Regulatory Affairs Graduate Programme at Aspen Pharma Group

About the Job

Aspen Pharma Group, a leading global specialty and branded pharmaceutical company, is excited to announce its Regulatory Affairs Graduate Programme. This initiative is designed to cultivate the next generation of pharmaceutical professionals, equipping them with critical skills in a rapidly evolving regulatory landscape. As a graduate, you will be immersed in a dynamic environment, contributing to the health of patients worldwide through high-quality, affordable medicines. This programme is a testament to Aspen's commitment to skills development and integration, particularly in scarce and critical areas such as Intellectual Property, Dossier Management, Quality, and Safety & Compliance within the pharmaceutical and healthcare sectors in South Africa.

Participants will gain invaluable hands-on experience, working alongside seasoned experts in a highly regulated industry. The programme offers a unique opportunity to understand the intricacies of pharmaceutical product registration, compliance, and post-market surveillance. You will learn how to navigate complex legal frameworks, prepare comprehensive regulatory submissions, and ensure that Aspen's products meet the highest standards of safety and efficacy. This role is ideal for driven individuals passionate about making a tangible impact on public health and eager to build a robust career foundation in a global pharmaceutical powerhouse.

Key Responsibilities

• Assist in the preparation and submission of regulatory dossiers for new products and variations.
• Support the maintenance of existing product registrations, ensuring ongoing compliance with local and international regulations.
• Conduct research on regulatory guidelines and requirements, providing insights to internal teams.
• Participate in cross-functional projects related to product development, quality assurance, and market access.
• Contribute to the development and implementation of regulatory strategies.
• Assist with the review of promotional materials and product labelling for regulatory compliance.
• Maintain accurate and up-to-date regulatory databases and documentation.
• Collaborate with various departments, including R&D, Quality Control, and Commercial, to ensure regulatory alignment.

Why Join the Company

Joining Aspen Pharma Group means becoming part of a dynamic organisation built on entrepreneurial strength and forward-thinking minds. Aspen attracts high-performing individuals who are passionate about their careers and driven to exceed expectations. The company prides itself on not only sourcing the best talent but also providing a host of opportunities for continuous development and career progression. With approximately 9,100 employees across 69 established offices in over 50 countries, Aspen offers a truly global perspective and diverse career paths. You will be part of a team that improves the health of patients in more than 150 countries, contributing to a meaningful purpose. Aspen fosters a culture of innovation, collaboration, and excellence, where your contributions are valued, and your growth is prioritised. The company's commitment to quality and affordability in medicines makes it a leader in the pharmaceutical industry, offering a stable and rewarding career environment.

How to Apply

Please apply using the Quick Apply button on this page. Note that if you have not heard from the Talent Acquisition department within 30 days of this advert closing, your application has unfortunately been unsuccessful. Internal Applications must be completed using an Aspen mailing address after applicants have informed their direct line managers of their application for this specific role.

• Matric / National Senior Certificate
• Science related tertiary qualification (either a BSC or National Diploma in Science)
• Computer literate and proficient in the Microsoft Office bundle (Word, Excel, PPT, Teams & Outlook)
• South African Citizen
• Must not have participated in a learnership/ internship before
• No criminal record
• Able to travel to the office in Woodmead, from Monday to Friday (8:00 to 17:00)
• Advanced verbal & written communication skills
• Confident with good interpersonal skills
• Able to work in a team environment and independently
• Good at planning, prioritizing, multi-tasking and implementing
• Have a high attention to detail
• Work in a highly regulated environment with a compliance mindset
• Good at decision making, problem solving and executing
• Have a high tolerance to stress
• Driven, determined and results oriented
• Ability to deal with and resolve conflict situations.