This internship opportunity within the Quality Management Systems (QMS) department offers hands-on experience in quality systems, documentation management, training management, and risk management. The role is designed to provide a comprehensive understanding of the QMS framework and its integration with site operations, ensuring compliance with industry standards and company policies. The intern will gain exposure to controlled document management, training coordination, risk assessment, and quality system improvements, contributing to the overall effectiveness of the quality function.
Key Responsibilities:
- Develop a clear understanding of the overall Quality Management System framework and how it interacts with site operations.
- Familiarize with Abbott Quality Policies, current Good Manufacturing Practices (cGMP), and site-specific quality procedures.
- Assist in managing controlled documents, including the issuance, revision, review, and archival of Standard Operating Procedures (SOPs).
- Participate in training management activities using ISOtrain and related systems to ensure compliance and tracking.
- Support Quality Risk Assessment activities and contribute to risk management processes.
- Understand and apply document control requirements and Good Documentation Practices (GDP).
- Assist in the review and maintenance of the Site Master File and Site Quality Manual.
- Track various QMS activities such as training compliance, SOP periodic reviews, and risk management actions.
- Support initiatives aimed at improving quality systems and monitoring compliance.
- Independently complete a defined project related to Quality Management Systems, demonstrating practical application of learning.
Required Qualifications:
- Pharm D degree.
- Fresh graduates or candidates with prior internship experience in the pharmaceutical or related industry.
Duration:
- The internship period is 5 to 6 months, providing sufficient time to gain meaningful experience and contribute to ongoing quality initiatives.
This internship is ideal for candidates looking to build a career in quality assurance within the pharmaceutical sector, offering valuable exposure to industry practices and regulatory requirements.