Job Description
Were currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Mayo. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do Key Activities Provide technical assistance to the manufacturing areas relating to the process and equipment to address issues and exceptions or support improvements. Develop and implement changes that will enhance equipment performance, product quality, reduce manufacturing costs and maximize efficiencies. Develop and modify procedures as needed to support the manufacturing areas. Submit Change plans and create investigation reports. Support the transfer of new products to the manufacturing area. Participate in process, equipment and facilities validation efforts and project implementation. Maintain manufacturing area equipment in compliance with site calibration and maintenance program Provide support to Technical Shift Leads on batch records Provide assistance and present when required at Regulatory Inspections Comply with policies and procedures and regulatory agency regulations. Evaluation and implement new equipment and process technology. Initiate capital project ideas dealing with safety, quality improvements, increases in capacity and/or cost reduction. Education and Experience: Bachelors degree in chemical, Mechanical Engineering, or a related discipline is required A minimum of 2 years experience in process / equipment engineering in a manufacturing environment of biotechnology, pharmaceutical plant desired. Lean Six Sigma/ Continuous Improvement experience is desirable Detailed knowledge of CGMP and regulatory requirements relating to the pharmaceutical industry is required for this role. Possess strong technical knowledge and application of concepts, practices, and procedures. Good interpersonal skills to develop working relationships with people at all levels. Ability to lead projects. Ability to quickly adopt to changing business / project demands. If interested in this posting, please feel free to contact Jack Caffrey at or for further information. Skills: Aseptic Clean room Fill Finish Validation Benefits: See Description