Compliance Specialist – Pharmaceutical Manufacturing (2nd Shift)

Aequor; Swiftwater (Monroe County); On-site; USD 30,000 - 47,000; Full time

Job summary

Aequor in Swiftwater, PA seeks a Compliance Specialist II for the 2nd shift to perform audits ensuring manufacturing procedures meet in-house specs and government regulations. This contract role requires establishing auditing requirements and maintaining quality standards.

You will conduct internal audits, review documentation, and inspect returned goods, interpreting complex documents to ensure compliance.

Responsibilities

• 2nd Shift: Perform audits necessary to ensure the compliance of manufacturing procedures to in-house specifications and government regulation.
• Establish auditing requirements, quality standards and test methods in accordance with regulations and relevant quality requirements.
• Conduct internal audits of manufacturing processes to ensure compliance.
• Review document and complete inspection of returned goods.
• Interpret complex, explicit documentation to ensure quality standards and compliance.
• Work under only very general supervision.
• Work is reviewed for soundness of judgment and overall adequacy and accuracy.
• Contribute to the completion of organizational projects and goals.
• Errors in judgment or failure to achieve results would normally require a moderate expenditure of resources to rectify.
• Frequent internal company and external contacts.
• Represent organization on specific projects.

Job description

Job Title- Compliance Specialist II 2nd Shift

Location: Swiftwater, PA 18370

Duration: Contract till Apr 2027 with possibility to extend

2nd Shift: Perform audits necessary to ensure the compliance of manufacturing procedures to in-house specifications and government regulation. Establish auditing requirements, quality standards and test methods in accordance with regulations and relevant quality requirements. Conduct internal audits of manufacturing processes to ensure compliance. Review document and complete inspection of returned goods. Interpret complex, explicit documentation to ensure quality standards and compliance. Work under only very general supervision. Work is reviewed for soundness of judgment and overall adequacy and accuracy. Contribute to the completion of organizational projects and goals. Errors in judgment or failure to achieve results would normally require a moderate expenditure of resources to rectify. Frequent internal company and external contacts. Represent organization on specific projects. Represent organization on specific projects. Years of Experience: 3 - 6 Years