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Roche Student Internship IP2TIS 2024

Posted on Mon 11th Mar, 2024 - hotnigerianjobs.com --- (0 comments)


Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible. Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management.

Founded in 1896, Roche continues to search for better ways to prevent, diagnose and treat diseases and make a sustainable contribution to society. The company also aims to improve patient access to medical innovations by working with all relevant stakeholders. Thirty medicines developed by Roche are included in the World Health Organization Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and cancer medicines. Roche has been recognised as the Group Leader in sustainability within the Pharmaceuticals, Biotechnology & Life Sciences Industry ten years in a row by the Dow Jones Sustainability Indices (DJSI).

Applications are invited for:

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

Location: Lagos
Employment Type: Full-time

Job Description

  • 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

Application Closing Date
Not Specified.

Method of Application
Interested and qualified candidates should:
Click here to apply online


  

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