Regulatory Compliance Officer (Post Market Surveillance) Job

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Regulatory Compliance Officer (Post Market Surveillance)

Job Posted: a month ago

  • Salary: Competitive

    Job Type: Permanent

  • Location: Edinburgh

Expire in: 3 days

Job Description

Regulatory Compliance Officer (Post Market Surveillance) Location: Edinburgh area - hybrid working Type: Full-time, Permanent, 37.5 hours per week. SRG is working with a leading Biotechnology company based in the Edinburgh area who are looking for a Regulatory affairs officer to join their team on a permanent basis. The regulatory compliance officer is responsible for implementing and maintaining regulatory compliance processes including regulatory evaluation of non-conformances, post market surveillance, vigilance and associated reporting, regulatory and standard watch. The Role: Act as the main contact for regulatory compliance issues Maintain the post market surveillance processes Provide PMS documentation according to IVDR requirements Lead and coordinate the vigilance process in interface with the complaint handling process Interface with Competent Authorities for reporting incidents and field safety actions, including FSCA, FSN, recalls, MDRs (medical device reporting), BPDR (biological products deviation reports) Evaluate product/process non-conformances and determine whether they need to be reported to the Competent Authorities Support QMS organisation during regulatory inspections or certification audits Liaise with regulatory authorities and external contract bodies and, in response to requests from these, to collate and interpret specialised information Contribute to the design and implementation of regulatory processes and identify areas for potential improvement Requirements: Scientific degree Previous regulatory experience within Medical Devices / IVD Experience of working within an FDA licensed manufacturing facility. Specialist knowledge of regulations as applied to medical devices, in vitro diagnostic medical devices, or Biologics (93/42/EC, 98/79/EC directives, 510(k), PMA, BLA, CMDR, etc.) Experience in meeting with and negotiating with regulators Benefits: Private Medical cover Life assurance Additional annual leave Cycle to work scheme + more.Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy
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