Quality Auditor at Theramex
London SW1H, , United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

03 Oct, 25

Salary

0.0

Posted On

04 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Root, Cross Functional Relationships, Regulated Industry, Auditing, Communication Skills

Industry

Pharmaceuticals

Description

WHY JOIN US?

Be part of a dynamic team at Theramex, where you’ll have the opportunity to make a significant impact on women’s health. We offer:

  • A fast-paced environment, with broad exposure, where you can develop professionally – even outside your area of expertise.
  • We support you as you grow and learn, and we love to celebrate success and recognize performance.
  • We provide opportunities for driven and talented professionals who want to be part of our exciting journey.

SKILLS / QUALIFICATIONS:

  • Experience in a quality function within the pharmaceutical or a regulated industry.
  • Proven experience in auditing and root cause analysis.
  • Strong attention to detail and organizational skills.
  • Excellent interpersonal, verbal, and written communication skills.
  • Ability to build strong cross-functional relationships.
  • A degree or equivalent in a life science subject is desirable.
Responsibilities

ABOUT THE ROLE:

As a Quality Auditor at Theramex, based in London, you will be responsible for managing and executing the self-inspection program across multiple departments and global affiliates. You will lead audits, support continuous improvement initiatives, and coordinate external audits with suppliers, customers, and regulatory authorities.

KEY RESPONSIBILITIES:

  • Manage and maintain the Theramex self-inspection schedule and process.
  • Plan and conduct self-inspections across various departments including QA, Compliance, Medical Affairs, Pharmacovigilance, Regulatory Affairs, IT, HR and more.
  • Facilitate root cause analysis and CAPA identification for non-conformances.
  • Support hosting of audits by customers and regulatory authorities.
  • Notify relevant partners of critical inspection findings.
  • Maintain auditor approval records.
  • Coordinate external supplier audit schedules and risk assessments.
  • Provide support to the wider QMS team, including mailbox management and complaint logging.
  • Stay current with regulatory updates and support implementation.
  • Confirm completion of actions and CAPAs with supporting evidence.
  • Occasional international travel (2–3 trips per year) to local Theramex affiliates.
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