At a Glance
- 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 12-month contract with opportunities for career advancement and a supportive work environment.
- Why this job: Be part of a mission-driven team making a real impact in healthcare while developing your skills.
- Qualifications: Experience in liquid drug product development and knowledge of cGMP manufacturing is essential.
- Other info: This role offers a chance to collaborate with diverse stakeholders in a dynamic setting.
The predicted salary is between 36000 - 60000 Β£ per year.
Scientist β Drug Product Process Development
Scientist β Drug Product Process Development
1 week ago Be among the first 25 applicants
Get AI-powered advice on this job and more exclusive features.
Scientist,Drug Product Process Development β Berkshire, England β 12 Months Contract
We are looking for an experienced Scientist β Drug Product Process Development for a fantastic 12 months contract based in Berkshire.
You will be working with our client who are 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!
Seniority level
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Seniority level
Mid-Senior level
Employment type
-
Employment type
Contract
Job function
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Job function
Research, Analyst, and Information Technology
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Industries
Staffing and Recruiting
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Scientist - Drug Product Process Development employer: QCS Staffing
Contact Detail:
QCS Staffing Recruiting Team
StudySmarter Expert Advice π€«
We think this is how you could land Scientist - Drug Product Process Development
β¨Tip Number 1
Network with professionals in the biopharmaceutical industry. Attend relevant conferences or webinars to meet potential colleagues and learn about the latest trends in drug product development.
β¨Tip Number 2
Familiarise yourself with the specific technologies and methodologies used in injectable drug product development. This could include understanding aseptic techniques and cGMP regulations, which are crucial for this role.
β¨Tip Number 3
Prepare to discuss your previous experiences in drug product development during interviews. Be ready to provide examples of how you've successfully managed projects or collaborated with cross-functional teams.
β¨Tip Number 4
Research the companyβs recent projects and initiatives in drug product development. Showing that you understand their work and values can set you apart from other candidates.
We think you need these skills to ace Scientist - Drug Product Process Development
Some tips for your application π«‘
Tailor Your CV: Make sure your CV highlights relevant experience in drug product development and manufacturing. Emphasise any specific projects or roles that align with the responsibilities mentioned in the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for biopharmaceuticals and your understanding of the role. Mention how your skills and experiences make you a perfect fit for the position, particularly in relation to injectable drug products.
Highlight Technical Expertise: In your application, clearly outline your technical knowledge and experience in liquid drug product development, cGMP manufacturing, and aseptic conditions. Use specific examples to demonstrate your expertise.
Proofread and Edit: Before submitting your application, thoroughly proofread your documents. Check for any spelling or grammatical errors, and ensure that all information is clear and concise. A polished application reflects professionalism.
How to prepare for a job interview at QCS Staffing
β¨Showcase Your Technical Expertise
Be prepared to discuss your experience in liquid drug product development and cGMP manufacturing. Highlight specific projects where you established robust manufacturing processes, as this will demonstrate your technical knowledge and suitability for the role.
β¨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think of examples where you had to design lab studies or perform process risk assessments, and be ready to explain your thought process and outcomes.
β¨Familiarise Yourself with Stakeholder Collaboration
Since the role involves working with various internal and external stakeholders, prepare to discuss your experience in team settings. Share examples of how you effectively communicated and collaborated with contract manufacturing organisations or other project teams.
β¨Understand the Companyβs Mission
Research the biopharmaceutical organisation's commitment to improving lives through innovative solutions. Be ready to express how your values align with theirs and how you can contribute to their mission in drug product process development.