

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
Your duties as the C&Q Engineer will be varied however the key duties and responsibilities are as follows:
- 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
To be successful in your application to this exciting role as the C&Q Engineer we are looking to identify the following on your profile and past history:
- 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
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career"
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.


