Assay Validation Scientist - Glasgow
at Merck Group
Glasgow, Scotland, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Apr, 2025 | Not Specified | 30 Jan, 2025 | N/A | Regulatory Requirements,Adherence,Regulatory Standards,Biologics | No | No |
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Description:
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 are seeking an experienced Assay Validation Scientist to join our Glasgow team and provide expert oversight of assay validation, ensuring that projects are conducted in compliance with scientific and regulatory standards. You will be responsible for on-time delivery and adherence to quality standards, with key responsibilities including:
- Monitoring compliance of assay validations with Quality and Regulatory functions.
- Managing and completing assay updates within agreed timelines.
- Interacting with operational staff to ensure successful completion of assay validation projects for UK and global facilities.
- Designing protocols and templates for assay validation studies.
- Ensuring timely delivery of client products and reports that meet quality and regulatory requirements.
- Acting as a consultant for clients on assay validation design.
- Supporting lab investigations and providing scientific coaching to team members.
- Promoting continuous improvement initiatives within Biologics.
Responsibilities:
- Monitoring compliance of assay validations with Quality and Regulatory functions.
- Managing and completing assay updates within agreed timelines.
- Interacting with operational staff to ensure successful completion of assay validation projects for UK and global facilities.
- Designing protocols and templates for assay validation studies.
- Ensuring timely delivery of client products and reports that meet quality and regulatory requirements.
- Acting as a consultant for clients on assay validation design.
- Supporting lab investigations and providing scientific coaching to team members.
- Promoting continuous improvement initiatives within Biologics
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Graduate
Proficient
1
Glasgow, United Kingdom