Project Manager, Pharmaceutical Development and Supply.

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Company Overview Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we save precious time and money in getting drugs to patients. As a growing and successful business, we employ more than 1,100 talented individuals globally, located at state-of-the-art development, manufacturing and clinical facilities in the UK and USA. Science, Agility and Culture are the core components that define Quotient Sciences, enabling us to do what we do in the way that we do it. People join Quotient Sciences because we are a respected member of the drug development community, driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast. Because humanity needs solutions, fast. The Role Quotient Sciences has a fantastic career opportunity for a Project Manager, Pharmaceutical Development and Supply. Reporting to a Director Project Management, you will be responsible for managing study execution to ensure formulation development, analytical testing, regulatory approvals, clinical trial manufactures, clinical supply and reporting are completed on time. You will be the primary contact with the Sponsor from project initiation to operational close out for allocated projects. You will develop a project plan and lead a multifunctional internal project team to deliver that plan to time, cost and quality and comply and adhere to GXP guidelines and regulations as required of this role. Other tasks and responsibilities include: Scheduling of allocated studies to ensure the efficient utilisation of resources. Monitoring and control of project progress - time/ quality/ cost Generation, review and approval of appropriate study-related documentation and reports in line with SOP requirements. Documentation of study related communication e.g. minutes, t-cons in a timely manner. Management of all third party and internal suppliers. Invoicing and debtor management. Tracking of allocated projects in MS Project on a real time basis. Maintenance of the Site File. Management of closedown activities for allocated studies and to ensure post-study reporting to the regulatory authorities and archiving are completed in a timely manner. Application of lessons learned from previous studies to ensure continuous improvement in delivery. The Candidate The successful candidate will be a driven and talented individual who thrives in a fast paced, delivery driven environment. You will be qualified to at least degree level in a science subject and have project management experience in a Contract Development Manufacturing Organisation (CDMO). A good understanding of the drug development process is essential for this role. Other skills and experience required: Excellent project management, customer service, communication and financial management skills Excellent written and verbal communication skills Excellent time management and organization skills Ability to effectively prioritise your own workload Self-sufficient and capable of working within an environment where deadlines are critical Energetic personality with strong personal presence and lots of enthusiasm Ability to build strong customer and stakeholder relationships You must have the right to work in the UK at the time of being offered employment. This role will be a blend of remote working and onsite working at our site in Nottingham, with an average of 2 days per week on site (post release of lockdown restrictions). Company benefits In return you will receive a competitive salary, a generous benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business. This job was originally posted as

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