CQV Engineer - Process Development (Travel Required)

Cpl Group; Ireland; Remote; EUR 50,000 - 70,000; Full time

Benefits offered by this job

Extensive travel opportunities

Ongoing technical development

Long-term career progression

Job summary

CPL Group is recruiting for a C&Q (Process Development) Engineer to support pharmaceutical and biopharmaceutical projects across Ireland, the UK and Europe. The role focuses on process development, thermal mapping, equipment qualification and validation within GMP-regulated manufacturing environments.

You will work with customers and technical teams to optimise critical process systems, including sterilisation and washing equipment, while advancing projects and contributing to technical reports

Qualifications

• Degree or equivalent qualification in Engineering, Validation, Science or related technical discipline.
• Experience within pharmaceutical or biopharmaceutical environments.
• Understanding of equipment qualification and validation activities.
• Strong technical writing and report writing skills.
• Ability to interpret technical documentation, drawings and specifications.
• Experience working within GMP environments.
• Strong analytical and problem-solving skills.
• Excellent communication and customer-facing abilities.
• Ability to work independently and manage multiple priorities.
• Full driving licence.
• Willingness to travel extensively and spend extended periods on customer sites.

Responsibilities

• Perform thermal mapping and process development activities.
• Support commissioning, qualification and validation projects.
• Execute cycle development and performance qualification studies.
• Support autoclave, washer and process equipment qualification activities.
• Analyse validation data and produce technical reports.
• Troubleshoot process performance issues and implement improvements.
• Execute validation protocols and prepare qualification documentation.
• Perform thermocouple calibration and verification activities.
• Support equipment qualification lifecycle activities.
• Liaise with clients, suppliers and internal technical specialists.
• Participate in customer meetings and technical presentations.
• Ensure work is completed in line with GMP requirements and quality standards.
• Support wider commissioning and qualification activities where required.

Skills

Process development

Technical writing

GMP environments

Analytical skills

Customer-facing

Independent worker

Travel readiness

Education

Engineering degree

Tools

E-Val Pro

Job description

CPL Group is recruiting for a C&Q (Process Development) Engineer to support pharmaceutical and biopharmaceutical projects across Ireland, the UK and Europe. The role focuses on process development, thermal mapping, equipment qualification and validation within GMP-regulated manufacturing environments.

You will work with customers and technical teams to optimise critical process systems, including sterilisation and washing equipment, while advancing projects and contributing to technical reports