QA Supply Chain Co-op Spring 2027

***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- NO RELOCATION STIPEND PROVIDED***

MilliporeSigma is a global leader in life science research and biopharmaceutical manufacturing. Our culture thrives on creativity and a shared passion for advancing scientific discovery. We are seeking a co-op to join our dynamic Research & Development team. This role supports the Life Science Biology franchise within MilliporeSigma.

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.

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

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