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ConvaTec Quality Project Manager – Medical Devices in Søborg, Denmark

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Are you passionate about leading people and driving quality projects to success? Do you want to join a world leading company specialised in treatment of chronic diseases such as Diabetes and Parkinson’s Disease? Then you might be the right candidate to join our Quality organisation as Project Manager.

At ConvaTec Infusion Care, we are transforming our business for the better. Better products. Higher Quality. Better ways of working. Join us on this transformative journey as our New Quality Project Manager and help shape the future of the company and our patients.

About the role

We are looking for an experienced Project Manager to drive quality projects for sterilised medical devices.

You will lead a cross functional Project Team for our most critical quality projects, such as Sterilisation validation, MDR implementation and continuous improvements to our system and processes and compliance projects in general. Your responsibility will be to ensure timely deliveries according to our quality and compliance plans.

Together with your team, including external stakeholders, you will create a clear and ambitious plan and ensure that the project is delivered successfully on time with agreed quality, documentation, and cost.

We offer you a central role in an exciting company in constant growth. You will work in a dynamic company and together with an experienced QA and RA team and have close collaboration with our key suppliers, the management team and highly competent subject matter experts within the organisation.

You will report to the Business Unit Quality Lead – IC, with a dotted line to the VP, Global Quality for Convatec. The current location is in Denmark (either Søborg or Osted). We offer flexible working hours and environments.

Your key responsibilities

  • Lead quality project teams, bring structure and motivation to the project and facilitate cross-functional teamwork

  • Establish and maintain a productive relation with the relevant stakeholders based on trust and respect.

  • Ensuring that project plans, including scope, success criteria, project schedule, resource plan, project risk plan are performed with involvement of key stakeholders

  • Aligning on resource plan for the projects with line managers

  • Managing project deliverables with accountability and ensuring timely mitigation on deviations and risks via the maintenance of an effective risk register

  • Managing expectations and stakeholders, and communicating project status, progress, and unexpected difficulties effectively

  • Reporting project status on monthly basis (or as needed) to the steering group

  • Supporting the global quality team with creation, consolidation, and simplification of strategies and company wide quality programs/projects

  • Partner with other project managers within and outside of global quality

What you bring

Besides having a proven track record as a Project Manager delivering projects successfully on time with agreed quality, scope and cost you are a team player with a holistic mindset. You apply best project management practices to lead and steer the Project Team safely and with motivation and good spirit through all stages of the project/programs in accordance with our QMS. You utilise your good collaborations skills, to build strong collaboration with other functions like production, sourcing, R&D and marketing. You must also be able to establish build a strong partnership with external suppliers, such as Sterilisation suppliers.

You are pragmatic and operate with a high sense of urgency to meet your deadlines. You enjoy a busy working day and can progress several tasks in parallel. You have proven analytical and problem-solving skills that will help you to take fast and well-founded decisions. You understand the importance of good documentation practices and have excellent written and verbal communication skills in English.

Qualification & Experience

You hold a Master’s or Bachelor’s degree in mechanical, chemistry, biology, pharmacy or similar. Alternatively, or in addition, you have a formal Project Manager background combined with hands-on experience from the medical device industry. This combined with most of the following increases you chance of success in the job:

  • 3+ years of experience in Medical Device Quality Assurance (Class II or higher)

  • 3+ years of proven experience as Project Manager, successfully leading projects, preferably within the medical device industry

  • Knowledge with sterilised medical devices is an advantage

About us

We offer you a position in a dynamic and global company 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.

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.

Interviews will be conducted continuously, so we encourage you to submit your application by using the apply button as soon possible. We look forward to receiving your application, CV and other relevant documents.

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 with deeply personal and challenging medical conditions, helping to improve care for them and giving them greater confidence, freedom and mobility.

Convatec, Infusion Care (Unomedical a/s) is a part of a global medical technology business focused on serving people and care givers. We develop and market sterile disposable products for subcutaneous infusion of various medications. Specialised in the treatment of chronic diseases, such as Diabetes Mellitus and Parkinson’s Disease. Our manufacturing facilities in Denmark and Mexico produce more than 100 million infusion sets per year, making us the world leader within this field. Further information about the company can be found at our website , or

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 .

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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