Chemical Compliance Technician
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Søborg
Chemical Compliance Technician
Do you want to be a part of the Biosafety team within Product Development in a company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, ready to invest in you. Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.
Every 2nd second Ferrosan Medical Devices’ products help surgeons and nurses control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team!
Chemical Compliance ownership
Chemical Regulatory Compliance means legal compliance with substance restrictions, enforced obsolescence, safe use of chemicals, responsible sourcing and supply chain management. As a Medical Devices manufacturer, FeMD faces the ever-growing, complex and frequent changes to regulatory and end-client requirements concerning material choices and chemical substance use, responsible sourcing and durability/recyclability which can directly impact product design and drastically affect costs and delivery.
As our new Chemical Compliance Technician, you will be an important member of our Biosafety team, which is part of the larger Product Development Department, consisting of 20 professionals working with Design & Development, Biosafety, Chemical Compliance and Labelling. In this role, you will support and optimize the chemical compliance process, coordinate chemical compliance initiatives, and engage proactively in the implementation of updates to our chemical compliance system. You will be instrumental in supporting the Product Development department and drive and own the chemical compliance process that contribute to the entire team's success. Your primary stakeholders will mostly be your colleagues in the Product Development department, our clinical insights and commercial specialists, quality assurance specialists, suppliers, and operations department. You will also engage with various cross-functional projects related to chemical compliance and it is therefore important that you thrive working in project teams.
Your role
In the role as our new Chemical Compliance Technician, your primary tasks will be to:
About you
You have a natural flair for working independently and you have an eye for detail in your work. Your entry to this job does not depend on a specific education – relevant practical experience can be sufficient.
Line of study is not as important as the interest in chemical compliance and product safety is. You will probably meet some of the below requirements:
Don’t meet every single requirement? If you are excited about this role, but you cannot meet all requirements, we encourage you to apply for the role anyway. You may be just the right candidate for this role.
We offer a truly purpose driven workplace where you can have real impact
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun 😊
Some of the facts and a little piece of history
Ferrosan Medical Devices develops and produces a portfolio of medical devices used in surgical care. Our portfolio consists of various hemostatic products to minimize bleeding challenges in surgery and electromechanical medical devices to perform breast biopsies. We are an international company with products registered in more than 100 countries. Our products are marketed in collaboration with global medtech partners. New ideas are developed and matured from the first thought to finished implementation in production. And we manage the business with an uncompromising focus on quality based on current GMP requirements.
Want to join our team?
Send your application along with your CV latest on August 31, 2024. We will process the applications as we receive them.
Questions? Please do not hesitate to contact us:
Katja Hvid Hinna
Manager, Biosafety & Labelling
+45 25 44 83 45
We look forward to hearing from you.
Read more about us here
Do you want to be a part of the Biosafety team within Product Development in a company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, ready to invest in you. Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.
Every 2nd second Ferrosan Medical Devices’ products help surgeons and nurses control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team!
Chemical Compliance ownership
Chemical Regulatory Compliance means legal compliance with substance restrictions, enforced obsolescence, safe use of chemicals, responsible sourcing and supply chain management. As a Medical Devices manufacturer, FeMD faces the ever-growing, complex and frequent changes to regulatory and end-client requirements concerning material choices and chemical substance use, responsible sourcing and durability/recyclability which can directly impact product design and drastically affect costs and delivery.
As our new Chemical Compliance Technician, you will be an important member of our Biosafety team, which is part of the larger Product Development Department, consisting of 20 professionals working with Design & Development, Biosafety, Chemical Compliance and Labelling. In this role, you will support and optimize the chemical compliance process, coordinate chemical compliance initiatives, and engage proactively in the implementation of updates to our chemical compliance system. You will be instrumental in supporting the Product Development department and drive and own the chemical compliance process that contribute to the entire team's success. Your primary stakeholders will mostly be your colleagues in the Product Development department, our clinical insights and commercial specialists, quality assurance specialists, suppliers, and operations department. You will also engage with various cross-functional projects related to chemical compliance and it is therefore important that you thrive working in project teams.
Your role
In the role as our new Chemical Compliance Technician, your primary tasks will be to:
- Drive and execute tasks to ensure compliance to chemical regulations, as well as update and maintain such documentation.
- Support the Product Development team with documentation tasks related to chemical compliance of Class III medical devices and gain insights into the complexities of the medical device industry.
- Coordinate Chemical compliance initiatives with external stakeholder such as suppliers.
- Acting as the lead for the development of a new chemical database, in cooperation with internal stakeholders; and supporting colleagues by maintaining in the chemical compliance system during life-cycle management.
- Managing cases regarding chemical compliance such as CLP-regulation and REACH and ensuring that documents such as declarations and statements meet the legal requirements.
- Collaborate with different departments and maintain a high level of communication.
- Project collaboration in a cross-functional setting.
About you
You have a natural flair for working independently and you have an eye for detail in your work. Your entry to this job does not depend on a specific education – relevant practical experience can be sufficient.
Line of study is not as important as the interest in chemical compliance and product safety is. You will probably meet some of the below requirements:
- Self-driven and outgoing with a positive, can-do attitude.
- The ability to work independently and thoroughly, with a high-quality mindset.
- Deep understanding of chemical regulations e.g., ability to identify chemicals listed in different regulations such as CLP regulation, REACH, California Proposition 65, etc.
- Ability to manage relations with external stakeholders i.e., suppliers.
- Structured mindset, with a keen eye for details.
- Possibly experience with managing chemical compliance system.
- Excellent communication skills, both written and verbal, Danish and English.
- Familiarity with Office SharePoint & SAP is a plus.
- Experience with GMP/GDP in the pharmaceutical or medical device industry is an advantage.
Don’t meet every single requirement? If you are excited about this role, but you cannot meet all requirements, we encourage you to apply for the role anyway. You may be just the right candidate for this role.
We offer a truly purpose driven workplace where you can have real impact
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun 😊
Some of the facts and a little piece of history
Ferrosan Medical Devices develops and produces a portfolio of medical devices used in surgical care. Our portfolio consists of various hemostatic products to minimize bleeding challenges in surgery and electromechanical medical devices to perform breast biopsies. We are an international company with products registered in more than 100 countries. Our products are marketed in collaboration with global medtech partners. New ideas are developed and matured from the first thought to finished implementation in production. And we manage the business with an uncompromising focus on quality based on current GMP requirements.
Want to join our team?
Send your application along with your CV latest on August 31, 2024. We will process the applications as we receive them.
Questions? Please do not hesitate to contact us:
Katja Hvid Hinna
Manager, Biosafety & Labelling
+45 25 44 83 45
We look forward to hearing from you.
Read more about us here
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 6.7.2024, 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.
- Øvrige
- Søborg
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