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
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.
Sales representative â€“ Medical â€“Device - Benelux
i-Pharm Consulting is seeking on behalf of a leading Medical device company in his market a SALE REPRESENTATIVE to join their operations on a permanent basis. This role will give the chosen individual the opportunity to work on the industryâ€™s most relevant and innovative medical device. ...
This is an exciting position where you can excel your career! My client is looking for an experienced professional within quality assurance to join their expanding team as the quality assurance manager. My client is a leader within their field and not only offers a stable environment and international opportunities but also a broad role working within biologics.
This is an exciting position where you can excel your career! My client is looking for an experienced professional within quality assurance to join their expanding team as the quality assurance manager. My client is a leader within their field and not only offers a stable environment and international opportunities but also a broad role working on several dosage forms and products.
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.
Responsible for developing, implementing and managing appropriate quality systems and practices to ensure that the Site is in substantially compliance to the Quality Manual and all relevant regulatory and notified body requirements.
An outstanding and highly coveted Biopharmaceutical company in the San Francisco Bay Area is looking to bring on a Sr. Statistical Programmer to join their experienced group. This is a full-time, onsite role.
* Acts as lead statistical programmer for a project. * May participate in sub-team meetings as a representative of Statistical Programming group. * Provides consistency and quality assurance across various studies. ...
I am working with a very interesting and exciting Pan European service provider based in Cambridge, who are actively seeking a Quality and Pharmacovigilance Manager to join their team. The ideal candidate here will have extensive experience in PV Audits and Inspections plus a solid working knowledge of GCP QA. As an expanding and developing organisation, my client can offer an excellent package, plus the chance of progression further down the line.
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