Analytical Study Manager

Job Title:Analytical Study Manager
Location UK ~ Nottingham
Type: Full Time, Permanent

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

Due to business growth, we have a brand-new exciting career opportunity for a Analytical Study Manager. This role will be based at our site in Nottingham.

The Analytical Study Manager is a client facing role.  You will be responsible for project development aspects of studies leading up to CMC activities within Pharmaceutical Sciences. This will include review of analytical qualification protocols, reports, laboratory write ups and analytical methods. You will also have line management responsibilities of development team members.

Main tasks and responsibilities include:

  • Delivery of analytical data and updates to the project team
  • Writing of analytical up updates for the project team and client
  • Attending project calls and providing updates and information to the client
  • Checking schedules to ensure that all project work is captured correctly and updated as required
  • Writing, review and approval of analytical test protocols and reports
  • Laboratory write ups, checking and approving of data
  • Writing and updating SOP’s and analytical methods
  • Completion/review of LIRs and QEs where appropriate

The Candidate

The successful candidate will have previous analytical development experience in a pharmaceutical environment. A minimum HNC/D science qualification and considerable experience in CMC product development or as a study lead is required.

Other skills and experience required:

  • Ability to work to strict and tight deadlines whilst juggling a range of tasks simultaneously
  • Excellent attention to detail
  • Good communication skills both written and verbal
  • Able to work as part of a multifunctional team
  • Client facing experience is preferred

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.

Our Commitment to Diversity & Inclusion

Quotient Sciences are advocates for positive change and conscious inclusion.

We strive to create a diverse Quotient family by remaining committed to the development of our culture, equality, mindset, diversity & inclusion in the workplace.

As a global employer, we recognise the value in having an organisation that is a true reflection and representation of our society today. All applicants welcome.