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- Tasks: Support stability study lifecycles and perform data analysis in a collaborative environment.
- Company: Join CSL Seqirus, a leading global influenza vaccine provider.
- Benefits: Enjoy competitive benefits, including health support and a focus on well-being.
- Other info: Three positions available; embrace a culture of inclusion and belonging.
- Why this job: Make a real impact in biopharmaceuticals while developing your scientific skills.
- Qualifications: Science-related degree or equivalent experience in pharmaceutical stability programs.
The predicted salary is between 30000 - 42000 £ 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.
Main Responsibilities and Accountabilities
- Support a variety of tasks associated with ongoing stability programs:
- Able to prepare routine stability protocols and compile data throughout the 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.
- 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.
- 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.
- 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.
Position Qualifications and Experience Requirements:
- Education Requirements:
- 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.
- 2+ years’ experience in the pharmaceutical manufacturing industry with direct exposure to Stability program development and management preferred.
- 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.
- Fluency in English in both writing and oral communications.
QC Stability Associate in Saint Helens employer: CSL Seqirus
Contact Detail:
CSL Seqirus Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Stability Associate in Saint Helens
✨Tip Number 1
Get to know the company inside out! Before your interview, dive into CSL Seqirus' mission and values. This will help you connect your skills with their goals, showing them you're not just another candidate but a perfect fit for their team.
✨Tip Number 2
Practice makes perfect! Run through common interview questions related to stability principles and data analysis. We can even help you with mock interviews to boost your confidence and ensure you nail those tricky questions.
✨Tip Number 3
Show off your teamwork skills! Be ready to share examples of how you've collaborated in past roles. Highlighting your ability to work well with others will resonate with the collaborative culture at CSL Seqirus.
✨Tip Number 4
Don’t forget to follow up! After your interview, drop a quick thank-you email to express your appreciation. It’s a simple gesture that keeps you on their radar and shows your enthusiasm for the role.
We think you need these skills to ace QC Stability Associate in Saint Helens
Some tips for your application 🫡
Know Your Stuff: Before you start writing, make sure you understand the basics of stability principles and the role itself. This will help you tailor your application to show that you’re the right fit for the QC Stability Associate position.
Be Clear and Concise: When you're putting together your application, keep it straightforward. Use clear language and avoid jargon unless it's relevant. We want to see your skills and experience shine through without any fluff!
Show Your Team Spirit: Since collaboration is key in this role, highlight any experiences where you've worked well in a team. Share examples that demonstrate your ability to communicate effectively and contribute to a cohesive environment.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you’ll find all the info you need about the role and our company there!
How to prepare for a job interview at CSL Seqirus
✨Know Your Stability Principles
Before the interview, brush up on your understanding of stability principles and regulatory expectations. Be ready to discuss how these concepts apply to the role and share any relevant experiences you have in stability study lifecycles.
✨Showcase Your Data Skills
Prepare to talk about 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. This will demonstrate your ability to handle the technical aspects of the job.
✨Emphasise Team Collaboration
Highlight your teamwork skills during the interview. Share specific instances where you've worked collaboratively with colleagues to achieve objectives, particularly in a QC or stability context. This shows that you can contribute to a cohesive team environment.
✨Be Ready to Problem Solve
Expect questions about how you would handle unexpected results or deviations in stability studies. Prepare examples of past challenges you've faced and how you escalated issues appropriately. This will showcase your problem recognition skills and your proactive approach.