Role OverviewThe QA Associate will work closely with the QA Supervisor to ensure site compliance with regulations, ISO standards, and organizational SOPs. They will also champion and develop the organization's Quality Mindset and 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, strong written and oral communication skills, and the ability to work autonomously. They will also be able to influence positive outcomes without direct reporting authority and possess a demonstrated ability in process owners and subject matter experts.
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.)
- Visual acuity of 20/20 or better, with or without corrective lenses, as well as color vision
Benefits
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