Quality Engineer
at AliveDx
Penicuik EH26, Scotland, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 25 Jun, 2024 | Not Specified | 26 Mar, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
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