At a Glance
- Tasks: Conduct analytical testing on therapeutic proteins and support quality assurance in a lab environment.
- Company: Join Lonza, a global leader in pharmaceutical manufacturing with a focus on collaboration.
- Benefits: Competitive pay, professional development, and a supportive, inclusive workplace.
- Other info: Dynamic team environment with opportunities for mentorship and continuous improvement.
- Why this job: Make a real difference in patients' lives by ensuring the quality of life-saving medicines.
- Qualifications: Degree in Chemistry or related field; experience in GMP-regulated labs preferred.
The predicted salary is between 35000 - 42000 £ per year.
- Scientist - QC Product Testing & Stability
- Slough, United Kingdom
Join Lonza's QC Product Testing & Stability team in Slough and play a key role in ensuring the quality and stability of therapeutic protein products that help improve patients' lives.
This is an exciting opportunity for a laboratory-based scientist to apply analytical expertise in a regulated GMP environment while developing technical and quality assurance experience.
This is a fully site-based role.
Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
- What you will get
- An agile career with opportunities for technical and professional development.
- A collaborative, inclusive and ethical working environment.
- Competitive compensation and recognition for high performance.
- A comprehensive range of benefits relevant to your role and location.
- Opportunities to contribute to continuous improvement projects and develop mentoring experience.
• The full list of our global benefits can be found here
What you will do
- Perform analytical testing on therapeutic protein samples using techniques including HPLC, capillary electrophoresis, spectrophotometry and other physicochemical methods in accordance with GMP requirements, SOPs and study protocols.
- Review analytical data for technical accuracy, interpret results against specifications, identify trends and communicate observations to key stakeholders including Study Directors, Quality Assurance and Manufacturing.
- Prepare stability study protocols, testing summaries and technical reports to support product quality and stability programmes.
- Support investigations, deviations, CAPAs and change controls, independently leading routine quality investigations where appropriate.
- Mentor and support colleagues by sharing technical knowledge, providing training and promoting best laboratory practices.
- Contribute to laboratory operations through equipment monitoring, reagent and consumable management, housekeeping and continuous improvement initiatives.
- Work collaboratively across Quality Control, Quality Assurance and Manufacturing to ensure customer, regulatory and business requirements are consistently met.
- What we are looking for
- Degree in Chemistry, Biochemistry or another relevant scientific discipline, or equivalent relevant laboratory experience.
- Experience working within a GMP-regulated pharmaceutical or biological laboratory environment.
- Practical knowledge of analytical techniques such as HPLC, capillary electrophoresis, spectrophotometry or other protein characterisation methods.
- Understanding of c GMP principles and their application within a quality-controlled laboratory.
- Strong analytical and problem-solving skills with the ability to interpret data and identify trends.
- Excellent organisational and communication skills with the ability to prioritise work and collaborate effectively within a multidisciplinary team.
- A proactive mindset with a commitment to continuous learning, quality, safety and process improvement.
- About Lonza
At Lonza, our people are our greatest strength.
With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow.
Our core values of
Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table.
At Lonza, we value diversity and are committed to creating an inclusive environment for all employees.
If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
QC Scientist in Slough employer: SwiftCruit
At Global, we pride ourselves on being an exceptional employer, offering a dynamic work environment in the heart of London that fosters innovation and collaboration. As a Senior Machine Learning Engineer, you'll not only have the opportunity to influence millions through cutting-edge AI solutions but also benefit from a culture that encourages professional growth, cross-functional partnerships, and the development of reusable engineering standards. With a commitment to employee development and a focus on impactful projects, Global is the ideal place for those seeking meaningful and rewarding careers in data science and machine learning.
StudySmarter Expert Advice🤫
We think this is how you could land QC Scientist in Slough
✨Unlock Networking Opportunities
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We think you need these skills to ace QC Scientist in Slough
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at SwiftCruit!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show SwiftCruit that you're not just a fit for the job but also a safety-conscious candidate!
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Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At SwiftCruit, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at SwiftCruit
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at SwiftCruit that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
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✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
