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　　Are you compliance-driven and passionate about the development and maintenance of quality management systems (QMS)? And do you have what it takes to manage and support the development of innovative products that improve people’s lives? Do you want to join a world leading company specializing in treatment of chronic diseases such as Diabetes and Parkinson’s Disease? Then you might be our new QMS Coordinator.

　　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 QMS Coordinator and you’ll do the same.

　　As our QMS Coordinator, you will be responsible for preparing, reviewing and issuing required documentation such as good practice quality guidelines and regulations (GxP) procedure manuals, quality control manuals, engineering documents, production instructions, and change authorizations in accordance with company policies, quality systems and government regulations. You will be responsible for implementing related periodic documentation reviews and implementing change change control processes. You will have a key role in providing input on quality control procedures and R&D documentation, while applying practical knowledge obtained through advanced education and work experience. You will report to the Site Quality Director and and be part of our global Quality organisation with a strong professional foundation. The primary workplace is in Osted, Denmark and this is an onsite position.

　　Key responsibilities

　　Approve documents in the QMS as QA Manager (formalities, system coherence, standards etc.)

　　Develop quality procedures and processes, where necessary in close cooperation with corporate RA/QA.

　　Ensure coherence and structure in the documents of the QMS and that all elements and requirements in relevant standards are implemented and maintained in the QMS.

　　Plan and carry through training of employees in the QMS.

　　Maintain Quality Manual, Cross Reference lists between QMS and applicable standards/regulation.

　　Ensure that internal audits are performed for all areas of the quality system.

　　Participate in planning and completion of external audits (Notified Body, Authorities, Customers).

　　Ensure constant development and maintenance of the quality management system (QMS).

　　Ensure that the QMS is in compliance with regulatory requirements in the countries where the company´s products are marketed.

　　Ensure simplification of procedures and processes, so the QMS always aims at and reflects best practice.

　　We offer you a position in a dynamic and global company with great benefits and flexibilities for the employees and where the days are never the same. Convatec will provide you with challenges and development opportunities and the chance to influence your own role. You will be a part of a great community where we all help and support each other – while continuously building on our competences and network.

　　Interviews will be conducted continuously, so we encourage you to submit your application (in English) as soon possible. In case of questions to the position, please contact Dani Booker-Perry at [email protected] . We look forward hearing from you! You do not need to attach a cover letter to your application, but please include your motivation applying for the job in your CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.

　　At Convatec, our vision is to develop pioneering trusted medical solutions to improve the lives we touch. We devise, develop, and manufacture innovative products and services that support people.

　　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-DB1

　　#LI-Onsite

　　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 [email protected] .

　　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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