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- Tasks: Lead the digital transformation of biopharma with innovative technology platforms.
- Company: Join FUJIFILM Biotechnologies, a global leader in healthcare and innovation.
- Benefits: Enjoy competitive salary, 35 days holiday, and a supportive work environment.
- Why this job: Make a real impact on life-saving therapies while working with cutting-edge technology.
- Qualifications: Bachelor's degree in Engineering or Science and 5+ years in IT for life sciences.
- Other info: Dynamic global role with excellent training and career development opportunities.
The predicted salary is between 60000 - 75000 ÂŁ per year.
The work we do at FUJIFILM Biotechnologies has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FUJIFILM Biotechnologies and help make the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe.
About Us
Help build the digital backbone of next‑generation biopharma. As our System Manager, you will own and elevate core Product Technology platforms—PDLM, ELN, and Risk Management—that power Process Development and MSAT. You’ll translate real-world science into robust, compliant digital solutions, weave data integrity through every workflow, and enable a new, standardized way of working across global teams.
Role & Responsibilities
- If you’re passionate about turning complex requirements into elegant, validated systems—and you thrive in a collaborative, matrixed environment—this role is your opportunity to make a visible impact on tech transfer timelines, batch right‑first‑time performance, and regulatory readiness.
Why you’ll love it here
- Shape how development knowledge (DoE, QbD) flows into manufacturing execution and CPV
- Own high‑value platforms with direct line of sight to business outcomes
- Partner across PD, MSAT, Automation/Engineering, QA/Validation, and IT/OT
- Drive standardization at scale with class‑based, globally reusable configurations
- Operate with autonomy while influencing best practices across sites
What you’ll do
- Design, configure, implement, and maintain PDLM, ELN, and Risk Management platforms to meet user and compliance requirements
- Translate business needs into scalable, class‑based configurations and reusable library objects that enable data standardization
- Ensure cGxP, data integrity (ALCOA+), and data security across integrations; partner with QA/CSV on risk‑based validation (GAMP 5, CSA) and audit readiness
- Define and enforce standards, templates, libraries, and master data structures in partnership with Master Data teams
- Deploy class‑based data structures to deliver recipe data models and master data (materials, specs, equipment classes)
- Develop training, job aids, and adoption materials; coach teams on ISA‑88 and digital recipe best practices
- Manage external partners and solution vendors; define user requirements, participate in design reviews, and ensure delivery to standards and timelines
- Contribute to digital thread initiatives linking development knowledge to manufacturing execution and CPV; support regulatory inspections and filings
- Drive harmonization and standard work across sites (templates, test protocols, UAT scripts) to reduce cycle times and deviations
- Champion continuous improvement through metrics, KPIs, and standardized ways of working
What success looks like
- Seamless, compliant platforms that accelerate development and tech transfer
- Standardized data models and libraries that scale globally
- Strong adoption and user satisfaction through clear training and enablement
- Audit‑ready documentation and validated configurations
- Reduced cycle times, deviations, and rework through harmonized processes
Qualifications And Experience
Minimum Qualification Requirements
- Bachelors Degree in Engineering or Scientific related field
- 5+ years’ of relevant experience in Information Technology implementing and sustaining GxP impacted systems in life sciences or closely related industries.
- Demonstrated experience with Computer System Validation (CSV) and data integrity principles (ALCOA+).
- Proven experience with one or more: PDLM/PLM, ELN, or Risk Management Platforms
Preferred Requirements
- Experience in manufacturing or process development systems preferred (MES/LIMS/QMS/data platforms)
- Preferred experience in pharmaceutical industry, IT CSV
- Familiarity with ISA-88/ISA-95 standards and digital recipe/data modelling
- Certifications: GxP/CSV (e.g., ISPE/GAMP), Agile/Scrum, ITIL, PMP/PRINCE2, or data integrity.
What you’ll bring
- Deep understanding of PDLM/PLM and ELN platforms and their application to Process Development/MSAT
- Strong knowledge of CSV, data integrity (ALCOA+), and risk‑based validation (GAMP 5, CSA)
- Knowledge of ISA‑88/ISA‑95 and digital recipe principles
- Excellent stakeholder communication and facilitation skills; ability to influence without authority
- Strong problem‑solving and analytical skills; experience with KPIs and continuous improvement
- Comfort operating in a global, matrixed environment
Why work with us?
As part of any recruitment process, FUJIFILM Biotechnologies collects and processes personal data relating to job applicants. The organisation is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations and may share this as part of the global recruitment process with hiring managers in Europe and the United States.
This is a global position that will support all FUJIFILM Biotechnologies sites. This position can be based at any of our locations around the globe. Benefits and compensation will be governed by the location that you are based from and considered your home site.
At FUJIFILM Biotechnologies, your passion – your Genki – is your power and we empower you to define what Genki means to you. When You Join Us, We Will Train, Develop And Support You To Become The Best You Can Possibly Be. We Offer a Structured New Starter Induction Programme As Well As On-going Development Training.
In Addition To This, We Offer
- Competitive salary plus company bonus scheme
- 35 days of holiday, plus bank holidays.
- Salary Sacrifice scheme offering, healthcare, bikes, dental etc.
- Generous pension scheme
- Free parking and electric charging points
Closing date 8th April 2026
System Manager - Digital Product Applications in Billingham employer: FUJIFILM Biotechnologies
Contact Detail:
FUJIFILM Biotechnologies Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land System Manager - Digital Product Applications in Billingham
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their mission and values, especially how they relate to biopharma. This will help you tailor your answers and show you're genuinely interested.
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online resources. Focus on articulating your experience with PDLM, ELN, and Risk Management platforms, as these are key for the System Manager role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining FUJIFILM Biotechnologies and contributing to something meaningful.
We think you need these skills to ace System Manager - Digital Product Applications in Billingham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the System Manager role. Highlight your experience with PDLM, ELN, and Risk Management platforms, and don’t forget to showcase your understanding of data integrity principles. We want to see how your skills align with what we’re looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you’re passionate about biopharma and how you can contribute to our mission. Be specific about your past experiences and how they relate to the role. Let your personality come through!
Showcase Your Problem-Solving Skills: In your application, give examples of how you've tackled complex challenges in previous roles. We love candidates who can think critically and drive continuous improvement. Share metrics or KPIs that demonstrate your impact!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining our team at FUJIFILM Biotechnologies.
How to prepare for a job interview at FUJIFILM Biotechnologies
✨Know Your Platforms
Make sure you have a solid understanding of PDLM, ELN, and Risk Management platforms. Be ready to discuss how you've used these systems in your previous roles and how they can be applied to enhance process development and tech transfer.
✨Showcase Your Compliance Knowledge
Familiarise yourself with GxP, data integrity principles (ALCOA+), and risk-based validation (GAMP 5). Prepare examples of how you've ensured compliance in past projects, as this will demonstrate your ability to maintain high standards in a regulated environment.
✨Communicate Effectively
Since this role involves collaboration across various teams, practice articulating your thoughts clearly. Think about how you can influence stakeholders without direct authority and prepare to share examples of successful teamwork from your experience.
✨Emphasise Continuous Improvement
Be ready to discuss how you've driven continuous improvement in your previous roles. Highlight any metrics or KPIs you've worked with and how you've used them to enhance processes, reduce cycle times, or improve user satisfaction.