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ComplianceEnglishLean / Six SigmaRecruitment
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About the role
As Data Integrity Specialist, You will lead data integrity activities to protect the completeness, accuracy and availability of quality and manufacturing data. You will work closely with site quality, IT, manufacturing and global quality teams. We value clear thinkers who act with integrity, who can teach others, and who enjoy improving systems and processes.
This role offers growth through cross-functional projects, meaningful impact on product quality systems, and alignment with GSK’s mission of uniting science, technology and talent to get ahead of disease together.
Responsibilities:
- Being Single Point of Contact (SPOC) for any topic related to Data Integrity
- Maintain and drive the site data integrity program to meet regulatory expectations and company standards.
- Assess computerised systems and paper records for data integrity risk, and support validation and change control activities.
- Write, review and approve procedures, work instructions and training materials related to data integrity.
- Lead investigations of data integrity issues and support corrective and preventive actions (CAPA).
- Deliver training and coaching for site colleagues to build data integrity awareness and good practices.
- Participate in internal audits and support readiness for regulatory inspections.
Why You?
Basic Qualifications & Skills:
- Bachelor’s degree in a scientific, technical or engineering discipline, or equivalent experience.
- Minimum 2–5 years’ experience in pharmaceutical quality, compliance, IT validation or related area.
- Practical knowledge of Good Manufacturing Practice (GMP) principles and how they apply to data and records.
- Experience assessing computerised systems, electronic records, or paper record controls.
- Fluent Hungarian and strong English language skills.
Preferred Qualifications & Skills:
- Experience specifically in data integrity programs or audits in a regulated environment.
- Knowledge of electronic quality management systems, laboratory systems or manufacturing execution systems.
- Hands-on experience with system validation, CSV (computerised system validation) or IQ/OQ/PQ activities.
- Practical skills in risk assessment and root cause analysis for data issues.
- Strong coaching and training experience to upskill site colleagues.
What we offer:
• Hybrid working model with a mix of 2 days on-site presence and 3 days working in HO. Exact on-site schedule will be discussed during hiring.
• A collaborative and supportive team that values learning and development.
• Opportunities to lead projects that improve quality systems and digital ways of working.
• Cafeteria package
• Annual bonus and annual salary review
• Group life and accident insurance package
• Voluntary pension fund contribution
• Health and wellbeing services
• Inclusive, diverse, and supportive company culture
• Commuting support (company shuttle buses from Budapest and surrounding towns or fuel reimbursement for private car usage)
• Permanent employment contract
• Paid parental leave and caregiver leave
Skills
Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Influencing Without Authority, Lean Management, Pharmaceutical Regulatory Compliance, Problem Solving, Quality Assurance (QA), Risk Awareness, Technical Writing
Hungarian Salary Range / Magyarországi bérsáv: HUF 12,132,000 to HUF 20,220,000The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the
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