Test Method Specialist
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Humlebæk
Test Method Specialist for Global Research and Development (R&D) – Chronic Care and Wound Care
Would you like to provide documentation to help one of the best-performing medical device companies in the world ensure product safety for wound care and chronic care globally?
Pursue a career within one of the best-performing medical device companies in the world and be part of the entire development process – from initial concept tests to final product. Feel the pride and see your efforts help make a difference to people with intimate health care needs.
Join our Materials department in Technology
Joining our Materials department, you will work alongside 39 skilled colleagues. Here, we ensure proper design and documentation of our new products within the chronic care and wound care business areas. Thus, you will collaborate closely with other parts of Global R&D in the design process but also with our 4 other test method specialists, who are based in Humlebæk, Denmark.
“Before new or existing products are brought to the market, we ensure the right documentation for our design verification and production test methods. This is crucial for us to make sure our customers can put their trust in our products,” explains Senior Test Method Validation Manager Kirsten Stuckert.
Ensure the quality of our test methods
As a test method specialist, you are responsible for ensuring documentation at the right level concerning the design and validation of test methods used for design verification in our productions. This means that you participate in creating documentation for test methods and related procedures and instructions.
Participating in the constant development of test method principles and structures in Global R&D, you will:
Scientific background and a flair for test methods
As you will not carry out the design part yourself, you must be able to work well with colleagues, give your feedback to ensure we create just the right test methods – and meet deadlines. Also, you will be responsible for the validation documentation at different stages in several projects at a time, so structure is crucial. Finally, you can expect to travel up to 15 days a year to liaise with our different production sites.
We imagine that you:
Interested?
At Coloplast, we make sure that you can be you. That is why we encourage applications from suitably qualified and eligible candidates regardless of sex, race, ethnicity, disability, age, sexual orientation, gender reassignment, religion or belief or marital status.
If you would like to know more about the position, please call Senior Lab. & Validation Manager, Kirsten Stuckert, at +45 4911 1331. We will take candidates into the recruitment process continuously, so do not hesitate to apply. This position will remain open until a suitable candidate has been found.
Pursuing an ambitious growth agenda, Coloplast develops and markets products and services that make life easier for people with very private and personal medical conditions. Employing more than 12,000 people and with products available in more than 140 countries, we are one of the world´s leading medical device companies. We are constantly growing our business and always looking for new ways to move forward – we explore, learn and look for new ways of doing things. Curiosity works here.
Visit us on Coloplast.com. Follow us on LinkedIn. Like us on Facebook.
Would you like to provide documentation to help one of the best-performing medical device companies in the world ensure product safety for wound care and chronic care globally?
Pursue a career within one of the best-performing medical device companies in the world and be part of the entire development process – from initial concept tests to final product. Feel the pride and see your efforts help make a difference to people with intimate health care needs.
Join our Materials department in Technology
Joining our Materials department, you will work alongside 39 skilled colleagues. Here, we ensure proper design and documentation of our new products within the chronic care and wound care business areas. Thus, you will collaborate closely with other parts of Global R&D in the design process but also with our 4 other test method specialists, who are based in Humlebæk, Denmark.
“Before new or existing products are brought to the market, we ensure the right documentation for our design verification and production test methods. This is crucial for us to make sure our customers can put their trust in our products,” explains Senior Test Method Validation Manager Kirsten Stuckert.
Ensure the quality of our test methods
As a test method specialist, you are responsible for ensuring documentation at the right level concerning the design and validation of test methods used for design verification in our productions. This means that you participate in creating documentation for test methods and related procedures and instructions.
Participating in the constant development of test method principles and structures in Global R&D, you will:
- Be responsible for creating and approving validation documentation for design verification and production-related test methods and equipment for medical devices
- Partake in projects and the ongoing maintenance of test methods implemented in our production
- Assist in troubleshooting of laboratory equipment as well as in the design of new test equipment/test methods
- Aid in the training of colleagues in Global R&D in test methods and procedures as well as in the design of new test methods
- Set best practices and create or update procedures for our test methods together with test method specialists from other departments
Scientific background and a flair for test methods
As you will not carry out the design part yourself, you must be able to work well with colleagues, give your feedback to ensure we create just the right test methods – and meet deadlines. Also, you will be responsible for the validation documentation at different stages in several projects at a time, so structure is crucial. Finally, you can expect to travel up to 15 days a year to liaise with our different production sites.
We imagine that you:
- Hold a master’s degree within science (e.g. mechanics/physical, chemistry, pharmacy or similar)
- Have knowledge of statistics and statistical software related to method validation (e.g. SAS.jmp)
- Probably have knowledge of polymers and mechanical testing – but we would also like to hear from you if you have knowledge of chemical testing and Six Sigma
- Have knowledge of ISO 9001 and, preferably, also ISO 13485 and GMP
- Have good English reading and writing skills
Interested?
At Coloplast, we make sure that you can be you. That is why we encourage applications from suitably qualified and eligible candidates regardless of sex, race, ethnicity, disability, age, sexual orientation, gender reassignment, religion or belief or marital status.
If you would like to know more about the position, please call Senior Lab. & Validation Manager, Kirsten Stuckert, at +45 4911 1331. We will take candidates into the recruitment process continuously, so do not hesitate to apply. This position will remain open until a suitable candidate has been found.
Pursuing an ambitious growth agenda, Coloplast develops and markets products and services that make life easier for people with very private and personal medical conditions. Employing more than 12,000 people and with products available in more than 140 countries, we are one of the world´s leading medical device companies. We are constantly growing our business and always looking for new ways to move forward – we explore, learn and look for new ways of doing things. Curiosity works here.
Visit us on Coloplast.com. Follow us on LinkedIn. Like us on Facebook.
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Humlebæk.
Jobbet er oprettet på vores service den 18.12.2019, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Forretningsudvikler
- Humlebæk
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