Nighttime Operators for Upstream, Downstream & Solution Prep - Join Our Pipeline!

FLBD FUJIFILM Life Sciences Biotechnologies Denmark ApS; Hillerød; On-site; DKK 320,000 - 520,000; Full time

Job summary

FUJIFILM Biotechnologies is expanding its biopharmaceutical production teams in Hillerød, Denmark, inviting applicants for Nighttime Operator roles across Upstream, Downstream and Solution Preparation. You will participate in cGMP activities, handle batch documentation, perform sampling and contribute to validation and optimization projects.

The schedule includes night shifts with a training period, and prior experience in GMP or life sciences is a plus.

Qualifications

• You double-check the details and ensure nothing slips through the cracks.
• You take initiative and step in when something needs to be done.
• You explain things clearly, keep people in the loop, and learn new digital tools quickly.
• You can read and understand work instructions in English.
• Experience with GMP and SOPs is advantageous.
• Experience with cGMP, chromatography, filtration or fermentation is a plus.

Responsibilities

• Execute and revise cGMP documents.
• Handle and complete batch documentation.
• Perform in-process sampling and analytical measurements.
• Execute validation protocols.
• Mix solutions to support Upstream and Downstream operations.
• CiP/SiP of equipment.
• Train new colleagues.
• Report deviations.
• Contribute to process optimization or continuous improvements.

Skills

Attention to detail

Proactive approach

Clear communication

Read English work instructions

GMP/SOP awareness

Process understanding

Education

Life Science graduate

Job description

Are you a night owl who thrives when the stars are out? Does it sound attractive catching the sunrise before the world awakens? Do you enjoy having time off when most others are working? Then keep reading. We’re continuously seeking motivated Nighttime Operators (Manufacturing Associates) to join our biopharmaceutical production teams in Upstream, Downstream and Solution Preparation. If you are interested in being part of our exciting expansion at a pivotal time of growth, you now have the chance to submit your application to join our talent pool. We will reach out if your profile matches our current openings.

About us

FUJIFILM Biotechnologies is expanding its capacity in Hillerød by adding 14 x 20,000L bioreactors and three additional downstream processing lines. This makes us Europe’s largest end-to-end CDMO, offering a total of 20 x 20,000L bioreactors for drug substance production complemented by comprehensive drug product and finished goods services. This is an excellent opportunity to join our company at a pivotal time of growth and be part of an exciting journey – and all while only working 7 days during a 14-day period.

FUJIFILM 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.

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 we 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 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.

We are part of the Fujifilm Group, and we all share the same purpose. Giving our world more smiles. We bring diverse ideas, unique capabilities, and extraordinary people together to change the world. FUJIFILM Biotechnologies works in strategic collaboration with biopharmaceutical and biotech companies to develop and manufacture the latest in biologics, advanced therapies and vaccines.

With production facilities in the US and Europe, we give our customers everything they need to develop and commercialize treatments and therapies effectively and efficiently to make patients’ lives better. We are driven to revolutionize the industry through our Partners for Life mindset, seeking to build global partnerships based on trust with our customers. Our global teams fully embrace our aspiration of being the leading and most trusted Partners for Life in the biopharmaceutical industry.

Tasks

• Execution and revision of cGMP documents.
• Handling and completion of batch documentation.
• In-process sampling and analytical measurements.
• Execution of validation protocols.
• Mixing of solutions to support Upstream and Downstream operations.
• CiP/SiP of equipment.
• Training new colleagues.
• Reporting deviations.
• Possibility of being a part of different projects such as process optimization, red lining SOPs, 5S and continuous improvements.

Qualifications

• You’re the type who double-checks the details and makes sure things don’t slip through the cracks.
• You don’t wait to be asked, but step in when something needs to be done.
• You explain things clearly, keep people in the loop, and you are quick to pick up new digital tools.
• People trust you to do what you say and handle things the right way.
• You show up with focus and give it your all - even on the routine stuff.
• You are enthusiastic about working under GMP and you enjoy working with math and IT tools.
• You have flair for understanding process flows.
• You can read and understand work instructions in English.
• Experience with working night shifts is a plus.
• Preferably, you are experienced in pharmaceutical production or regulated industries OR you are a Life Science Graduate ready to start your career in production.
• It is a plus if you have experience with cGMP, SOPs, chromatography, filtration or fermentation processes.

Schedule & Application

As an operator (Manufacturing Associate) your work will follow below schedule:

Week 1: Monday, Tuesday, Friday, Saturday, Sunday

Week 2: Wednesday and Thursday

Furthermore, you will either work on Night 1 (18:30 - 04:43) or Night 2 (20:05 - 06:18).

Note: First four weeks include comprehensive training from 8:00 - 16:00.