How to Apply for Roche Student Internship IP2TIS 2024

How to Apply for Roche Student Internship IP2TIS 2024 Roche, a global leader in pharmaceuticals and diagnostics, is dedicated to advancing scientific research to enhance the quality of life for individuals. By integrating pharmaceuticals and diagnostics, Roche has become a frontrunner in personalized healthcare, striving to tailor treatments to each patient’s specific needs. As the largest biotech company worldwide, Roche specializes in groundbreaking medicines for oncology, immunology, infectious diseases, ophthalmology, and central nervous system disorders. Additionally, Roche leads in vitro diagnostics and tissue-based cancer diagnostics and is at the forefront of diabetes management.

Established in 1896, Roche remains committed to discovering innovative methods for disease prevention, diagnosis, and treatment while promoting sustainability. The company collaborates with various stakeholders to enhance patient access to medical breakthroughs. Thirty Roche-developed medicines, including vital antibiotics, antimalarials, and cancer treatments, are listed in the World Health Organization Model Lists of Essential Medicines. Furthermore, Roche has been consistently recognized as the Group Leader in sustainability within the Pharmaceuticals, Biotechnology & Life Sciences Industry by the Dow Jones Sustainability Indices (DJSI) for ten consecutive years.

Internship Opportunity:

Position Title: Student Internship IP2TIS 2024 – Reduction of Post-Registration Import Sample Quantities in Emerging Markets

Location: Nigeria

Employment Type: Full-time

Job Description:

We are looking for a highly motivated intern to support our post-registration laboratory testing efforts for medicines, primarily focusing on Nigeria and broader African markets. The intern will collaborate closely with a diverse team to assist in ensuring quality control and regulatory compliance in pharmaceutical products.

Key Responsibilities:

• Research and document regulatory requirements for post-registration import sample testing in Nigeria and other African countries.
• Conduct thorough research on the regulatory frameworks, guidelines, and practices governing post-registration laboratory testing of medicines in Nigeria and across Africa.
• Gather and analyze data on the quality, safety, and efficacy of pharmaceutical products available in Nigerian and African markets.
• Lead the development and execution of sampling plans, testing protocols, and quality assurance procedures for post-registration laboratory testing.
  • Work collaboratively with internal teams and external partners to exchange information, adopt best practices, and address emerging issues in pharmaceutical quality control.
  • Prepare comprehensive reports, presentations, and recommendations based on research findings and analysis of post-registration laboratory testing data.
  • Stay updated on industry trends, regulatory advancements, and new technologies in pharmaceutical quality control and testing.

Join us in making a meaningful impact in ensuring the quality and compliance of pharmaceutical products in Nigeria and across Africa.

About You

If you’ve recently completed your Bachelor’s or Master’s degree, particularly in fields such as life sciences (Biochemistry, Microbiology), Chemistry, Pharmacy, Pharmaceutical sciences, or Public health, and are keen on applying your knowledge in a contemporary work setting through an internship lasting at least 3 months, while also delving into the pharmaceutical industry, then you’re the one we’re looking for.

Moreover, you possess:

• Familiarity with the regulatory framework of the African continent and a strong desire to contribute positively to regulatory policies.
• Exceptional organizational abilities and a flexible approach to managing tasks and their execution.
• Capability to work autonomously and collaborate efficiently within a highly motivated team.
• Proficient communication skills, with fluency in both written and verbal English; proficiency in local languages is an added advantage.
• Proficiency in Microsoft Office and Google Software applications is essential.
• Regulatory certifications and prior experience in Drug Quality Control Laboratory testing are advantageous.