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BSI

Product Certification Auditor (AMR)

BSI

Ireland, England, United Kingdom ・ フルタイム

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経験
2年以上
給料
求人情報
1
投稿済み
3週間前
作業モード
在任中
資格
Professionals with at least 2 years of experience in a regulated industry such as pharmaceuticals, chemicals, biotechnology, or a similar field, and who are willing to undertake extensive onboarding and frequent European travel.
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仕事内容

Role overview

BSI is seeking a Product Certification Auditor focused on antimicrobial resistance (AMR) certification. In this role, you will help uphold product quality and support responsible antibiotic manufacturing practices across the AMR Kitemark scheme. The position is part of a long-established global standards organization that continues to expand its impact across industries and countries.

This is a field-based position with frequent international travel, mainly across Europe. The role is available in Spain, Ireland, the UK, Germany, Italy, and the Netherlands.

Salary is a competitive base package aligned to experience.

What you will do

  • Carry out product assessment audits and present findings to clients in a clear, actionable way.
  • Explain assessment outcomes and recommend corrective actions where needed.
  • Advise on whether certificates should be issued, renewed, or withdrawn, and submit recommendations within BSI policy and timelines.
  • Take responsibility for assigned client accounts and support strong, effective partnerships.
  • Deliver high-quality service while contributing to account development and revenue growth.
  • Organise workloads and schedules to use time efficiently and maximise billable activity.
  • Complete a structured onboarding pathway and work toward Lead Assessor status.
  • Demonstrate the knowledge and skills required for standardised assessments and audit practice evaluations.
  • Manage a portfolio of clients based on geography and contractual fit.
  • Coordinate client contact, plan visits, arrange travel, conduct assessments, and manage reporting and follow-up efficiently.

What we are looking for

  • At least 2 years of relevant experience in the pharmaceutical, chemical, biotechnology, or another regulated sector.
  • Exposure to auditing, operational, or technical work in one or more of these industries.
  • Working knowledge of ISO 14001 auditing; Lead Auditor certification is an advantage.
  • Professional qualifications such as PSCI-HSE or PSCI Supplier Audit Training – EHS are strongly preferred.
  • Experience or familiarity with manufacturing/production, quality control, quality assurance, environment, health and safety, or regulatory affairs.
  • Understanding of end-to-end pharmaceutical manufacturing, including waste management systems, controls, and compliance requirements.
  • Willingness to travel internationally and work in a field-based role.

About the employer

BSI is a global business improvement and standards organisation with a long history of helping organisations perform better, improve safety, and build trust. The company works with clients across many countries and sectors, supporting progress toward a more sustainable and trusted world.

What you can expect

  • Competitive overall reward package.
  • Independent and varied work in an international environment.
  • Flexible working hours.
  • Ongoing training and development.
  • Generous benefits package.
  • Annual bonus.

Additional information

BSI celebrates 125 years of excellence and remains committed to client-centricity, agility, and collaboration. The organisation is dedicated to equal opportunity and to maintaining a diverse and inclusive workplace.

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