Position: Product Certification Auditor (AMR – Antimicrobial Resistance)
Location: Spain, Ireland, UK, Germany, Italy, Netherlands
Salary: Competitive basic salary based on experience
Essential Responsibilities
- Prepare assessment reports and deliver findings to clients to ensure client understanding of the assessment decision and clear direction to particular items of corrective action where appropriate
- Recommend the issue, re‑issue or withdrawal of certificates, and report recommendations in accordance with BSI policy, procedures and prescribed time frame.
- Maintain overall account responsibility and accountability for nominated accounts to ensure an effective partnership, whilst ensuring excellent service delivery and account growth.
- Plan/schedule workloads to make best use of own time and maximise revenue‑earning activity.
- Must be willing to go through extensive onboarding plan in order to reach Lead Assessor status through the prescribed program (based on the knowledge, skills and experience they have as well as the requirements of the appropriate schemes)
- Must be able to demonstrate knowledge and skills, to include preparation for and taking standardised assessments related to knowledge and application of audit practices
- Responsible for managing a portfolio of assigned clients based on location and a match of qualifications and client contract requirements
- Responsible for contacting clients and scheduling the visits, planning the assessments, making travel plans, conducting the assessments and reporting and managing the results in an efficient manner.
- This is a field based position that requires regular international travel, primarily within Europe.
Candidate Requirements
- Minimum 2 years of relevant industry experience in the Pharmaceutical, Chemical, Biotechnology, or similar regulated sectors. (Essential)
- Additional professional qualifications such as PSCI‑HSE or PSCI Supplier Audit Training – EHS are highly desirable
- ISO 14001 auditing knowledge. Lead Auditor Certification is highly desirable
- Experience may include:
- Direct operational or technical work within these industries.
- Auditing activities carried out within these sectors.
- Candidates should ideally have exposure to one or more of the following functions:
- Manufacturing / Production
- Quality Control (QC) / Quality Assurance (QA)
- Environment, Health & Safety (EHS)
- Regulatory Affairs
We emphasize a solid understanding of end‑to‑end pharmaceutical manufacturing processes including waste management systems, controls, and compliance requirements.
Benefits
BSI offers a competitive total reward package, an independent and varied job in an international environment, versátil working hours, ongoing training, and development with a generous benefits package and annual bonus.
Equal Opportunity Employer
BSI is an Equal Opportunity Employer dedicated to fostering a diverse and inclusive workplace.
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