QA Co-op: cGMP Documentation & Compliance (6-Month)

Randstad USA; Indianapolis (IN); On-site; USD 36,000 - 45,000; Part time

Job summary

MilliporeSigma is seeking a detail-oriented QA Co-op to join the Quality Assurance team at our Indianapolis facility. The role supports cGMP documentation systems and regulatory readiness during a 6-month coop from January 4, 2027 through June 25, 2027.

Active enrollment in an academic program is required. The successful candidate will assist with document processing, review, and change control, while gaining exposure to pharmaceutical quality systems and regulatory compliance in a controlled

Qualifications

• Currently pursuing a Bachelor's degree in Life Sciences, Quality Systems, or related field.
• Basic understanding of Quality Management Systems and cGMP principles.
• Strong attention to detail and organizational skills.
• Proficiency with Microsoft Office applications (Excel, Word, PowerPoint).
• Excellent written and verbal communication skills.
• Ability to follow established procedures and maintain confidentiality.
• Demonstrated analytical thinking and problem-solving abilities.

Responsibilities

• Assist in processing, editing, updating, tracking, and filing of quality documents per cGMP.
• Support document review and approval through the electronic document management system.
• Participate in change control procedures and revision history maintenance.
• Perform periodic reviews of controlled documents for regulatory compliance.
• Update the Approved Supplier List by coordinating with vendors and Inventory Management.
• Prepare documentation for regulatory inspections and internal audits.
• Contribute to continuous improvement initiatives for Quality Management Systems.

Skills

Quality Management Systems

cGMP principles

Attention to detail

MS Office

Written and verbal communication

Analytical thinking

Problem solving

Education

Bachelor's degree in Life Sciences/Quality Systems

Tools

Electronic document management systems

Job description

MilliporeSigma is seeking a detail-oriented QA Co-op to join the Quality Assurance team at our Indianapolis facility. The role supports cGMP documentation systems and regulatory readiness during a 6-month coop from January 4, 2027 through June 25, 2027.

Active enrollment in an academic program is required. The successful candidate will assist with document processing, review, and change control, while gaining exposure to pharmaceutical quality systems and regulatory compliance in a controlled