QA Associate - Pharmaceuticals Job at Harba Solutions
Job Responsibilities:
- Review of production activities, including area clearance, issuance, and review of batch records
- Deviation triage, tracking/trending, and investigation support
- Review of Facilities and Engineering assets, work, and records
- Review of QC documentation/test records
- Support Raw material sampling and coordination with material management for the release
- Review and approval of Materials Management and Supply Chain activities
- Support of Environmental Monitoring Program
- Ensure documents comply with company style guide and business practices
- Communicate with all relevant stakeholders to understand the documentation needs
Qualifications:
- B.S. in Biology, Biochemistry, Biotechnology, Chemistry, or related field desired
- Minimum of 3 years of Quality Assurance experience in biopharma or similarly regulated industry.
- GMP-related documentation
- Hands-on experience with aseptic manufacturing Quality.
- Proficient in Microsoft Office Suite, especially Microsoft Excel.
- Ability to collaborate with a team and individuals.
Job Type: Full-time
Pay: $60,000.00 - $80,000.00 per year
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Vision insurance
Schedule:
- 8 hour shift
- Day shift
- Evening shift
- Monday to Friday
Ability to commute/relocate:
- Indianapolis, IN 46260: Reliably commute or planning to relocate before starting work (Required)
Education:
- Bachelor's (Required)
Experience:
- GMP: 2 years (Required)
Work Location: One location
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