At a Glance
- Tasks: Ensure GxP systems and lab software compliance while managing user access and troubleshooting.
- Company: Innovative global leader in Healthcare, Life Science, and Electronics.
- Benefits: Inclusive culture, career growth opportunities, and a chance to impact millions.
- Other info: Embrace diversity and innovation in a collaborative environment.
- Why this job: Join a dynamic team and work with cutting-edge technology to drive real change.
- Qualifications: Bachelor's degree in science or IT and 2 years in a technical role.
The predicted salary is between 42840 - 52360 £ per year.
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
Join our dynamic team to ensure our GxP computer systems and lab software remain compliant across their entire lifecycle. In this hands-on position, you’ll handle system administration, manage user access, maintain critical quality records, and perform essential software troubleshooting. You'll act as the key liaison between laboratory users, IT, Validation, and external vendors to drive seamless system implementations and upgrades. Working across global departments, your expertise directly protects data integrity and streamlines site operations.
Key responsibilities
- Perform administration tasks for a variety of GxP systems and associated software in a regulated (GxP) environment following defined procedures.
- Defining, assigning, installing, configuring, documenting and managing user access across CTS.
Who You Are
Minimum Qualifications:
- Bachelor of Science/IT (B.S.) or Bachelor of Arts (B.A.) degree in science or technical area.
- 2 years’ in a technical role supporting regulated software applications or laboratory systems.
- Proven hands-on experience in GxP system administration, user access management, and troubleshooting.
Preferred Qualifications
- Excellent communication and facilitation skills (ability to lead cross-functional meetings, demonstrated ability to bring consensus among diverse cross-functional teams).
- Proficient knowledge and application of FDA and EU regulations (cGMP, GLP).
- Advanced knowledge and application of data integrity regulatory guidance (e.g., FDA, MHRA, WHO).
- Understand quality standards for GxP software applications and systems.
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!
Global GxP System Engineer (all gendesr) in Glasgow employer: Merck Life Science
As a Production Planning Specialist, you will thrive in a dynamic environment that values diverse perspectives and fosters innovation. Our commitment to employee growth is reflected in our inclusive culture, where you can develop your skills at your own pace while contributing to meaningful projects that impact millions. Join us to be part of a team that champions human progress and supports your professional journey in a regulated production setting.
