QA Associate: Elevate cGMP & Quality

Artech Information System LLC; Morris Plains (NJ); On-site; USD 55,000 - 75,000; Full time

Job summary

A leading IT staffing company is seeking a candidate with 0-3 years of GMP manufacturing or QA experience for a role in compliance and quality assurance. Responsibilities include ensuring adherence to regulatory requirements, coordinating batch records, and approving documents for raw materials. A BS/BA in Biological Sciences or equivalent experience is required. This position is critical to maintaining product quality and compliance with site standards.

Qualifications

• 0-3 years GMP manufacturing and/or QA related experience.

Responsibilities

• Ensure compliance with cGMP legal and regulatory requirements.
• Coordinate and perform batch record issuance for internally manufactured products.
• Review and approve manufacturing and QC documents for raw material disposition.
• Perform administrative functions for filing and maintenance of records.
• Control costs within the department to meet budget.
• Complete training in electronic database and GMP, safety, and Compliance courses.
• Support tasks necessary for product quality and cGMP compliance.

Education

BS/BA in Biological Sciences or equivalent relevant career experience

Job description

A leading IT staffing company is seeking a candidate with 0-3 years of GMP manufacturing or QA experience for a role in compliance and quality assurance. Responsibilities include ensuring adherence to regulatory requirements, coordinating batch records, and approving documents for raw materials. A BS/BA in Biological Sciences or equivalent experience is required. This position is critical to maintaining product quality and compliance with site standards.