job description
Join GSK, a global leader in healthcare innovation, for a transformative 6-month QA Operations Internship in Denpasar, Bali. This role offers a unique opportunity to contribute to clinical research excellence by leading critical biosampling activities for international studies.
As a QA Operations Intern, you will play a pivotal role in designing and executing biosampling protocols and sample logistics plans that ensure the integrity, compliance, and efficiency of clinical trials. You’ll collaborate with cross-functional teams, including clinical operations, laboratory services, and regulatory affairs, to uphold GSK’s commitment to patient safety and data accuracy.
This internship is ideal for aspiring healthcare professionals or biomedical/pharmacy students seeking hands-on experience in quality assurance, clinical logistics, and global health research. Based in Bali’s dynamic healthcare hub, you’ll gain exposure to international standards (GCP, GLP) while contributing to life-changing medical advancements.
Internship Duration: January – June 2027 (6 months)
Location: Hybrid (Denpasar, Bali with potential travel for training)
Responsibility
- Lead the design and implementation of biosampling strategies for clinical studies, ensuring alignment with protocol requirements and regulatory standards.
- Develop and maintain sample logistics plans, including transportation, storage, and tracking systems to guarantee sample integrity.
- Collaborate with clinical sites, laboratories, and vendors to coordinate sample collection, processing, and shipping timelines.
- Conduct risk assessments and implement mitigation strategies for biosampling activities to minimize errors and delays.
- Monitor and report on sample management KPIs, such as turnaround times, temperature excursions, and compliance metrics.
- Assist in audit preparations and inspections by ensuring documentation and processes adhere to GSK’s quality standards and global regulations.
- Support the training of site staff on biosampling procedures, equipment use, and data recording best practices.
- Contribute to process improvement initiatives by identifying inefficiencies in sample handling workflows.
Qualifications
- Education: Currently enrolled in a Bachelor’s or Master’s degree in Pharmacy, Biomedical Sciences, Biology, or a related field.
- Technical Knowledge: Familiarity with Good Clinical Practice (GCP), Good Laboratory Practice (GLP), or quality assurance principles is a plus.
- Analytical Skills: Ability to interpret clinical protocols, SOPs, and regulatory guidelines with attention to detail.
- Communication: Excellent written and verbal English skills to liaise with global teams and document findings.
- Problem-Solving: Proactive approach to identifying and resolving logistical or compliance challenges.
- Software: Proficiency in Microsoft Office (Excel, Word) and basic data analysis tools.
- Availability: Commitment to a full-time, 6-month internship from January to June 2027.
- Soft Skills: Strong organizational, time-management, and teamwork abilities in a fast-paced environment.