Medicon Village

Quality Engineer

Apply here: LinkedIn

Do you want to be part of our journey of restoring health to improve the quality of life for patients with bone disorders? BONESUPPORT is looking for a Quality Engineer to support us for a time-limited (1 year) assignment. We are looking for you who want to contribute with your experience and expertise in a fast-growing company with extraordinary products, that make a real difference for people.

Become part of our team!

As a Quality Engineer at BONESUPPORT, you will pay a key role in ensuring that the products that reach the market has gone through rigorous quality assurance, meeting strict quality, safety and regulatory standards. As part of the Global Operations team, you will work in close collaboration with Quality Management, Research & development, contract manufacturers and suppliers. Your mission is to ensure that all processes remain stable, secure, and documented to the highest industry standards.

You will join our dedicated Global Operations team in Lund that manages the entire supply chain, from procurement and production planning to final approval. The team is characterized by a high level of expertise, a supportive atmosphere and a strong sense of community. Working closely with your peers, you will ensure a smooth flow of information and contribute to the positive, collaborative team spirit.

Your key tasks will include:

  • Quality Operations: Review batch documentation and manage deviations, CAPAs, and Change Orders. You investigate technical issues in production and help find sustainable, long-term solutions.
  • Project work: related to improving and/or sustaining our processes and tools, which could for example include supporting the development of our manufacturing process risk process, and implementing new tools to streamline our quality assurance process.

You are offered

  • A stimulating workplace supporting our company growth agenda, where you are challenged and developed daily.
  • Working with products based on a scientifically trustworthy foundation that truly changes patients' lives.

To succeed in the role, it is expected that you:

  • Are a self-driven, collaborative individual with an analytical mindset, high attention to detail and ability to see patterns and critically assess data
  • Are goal oriented, responsible and assertive in your daily work
  • Have a good ability to find solutions to a variety of problems and challenges
  • Have a flexible mindset and “can do-attitude” with the ability to quickly move between tasks as priorities changes

Further we see that you:

  • Hold an M.Sc. or B.Sc. in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or a similar field.
  • Have previous experience from working with quality or a similar role in a regulated industry (MedTech, Pharma, or similar), where experience in microbiology, sterilization processes, process improvements, process validations and similar are meritorious
  • Are fluent in English and communicates clearly, both written and oral (Swedish fluency is a plus but not a requirement)
  • Have experience working in as well as leading projects, delivering against specific deadlines.
  • Training and experience from writing, executing, and approving documentation

We review applications on an ongoing basis, so we encourage you to apply as soon as possible. The position will remain open until it has been filled.

About BONESUPPORT

BONESUPPORT (Nasdaq Stockholm: BONEX) develops and commercializes innovative injectable bio-ceramic bone graft substitutes that remodel to the patient’s own bone and have the capability of eluting drugs. BONESUPPORT’s bone graft substitutes are based on the patented technology platform CERAMENT. The company is conducting several clinical studies to further demonstrate the clinical and health economic benefits its products deliver. Bonesupport has around 170 employees and almost half of them are based in Lund at the company headquarters.

BONESUPPORT and CERAMENT are registered trademarks of BONESUPPORT AB