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Job summary
A leading pharmaceuticals company seeks a Quality Assurance Senior Associate in West Greenwich, RI. In this role, you will provide crucial quality oversight for manufacturing operations and ensure compliance with regulatory standards. Responsibilities include reviewing quality documentation, collaborating with various departments, and maintaining GMP practices. Ideal candidates have a Bachelor's degree, at least 2 years of relevant experience, and familiarity with industry systems. This position offers opportunities for growth in a dynamic environment.
Qualifications
Minimum of 2 years of experience in Quality or Manufacturing.
Strong understanding of cGMP principles and regulatory expectations.
Experience utilizing enterprise systems like Maximo and MES.
Responsibilities
Provide quality oversight for F&E and IQA Warehouse areas.
Ensure facilities comply with cGMP standards.
Review and approve work orders and job plans.
Skills
Ability to prioritize and navigate ambiguity
Exposure to F&E operations
GMP experience
Strong communication skills
Proficient in Microsoft Office
Education
Bachelor's Degree in a relevant field
Tools
Maximo
MES
Job description
A leading pharmaceuticals company seeks a Quality Assurance Senior Associate in West Greenwich, RI. In this role, you will provide crucial quality oversight for manufacturing operations and ensure compliance with regulatory standards. Responsibilities include reviewing quality documentation, collaborating with various departments, and maintaining GMP practices. Ideal candidates have a Bachelor's degree, at least 2 years of relevant experience, and familiarity with industry systems. This position offers opportunities for growth in a dynamic environment.