Quality Assurance Technician
at BioVectra Inc
Windsor, NS, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 29 Nov, 2024 | Not Specified | 31 Aug, 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 BIOVECTRA, we are passionate about improving patient care by making better therapeutics as a contract drug manufacturing organization (CDMO) that supports the top pharmaceutical and biotech companies in the world. Be part of a team with a global reach that also has a great community vibe. We care about each other and live our values of teamwork, respect, professionalism, and quality. Diversity is one of our strengths as we strive to offer a welcoming and inclusive environment.
We have an opening for Quality Assurance Technician. This is a 12 month-term position based out of our Windsor, Nova Scotia facility.
Responsibilities:
You will responsible for supporting the Quality Unit teams, including document control, quality electronic systems, quality system programs such as change control and supplier management, and batch review. You will identify and correct deficiencies within the Quality Management System.
- Performing GMP batch record and data review as per assignment and training for release of products.
- Identifying, acknowledging and escalating deviations and other quality system incidents as needed, and assisting in incident resolution.
- Scanning BPRs for archive and retrieving files to support audit and client requests.
- Supporting the documentation archive program.
- Issuing QA controlled documents for activities supporting GMP production.
- Supporting quality system programs including change control, incidents, supplier management, and client requests.
- Assembling data tables in support of PVR/APR for new projects.
- Supporting the CAPA program.
- Providing support for daily administration of quality electronic systems and participating in related project plans.
- Reviewing and initiating revisions to SOPs.
- Participating in the Facility Inspection Program.
- Inspecting and approving manufacturing suites for use.
- Participating in internal and external audits.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Windsor, NS, Canada