At a Glance
- Tasks: Support stability study lifecycles and perform data analysis in a dynamic environment.
- Company: Join a leading biotech firm committed to innovation and collaboration.
- Benefits: Enjoy competitive pay, health benefits, and opportunities for professional growth.
- Other info: Be part of a diverse team with a focus on learning and development.
- Why this job: Make a real impact in the pharmaceutical industry while developing your skills.
- Qualifications: Science-related degree and 2+ years in pharmaceutical stability programs required.
The predicted salary is between 30000 - 40000 £ per year.
The Stability Associate is responsible for executing day-to-day activities to support stability study lifecycles. This role requires a basic understanding of stability principles and has the ability to work well independently but under instruction and guidance of the line manager. The position focuses on preparing routine protocols, compiling data, basic statistical analysis, and escalating issues promptly.
Responsibilities
- Able to prepare routine stability protocols and compile data throughout study, keeping data tables up to date.
- Understand different trends associated with the data highlighting to senior members of the team.
- Perform basic statistical analysis to support data interpretation and decision‑making.
- Be aware of pull dates and associated testing, and which laboratories are responsible for conducting the different test methods.
- Maintain compliance with GMP, ICH guidelines, and internal procedures.
- Support investigations into stability‑related deviations under guidance.
- Familiarity with electronic systems (e.g. LIMS, JMP) for data management.
Knowledge & Understanding
- Basic understanding of stability principles and regulatory expectations.
- General awareness of stability‑indicating parameters and expected product profiles.
- Ability to recognize unexpected results and escalate appropriately.
- Basic knowledge of risk‑based assessments and change control processes.
Working Collaboratively
- Coordinate with QC Operations to monitor progress of stability samples.
- Ensure routine stability studies are set up correctly and data available at all timepoints.
- Collaborate well with colleagues to achieve stability program objectives.
- Work effectively, demonstrating initiative and accountability.
Competencies
- Attention to Detail: Ensures accuracy in data compilation and reporting.
- Problem Recognition: Identifies issues and escalates promptly.
- Collaboration and Teamwork: Communicates clearly, contributing to a cohesive team environment.
- Learning Agility: Shows readiness to develop scientific and technical knowledge over time.
Qualifications
- Associate degree (Foundation degree HND/HNC or equivalent Level 5 vocational qualification in science related subject) essential.
- Science degree (e.g., Bachelor) in pharmacy, pharmaceutical technology, biology, chemistry or comparable education preferred.
Experience Required
- 2+ years’ experience in the pharmaceutical manufacturing industry with direct exposure to stability program development and management.
- Basic understanding of product lifecycle management in a global biotech or pharmaceutical GMP environment.
- Awareness of current regulations and guidelines of stability monitoring of biopharmaceutical products.
Other Essential Knowledge
- Fluency in English in both writing and oral communications.
QC Stability Associate (18 month fixed-term contract) in Liverpool employer: CSL
CSL is an exceptional employer that prioritises employee well-being and professional growth, offering a collaborative work culture where innovation thrives. As a QC Stability Associate, you will benefit from comprehensive training, access to cutting-edge technology, and the opportunity to contribute to meaningful projects in the pharmaceutical industry. Located in a vibrant area, CSL fosters a supportive environment that encourages continuous learning and development, making it an ideal place for those seeking a rewarding career in science.
StudySmarter Expert Advice🤫
We think this is how you could land QC Stability Associate (18 month fixed-term contract) in Liverpool
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who know about stability studies. A friendly chat can lead to insider info on job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of stability principles and GMP guidelines. We recommend practising common interview questions related to data analysis and problem-solving to show you’re ready to tackle challenges head-on.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you, and tailor your approach to each one to stand out from the crowd.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you fresh in the interviewer’s mind. Plus, it shows your enthusiasm for the role and your commitment to joining their team.
We think you need these skills to ace QC Stability Associate (18 month fixed-term contract) in Liverpool
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience with stability studies and data management. We want to see how your background aligns with the role, so don’t hold back on showcasing relevant skills!
Show Off Your Attention to Detail:Since this role requires accuracy in data compilation, emphasise your attention to detail in your application. Mention any specific examples where you’ve successfully managed data or identified issues in previous roles.
Highlight Your Teamwork Skills:Collaboration is key in this position, so be sure to include experiences where you’ve worked effectively with others. We love seeing candidates who can communicate well and contribute to a cohesive team environment!
Apply Through Our Website:We encourage you to submit your application through our website for the best chance of being noticed. It’s the easiest way for us to keep track of your application and get back to you quickly!
How to prepare for a job interview at CSL
✨Know Your Stability Principles
Before the interview, brush up on your understanding of stability principles and regulatory expectations. This will not only help you answer questions confidently but also show that you're genuinely interested in the role.
✨Showcase Your Data Skills
Be prepared to discuss your experience with data compilation and basic statistical analysis. Bring examples of how you've managed data in previous roles, especially if you've used electronic systems like LIMS or JMP.
✨Demonstrate Attention to Detail
During the interview, highlight instances where your attention to detail made a difference in your work. Discuss how you ensure accuracy in data reporting and how you handle unexpected results.
✨Emphasise Collaboration
Since this role involves working closely with QC Operations and other team members, be ready to share examples of how you've successfully collaborated in the past. Show that you can communicate clearly and contribute to a cohesive team environment.
