Validation QC specialist
at CRYOPAK INC
Anjou, QC, Canada -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 25 Oct, 2024 | Not Specified | 30 Jul, 2024 | 3 year(s) or above | Process Validation,English,French,Excel,Writing,Microsoft Word,Technical Operations | 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:
.Job Overview:We are seeking a dedicated Quality/Validation Coordinator to manage and implement quality and validation processes. This role ensures that products and services meet regulatory agency requirements, internal standards, and current industry practices. The ideal candidate will coordinate with regulatory, service, instrumentation, and R&D teams to review and improve quality/validation processes.
MINIMUM REQUIREMENTS:
- Education: College diploma in science, industrial pharmacy, or related discipline.
- Experience: 3+ years in pharmaceutical/biotechnology technical operations (QA/QC/validation).
- Skills:
- Bilingual (French & English).
- Knowledge of GMP guidelines and process validation/QC.
- Experience in writing protocols and reports.
- Proficient in Microsoft Word, Excel, and computerized monitoring systems.
- Excellent organizational and prioritization skills.
- Clean driver’s license (50% travel).
Responsibilities:
REQUIREMENT SUMMARY
Min:3.0Max:8.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Diploma
Proficient
1
Anjou, QC, Canada
