Job Description
Would you like to be involved in, coordinate and managing our supplier and audit documentation?
As well as engage with internal stakeholder across sites and suppliers? And do you strive to strengthen and ensure quality compliance through change controls and related quality systems?
Then we hope you will join us!
About the Role
Through your sound judgement and risk-based approach, you will help ensure that both our internal stakeholders and suppliers comply with the relevant legislation (API, drug, medical devices, etc.), thanks to your proactive quality mindset and hands-on approach.
You will be based at our manufacturing site in Hillerød in our activity based working environment.
This is a fixed-term parental cover position lasting until December 2026.

Primary Responsibilities

• Support and manage/coordinate change controls, quality agreement revisions, assessment of vendor changes and impact assessments
• Management and negotiation of supplier quality agreements with suppliers and internal stakeholders
• Support maintenance of the approved GMP supplier list
• Support and coordinate TrackWise workflows and maintain relevant supplier process, GxP records and archiving
• Review and approve minor audit observation responses and audit CAPA’s
• Support and ensure follow up on KPI and QMR data
• Manage and ensure quality system procedures updates and driving updates

Skills & Knowledge, we hope you possess

• You have a relevant scientific background (BSc or MSc degree within life science)
• 3-5 years of experience with GxP QA and supplier/auditing management, project related work
• We are an international company and fluency in English is required
• Fluency in Danish is preferred
• Strong interpersonal skills
• Positive mindset

We hope you are
someone who embraces tasks and interactions with openness and vibrant energy. You hold an analytical mindset, finding the balance between independent work and being a valuable team player when collaboration is key. Understanding the importance of engaging stakeholders in your daily activities shows your commitment to a collective success.
About the Team
You’ll join a great, expanding, hard-working and self-managed team of competent colleagues. We are a team of 12 experienced individuals covering a variety of tasks, we are driven by our curiosity, humor and commitment to the patient and quality. We’re there for each other, always ready to lend a hand.
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.
Your application
Has this sparked your interest? Then please upload your CV and cover letter as soon as possible as we conduct interviews on an ongoing basis and will take down the advert when we have found the right candidate.
In case you have any questions, please do not hesitate to reach out to Betina Hilligsøe,
betina.hilligsoee@fujifilm.com
, phone: +45 22 18 32 81
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://fujifilmdiosynth.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.
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.
About Us
FUJIFILM Biotechnologies is an industry-leading Biologics Contract Development and Manufacturing Organization (CDMO) with locations in Hillerød, Denmark, Teesside, UK, RTP, North Carolina, Toyama, Japan and College Station, Texas, USA. We use our skills, dedication and ambition to enable impact for the world’s most innovative biotech and biopharma companies reimagining healthcare’s potential. We work across the entire lifecycle of our customers’ products – enabling success throughout. Every cure, vaccine, biologic, and advancement we contribute to starts with our people and our passion. We fuel one another’s passion, help accelerate progress, expand capabilities, strengthen innovation, and improve processes to improve lives.
Our site in Hillerød, Denmark, brings together expertise, capabilities and technologies to manufacture advanced biologics. The large scale manufacturing facility has a capacity of 120,000 liters to reliably manufacture biologics for late phase and commercial use. We commenced 6 billion DKK projects to double our manufacturing capacity and to add fill finish to the site.
We offer the chance to be part of a global workplace where passion, drive and commitment are met with opportunities for professional and personal development. Deeply committed to diversity and inclusion, we ensure that everyone no matter their background or gender has an opportunity to develop. We take pride in enriching our communities, caring for our environment, and cultivating a world of opportunity for future generations.
We aim to foster a collaborative, innovative and rewarding environment, where diverse perspectives and people come together united by a common purpose and shared values. We pursue our fullest potential as individual contributors and team members. We strive to be the employer of choice and offer a competitive compensation and benefit package.
As we continue to enhance and expand our capabilities, we are looking for people who share our passion, drive, and energy – what we call Genki – to join our team.

• Support and manage/coordinate change controls, quality agreement revisions, assessment of vendor changes and impact assessments
• Management and negotiation of supplier quality agreements with suppliers and internal stakeholders
• Support maintenance of the approved GMP supplier list
• Support and coordinate TrackWise workflows and maintain relevant supplier process, GxP records and archiving
• Review and approve minor audit observation responses and audit CAPA’s
• Support and ensure follow up on KPI and QMR data
• Manage and ensure quality system procedures updates and driving update