Junior Validation Engineer
at Biocrucible
SWC1, , United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 31 Jan, 2025 | Not Specified | 01 Nov, 2024 | N/A | Manufacturing,Regulations | No | No |
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Description:
We love people who crave autonomy, it is our job to empower you to get the job done.
We view this role as a stepping stone for someone keen to start or enhance their early career in Validation.
We are seeking a Junior Validation Engineer to join our small but growing team. You will be very close to the action. Possibly you’ve worked in manufacturing, in labs, or a quality team and keen to start a career in validation. This is your opportunity to take that step.
ABOUT US:
Sapphiros UK is the fusion of two innovative entities - Biocrucible in Cambridge and Flexotronix in Hove. Biocrucible specialises in molecular detection technologies for near-patient and at-home testing, while Flexotronix is a center of excellence in high-speed printed electronics manufacturing. Together, they form Sapphiros UK, a company committed to pushing the boundaries of diagnostics.
Sapphiros’s portfolio of capabilities and technologies includes novel sample collection, next generation diagnostics, computational biology, and printed electronics.
With a ‘fail fast’ attitude we make decisions and progress quickly. We encourage our team to challenge the status quo and explore ways to improve our outcomes in a calculated manner, producing data to generate insights and acting rapidly on findings.
QUALIFICATIONS AND EXPERIENCE:
- Some experience in engineering, labs, quality or manufacturing environments
- Experience of working in highly regulated roles and environments.
- Knowledge of regulations
- Bachelor’s Degree or higher in a STEM discipline
Responsibilities:
- Working to develop and implement the sites validation strategy for all pipeline and future products.
- Support harmonisation of the validation and risk approaches across multiple sites.
- Execution of protocols to qualify equipment and validate manufacturing processes.
- Assessing new and existing manufacturing processes and workflows.
- Review compliance and adherence to safety and quality standards.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Graduate
A stem discipline
Proficient
1
Saffron Walden CB10 1XL, United Kingdom