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Validation supervisor

Wicklow
Mason Alexander
Supervisor
€60,000 - €80,000 a year
Posted: 21h ago
Offer description

I have an exciting opening for a ASL Stability/Validation Supervisor with a pharmaceutical company based in Wicklow. Reporting to the ASL Manager, the Stability/Validation Supervisor will be responsible for control of all Reports & Protocols, adherence to site plans, scheduling/release of all associated batches and control of Group Performance. Leading a Team & working in collaboration with other groups and departments, they will ensure that batches are tested in a timely manner to meet all related targets and deadlines.

Key Responsibilities:

* Oversee the Stability Program ensuring samples are entered/removed from Stability Cabinets and tested/approved within target windows.
* Oversee all Laboratory validation related activities relating to Process Validation, Analytical Method Validation and Cleaning Validation.
* Ensure adherence to Validation Site Master plan.
* Ensure all Validation/Stability protocols & reports are available in a timely manner to meet in-house and regulatory due dates.
* Process all Validation/Stability Regulatory requests.
* Process all DRF’s, LIR’s, OOS’s, CC’s etc in a timely manner so as to meet site targets.
* Attend all regulatory and customer audits as group representative, ensuring that the Group is audit ready at all times.
* Manage & control training within the Group.
* Schedule & Host all Group ‘Piloting’ meetings to facilitate performance and ensure all KPI targets are achieved.Carry out Daily capacity planning based on a standard work approach.
* Process all TMS and HR.net related activity for the Group.
* Continuously develop the Group as a Team and optimize resources in order to achieve targets.
* Responsible for Annual Yearly Development reviews for the Group (YDR)
* Review and update all relevant documentation as necessary, eg SOP’s, Methods/Specifications etc
* Attend Meetings with other departments (Planning, QA Validation etc) to assist in efficient planning to achieve site validation master plan & stability requirements.
* Act as SME for Stability/Validation during Audit Visits, Laboratory Tours etc

Position Requirements

Essential:

* Degree in Chemistry/Analytical Science/ Pharmaceutical Science or Forensic Science
* Strong IT skills
* Strong attention to detail
* Demonstrate strong use of initiative/self-motivation and a disciplined approach
* Good communication skills
* Strong positive attitude is essential for this position.
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