Life Science jobs in United Kingdom
Regulatory Affairs Manager
Kindeva Drug Delivery Company
Solution Design Associate Director
Novartis Farmacéutica
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PM Group
Pediatric / Neuromuscular Neurology Physician
Medpace Inc.
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Tétris SA
QC Scientist – IVD qPCR Manufacturing & Compliance
TRUPCR Europe Ltd
Analyst / Associate – Real Estate
Hanningrecruitment
Strategic Cost Manager — Life Sciences Projects (UK/EU)
Arcadis
Field Service Engineer – Lab Instruments (Remote Options)
Sartorius
Investment Banker, EMEA Healthcare Coverage, Associate
LGBT Great
Senior Project Manager
Morgan Sindall Group Plc
Mechanical Design Engineer - Life Science Instruments
The Technical Partnership
Manager, Clinical Monitoring (English And French Speaking) - Clinical Trial Services
Thepharmadaily LLP
Senior Project Cost Manager - Life Sciences Facilities
Arcadis
CSV Auditor
Job summary
A leading clinical research organization is seeking CSV Auditors to join their consultant network. Candidates will conduct audits, ensure compliance with regulations, and collaborate with client teams. The ideal candidate has at least 10 years of Quality Assurance experience and 5 years in auditing. This role is open to candidates in the EU region.
Qualifications
- Minimum 10 years of experience in Quality Assurance and/or GxP in life sciences.
- Minimum 5 years of experience in Quality Assurance auditing.
Responsibilities
- Conduct Computer System Validation (CSV) audits for life science clients.
- Assess compliance with GxP regulations and client requirements.
- Develop audit reports and provide recommendations.
- Collaborate with client teams to ensure remediation actions are implemented.
Skills
At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact.
Our people--both employees and consultants—are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.
Advarra is seeking CSV Auditors to join our consultant network for EU-based projects. Auditors ensure compliance with GxP regulations and provide expertise across clinical, laboratory, and manufacturing systems.
- Conduct Computer System Validation (CSV) audits for life science clients.
- Assess compliance with GxP regulations and client requirements.
- Develop audit reports and provide recommendations.
- Collaborate with client teams to ensure remediation actions are implemented.
This evergreen role is open to candidates based in the EU region.
- Minimum ten (10) years of Quality Assurance and/or GxP experience in life sciences.
- Minimum five (5) years of Quality Assurance auditing experience.
- Strong interpersonal and client interaction skills.
- Excellent verbal and written communication in English.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.