Lead Auditor
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Søborg
Lead Auditor to drive our Audit team
Do you want to be a part of a dedicated team of auditors 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. As our new Auditor you will lead our internal and CMO / Supplier audit programs.
Every 3rd 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!
Lead our internal and supplier audit program
We cover it all in our QA department; we ensure quality across the entire company - from product development to market release. In close cooperation with your 15 dedicated colleagues, counting both QA specialists and technicians, you are involved in daily operations, supporting development projects and securing compliance at suppliers and manufacturers.
You can expect a warm welcome, we are helpful, and we have a team spirit focused on having a good time while creating the best results together.
Your role
As our auditor, you will be responsible for planning and executing audits as lead auditor and potential follow-ups. You enjoy - and have previous experience - orchestrating all phases of our internal and supplier audits of our CMOs and suppliers, from planning to execution and follow-ups. A task you set your personal mark on. Additionally, you
- Ensure quality supplier management
- Optimise our quality management system based on your audit activities
- Secure qualified suppliers in various product development projects
About you
You are a strong communicator and have excellent business acumen and situational awareness. You thrive leading audits with a natural authority, and you manage stakeholders such as our suppliers and department managers with ease.
You are structured and plan large aspects of the audit planning on your own, which requires you to appreciate the responsibility and understand how to effectively manage your tasks. You have strong analytical skills and apply these persistently and vigorously in audit situations. You are oriented towards reaching results and aiming to keep deadlines with high level of quality and compliance. You set directions for the auditor teams and secure that new requirements are incorporated in the audit plan.
Furthermore, you bring:
- Experience as an auditor within a medical device or pharmaceutical company
- A master’s degree within pharmacy, biology, engineering, chemistry or similar
- Experience in working with supplier management
- Experience with ISO 13485 and 21 CFR Part 820 as well as knowledge of the requirements for complying
- Experience with MDSAP audits
- Fluency in Danish and English, written and verbally
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 haemostatic 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 24 January 2023. We will process the applications as we receive them.
Questions? Please do not hesitate to contact Director of QA, Hans Georg Madsen, on +45 22 89 27 72.
We look forward to hearing from you.
Read more about us here
Information og data
Denne ledige stilling har jobtypen "Regnskabsmedarbejder", og befinder sig i kategorien "Økonomi og jura".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 21.12.2022, 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.
- Regnskabsmedarbejder
- Søborg
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