Incoming Quality & Documentation Specialist

Alcami-5; Michigan; On-site; USD 52,000 - 72,000; Full time

Job summary

Alcami is seeking an Incoming Quality Specialist to join our QA team. This 100% on-site position focuses on ensuring incoming materials, packaging components, and documentation meet GMP standards prior to release for manufacturing and packaging operations.

The role emphasizes documentation control, cross-functional collaboration, and clear communication with internal teams and customers to support patient safety and regulatory expectations.

Qualifications

• At least one year of pharma cGMP regulatory experience required.
• Experience with documentation processes or controlled document systems.
• High school diploma or equivalent required.

Responsibilities

• Incoming Quality & Product Control: perform checks prior to release.
• Inspect packaging, bulk, and components against specifications.
• Verify materials and documentation meet GMP requirements.

Skills

Attention to detail

Quality Assurance

Documentation

English proficiency

Cross-functional collaboration

Education

High school diploma or equivalent

Tools

Document control systems

Job description

Alcami is seeking an Incoming Quality Specialist to join our QA team. This 100% on-site position focuses on ensuring incoming materials, packaging components, and documentation meet GMP standards prior to release for manufacturing and packaging operations.

The role emphasizes documentation control, cross-functional collaboration, and clear communication with internal teams and customers to support patient safety and regulatory expectations.