Senior Medical Writer I at Langland
belfast, Belfast, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

24 Jan, 27

Salary

60000.0

Posted On

26 Oct, 26

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Pharmaceutical Manufacturing

Description

bout the job

Regulatory Compliance SpecialistBiotechnology | Biobanking | Remote UK

We are seeking a Regulatory Compliance Specialist to support international biospecimen procurement and biobanking operations, ensuring ethical sourcing, regulatory compliance and robust quality standards across a global vendor network.

  • Key ResponsibilitiesMonitor international regulations governing human biological materials, biobanking and cross border transport.
  • Conduct remote vendor audits, compliance reviews and supplier qualification.
  • Review vendor licences, accreditations, informed consent forms and IRB/IEC approvals.
  • Assess regulatory and ethical risks associated with biospecimen sourcing.
  • Develop, review and maintain SOPs, compliance checklists and quality documentation.
  • Support eQMS/document control and CAPA tracking.


  • RequirementsBachelor’s or Master’s degree in Life Sciences, Biotechnology or a related discipline.
  • 5+ years’ experience in Regulatory Affairs, QA or Compliance within biotech, pharma, CRO or biobanking.
  • Knowledge of GCP/GCLP, ISO 20387, GDPR/HIPAA and human sample ethics.
  • Experience with vendor audits, informed consent documentation and SOP development.
  • Familiarity with eQMS platforms; Cognidox experience is an advantage.
  • Excellent written and spoken English, strong attention to detail and independent working skills.


  • What’s OfferedFully remote working.
  • Competitive compensation.
  • Professional development opportunities.
  • Collaboration with an international team supporting biomedical research and diagnostics.



Responsibilities
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