QA Supply Chain Co-op Spring 2027

Randstad USA; Indianapolis (IN); On-site; USD 34,000 - 44,000; Part time

Job summary

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

Qualifications

• 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.

Responsibilities

• 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

Skills

GxP

MS Office

ERP system

Education

High School

Job description

***THIS IS A 6-MONTH CO-OP STARTING JANUARY 4, 2027 THROUGH JUNE 25TH, 2027. TO QUALIFY, THE CANDIDATE HAS TO BE ACTIVELY ENROLLED IN AN ACADEMIC PROGRAM*** At MilliporeSigma, they are at the forefront of life sciences, working tirelessly to tackle the industry's toughest challenges. By collaborating with the global scientific community, they strive to enhance health access worldwide. Their mission is clear: to equip scientists and engineers with top-notch lab materials, technologies, and services, making research and biotech production simpler, faster, and more successful. With a dedication to shaping the future of drug development, they’re with our customers every step of the way, pioneering tomorrow's possibilities. We are seeking a detail-oriented QA Co-op to join the Quality Assurance department of our commercial drug product manufacturing facility. The successful candidate will assist in creating and updating material specification documentation while gaining valuable experience in pharmaceutical quality and materials management.

Required Qualifications

• 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 management 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

Preferred Qualifications

• Previous exposure to pharmaceutical or regulated manufacturing environment
• Experience with SAP or other ERP
• Experience with data entry and records management

Learning Opportunities

• Gain hands-on experience with cGMP documentation requirements
• Develop understanding of pharmaceutical material receipt and release process
• Develop material evaluation and receipt requirements
• Build knowledge of quality systems and materials management
• Network with professionals in pharmaceutical manufacturing

Compensation and Working Hours

• salary: $25 - $32 per hour
• shift: First
• work hours: 8 AM - 5 PM
• education: High School

Responsibilities

• 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

Skills

• GxP (6 months of experience is preferred)
• MS Office (6 months of experience is preferred)
• ERP system (6 months of experience is preferred)

Qualifications

• Years of experience: 0 years
• Experience level: Entry Level

Education

• High School (required)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.