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- Germany
- Posted 16 days ago
QA/RA – Manager (SaMD) Tasks: · Responsibility for international approvals/registrations of our software and medical devices including the coordination of the preparation and compilation of the required documents. · Assessment of the conformity of the documentation with the appli...
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- Posted 16 days ago
Head of Department (m/f/d) Regulatory Affairs Your tasks: · You will take over the management of the Regulatory Affairs department and coordinate the approval of medical devices under MDR while adhering to the agreed deadlines · You lead the employees of the Regulatory Affairs de...
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- Posted 16 days ago
Cloud Engineer (m/w/d) Your tasks: · Project management of software development projects in medical technology · Operation and further development of our development infrastructure (CI/CD-Pipelines for Java and AI) · Carrying out risk management according to ISO 14971 for S...
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- Chester
- Posted 16 days ago
Location:UK Salary:46,000-56,000 Qualifications: Bachelor's degree in a relevant field (e.g., Business, Engineering, Information Technology) or equivalent work experience. Minimum of 4 years of experience in project management, with a proven track record of successfully delivering projects on ...
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- Massachusetts
- Posted 16 days ago
Overview: We are seeking a highly skilled and experienced Vice President of Quality Assurance specializing in In Vitro Diagnostics (IVD) consultancy services. This role will lead our quality assurance efforts for IVD products and provide strategic guidance to our clients in the IVD industry. R...
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- Chester
- Posted 16 days ago
We are a leading Life Science Recruitment Company seeking a Senior Scientific Services Team Lead on behalf of our client, a highly reputable medical communication company. The successful candidate will be responsible for leading a team of scientific services professionals to deliver high-quality ...
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- Chester
- Posted 16 days ago
Location:UK Salary:60,000-68,000 Qualifications: Ph.D. or equivalent advanced degree in a relevant scientific field (e.g., Biology, Chemistry, Pharmacology, or a related discipline). Minimum of 4 years of experience in scientific research and project management, preferably in the pharmaceutical...
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- Posted 16 days ago
Melio Life Science are partnered with a leading mid-size medical device company specializing in respiratory solutions, is dedicated to delivering high-quality healthcare products. They are seeking an experienced and detail-oriented Supplier Quality Engineer to join their growing team! Position...
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- City of London
- Competitive
- Posted 16 days ago
Our client is looking for an experienced and dedicated Quality Manager Associate to join their team in London & Greater London.
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- Massachusetts
- Posted 16 days ago
Overview: We’re seeking a detail-oriented Quality Assurance Specialist to ensure the quality and compliance of our medical devices. The ideal candidate will be responsible for conducting tests, analyzing results, and implementing quality processes to uphold the reliability and safety of our produ...
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- Massachusetts
- Posted 16 days ago
Overview: We’re looking for an experienced Senior Quality Engineer to lead our quality assurance efforts in the development and manufacturing of medical devices. The ideal candidate will play a key role in ensuring compliance with regulations, driving process improvements, and maintaining the hi...
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- City of London
- Competitive
- Posted 16 days ago
Our client is looking for an experienced and dedicated experienced Head of Quality to join their team in London & Greater London.
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- Slough
- Posted 16 days ago
Our client, a leading life sciences company, is seeking a talented Regulatory Affairs Manager to join their team in Slough. This is a unique opportunity that allows for flexibility in working arrangements, with a combination of remote and on-site work. Responsibilities: Develop and implement r...
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- Massachusetts
- Posted 16 days ago
Melio Life Science has partnered with a leading innovator in the medical device industry, committed to advancing healthcare through cutting-edge technologies. They are seeking a highly skilled and experienced Senior Regulatory Manager to join their dynamic team. Overview The successful candidate ...
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- Posted 16 days ago
Head of Regulatory Affairs Your tasks: · Technical and disciplinary management of employees in the Regulatory Affairs EU/EMEA group · Ensuring compliance with MDR requirements for product certification and re-certification, registration, and re-registration of medical devices · ...
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- United States of America
- Posted 16 days ago
Melio Life Science is partnered with a leading mid-sized medical device company specialising in the manufacturing of catheters. Recently acquiring an office in Europe, they are looking for a Regulatory Affairs Manager to join their team. Position Overview: They are seeking a highly skilled and...
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- Massachusetts
- Posted 16 days ago
Melio Life Science have partnered with a leading mid-size medical device company who are seeking an experienced and highly skilled Principal Quality Engineer to join their dynamic team. Overview: As a key member of their Quality Assurance department, you will play a crucial role in ensuring...
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- Massachusetts
- Posted 16 days ago
Overview: We are seeking a highly skilled and experienced professional to join our team as the Director of Quality Affairs. Headquartered in Massachusetts, we are committed to developing innovative and life-changing medical devices that meet the highest standards of quality and compliance. Respo...
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- Illinois
- Posted 16 days ago
Job Title: Associate Director, Quality Assurance and Regulatory Affairs Location: Illinois (Hybrid) Melio Life Science is partnered with a leading FDA approved medical device company specialising in cardiology. Overview: They are seeking an experienced Associate Director of Quality Assuran...