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Nexus Life Sciences

QC Validation & Systems Lead

Cheshire West And Chester
£42k – £48k/yr
Posted 1 day ago
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QC Validation & Systems Lead – Pharmaceutical / GMP Laboratory

📍 North West | 💷 £42,000–£48,000 | 🧪 Permanent -100% site based

Are you an experienced QC professional with a passion for equipment validation, data integrity and keeping GMP labs inspection‑ready? One of our long‑standing pharmaceutical partners is expanding and now seeking a QC Validation & Systems Lead to take ownership of QC systems, equipment lifecycles and computerized platforms across a busy GMP environment.

This is a hands‑on, senior role with real influence — perfect for someone who thrives on improving systems, leading validation strategy, and ensuring compliance excellence.

What You’ll Be Doing

  • Leading the full lifecycle of QC laboratory equipment, especially HPLC systems — from procurement and qualification through to maintenance, change control and retirement.
  • Managing and executing validation activities (IQ/OQ/PQ) and overseeing site calibration programmes, including external service providers.
  • Acting as system owner for key QC platforms (e.g., Empower, LabX), driving CSV, data integrity and regulatory compliance.
  • Maintaining QC equipment and validation status within electronic systems such as LIMS, ensuring audit readiness at all times.
  • Authoring and approving validation documentation, leading deviation investigations, impact assessments and CAPAs.
  • Providing technical leadership and line management to a small QC systems team, and representing QC during internal and external audits.

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The ideal candidate will have:

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  • Degree (BSc or equivalent) in Chemistry or a related scientific discipline.
  • Strong experience using HPLC, including troubleshooting and maintenance, in a GMP‑regulated QC laboratory.
  • Team Leadership or supervisory experience.
  • Proven background in equipment qualification, validation, calibration and troubleshooting.
  • Hands‑on experience with QC computerized systems (Empower, LabX or CDS systems) and solid understanding of CSV and Data Integrity principles.
  • Confident communicator with experience supporting audits; previous supervisory experience is beneficial.

❗ Please note: Sponsorship is not available for this role.

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Skills

Equipment Validation
Data Integrity
GMP Compliance
HPLC
IQ/OQ/PQ
CSV
Empower
LabX
LIMS
Calibration
Change Control
CAPA
Team Leadership
Audit Support
Deviation Investigations
Impact Assessments

Location

Cheshire West and Chester, England, United Kingdom

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