Injectable Drug Product Process Development
Injectable Drug Product Process Development

Injectable Drug Product Process Development

Slough Temporary No home office possible
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At a Glance

  • Tasks: Join us as a Drug Product Development Scientist, designing and executing lab studies.
  • Company: Work with a global biopharmaceutical company focused on severe diseases in immunology and neurology.
  • Benefits: Earn from £20.68 per hour PAYE or £28.16 via umbrella; great career growth opportunities.
  • Why this job: Make a real impact in drug development while working in a dynamic, innovative environment.
  • Qualifications: A relevant scientific degree or equivalent experience in liquid drug product development is essential.
  • Other info: This role is based in Slough; applicants must have the right to work in the UK.

CK Group are 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.

Drug Product Development Scientist Role:

  • Design and execution of lab studies in relation to drug product development activities, capture and analyse data and author related documentation.
  • Capture and analyse critical manufacturing process data for process understanding and process characterization.
  • Design DP processes for sterile injectable drug products in liquid or lyophilized powder form, in vials, pre-filled syringes or as combination products.
  • Provide support in the completion of the relevant sections of the CMC regulatory submissions and regulatory briefing documents.
  • Provide support in investigations of deviations and complaints related to DP quality.

Your Background:

  • Hold a relevant scientific degree or have equivalent working experience.
  • Experience in liquid drug product development or manufacturing in the pharmaceutical industry.
  • Knowledge and technical experience in liquid drug product development and cGMP manufacturing under aseptic conditions (such as vial, cartridge and pre-filled syringe filling).
  • Technical knowledge of sterile DP development covering DP components, process transfer, scale-up and optimisation is an advantage.

Company: Our client is a global biopharmaceutical company, focused on creating value for people living with severe diseases in immunology and neurology, now and into the future.

Location: This role is based at our client’s site in Slough.

Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 130 081 in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

If this position isn’t suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.

Injectable Drug Product Process Development employer: CK Group

As a leading global biopharmaceutical company based in Slough, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make a meaningful impact in the lives of those affected by severe diseases. With competitive pay rates and a commitment to professional development, we offer exceptional growth opportunities and support for our team members, ensuring they thrive in their careers while contributing to groundbreaking advancements in drug product development.
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Contact Detail:

CK Group Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Injectable Drug Product Process Development

✨Tip Number 1

Network with professionals in the pharmaceutical industry, especially those involved in drug product development. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest trends in injectable drug products.

✨Tip Number 2

Familiarise yourself with the specific regulatory requirements for CMC submissions in the UK. Understanding these regulations can give you an edge during interviews, as it shows your commitment to compliance and quality in drug development.

✨Tip Number 3

Prepare to discuss your hands-on experience with aseptic manufacturing processes. Be ready to provide examples of how you've contributed to process optimisation or troubleshooting in previous roles, as this is crucial for the position.

✨Tip Number 4

Research the company’s recent projects and innovations in immunology and neurology. Being knowledgeable about their work will not only help you tailor your responses but also demonstrate your genuine interest in contributing to their mission.

We think you need these skills to ace Injectable Drug Product Process Development

Drug Product Development
Laboratory Skills
Data Analysis
Documentation Authoring
Process Characterisation
Regulatory Submissions Knowledge
cGMP Manufacturing
Aseptic Techniques
Sterile Injectable Drug Products
Problem-Solving Skills
Attention to Detail
Technical Knowledge of DP Components
Process Transfer and Scale-Up
Quality Investigation Support

Some tips for your application 🫡

Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the Drug Product Development Scientist position. Tailor your application to highlight relevant experiences and skills that match these criteria.

Highlight Relevant Experience: In your CV and cover letter, emphasise any experience you have in liquid drug product development or manufacturing. Mention specific projects or roles where you applied your knowledge of cGMP manufacturing and aseptic conditions.

Showcase Technical Skills: Detail your technical knowledge related to sterile drug product development, including process transfer and optimisation. Use specific examples to demonstrate your expertise in designing DP processes for injectable products.

Proofread Your Application: Before submitting, carefully proofread your application materials for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial in the pharmaceutical industry.

How to prepare for a job interview at CK Group

✨Showcase Your Technical Knowledge

Make sure to highlight your understanding of liquid drug product development and cGMP manufacturing. Be prepared to discuss specific processes you've worked on, especially those involving sterile injectable products.

✨Prepare for Regulatory Questions

Since the role involves supporting CMC regulatory submissions, brush up on your knowledge of regulatory requirements. Be ready to explain how you've contributed to compliance in past roles.

✨Demonstrate Problem-Solving Skills

The job requires support in investigations of deviations and complaints. Think of examples where you've successfully resolved issues in a lab setting and be ready to share these during the interview.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's drug product development processes and future projects. This shows your genuine interest in the role and helps you assess if it's the right fit for you.

Injectable Drug Product Process Development
CK Group
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  • Injectable Drug Product Process Development

    Slough
    Temporary

    Application deadline: 2027-04-16

  • C

    CK Group

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