Deeside, Wales, United Kingdom
13 days ago
Engineer II – Research and Development
Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring.
Our solutions provide a range of benefits, from infection prevention and protection of at risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC).
To learn more about Convatec, please visit http://www.convatecgroup.com

Change is everywhere at Convatec. It’s transforming our business, and helping us improve millions of lives. And we’re nowhere near finished. Across every part of our business, we’re pushing for better. Join us on our journey to #ForeverCaring as a Engineer II – Research and Development and you’ll do the same.


 

The Engineer II – Research and Development provides both New and Existing Product Development support, remediation activities performance, participates in Material change and Base Business projects relating to Accessories and 3rd Party manufactured products. This position focuses on development of design documentation and test-methods to verify the Product compliance with international standards and established company procedure.

Key Responsibilities: 
•    Design and development of new or improvement of existing products, systems, and process components.
•    Development of process specifications for new products and improved processes/products, ensuring the accurate completion of the required documentation to ensure transition of processes and design from R&D to manufacturing
•    Preparation of prototyping lines and prototypes of product
•    To perform laboratory tests at site in cooperation with Quality Management
•    To ensure that design documentation is prepared according to required standards and established company procedures
•    To Perform good and seamless communication, Global T&I, Global Marketing, Global and local Quality, Regulatory and Clinical as well as functions in Global and Local Manufacturing and Supply Chain
•    To participate in Risk Assessments
•    To update / create drawings in cooperation with Global R&D Engineering
•    To create specification of products, raw materials, semi-finished goods etc.
•    To develop test methods
•    To perform the Design review of drawings / measurement / test methods etc.
•    To initiate and perform shelf-life testing
•    To initiate and perform biocompatibility testing (external contracting)
•    To determine effects of (re)-sterilization
•    To ensure compliance with the legislative and internal requirements of the EHS and to participate in the fulfillment of the company's targets in the EHS area

For Existing Product remediation purpose:
•    To develop Product design Inputs/Outputs
•    To perform Product design verification
•    To perform Product design validation
•    To perform Final Design Review
•    To perform any other duties assigned by the immediate superior

Authority:
•    R&D Approver / technical Approver
•    R&D Owner Change Control Record (CCR´s and ECCF’s)


Skills & Experience: 
•    Good analytical skills and technical knowledge in product development and especial in design, materials and processes
•    Proficien in compuer systems such as Microsoft office, Microsoft Excel, Minitab (or equivalent) and Solidworks (AutoCAD)
•    Ability to communicate effectively in English
•    Able to work independently though still be a team player 
•    Able to work cooperatively with other departments to achieve results

Desirable but not required:
•    Experience within product / process development.  
•    Experience in Product and/or process development in a highly regulated area such as Medical products, Pharmaceuticals, Food

Qualifications/Education:
•    Bachelor of science in Engineering, Plastic, Mechanical or related field
•    Analytical mind, technical and communicative skills
•    Self-development through continuous learning and knowledge sharing
•    General PC experience and specific experience in spreadsheets
•    Statistical know-how and beneficial if experience into Statistics programs

Preferred training requirements:
•    Introduction training for administrative employees
•    Quality System documents and procedures relevant to all employees (local and Convatec corporate e.g. Code of Ethics and Business Conduct, Quality Policy, Complaints, relevant GxP documents), including regular re-training when required
•    Quality System documents and procedures relevant to job performance
 

Principal Contacts & Purpose of Contact
•    Internal – Global T&I, Global Marketing, Global Quality, Global Supply, Advanced operations  - general daily projects related communication
•    External – 3rd Party Suppliers of Accessory products – project specific communication

Travel Requirements
•    Position may involve travel up to 25% of the time, mostly within Europe but overseas travel is expected.(variable and project related) Most trips will include overnight travel

Languages
•    Speaking:        Yes        English*
•    Writing/Reading:    Yes        English*
*additional languages as required or nice to have

Working Conditions:
•    Office based position with home office possibilities based on the local home office policy 
•    Flexible working hours

Special Factors
Supporting manufacturing trials may require working atypical hours, across multiple shifts, on weekends or on holidays.
 


 

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-DS4

#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 careers@Convatec.com.

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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