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ConvaTec Quality Engineer, Business Quality (Fixed-term Contract) in Deeside, United Kingdom

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 atrisk 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.

Our search for better is changing the lives of our customers. It’s changing the careers of our people too –creating new challenges and opportunities all the time. We’re a business that never stands still. Join us on our journey to #ForeverCaring as Quality Engineer, Business Quality, and you won’t either.

Job Summary:

This is a key role within the Global Quality function, where you will uphold a state of audit readiness by maintaining Quality Systems, including, Internal audit, change control, EDMS and validation and represent Quality Management on the more complex projects that involve coordination of several quality resources. This role will drive the internal audit process for the site. This is a fixed term contract for 12 months .

About the Role:

Key Duties & Responsibilities

  • Manage the Internal Audit system

  • Support documentation systems

  • Provide a QA review and approval of documents (e.g. procedures within the EDMS, Laboratory Equipment qualification documentation, QA review/QA manager review for NCs within Trackwise)

  • Maintain an audit readiness state

  • Key person for Documentation storage

  • Responsible for SAP ordering and invoicing

  • Maintain an excellent up to date knowledge of international Quality Regulations and advises management of implications for the site

  • Work closely with other functions on site, to communicate and implement relevant Quality Systems

  • Support the general activities with the Quality Department

  • Prepare routine metrics relating to the Quality System and the routine Management Reviews

  • Support inspections by regulation bodies, including BSI

  • Proficient in EDMS, TRACKWISE, SAP, and spreadsheet / database software

About You:

The ideal candidate should bring the following qualities to the role:

  • Keen sense for attention to detail and ability to apply skillset to document and record reviews.

  • Excellent sense of prioritization and time management, operating against multiple deadlines.

  • Demonstrated experience of project management and/or leading project implementations.

  • Ability to deal and lead through difficult situations with tact and professionalism.

  • Analytical mindset and able to influence others using data driven decisions.

  • Demonstrate problem solving and trouble shooting skills.

  • Experience of using electronic quality management system software.

Travel Requirements

Not Applicable

Education/Qualifications

  • Degree, or equivalent, in Science or Engineering

  • Demonstrated experience in Medtech industry

  • Knowledge and experience of working with a Quality Management System within Medical Devices

  • ISO 13485 lead auditor or internal auditor qualification

Working Conditions:

This is a Hybrid position, working in an office environment (CTEC Deeside)/work from home

This is a fixed term contract for 12 months

Language Skills Required:

Speaking: Yes English

Writing/Reading: Yes English

Our ambitions will bring the very best out in you. You’ll be pushed to aim higher and really own your work. You’ll be encouraged and supported to make things happen too. It can be challenging. But, as the progress you make will help improve the lives of millions, it’ll be worth it.

This is stepping up to a challenge.

This is work that’ll move you.

#ForeverCaring #ForeverConvatec #WeAreConvatec

#LI-DB1

#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.

Already a Convatec employee?

If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

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