An exciting opportunity to join a growing site in Tipperary. This is a contract role with an immediate start. HPLC experience is required. Job Duties. • Supports Laboratory Set-up activities. • Prepares Laboratory procedures, specifications, protocols & reports as required. • Performs Laboratory testing and investigations per SOP, applicable regulations and cGMP. • Performs peer review of documentation as required. • Performs Analytical method verification, validation and technical transfer as required. • Supports Laboratory/Site EHS governance. • Performs management of Laboratory consumables ordering and tracking. • Assists in Equipment Qualification activities, ordering and tracking as required. • Supports preparation for regulatory audits/visits ad ongoing audit readiness. • Supports development of QC Testing processes. • Liaises with Contract Research Organisations and audits where appropriate. • Ensure all required training has been carried out to ensure that procedures are followed and meet all quality requirements. • Follow documented policies and procedures as designated by the company’s Quality Management System. • Complete required documentation relating to business and regulatory requirements and as per Good Documentation Practice procedures. Qualifications/Experience: • Degree in Chemistry or equivalent. • 3 years+ experience within the pharmaceutical industry in a similar role in a QC laboratory. • Experience of working in an FDA/HPRA regulated site. Skills: • Ability to work well with others in a team environment. • Excellent communication and problem solving skills. • Good Organisational skills. For more on the role call Nigel on 021 4221000 or send your CV for consideration. This job originally appeared on RecruitIreland.com.
7 days ago