Teva Pharmaceutical Industries Ltd.
Location
United Kingdom | United States
Job description
We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us. We’re Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world and we currently have a fantastic opportunity for a Qualified Person to join our team on a Full Time, Permanent basis in Runcorn.
At Teva Runcorn, we develop, manufacture and market innovative and affordable medicines, specialising in sterile liquid products mainly used for treating respiratory conditions using Blow-Fill-Seal technology as well as injectable Combination Products such as our MS treatment Copaxone.
You'll be performing final QP Batch Certification daily to ensure that all products released to market comply with the requirements of the Manufacturer's Licence, Marketing Authorisations, ANDAs, Technical Agreements, CE certification, in accordance with EU, USA, or other requirements e.g. Russia, Brazil, Canada.
Key Responsibilities
Ensure the principles and guidelines of cGMP have been met during manufacturing, packaging and testing operations.
Verify all batch related documentation is compliant with the requirements of the regulatory authorities.
Review and certify batches in line with business shipment schedules.
Responsibility for planned changes or deviations being supported by appropriate sampling, inspection, testing and compliance adherence, in line with the requirements of the regulatory authorities.
Do you have:
A degree in a Science based discipline.
Membership of appropriate professional body.
Significant experience in a senior Quality role, a Quality Leader, in a modern manufacturing environment.
Registration as a Qualified Person, with acceptability to the Licensing Authority.
Experience with aseptic processing, sterile medicinal products and combination products is highly preferable.
Are you:
We're looking for a strong personality that is driven to set and deliver high performance standards relating to quality, safety, cost and customer service
A creative, visionary thinker that will proactively make suggestions/changes that take a long term strategic view for the overall improvement of quality processes
A confident communicator that defends their opinions to internal stakeholders
You'll be part of a small QP team, which translates to having a big influence across the business, including (but not limited to) involvement with initiatives to improve the site and the introduction of new products
If so - we would value hearing from you!
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
The deadline for internal application for this role will be Friday 10th November 2023#TJ
At Teva, we pride ourselves on being a company where we can all thrive, and where everyone feels comfortable being their true self.
Diversity and inclusion sits at the heart of everything we do. By valuing difference, we can be a better employer for our colleagues, and provide a better service for our customers and patients. That is why we are constantly looking for ways in which we can learn from each other, embrace what makes us unique and contribute to a fairer society free from discrimination and prejudice.
Job tags
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