Senior QA Specialist
Søborg
We are expanding our QA Organisation, and we are looking for a new colleague that is passionate about quality and production of Medical Devices. We are a team of dedicated QA Specialists and technicians who support our Production and ensure compliance in our documentation.
At Ferrosan, we make a difference in the surgical care area, we are ready to invest in you and will support your development and help you grow your own skills. Every 2nd second, Ferrosan Medical Devices’ products help surgeons and nurses control bleedings and avoid complications in surgical procedures. Our products make seconds count in surgical care - and we need you on our team to continue our successfully journey.
Our team
You will be part of our QA Operations Support Team. We participate in all aspects of support to our production e.g., handling of non-conformities, qualification and validation of utilities and equipment and product release. Furthermore, we participate in projects both as quality and compliance experts as well as ensure that our documentation complies with the requirements for Class III Medical Devices.
Our team consists of 8 QA Specialists and technicians with broad knowledge about quality requirements for Medical Devices. You will refer to the Senior Manager for QA Operations Support.
Your role
As a Senior QA Specialist, you will impact the daily production of our products – the heart of our company. You will
In this role, you will be in contact with a great part of our organization and your main stakeholders will be our colleagues in our Production.
About you
You have a proven track record from working within QA. You have knowledge about ISO 13485, MDR and preferably the requirements covered by MDSAP. As our products are based on raw material from animal origin and are used at the operating theatre, experience working with Class III products is an advantage.
You are a strong communicator with good analytical skills. You thrive in a dynamic workplace, practice go look see / go to gemba, and like to improve and align work processes. You are oriented towards reaching results and aiming to keep deadlines with high level of quality and compliance.
In short, you bring:
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?
Apply for the position by submitting your CV including your motivation no later than July 31, 2024. We will process applications on an ongoing basis, so don’t wait too long. The job ad will be reposted until the position is filled.
If you have any questions, please do not hesitate to contact:
Anne Mette Wolsing
Senior Manager, QA Operations Support
+
At Ferrosan, we make a difference in the surgical care area, we are ready to invest in you and will support your development and help you grow your own skills. Every 2nd second, Ferrosan Medical Devices’ products help surgeons and nurses control bleedings and avoid complications in surgical procedures. Our products make seconds count in surgical care - and we need you on our team to continue our successfully journey.
Our team
You will be part of our QA Operations Support Team. We participate in all aspects of support to our production e.g., handling of non-conformities, qualification and validation of utilities and equipment and product release. Furthermore, we participate in projects both as quality and compliance experts as well as ensure that our documentation complies with the requirements for Class III Medical Devices.
Our team consists of 8 QA Specialists and technicians with broad knowledge about quality requirements for Medical Devices. You will refer to the Senior Manager for QA Operations Support.
Your role
As a Senior QA Specialist, you will impact the daily production of our products – the heart of our company. You will
- Participate in qualification and validation projects ensuring that our validation activities are completed on time and in the right quality as a subject matter expert (SME) and as an approver of documentation.
- Review and approve change controls, non-conformities, CAPAs, complaints and SOPs.
- Be a good and constructive sparring partner for the organisation regarding quality related matters, train colleagues in QA processes, maintain QA process and drive a Quality Mindset.
In this role, you will be in contact with a great part of our organization and your main stakeholders will be our colleagues in our Production.
About you
You have a proven track record from working within QA. You have knowledge about ISO 13485, MDR and preferably the requirements covered by MDSAP. As our products are based on raw material from animal origin and are used at the operating theatre, experience working with Class III products is an advantage.
You are a strong communicator with good analytical skills. You thrive in a dynamic workplace, practice go look see / go to gemba, and like to improve and align work processes. You are oriented towards reaching results and aiming to keep deadlines with high level of quality and compliance.
In short, you bring:
- A master’s degree within pharmacy, biology, engineering, chemistry or similar
- More than 5 years of QA experience within the Medical Device industry
- Experience within qualification and validation of equipment and processes.
- Statistical skills for qualification and validation.
- Experience with CAPA, change control and complaints.
- Fluency in Danish and English, written and verbally.
- Quality, improvement - and a want-to-succeed-together mindset.
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?
Apply for the position by submitting your CV including your motivation no later than July 31, 2024. We will process applications on an ongoing basis, so don’t wait too long. The job ad will be reposted until the position is filled.
If you have any questions, please do not hesitate to contact:
Anne Mette Wolsing
Senior Manager, QA Operations Support
+
Information og data
Denne ledige stilling har jobtypen "Produktspecialist", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- 25.06.2024
- Produktspecialist
- Søborg