Onsite IPQA Associate - 2nd Shift Quality

SUN PHARMA

New Brunswick (NJ)

On-site

USD 85,962,000 - 106,020,000

Full time

4 days ago

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Job summary

Sun Pharma is seeking a detail-oriented IPQA Associate I to support in-process quality assurance activities across our pharmaceutical manufacturing operations. This role is onsite in New Jersey on 2nd shift (Mon-Fri, 3:15-11:45pm).

You will monitor manufacturing and packaging activities, ensuring compliance with cGMP requirements and quality standards to protect product integrity. This position offers collaboration with cross-functional teams, close work on the production floor, and active

Qualifications

Bachelor's degree in a science related major required.
Minimum 2 years of experience in a pharmaceutical quality role.
Experience with GMP quality systems and validated documentation.
Ability to work in a regulated environment and communicate clearly.

Responsibilities

Perform routine area assessments to ensure compliance with cGMP requirements, SOPs, policies, and procedures.
Provide line clearance authorization prior to manufacturing and packaging operations.
Conduct conditional and final release inspections of packaging lines.
Support and monitor in-process quality checks during manufacturing and packaging activities.
Collaborate with Production and Packaging teams to resolve quality-related issues and ensure compliance throughout operations.
Review and approve controlled documents, including manufacturing and packaging batch records.