Intern, Quality Assurance

Exela Pharma SciencesLenoir, NC
3h

About The Position

As a Quality Assurance Intern, you will work closely with the QA team to support and learn the various aspects of quality control and regulatory compliance in the pharmaceutical industry. This internship will provide you with exposure to industry standards, quality systems, and the opportunity to contribute to ensuring the quality and safety of our products. Priority consideration will be given to candidates who are in their final year of study or have recently completed their degree.

Requirements

  • Currently pursuing a degree in Pharmaceutical Sciences, Chemistry, Biology, Biotech, or a related field.
  • Strong attention to detail and a passion for quality and compliance.
  • Good understanding of cGMP (current Good Manufacturing Practices) and FDA regulations (preferred).
  • Excellent communication skills (both written and verbal).
  • Ability to work independently and as part of a team.
  • Strong organizational and time-management skills.
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint).

Nice To Haves

  • Prior internship or experience in a pharmaceutical or healthcare environment is a plus, but not required.

Responsibilities

  • Assist in the review and development of standard operating procedures (SOPs) and quality documentation.
  • Support the preparation for and execution of internal and external audits.
  • Participate in investigations of deviations, non-conformances, and CAPAs (Corrective and Preventive Actions).
  • Review batch records, test results, and other quality-related documents for compliance.
  • Support the QA team in maintaining and improving quality systems.
  • Assist with data analysis to identify trends, process improvements, and compliance gaps.
  • Collaborate with cross-functional teams (e.g., Manufacturing, R&D, and Regulatory Affairs) to ensure product quality and compliance.
  • Help with the preparation of quality reports and presentations for internal stakeholders.
  • Participate in product release processes and documentation reviews to ensure compliance with regulatory standards.
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