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- Tasks: Join a dynamic team to support stability testing and quality control in pharmaceuticals.
- Company: Leading European contract manufacturer in the pharmaceutical and biotech sectors.
- Benefits: Exciting work environment, career growth, and opportunities to make an impact.
- Why this job: Be part of a passionate team driving innovation in healthcare.
- Qualifications: Relevant science qualification and experience in analytical techniques required.
- Other info: Fast-paced environment with a focus on quality and teamwork.
The predicted salary is between 30000 - 40000 £ per year.
Are you looking for an exciting professional challenge? We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,300 employees in Germany, France, Finland, UK and Norway. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.
Job Purpose
To support the on-going stability program for commercial, clinical and technical products. In addition, support of quality control testing of both development and market finished products under GMP conditions.
Key Responsibilities And Accountabilities
- Work as part of a team alongside quality control and micro departments.
- Actively involved in performing analytical activities for stability analysis of drug products.
- Must be technically competent in analytical activities (e.g. pharmacopoeial wet chemistry, HPLC, GC, Dissolution, KF) for stability testing of finished products.
- All activities to be performed under current cGMP, in-house SOP’s and/or pharmacopoeia.
- Writing of stability summaries, protocols and reports.
- Performing set down of new stability studies, receipt of stability samples being returned from storage facility and disposal of samples following reporting of analysis.
- Checking of data for stability, QC and micro departments.
- Ordering of lab supplies to ensure continued availability of materials for timely analysis.
- Comply with company health and safety procedures.
Person Profile: Quality Control Analyst (Stability)
- Results oriented with a positive outlook and clear focus on high quality output.
- Solid planning and organizational ability; reliable, tolerant and dependable.
- Comfortable dealing with senior managers and customers; enjoy working in a fast, stimulating environment.
- Goal-oriented; able to work under pressure and meet deadlines.
- Excellent communication/presentation skills.
- Able to get on with others and be a team player, but is equally comfortable working independently.
- Flexible and able to work extended hours when required.
- Must be eligible to work in the UK.
Specific Job Skills
- Relevant qualification, HNC/HND/Science Degree or Equivalent.
- An understanding of drug development and stability processes.
- Demonstrated technical competence of the technical and practical skills involved in analytical activities to prescribed quality standards.
- Must be skilled in analytical techniques e.g. HPLC, Dissolution, Gas Chromatography, KF and wet chemistry techniques.
- Able to communicate well with others, both laboratory and non-laboratory based.
- Able to work with minimal supervision.
- Good understanding of quality control, SOP and GMP adherence.
Desired
- Have a broad knowledge with and experience of working within a cGMP/GLP environment.
- 2-3 years experience of working within a pharmaceutical or biotechnology industry.
- Ability to work to key regulatory and compliance requirements.
- Experience of quality control/Stability within a pharmaceutical environment.
- Experience of Chromeleon software.
- Experience of data reporting and checking data within a QC environment.
- Understand and demonstrate a pragmatic approach to problem solving with GMP constraints.
Computer skills
- Must be competent in the use of MS Office, particularly Excel and Word, e-mail and internet.
Literacy and Numeracy
- Must be competent in writing reports both for internal use and for customers.
- Must be competent in the interpretation of analytical data.
Business Presentation Skills
- Must be an excellent face-to-face and telephone communicator.
Only candidates with a permanent right to work in the UK will be considered.
It’s Time For Your Next Chapter. We look forward to receiving your application.
QC Stability Analyst in Livingston employer: NextPharma
Contact Detail:
NextPharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Stability Analyst in Livingston
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and practising common questions. Show them your passion for quality control and stability analysis – it’s all about making that personal connection!
✨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.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. It shows you’re genuinely interested and professional – traits that employers love!
We think you need these skills to ace QC Stability Analyst in Livingston
Some tips for your application 🫡
Show Your Passion: When you're writing your application, let your passion for quality control and stability analysis shine through. We want to see that you’re excited about the role and how you can contribute to our team at NextPharma.
Tailor Your CV: Make sure your CV is tailored to highlight your relevant experience in analytical techniques like HPLC and GC. We love seeing candidates who can demonstrate their technical competence and understanding of GMP standards.
Be Clear and Concise: In your written application, clarity is key! Use straightforward language and structure your thoughts well. This will help us understand your qualifications and how you fit into our fast-paced environment.
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the QC Stability Analyst position. We can’t wait to hear from you!
How to prepare for a job interview at NextPharma
✨Know Your Analytical Techniques
Make sure you brush up on your knowledge of analytical techniques like HPLC, GC, and wet chemistry. Be ready to discuss how you've used these methods in past roles, as this will show your technical competence and understanding of the stability testing process.
✨Familiarise Yourself with cGMP Standards
Since the role involves working under current cGMP conditions, it’s crucial to understand these regulations inside out. Prepare examples of how you've adhered to quality control standards in previous positions, as this will demonstrate your commitment to compliance.
✨Prepare for Team Dynamics
This position requires collaboration with various departments. Think of instances where you've successfully worked in a team, especially under pressure. Highlight your communication skills and how you can contribute positively to a fast-paced environment.
✨Showcase Your Problem-Solving Skills
Be ready to discuss specific challenges you've faced in a laboratory setting and how you approached them. This could involve troubleshooting analytical issues or managing tight deadlines. A pragmatic approach to problem-solving is key in this role, so make sure to convey that.