Disclaimer: Hunt UK Visa Sponsors aggregates job listings from publicly available sources, such as search engines, to assist with your job hunting. We do not claim affiliation with Lonza. For the most up-to-date job details, please visit the official website by clicking "Apply Now."
United Kingdom, Slough
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
The Role
Working as part of the QA Documentation Control Team. You will be responsible for proactively issuing documents and labels to Manufacturing based on the schedule and defined timelines obtained from customer departments. You will also be responsible for ensuring a high standard of documentation issuing is adhered to by yourself and others.
Key Responsibilities
- Proactively issue approved/effective GMP documents for use in Manufacturing, ensuring all deadlines are strictly met.
- Print labels for the Manufacturing process, including finished product labels to maintain the highest standards.
- Check the accuracy of issued documentation and labels to ensure flawless compliance.
- Issue effective logbooks as required according to GMP procedures.
- Print and issue other GMP documentation as required, meeting business timelines.
- Lead and manage quality records such as Deviations, CAPA, Change Controls, and Investigations.
- Author, review, and approve GMP documentation to support our ambitious goals.
- Prioritize workload to ensure all deadlines are met successfully.
- Act as a point of contact for general queries relating to document issuing.
- Maintain issuing supplies to ensure materials are always available, enabling timely issuing of documents.
Key requirements:
- Bachelor of Science or equivalent experience.
- IT literate with proficiency in MS Office (Word, Explorer, Excel, Access, Outlook) and familiarity with database entries.
- Previous work experience in QA / GMP is useful though not essential.
- Proven ability to prioritize and manage workload efficiently.
- Outstanding attention to detail and strict adherence to procedures and timelines.
- Strong communication skills and ability to collaborate effectively.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Reference: R67271
Apply