Role OverviewThe QA Associate will work closely with the QA Supervisor to ensure site compliance with Regulations, ISO Standards, and organizations SOPs. They will also support the development of a Quality Mindset and a culture of efficiency, attention to detail, and on-time delivery.
What You Will Do
The QA Associate will maintain a Quality Assurance presence on the manufacturing floor, review and approve documentation for Quality approval, and collaborate with the Manufacturing/Operations team to resolve equipment and process-related deviations.
Why It Might Be a Fit
The ideal candidate will have excellent interpersonal skills, be able to develop productive working relationships, and demonstrate excellent written and oral communication skills. They will also be able to thrive in a team environment and work autonomously.
Requirements
- Bachelor's Degree in Science (Chemistry, Biology, Biochemistry, Microbiology etc.)
- Minimum of 2 years of experience working as Quality in a GMP Manufacturing environment, and/or as an Operator within a Pharmaceutical Manufacturing environment
- Moderate knowledge of regulations and quality systems such as deviations, Non-Conformance, CAPA, etc.
- Understanding of Good Documentation Practices (GDPs) and its criticality
- Excellent written and verbal communication skills
- General computer skills evidenced by hands-on work with computerized Operations equipment (SCADA); and reporting and data analysis software (Word, Excel, Visio, JMP, Minitab, etc.)
Benefits
- Smoke-free campus
- Equal Opportunity Employer
- Prohibits discrimination and harassment of any kind
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