Contract QA Specialist,
Job Location:
Somerset, NJ - USA
Monthly Salary:
Not provided by the employer
Posted:
23 October 2026 (12 hours ago)
Application Deadline:
20 January 2027
Vacancies:
1 Vacancy
Job Summary
Role and Responsibilities
The Contract QA Specialist Validation / Qualification is responsible to provide quality oversight and ensure that validation and qualification activities conducted at Lupin Somerset are in compliance with FDA regulations guidance and other recognized industry standards. *This is a Contract role for Monday-Friday Work Week* Responsibilities and Duties: Provide Quality oversight for Validation and Qualification of Facilities and Utilities Equipment Manufacturing Packaging and Cleaning Processes and Computer Systems. Implement policies and procedures for Validation and Qualification systems consistent with FDA regulations Corporate and Site requirements. Review and approve all protocols plans risk assessments and reports pertaining to Validation and Qualification of the above systems. Review and approve applicable Change Controls including an impact assessment regarding changes to validated systems and processes. Ensure that the knowledge acquired during validation / qualification is incorporated in to batch records SOPs to ensure the validated state of the processes is maintained throughout lifecycle. Collaborate with SMEs from various functional departments to ensure that Validation and Qualification activities are consistent with requirements of Site / Corporate SOPs. Other duties as assigned by leadership Minimum Education and Experience Requirements Minimum Bachelor Degree in a scientific or technical field; graduate degree desired 3 years of extensive experience in the pharmaceutical industry in Quality Assurance. Cross functional experience in Engineering Technical Operations or Product development is a plus Working knowledge of FDA and applicable non-US regulations guidance and industry standards pertaining to pharmaceutical drug manufacturing. Experience with Process / Method validation or Equipment / Facility Qualification is a big plus Experience in using electronic Quality Management System ERP system MS Office applications Excellent analytical coordination and influential skills; Must be able to persuade cross functional
The Contract QA Specialist Validation / Qualification is responsible to provide quality oversight and ensure that validation and qualification activities conducted at Lupin Somerset are in compliance with FDA regulations guidance and other recognized industry standards. *This is a Contract role for Monday-Friday Work Week* Responsibilities and Duties: Provide Quality oversight for Validation and Qualification of Facilities and Utilities Equipment Manufacturing Packaging and Cleaning Processes and Computer Systems. Implement policies and procedures for Validation and Qualification systems consistent with FDA regulations Corporate and Site requirements. Review and approve all protocols plans risk assessments and reports pertaining to Validation and Qualification of the above systems. Review and approve applicable Change Controls including an impact assessment regarding changes to validated systems and processes. Ensure that the knowledge acquired during validation / qualification is incorporated in to batch records SOPs to ensure the validated state of the processes is maintained throughout lifecycle. Collaborate with SMEs from various functional departments to ensure that Validation and Qualification activities are consistent with requirements of Site / Corporate SOPs. Other duties as assigned by leadership Minimum Education and Experience Requirements Minimum Bachelor Degree in a scientific or technical field; graduate degree desired 3 years of extensive experience in the pharmaceutical industry in Quality Assurance. Cross functional experience in Engineering Technical Operations or Product development is a plus Working knowledge of FDA and applicable non-US regulations guidance and industry standards pertaining to pharmaceutical drug manufacturing. Experience with Process / Method validation or Equipment / Facility Qualification is a big plus Experience in using electronic Quality Management System ERP system MS Office applications Excellent analytical coordination and influential skills; Must be able to persuade cross functional
Required Experience:
IC
About Company
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