Manufacturing Process Engineer
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| Job Type | Permanent |
| Location | Mayo |
| Area | Mayo, Ireland |
| Sector | EngineeringOperations & Manufacturing |
| Start Date | |
| Advertiser | Darcy Ainscough-Denton |
| Telephone | 01 574 6266 |
| Job Ref | 1003194 |
| Job Views | 678 |
- Description
- Team Horizon is seeking a Manufacturing Process Engineer in Mayo for our client who are a global leader in the biopharmaceutical industry. In the role, you will have the opportunity to optimize and improve the efficiency of manufacturing processes within a multi-product aseptic environment across a wide range of process and equipment types. You will be required to ensure efficient operation of aseptic Filling lines and associated equipment. In this role you will become a ‘Subject Matter Expert’ across critical aseptic processes and will identify and lead the implementation of process improvement projects. The position will require dealing with challenging technical problems within a highly regulated environment. The successful candidate will have the ability to co-ordinate with multiple stakeholders and varying levels and areas of expertise, ensuring that the necessary skill sets for successful project delivery are available.
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
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 maximise 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 company 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.
Any other duties as assigned.
What you need to apply:
Bachelor’s 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 quicky adopt to changing business / project demands.
