Quality Manager
Posted on Jun 11, 2026 by CV-Library
Cwmbran, Gwent, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
Quality Manager - Cwmbran (Near Newport, South Wales)
A leading CRO is looking for a Quality Manager to join its Cwmbran team, taking ownership of day‑to‑day Quality Assurance operations and ensuring both GMP and non‑GMP activities meet the highest standards of compliance, integrity, and client commitment.
In this pivotal role, you'll provide hands‑on QA leadership across the full spectrum of quality system activities - from laboratory oversight and supplier audits to inspection readiness and documentation review. You'll be expected to apply pragmatic, risk‑based judgement suited to a dynamic contract laboratory environment where regulated and non‑regulated activities coexist.
As a senior quality practitioner and people manager, you'll guide operational teams, coach staff on GMP and non‑GMP expectations, and step in to deputise for the Head of Quality when required. This is a role for someone who thrives on responsibility, collaboration, and driving a culture of compliance and continuous improvement.
Key Responsibilities
Provide routine QA oversight of GMP and non‑GMP laboratory activities
Maintain and improve the Pharmaceutical Quality System (PQS), including deviations, CAPAs, change controls, and investigations
Arrange, host, and respond to client audits and regulatory inspections
Lead, perform, and report on internal audits in line with the site audit programme
Conduct supplier audits, oversee supplier qualification, and maintain the Approved Supplier List
Apply data integrity and CSV principles across GxP systems
Support or lead implementation of electronic Quality Management Systems (eQMS)
Line‑manage 2 QA direct reports and mentor up to 4 indirect reports
Identify training needs, coach staff, and promote a strong quality culture
Drive continuous improvement initiatives across QA processes and systems
What We're Looking For
Significant QA experience within a GMP‑regulated environment
Experience in a contract laboratory or service‑based organisation conducting GMP and non‑GMP activities
Demonstrable experience conducting internal and supplier audits
Proven track record supporting and hosting client and regulatory inspections
Strong working knowledge of EU GMP, FDA CFRs, Annex 11, and ICH Q8-Q10
Sound understanding of data integrity and CSV principles
Approachable, credible, and collaborative leadership style
Confident communicator with internal stakeholders, clients, and regulators
Practical, solution‑focused, and calm under inspection conditions
Desirable:
Experience implementing or enhancing electronic Quality Management Systems (eQMS)
QMS Lead Auditor qualification
Certified training within GxP
A leading CRO is looking for a Quality Manager to join its Cwmbran team, taking ownership of day‑to‑day Quality Assurance operations and ensuring both GMP and non‑GMP activities meet the highest standards of compliance, integrity, and client commitment.
In this pivotal role, you'll provide hands‑on QA leadership across the full spectrum of quality system activities - from laboratory oversight and supplier audits to inspection readiness and documentation review. You'll be expected to apply pragmatic, risk‑based judgement suited to a dynamic contract laboratory environment where regulated and non‑regulated activities coexist.
As a senior quality practitioner and people manager, you'll guide operational teams, coach staff on GMP and non‑GMP expectations, and step in to deputise for the Head of Quality when required. This is a role for someone who thrives on responsibility, collaboration, and driving a culture of compliance and continuous improvement.
Key Responsibilities
Provide routine QA oversight of GMP and non‑GMP laboratory activities
Maintain and improve the Pharmaceutical Quality System (PQS), including deviations, CAPAs, change controls, and investigations
Arrange, host, and respond to client audits and regulatory inspections
Lead, perform, and report on internal audits in line with the site audit programme
Conduct supplier audits, oversee supplier qualification, and maintain the Approved Supplier List
Apply data integrity and CSV principles across GxP systems
Support or lead implementation of electronic Quality Management Systems (eQMS)
Line‑manage 2 QA direct reports and mentor up to 4 indirect reports
Identify training needs, coach staff, and promote a strong quality culture
Drive continuous improvement initiatives across QA processes and systems
What We're Looking For
Significant QA experience within a GMP‑regulated environment
Experience in a contract laboratory or service‑based organisation conducting GMP and non‑GMP activities
Demonstrable experience conducting internal and supplier audits
Proven track record supporting and hosting client and regulatory inspections
Strong working knowledge of EU GMP, FDA CFRs, Annex 11, and ICH Q8-Q10
Sound understanding of data integrity and CSV principles
Approachable, credible, and collaborative leadership style
Confident communicator with internal stakeholders, clients, and regulators
Practical, solution‑focused, and calm under inspection conditions
Desirable:
Experience implementing or enhancing electronic Quality Management Systems (eQMS)
QMS Lead Auditor qualification
Certified training within GxP
Reference: 225237742
https://jobs.careeraddict.com/post/113396845
Quality Manager
Posted on Jun 11, 2026 by CV-Library
Cwmbran, Gwent, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
Quality Manager - Cwmbran (Near Newport, South Wales)
A leading CRO is looking for a Quality Manager to join its Cwmbran team, taking ownership of day‑to‑day Quality Assurance operations and ensuring both GMP and non‑GMP activities meet the highest standards of compliance, integrity, and client commitment.
In this pivotal role, you'll provide hands‑on QA leadership across the full spectrum of quality system activities - from laboratory oversight and supplier audits to inspection readiness and documentation review. You'll be expected to apply pragmatic, risk‑based judgement suited to a dynamic contract laboratory environment where regulated and non‑regulated activities coexist.
As a senior quality practitioner and people manager, you'll guide operational teams, coach staff on GMP and non‑GMP expectations, and step in to deputise for the Head of Quality when required. This is a role for someone who thrives on responsibility, collaboration, and driving a culture of compliance and continuous improvement.
Key Responsibilities
Provide routine QA oversight of GMP and non‑GMP laboratory activities
Maintain and improve the Pharmaceutical Quality System (PQS), including deviations, CAPAs, change controls, and investigations
Arrange, host, and respond to client audits and regulatory inspections
Lead, perform, and report on internal audits in line with the site audit programme
Conduct supplier audits, oversee supplier qualification, and maintain the Approved Supplier List
Apply data integrity and CSV principles across GxP systems
Support or lead implementation of electronic Quality Management Systems (eQMS)
Line‑manage 2 QA direct reports and mentor up to 4 indirect reports
Identify training needs, coach staff, and promote a strong quality culture
Drive continuous improvement initiatives across QA processes and systems
What We're Looking For
Significant QA experience within a GMP‑regulated environment
Experience in a contract laboratory or service‑based organisation conducting GMP and non‑GMP activities
Demonstrable experience conducting internal and supplier audits
Proven track record supporting and hosting client and regulatory inspections
Strong working knowledge of EU GMP, FDA CFRs, Annex 11, and ICH Q8-Q10
Sound understanding of data integrity and CSV principles
Approachable, credible, and collaborative leadership style
Confident communicator with internal stakeholders, clients, and regulators
Practical, solution‑focused, and calm under inspection conditions
Desirable:
Experience implementing or enhancing electronic Quality Management Systems (eQMS)
QMS Lead Auditor qualification
Certified training within GxP
A leading CRO is looking for a Quality Manager to join its Cwmbran team, taking ownership of day‑to‑day Quality Assurance operations and ensuring both GMP and non‑GMP activities meet the highest standards of compliance, integrity, and client commitment.
In this pivotal role, you'll provide hands‑on QA leadership across the full spectrum of quality system activities - from laboratory oversight and supplier audits to inspection readiness and documentation review. You'll be expected to apply pragmatic, risk‑based judgement suited to a dynamic contract laboratory environment where regulated and non‑regulated activities coexist.
As a senior quality practitioner and people manager, you'll guide operational teams, coach staff on GMP and non‑GMP expectations, and step in to deputise for the Head of Quality when required. This is a role for someone who thrives on responsibility, collaboration, and driving a culture of compliance and continuous improvement.
Key Responsibilities
Provide routine QA oversight of GMP and non‑GMP laboratory activities
Maintain and improve the Pharmaceutical Quality System (PQS), including deviations, CAPAs, change controls, and investigations
Arrange, host, and respond to client audits and regulatory inspections
Lead, perform, and report on internal audits in line with the site audit programme
Conduct supplier audits, oversee supplier qualification, and maintain the Approved Supplier List
Apply data integrity and CSV principles across GxP systems
Support or lead implementation of electronic Quality Management Systems (eQMS)
Line‑manage 2 QA direct reports and mentor up to 4 indirect reports
Identify training needs, coach staff, and promote a strong quality culture
Drive continuous improvement initiatives across QA processes and systems
What We're Looking For
Significant QA experience within a GMP‑regulated environment
Experience in a contract laboratory or service‑based organisation conducting GMP and non‑GMP activities
Demonstrable experience conducting internal and supplier audits
Proven track record supporting and hosting client and regulatory inspections
Strong working knowledge of EU GMP, FDA CFRs, Annex 11, and ICH Q8-Q10
Sound understanding of data integrity and CSV principles
Approachable, credible, and collaborative leadership style
Confident communicator with internal stakeholders, clients, and regulators
Practical, solution‑focused, and calm under inspection conditions
Desirable:
Experience implementing or enhancing electronic Quality Management Systems (eQMS)
QMS Lead Auditor qualification
Certified training within GxP
Reference: 225237742
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