CSV Engineer - 12 Month FTC

Work Your Magic with us!  

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

Your role:

We have an exciting new opportunity for a CSV Engineer to join us on a 12 Month Fixed Term Contract which can be fully remote in the UK or hybrid in Glasgow. In this role, you will join our project team to remotely support new infrastructure being implemented in our head office in Darmstadt, Germany. You will provide validation testing and quality expertise to ensure that the laboratory systems are installed and remain compliant to the required pharmaceutical regulations as outlined by site procedures as well as supporting audit preparation and readiness.

Other key responsibilities include:

• Work in conjunction with onsite IT & Laboratory teams as well as the wider project groups to ensure that the site is aligned with our corporate strategy for plant digitization processes.
• Support with Development of gap analysis / action plan to address any compliance gaps identified.
• Help to determine most appropriate testing, writing protocols to be utilized for each system/integration and reporting outcomes.
• Support with the integration of existing systems into a new framework.
• Align with project timelines and report on progress.
• Flexibility with scheduling meetings as you will be working with global teams.

Who you are:

• Bachelor’s degree or above in business, Life Science, IT or engineering subject.
• Advanced knowledge of Laboratory platforms / LIMS – instrumentation and stand-alone systems.
• Work experience in regulated environments.
• Advanced knowledge of Data Integrity, GAMP / 21 CFR 11, ISO 13845.
• Knowledge of preparation of URS / FDS.
• Experienced in authoring & executing Validation protocols (IQ/OQ/PQ) and preparation of VP, VSR, SOPs, Risk Assessment.
• Knowledge of traceability matrix.
• Team Player who is result oriented with a strong affinity to transparency.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!