Project Scientist

Quotient Sciences; Nottingham; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading pharmaceutical sciences company in Nottingham is seeking an experienced Project Scientist to support project activities and facilitate the transition from development to GMP operations. The role involves developing and overseeing formulation plans, analytical testing, and project documentation while training staff and ensuring compliance with operational standards. Candidates should possess a minimum of HNC/D in a science discipline and at least 3 years of relevant experience in CMC product development.

Qualifications

• Minimum HNC/D in a science discipline or equivalent industrial experience.
• At least 3 years' experience in CMC product development or as a study lead.

Responsibilities

• Lead project development activities ahead of CMC operations.
• Provide development plans, reports, and laboratory documentation.
• Oversee formulation development and draft batch records for manufacturing.
• Deliver project updates to the Project Manager.
• Write and review analytical and formulation test protocols.

Skills

Project management

Formulation development

Analytical testing

SOP writing

Staff training

Education

HNC/D in a science discipline

Job description

We are looking for a Project Scientist to join our Pharmaceutical Sciences team in Nottingham. This client‑facing role is pivotal in supporting project set‑up activities and ensuring seamless transition from development to GMP operations.

Responsibilities

• Lead project development activities ahead of CMC operations.
• Provide development plans, reports, analytical qualification protocols, and laboratory documentation.
• Oversee formulation development and draft batch records for manufacturing.
• Deliver development plans, reports, and project updates to the Project Manager.
• Write and review analytical and formulation test protocols and reports.
• Identify excipients and prepare specifications aligned with study requirements.
• Transfer programmes to manufacturing operations, including batch records and draft IMP labels.
• Perform in‑vitro and analytical testing (e.g., dissolution, PSD) to meet deadlines.
• Complete and check laboratory write‑ups.
• Train new and existing staff.
• Write and update SOPs and analytical methods.
• Complete and review LIRs and QIs as appropriate.

Qualifications

• Minimum HNC/D in a science discipline or equivalent industrial experience.
• At least 3 years' experience in CMC product development or as a study lead.