Project Engineer

at  Harmac Medical Products

QUALIFICATIONS AND EXPERIENCE REQUIRED:

• Level 8 or equivalent Degree in Engineering or similar discipline is desirable
• 3 years’ experience in a medical device manufacturing engineering role is desirable
• Knowledge of medical device validation protocols and associated documentation
• Implementation experience of validation protocols
• Knowledge of AutoCAD and Solid Works is desirable
• Lean and six sigma knowledge
• Strong process engineering background
• New product introduction experience
• Strong team player, with the ability to work on own initiative
• Guided by the disciplines of due diligence and compliance in all aspects of work.
• To be a good team member, fully motivated to achieve and demonstrate best practices

in line with the department and site objectives.

• Ability to work with cross-functional teams, including quality, production and supply

chain.

• Excellent interpersonal skills.
• Ability to plan, organise, and prioritise own daily work routine to meet established

schedule.

• Good understanding of ISO 9001: 2008 and ISO 13485.
• Excellent knowledge of MS Office

• Provide manufacturing support over a range of manufacturing processes
• Lead process improvement initiatives to reduce cost and to improve manufacturing

efficiency by using data analysis

• Manage projects and lead new product introduction projects introducing new processes

as appropriate

• Carry out process and product validations
• Implement product, process and material changes through validation, change control and

documentation updates

• Familiarize yourself with a variety of processes to allow you to work across a number of

product lines

• Conform to the requirements of the quality and environmental management system
• Additional ad hoc duties and projects as assigned