Quality Compliance Jobs in Puerto Rico

Execute Quality disposition (approval or rejection) of bulk drug substances. Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured tested stored and managed according to current Good Manufacturing Practices (cGMP) Good Lab...

Preferred qualification in experience with Inspection Development process. Basic Knowledge in statistics using Minitab JMP or other statistical software Project Management Skills Knowledge in development documentation protocols and reports Excellent Communication and Teamwork skills Good Documentat...

SummaryThe Quality Applications Specialist supports quality systems and product transfer activities by ensuring compliant validation of computerized systems and manufacturing processes. The role focuses on sterilization equipment process validation and quality system compliance in regulated environm...

The Packaging Engineer will be responsible for designing developing validating and optimizing packaging systems to support Product Transfer and New Product Introduction (NPI) initiatives. This role requires hands-on experience working with packaging lines filling equipment automation systems and man...

Expericence in Quality and ComplianceExperience with validation protocols and reports for clean utilities manufacturing processes cleaning processes equipment computerized systems change control records deviationsetc. Experience in biological processes is desired.RequirementsDoctorate OR Masters 2...

QRC Group is a leading provider of consulting engineering validation quality and talent solutions for the pharmaceutical biotechnology and regulated manufacturing industries. Our mission is to connect top-tier talent with essential projects that drive innovation quality and operational excellence fo...

Lead and execute Computer System Validation (CSV) activities for Quality Information Technology systems in compliance with FDA GxP ISO and global regulatory requirements.Conduct and maintain formal validation documentation including Validation Plans Risk Assessments IQ OQ PQ protocols and reports an...

Description:Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on incident triage team....