At a Glance
- Tasks: Conduct lab tests on therapeutic proteins and ensure quality and stability.
- Company: Leading pharmaceutical company focused on innovation and compliance.
- Benefits: Competitive pay, hands-on experience, and opportunities for professional growth.
- Other info: Collaborative environment with mentorship opportunities and career advancement.
- Why this job: Join a dynamic team and make a real difference in healthcare.
- Qualifications: BSc in Chemistry/Biochemistry or relevant experience; knowledge of GMP preferred.
The predicted salary is between 37000 - 40000 € per year.
Location: Slough
Contract Length: 12 months
Working Hours: 37.5 hours/week
Pay: £17.96 per hour
About The Role
The role is predominantly lab based for the execution of analytic testing e.g. HPLC (size exclusion, ion exchange etc.), electrophoresis (e.g. CE SDS, icIEF), spectrophotometry and general characteristic analysis (e.g. visual appearance, pH, Osmolality) for the purpose of assessing the quality and stability of therapeutic proteins. All work is expected to be carried out in a safe and compliant manner in accordance with local EHS policies and cGMP guidelines. In addition, some time will be spent technically reviewing other analysts' assays, writing stability study protocols and data summary reports, SOP updates, and assisting with quality records.
Key Responsibilities
- Performs experimental work independently in accordance with SOPs and study protocols on a variety of sample types.
- Performs work in a safe, compliant manner, ensuring training profile is maintained and up to date at all times.
- Plans and completes assigned tasks within the required timeframe.
- Communicates progress and escalates challenges to Line Manager and/or scientific lead as appropriate.
- Technically reviews assays against SOPs, protocols and GMP principles and liaises with operators and study directors to close out technical review of assays.
- Interprets data against specifications, critically assesses results and identifies trends within data, reporting any observations and concerns to QC management, SDs, QC representative in a timely manner.
- Writes stability study protocols, reports, testing summaries etc.
- Acts as a mentor and/or trainer to newer or more junior members of the team and provides help and support to teammates.
- Supports improvement projects within the department and encourages best practice and corrects incorrect/bad practice.
- Supports, as needed, with the timely completion of investigations, deviations, CAPAs and change controls and may independently lead and complete minor investigations e.g. pipette calibration failure, storage equipment temperature excursions.
- Actively contributes to QC department general lab housekeeping, ensuring the laboratory is adequately stocked with reagents and consumables as needed.
- Performs monitoring and maintenance of equipment and may take on system owner responsibilities.
- Works collaboratively in a team to ensure business, regulatory and customer needs are met.
- Performs other duties as assigned.
Education/Experience Required
BSc in relevant scientific discipline or relevant previous experience - Chemistry / Biochemistry Experience - GMP, Pharmaceutical, Biological.
Scientist (QC Product Testing and Stability) employer: Carbon
Join a dynamic and innovative team in Slough, where we prioritise employee growth and development in the field of quality control for therapeutic proteins. Our collaborative work culture fosters mentorship and continuous learning, ensuring that you not only contribute to meaningful projects but also advance your career in a supportive environment. With a commitment to safety and compliance, we offer a rewarding workplace that values your expertise and encourages best practices.
StudySmarter Expert Advice🤫
We think this is how you could land Scientist (QC Product Testing and Stability)
✨Tip Number 1
Network like a pro! Reach out to professionals in the QC and pharmaceutical fields on LinkedIn. Join relevant groups and participate in discussions to get your name out there and show off your expertise.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge. Be ready to discuss HPLC, electrophoresis, and other techniques mentioned in the job description. We want you to shine when they ask about your experience!
✨Tip Number 3
Don’t forget to showcase your soft skills! Communication and teamwork are key in this role. Think of examples where you've successfully collaborated or mentored others, and be ready to share those stories.
✨Tip Number 4
Apply through our website for the best chance at landing the job! We love seeing candidates who take the initiative to connect directly with us. Plus, it shows you're serious about joining our team.
We think you need these skills to ace Scientist (QC Product Testing and Stability)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights relevant experience in QC product testing and stability. We want to see how your skills match the job description, so don’t be shy about showcasing your expertise in HPLC, electrophoresis, and other analytical techniques!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality control in the pharmaceutical industry. We love seeing candidates who can connect their personal experiences to our mission at StudySmarter.
Showcase Your Team Spirit:Since collaboration is key in this role, make sure to mention any team projects or mentoring experiences you've had. We value teamwork and want to know how you can contribute to our supportive environment!
Apply Through Our Website:Don’t forget to submit your application through our website! It’s the best way for us to keep track of your application and ensure it gets the attention it deserves. We can’t wait to hear from you!
How to prepare for a job interview at Carbon
✨Know Your Techniques
Make sure you brush up on the specific analytical techniques mentioned in the job description, like HPLC and electrophoresis. Be ready to discuss your hands-on experience with these methods and how you've applied them in previous roles.
✨Understand Compliance and Safety
Familiarise yourself with cGMP guidelines and EHS policies. During the interview, be prepared to explain how you ensure compliance in your work and share examples of how you've maintained safety standards in a lab environment.
✨Showcase Your Problem-Solving Skills
Think of examples where you've faced challenges in your previous roles, especially related to data interpretation or technical reviews. Highlight how you approached these issues and what the outcomes were, demonstrating your critical thinking abilities.
✨Team Player Mindset
Since collaboration is key in this role, be ready to discuss your experience working in teams. Share instances where you've mentored others or contributed to team projects, showing that you're not just a great scientist but also a supportive colleague.
