Product Quality Specialist

at  ConvaTec

Pioneering trusted medical solutions to improve the lives we touch: Unomedical s.r.o. is a member of Convatec which 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
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. With us, you will not only could influence the production and development of our products - you will also have the opportunity to develop in our QC Support team
We’re a business that never stands still. Join us on our journey to #ForeverCaring as Quality Specialist, and you won’t either.

ABOUT THE ROLE

As a quality Specialist you will be responsible for, the validation of documentation, revalidations, and risk assessments for the specific process. You will also be responsible for systematic problem solving, deviation management, optimization of equipment and processes as well as general support for production and organizational projects. You will have a central and cross-organizational role in connection with development projects and the implementation of new products and act as a link between production, the support team, project team, development, and maintenance.

KEY RESPONSIBILITIES:

• Improve activities in QC, including facilitation of problem solving.
• Identify potential improvements by analyzing data in release process.
• Confident presenter when QC are audited or inspected by customer/authorities.
• Handle deviations; includes close sparring with operators, technical department, QA etc.
• Prepare and maintain documentation e.g., risk assessments and periodic evaluation
• Change Control Request (CCR) with associated documentation
• QC specialist in connection with development and equipment projects