At a Glance
- Tasks: Ensure compliance of computerised systems to safeguard patient safety and data integrity.
- Company: Join Pharmanovia, a fast-growing global pharmaceutical company with a supportive culture.
- Benefits: Competitive salary, bonuses, hybrid working, and employee recognition awards.
- Other info: Be part of a diverse team focused on innovation and accountability.
- Why this job: Play a vital role in patient safety and regulatory compliance in a dynamic environment.
- Qualifications: Experience in GxP compliance and strong stakeholder management skills required.
The predicted salary is between 50000 - 60000 £ per year.
Basildon – (Hybrid role: 3 days office, 2 days home per week)
About the Company
Pharmanovia is a dynamic, fast‑growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried‑and‑trusted medicines. Our core behaviours are:
- We act decisively, but we never compromise on quality.
- We keep our promises and do as we say.
- We value our heritage and foster an entrepreneurial spirit.
- We reinvest in our future – in our products, our brands and our people.
- We give back to our communities.
Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high‑quality branded prescription medicines to patients, prescribers, and healthcare providers worldwide. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees from 29 nationalities and operates from offices in the UK, Denmark, the Netherlands, Switzerland, Italy, Spain, Germany, the U.A.E., India, Australia, and Singapore. We are an agile, committed, and innovative global speciality pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to engage extensively with clinical communities to communicate product improvements and to prioritise environmental, social, and governance considerations across the business and workforce. Pharmanovia’s therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology.
About the Role
We are looking for an experienced Computerised Systems Compliance Manager to help safeguard patient safety through GxP compliance and data integrity.
Responsibilities
- Provide overall compliance oversight for all GxP computerised systems across Pharmanovia
- Ensure systems comply with regulatory expectations, including EU Annex 11, 21 CFR Part 11, GAMP and MHRA data integrity guidance
- Develop, implement and maintain computerised systems validation and lifecycle management processes
- Act as the organisation’s subject matter expert (SME) and primary point of contact for computerised systems compliance
- Own and maintain the Site Validation Master File and validation documentation
- Lead and support internal, client and regulatory audits relating to computerised systems
- Review and approve system implementation plans, upgrades and change control activities
- Identify compliance gaps and support remediation, CAPA planning, and execution
- Conduct and communicate risk assessments associated with computerised systems
- Establish and report KPIs related to computerised systems at Quality Review Meetings
- Support supplier and system onboarding due diligence from a compliance perspective
Qualifications
Essential Experience & Knowledge
- Demonstrated experience managing computerised systems validation in a pharmaceutical, biotech, or life sciences environment, with a strong focus on GxP compliance and validation processes.
- Previous QA experience in the management of (CAPA, Deviation, Change Controls, Complaints, PQRs)
- Strong knowledge of:
- Good Manufacturing Practice (GMP) and GxP
- EU Annex 11
- 21 CFR Part 11
- GAMP 5
- Data integrity principles and MHRA expectations
- Experience supporting or leading regulatory inspections and audits
Required Skills
- Ability to translate complex technical and regulatory concepts into clear, practical guidance
- Strong stakeholder management and cross‑functional collaboration skills
- High attention to detail and strong documentation practices
- Ability to work independently while influencing multiple levels of the organisation
- Professional, reliable and committed to maintaining quality and compliance standards
Why Join Pharmanovia
- Be part of a growing global pharmaceutical organisation with a strong pipeline and expanding footprint
- Work in a collaborative, people‑focused culture that encourages innovation and accountability
- Play a key role in ensuring patient safety and regulatory compliance across a diverse portfolio of established medicines
Pay range and compensation package
We offer a competitive salary plus a bonus and rewards package, including holidays, employee recognition awards, social events, a pension scheme, and hybrid working.
Pharmanovia is an equal‑opportunity employer. Pharmanovia does not unlawfully discriminate against employees or applicants for employment based on an individual’s race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. Pharmanovia will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.
Computer Systems Validation Specialist Basildon employer: Meeveem Limited
Pharmanovia is an exceptional employer, offering a dynamic and supportive work environment in Basildon that fosters innovation and accountability. With a strong commitment to employee growth and a collaborative culture, team members are empowered to play a vital role in ensuring patient safety and regulatory compliance across a diverse portfolio of established medicines. The company provides competitive compensation, a comprehensive benefits package, and the flexibility of a hybrid working model, making it an attractive choice for those seeking meaningful and rewarding employment in the pharmaceutical industry.
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