SIP expertise
Equipment qualification
PPQ & tech transfer
Investigations & CAPAs
Risk assessments
Coaching & knowledge share

Education

Master's degree in Chemical/ Bioprocess/ Process/ Mechanical Eng

Tools

CIP/SIP systems
Process equipment & instrumentation

Job description

Bavarian Nordic is seeking an Engineering Specialist to strengthen our Drug Substance manufacturing processes in Denmark. The role combines hands-on problem solving with technical leadership to ensure reliable performance, quality, and GMP compliance.

You will lead process design and optimization, oversee CIP/SIP strategies, support equipment introduction and validation, and contribute to technology transfer and investigations.

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