QA Supply Chain Co-op Spring 2027

Randstad USA; Indianapolis (IN); Sur place; USD 34 000 - 44 000; Plein temps

Avantages offerts par ce poste

Medical, prescription, dental, vision,

401K plan

Résumé du poste

Randstad USA is seeking a detail-oriented QA Co-op to join the Quality Assurance department at our Indianapolis location. The role focuses on creating and updating material specification documents and gaining exposure to pharmaceutical quality and materials management.

Candidate must be actively enrolled in an academic program and pursuing a degree related to Life Sciences or Engineering; the program runs January through June 2027 with a shift from 8 AM to 4 PM and a pay rate of $25–$32 per hour.

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

Responsabilités

• 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

Connaissances

GxP

MS Office

ERP system

Formation

High School

Outils

SAP

Description du poste

***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

salary: $25 - $32 per hour

shift: First

work hours: 8 AM - 4 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

Experience

• 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.