Incoming QA Specialist – GMP & Documentation Focus

Tjoapack; Michigan; On-site; USD 55,000 - 70,000; Full time

Job summary

Tjoapack is seeking an Incoming QA Specialist in Clinton, TN to ensure all incoming materials meet GMP standards before release for manufacturing and packaging. This role emphasizes documentation control, inspection, and cross-functional communication with Planning, Warehouse, Production, Customer Service, and QA teams.

You will verify documentation and materials against specifications, prepare batch records for submission, and maintain compliant records to support patient safety and regulatory

Qualifications

• Experience in a pharmaceutical cGMP environment is required.
• Strong attention to detail and accurate information processing.
• Clear written and verbal communication in English.

Responsibilities

• Perform incoming product checks prior to release for use.
• Inspect packaging, bulk, and components against specifications.
• Verify materials meet quality and GMP requirements.
• Support documentation review, release decisions, and archiving.

Skills

Attention to detail

Documentation management

English proficiency

Communication skills

GMP knowledge

Job description

Tjoapack is seeking an Incoming QA Specialist in Clinton, TN to ensure all incoming materials meet GMP standards before release for manufacturing and packaging. This role emphasizes documentation control, inspection, and cross-functional communication with Planning, Warehouse, Production, Customer Service, and QA teams.

You will verify documentation and materials against specifications, prepare batch records for submission, and maintain compliant records to support patient safety and regulatory