.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 Convatec Group.Main Responsibilities:The Team Lead will assure the good environment of the quality engineering team is established.Maintain trained and motivated personnel in the areas to her/his responsibility.Main leader assuring the compliance for regulations, standards, QMS internal procedures on a New Project (CCR), Process Improvements (OFI), Validation & Revalidations, Risk Management, Customer complaints investigations which are directly handled by his team - Projects Quality Engineer (PQE).Assure that quality issues are well handled from a non-conformity, maintain quality indicators and internal deviations ensuring the activities are taken in a proper manner and time.Requirements:Bachelor's degree (Mechanical, Electronic, Industrial area or similar education) required.Min.
3 years' experience in Engineering areas, required.Strong experience in handling of QMS (Quality Management System), required.Strong experience with Quality Control Charts (histogram, pareto, process capability calculations, control charts, etc.
), required.Strong experience with Quality Management Tools (brainstorms, flow diagrams, cause and effect diagrams, etc.
), required.Focus on continuous improvement mindset, required.Verbal and written English, required.Strong ability to capture, describe and communicate ideas to the teamwork, preferred.Auditor skills, preferred.Supervisor experience, preferred.Training/Knowledge on MDSAP, MDR, FDA QSR's and GMP's, ISO 13485, J-PAL/Ordinance No.169, EU and Canadian medical devices regulation, or similar regulations, preferred.Familiar with common computer software packages.
MS Office, Lotus Notes, etc., required.Molding process knowledge preferred.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 ******