QC Validation & Systems Lead
Posted on Jun 16, 2026 by CV-Library
Cheshire West and Chester, Cheshire, United Kingdom
Pharmaceutical
Immediate Start
£40k - £50k Annual
Full-Time
QC Validation & Systems Lead
Cheshire
£40,000 – £50,000
Pharmaceutical / GMP Laboratory
The Role
We are seeking an experienced QC Validation & Systems Lead to take ownership of QC laboratory equipment lifecycles and computerized systems within a GMP-regulated environment.
This senior, hands-on role blends equipment validation, CSV, data integrity, and team leadership, ensuring QC operations remain compliant, efficient and inspection-ready at all times.
Key Responsibilities
* Own the full lifecycle of QC laboratory equipment, including procurement, qualification, maintenance, change control, and retirement
* Lead equipment validation activities (IQ/OQ/PQ) and manage site calibration programmes, including oversight of external service providers
* Manage QC equipment and validation status using electronic systems (e.g. LIMS), ensuring GMP compliance and inspection readiness
* Lead Computer System Validation (CSV) and administration for QC systems such as Empower and LabX, ensuring data integrity and regulatory compliance
* Author and approve validation and GMP documentation, and lead deviation investigations, impact assessments, and CAPA related to equipment and systems
* Provide technical leadership and line management to a small QC systems team and act as SME during internal and regulatory audits
The QC Validation Lead must have:
* Degree (BSc or equivalent) in Chemistry or a relevant scientific discipline, with essential HPLC experience in a pharmaceutical or GMP-regulated laboratory
* Strong working knowledge of GMP, Health & Safety and COSHH requirements
* Proven experience in laboratory equipment qualification, validation, calibration, and troubleshooting especially for HPLC systems
* Hands-on experience with QC computerized systems (e.g. Empower, LabX), including CSV and a solid understanding of Data Integrity principles
* Confidence representing QC during audits and inspections, with previous supervisory or team leadership experience preferred
Please note: my client is unable to offer sponsorship on this role
Cheshire
£40,000 – £50,000
Pharmaceutical / GMP Laboratory
The Role
We are seeking an experienced QC Validation & Systems Lead to take ownership of QC laboratory equipment lifecycles and computerized systems within a GMP-regulated environment.
This senior, hands-on role blends equipment validation, CSV, data integrity, and team leadership, ensuring QC operations remain compliant, efficient and inspection-ready at all times.
Key Responsibilities
* Own the full lifecycle of QC laboratory equipment, including procurement, qualification, maintenance, change control, and retirement
* Lead equipment validation activities (IQ/OQ/PQ) and manage site calibration programmes, including oversight of external service providers
* Manage QC equipment and validation status using electronic systems (e.g. LIMS), ensuring GMP compliance and inspection readiness
* Lead Computer System Validation (CSV) and administration for QC systems such as Empower and LabX, ensuring data integrity and regulatory compliance
* Author and approve validation and GMP documentation, and lead deviation investigations, impact assessments, and CAPA related to equipment and systems
* Provide technical leadership and line management to a small QC systems team and act as SME during internal and regulatory audits
The QC Validation Lead must have:
* Degree (BSc or equivalent) in Chemistry or a relevant scientific discipline, with essential HPLC experience in a pharmaceutical or GMP-regulated laboratory
* Strong working knowledge of GMP, Health & Safety and COSHH requirements
* Proven experience in laboratory equipment qualification, validation, calibration, and troubleshooting especially for HPLC systems
* Hands-on experience with QC computerized systems (e.g. Empower, LabX), including CSV and a solid understanding of Data Integrity principles
* Confidence representing QC during audits and inspections, with previous supervisory or team leadership experience preferred
Please note: my client is unable to offer sponsorship on this role
Reference: 224720657
https://jobs.careeraddict.com/post/113418034
QC Validation & Systems Lead
Posted on Jun 16, 2026 by CV-Library
Cheshire West and Chester, Cheshire, United Kingdom
Pharmaceutical
Immediate Start
£40k - £50k Annual
Full-Time
QC Validation & Systems Lead
Cheshire
£40,000 – £50,000
Pharmaceutical / GMP Laboratory
The Role
We are seeking an experienced QC Validation & Systems Lead to take ownership of QC laboratory equipment lifecycles and computerized systems within a GMP-regulated environment.
This senior, hands-on role blends equipment validation, CSV, data integrity, and team leadership, ensuring QC operations remain compliant, efficient and inspection-ready at all times.
Key Responsibilities
* Own the full lifecycle of QC laboratory equipment, including procurement, qualification, maintenance, change control, and retirement
* Lead equipment validation activities (IQ/OQ/PQ) and manage site calibration programmes, including oversight of external service providers
* Manage QC equipment and validation status using electronic systems (e.g. LIMS), ensuring GMP compliance and inspection readiness
* Lead Computer System Validation (CSV) and administration for QC systems such as Empower and LabX, ensuring data integrity and regulatory compliance
* Author and approve validation and GMP documentation, and lead deviation investigations, impact assessments, and CAPA related to equipment and systems
* Provide technical leadership and line management to a small QC systems team and act as SME during internal and regulatory audits
The QC Validation Lead must have:
* Degree (BSc or equivalent) in Chemistry or a relevant scientific discipline, with essential HPLC experience in a pharmaceutical or GMP-regulated laboratory
* Strong working knowledge of GMP, Health & Safety and COSHH requirements
* Proven experience in laboratory equipment qualification, validation, calibration, and troubleshooting especially for HPLC systems
* Hands-on experience with QC computerized systems (e.g. Empower, LabX), including CSV and a solid understanding of Data Integrity principles
* Confidence representing QC during audits and inspections, with previous supervisory or team leadership experience preferred
Please note: my client is unable to offer sponsorship on this role
Cheshire
£40,000 – £50,000
Pharmaceutical / GMP Laboratory
The Role
We are seeking an experienced QC Validation & Systems Lead to take ownership of QC laboratory equipment lifecycles and computerized systems within a GMP-regulated environment.
This senior, hands-on role blends equipment validation, CSV, data integrity, and team leadership, ensuring QC operations remain compliant, efficient and inspection-ready at all times.
Key Responsibilities
* Own the full lifecycle of QC laboratory equipment, including procurement, qualification, maintenance, change control, and retirement
* Lead equipment validation activities (IQ/OQ/PQ) and manage site calibration programmes, including oversight of external service providers
* Manage QC equipment and validation status using electronic systems (e.g. LIMS), ensuring GMP compliance and inspection readiness
* Lead Computer System Validation (CSV) and administration for QC systems such as Empower and LabX, ensuring data integrity and regulatory compliance
* Author and approve validation and GMP documentation, and lead deviation investigations, impact assessments, and CAPA related to equipment and systems
* Provide technical leadership and line management to a small QC systems team and act as SME during internal and regulatory audits
The QC Validation Lead must have:
* Degree (BSc or equivalent) in Chemistry or a relevant scientific discipline, with essential HPLC experience in a pharmaceutical or GMP-regulated laboratory
* Strong working knowledge of GMP, Health & Safety and COSHH requirements
* Proven experience in laboratory equipment qualification, validation, calibration, and troubleshooting especially for HPLC systems
* Hands-on experience with QC computerized systems (e.g. Empower, LabX), including CSV and a solid understanding of Data Integrity principles
* Confidence representing QC during audits and inspections, with previous supervisory or team leadership experience preferred
Please note: my client is unable to offer sponsorship on this role
Reference: 224720657
Share this job:
Alert me to jobs like this:
Amplify your job search:
Expert career advice
Increase interview chances with our downloads and specialist services.
Visit Blog