We are currently recruiting for a GCP AUDITOR/QA AUDITOR to join our industry-leading client. They are a well-recognised, high performing BIOTECH who have grown exponentially in the last five years. They are looking to further that growth by bringing in an experienced GCP/QA AUDITOR.
A Global CRO is looking for a Junior/Trainee GCP Auditor to join their expanding and successful Quality Assurance team. The role will require a candidate who is clued up on GCP regulations and is capable of Auditing to GCP Standards European wide or ideally Globally. A professional who has conducted audits already will have a significant advantage for this role.
GCP Auditor/Clinical Compliance Auditor/QA Auditor: This is a great opportunity to join a friendly CRO that is currently growing its presence in the UK. You will be carrying out GCP audits both internally and externally to ensure the highest quality and compliance.
I am currently working with one of the biggest and most successful Biopharmaceutical companies in the World to recruit a Senior Clinical Quality Assurance Auditor for a great new position based in New Jersey. The ideal candidate will have a solid GCP Auditing background with good Pharmaceutical/Biopharmaceutical experience. A piece of specific information which is vital is the candidate must have experience working with Metrics and presenting data and metric reports to Senior Management.
My client is currently recruiting for a GCP Compliance Manager. You will be responsible for the compliance and QA activities throughout Europe. This is an excellent opportunity to join a company that offers excellent rewards to its employees as well as a great working environment.
We are looking for professional qualified and enthusiastic candidates to take up a full-time position of a QA/GCP Auditor. A person at this position is responsible for scheduling, planning, conduct, and reporting quality assurance audits of clinical trials and vendor qualification audits. They may also be required to participate in internal systems audits or internal audits of PSI locations.
Office-based in Oxfordshire/Kidlington or home-based UK wide
We are working with a TOP 10 CRO and are a leading organisation with offices in over 20 countries and on-going clinical studies in over 45 countries. They are looking to expand their QA Auditing division in Germany. You will be given the chance to monitor therapeutic areas and from Phase I to Phase IV, conducting auditing visits on a number of large scale studies, as well as being involved in internal audits
A Global CRO is looking for a Junior GCP Auditor to join their expanding and successful Quality Assurance team. The role will require a candidate who is experienced in GCP regulations and is capable of Auditing to GCP Standards European wide or ideally Globally. A professional who has conducted investigator site audits already will have a significant advantage for this role.
I am currently working with a very interesting and expanding CRO who are seeking an experienced Quality Assurance Professionals for a Senior GCP Auditor position, based in Europe. The candidate will ideally be located in Central Europe however experienced candidates across Europe will be considered. The company is looking for a professional with around 3 years GCP Auditing experience and a solid grounding within the pharmaceutical industry.
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