GMP Process Engineering Specialist – CIP/SIP Expert

Bavarian Nordic; Kvistgård; On-site; DKK 900,000 - 1,200,000; Full time

Job summary

Bavarian Nordic is seeking an Engineering Specialist to strengthen Drug Substance manufacturing processes and support equipment introduction and new technologies. You will join Material & Sterile Operation and lead hands-on problem solving with technical leadership to ensure GMP-compliant, reliable manufacturing.

You will develop, validate, and maintain processes, challenge existing solutions, and drive improvements across Manufacturing, Engineering, Automation, and Quality teams.

Qualifications

• At least 10 years of industrial GMP process engineering experience.
• Strong track record in process design, optimization, and troubleshooting within pharma/biotech.
• Extensive hands-on CIP/SIP design and operation experience.
• Knowledge of process equipment, piping, valves, instrumentation, and automation interactions.

Responsibilities

• Lead process design and optimization to improve efficiency, reliability, and quality.
• Act as SME for CIP/SIP systems and improve cleaning/sterilization strategies.
• Guide equipment introduction, qualification, validation, PPQ, and tech transfer activities.

Skills

Process design

Process optimization

Troubleshooting

CIP/SIP design

Equipment qualification

Technology transfer

Regulatory compliance

Cross-functional collaboration

Education

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

Job description

Bavarian Nordic is seeking an Engineering Specialist to strengthen Drug Substance manufacturing processes and support equipment introduction and new technologies. You will join Material & Sterile Operation and lead hands-on problem solving with technical leadership to ensure GMP-compliant, reliable manufacturing.

You will develop, validate, and maintain processes, challenge existing solutions, and drive improvements across Manufacturing, Engineering, Automation, and Quality teams.