Responsible Engineer For Automatic Inspection In Drug Product Manufacturing

Engineer In Drug Product Manufacturing

Can you envision yourself taking technical ownership of state-of-the-art Automatic Inspection equipment in our Drug Product manufacturing suite?

And would you like to play a pivotal role in ensuring these systems maintain top operational performance while supporting critical GMP events and manufacturing processes?

Then we hope you are our new Engineer colleague in Drug Product Manufacturing!

Your New Role

You will have the technical ownership of the Automatic Inspection equipment operating in the Drug Product manufacturing suite. You will ensure to maintain validated state and operational performance of automatic inspection equipment as well as provide technical support to Operations, QC, and Quality for GMP and manufacturing events.

Main Tasks:

• Develops and maintains equipment-related Recipes.
• Provides operational support for the automated inspection equipment including establishment of maintenance programs, spare part assessment and management, preparation of procedures, training, etc.
• Acts as second line support to maintenance organization in complex and unforeseen equipment issues—leading troubleshooting teams and activities and being the point of contact to suppliers. Responsible for driving and supporting GMP events related to equipment in scope such as Deviations, change controls, events, inspections.
• Provides support to tech transfer programs and Operations as Equipment owner.
• Participates in Operational board meetings and validation activities as well as acts as technical support to GMP events when validated state is impacted.

Your Skills & Talent

• +3 years' experience as Senior Technician or + 2y as Engineer in Drug Product or Fill Finish manufacturing
• Knowledge of Validation and Risk Assessment of manufacturing equipment in GMP
• Vision engineering and / or Automatic inspection experience
• Have a technical background and appreciate dealing with technical challenges on the shopfloor

We Hope You Are

A positive team player with a can-do attitude eager to sharpen your technical skills and thrive in a very dynamic environment with plenty of opportunity to take ownership

Your New Team & Department

DP MSAT covers a broad scope and play a central part in Drug Product Manufacturing. Our team is composed of process owners, responsible engineers, technology specialists, CQV leads and Pilot laboratory scientists.

We are in expansion phase as we get closer to clinical and commercial drug product manufacturing operations starting early 2026. The work environment is international and informal. We keep a high pace and focus on a vital life balance while having fun. We put a strong emphasis on psychological safety through trust and empowerment within our teams and hope that this is something that speaks to you as well.

Application

Has this sparked your interest, then please upload your CV and cover letter in English as soon as possible, as we screen candidates on a continuous basis and call in for interviews. If you have any questions, do not hesitate to reach out to the hiring manager Frédéric Osuch +45 20723569

FUJIFILM Biotechnologies is a global leader in biologics contract development and manufacturing Organization (CDMO), partnering with innovative biotech and biopharma companies to transform healthcare. With locations in Denmark, the UK, and the USA, we support every stage of our customers' product lifecycle, from breakthrough cures to life-saving vaccines.

Our success starts with our people—their passion drives progress, innovation, and impact. Join a diverse, inclusive workplace that values collaboration, fosters growth, and empowers future generations. Together, we're enriching communities, protecting the environment, and reimagining healthcare's potential.

Shape the future with us—your drive meets boundless opportunity here https://fujifilmbiotechnologies.fujifilm.com/

FUJIFILM Biotechnologies Denmark is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identify or any other protected class.