QC Project Lead: Lab Systems & GMP Innovation

Blackfield Associates

England

On-site

GBP 65,000 - 90,000

Full time

14 days+

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Job summary

Blackfield Associates is recruiting a QC Technical Project Manager for a leading pharmaceutical manufacturing organisation. You will lead technical projects in the QC laboratory, manage laboratory systems (LIMS and CDS) and drive compliance with GMP and Data Integrity standards.

You will oversee a team of QC specialists, coordinate equipment lifecycle plans and qualification/validation activities, and collaborate with IT, vendors and cross-functional teams to ensure compliant, high‑quality

Qualifications

  • Degree in a scientific discipline or equivalent industry experience.
  • Strong knowledge of pharmaceutical QC equipment and laboratory systems.
  • Experience with qualification and validation activities.
  • Experience managing QC equipment and electronic systems in regulated environments.
  • Proficiency with LIMS and CDS platforms.
  • Good understanding of GMP and Data Integrity principles.
  • Proven ability to lead technical projects to timelines.
  • Strong communication and stakeholder management skills.

Responsibilities

  • Lead and develop a team of QC Technical Specialists.
  • Oversee laboratory equipment and electronic systems compliance.
  • Deliver projects involving procurement, qualification, validation, and implementation.
  • Maintain long-term equipment replacement strategies.
  • Lead new product introductions, method transfer and compliance activities.
  • Oversee change controls, deviations, and validation activities for lab systems.

Skills

Quality Control
Project Management
Stakeholder management
Analytical methods
LIMS experience
CDS experience
GMP compliance
Leadership

Education

Degree in a scientific discipline

Tools

LIMS
CDS

Job description

Blackfield Associates is recruiting a QC Technical Project Manager for a leading pharmaceutical manufacturing organisation. You will lead technical projects in the QC laboratory, manage laboratory systems (LIMS and CDS) and drive compliance with GMP and Data Integrity standards.

You will oversee a team of QC specialists, coordinate equipment lifecycle plans and qualification/validation activities, and collaborate with IT, vendors and cross-functional teams to ensure compliant, high‑quality

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