|GCP QA Auditor|
International Research & Development based company is currently recruiting for a Quality Auditor Clinical Development. Our client is leader of large programs in oncology, inflammatory and neurodegenerative diseases as well as human and veterinary medicine. It is a wonderful opportunity to work on different projects, work from home and on site in France.
|Senior Global Auditor, GCP, PV and GLP|
Senior Global Auditor, GCP, PV and GLP We are actively looking to recruit an Experienced Senior Global Auditor to join a global leading pharmaceutical company based in the UK. This position will require 40-50% international travel. This is a permanent office based role.
|Clinical Quality Assurance Auditor|
Clinical Quality Assurance Auditor - 18 month Fixed Term
International Research & Development based company is currently recruiting for a Quality Auditor Clinical Development. Our client is leader of large programs in oncology, inflammatory and neurodegenerative diseases as well as human and veterinary medicine. It is a wonderful opportunity work for a dynamic company as a home-based freelancer in France.
|Freelance GCP Auditor- French Speaking|
Freelance GCP Auditor- French Speaking
A growing Pharma company are currently seeking a short term contractor to lead and carry out a number of audits over the coming months. Working largely across France, you should have a strong Clinical Auditing and CQA background and speak fluent English and French.
|GCP Auditor- International Role|
GCP Auditor- International Role
A leading Pharmaceutical company in Germany are recruiting for a GCP Auditor to work internationally on a number of high level and interesting clinical studies. Across different Therapeutic areas, this is a company and position who will progress your career and continue to provide you with strong exposure within the industry.
|QA Auditor - Pharmaceutical|
QA Auditor - Pharmaceutical
6 month FTC
|Home-Based - International Senior GCP Auditor/QA Auditor â€“ CRO |
We are currently recruiting for a Senior GCP Auditor to join our top 10 global CRO. You will be responsible for the full life cycle of audits from planning audits through to hosting them. This role will require carrying out vendor/system/facility/investigative audits across many therapeutic areas. This role also involves much travelling across Europe.
My client is looking for a home-based pharmacovigliance auditor to join an expanding team, with offices based in the South East of England. You will conduct audits at the site of clients to ensure compliance with all pharmacovigilance regulations. You will be expecting to partake in ongoing training as required, and maintain a clear understanding of UK, EU and international regulatory requirements.
|GCP QA Auditor - Consultant|
In this position you will be responsible for planning, conducting and auditing various Life Science organisations across the globe - the position is based in Berkshire, but you will need to be prepared to travel. In order to be considered for this position you will have extensive experience in conducting GCP Audits, Investigator Site Audits, CRO and Vendor Audits. You will also have excellent experience within working to SOPs in a highly regulated environment.
|GMP QA Auditor|
In this role you will be responsible for performing the activities related to Supplier Quality. Ensure an economical operation and performance in accordance with established Global Quality, and regional requirements in Europe, Middle East and Africa. You will make recommendations to be implements post audit, and highlight procedural areas for improvement.
|GCP Auditor - Cambridge|
GCP Auditor needed in Cambridge
|Senior GCP Auditor - Switzerland - Excellent Salary, Bonus + Relocation Packages|
I am currently working with a market leader in the Pharmaceutical industry who are active in seeking a Senior GCP professional to join their team. This company is currently experiencing some fantastic growth and the pipeline for the next few years is truly staggering. The ideal candidate will have extensive auditing experience, including investigator site, vendor and process audits. The company will offer full relocation to candidates from outside of Switzerland.
|GMP Auditor-Theorem Clinical Research-Bad Soden|
GMP Auditor-Bad Soden-Theorem Clinical Research
|Quality Assurance GMP Auditor |
A leading pharmaceutical company with a strong pipeline, known for attracting & retaining the brightest individuals currently has an exciting opportunity for a Quality GMP Auditor. This role is an initial office based 6 month extend-able contract in my clients cutting edge manufacturing site in leafy Hertfordshire.
|QA Auditor/GMP Auditor/Quality Assurance Auditor â€“ Leading Pharma â€“ North West England|
QA Auditor/GMP Auditor/Quality Assurance Auditor â€“ Leading Pharma â€“ North West England We are currently recruiting for an experienced GMP Auditor/QA Auditor. This role will be to join our global and reputable BioPharmaceutical with an extensive product portfolio and who work across multiple therapeutic areas.
|Clinical Quality Auditor Cambridge|
Cambridge, London, England
Clinical Quality Auditor Cambridge
|GCP Auditor/Manager UK-London/Scotland|
London, Scotland, England
London or Scotland based GCP Auditor/Manager
|Senior Clinical Quality Assurance Auditor - Switzerland|
I am working with one of, if not THE, top Biopharmaceutical companies globally, to recruit another Senior GCP Auditor for the team based in Switzerland. The ideal candidate for the role will have 10 years industry experience and a solid Auditing background within Clinical QA. The ideal experience will be Investigator Site Auditing, Vendor, System and Process Audits are a large aspect too.
|Prinicpal Auditor Of QA- New Jersey Area Perm position |
My client is a leading pharma company in New Jersey that is looking to bring on board an experiences QA GCP Principal Auditor to help run the department. Experience in GCP auditing must not be below 3yrs to qualify. You must have a bachelors degree, and experience with site audits, vendor audits, internal and external audits, as well as working along ICH guidelines & FDA inspections. ...
|Corporate Quality and Compliance Internal Auditor - Gold Level|
Frankfurt am Main
Currently recruiting, are a global pharmaceutical company who takes pride in its forward thinking research in developing ways to improve the quality of the lives of those who are chronically or critically ill. They are looking to build a team of 4/5 Global Auditors to supplement their internal audit program, each of them specialized in their own fields ranging from "computerized systems" to "U.S. FDA"
|GMP - Auditor (m/w)|
FĂĽr meinen Kunden, ein international fĂĽhrendes, forschendes Pharmaunternehmen in Hessen suche ich derzeit einen GMP-Auditor fĂĽr die kontinuierliche und wertschĂ¶pfende Verbesserung der Prozesse am eigenen Produktionsstandort
A Pharmaceutical company based in London is looking for a Pharmacovigilance Auditor to join their safety team and take responsibility for the PV audit program and conduct audits of their PV partners to ensure compliance with their Safety Data Exchange Agreements.
The ideal candidate would be an experienced Pharmacovigilance professional with a very strong knowledge of current regulations and previous experience of external PV auditing.
|GCP Auditor of Quality Assurance- Up to 140K |
Looking for experienced GCP auditors. GCP experience is necessary not GLP or GMP.
I am working on multiple positions at various levels so experience within 3-5 years and/or 7+ years will be the most appropriate for the positions avaliable now.
The positions avaliable are located on the East Coast and will be filled in a matter of a week or so due to the popular demand of the companies that are offering these openings. ...
|Clinical Quality Assurance Auditor (GCP and GLP) - Berkshire|
Clinical Quality Assurance Auditor (GCP & GLP)
We are looking to hire an excellent experienced Clinical Quality Assurance Auditor for our Berkshire based client.
|Quality Auditor and Distributors Quality Contact - Almere, Netherlands |
The QA operations organization deals with compliance of all Quality Systems (QS) in different areas and departments. Their main tasks are 1. to ensure that Quality Systems are properly implemented within the Distributors and 2. To support â€śsupplierâ€ť audits. In this you will coordinate, provide directions and leadership for the compliance of the pharma and devices distributors within the EMEA region
| Clinical Quality Assurance Auditor |
South East UK
This is a brilliant opportunity for a Clinical Quality Assurance Auditor to move forward and progress their career with a very successful and exciting pharmaceutical company. Based in the South East of the UK, this is an excellent opportunity to join an expanding Quality Assurance team, with options to progress into Management roles available regularly in the company. There is a possibility for an ideal candidate to be home based.
One of the fastest growing and successful pharmaceutical companies is seeking a PV Auditor to be based at their Central London Site. With easy transport links and a vibrant, progression driven environment, this is a perfect role for a Pharmacovigilance professional with Auditing experience to develop and grow their career. The ideal candidate will have a PV background and auditing experience. You will also be working closely with a QPPV in your current role.
|GCP Auditor Biopharmaceutical - UK|
An exciting and challenging opportunity has arisen to join the International Compliance team with a leading biopharmaceutical company. This position is based in the UK.
|Senior Quality Assurance Auditor - Europe - Any INC Office|
Conducts audits of on-going Company projects, and assist with other QA program initiatives. Provides guidance to less experience staff.
|Senior Auditor - GCP - office/ home based|
PAREXEL is looking for Senior Auditor (GCP) - position can be office or home based in any location in Europe.
|Global PV Auditor|
Global PV Auditor - Prostrakan Scotland
|SENIOR / QUALITY ASSURANCE AUDITOR - (Reading, UK), (Mannheim, Germany), (Paris, France), (Milan, Italy), (Madrid, Spain)|
An outstanding opportunity to join one of the worldâ€™s leading contract research organisations and be part of a dynamic and growing international company. Join PRA as a Quality Assurance Auditor and help realize your career potential.
|Global Quality Auditor|
A Global leader within in the pharmceutical industry is seeking a Global Quality Auditor.
ESSENTIAL DUTIES AND RESPONSIBILITIES
-Prepare and conduct internal and external audits for the company
-Perform independent research of required topics and FDA, EMEA, TGA, Health Canada, WHO, PIC/S, MHLW, and other national, international, or supranational regulations (GxP and ICH) including assessment of applicability and impact on systems being audited. ...
|Senior Quality Auditor for inVentiv Health Clinical, Eastern Europe (flexible location, home or office based)|
Senior Quality Auditor at inVentiv Health Clinical will require minimum supervision while delivering exceptional results and ensuring that the Quality of Research is maintained. You will successfully complete your role by conducting site audits, auditing documents and internal procedures, as well as identifying training and development needs for a continuous understanding of the ICH GCP guidelines.
|Principal Quality Assurance Auditor (Home or Office Based UK)|
Home or Office Based UK
To assist with the development and maintenance of audit programmes (internal and external) as part of the Quality Assurance program within the Pharm-Olam Group of companies. Responsible for scheduling and conducting study related audits to support Pharm-Olam/MBQ Sponsors
|Senior GCP Auditor (m/f)|
homebased (Eastern Europe)
Our client is headquartered near Boston, Massachusetts and operates in 76 locations with more than 15,000 employees in 50 countries worldwide. Our clientsâ€™ global regulatory expertise, Phase I-IV clinical research services, integrated eClinical technologies, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.
QA Auditor to be based in the Midlands
|Quality Auditor |
We currently have an opportunity for Quality Auditor to join our team in Leamington Spa.
|Senior Clinical Quality Assurance Auditor (GCP)|
Senior Clinical GCP Quality Assurance Auditor East Anglia 2 Year fixed Term Contract firstname.lastname@example.org for further information
|QA Auditor |
Key People are recruiting for an QA Auditor (Entry Level) for our medium global CRO client