At a Glance
- Tasks: Ensure GMP quality and compliance in biopharmaceutical processes while collaborating with various teams.
- Company: Join Lonza, a global leader in life sciences with a focus on innovation and collaboration.
- Benefits: Enjoy an agile career, competitive compensation, and a variety of benefits tailored to your role.
- Other info: Be part of a diverse team dedicated to improving lives through innovative therapies.
- Why this job: Make a real impact in the biopharmaceutical industry while working in a dynamic and inclusive environment.
- Qualifications: BSc in Life Sciences and experience in Quality Assurance within the pharmaceutical sector.
The predicted salary is between 40000 - 50000 £ per year.
The Senior Quality Assurance Specialist will be responsible for supporting the Centre of Excellence for biopharmaceutical process development and small-scale GMP manufacturing in Slough, ensuring the effective management of GMP quality and compliance activities across the site. The role enables operational performance by providing expert oversight of GMP issues through Quality Management System (QMS) processes, site governance, and quality leadership. Working collaboratively with GMP Manufacturing, Quality Control, MSAT, Procurement, and Warehouse teams, the position provides comprehensive Quality Assurance support, helping to maintain regulatory compliance, uphold quality standards, and drive continuous improvement across site operations.
What you will get:
- An agile career and dynamic working culture
- An inclusive and ethical workplace
- Compensation programs that recognize high performance
- A variety of benefits dependant on role and location
Key responsibilities:
- To provide shoulder to shoulder review of documentation generated during manufacturing processes, development and laboratory processes
- Review, approve and provide QA support to key business partners for the management of quality records e.g. Deviations, CAPA, Change Controls, Investigations.
- Utilise knowledge of GMP and quality processes within the functional areas to manage and escalate Major and Critical compliance issues through the site QMS processes e.g. deviations and CAPAs
- To actively identify, suggest and participate in continuous improvement activities
- Mentor and coach business partners in cGMP practices to maintain and develop a cGMP environment
- Maintain and promote a state of audit readiness
- Actively suggest, initiate, participate and contribute to PQS process improvements initiatives and projects
- Provide QA SME support at departmental Local Quality Councils and project meetings
What we need you to have:
- BSc life Sciences qualified
- Quality Assurance, preferably within a CDMO or Pharmaceutical industry sector
- Hands on experience with batch documentation is essential and CAPA’s and Deviations is highly desirable but essential
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.
Ready to shape the future of life sciences? Apply now.
Senior QA Specialist - Night Shift in Slough employer: Lonza
Lonza is an exceptional employer, providing a vibrant work culture in Cambridge where innovation thrives. Employees benefit from a competitive package and ample opportunities for professional growth, all while contributing to groundbreaking advancements in therapies that impact patients worldwide.
StudySmarter Expert Advice🤫
We think this is how you could land Senior QA Specialist - Night Shift in Slough
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Lonza. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Lonza.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Lonza. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Lonza is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Senior QA Specialist - Night Shift 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 Lonza!
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 Lonza that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Lonza!
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 Lonza, 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 Lonza
✨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 Lonza 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
Take some time to familiarise yourself with Lonza’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨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.
