Senior Commissioning and Qualification Engineer

Job Title: Senior Commissioning and Qualification Engineer
Contract Type: Permanent
Location: Dublin
REF: 123641
Contact Name: Larry O’Leary
Contact Email:
Job Published: almost 3 years ago

Job Description

Senior Commissioning and Qualification Engineer
Our client, an established consulting organization who provides focused support in Pharmaceutical, Biotechnology and Medical Devices industries, now seeks Senior Commissioning and Qualification Engineers for Process and Automation related lifecycle projects in FDA regulated industry.

The successful candidates will work within an existing project teams who are responsible for a wide range of projects, hence experience in general process/building services commissioning/ qualification is highly desirable.

This hire will be responsible for leading the generation and execution of documentation for cGMP validation of systems, equipment & manufacturing processes, including validation plans, protocols and reports.

This role will suit experienced pharma / biotech professionals with strong knowledge of processing equipment and utility systems gained within pharmaceutical sector, who are highly motivated with a clear desire for career development and progression.

Excellent opportunities currently exist for professionals at all levels with the right blend of skills and experience in process and technology related regulated industries.

These opportunities exist for full-time permanent (with benefits) employees and contractor staff to contribute to a wide variety of diverse projects located throughout Ireland and UK if desirable.

Please note: there a number of large projects located in greater Dublin area.

Requirements for Senior Commissioning and Qualification Engineer:
B.Sc. degree qualifications in science, engineering, quality, technical or other related life sciences / engineering discipline.
5+ year commissioning, qualification, validation and/or project life cycle experience, ideally with pharma/biopharma FDA regulated environment.
Proven experience in providing technical advice, in preparation and execution of associated Commissioning and Qualification lifecycle documentation.
Experienced in completion and delivery of documentation and reports to required regulatory standards.
Excellent communication skills and the ability to be analytical.

Please contact Larry on 01-2302400 /

The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors.