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Bioassay QC Scientist/ Sr. Associate

Scientist for QC Bioassay & Virology
Are you eager to join a fast-growing pharmaceutical company? Now you have a unique opportunity as we are looking for a bioassay scientist/senior scientist who shares our passion, drive, and energy – what we call Genki – to join QC Bioassay & Virology.
Your New Role
When working at FUJIFILM Diosynth Biotechnologies Denmark you will, besides from the tasks listed below, onboard new customers and products to the site, build a network across QC and FDBD, support our site expansion project, and assist in finding new and innovative ways of working smarter in a complex everyday life.
Your primary tasks will be but not limited to:
  • You will be scientific responsible (SME) on assays performed in QC Bioassay & Virology. This includes support to testing, improvements, troubleshooting and investigations - all in compliance with cGMP
  • Laboratory support if unexpected analytical method trends are observed
  • Daily QC manager approval of test results for commercial product.
  • Handling deviations, Invalid assays, Laboratory exceptions, CAPAs and Change Controls
  • Be the QC SME/project lead in close collaboration with our Analytical Development department when transferring new methods for testing in QC laboratories
  • Implementation of new instruments in close collaboration with the QC Instrument supporting team
  • Author technical protocols and reports as well as change control requests for ensuring successful execution of qualification and analytical improvement projects
  • Drive continuous improvements of practice in collaboration with management
  • Ensure compliance with cGMP and participate in audits and inspections
Skills & Knowledge, we hope you possess:
  • Master’s degree in Biochemistry, Biology, Biotechnology, Pharmaceutical Sciences or similar combined with experience from the pharmaceutical industry, preferably experience from QC.
  • Experience working under cGMP
  • Knowledge of cell-based assays, ADCC, ELISA and qPCR testing related to DS/DP is an advantage.
We are looking for a person with the right attitude and energy, and who understands the requirements in a cGMP QC laboratory. You thrive in a busy environment with many changing priorities and can keep your spirit and overview while still paying attention to details. You should possess excellent collaboration skills nurture our OneQC mind-set, where we aim at helping cross-functionally. You are curious, self-driven, dedicated, thorough and systematic and can plan your projects and deliverables in a structured way. Fluency in English is required as English is our corporate language.
The work environment is international and informal. We keep a high pace and focus on a vital work 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.
About the team
The QC Bioassay & Virology team currently consists of > 20 dedicated employees (16 analysts, 6 scientists, 2 team leader and 1 manager). The team supports the global release of commercial products (DS/DP) for our customers with various potency and ID testing (e.g. cell-based assays, ADCC assays, ELISA based assays and dot blot) as well as the support to the on-site biologic Drug Substance (DS) manufacturing by ensuring viral safety on products with Adventitious Virus testing, MMV testing and qPCR testing for impurity of in-process samples (IPT). Method transfers and product specific qualification as well as generation of cell banks are becoming a key deliverable for the team with the many new customers. And not least we perform qualification of controls and reference standards, handle deviations, CAPAs, invalid assays, OOS and Change Controls and much more. All this is part of our daily activities in respect of getting the commercial products out to the patients.
Our Quality Control (QC) department at site Hillerød consists of approximately 200 employees divided into different support teams and four testing teams. In QC we strive towards a OneQC team spirit where we help and support each other across teams not only to reach our goals but also to support a high level of collaboration and possibilities for personal development. The pillar in our QC department is our employees – our success is only possible due to competent and dedicated colleagues, who wants to make a difference for QC, our site, our customers, and patients all over the globe. As a leading CDMO company we, in QC, are obligated to continuously improve our way of working creating a dynamic and inspiring environment with huge individual co-decision making due to our flat organizational structure.
Application
Has this sparked your interest? Then we urge you to send an updated CV and cover letter as soon as possible. We will continuously invite relevant candidates for job interviews and will close the position as soon as we have found the right candidate.
In case you have any questions, please do not hesitate to contact Manager Trine Kvist +45 41949508
Please accept some delayed response time due to vacations. We hope you have a great Summer.
About FUJIFILM Diosynth Biotechnologies
We are 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 Manufacturing site in Hillerød, Denmark, brings together a complete range of expertise, capabilities, and technologies to manufacture advanced biologics. 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. Learn more at https://fujifilmdiosynth.com/
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.
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.
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CEO of Fujifilm Diosynth Biotechnologies
Fujifilm Diosynth Biotechnologies CEO photo
Lars Petersen
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At FUJIFILM Diosynth Biotechnologies our mission is to become the leading and most trusted global CDMO in the industry, and our purpose is to become Partners for Life, Advancing Tomorrow’s Medicine

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DATE POSTED
July 4, 2023

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