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Clinical QA Manager / Auditor - Germany - 6 Months - Oferta z Jobs.pl

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Clinical QA Manager / Auditor - Germany - 6 Months

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  • Clinical QA Manager / Auditor - Germany - 6 Months

    Please contact Matt Lowe-Lauri on () or email if you would like to know more about this opportunity.

    My client is a leading Biotechnology company based in South West Germany. Currently at the forefront of the industry, this company specialises in highly scientific and complex studies within Oncology. They are currently one of Germany's fastest growing organisations with heavy investment in their clinical operations and have 3 key studies coming to close out. Consequently, they're looking to recruit an experienced Clinical QA Manager who is qualified to audit, to ensure they maintain GCP Compliance and deliver successful trial close-outs.

    Company Background

    This company has rapidly become one of the more innovative biotechnology companies in Germany. Having developed strong relationships with local German universities they are specialists within oncology and have a strong track of bringing effective and innovative drugs to market.

    Roles and responsibilities

    · Provide GCP Compliance oversight to study close-out

    · Act as Clinical QA Manager, ensuring compliance GCP

    · Managing QMS

    · Manage internal SOPs

    Skills Desired

    · Extensive experience within clinical QA environments

    · Extensive GCP auditing experience


    Location - Russia

    Pay - Lucrative daily rate

    Length - 1 Month contract

    NOTE-This role is required to be filled URGENTLY. Apply immediately to avoid missing out.

    Please contact Matt Lowe-Lauri on () or email if you would like to know more about this opportunity.

    Full job description and company details are available upon application, apply below. This position is being dealt with by Matt Lowe-Lauri at meet, call on or email directly at to discuss in confidence.

    Meet is a European wide recruitment agency who specialise purely in the pharmaceutical sector. We work in a number of regions across Europe placing both permanent and freelance candidates into Clinical, Regulatory and Data management teams within CRO's, Pharmaceutical, Generic and Biotech companies.

    If this vacancy isn't quite suitable for your experience, then we are currently working on a wide range of other positions too. Please apply through our website, or alternatively call Matt Lowe-Lauri to find out more.

    Find out more about us at

    Associated keywords: Associated keywords: Quality Assurance; QA; Quality; Quality; QA Advisor; GXP; GMP; Good Clinical Practice; Quality Management Systems, Pharma; Biotech; Freelance; Temporary; Contract; Qualified Person; CAPAs; SOPs; FDA; Inspection; Remediation; GCP; Clinical; Good Clinical Practice


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