Quality Assurance (QA) Manager to Inossia AB
QriosOm tjänsten
Inossia is now recruiting a Quality Assurance (QA) Manager to the company. The position is full-time and based in our
headquartered office in Stockholm and we are looking for a new colleague to join the team at Inossia.
Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life. Inossia® provides
vertebral augmentation solutions that have been adapted to the mechanical properties of bone that will give Better fracture
treatment for Osteporotic Bone. The company is entering a pivotal phase of its growth, with the upcoming launch of its first
product and the transition from development to commercial operations. While moving toward market introduction, the company remains
committed to ongoing research and development to advance solutions in spine care
As a QA Manager, you will be responsible for managing our QMS and overseeing product releases. You will lead training on new SOPs
and collaborate closely with our Production Manager to ensure accurate and compliant documentation. Additionally, your
responsibilities will include preparing the organization for audits and conducting supplier audits.
At Inossia, you will get the unique opportunity to build, shape and optimize our processes from the inside out, make a positive
impact and apply your experience and expertise within QA to ensure the highest quality standards. If this sounds interesting to
you - Come join us and be part of our mission of improving fracture treatment for osteoporotic patients so that they can live an
active life.
We will interview candidates continuously and welcome your application today!
RESPONSIBILITIES
The QA Manager will have a central role in oversight and management of manufacturing and analytical activities from a quality
perspective. You will report directly to the Director of QA/RA at Inossia.
Your main responsibilities will include:
- Lead, maintain, and continuously improve the Quality Management System in accordance with ISO 13485 and applicable medical
device regulations
- Ensure compliance throughout the medical device product lifecycle, from development and design through manufacturing, release,
and post-market activities
YOUR PROFILE
Key Qualifications for the position include:
We are looking for someone with a can-do attitude, strong organizational skills and a quality-driven mindset. You enjoy taking
ownership and accountability to drive continuous improvement of the quality system and work well both independently and in team
settings. You can handle multiple tasks and manage priorities in a timely manner and have excellent collaboration and
communication skills. You are analytical, detail- and result-oriented and can effectively combine flexibility with a strong
decision-making ability. Importantly, you enjoy a dynamic place of work where people matter, and your contributions will make a
positive impact.
If you are passionate about making a difference in the lives of patients and have the skills and experience to excel in this role,
we invite you to apply today!
ABOUT INOSSIA AB
Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life.
Inossia is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from
development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research
and development to advance solutions in spine care
To learn more, please visit www.Inossia.com
FOR MORE INFORMATION ABOUT THE POSITION, PLEASE CONTACT:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: +46 (0)72-070 16 53
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