At a Glance
- Tasks: Oversee quality processes and digital solutions in compliance with global standards.
- Company: Join Sanofi, a leading biopharma company dedicated to improving lives.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Be part of a dynamic team driving continuous improvement in QC processes.
- Why this job: Make a real impact on medicine delivery and improve lives globally.
- Qualifications: Experience in quality control and knowledge of GMP regulations required.
The predicted salary is between 40500 - 49500 £ per year.
Location: Waterford, Ireland
Working Arrangement: Hybrid - 3 Days On-Site, 2 Days Working From Home Remotely
Job type: Full-Time, 12-Month Fixed Term Contract
About the job
The Quality Control system team will have responsibility to oversee all quality processes and digital solutions related to quality control management and to ensure compliance with the Sanofi global processes. The team also supports the delivery of ongoing QC continuous improvement initiatives.
Main responsibilities:
- Overseeing all quality processes and digital solutions related to quality control management in compliance with the Sanofi global processes and quality control tools.
- Ensuring issuance and approval of all appropriate local quality control documentation, such as local procedures, templates, to support the QC processes and QC digital system usage, in the QC labs, in accordance with the Sanofi global processes.
- Ensuring quality control processes supported by appropriate procedures are implemented locally and maintained, in line with Sanofi global and regulatory requirements.
- Ensuring implementation and maintenance of QC digital solution (core model and local) including data management and end-user management.
- Ensuring archiving of all QC documentation, in compliance with the Sanofi global requirements and regulatory.
- Ensuring training and support of end-users on QC processes and tools, in coordination with Sanofi global teams.
- Investigating on a timely manner and resolving any quality control events, issues or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs.
- Providing support during regulatory inspections and audits by presenting QC processes and QC digital solution documents and records.
- Leading initiatives for continuous improvement in QC processes and tools usage, in coordination with QC excellence team.
- Being representative of the site in the related CoPs led by the global, for the process in his/her scope, and if requested participating in the CoEs, and ensuring local communication.
- Being representative of QC for the processes led by QMS team at site level.
About you
- Demonstrable experience in quality control within the pharmaceutical industry, including knowledge of Good Manufacturing Practices (GMP) and regulatory requirements.
- Third level qualification (degree in science or related discipline) or appropriate relevant experience supplementing lower grade scientific qualification.
- Ability to analyze complex data and laboratory results to make informed decisions and identify areas for improvement.
- Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements.
- Proficiency in identifying issues and implementing effective solutions to resolve quality control problems.
Why choose us?
Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply. Transform lives worldwide by delivering life-changing treatments anywhere, anytime. Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride. Help deliver 30+ new product launches by 2030, ensuring patients get treatments faster than ever.
Quality Control System Supervisor in Slough employer: Sanofi EU
Sanofi Waterford is an exceptional employer, offering a dynamic and supportive environment for MSAT Graduates to thrive. With a strong commitment to employee wellbeing, the company provides flexible working arrangements, access to an onsite gym and medical centre, and numerous opportunities for professional growth through structured training and mentorship. The collaborative work culture fosters innovation and teamwork, making it an ideal place for graduates to launch their careers in the biopharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Control System Supervisor in Slough
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We think you need these skills to ace Quality Control System Supervisor 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 Sanofi EU!
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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 Sanofi EU, 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 Sanofi EU
✨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 Sanofi EU that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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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.
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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.
