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Quality Assurance Associate
40 Technology Way West Greenwich, RI 02817 US
Job Description
*Depending on experience
Fully Onsite - Rhode Island - 9-5 standard working hours
Experience: Associates degree at a minimum. Basic GMP experience, Document management experience, Familiar with working within a regulated industry, Strong attention to detail.
Job Details: Responsible for the maintenance of all required documentation for the Rhode Island site under the direction of Quality Management with coaching from the Document Management Subject Matter Expert. Provide comprehensive services in accordance with Good Manufacturing Practices (GMP) within Document Management with ability to flex support as needed within the Quality System space.
The staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.
Planet Pharma is an equal opportunity employer. It is our practice not to discriminate against any employee or applicant based on any criteria, condition or basis protected by laws or regulations in the locations where we do business. All qualified applicants are encouraged to apply. We celebrate diversity and are committed to providing an environment of mutual respect. We believe that diversity, equity and inclusion enable us to better meet our mission and values while serving our clients across the globe. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter, or contact us, so that we can discuss the appropriate alternatives available.
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