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- Tasks: Lead the development of injectable drug products from initial studies to approval.
- Company: Join a global biopharmaceutical leader dedicated to improving lives through innovative therapies.
- Benefits: Enjoy a supportive work environment with opportunities for career advancement and professional growth.
- Why this job: Be part of a mission-driven team making a real impact in healthcare and drug development.
- Qualifications: Must have extensive experience in liquid drug product development within the pharmaceutical industry.
- Other info: This is a 12-month contract role based in Berkshire, England.
The predicted salary is between 36000 - 60000 £ per year.
Scientist, Drug Product Process Development – Berkshire, England – 12 Months Contract
We are looking for an experienced Scientist – Drug Product Process Development for a fantastic 12 months contract based in Berkshire.
You will be working with our client who is a global biopharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease.
This is a superb opportunity if you are looking to advance your career in the field with a supportive and innovative company that will put you first.
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 organisations, 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 characterisation.
- 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.
Requirements:
- Extensive 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 optimisation is an advantage.
If this role is of interest to you, please apply now!
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Scientist - Drug Product Process Development employer: Quanta Consultancy Services Ltd
Contact Detail:
Quanta Consultancy Services Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Scientist - Drug Product Process Development
✨Tip Number 1
Network with professionals in the biopharmaceutical industry, especially those who have experience in drug product process development. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest trends in the field.
✨Tip Number 2
Familiarise yourself with the specific technologies and methodologies used in liquid drug product development. Being able to discuss these in detail during an interview will demonstrate your expertise and enthusiasm for the role.
✨Tip Number 3
Prepare to discuss your previous experiences with aseptic manufacturing processes and how you’ve contributed to successful drug product development projects. Real-life examples can make a strong impression on interviewers.
✨Tip Number 4
Research the company’s recent projects and initiatives in drug product development. Showing that you understand their work and how you can contribute will set you apart from other candidates.
We think you need these skills to ace Scientist - Drug Product Process Development
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your extensive experience in liquid drug product development and manufacturing. Emphasise any relevant roles or projects that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for biopharmaceuticals and your technical expertise. Mention specific experiences that demonstrate your ability to design and execute lab studies, as well as your familiarity with cGMP manufacturing.
Highlight Relevant Skills: In your application, clearly outline your knowledge of sterile drug product development and any experience with aseptic conditions. Use keywords from the job description to ensure your application stands out to hiring managers.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail, which is crucial in the pharmaceutical industry.
How to prepare for a job interview at Quanta Consultancy Services Ltd
✨Showcase Your Technical Expertise
Be prepared to discuss your experience in liquid drug product development and manufacturing. Highlight specific projects where you established robust manufacturing processes, and be ready to explain the methodologies you used.
✨Understand the Company’s Focus
Research the biopharmaceutical organisation's recent projects and their commitment to neurological and immunological diseases. This will help you align your answers with their mission and demonstrate your genuine interest in their work.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think of examples where you had to cooperate with stakeholders or design lab studies, and be ready to discuss the outcomes and what you learned.
✨Emphasise Compliance and Quality Control
Since the role involves cGMP manufacturing, be sure to discuss your understanding of compliance and quality control measures. Share experiences where you ensured adherence to regulations during drug product development.
