Job Description
Our client, an established consulting organization who provides focused support in Pharmaceutical, Biotechnology and Medical Devices industries, now seeks QA Lab Validation Specialist. This client is flexible to hire full-time permanent (with benefits) employees and/or contractor staff in the greater Dublin / north Leinster areas.
The successful candidates will work within an existing integrated project team who are responsible for the qualification of new instrumentation within the Quality Control Labs.
This hire will be responsible for generate and execute documentation for cGLP/cGMP validation of systems, laboratory equipment, including validation plans, protocols and reports.
Excellent opportunities exist for professionals at all levels with the right blend of skills and experience in: laboratory, systems, process and/or technology cGLP/cGMP industries.
This role will suit experienced pharma / biotech professionals who are highly motivated with a clear desire for career development and progression.
Requirements for QA Lab Validation Specialist:
B.Sc. degree qualifications in science, engineering, quality, technical or other related life sciences or engineering discipline.
3+ year validation or qualification experience with laboratory instrumentation, validation and project life cycle, ideally with pharma/biopharma FDA regulated environment.
Proven experience in updating documentation and reports.
Good working knowledge of IT systems and their interactions with laboratory instrumentation would be considered an advantage but not essential.
Excellent communication skills and the ability to be analytical.
For further details, contact Larry on +353 1-2302400 / larry@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. www.rftgroup.ie
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