Quality Engineer

at  AliveDx

Penicuik EH26, Scotland, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate25 Jun, 2024Not Specified26 Mar, 2024N/AGood communication skillsNoNo
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Description:

At AliveDx, we empower diagnostic insights, transform patient care, and innovate for life. With over 30-years in in-vitro diagnostics, we put the health of patients first by creating innovative solutions designed for faster diagnostic results. Alba–– our blood bank reagents portfolio–– and MosaiQ®–– one of the first multiplexing and multimodality automated testing platforms––are designed to make labs more efficient and clinical decision-making more effective. Our journey started as Alba Bioscience, and later, Quotient. Today, as AliveDx, we innovate for life.

Responsibilities:

  • Has Working Knowledge of Quality Management System Concepts and Procedures; performs a variety of routine tasks or assignments.
  • Non-Conformance assessment and progression
  • Change Control assessment and progression.
  • Quality Meeting facilitation
  • Follows prescribed guidelines or procedures to provide solutions to problems.
  • Root Cause Analysis.
  • Trend quality data from key data (e.g. non-conformance, CA/PA)
  • Works with moderate level of guidance
  • Ownership of Issues
  • Internal auditing
  • Continues to build knowledge of the business, processes and customers (internal and external)
  • Assist during internal/external audits from customers and regulatory bodies.
  • Compile and contribute to quality metrics and trending accordingly to her activities.
  • Identify areas for improvement and contribute to a culture of continuous improvement.
  • Demonstrate and exhibit all key behaviours as defined by the business.
  • Participate in an ‘in-house’ programme of continuous training and assessment.
  • Conduct all duties in compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP) and appropriate regulatory requirements including statutory Health & Safety legislation and internal practice.
  • Perform any other duties as reasonably requested from the Company from time to time


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Proficient

1

Penicuik EH26, United Kingdom