Visual Inspection Operator in Drug Product Manufacturing

Would you like to influence our future processes and routines in Drug Product Operations?

And do you have experience from Visual Inspection and/or other aspects of aseptic drug product manufacturing combined with solid GMP understanding?

Then we hope you will join us soon

Your New Role

You'll support the onboarding of new products in the visual inspection area, initially focusing on manual visual inspection and transitioning to automated visual inspection.

You'll have the unique opportunity to help establish all our processes, structures, and daily routines as our business area develops, working closely with your colleagues, including both operators and supporters.

Our Work Schedule

The position is based on a fixed weekday shift, with working hours from 10:00 to 18:00, Monday to Thursday, and Friday from 10.00 to 17.30.

Main Responsibilities:

• Perform manual inspection activities related to on-boarding of new products.
• Perform visual inspection related to on-going production (automated and manual visual inspection)
• Documentation of tasks performed as per established Good Documentation Practices
• Assist in the execution of equipment/process qualification, APS, validation, and studies as required
• Participate in creation and development of departmental procedures to include but not limited to SOPs, OJTs, and work instructions.

Your Talent & Skills

• Certified per eye-sight requirements in FDBD
• Able to read, write and talk in English (SOP/WI/MBR are in English).
• Experience as an operator within Visual Inspection or from work within working under Aseptic conditions.
• You are e.g. certified for visual Inspection, process technologists, process operators, industrial operators, or other related backgrounds.
• A minimum 1-2 years of direct hands-on experience within GMP governed pharmaceutical manufacturing.
• It is an advantage if you have experience with operating and running automated processes.
• You have a strong quality mindset.

We hope you are

A positive and independent team player with a "can-do" attitude, eager to lean new skills and take ownership of tasks.

Your New Team & Department

The Drug Product Manufacturing Department consist of more than 40 dedicated and enthusiastic employees organized in 3 teams covering Wash & Sterilization, Formulation, filling, and Inspection.

The department continuously strives to identify opportunities to improve systems and practices to optimize and streamline our operation.

We emphasize psychological safety, personal development, and a people-first culture. We are a multicultural, supportive, and flexible environment and strive to lead by example.

Application

If this opportunity excites you, please upload your CV and cover letter as soon as possible. We review applications continuously and will contact candidates for interviews.

If you have any questions, please reach out to Kristoffer Kielland, at

FUJIFILM Diosynth 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 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 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.