Senior Process C&Q Engineer

Dillon Engineering Services; Munster; On-site; EUR 110,000 - 138,000; Full time

Job summary

Dillon Engineering Services is seeking an experienced Senior Process C&Q Engineer / CQV API Project Lead for a contract in Tipperary, Ireland. The role focuses on commissioning and qualification of API process equipment and utilities, from construction handover through start‑up and final handover.

The ideal candidate will have extensive C&Q experience in pharma/API environments, with hands‑on knowledge of Filter Dryers and ANFDs, and a strong track record supporting GMP/QA requirements.

Qualifications

• Minimum 10 years' experience in Commissioning & Qualification (C&Q/CQV).
• Experience with API process equipment and pharmaceutical utilities.
• Experience leading C&Q activities on large pharmaceutical projects.
• Knowledge of GMP, GEP and regulatory requirements.

Responsibilities

• Prepare, review and execute commissioning and qualification documentation for API equipment and utilities.
• Develop and execute IOC/IOQ protocols and installation verification.
• Lead field walkdowns, start‑up, and qualification activities.
• Coordinate contractors and vendors for commissioning tasks.
• Ensure safety, compliance and smooth project handover.
• Provide technical guidance to C&Q personnel.

Skills

C&Q experience

API equipment

Project leadership

GMP/GEP knowledge

Document control

Troubleshooting

Communication skills

Education

Engineering or science degree

Job description

Hourly Rate: €80–€100 per hour (depending on experience)

Industry: Pharmaceutical / API Manufacturing

Job Overview

Dillon Engineering Services is currently seeking an experienced Senior Process C&Q Engineer / CQV API Project Lead for a contract opportunity supporting a major pharmaceutical API manufacturing project in Tipperary.

The successful candidate will be responsible for the commissioning and qualification of API process equipment and associated utility systems, supporting activities from construction handover through system start-up, qualification and final handover.

This is a hands‑on technical role requiring extensive C&Q experience within pharmaceutical or API manufacturing environments. Previous experience with Filter Dryers and/or pharmaceutical utilities would be a distinct advantage.

Key Responsibilities

• Prepare, review and execute commissioning and qualification documentation for API process equipment and associated utility systems.
• Develop and execute electronic commissioning and qualification protocols, including IOC and IOQ.
• Perform field walkdowns, installation verification and system inspections to support construction handover.
• Coordinate and support system start‑up, functional testing, commissioning and qualification activities.
• Ensure the safe operation of equipment and systems throughout commissioning, start‑up and qualification phases.
• Support C&Q activities for API process equipment, including filtration, drying and associated process systems.
• Manage change control activities throughout the project lifecycle.
• Prepare C&Q summary reports and associated technical documentation.
• Plan, organise and track daily commissioning and qualification activities to ensure project milestones are achieved.
• Coordinate contractors, equipment vendors and other technical personnel.
• Troubleshoot technical issues arising during commissioning and qualification.
• Liaise with Construction, Engineering, Automation, Quality, Validation and End User teams throughout the project lifecycle.
• Ensure all activities comply with GMP, Good Engineering Practice (GEP), site procedures and relevant safety requirements.
• Provide technical guidance and support to other C&Q personnel as required.

Qualifications & Experience

• Degree in Engineering, Science or a related discipline, or equivalent technical qualification supported by relevant industry experience.
• Minimum of 10 years' experience in Commissioning & Qualification (C&Q/CQV) within pharmaceutical, biotechnology or API manufacturing environments.
• Proven hands‑on C&Q experience on large‑scale pharmaceutical projects.
• Strong technical knowledge of API process equipment, pharmaceutical utilities and/or facilities systems.
• Experience preparing and executing commissioning and qualification protocols, including IOC, IOQ and installation verification.
• Experience with equipment walkdowns, system start‑up, functional testing and construction handover.
• Good understanding of GMP, GEP and relevant pharmaceutical regulatory requirements.
• Strong troubleshooting, technical documentation and problem‑solving skills.
• Ability to work independently, manage assigned activities and coordinate effectively with multidisciplinary project teams.
• Excellent communication, organisational and interpersonal skills.
• Hands‑on commissioning and qualification experience with Filter Dryers, particularly Agitated Nutsche Filter Dryers (ANFDs).
• Experience with API manufacturing equipment, including reactors, centrifuges, filtration systems, dryers and process vessels.
• Experience commissioning and qualifying pharmaceutical clean and/or black utility systems.
• Familiarity with electronic C&Q documentation and execution systems.
• Previous experience in a Senior C&Q Engineer or technical lead capacity.

For more information, please contact Jessica on 094 931 6003 or [e-mail].

Note: Only candidates who are legally authorised to work in Ireland will be considered for this role.