Process Engineer - Medical Devices

Process Engineer - Medical Devices
Ref No.: DJ05641
Location: Westmeath, Longford, Offaly
Salary:
Experience required: 5 - 6 years
Job Type: Permanent

Summary: Our client based in the Midlands is currently looking to recruit a Principal Process Engineer.

Description:
Process Engineer - Medical Devices
Our client based in the Midlands is currently looking to recruit a Principal Process Engineer.
Responsibilities:
Manage and co-ordinate technical support for the introduction of new products
Develop resource allocation and a critical path so as to effectively manage the introduction of technology on loads, modifications and process improvements.
Develop manufacturing technical capabilities and skills so as to ensure ongoing process requirements can be effectively achieved.
Select, motivate and develop competent personnel and develop appropriate engineering organisational structures
Ensure all process engineering activities are managed so as to comply with Corporate, Regulatory and GMP requirements.
Assume responsibility for all manufacturing/process engineer training and development including timely completion of staff appraisals, which will help motivation and enhance staff performance.
Develop strong links with our sister plants so as to ensure effective ongoing transfer and sharing of products, processes and systems.
Ensure that process validations and work methods are adequate to maintain the highest quality standards.
Provide technical support in field related activities such as clinical programmes and complaint investigations.
Ensure safety standards and awareness within the manufacturing/process engineering group are in compliance with legislation and issues effectively dealt with.
Prepare technical documentation such as standard operating procedures, safety programmes, validation protocols, technical reports, engineering calculations, change controls and other documentation as required.
Provide technical leadership for operations personnel involved in process engineering and development activities.

Requirements:
Degree in relevant engineering discipline.
Minimum of 5-7 years experience in medical device or similar industry with an established track record.
Established knowledge of cGMP and safety standards applicable to a clean-room/controlled environment and associated manufacturing processes and procedures.
Ability to share technical expertise with colleagues
Good problem solving abilities
Team and results orientated - committed and energetic approach to work with positive attitude.
Proven reliability – efficient, results-orientated and manages own time well.
Ability to deal effectively with all employees and external business contacts while conveying a positive, service-oriented attitude.
Strong computer skills
Six Sigma/lean expertises demonstrated in the manufacturing and design of new products is highly desired.