Commissioning & Qualification Engineer
|Contact Name:||Larry O’Leary|
Our client, a third party contractor, now seeks commissioning & qualification engineer for a technical support role. This role will focus on representing the user group in walkdowns, functional testing, OQ and PQ executions
The successful candidate will be responsible for generate and execute documentation for cGMP validation of systems, equipment & manufacturing processes, including validation plans, protocols and reports.
Opportunities exist for full-time permanent and contract employees in Dublin.
Responsibilities of Commissioning & Qualification Engineer:
Generate and execute documentation for cGMP commissioning & qualification of systems, equipment & manufacturing processes, including validation plans, protocols and reports.
Participate in commissioning & qualification teams involved in specific projects outside this scope such as process validation.
Provide technical and compliance review of contract generated testing protocols and reports.
Co-ordinate activities of teams for specific projects, as necessary.
Operate according to SOPs developed for validated manufacturing operations and cGMP compliance.
Requirements for Commissioning & Qualification Engineer:
B.Sc. degree in life sciences or engineering discipline.
3+ year commissioning & qualification experience in GMP environment.
Ideally experienced with pharmaceutical FDA regulations.
Excellent communication skills and experienced in updating documentation and reports.
Please contact Larry on 01-2302400 / firstname.lastname@example.org / www.rftgroup.ie
The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors.