Process Supporters to Drug Product Manufacturing

Are you looking for an opportunity to join a growing pharmaceutical organization at a pivotal moment?

At FUJIFILM Life Sciences Biotechnologies Denmark in Hillerød, we are entering an exciting phase where our Drug Product Manufacturing Facility is coming into operation.

You now have the chance to be a part of this journey and contribute to filling the facility with new products, Genki and purpose.

We are currently looking for Process Supporters to join our team. You will play a key role in helping us onboard new products and support operations in our DP manufacturing area.

Your New Role

We are looking for process supporters for all main operational processes including wash and sterilization, formulation, filling and manual/automated visual inspection.

You will be part of our support organization which is responsible for implementation of operational processes and creation of procedures within the DP manufacturing area. You will support and participate in the design and creation of our electronic Master Batch Records. Work in close cooperation with our stakeholders to get all supporting documentation ready for operation and support Tech Transfer activities for the DP area.

The team is also responsible for supporting the daily operations in the DP area.

Primary tasks will be:

Develop and implement operational documentation package (SOP’s and WI’s)

Design and built electronical Master Batch Records (PAS-X)

Participate and support the execution of qualification of equipment and processes.

Participate and support activities related to initial and ongoing Aseptic Process Simulation (APS).

Participate in Tech transfer activities and implementation of new programs for our area.

Participate and contribute to Risk assessments related to ongoing manufacturing and new products.

Fist line supporting role for DP operation including Training of colleges.

Handling of events and deviations

Continues Improvements on e.g. flows of personnel, materials and equipment, CMR’s and document updates

Identification and implementation of corrective and preventive actions (CAPA’s) to prevent re-occurrence and improve compliance.

Your Talent & Skills

You have a bachelor’s or master’s degree within Pharmaceutical Sciences, Process Engineering, or similar degree.

As a minimum you have a few years of experience within GMP manufacturing in the Pharmaceutical/Biotech industry.

Preferable you have experience related to Drug product manufacturing and maybee even PAS-X.

You can work independently on compliance related tasks, events, and optimization projects.

You are able to manage multiple stakeholders and is motivated by the interface between QA, MSAT and Manufacturing.

You understand and are able to execute against regulatory requirements.

You have a high level of technical writing skills and excellent communication skills in English and Danish (spoken and written).

We hope you are

Curious of nature, meet and greet people with a smile and have a can do attitude. You work with humility and respect for the people around you. You are flexibile and able to prioritize tasks to meet defined timelines. You work structured with a quality mind set and enjoy working independently and proactive in a dynamic entrepreneurial environment.

Your New Team & Department

The Drug Product Manufacturing department consist of approx. 50 dedicated and enthusiastic employees divided into three areas, DPM shopfloor, DPM Process support and DPM Wash & Sterilization and Area support.

The common denominator of the five teams is the acknowledgement and development of each employee and the diversity of the employees who have different experiences and educational backgrounds but collaborate closely on getting our medicine safely and quickly to the market.

Our ambition is that the Drug Product Facility will be state of the art, with automated isolator filling line and inspection line. The department continuously strives to identify opportunities to improve systems and practices to optimize and streamline our operation.

We are team players, entrepreneurs, and people who both like details and like taking greater responsibility beyond your scope of work. 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 as soon as possible as we screen candidates on a continuous basis and call in for interviews. If you have any questions, please do not hesitate to reach out to Associate Director Christina Madsen +45 22200717

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

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.

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

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