Vacancies

Manufacturing Supervisor

Job Title:Manufacturing Supervisor
Reference:QUO01384
Location UK ~ Reading
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 our continued growth and success a great opportunity has arisen for a Manufacturing Supervisor to join our Manufacturing team based in Reading. In this role you will be responsible for the manufacture of Investigational Medicinal Products for all types of clinical studies.

You will be responsible for overseeing and completing the operational setup, operation, control, monitoring and cleaning of various manufacturing process equipment to produce solids, liquids, creams, gels and inhalation dosage forms following Standard Operating Procedures (SOP’s).

Other main tasks and responsibilities include:

  • Oversee GMP Manufacturing operators to ensure that all operations during the manufacture or packaging of a batch are conducted in strict accordance with the instructions in the batch manufacturing record and that all activities are appropriately recorded.
  • Ensure that all operatives taking part in a manufacturing activity have the appropriate understanding of the specific activities that they will be undertaking.
  • Ensure manufacturing facility is maintained to a high level of hygiene at all times
  • Complete technical documentation to support manufacturing processes (including batch manufacturing records and process/equipment qualification documentation)
  • Review master batch records and executed batch records
  • Supervise day to day operations, general housekeeping and maintain/improve standards of manufacturing through training and development of the team members
  • Maintain equipment and area usage logs and action any recalibration requirements in liaison with the facilities co-ordinator
  • Maintain equipment operational status and documentation in conjunction with QA
  • Assist in the preparation of SOPs for new equipment and procedures and update them periodically

The Candidate

The ideal candidate will have Clinical Trial Manufacturing experience and will have substantial experience in a pharmaceutical GMP supervisory role.

Applicants must have the right to work in the UK upon being offered employment.

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

Applicants must have the right to work in the UK upon being offered employment.

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.