The role
PE Global is currently recruiting for a QC Lab Support Supervisor on behalf of a leading pharmaceutical company based in Sligo.
This is an initial 9-month contract role.
Job Summary
To provide an effective testing and analytical service to the plant ensuring that products manufactured are tested to specification on time and plant quality and safety goals are met.
Ensure that all raw materials, in-process, finished product testing is carried out per schedule, and records are maintained to appropriate requirements.
Ensure that technical and systems excellence is maintained in the laboratory by ensuring own skills are maintained, by coaching and training analysts to ensure right first-time behaviour and by implementing improved working practices in terms of efficiency, compliance and Right First Time.
This position will take full responsibility for Compliance, Documentation, Equipment troubleshooting, Planning and Scheduling, LIMS and LES updates and System Training as required within the QC Lab.
Other responsibilities may be assigned as required.
Responsibilities
Ensure Laboratory Documentation and Computerized Systems compliance with Data Integrity policies and regulatory requirements.
Understand Regulations and business processes required to maintain Laboratory Data Integrity.
Ensure that analysts working in the assigned team are performing to the best of their ability, coaching and providing guidance where issues occur such as poor set-up or test execution performance.
Improve the overall efficiency and velocity within the assigned team.
Ensure that the agreed schedule timelines, and identify recovery paths when required, to bring test schedules back into alignment with plant requirements.
Identify weaknesses in laboratory performance and work with the laboratory manager to rectify.
Act as designee for the Laboratory Supervisor as assigned.
Instill a quality culture of Zero, Believe it, Achieve it amongst the QC laboratory team.
Execute and/or support projects as assigned by the laboratory manager.
Develop and change in-house laboratory procedures as appropriate.
Complete project work.
Adhere to and support all EHS standards, procedures, and policies.
Develop and review training material.
Supervision Received
Operate in an environment which is essentially self-managed but with supervision through the Laboratory Manager.
Liaise with Laboratory supervisors and Laboratory manager to meet department timelines.
Education and Experience
3rd level qualification in a relevant Science discipline.
Minimum 4 years analytical experience in the pharmaceutical industry.
Proven track record in an analytical role.
Must be expert in HPLC and GC.
Strong knowledge of regulatory requirements.
Proficient in using analytical equipment in the QC lab.
Interested candidates should submit an updated CV.
Please click the link below to apply, call Kellie on ********** or alternatively send an up-to-date CV to ******.
Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland.
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