QUALITY ASSURANCE SPECIALIST
at Bond Williams
Oxford, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 17 Jul, 2024 | GBP 45000 Annual | 18 Apr, 2024 | N/A | Change Control | 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:
Other responsibilities as Quality Assurance Specialist include:
- Provide support to new product development activities and processes
- Review and approve Design and Development documentation
- Review and approve Change Control documentation for Quality Assurance
- Support the maintenance of Quality System documentation
- Analyse and communicate proposed, new or changing requirements
- Review and approve CAPA documentation
- Provide support to routine manufacturing activities, projects, development and training
Experience required:
- Experience working in Quality Assurance
- Experience operating in ISO9001 environment
- Excellent working knowledge of document management systems, change control and CAPA systems
- Knowledge and experience of working in an ISO13485 environment is advantageous
- Good team player and able to work in a fast-paced environment with minimal supervision
Keywords: Quality Assurance Specialist, QA Specialist, Regulatory Specialist, Quality Assurance Manager, QA Manager, ISO9001, ISO 13485
Bond Williams Professional Recruitment are an equal opportunity employer and operate as an Employment Business and Recruitment Agency
Responsibilities:
- Provide support to new product development activities and processes
- Review and approve Design and Development documentation
- Review and approve Change Control documentation for Quality Assurance
- Support the maintenance of Quality System documentation
- Analyse and communicate proposed, new or changing requirements
- Review and approve CAPA documentation
- Provide support to routine manufacturing activities, projects, development and trainin
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
IT Software - QA & Testing
Software Testing, Clinical Pharmacy
Graduate
Proficient
1
Oxford, United Kingdom