Scientist for QC Tech Transfer & Sample Support Team (Maternity Cover 12 months)

at  Fujifilm Diosynth Biotechnologies

Join Our Mission to Make a Global Impact in Pharmaceuticals!
This position is a maternity cover with the potential for a permanent role.
Are you ready to take on a proactive role that not only challenges you but also allows you to make a significant difference in people’s lives around the world? At our company, we strive to empower our team members to take ownership of their tasks while fostering a supportive and collaborative environment. If you’re passionate about pharmaceuticals and want to contribute to meaningful projects, we want to hear from you!
About the Role:
We are looking for a talented scientist who is eager to drive change and manage stakeholder relationships effectively. If you have experience with GMP and process flows in the pharmaceutical industry, you could be the perfect fit for our QC Tech Transfer & Sample Support team. In this role, you will actively ensure that the right samples are obtained and tested according to specifications, and Planned Sample Plans all while maintaining a positive and energetic spirit in a fast-paced environment.
We believe that a meaningful life goes hand in hand with a fulfilling work life. That’s why we value a healthy integration of work and personal life and offer flexible working hours, allowing you to prioritize both your professional development and personal well-being. Here, it’s important that you have the opportunity to live life to the fullest while contributing to our shared mission of making a difference in the world.
What Makes You a Great Fit:
To succeed in this role, you should possess qualities such as proactivity, patience, curiosity, and a strong sense of responsibility for your own development. These traits are essential for navigating the exciting and busy future that lies ahead with our new production facilities.

Your primary responsibilities will include:

• Driving and coordinating the preparation of QC Sample Plans and specifications, ensuring effective communication with customers and stakeholders throughout the tech transfer process and into commercial manufacturing
• Managing QC change controls for both internal and external changes related to Sample Plans and specifications
• Creating and maintaining GMP documents in collaboration with stakeholders and QA
• Identifying potential optimizations and implementing improved processes.
• Supporting investigations as necessary while ensuring high compliance with cGMP standards.

Preferred Qualifications:

• Bachelor’s or Master’s degree in pharmacy, biochemistry, biotechnology, process engineering, or a related field.
• Experience in optimizing and implementing processes.
• Project management experience is a plus.
• Several years of experience in pharmaceutical manufacturing and GMP compliance.
• Fluency in English is required; our company operates internationally.
• Familiarity with QC data systems such as LIMS and metrics tools like Tableau is advantageous.

Why Join Us?
If you’re looking for a company that values your input, encourages your growth, and is committed to making a positive impact in the world, this is the place for you. Together, we can work on meaningful tasks that improve and save lives globally. Join us in this exciting journey and help us shape the future of pharmaceuticals!
Apply today and be a part of something bigger!
Application
If you have any further questions, please reach out to Nicolaj Ørsted Larsen,
Email:
Nicolaj.larsen@fujifilm.com
Mobile: +45 41945462
FUJIFILM Diosynth Biotechnologies is an industry-leading Biologics Contract Development and Manufacturing Organization (CDMO) with locations in Hillerød, Denmark, Teesside, UK, RTP, North Carolina 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.
FUJIFILM Diosynth Biotechnologies Denmark (FDBD) 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 Diosynth Biotechnologies is an industry-leading Biologics Contract Development and Manufacturing Organization (CDMO) with locations in Hillerød, Denmark, Teesside, UK, RTP, North Carolina 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.

• Driving and coordinating the preparation of QC Sample Plans and specifications, ensuring effective communication with customers and stakeholders throughout the tech transfer process and into commercial manufacturing
• Managing QC change controls for both internal and external changes related to Sample Plans and specifications
• Creating and maintaining GMP documents in collaboration with stakeholders and QA
• Identifying potential optimizations and implementing improved processes.
• Supporting investigations as necessary while ensuring high compliance with cGMP standards