Senior Project Engineer - GMP & Capital Projects Lead

CSL

Liverpool

On-site

GBP 70,000 - 110,000

Full time

14 days+

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Job summary

CSL Seqirus is seeking a Senior Project Engineer to lead capital GMP projects at the LVP site, focusing on scoping, delivery and cost control in line with cGMP, EHS and business continuity standards. You will head cross‑functional teams across GMP disciplines, oversee commissioning and qualification, and ensure training, drawings and documentation are provided for validation and operation.

The role requires an MSc/BSc in Engineering and 5+ years in the pharmaceutical industry with strong project

Qualifications

  • MSc/BSc/BA in Engineering preferred or local equivalent.
  • 5+ years practical and leadership experience in pharmaceutical industry.
  • Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility Pharmaceutical/biotech industry experience preferred
  • Understanding of project management principles and project lifecycle phases
  • Knowledge of Validation, and facility regulatory submission requirements

Responsibilities

  • Create accurate and timely proposals for investment projects to ensure submission for approval in line with the capital expenditure plan.
  • Budget and schedule responsibility for approved multi-disciplinary GMP projects, including cashflow forecasting and tracking.
  • Manage commissioning, qualification and handover processes with QA, production management and maintenance, ensuring training, drawings and documentation are provided for validation, operation and maintenance.
  • Ensure GMP, housekeeping, safety and discipline standards are maintained within the department and operational areas.

Skills

Project leadership
Project management
GMP knowledge
Validation knowledge
Cross-functional collaboration

Education

Engineering degree

Job description

CSL Seqirus is seeking a Senior Project Engineer to lead capital GMP projects at the LVP site, focusing on scoping, delivery and cost control in line with cGMP, EHS and business continuity standards. You will head cross‑functional teams across GMP disciplines, oversee commissioning and qualification, and ensure training, drawings and documentation are provided for validation and operation.

The role requires an MSc/BSc in Engineering and 5+ years in the pharmaceutical industry with strong project

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