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The QA Validation Intern will support validation activities by organizing and tracking documentation, assisting with QA release processes, and maintaining compliance records. This role provides exposure to GMP documentation practices and quality assurance workflows within the biotechnology industry.
Responsibilities
- Organize and track document spreadsheets for validation activities
- Print QA release labels and file release copies to Cartna
- Pick up and deliver documents between departments and buildings
- Compose a list of site SOPs sorted by topic
- Support QA team with administrative and compliance tasks
Requirements
- Enrollment in an undergraduate program
- Strong working knowledge of Excel
- Ability to work collaboratively in a team environment
- Strong organizational and presentation skills
Qualifications
- Undergraduate program
- Enrolled in an undergraduate program (Desired Academic Grade Level: Junior/ Senior)
Skills
Excel
*
* Required skills
Benefits
Dental Insurance
Medical Insurance
Accident insurance
Hospital indemnity insurance
Long-term disability coverage
Paid parental leave (8 weeks)
Peer-to-peer recognition programs
Vision Insurance
AD&D Insurance
Flexible spending accounts
401k retirement plan with company match
Health Savings Accounts
Well-being initiatives
Paid time off (vacation, personal, sick, floating holidays)
Life Insurance
Commuter Benefits
Pet insurance
Critical illness insurance
Short-term disability coverage
Legal assistance
Family planning and care resources
Eleven company holidays
About BioSpace
Lilly is a global healthcare leader headquartered in Indianapolis, Indiana, specializing in discovering and bringing life-changing medicines to patients worldwide. They are investing over $1 billion to create a new state-of-the-art manufacturing site in Concord, NC, focusing on parenteral medication...
Healthcare
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