Are you looking for a challenging role, related with designing and developing the customer focused sterile and non-sterile medical devices, across multiple locations?
As Development Engineer you will be part of a team supporting the maintenance of existing products in the market.
Key duties and responsibilities of Development Engineerinclude :
Designing and development of customer focused sterile and non-sterile medical devices, across multiple locations, from concept through to commercialization, project managing technical elements of development projects (time, budget and resources)
Carryingout project activities within a Design Controls Framework in accordance with ISO 13485 & 21CFR820 Quality Systems
Problem solving activities & ideas generation to deliver practical solutions
Leading for design for manufacturing, including process flowcharts
Identifying & generating new Intellectual Property (IP) and translating novel ideas into valuable & protectable IP
Development & Validation of new test methods, etc.
Developing and maintaining good working relationships with all key internal and external organizational stakeholders
Liaising with other business functions to effectively execute projects
To be successful in thisroleyou need to have :
Bachelor’s Degree in Science and / or Engineering (or equivalent)
Experience working within the Medical Devices or equivalent regulated industry, within device design control and / or manufacturing processes
Demonstrable experience of on-time delivery of complex technical projects and activities
Ability to build productive relationships with external parties (e.g. design houses and contract development and manufacturing organizations (CDMO’s)
Experience in application of CAD packages and Technical Drawing Management Systems
Knowledge in the area of applying a range of statistical techniques incl. Design of Experiments (DoE) to product / process development activities
Highly structured ability to progress tasks in parallel, and proven problem-solving skills
Experience of Product & Process Validation activities
The ability to communicate effectively in English (verbal and written) is essential
Computerliteracy i.e. Microsoft Office (Outlook, Excel, Word, and PowerPoint)
What is great about being part ofConvaTec?
ConvaTecenvironment is fully focused on a company mission which is based on creating an incredibly valuable patient-orientedorganisationwhich enables us to become the market leader by offering high value products to our customers
As aConvaTecemployee you will become a part of fast-paced medical devices sector with a spotlight on making people’slifesbetter
You will have access to series of trainings and personal development opportunities
ConvaTec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
Notice to Agency and Search Firm Representatives : ConvaTec is not accepting unsolicited resumes from agencies and / or search firms for this job posting.
Resumes submitted to any ConvaTec employee by a third party agency and / or search firm without a valid written and signed search agreement, will become the sole property of ConvaTec.
No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.