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RQM+ General Application Form

Remote: 
Full Remote
Contract: 
Full time
Work from: 
Europe

Offer summary

Qualifications:

Background in Regulatory Affairs, Quality Assurance, Clinical Trials, Auditing, Medical Writing, or Laboratory services..
RQM+ logo
RQM+ SME https://www.rqmplus.com/
501 - 1000 Employees
About RQM+
RQM+ is a global MedTech service provider accelerating compliance and market success. Through our unparalleled expertise and industry knowledge, we deliver specialized solutions and expedite the journey along the full product lifecycle for Med Device and IVD companies, from concept to commercialization to post-market. Our portfolio of services enables the delivery of end-to-end solutions across the complete med device product lifecycle, with our:​ + Regulatory and Quality Consulting​ + Lab Services (Jordi Labs)​ + Clinical Trials​ + Reimbursement​ + Technology Solutions​
See more RQM+ offers

Job description

RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to promote economic growth through regional partnerships, provide a rewarding place to work, and improve our communities.
 
We are always interested in speaking to expert personnel with backgrounds in either Regulatory Affairs, Quality Assurance, Clinical Trials, Auditing, Medical Writing and Laboratory services.

Required profile

Experience

Spoken language(s):
English
Check out the description to know which languages are mandatory.

Hard Skills

Clinical TrialsMedical LaboratoryAuditingMedical WritingRegulatory Affairs

Other Skills

  • Quality Assurance
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