Incoming QA Specialist: Materials & Documentation

Alcami Corporation; Clinton (TN); On-site; USD 45,000 - 70,000; Full time

Job summary

Alcami Corporation is seeking an Incoming QA Specialist to join its Quality Assurance team in Clinton, TN. The role ensures all incoming materials meet GMP standards before release, handling documentation control and cross-functional coordination.

You will work on-site, with first shift hours, collaborating with Planning, Warehouse, Production, and Customer Service to maintain traceability and regulatory compliance for packaging components, bulk products, and materials.

Qualifications

• Minimum of 1 year of pharmaceutical cGMP regulatory experience.
• Experience with documentation processes or controlled document systems.
• High school diploma or equivalent is required.

Responsibilities

• Perform incoming quality checks for materials prior to release.
• Review and control documentation to ensure accuracy and compliance.
• Coordinate with cross-functional teams to ensure timely release and archiving.
• Communicate quality findings to internal teams and customers.

Skills

Planning & Scheduling

Attention to detail

English communication

Education

High school diploma or equivalent

Job description

Alcami Corporation is seeking an Incoming QA Specialist to join its Quality Assurance team in Clinton, TN. The role ensures all incoming materials meet GMP standards before release, handling documentation control and cross-functional coordination.

You will work on-site, with first shift hours, collaborating with Planning, Warehouse, Production, and Customer Service to maintain traceability and regulatory compliance for packaging components, bulk products, and materials.