QA Co-op: Pharma Materials & Supply Chain (Spring 2027)

Randstad USA; Indianapolis (IN); In loco; USD 34.000 - 44.000; Part-time

Descrizione del lavoro

Randstad USA is seeking a detail-oriented QA Co-op to support the Quality Assurance department at a pharmaceutical manufacturing facility in Indianapolis, IN. The six-month program runs January 4, 2027 through June 25, 2027 and requires active enrollment in an academic program.

The role involves assisting with material specification documentation, GMP compliance, and document control processes. You will gain hands-on exposure to cGMP documentation, product release procedures, and regulatory

Competenze

• Currently pursuing a Bachelor's degree in Life Sciences, Engineering, or related field.
• Basic understanding of Quality Management Systems and cGMP principles.
• Strong attention to detail and organizational skills.
• Ability to track and manage project progress.
• 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.

Mansioni

• Assist in the receipt and evaluation of item coded materials for quality acceptance or rejection.
• Participate in document change control procedures and revision history maintenance.
• Assist in periodic reviews of controlled documents to ensure compliance with current regulations.
• Update controlled item specification documents to conform with updated site requirements.
• Perform quality oversight tasks for GMP warehouses.
• Help prepare documentation for regulatory inspections and internal audits.
• Contribute to continuous improvement initiatives for Quality Inspection team

Conoscenze

GxP

MS Office

ERP system

Formazione

High School

Descrizione del lavoro

Randstad USA is seeking a detail-oriented QA Co-op to support the Quality Assurance department at a pharmaceutical manufacturing facility in Indianapolis, IN. The six-month program runs January 4, 2027 through June 25, 2027 and requires active enrollment in an academic program.

The role involves assisting with material specification documentation, GMP compliance, and document control processes. You will gain hands-on exposure to cGMP documentation, product release procedures, and regulatory