Injectable Drug Product Process Development

TN United Kingdom; Slough; On-site; GBP 80,000 - 100,000; Full time

Job summary

An innovative global biopharmaceutical company is seeking a Drug Product Development Scientist to join their team in Slough. This exciting role involves designing and executing lab studies, analyzing critical data, and supporting regulatory submissions for sterile injectable drug products. As part of a forward-thinking organization focused on improving the lives of patients with severe diseases, you will have the opportunity to contribute to meaningful projects in immunology and neurology. If you are passionate about drug development and eager to make a difference, this role is for you.

Qualifications

• Experience in liquid drug product development or manufacturing.
• Knowledge of cGMP manufacturing in aseptic conditions.

Responsibilities

• Design and execute lab studies related to drug product development.
• Capture and analyze critical manufacturing process data.
• Support completion of CMC regulatory submissions.

Skills

Drug Product Development

Data Analysis

cGMP Manufacturing

Process Design

Education

Relevant Scientific Degree

Job description

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Injectable Drug Product Process Development, Slough

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Client:

CK Group

Location:

Slough, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

9f0f2f35ff4c

Job Views:

3

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

CK Group is recruiting for a Drug Product Development Scientist to join a global pharmaceutical company based in Slough on a contract basis, initially for 12 months.

Salary from £20.68 per hour, PAYE, or from £28.16 per hour via umbrella.

Role Responsibilities:

• Design and execute lab studies related to drug product development, analyze data, and document findings.
• Capture and analyze critical manufacturing process data for understanding and characterization.
• Design DP processes for sterile injectable drug products in liquid or lyophilized powder form, in vials, pre-filled syringes, or as combination products.
• Support completion of relevant sections of CMC regulatory submissions and briefing documents.
• Assist in investigations of deviations and complaints related to DP quality.

Qualifications and Experience:

• Relevant scientific degree or equivalent working experience.
• Experience in liquid drug product development or manufacturing within the pharmaceutical industry.
• Knowledge of cGMP manufacturing in aseptic conditions (vials, cartridges, pre-filled syringes).
• Technical knowledge of sterile DP development, including components, process transfer, scale-up, and optimization, is advantageous.

Company:

A global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology.

Location:

This role is based at the company's site in Slough.