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Regulatory Affairs Specialist

2 months ago

Edinburgh, Edinburgh, United Kingdom Cpl Life Sciences Full time £35,000 - £40,000
Job Title: Senior Regulatory Compliance Officer - IVDs

Job Type: 12 month fixed term contract

Location: Outskirts of Edinburgh (Hybrid)

About the Role:

We are seeking a highly skilled and experienced Regulatory Affairs Specialist to join our growing Regulatory Affairs Department at Cpl Life Sciences. As a Senior Regulatory Compliance Officer, you will be responsible for delivering end-to-end regulatory packages under the ODM-Distributor scheme in compliance with established quality management systems.

Key Responsibilities:

  • Deliver end-to-end regulatory packages under the ODM-Distributor scheme in compliance with established quality management systems.
  • Oversee the initial compilation of design control evidences, supplier management, incoming inspection and product release process, product submission, post-market surveillance, vigilance, and associated reporting.
  • Maintain product and site regulatory & quality compliance to maintain license/registration once granted.
  • Prepare and compile regulatory documentation, coordinate and execute regulatory submission in compliance with ISO13485, IVD 2017/746 Regulation, FDA 21 Code of Federal Regulations (CFRs), Medical Device Approvals (510(k)), and other country requirements as appropriate.
  • Advise staff and project team members on data and information required for successful license applications and coordinate their efforts to ensure that their contributions to regulatory applications are produced to an appropriate standard for submission.
  • Ensure Quality Assurance release of incoming goods, intermediate, and final product obligations.
  • Be a point of contact for regulatory & quality compliance issues.
  • Interface with Competent Authorities for reporting incidents, and field safety actions, including FSCA, FSN, recalls, MDRs (medical device reporting).
  • Support QMS organization during regulatory inspections or certifications audits.
  • Conduct all duties in compliance with company Quality Management System and cGMP, GCP and ISO13485 requirements.

Requirements:

  • Master's degree or equivalent in life sciences and 3/5 years of experience in a regulatory/quality role.
  • Level required in the function (e.g.: validation, finance, quality control)
  • Experience in the medical device / IVD / biotech industry
  • Specific technical competencies required for the role (e.g.: GMP, GLP exposure, FDA exposure, IT packages, technical writing skills)
  • Significant specialist knowledge of regulation as applied to medical devices, in vitro diagnostic medical devices, or Biologics (93/42/EC, 98/79/EC directives, 510(k), PMA, CMDR, etc..)

What We Offer:

We offer a competitive salary and benefits package, as well as opportunities for professional growth and development in a dynamic and supportive team environment.