At a Glance
- Tasks: Conduct lab-based analytical testing and ensure quality of therapeutic proteins.
- Company: Leading pharmaceutical company focused on innovation and compliance.
- Benefits: Gain hands-on experience, mentorship, and opportunities for career advancement.
- Other info: Collaborative environment with a focus on safety and best practices.
- Why this job: Join a dynamic team and contribute to impactful scientific research.
- Qualifications: BSc in Chemistry/Biochemistry or relevant experience required.
The predicted salary is between 28000 - 35000 € per year.
The role is predominantly lab based for the execution of analytical 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.
- 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. In addition, 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.
Degree BSc in relevant scientific discipline or relevant previous experience. Field of Study: Chemistry / Biochemistry. Work experience Area: GMP, Pharmaceutical, Biological. Level: Entry Level.
Scientist in Edinburgh employer: LanceSoft UK
As a Scientist at our Slough location, you will be part of a dynamic and innovative team dedicated to advancing therapeutic protein quality and stability. We pride ourselves on fostering a collaborative work culture that encourages professional growth through mentorship and continuous learning opportunities, all while adhering to the highest safety and compliance standards. Our commitment to employee well-being is reflected in our supportive environment and comprehensive benefits, making us an exceptional employer for those seeking meaningful and rewarding careers in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Scientist in Edinburgh
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can help you land that scientist role.
✨Tip Number 2
Prepare for interviews by brushing up on your technical skills and understanding the latest trends in analytical testing. We recommend practising common interview questions and even doing mock interviews with friends or mentors to boost your confidence.
✨Tip Number 3
Showcase your passion for science! During interviews, share your experiences and projects that highlight your analytical skills and compliance with GMP guidelines. We want to see your enthusiasm for quality control and how you can contribute to the team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive and take the initiative to connect directly with us.
We think you need these skills to ace Scientist in Edinburgh
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights relevant experience and skills that match the Scientist role. We want to see how your background in analytical testing and compliance aligns with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about the role and how your expertise in HPLC, electrophoresis, and other techniques can contribute to our team at StudySmarter.
Showcase Your Team Spirit:Since collaboration is key in our lab, mention any experiences where you've worked well in a team. We love seeing candidates who can support their teammates and contribute to a positive work environment!
Apply Through Our Website:Don't forget to submit your application through our website! It’s the best way for us to receive your details and get you into our system quickly. We can't wait to hear from you!
How to prepare for a job interview at LanceSoft UK
✨Know Your Techniques
Make sure you brush up on the analytical techniques mentioned in the job description, like HPLC and electrophoresis. Be ready to discuss your experience with these methods and how you've applied them in previous roles or studies.
✨Understand Compliance Standards
Familiarise yourself with cGMP guidelines and EHS policies. During the interview, demonstrate your understanding of these standards and how you ensure compliance in your work. This shows that you take safety and quality seriously.
✨Prepare for Technical Reviews
Since the role involves reviewing assays and writing protocols, think about examples where you've had to critically assess data or mentor others. Be prepared to discuss how you approach technical reviews and what steps you take to ensure accuracy.
✨Show Team Spirit
Collaboration is key in this role, so be ready to share experiences where you've worked effectively in a team. Highlight any instances where you've supported colleagues or contributed to improvement projects, as this will show you're a team player.
