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- Tasks: Join us as a Development Scientist, focusing on injectable drug product processes.
- Company: Be part of a leading pharmaceutical development team making a real impact.
- Benefits: Enjoy a 12-month contract with flexible working hours and opportunities for growth.
- Why this job: Contribute to innovative drug development while collaborating with diverse teams.
- Qualifications: Experience in liquid drug product development is essential; bio-pharmaceutical experience is a plus.
- Other info: The site will relocate to Windlesham in 2026/7, so flexibility is key.
The predicted salary is between 36000 - 60000 £ per year.
Are you interested in working within Pharmaceutical Development Sciences? Do you have experience in liquid drug product development and/or manufacturing within the pharmaceutical industry? If so, we would love to hear from you!
We are recruiting for a Development Scientist to work on the development of our clients Injectable Drug Product Process. This role is offered on a contract basis working 37.5 hours per week for 12 months. (Inside IR35).
Responsibilities:- Technical expert in the establishment of robust, fit for purpose injectable drug product manufacturing processes from toxicology studies or first in human until BLA approval.
- Define and select drug product manufacturing processes and parameters for clinical manufacture.
- Cooperate with a wide range of internal and external stakeholders, including contract manufacturing organizations, as part of a project team.
- Design and execution of lab studies in relation to drug product development activities, capture and analyze data and author related documentation (write-ups, protocols, reports (eg filter selection and sizing, target fill volume assessment, compatibility assessments, clinical blinding, etc).
- Capture and analyse critical manufacturing process data for process understanding and process characterization.
- Perform process risk assessments.
- Design DP processes for sterile injectable drug products in liquid or lyophilized powder form, in vials, pre-filled syringes or as combination products.
- Define the investigational medicine product preparation process in clinical trials.
- Provide support to ensure timely manufacture of stability and clinical DP batches.
- Provide support to process performance qualification/validation.
- Ensure products are manufactured in accordance with our clients quality system, cGMP and latest regulatory requirements.
- Provide support in the completion of the relevant sections of the CMC regulatory submissions and regulatory briefing documents and response to questions from authorities.
- Provide support in investigations of deviations and complaints related to DP quality.
- Support knowledge transfer from late phase development to commercial for validated DP processes.
- Experience in liquid drug product development and/or manufacturing within the pharmaceutical industry is required.
- Experience within the bio pharmaceutical industry is an advantage.
- Knowledge and technical experience in liquid drug product development and cGMP manufacturing under aseptic conditions (such as vial, cartridge and pre-filled syringe filling) is an advantage.
- Technical knowledge of sterile DP development covering DP components, process transfer, scale-up and optimization is an advantage.
In 2026/7, this site will relocate from Slough to Windlesham Surrey so applicants must be able to get to both locations.
Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.
Candidates must be eligible to live and work in the UK.
For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Process Development Scientist employer: CV-Library
Contact Detail:
CV-Library Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Process Development Scientist
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those involved in drug product development. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and technologies.
✨Tip Number 2
Familiarise yourself with the specific regulatory requirements and cGMP standards relevant to injectable drug products. This knowledge will not only enhance your understanding but also demonstrate your commitment to quality and compliance during interviews.
✨Tip Number 3
Prepare to discuss your previous experiences in liquid drug product development in detail. Be ready to share specific examples of challenges you faced and how you overcame them, as this will showcase your problem-solving skills and technical expertise.
✨Tip Number 4
Research StudySmarter and our clients thoroughly. Understanding our mission and values will help you align your answers during interviews and show that you're genuinely interested in contributing to our goals.
We think you need these skills to ace Process Development Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in liquid drug product development and manufacturing. Use specific examples that demonstrate your technical expertise and familiarity with cGMP practices.
Craft a Compelling Cover Letter: Write a cover letter that clearly outlines your motivation for applying to this role. Mention your relevant experience and how it aligns with the responsibilities listed in the job description, such as process risk assessments and data analysis.
Highlight Relevant Skills: In your application, emphasise skills that are particularly relevant to the role, such as knowledge of sterile injectable drug products, process transfer, and scale-up. This will show that you understand the requirements of the position.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or 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 CV-Library
✨Showcase Your Technical Expertise
Be prepared to discuss your experience in liquid drug product development and manufacturing. Highlight specific projects where you played a key role, especially those involving aseptic conditions or cGMP compliance.
✨Understand the Regulatory Landscape
Familiarise yourself with the latest regulatory requirements and guidelines related to injectable drug products. Be ready to explain how you've navigated these in past roles, particularly in relation to CMC submissions.
✨Demonstrate Collaboration Skills
Since the role involves working with various stakeholders, prepare examples of how you've successfully collaborated with internal teams and external partners, such as contract manufacturing organisations, to achieve project goals.
✨Prepare for Process Risk Assessments
Brush up on your knowledge of process risk assessments and be ready to discuss how you've identified and mitigated risks in previous projects. This will show your proactive approach to ensuring quality and compliance.
