Overview
GSK are looking for a Quality Computer System Validation Senior Lead to join on a full-time and permanent basis. This is a strategic and global role with high visibility, dealing with a diverse mix of stakeholders across multiple functions. Given our hybrid working model, there is flexibility of the location of the role.
Responsibilities
* Provide quality oversight to support the implementation and maintenance of strategic computerised systems through the entire system life cycle.
* Collaborate with end users and IT/Tech teams to develop global business processes for GxP operations that are supported by IT systems (e.g., eBRS, LES, M-ERP).
* Ensure that processes and automated solutions satisfy applicable compliance requirements and regulatory constraints.
* Offer expert advice and support to GSC sites on business processes supporting the Quality IT Strategy to achieve consistent application of processes and systems and to share best practices.
* Apply GEMBA and other methods to identify improvements in automated processes to reduce costs, improve user experience, and enhance Quality understanding and performance; drive improvements to business benefits.
* Establish quality standards for data management (data formatting, data cleaning, standardization and analysis) and educate users; work with IT teams and GSC to enforce these standards.
* Implement proactive risk management processes; clearly define and communicate risks to stakeholders and manage risks through problem solving and mitigations.
Qualifications
Required:
* Proven ability to organize and manage validation, deployment, and change management of large, complex, computerised systems across multiple locations, prioritising conflicting demands in a data-driven, business-focused way.
* Understanding of pharmaceutical manufacturing, laboratory and distribution regulations, guidelines, principles and expectations with the ability to interpret and apply company guidelines and expectations.
* Ability to analyse complex data/information/scenarios and make rational, risk-based decisions with clear communication and escalation as needed; able to address challenges to Quality and compliance decisions confidently.
* Proven ability to communicate effectively and collaborate with diverse stakeholders to achieve win-win outcomes and business objectives.
* Experience in coaching/mentoring teams in quality and validation principles and activities.
Preferred:
* B.S. or advanced degree in Computer Science, Engineering, Pharmacology or related sciences.
* Strong interpersonal skills with the ability to influence and negotiate at all levels.
* Ability to work well under pressure with tight timelines; strong consultative, listening, analytical skills; flexible and a team player.
* Coaching and involving team members to understand the need for improvement and encourage idea contributions.
Closing Date for Applications – Wednesday 17th September 2025 (COB).
When applying, use the cover letter or CV to describe how you meet the competencies outlined above. The information provided will be used to assess your application.
Why GSK?
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We are committed to creating an environment where our people can thrive, and we focus on being ambitious for patients, accountable for impact and doing the right thing.
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information, military service or any basis prohibited under federal, state or local law. We also offer a hybrid working model and adjustments process for applicants as needed.
GSK does not accept referrals from employment businesses/agencies unless prior written authorization is obtained. For inclusivity, see our UK Recruitment FAQ guide for common questions.
Seniority level: Not Applicable
Employment type: Full-time
Job function: Quality Assurance
Industries: Pharmaceutical Manufacturing
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