C&Q Engineer

Hyper Recruitment Solutions Ltd; Waterford; On-site; EUR 60,000 - 80,000; Full time

Job summary

Hyper Recruitment Solutions Ltd is seeking a Commissioning & Qualification (C&Q) Engineer for a leading Pharmaceutical company in County Waterford, Ireland, on an initial 12-month on-site contract. The role focuses on GMP-compliant commissioning, qualification, and validation activities for laboratory systems, utilities, and manufacturing equipment.

The successful candidate will develop and implement validation protocols, support CAPEX projects, and collaborate with cross-functional teams to

Qualifications

• Degree or higher in Engineering, Life Sciences, or related technical discipline.
• Proven experience on qualification activities within a GMP-regulated environment.
• Experience supporting CAPEX projects and lifecycle documentation.

Responsibilities

• Oversee and execute commissioning and qualification activities for manufacturing equipment, utilities, and laboratory systems to ensure GMP compliance.
• Develop, review, and execute validation protocols and reports for systems such as autoclaves, clean utilities, and production infrastructure.
• Support CAPEX projects by providing technical expertise during installation, commissioning, and qualification phases.

Skills

GMP knowledge

CAPEX projects experience

Validation protocols

Cross-functional collaboration

On-site execution

Education

Engineering or Life Sciences degree

Job description

We are looking for a Commissioning & Qualification (C&Q) Engineer to join a leading Pharmaceutical company in County Waterford on an initial 12 month contract. This is an opportunity to contribute to critical commissioning and qualification activities within a fast-paced GMP environment. The role is primarily on-site, offering a collaborative and dynamic environment for those looking to further their expertise in quality assurance, validation, and engineering. This position provides the chance to work on CAPEX projects involving laboratory systems, utilities, and manufacturing equipment.

KEY DUTIES AND RESPONSIBILITIES

• As the C&Q Engineer, you will oversee and execute commissioning and qualification activities for manufacturing equipment, utilities, and laboratory systems to ensure compliance with GMP standards.
• As the C&Q Engineer, you will develop, review, and execute validation protocols and reports for systems such as autoclaves, clean utilities (PW, WFI, steam, gases), and other production-related infrastructure.
• As the C&Q Engineer, you will support CAPEX projects by providing technical expertise during installation, commissioning, and qualification phases.
• As the C&Q Engineer, you will collaborate with cross-functional teams to ensure project milestones are met and documentation is compliant with regulatory requirements.
• As the C&Q Engineer, you will contribute to continuous improvement initiatives while maintaining the integrity of qualification lifecycle activities.

ROLE REQUIREMENTS

• A Degree or higher level in Engineering, Life Sciences, or a related technical discipline.
• Proven experience working on qualification activities within a GMP-regulated environment, specifically involving laboratory systems, utilities, or manufacturing equipment.
• Strong knowledge of GMP, qualification processes, and lifecycle activities, with experience supporting CAPEX projects.

Key Words: Commissioning / Qualification / GMP / Validation / CAPEX / Laboratory Systems / Utilities / Pharmaceutical / Biotech / Manufacturing Equipment / On-site / Regulated Environments / CQV / C&Q / Validation / Commissioning and Qualification / Commissioning and Qualification Validation / Engineering / Pharma / Pharmaceutical / Biopharma / Biologics / Biopharmaceutical / Biotechnology