Michael Page Life Sciences is recruiting for a Basingstoke based Pharmaceutical organisation who are undergoing significant growth. Responsibilities - Edit word processes and perform quality control checks of documents for.
The Senior Supplier Quality Specialist will provide Quality Assurance and Technical support globally, under the direction of the Global QA Manager to the third party suppliers. The Senior Supplier Quality Specialist will ensure that products are manufactured and in compliance with their Registered approvals (NDA or MA), National or European, and the principles and guidelines of current Good Manufacturing Practices.
Michael Page Life Sciences is recruiting for a Basingstoke based Pharmaceutical business who are looking for a Clinical Document Management Specialist to join the team. The Clinical Document Management Specialist position reports to the Clinical Document Manager and will act as advisor/mentor to the Specialists in the UK team ensuring timelines are met and assisting in resolving technical problems.
The purpose of this role is to support the growth of the Finance department and ensure that projects and deadlines are met whilst maintaining current service level during this growth period.
This position will be the primary technical point of contact for the Global Supply Chain organization with our internal, Pharmaceutical Sciences and external, Contract Manufacturing Organizations.The primary role of this individual will be to own, understand and continuously improve the process capability and supply chain resiliency for the products within their assigned product portfolio.
As part of the Biostatistics & Statistical Programming, Clinical Development Operations & Biometrics function we are recruiting an Associate Director, Biostatistics who will report to a UK based Group Leader, Biostatistics.
Primary RoleTo provide QA and Technical support globally, under the direction of the GQA Manager (Drug Product, Site GMP Support), to Shire’s external suppliers of commercial drug product.
This specialist agency is looking for a Pharma Recruitment Consultant to join a very successful team in Basingstoke. With a strong brand and an excellent reputation they offer a supportive culture, on going training and opportunities for career development.
A methodical project manager who has previously managed European / Global projects who is detail oriented as well as focused on quality delivery is essential for success in this role. As this position will be working as part of a cross functional team, an excellent relationship builder with the ability to negotiate, collaborate and influence at a variety of levels and cultures is key.
Responsible for the planning, implementation, execution and management of clinical research study/studies and/or programs. Manages clinical outsourcing to CROs or other clinical vendors such as labs, IRBs, etc and oversees the financial and budgetary aspects of the study/studies Authors/oversees protocols, informed consent forms, sections of investigational drug brochures, study report writing and integrated summaries for regulatory submissions.
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