Working on behalf of a client in Cork, Headcount Solutions is seeking
a Validation Engineer for a biotech facility. Reporting to the CQ&V
Team Lead, this person will provide thermal mapping validation support
to a number of activities across the site.
Responsibilities:
* Preparation and review of Qualification protocols (IQ, OQ, PQ)
* Preparation and review of Requalification protocols.
* Execution of thermal mapping activities, including Controlled
Temperature Units, Autoclaves, Depyrogenation Ovens.
* Analyses the results of testing and determines the acceptability of
results against predetermined criteria.
* Investigates and troubleshoots problems which occur and determines
solutions or recommendations for changes and/or improvements.
Requirements:
* Degree in an Engineering or other relevant discipline.
* Minimum 2 years&#**Apply on the website**; experience in a similar
role.
* Experience in a GMP environment is essential.
* Use and operation of Kaye Validator **Apply on the website** data
logger (or equivalent) is an advantage.
* Demonstrated knowledge in pharmaceutical / biopharmaceutical
technical / manufacturing operations, with experience of successfully
delivering technical projects.
* Knowledge of Regulations and applicable standards for Quality,
Safety, Regulatory.
To express an interest in this position, please forward details to or,
alternatively, please contact Mick on (phone number removed) Validation Engineer - Thermal Mapping
Working on behalf of a client in Cork, Headcount Solutions is seeking
a Validation Engineer for a biotech facility. Reporting to the CQ&V
Team Lead, this person will provide thermal mapping validation support
to a number of activities across the site.
Responsibilities:
* Preparation and review of Qualification protocols (IQ, OQ, PQ)
* Preparation and review of Requalification protocols.
* Execution of thermal mapping activities, including Controlled
Temperature Units, Autoclaves, Depyrogenation Ovens.
* Analyses the results of testing and determines the acceptability of
results against predetermined criteria.
* Investigates and troubleshoots problems which occur and determines
solutions or recommendations for changes and/or improvements.
Requirements:
* Degree in an Engineering or other relevant discipline.
* Minimum 2 years&#**Apply on the website**; experience in a similar
role.
* Experience in a GMP environment is essential.
* Use and operation of Kaye Validator **Apply on the website** data
logger (or equivalent) is an advantage.
* Demonstrated knowledge in pharmaceutical / biopharmaceutical
technical / manufacturing operations, with experience of successfully
delivering technical projects.
* Knowledge of Regulations and applicable standards for Quality,
Safety, Regulatory.
To express an interest in this position, please forward details to or,
alternatively, please contact Mick on (phone number removed)
We need : English (Good)
Type: Permanent
Payment:
Category: Others
