Shift Leader

Pe Global

Sligo

Currently assisting our client in recruiting and Shift leader in County Sligo. This role is a permanent position that will lead and facilitate the safe operations of the API manufacturing team in a pharmaceutical processing facility in line with all safety, regulatory and operational requirements. The Role: Supervision and execution of pharmaceutical processing activities in the API building and support locations, to meet clearly stated operating objectives. Daily reporting on the status of all operations and support activities. Team leadership, motivation and direction to maximise the effectiveness of their manufacturing team. Responsible for verification and update of manufacturing control system transactions accurately and in a timely fashion. Act as key point of technical contact for API Business Unit. Shift technicians report directly to this role. Communicate the departmental goals, to provide cost effective products as part of the AbbVie Class A supply chain system. Responsible for driving operation excellence and Key operations targets including OEE where applicable. Responsible for manufacturing compliance with all safety, environmental and quality related SOPs. Process improvement. Ensure successful review, amendment and implementation of changes to SOPs and managing CAPAs. Liase with the relevant departments & customers in the introduction and execution of NPIs Projects. Adheres to and supports all EHS & E standards, procedures and policies. Work closely with the other Technical Shift Leaders to ensure interdepartmental activities are planned and executed safely. Develop direct reports by securing appropriate training, assigning progressively challenging tasks and managing mid year and annual reviews. Assist and cooperate with HR in the management of employee relations issues. Interacts with internal and external customers, by meeting regularly, responding to requests and explaining procedures. Requirements: A minimum of 5 years experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry. Degree or equivalent in Life Sciences or a Process/ Chemical Engineering discipline. Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role. Background as a technical leader in either a process engineering, formulations and technical transfers capacity. Must be able to lead & project manage these activities. Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality requirements. If you are interested in this position please send CV to aoife.lomasney@peglobal.net or call Aoife 0214297900 to discuss. This job originally appeared on RecruitIreland.com.

2858 days ago