Pharmaceutical validation specialist Work, Jobs in England (with Salaries)

Validation Execution Specialist
BI AH UK Ltd —Ash
- Full-time
- Engineering
- Microsoft Office
- Bachelor's degree
Qualification & Validation Specialist
Bespak —Holmes Chapel
- £55,000 a year
- Free parking
- Life insurance
Quick apply
13d
Quality Assurance Specialist
Cytiva —Portsmouth
- Full-time
- Analysis skills
- Bachelor's degree
- Communication skills
Quality Specialist
Steris —Syston
- Full-time
- Microsoft Excel
- Communication skills
Quality Specialist- FCP
Indivior —Kingston upon Hull
- Full-time
- Bachelor's degree
- Travel
- APIs
5d
QA Specialist - NPI
GE HEALTHCARE —Chalfont Saint Giles
- Bachelor's degree
- Travel
- Contracts
Chemical Development Trace Analysis Scientist
Eurofins UK PSS —Macclesfield
- Full-time
- Laboratory experience
- Microsoft Office
- Analysis skills
- Free parking
- Employee assistance programme
Quick apply
6d
Advanced Therapy Quality Control Scientist
Guy's and St Thomas' NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Full-time
- Quality control
- Communication skills
7d
Computer Systems Validation Specialist
Pharmanovia —Basildon
- Hybrid work
Associate Scientist
Cyprotex —Macclesfield
- Full-time
- Laboratory experience
- Master's degree
- Bachelor's degree
- Referral programme
Quick apply
9d
Senior Technical Specialist - InVivo
Charles River Laboratories —Portishead
- Full-time
- Microsoft Word
- Microsoft Outlook
- Doctoral degree
- Paid training
- Annual leave
14d
Clinical Operations & Enablement Lead
Nucs AI —London
- Full-time
- Hybrid work
- Master's degree
- Presentation skills
- Bachelor's degree
Quick apply
QC Project Analyst
Dechra Pharmaceuticals PLC —Skipton
- £32,000 - £37,000 a year
- Monday to Friday
- Bachelor's degree
- Organisational skills
- Communication skills
- Free parking
- Annual leave
Product Support Specialist
LabLogic Systems —Sheffield
- Full-time
- Oracle
- Laboratory experience
- Windows
Quality Supplier Officer
MICRONCLEAN LIMITED —Skegness
- £36,000 - £40,000 a year
- Overtime
- Microsoft Powerpoint
- ERP systems
- SharePoint
- Relocation assistance
- Annual leave
QC Technical Specialist
Dechra Pharmaceuticals PLC —Skipton
- Computer literacy
- Maintenance
Research Fellow in Biophysics and Translational Mechanobiology
University College London —London
- £43,981 - £52,586 a year
- Full-time
- Doctoral degree
- Annual leave
- Employee assistance programme
1d
Qualification and Validation Professionals
Scitech Engineering Ltd —Godalming
- Full-time
Quick apply
QA Manager - Projects and NPI Support
Bespak —Holmes Chapel
- £55,000 a year
- Leadership
- Free parking
Quick apply
Imaging Scientist II
Perspectum —Oxford
- £45,000 - £55,000 a year
- Full-time
- Doctoral degree
- Master's degree
- Analysis skills
Quick apply

I want to receive the latest job alerts for pharmaceutical validation specialist in england

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Validation Execution Specialist

BI AH UK Ltd -
Ash

Apply Now

Job details

Full-time

Qualifications

Engineering
Microsoft Office
Quality assurance
Bachelor's degree
HVAC
Water systems
Communication skills
FDA regulations

Full job description

THE POSITION

To support validation activities at the Pirbright Site, the Validation Execution Specialist will generate and/or revise validation documentation for utilities, facilities, processes, and equipment, ensuring delivery of commitments in line with timelines and internal/external validation regulations.

This is a fixed-term contract until December 2027.

Tasks & responsibilities

Responsible for the successful delivery of the validation and qualification activities according to the Site Validation Master Plan (SVMP) for the Pirbright Site.

Coordinate and support Validation activities for utilities and facilities revalidation (Water systems, Gases, HVAC, TCUs, SIP, Sterilisers etc).
Ensure HVAC validation activities are coordinated efficiently to maintain classified rooms/zones (A,B,C,D) in compliance and according to contamination control strategy of the site (from both physical and microbiological point of view).
Manage external parties supporting validation activities.

Responsible for providing support for the successful delivery of the Validation activities for systems, processes and procedures.

Support Process validation activities for new products by writing, reviewing or approving validation documents.
Support Computerised systems and Spread sheets validation.
Support cross functional teams to establish protocols for miscellaneous validation activities such as Gowning qualification and disinfectant validation.

Generation, review and/or approval of Validation documentation (Validation Plan, Protocols, Reports, Impact assessment, Risk assessment, URS, IQ, OQ, PQ, RA, Traceability Matrix, Periodic Reviews, etc) for the validation/qualification, when applicable.

Ensure validation related activities are captured into change controls and new projects.

Support change / project owners to identify validation needs.
Act as a validation SME for new projects and change controls as appropriate.
Support and provide guidance to validation contractors, End users, Engineers in the delivery of validation documentation ensuring that a consistent and best practice approach is adopted with regards to generation of validation documentation.

Review documentation such as SAT, FAT, Commissioning, Decommissioning Documents.

Interpret and apply regulation/policies/corporate and local procedures during cross-functional meetings building a culture of quality and validation compliance ensuring the fulfilment of the cGMP requirements.

Guide and influence teams on GxP compliance .

Support colleagues to resolve issues, Risk assessment, Periodic Reviews, Investigations, etc to support CAPA, Change Controls, Deviations and other Quality systems.

Guide colleagues/ QMS records owners to delivering compliant, regulatory acceptable records and documentation within the regulated areas.

Act as the Validation member / validation SME of different forums such as Water committee, change control committee, QMR etc.

Actively support audit preparations and act as SME for validation, qualification, contamination control, classified room validation audit topics as needed.

Requirements

Bachelor’s degree in Sciences, Engineering, Microbiology, or related field, or formal validation qualification.
Significant experience in Quality Assurance/Manufacturing in a pharmaceutical company.
Good knowledge & experience in Validation.
Excellent knowledge of MS Office Suite.
Excellent written and verbal communication skills; experience authoring technical documentation.
In‑depth knowledge of the regulated pharmaceutical industry and compliance expectations (VMD, FDA, Eudralex Annex 1).
Good understanding of industry guidelines (ISPE, PDA, ISO, HTM).
Good understanding of GxP water systems, HVAC systems, pharmaceutical gases, etc.
Experience in Biologicals beneficial.
Experience in Sterile Manufacturing beneficial.

*A Disclosure and Barring Service (DBS) check will be required for the successful candidate. Any offer of employment will be subject to satisfactory DBS certificate.

WHY THIS IS A GREAT PLACE TO WORK

Boehringer Ingelheim has been recognised as a Top Employer in the UK, demonstrating our commitment to building an exceptional workplace through strong people practices and supportive HR policies.
Learn more: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work

Apply Now

Refine Your Search

pharmaceutical validation specialist jobs in england

Validation Execution Specialist

Qualification & Validation Specialist

Quality Assurance Specialist

Quality Specialist

Quality Specialist- FCP

QA Specialist - NPI

Chemical Development Trace Analysis Scientist

Advanced Therapy Quality Control Scientist

Computer Systems Validation Specialist

Associate Scientist

Senior Technical Specialist - InVivo

Clinical Operations & Enablement Lead

QC Project Analyst

Product Support Specialist

Quality Supplier Officer

QC Technical Specialist

Research Fellow in Biophysics and Translational Mechanobiology

Qualification and Validation Professionals

QA Manager - Projects and NPI Support

Imaging Scientist II

I want to receive the latest job alerts for pharmaceutical validation specialist in england

Explore jobs in more locations

THE POSITION

Jobseeker tools

Employer Tools

Browse

Stay Connected