PE Global is currently recruiting for an Analytical Analyst for a leading multi-national Pharma client based in Sligo.
This is a contract position.
RESPONSIBILITIES
Ensuring Analytical Laboratory Documentation and Computerized Systems compliance with Data Integrity policies and regulatory requirements.
Understanding Regulations and business processes required to maintain Laboratory Data Integrity.
Ensuring timely completion of all laboratory analysis assigned to shift.
Ensuring that analysts working in the assigned cell or 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.
Improving the overall efficiency and velocity within the assigned team.
Identifying and implementing improvements in analytical practices using ‘Zero, Believe it, Achieve it’
Ensuring that the agreed test schedule is adhered to and identifying recovery paths to bring test schedules back into alignment with plant requirements.
Identifying weaknesses in laboratory performance and working with the laboratory management to rectify.
Supporting & initiating analytical OOS issues as they arise in a timely manner both through practical work and through the quality system.
Ensuring 5S excellence is maintained across the Laboratory.
Instilling a quality culture of Zero, Believe it, Achieve it amongst the laboratory team
Ensuring that all laboratory test equipment is utilised and maintained correctly.
Maintaining up-to-date, complete and precise records of all tests performed.
Investigates Documentation related events in production that have quality or compliance impact.
Leads or participates IIA, RCI sessions.
Documents investigation outcomes.
Frequently interacts with functional peer groups. Interaction normally requires the ability to gain cooperation of others, conducting presentations of technical information concerning specific projects, schedules, etc.
Comply with policies and procedures, Standards and Specifications, Plant procedures, and regulatory agencies regulations and requirements.
REQUIREMENTS
Bachelor’s Degree or equivalent preferential, preferably in a Science or related field
Experience Level = 1+ Years
Experience within a GLP/GMP environment and knowledge of current EU/FDA/ICH/HPRA guidelines
Proven track record in an analytical role.
Proficient in using analytical equipment in a QC lab as well as troubleshooting.
Knowledgeable in instrumentation such as UHPLC, SoloVPE, TOC, and Identification techniques.
Experience in industry is essential.
Interested candidates should submit an updated CV.
Please click the link below to apply, or alternatively send an up to date CV to niamh.mcdonald@peglobal.net
***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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