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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 the leading MedTech service provider with the world’s largest global team of regulatory and quality experts. Building upon 40 years of regulatory expertise, we also provide comprehensive clinical trial, lab and reimbursement services – reducing risk and supporting market access throughout the entire product lifecycle for medical devices, digital therapeutics and diagnostics. With more former FDA, Medicines and Healthcare Products Regulatory Agency (MHRA) and notified body regulators than any other firm, the RQM+ team has deep expertise in all clinical specialties. RQM+ currently works for 19 of the top 20 medical device manufacturers and seven of the top 10 IVD companies.
See more RQM+ offers

Job description

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Your missions

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):
Check out the description to know which languages are mandatory.

Hard Skills

Medical LaboratoryClinical TrialsAuditingMedical WritingRegulatory Affairs

Soft Skills

  • Quality Assurance
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