Chemical Manufacturing Engineer
Sigmar Recruitment
Galway
The role will be responsible for researching and developing new and improved chemical manufacturing processes. manufacturing line products, processes, equipment, and documentation to meet quality, service and cost objectives for AOP targets. Key responsibilities. You will undertake specific projects as designated in support of the business unit objectives. You will contribute to and give technical support to required site visitor programs as required. demonstrate your ability to identify continuous improvement activities & lead or participate in cross-functional teams through implementation, qualification & validation. This will include cost reduction, process efficiency & operational excellence. monitor and improve chemical processes with respect to cycle times, machine utilization and yields. You will structure experiments for coating/impregnation processes, material performance improvements and develop new chemical processes for new products. lead and support root cause driven approaches to problem solving efforts for chemical issues. analyze and report on chemical, quality and technical issues within Manufacturing Departments. provide expertise to support product development cycles, technology transfers and Operations scale ups. perform laboratory studies of steps in manufacture of new product and test proposed process in small scale operation. prepare / critically review protocols / reports and co-ordinate qualification and validation activities in conjunction with Engineering / Quality team, providing expert chemical direction as appropriate. maintain expert up to date knowledge of developments in regulatory compliance requirements for product de-sign, development, transfer and commercialization activities. Key requirements. Qualified to third level 8 Degree/ Masters in Chemical Engineering/ Process Engineering or related discipline. With relevant experience in the pharma/chemical synthesis industry. 5 years relevant manufacturing experience in pharma industry (ideally API related. knowledge of Analytical test methods and Regulatory requirements (i.e. FDA/BSI Audits. experience with and effective application of Validation Protocol and Report creation, Equipment and Process Validations (IQ, OQ, PQ, and PV), GD&T, MSA, DOE's, Design and Process FMEA’s, SPC, Process Control Plans, Gauging applications, design, and construction, sampling methodologies, data analysis. dynamic team player and can work effectively and proactively on cross-functional teams. knowledge of medical device industry regulations, manufacturing engineering role and ability to manage self and others to achieve challenging targets is advantageous. To apply for this position please contact Majella Slevin at Sigmar RecruitmentT: +353 91 455300E: mslevin@sigmar.ie. All applications will be treated with the strictest of confidence. Sigmar will never forward your CV to a third party without prior consent. This job originally appeared on RecruitIreland.com.
2344 days ago