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ConvaTec Validation Engineer in Osted, Denmark

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. Group revenues in 2022 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

We are guided by our five core values, that shape the way we work, every day: Improve Care, Deliver Results, Grow Together, Own It and Do What’s Right.

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 Validation Engineer and you’ll do the same.

About the role:

We are expanding our Validation Engineering Team and are looking for 3 new Validation Engineers, to join the department Validation Engineering of 5 dedicated employees supporting innovation projects, capacity increase projects and customer projects.

As our new Validation Engineer, you will be responsible for validation and qualification of processes and equipment related to customer projects. You will be working closely with a dedicated project team to ensure progress of customer projects.

You will collaborate closely with cross-functional project teams, and key stakeholders in Denmark and globally, like QA, Regulatory Affairs, R&D, suppliers, and the production units.

We can offer you a central position in an exciting growth company, where you will have great influence on the projects and processes in which you take part.

You will refer to Team Lead – Validation Engineering, Infusion Care and your main work location is in Osted, south of Roskilde, where the Danish production is located. We offer some flexibility to work from home 1-2 days a week, as it fits your tasks or projects. Some travel activity is to be expected, visiting suppliers in primarily Denmark or Scandinavia. This will be agreed in timely manner with your manager.

Key responsibilities

Key responsibilities in this role include, but are not limited to:

  • Validation and Qualification of processes and equipment when implementing new material.

  • Perform Validation and ensure results are accurately documented.

  • Create validation documentation in collaboration with customer, project team, QA and production.

  • Ensure project documentation is adherent to applicable regulation and internal procedures.

  • Ensure high level of expertise and quality to the product, equipment and documentation.

  • Contribute to knowledge sharing across project teams and departments.

Key requirements

Essential competencies and characteristics that candidates must demonstrate to contribute to our diverse, inclusive culture and succeed in the role.

These may include:

  • We are looking for a structured and team-oriented professional, with a high focus on quality and an eye for detail. You are a positive person who looks for solutions rather than obstacles and sets a pride in being a specialist and aim to improve your professional skills.

  • You understand that key contributing factors to success are collaboration - and at the same time deliver high quality and timely solutions and deliverables. You have strong communicative skills in both English and Danish, where you can provide constructive feedback as well as further guidance.

  • You thrive in an informal culture with great degrees of freedom, a great degree of autonomy with the opportunity to make your own mark on your everyday life and tasks.

Education/ Qualifications

  • Education as Engineer, Laboratory Technician, or other relevant technical background.

  • You have +2 years’ experience from a similar role, working with validation in a regulated industry – preferably from medical device or pharma industry, alternatively other industries with legislative regulations and related documentation.

  • Experience with ISO 13485 and FDA requirements preferred.

  • A high level of language skills in Danish and English, both written and verbal.

We will make sure, that you will get a thorough on-boarding and we will provide you with the necessary training.

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 from day one. 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 as soon possible. We look forward to hear from you!

Apply with your CV and please include a few sentences on your motivation for applying for the job in your CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.

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.

#LI-SF1

#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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