Laboratory Supervisor - Waterford

Company: Confidential
Your Application: You have not applied yet
Location: Waterford, Irlanda
JOB DESCRIPTION

?This is a fantastic opportunity to join one of the most coveted employers in the South East as they undergo further expansion. In this full time permanent role as a Laboratory Supervisor you will bring your considerable Chemistry experience and your previous management experience to bear in a collegiate and collaborative work environment.
Working in a diverse, dynamic site you will coordinate the day to day running of a state of the art laboratory and also drive towards operational excellence along with the rest of the QC Management team.
Ideally you will bring a broad background in analytical chemistry along with at least 3 years of experience at supervisory level or above. Previous strong supervisory or management experience is a requirement for this role.
Duties and Responsibilities:

Supporting the Laboratory Manager in generating and executing on Instrument Qualification protocols or test method transfer protocols, generating standard Operating Instructions or implementing workflows.

Supervising a group of Analysts, with the goal of performing all analytical testing that is required to support plant operations. This includes batch release testing as well as testing of incoming materials

Analytical testing will cover wet chemical analysis, modern spectroscopic and chromatographic methods as well as functional testing.

Implementing processes and procedures to ensure on-time delivery of testing in compliance with
cGMP, the relevant Regulatory Guidelines/Industry Standards and the relevant local and global Safety Guidelines.

Guiding customer audits in the analytical laboratory area.

Investigating OOS/OOT results and implementing CAPAs related to analytical testing.

Executing/supporting qualification/validation activities within the laboratory, production clean rooms or water systems, e.g. cleaning validations.

Supporting other functions (e.g. R&D, TCS, process engineering) as a Subject Matter Expert

Contributing to the harmonization of test methods, equipment, infrastructure, etc. based on the strategy of the global laboratory organization.

Developing/implementing new test methods in alignment with global laboratory strategy.

Approval of Documents in the Laboratory Supervisor's (Micro/Particle) absence:
SOIs, ESOPs, EWIs, Attachments, Protocols, Reports, Strategy documents, Risk Assessments, OOS investigations, Deviations.

Compliance to all site Environmental, Health and Safety requirements, training and regulations.
About You:

5+ year experience is a similar role (analytical testing) within the pharmaceutical / medical devices / manufacturing industry.

Experience in a cGMP environment.

Strong competence in IT

Excellent interpersonal skills with the ability to work with all levels within the organisation.

Team player.

Structured way of working & strong Organisational skills
For more on the role call Nigel on 087 3618142 or send your CV for consideration.



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