implementation specialist Work, Jobs in fobbing, ess (with Salaries)

Computer Systems Validation Specialist
Pharmanovia —Basildon
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Mid and South Essex NHS Foundation Trust —Basildon
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Mid and South Essex NHS Foundation Trust —Westcliff-on-Sea
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IT Implementation Specialist VCM
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OSB Group —Chatham
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zendbox —Paddock Wood
- £38,000 - £40,000 a year
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Robosol Software UK Limited —Basildon
- From £50,000 a year
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Allvue Systems —London
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IT Implementation Specialist - Teamcenter
Leonardo UK Ltd —Basildon
- £50,000 - £70,000 a year
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Leonardo UK Ltd —Basildon
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Kyriba —London
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Ylem Group Limited —Coryton
- £12,480 - £31,200 a year
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- Annual leave
- Employee assistance programme
Quick apply
4d
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Janus Henderson —London
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NOVA Data Quality Assistant
Mid and South Essex NHS Foundation Trust —Wickford
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Information Security Governance, Risk, and Compliance (GRC) Specialist
Janus Henderson —London
- Hybrid work
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Onboarding Specialist
xpate —London
- Analysis skills
- Annual leave
- Flexible schedule
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Computer Systems Validation Specialist

Pharmanovia -
Basildon

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Job details

Benefits

Company pension

Qualifications

GAMP

Full job description

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.

Equal Opportunity Statement

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.

Apply Now

Refine Your Search

implementation specialist jobs in fobbing, ess

Computer Systems Validation Specialist

NOVA RTT Validator

Implementation Specialist

Implementation Specialist

Implementation Consultant - WFH - £70,000 pa

EPR Change Analyst

IT Implementation Specialist VCM

ESG and Sustainability Manager

Lead Appointed Person Lifting Operations

Implementation & QA Specialist

QMS Product Lead

Implementation Specialist III

IT Implementation Specialist - Teamcenter

IT Implementation Specialist - Manufacturing

Senior Specialist, Workday Finance

Site Operator - Part Time 16 Hours Essex

Associate, Governance & Oversight Specialist

NOVA Data Quality Assistant

Information Security Governance, Risk, and Compliance (GRC) Specialist

Onboarding Specialist

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