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Quality Engineer (Manufacturing, Science & Technology), West Yorkshire
Client: Thornton & Ross
Location: West Yorkshire, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Reference: d010ead30073
Job Views: 97
Posted: 03.03.2025
Job Description:
Quality Engineer
Manufacturing, Science & Technology
About the Company:
Thornton & Ross are one of the UK's fastest-growing, leading producers of household pharmaceutical products & own some of the country's most loved brands. We are also a trusted & reliable provider of prescription products, including emollients, bone health products & generics to the NHS with 100 years’ heritage behind us.
We are part of the STADA group, which focuses on a two-pillar strategy consisting of generics, including specialty pharmaceuticals & non-prescription consumer health products.
If you are ready for new challenges where you can make a difference to people’s health, you have come to the right place. We are looking for people with a great attitude and passion, who care about making a difference in the world.
About the Role:
The purpose of this role is to provide front line expert support for all process-specific issues to production within one or more production steps, ensuring execution of processes on-time, continuously improving in quality and efficiency, performed in compliance with cGMPs, SOPs and applicable guidelines. Responsibilities include:
* Provide front line support to manufacturing, working with the shift teams to ensure safe, timely, and compliant batch production.
* Support the completion of technology transfer projects, commercialization, and product launch of new products.
* Execute process validations, re-validations, and short-term improvement projects.
* Review and assure that validation protocols and reports are technically correct.
* Write Manufacturing Process Transfer Documents.
* Provide expertise and identify and implement innovative validation best practices.
* Execute process improvements and scale-up.
About You:
At STADA, we recognize our differences as a strength. Our values of Entrepreneurship, Integrity, Agility and One STADA ensure our uniqueness thrives. If you’re keen to add value and thrive in a busy fast-paced environment, bring those qualities along with:
* Degree in Pharmacy, Pharmaceutical Technology, Chemistry or equivalent scientific degree.
* Experience in Pharmaceutical (i.e., Validation / QA) or allied industries with exposure to cGMP and GDP.
* Strong knowledge of the pharmaceutical industry, specifically in production.
* Proficiency in English, both written and spoken.
* In-depth knowledge of cGMPs and current validation sciences.
* Proven process understanding (Pharma, GMP, Regulatory aspects).
What’s in it for you?
We offer a range of fantastic benefits, such as:
* 25 days annual leave (plus bank holidays) and the opportunity to buy an additional 5 days leave.
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