Quality Assurance Intern

Description

We are seeking a motivated and detail-oriented undergraduate student working towards a Pharmaceutical Manufacturing Certificate who is interested in gaining hands-on experience in Quality Assurance (QA) within the pharmaceutical industry. The successful candidate will assist the QA team with various projects related to qualification reviews, documentation support, and the setup of Quality Management System (QMS) documents.

Requirements

• Qualification Review Support: Assist in the review and assessment of qualification documents for manufacturing equipment, systems, and processes to ensure compliance with regulatory requirements and industry standards.
• Documentation Support: Provide assistance in organizing, preparing, and maintaining accurate QA documentation. This includes ensuring that records are complete, compliant, and ready for audits.
• QMS Document Setup: Support the setup and management of QMS documents, including Standard Operating Procedures (SOPs), work instructions, and other quality-related documentation. Ensure documents are up to date and follow proper formats.
• Data Entry and Tracking: Assist with tracking and updating key quality metrics, including document review cycles, qualification statuses, and other relevant data.
• Collaboration with Quality Teams: Work alongside experienced quality professionals to gain exposure to pharmaceutical quality standards and practices.
• Continuous Improvement: Contribute to ongoing efforts to improve quality systems, documentation processes, and overall efficiency.

Qualifications:

• Enrolled in an undergraduate program with a focus on Pharmaceutical Manufacturing or a related field.
• Interest in Quality Assurance and regulatory compliance within the pharmaceutical industry.
• Strong attention to detail and organizational skills.
• Ability to communicate effectively, both verbally and in writing.
• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
• Ability to work independently and as part of a team.
• Prior experience in pharmaceutical or manufacturing settings is a plus, but not required.

Schedule:

• 20 hours per week, with flexible hours to accommodate academic commitments

Benefits:

• Gain hands-on experience in pharmaceutical quality assurance and manufacturing.
• Opportunity to work with a dedicated and experienced team.
• Exposure to regulatory requirements and industry standards.
• Professional development and networking opportunities in the pharmaceutical industry.