Strides Pharma Inc.
Associate, Quality Assurance (QMS)
Strides Pharma Inc., Chestnut Ridge, New York, United States
Position Summary
The Entry-Level Associate, Quality Assurance supports the Quality Management System (QMS) and documentation processes at the Chestnut Ridge site. This role is designed for individuals beginning their career in pharmaceutical quality assurance and provides hands-on experience in maintaining compliance and supporting documentation workflows in a regulated environment.
Roles and Responsibilities Assist in organizing and maintaining
QMS documentation
including
SOPs, CAPAs, deviations, and complaints. Support the preparation and tracking of quality metrics and trending reports. Help coordinate internal audits and document audit responses. Participate in documenting product quality complaints and adverse event records. Aid in digitizing logbooks and checklists using electronic systems. Collaborate with cross-functional teams to ensure timely and accurate documentation updates. Provide administrative support for change control processes and quality-related meetings. Assist in preparing documentation for regulatory inspections and external audits. Maintain document control systems and ensure timely review and archival of QA records. Support training documentation and tracking for QA-related procedures. Help with data entry and analysis for quality reports using basic statistical tools. Monitor document lifecycle and ensure version control compliance. Participate in continuous improvement initiatives related to documentation and QMS processes. Education & Experience
Required Education: Bachelor's degree in Pharmaceutical Sciences or a related field. Preferred Education: Master's degree is a plus. Experience:
1-3 years in a pharmaceutical or regulated industry
(internships or co-op experience acceptable). Tools/Technologies:
Familiarity with QMS platforms and electronic documentation systems preferred. Physical Requirements
On-site role at Chestnut Ridge, NY. Standard work hours: 8 AM to 5 PM. No travel required. No lifting or driving responsibilities.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
The Entry-Level Associate, Quality Assurance supports the Quality Management System (QMS) and documentation processes at the Chestnut Ridge site. This role is designed for individuals beginning their career in pharmaceutical quality assurance and provides hands-on experience in maintaining compliance and supporting documentation workflows in a regulated environment.
Roles and Responsibilities Assist in organizing and maintaining
QMS documentation
including
SOPs, CAPAs, deviations, and complaints. Support the preparation and tracking of quality metrics and trending reports. Help coordinate internal audits and document audit responses. Participate in documenting product quality complaints and adverse event records. Aid in digitizing logbooks and checklists using electronic systems. Collaborate with cross-functional teams to ensure timely and accurate documentation updates. Provide administrative support for change control processes and quality-related meetings. Assist in preparing documentation for regulatory inspections and external audits. Maintain document control systems and ensure timely review and archival of QA records. Support training documentation and tracking for QA-related procedures. Help with data entry and analysis for quality reports using basic statistical tools. Monitor document lifecycle and ensure version control compliance. Participate in continuous improvement initiatives related to documentation and QMS processes. Education & Experience
Required Education: Bachelor's degree in Pharmaceutical Sciences or a related field. Preferred Education: Master's degree is a plus. Experience:
1-3 years in a pharmaceutical or regulated industry
(internships or co-op experience acceptable). Tools/Technologies:
Familiarity with QMS platforms and electronic documentation systems preferred. Physical Requirements
On-site role at Chestnut Ridge, NY. Standard work hours: 8 AM to 5 PM. No travel required. No lifting or driving responsibilities.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.