Remote opportunity at
ERGOMEDPharmacovigilance Auditor - Freelance Position (1FTE or 0.6 FTE and above)- remote in Spain
ADAMAS Consulting, part of the Ergomed Group, seeks a freelance Pharmacovigilance Auditor to execute audits throughout Europe. This freelance position is available at either full-time or…
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About This Role
ADAMAS Consulting, part of the Ergomed Group, seeks a freelance Pharmacovigilance Auditor to execute audits throughout Europe. This freelance position is available at either full-time or part-time capacity, specifically 0.6 FTE and above, with a remote working arrangement based in Spain. ADAMAS partners with biotechnology and pharmaceutical organizations to maintain rigorous standards in quality assurance, compliance, and patient safety. This role suits independent professionals who possess deep expertise in regulatory…
Job Description
ADAMAS Consulting, part of the Ergomed Group, seeks a freelance Pharmacovigilance Auditor to execute audits throughout Europe. This freelance position is available at either full-time or part-time capacity, specifically 0.6 FTE and above, with a remote working arrangement based in Spain. ADAMAS partners with biotechnology and pharmaceutical organizations to maintain rigorous standards in quality assurance, compliance, and patient safety.
This role suits independent professionals who possess deep expertise in regulatory standards and wish to help life sciences clients identify compliance risks. The selected auditor will handle the end-to-end audit lifecycle, ranging from initial preparation and planning to conduct, reporting, and follow-up activities such as CAPA plans. Additionally, the practitioner will execute Good Pharmacovigilance Practice quality assurance initiatives for industry clients.
Candidates must be capable of traveling up to 40 percent of the time and conducting remote audits as needed. Joining the Ergomed network places professionals among an expert team dedicated to advancing safe pharmaceutical treatments while upholding core values focused on quality, integrity, collaboration, and responsiveness.
Responsibilities
- Plan, prepare, conduct, report, and follow up on various Pharmacovigilance audits, including managing CAPA plans, within established timelines and quality standards
- Execute audits while demonstrating a thorough grasp of regulatory requirements and Good Pharmacovigilance Practice
- Carry out Good Pharmacovigilance Practice quality assurance projects for biotechnology and pharmaceutical client companies
- Conduct remote audits and travel up to 40 percent of the time
Requirements
- Experience in conducting and leading both internal and external Pharmacovigilance audits for multiple stakeholders
- Expert knowledge regarding national and international Pharmacovigilance legislation and guidelines
- Proficiency in project management to ensure timely delivery of work
- Ability to identify problems and deliver pragmatic solutions
Qualifications
- Bachelor Degree in Life Sciences is preferred
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, this role is remote in Spain, though it requires the ability to conduct remote audits and travel up to 40 percent of the time.
What is the employment type and schedule?
It is a freelance position offered on a full-time basis or part-time at 0.6 FTE and above.
What salary does this role offer?
The source posting does not specify the salary for this position.
What are the main duties of the Pharmacovigilance Auditor?
The auditor is responsible for planning, preparing, conducting, reporting, and following up on various Pharmacovigilance audits and CAPA plans, as well as performing GVP quality assurance projects for clients.
Sample Interview Questions
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