At Convatec, we're transforming our business for the better. Better products. Better ways of working. And better ways of delivering for our customers and each other. We're aiming for nothing short of excellence. Join us on our journey to
#ForeverCaring as a Development Engineer and you'll do the same.
Convatec is a developer, manufacturer and marketer of innovative medical products focused on therapies for the management of chronic conditions. Its four franchises provide products used for advanced chronic and acute wound care, ostomy care, continence and critical care and infusion devices used in the treatment of diabetes and other conditions.
Job Summary
Has experience in medical device product development and manufacturing processes and is part of a global team supporting the design, development, and maintenance of existing ostomy care products in the market. Duties and Responsibilities Perform moderately complicated engineering work exercising independent judgement and action.
Develop products following design controls framework to technical and functional requirements. Measure and analyze the reliability of designs, materials, processes, costs, and final products of production.
Provide technical solutions to a wide range of difficult problems. Identify and generate new intellectual property (IP).
Create project plans, technical reports, and document research. Summarize critical results and observations. Ensure research and design methodologies meet established scientific and engineering standards.
Work under only general direction. Independently determine and develop an approach to solutions.
Lead and conduct problem-solving efforts and propose practical solutions.
Propose, design, prioritize, conduct, and oversee multiple projects. Develop and validate new test methods.
Present information and effectively communicate cross-functionally to key stakeholders.
Drive growth, cost reduction, product quality improvements, and support capacity improvements.
Own Design History Files (DHF's) for commercially available ostomy products.
Ensure compliance with ISO 13485, FDA 21CFR820, and cGMP requirements.
Education / Experience / Qualifications Bachelor's Degree in Science and/or Engineering (or equivalent)
Experience working within the Medical Device industry (or a similarly regulated industry)
Experience in medical device design controls and/or manufacturing processes
Strong math and analytical skills
Strong organization and attention to detail
Ability to interface effectively with cross-functional groups to define and execute overall requirements.
Ability to communicate effectively in English (verbal and written)
Proficient in computer systems such as Microsoft Office, Microsoft Excel, Minitab (or equivalent), and AutoCAD / Solidworks
Desirable Experience in product design, detailed engineering design, quality function deployment, design for manufacture, and design transfer.
Experience in Ostomy Care
Experience with the selection and processing of materials including flexible films/fabrics, adhesives, and plastics.
Experience with manufacturing processes including injection molding, thermal heat welding, RF welding, registered rotary converting, and various printing processes.
Core Behaviors Team player – experience collaborating with diverse, global, cross-functional teams.
Customer focused.
Excellent communicator – verbal, written, presenting.
Curious and eager to learn.
Principal Contacts The nature of this role will require the individual to deal with a wide range of contacts at different levels of seniority within the organization. In addition, the individual will deal with contacts external to the organization where these may be external companies or government agencies.
Travel Requirements Yes: Up to 15% (variable and dependent on projects).
Language Skills Required Fluency in English is a requirement for the role.
Training Requirements A list of trainings that must be completed and documented to fulfill the duties and responsibilities of this role will be provided accordingly by HR.
Working Conditions This position is based at a Convatec core site (hybrid) working within an office, manufacturing, and laboratory environment.
Special Factors The candidate should also be flexible as travel may fall outside normal working hours.
Flexibility to support Operations across shifts and weekends if required.
Our transformation will change your career. For good. You'll be pushed to think bigger and aim for excellence. Your ideas will be heard, and you'll be supported to bring them to life. There'll be challenges. But, stretch yourself and embrace the opportunities, and you could make your biggest impact yet.
This is stepping outside of your comfort zone.
This is work that'll move you.
#LI-MF1
#LI-Hybrid
Beware of scams online or from individuals claiming to represent Convatec A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.
If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you're unsure, please contact us at ******.
Equal 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.
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