Continuous Improvement Scientist for Quality Control Analytical Development at FUJIFILM Diosynth Biotechnologies

Hillerød, Capital Region of Denmark, Denmark -

Full Time

Start Date

Immediate

Expiry Date

26 Dec, 25

Salary

0.0

Posted On

27 Sep, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, Communication Skills, Collaboration Skills, Curiosity, Self-Driven, Dedication, Thoroughness, Systematic Planning, LEAN Tools, CI Tools, Facilitating Workshops, PowerPoint Presentations

Industry

Biotechnology Research

Description

Are you eager to join a fast-growing pharmaceutical company with focus on Continuous Improvements (CI)? Now you have the opportunity as we are looking for a CI Scientist who shares our passion, drive, and energy – what we call Genki – to join Quality Control Analytical Development (QC AD). About FUJIFILM Biotechnologies and our QC Department FUJIFILM Biotechnologies is a world leading Contract Development Manufacturing Organization (CDMO) serving customers in the pharmaceutical industry – from pre-clinical investigations to commercial GMP production. Our overall mission is to “Advancing Tomorrow’s Medicines” and we like to invite you to be part of that journey. Our Quality Control (QC) department at site Hillerød consists of approximately 260 employees divided into different support teams, four testing teams, and four AD 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. The culture at our site is key if you ask our employees and besides a competitive salary and bonus package, we offer health insurance, massage and physiotherapy, health check, fitness center, possibility to work from home and most recently we invested in a mobile barista coffee van. We have site Friday brunch and monthly afternoon cake, just as we have a “bell ringing” tradition when reaching important milestones. About the QC AD Department QC AD Department consists of Projects team, Chemistry teams, Bioassay team, and a TOC & DP team – in total we are approximately 50 people. The various teams support testing of non-GXP samples from our Process Specialist, Manufacturing Science and Technology - Drug Substance & Drug Product teams. We work in close collaboration with the QC Testing teams where we lead method validation, qualification and transfer studies that enable in-process and release testing of Drug Substance Manufacturing and Drug Product Manufacturing. We have grown significantly over the last 4 years where we as a CDMO has implemented many new customers, and subsequently implemented all the methods associated with testing of the customers products. Due to the fast growth and the many new responsibilities that has come with new customers, methods, and complexity – then we need to move our department to next level. We need to do something differently and work more focused on working smarter not harder, and invest the time in optimizing our processes, procedures, and make sure we constantly have focus on continuous improvements. That is where you come into the picture! About the position We want a Continuous Improvement Scientist to help the 4 teams investigate various problems or processes, with the focus of supporting and driving the improvements projects locally or across the departments in QC. You will be reporting directly to the Director for the QC AD Department with the aim of making sure we prioritize the right projects across the 4 teams, and you will help the QC AD management team to make the right prioritizations of where we will have most gains. You will be part of a CI network and work closely with the entire QC Department and the QC CI partner. Lastly you will work very close with the SMEs and managers from the various departments on the optimization projects. Your primary tasks will be but not limited to: You will function as Project Manager for various improvement projects across the 4 teams. You will investigate, support, and drive and consequently maybe also execute on the projects – this will often also include updating of various processes, SOPs etc. to finalize the implementation. You will lead method transfer root cause investigations. You will help drive a CI culture with the QC AD management team. You will help making presentations and business cases where needed for large optimizations and communications to stakeholders or upper management in Fujifilm. Your will help QC AD Teams to move to a new level as a department that constantly look at making improvements. You will play a vital role in assuring we have focus on the strategic projects and must-win-battles for QC AD teams. Professional and Personal Qualifications The ideal candidate holds a master’s degree in Biochemistry, Biology, Biotechnology, Pharmaceutical Sciences or similar combined with experience from the pharmaceutical industry, preferably experience from QC. We are looking for a person who has the right attitude and energy and understands the requirements in a cGMP QC laboratory. Your qualifications are: You have project management skills and are used to running project across Teams and has experience with the common project management tools. You have good communication skills and are used to make very good PowerPoint presentations that can explain complexity in a simple manner. You possess excellent collaboration skills and understands the importance of OneTeam (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. You have previous experience either as LEAN responsible, CI partner, and knows the various CI/LEAN/Shingo tools. You have experience with facilitating workshops. Fluency in English is required as English is our corporate language. At FUJIFILM Biotechnologies we put #PeopleFirst and we always look for candidates with the right combination of personality and skills, and we have high focus on work-life balance despite that we are a busy company. We are many different nationalities and personalities at FUJIFILM Biotechnologies and for us to succeed we all need to focus on communication, take responsibility, and display great interpersonal skills. 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 Director, Mette Ottosen +45 4194 9913 FUJIFILM 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 https://fujifilmbiotechnologies.fujifilm.com/ 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. 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. 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.

Responsibilities

The Continuous Improvement Scientist will investigate and drive improvement projects across the Quality Control Analytical Development teams. They will prioritize projects and collaborate closely with management and subject matter experts to optimize processes.