Student Internship IP2TIS 2024 - Reduction of Post-Registration Import Sample Quantities in Emerging Markets at Roche

• We are seeking a highly motivated intern to support our efforts in post-registration laboratory testing of medicines, with a focus on Nigeria and broader African markets.
• The intern will work closely with a cross-functional team to assist in this ambitious project as it relates to quality control and regulatory compliance related to pharmaceutical products.

This internship position is located in Lagos, Nigeria, on site / hybrid.

Key Responsibilities

• Establish and document regulatory requirements for post-registration import sample testing in Nigeria and across Africa
• Conduct research on the regulatory framework, guidelines, and practices governing post-registration laboratory testing of medicines in Nigeria and other African countries
• Collection and analysis of data on the quality, safety, and efficacy of pharmaceutical products available in the Nigerian and African markets
• Drive the development and implementation of sampling plans, testing protocols, and quality assurance procedures for post-registration laboratory testing
• Collaborate with internal stakeholders and external partners to gather information, share best practices, and address emerging issues related to pharmaceutical quality control
• Prepare reports, presentations, and recommendations based on research findings and analysis of post-registration laboratory testing data
• Assess industry trends, regulatory developments, and emerging technologies in the field of pharmaceutical quality control and testing

Who You Are
You are enrolled or have completed your Bachelor’s or Master’s studies at a university, preferably in the field of life sciences (Biochemistry, Microbiology), Chemistry, Pharmacy, Pharmaceutical sciences or Public health within the last 12 months and are interested in applying your knowledge in a modern working environment as part of an internship of at least 3 months and getting to know the pharmaceutical industry.

Furthermore you are/have

• Experience in the regulatory landscape of the African continent and passionate desire to positively influence regulatory policy
• Excellent organizational skills and a flexible approach to task prioritization and execution
• Able to work independently and collaborate effectively within a highly motivated group
• Effective communication skills, both written and verbal English is required. Ability to communicate in local languages is a plus
• Good command of Microsoft office and Google Software applications is crucial
• Regulatory Certifications and experience with Drug Quality Control Laboratory testing is an advantag