Life Sciences Process Optimization Lead

Vulcain Engineering Group; København; On-site; DKK 700,000 - 1,100,000; Full time

Job summary

Consultys Denmark, part of the Vulcain Group, is seeking an Engineering Project Manager to lead cross‑functional teams in designing, developing, and optimizing manufacturing processes for the life sciences sector in Copenhagen.

You will drive process excellence, oversee scale‑up and technology transfer from development to production, ensure regulatory compliance, build robust documentation, and deliver high‑impact projects with a strong focus on quality and efficiency.

Qualifications

• Bachelor's or Master's degree in Chemical Engineering, Bioprocess Engineering, or related field.
• 5–10 years of process engineering experience in life sciences (pharma, biotech, etc.).
• Project management experience required.
• Knowledge of industry regulations and quality standards.
• Proficiency in process modeling and simulation tools.
• Strong analytical and communication skills.
• Ability to work within cross-functional teams and independently.
• Experience with process validation and technology transfer is a plus.

Responsibilities

• Lead cross-functional teams in designing, developing, and optimizing manufacturing processes in the life sciences sector.
• Oversee process simulations, evaluate and implement process improvements, and resolve complex operational issues.
• Develop and review comprehensive process documentation, including P&IDs, SOPs, and batch records.
• Ensure full compliance with industry regulations, quality standards, and regulatory requirements.
• Provide technical expertise in aseptic processing, downstream and upstream processing, filtration, sterilization, and purification techniques.
• Lead or participate in process validation activities to ensure product quality and regulatory compliance.
• Investigate deviations, incidents, and quality issues, and implement corrective and preventive actions.
• Coordinate process scale-up and technology transfer from development to production.
• Lead equipment selection, qualification, and maintenance efforts.
• Stay informed about industry trends and emerging technologies to continually enhance processes.

Skills

Project management

Process engineering

Regulatory compliance

Process modeling & simulation

Documentation

Communication

Education

Bachelor's or Master's in Chemical Engineering / Bioprocess Engineering

Tools

Aspen / COMSOL

Job description

Consultys Denmark is part of the Vulcain Group, a global consulting and engineering company dedicated to the Life Sciences industry. Since 2012 our team in Copenhagen has supported pharmaceutical, biotech and medical device companies with tailored solutions across development, production and compliance.

AL Engineering and AM Groupe are part of Consultys Denmark. Together we strengthen our local capabilities in design, automation and technical project execution, delivering high-impact services built on deep industry knowledge.

With over 750 Life Sciences experts globally and 63 specialists in Denmark, we bring experience, agility and commitment to every project. Our consultants average 8 years of experience and work closely with clients on long-term innovative assignments.

We are driven by respect, transparency and gratitude. These values help us build strong partnerships and deliver reliable results

We are seeking an Engineering Project Manager with a focus on process optimization and management expertise to join our team. In this role, you will lead cross-functional teams, drive process excellence, and ensure the successful execution of projects related to the production of multiple types of pharmaceutical products.

Responsibilities

• Lead and manage cross-functional teams in designing, developing, and optimizing manufacturing processes in the life sciences sector.
• Oversee process simulations, evaluate and implement process improvements, and resolve complex operational issues.
• Develop and review comprehensive process documentation, including P&IDs, standard operating procedures, and batch records.
• Ensure full compliance with industry-specific regulations, quality standards, and regulatory requirements.
• Provide technical expertise in areas such as aseptic processing, downstream and upstream processing, filtration, sterilization, and purification techniques.
• Lead or participate in process validation activities to ensure product quality and regulatory compliance.
• Investigate and address deviations, incidents, and quality issues, and recommend corrective and preventive actions.
• Coordinate process scale-up and technology transfer activities from development to commercial production.
• Lead equipment selection, qualification, and maintenance efforts.
• Stay informed about industry trends and emerging technologies to enhance processes and methodologies continually.
• Bachelor's or Master's degree in Chemical Engineering, Bioprocess Engineering, or a related field.
• Minimum of 5-10 years of process engineering experience in the life sciences industry (pharmaceuticals, food and beverage, cosmetics, etc.).
• Previous experience in managing projects and Project Manager or Project Engineer is needed
• Excellent knowledge of industry-specific regulations and quality standards.
• Proficiency in process modeling and simulation tools.
• Strong analytical and problem-solving skills.
• Excellent written and verbal communication abilities.
• Ability to work effectively within cross-functional teams and independently.
• Experience with process validation, technology transfer, and equipment qualification is a plus.
  
  

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