Quality Engineer (Manufacturing, Science & Technology)
Client:
Thornton & Ross
Location:
Huddersfield, United Kingdom
Job Category:
Other
EU work permit required:
Yes
Job Reference:
d010ead30073
Job Views:
112
Posted:
14.03.2025
Expiry Date:
28.04.2025
Job Description:
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 provider of prescription products, including emollients and generics to the NHS with 100 years’ heritage behind us.
We are part of the STADA group, focusing on generics and non-prescription consumer health products, selling in approximately 120 countries.
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. To implement the Technology Transfer/Commercialization of new products.
Main responsibilities include but are not limited to:
* Provide front line support to manufacturing, working with the shift teams, focusing on manufacturing each batch safely, on time, in compliance with the batch instructions and quality requirements.
* Support the completion of technology transfer projects, commercialization, and product launch of new products.
* Execute process validations, re-validations, Annual Monitoring Batch (AMB), and short-term improvement projects.
* Review and assure that validation protocols and reports are technically correct.
* Ensure protocols are executed as intended.
* Write Manufacturing Process Transfer Documents.
* Provide expertise and implement innovative validation best practices.
* Execute process improvements and scale-up.
About You:
At STADA, we value uniqueness. If you’re keen to add value, thrive in a busy environment, and have the can-do spirit, 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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