Validation Engineer

at  Biocrucible

Hove BN3 7ED, , United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate24 Dec, 2024Not Specified26 Sep, 2024N/AAutomation,Manufacturing ProcessesNoNo
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Description:

We love people who crave autonomy, it is our job to empower you to get the job done.
We are seeking an experienced hands on Validation Engineer to join our small but growing team. You will be close to the action and have creative freedom. This role would fit a multi-skilled individual with experience in validation, supported by process and/or materials experience.
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.

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.

QUALIFICATIONS AND EXPERIENCE:

  • Highly proficient with risk management practises (e.g. FMEA) .
  • Injection moulding, automation and/or software validation experience would be useful.
  • Experience validating materials used in product development and manufacturing processes would be beneficial.

Responsibilities:

We are able to offer this role with a hybrid working pattern to include at least 3 days per week onsite in Hove, and 1x day per month in Cambridge.

  • Develop and implement the sites validation strategy for all pipeline and future products.
  • Support harmonization of the validation and risk approaches across multiple sites.
  • Lead the 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)

Other Industry

Pharma / Biotech / Healthcare / Medical / R&D

Other

Graduate

Proficient

1

Hove BN3 7ED, United Kingdom