Closing Date: 22 Dec 16
Salary (£): Competitive
We are looking for a QC Scientist to join our team in Harrogate (http://www.visitharrogate.co.uk/) as part of QC Operations Group.
COVANCE is one of the world’s most comprehensive and experienced contract research organizations (CROs) with a tradition of innovation in the science and processes of drug development. We have the ability to offer wealth of services covering all aspects of drug development ranging from non-clinical research services through to post-marketing safety and commercialization services. We are currently the only CRO with this depth of service offerings.
Working as part of the QC Operations Group, the QC Scientist routinely manages a number of studies pertaining to common techniques. These techniques may comprise single studies or be part of a larger study / project working in conjunction with the Scientific Lead (SL). This may include but is not limited to; (complex) validation, transfer, batch release and stability studies. They will write protocols and reports for single studies with no assigned SL. The QC Scientist has in depth knowledge in a relevant field and is able to troubleshoot techniques in the area of their expertise. The QC Scientist is accountable for the approval and integrity of the data and associated quality documentation. They are also responsible for the preparation and review of analytical procedures.
In this role, the QC Scientist will provide internal Clients with a central scientific point of contact for techniques within their area of expertise. The individual is accountable for effective communication either directly with the Client or via the SL to ensure that Client requirements and deliverables are met. This involves discussion with the Client / SL to design proposals, working with the PMO, communication with the QC Section Managers and oversight of scientific progress of techniques / studies to ensure the successful, initiation, planning, execution, monitoring and completion of projects.
The QC Scientist ensures that the studies are carrried out to the required standards ensuring that all work is conducted in compliance with applicable regulatory requirements (GxP). The QC Scientist is required to have an expert knowledge of the GxP and regulatory guidelines. They are the main point of contact for internal and external clients where the molecule is not overseen by the SL. Where the molecule is overseen by a SL the QC Scientist will act as the main technical contact.
The QC Scientist will be responsible for overseeing the work of other QC Scientists where appropriate. They will be expected to train, coach and mentor members of the team and across functions as required.
The individual will identify and communicate scientific and regulatory developments within their field expertise to the molecule management team and the wider senior scientific group (Analytical Development and QC Scientists). There is an expectation that the senior members of the QC Scientist team will be required to travel to visit clients and attend conferences, and represent Covance by preparing and/or giving presentations and writing scientific papers in their area of expertise.
Covance is committed to diversity in the workplace and is an equal opportunity employer. Your confidentiality and privacy are important to us.
Keywords: Biacore, Surface Plasmon Resonance, SPR, BIO CMC, BioPharm, Harrogate, UK.
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