Mechanical Product Support Engineer

The group of companies combines core fields of expertise: research and development, production and service as well as distribution and training.

Job Purpose:
To provide design engineering input to ensure that changes required to released products to meet on-going business needs are conducted on time, within budget and with the required level of quality.

Your duties:
Provide design and development support to products post launch, coordinating design and manufacturing changes and improvements to meet defined device and manufacturing requirements.
Accept the introduction of new products and ensure their efficient on-going transition into regular production by appropriate provision of a design authority service to operations and quality.
Assessment of Non Conformance Reports (NCRs) and implementation of agreed corrective / preventative actions to maintain regulatory compliance.
Maintain a strong and current understanding of relevant new product development and manufacturing technologies and their application to medical device design to meet or exceed customer, company and project needs.
Evaluate and document the feasibility, reliability and risk to of changes to product designs and manufacturing processes through engineering design, analysis & testing to demonstrate the product performance, manufacturability, material selection, safety and cost are consistent with the customer and regulatory requirements.
Develop timelines and cost estimate for development tasks and appraise management of performance against plan to maintain compliance to project schedule.
Generate and review design history file documentation in compliance with Good Manufacturing Practice (GMP), Quality System Regulations (QSR), International Standards Organisation (ISO) and company Product Development Process (PDP) requirements throughout the project life cycle to ensure the design is fully documented.
To be responsible for customer contact with respect to company products to ensure maintenance of product line and communication and buy in of design change implementation where required.

Education/Qualification
Bachelors degree in an appropriate Engineering discipline or equivalent with a minimum of 2 years’ experience in a regulated and highly mechanical engineering design environment
Or
HNC/D in an appropriate Engineering discipline with a minimum of 5 years’ experience in a regulated and highly mechanical engineering design environment

Work Experience
Excellent knowledge of and ability to critique 2D engineering drawings and 3D modelling
Ideally cGMP, ISO 13485, and FDA QSR knowledge as practiced in the disposable medical device industry
Ideally medical device design or development experience

Skills
Competent in MS Word, Powerpoint and Excel
Good analytical and mathematical skills.
Understanding of a wide range of engineering technologies used in design and manufacturing
Knowledge of mechanical design relating particularly to mechanisms
Good planning, organisation and control skills
Able to use initiative
Strong problem solving skills
Excellent verbal and written communication skills