Preclinical R&D Quality Partner | Quality by Design

GlaxoSmithKline; Stevenage; On-site; GBP 70,000 - 90,000; Full time

Job summary

GlaxoSmithKline is seeking a Quality Business Partner to provide strategic quality guidance across R&D, embedding quality by design in key processes. You will collaborate with pre-clinical research and therapy area units to assess quality risks and drive continuous improvement within a cross-functional QMS.

Based at our Stevenage site with plans to relocate to Cambridge by early 2029, you will lead quality strategies, educate stakeholders, and ensure timely escalation of quality issues and CAPA

Qualifications

• Bachelor's degree or equivalent in scientific or quality-related field.
• Experience in drug development, regulatory compliance or quality management.
• Expert knowledge of non-clinical research practices, GLP/GCP or Animal Welfare requirements.
• Strong ability to influence diverse stakeholders and embed quality by design.

Responsibilities

• Serves as Quality Business Partner for Research across R&D.
• Defines activities to deliver quality strategies for R&D Research.
• Collaborates with Risk and Issue Management to drive quality by design.
• Shares learnings to drive simplification and best practices across the business.
• Works with business teams to provide expert quality information and support continuous improvement.
• Evaluates procedures to support an integrated, cross-functional QMS.
• Fosters a culture of quality across GSK and with third parties.
• Facilitates communication and knowledge sharing across teams.
• Supports due diligence and M&A activities.
• Works with R&D Data Analytics to define KPI, KQI and metrics needs.

Skills

Quality by Design

Risk management

Stakeholder management

Continuous improvement

GxP knowledge

Education

Bachelor's degree or equivalent in scientific/quality field

Job description

GlaxoSmithKline is seeking a Quality Business Partner to provide strategic quality guidance across R&D, embedding quality by design in key processes. You will collaborate with pre-clinical research and therapy area units to assess quality risks and drive continuous improvement within a cross-functional QMS.

Based at our Stevenage site with plans to relocate to Cambridge by early 2029, you will lead quality strategies, educate stakeholders, and ensure timely escalation of quality issues and CAPA