Quality Assurance Specialist - Biopharmaceutical Company - Békéscsaba
at Carbyne Consulting
Budapest, Közép-Magyarország, Hungary -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jun, 2024 | Not Specified | 19 Mar, 2024 | 2 year(s) or above | Continuous Monitoring,Adherence,Deviations,Document Preparation,Product Quality | 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:
LOOKING FOR A METICULOUS QUALITY ASSURANCE SPECIALIST TO JOIN A LEADING PLASMA-DERIVED CENTER IN BÉKÉS COUNTY! YOUR EXPERTISE WILL DRIVE ADHERENCE TO STRICT QUALITY, SAFETY, AND COMPLIANCE STANDARDS IN THE MANUFACTURING OF LIFE-SAVING PRODUCTS. COLLABORATE WITH A DYNAMIC TEAM TO ENSURE THE HIGHEST PRODUCT QUALITY.
Tasks Await You:
- Contribute to continuous monitoring of quality assurance system.
- Investigate and manage deviations, implement corrective measures.
- Prepare shipment release dossiers.
- Set exemplary standards for quality approach.
- Maintain Site Master File & quality system documentation.
- Assist in internal document preparation & administrative tasks.
- Ensure station operation compliance.
- Present processes & QA documentation during audits.
REQUIREMENTS:
- Relevant BSc/MSc degree (pharmacist, biologist, etc.)
- Minimum 2 years of part-time or full-time quality experience in ISO or GMP environment
- Residency in/around Békés county - or ability to commute and be on site 4 days a week
- Upper intermediate English oral and written skills
Responsibilities:
- Contribute to continuous monitoring of quality assurance system.
- Investigate and manage deviations, implement corrective measures.
- Prepare shipment release dossiers.
- Set exemplary standards for quality approach.
- Maintain Site Master File & quality system documentation.
- Assist in internal document preparation & administrative tasks.
- Ensure station operation compliance.
- Present processes & QA documentation during audits
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Budapest, Hungary