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Quality Control jobs in United Kingdom

Affiliate PV Partner Compliance Specialist

AbbVie

Maidenhead
On-site
GBP 60,000 - 80,000
15 days ago
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Document Controller

Advance Training & Recruitment Services

York and North Yorkshire
On-site
GBP 35,000 - 45,000
15 days ago

Assistant Project Manager

UK Power Networks

United Kingdom
Hybrid
GBP 66,000
10 days ago

Senior C&I Engineer

Snc-Lavalin

Bristol
On-site
GBP 55,000 - 75,000
14 days ago

Focus Technician/Maintenance Technician (Making Plant)

Unilever Brasil Ltda.

Port Sunlight
On-site
GBP 30,000 - 40,000
15 days ago
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Focus Technician/Maintenance Technician (Making Plant) Port Sunlight, Reino Unido

Unilever PLC

Port Sunlight
On-site
GBP 30,000 - 35,000
15 days ago

Laboratory Manager – Global Chemicals Leader CV-Library Laboratory Manager - Global Chemicals Leader

Scienceabode

Billericay
On-site
GBP 80,000 - 100,000
15 days ago

D365 Staff, Release Manager

Warner Bros Games

Leavesden
Hybrid
GBP 75,000 - 95,000
10 days ago
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Integration Developer

Transformationunitgm

Leicester
On-site
GBP 40,000 - 55,000
13 days ago

Vehicle Quality Controller / Trainee Workshop Controller

Activate Group

Kings Langley
On-site
GBP 30,000 - 40,000
14 days ago

Production Engineer

Celeros Flow Technology LLC

Glasgow
On-site
GBP 40,000 - 55,000
14 days ago

Civils Delivery Lead

OCU Group

Stockport
On-site
GBP 60,000 - 80,000
14 days ago

Global Quality CSV Engineer

Uniphar Group

England
Hybrid
GBP 60,000 - 80,000
14 days ago

Property Project Manager

The Old Station Nursery Limited

Theale
Hybrid
GBP 45,000 - 65,000
15 days ago

Senior Project Manager - Chorley

ESG Global Ltd

United Kingdom
Hybrid
GBP 70,000 - 90,000
15 days ago

Quantity Surveyor (Tiverton & Bristol)

Allison Homes Limited

Bristol
On-site
GBP 40,000 - 60,000
8 days ago

Clinical Pharmacist for Mental Health and Learning Disabilities

Transformationunitgm

Radlett
On-site
GBP 40,000 - 57,000
10 days ago

Associate Practitioner - Biochemistry

Haringey GP Federation

Gateshead
On-site
GBP 24,000 - 30,000
10 days ago

Associate Practitioner - Biochemistry

NHS

Gateshead
On-site
GBP 22,000 - 28,000
10 days ago

Assembly Operator

Watson-Marlow Fluid Technology Solutions

Huddersfield
On-site
GBP 40,000 - 60,000
10 days ago

Assembly Operator

Watson-Marlow Fluid Technology Solutions

Huddersfield
On-site
GBP 40,000 - 60,000
10 days ago

Production Supervisor

DCS Scaffolding

Leyland
On-site
GBP 60,000 - 80,000
10 days ago

Snr Manager, Manufacturing Engineering

Gonzalescomm

United Kingdom
On-site
GBP 70,000 - 90,000
12 days ago

Quality Manager - GMP Facilities & Equipment Qualification / Validation (FTC)

Haleon plc

Weybridge
On-site
GBP 50,000 - 70,000
12 days ago

Value Stream Shift Manager- Manufacturing- Late shift

Dechra Group

Skipton
On-site
GBP 51,000
12 days ago

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Affiliate PV Partner Compliance Specialist
AbbVie
Maidenhead
On-site
GBP 60,000 - 80,000
Full time
15 days ago

Job summary

A global biopharmaceutical company in Maidenhead is seeking a professional to oversee compliance and quality in pharmacovigilance services. You will manage outsourced processes, perform quality control, and support training sessions for external suppliers. The ideal candidate will have a science degree, fluency in Spanish, and several years of relevant experience in the pharmaceutical industry. This role emphasizes collaboration, regulatory knowledge, and strong analytical skills.

Qualifications

  • 3 years of pharmaceutical industry experience; including a minimum of 2 years in pharmacovigilance quality systems.
  • Good knowledge of global pharmacovigilance regulations.
  • Skilled at technical writing and authoring, including SOPs/procedural documents.

Responsibilities

  • Manage standards and oversee the monitoring of outsourced processes.
  • Support presentations of quality control results to senior stakeholders.
  • Perform quality control of all outsourced processes.

Skills

Fluency in Spanish
Technical writing
Data interrogation
Influencing stakeholders
Analytical skills

Education

Bachelor’s Degree in related science field
Job description
Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description
Purpose

Support the establishment and maintenance of effective compliance & oversight of external providers of pharmacovigilance services for AbbVie affiliates. At a minimum this system must ensure compliance with global regulatory requirements, AbbVie standards and local PV regulations. The scope extends to all externalized services and providers overseen by PPS on behalf of AbbVie affiliates, including adverse event management, reporting, and related operational activities, and spans all marketed products.

Responsibilities
  • Manages standards and oversees the monitoring of outsourced processes, investigates and leads the follow‑up of discrepancies.
  • Manages the monitoring of supplier performance via SLAs and other metrics, prepares routine and ad‑hoc reports, leads the investigation of trends, and escalates issues as appropriate.
  • Supports presentations of quality control results and trend analysis to senior, cross‑functional AbbVie stakeholders.
  • Support the establishment of AbbVie quality management processes for external suppliers of affiliate pharmacovigilance services that meet applicable PPS, RDQA, and affiliate standards and ensure reproducible, controlled, and timely delivery of high‑quality outputs.
  • Collaborate with suppliers and internal partners to implement vendor quality management processes which integrate with supplier and AbbVie processes wherever possible. Support the use of risk‑proportionate approaches for in‑line and retrospective evaluations.
  • Supports development of materials and delivers training sessions (through multiple modalities) in conjunction with supplier, including train‑the‑trainer, special‑topics, refresher, and internal AbbVie trainings as needed.
  • Manages issue investigation (eg CAPAs), coordinating between AbbVie and supplier systems. Supports the communication and collaborates across internal and partner stakeholders for prioritization of issues, as well as timely, effective, and permanent remediation actions.
  • Performs quality control (QC) of all outsourced processes reliable documents results; proactively identifies areas of process and technical improvement and supports the implementation of changes.
  • Proactively suggests changes in QC approaches to account for external and internal process, regulatory and business change.
  • Responsible as a member of the Affiliate PV Operations team for driving compliance and business excellence for all of outsourced affiliate PV activities.
Qualifications

Please note - candidates who are not fluent in Spanish cannot be considered for this role.

List required and preferred qualifications (up to 10). Include education, skills and experience.

  • Bachelor’s Degree or equivalent in related science field
  • 3 years pharmaceutical industry experience; including a minimum of 2 years in pharmacovigilance quality systems. Affiliate experience strongly preferred
  • Good knowledge of global pharmacovigilance regulations, including one or more countries with an excellent understanding of PV quality assurance systems
  • Skilled at technical writing and authoring, including SOPs/procedural documents, corrective actions plans / exception reports
  • Good Excel, data interrogation and interpretation skills and experience
  • Good influencer across multiple stakeholders; seen as a collaborative partner across the organization
  • Able to proactively identify, assess, and effectively manage compliance risks
  • Experienced in working in cross‑functional teams
  • Analytical with a high degree of attention to detail
  • Very good written and spoken English plus one other language
Key Stakeholders
  • PPS: Safety Compliance,ance Excellence, Vendor Management Team, Case Processing Center of Excellence, ODC Center of Excellence, EU QPPV.
  • RDQA: Pharmacovigilance & Regulatory Affairs Quality Assurance.
  • GMA: Area Medical Heads, Aff MD's.
Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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