Quality Control Compliance Specialist
at Sanofi
Waterford, County Waterford, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 26 Apr, 2025 | Not Specified | 26 Jan, 2025 | 2 year(s) or above | Interpersonal Skills,Communication Skills,Completion | 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:
KNOWLEDGE:
- Extensive knowledge of cGMP and GDP in a regulated environment.
- Working knowledge of quality systems in a regulated environment.
- Understand relevant quality/compliance regulations.
SKILLS AND COMPETENCIES:
- Excellent accuracy and attention to detail.
- Excellent interpersonal skills.
- Excellent Communication skills.
- Initiative – be able to work in a self-directed manner to see issues through to completion.
Responsibilities:
- Raising and management and on time closure of all Quality System processes including assigned Change Controls, Deviations, CAPAs, ILIs & QEs.
- Driving of all Quality Metrics for the department.
- Forward review of Quality Metrics to ensure no over-dues.
- Procedure effectiveness and simplification and actively contribute to continuous improvement initiative.
- Ensure effective co-ordination and support for external and internal audits for the department.
- Perform critical / constructive review of procedures and practices. Identify and lead projects to make step change improvements to the department’s Quality.
- Conduct duties in a safe manner and report all safety issues or concerns.
- Support leadership team in achieving goals / tasks.
- Actively contribute to continuous improvement initiatives utilizing lean methodologies where appropriate.
- Liaise with Quality Assurance Representative to support and improve RFT in the area and Always Audit Ready.
- Ensure all required training is completed on time.
- Maintain training in critical test activities as required in the laboratory (will be defined by head of QC).
- Complete all duties as per relevant SOPs and global procedures.
- Ensure compliance to cGMP at all times.
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Waterford, County Waterford, Ireland