Denmark Job Openings
Fujifilm Diosynth Biotechnologies
Scientist for QC Tech Transfer & Sample Support Team (Maternity Cover 12 months)
Hillerød
FULL TIME
October 2, 2024
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 c GMP 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!
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.
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.
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