📢 We’re Hiring | Regulatory Affairs Manager 📍 Location: Lusaka, Zambia 💼 Employment Type: Full-Time Levant Biotech LTD is seeking an experienced and motivated Regulatory Affairs Manager to lead regulatory activities and ensure compliance across our portfolio of pharmaceutical, medical device, and healthcare products. Key Responsibilities Manage product registrations, renewals, and regulatory submissions. Prepare and maintain regulatory documentation and dossiers. Liaise with regulatory authorities and business partners. Ensure compliance with applicable regulatory requirements. Review product labeling and promotional materials. Monitor regulatory changes and support new product launches. Qualifications Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related field. Minimum 3 years’ experience in Regulatory Affairs within the pharmaceutical or healthcare industry. Strong knowledge of regulatory requirements and product registration processes. Excellent communication, analytical, and organizational skills. Applicants must be Zambian nationals. How to Apply Send your CV and Cover Letter to hr@levantbiotech.com with the subject: Application – Regulatory Affairs Manager Only shortlisted candidates will be contacted.

Requirements

requirements. Review product labeling and promotional materials. Monitor regulatory changes and support new product launches. Qualifications Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related field. Minimum 3 years’ experience in Regulatory Affairs within the pharmaceutical or healthcare industry. Strong knowledge of regulatory requirements and product registration processes. Excellent communication, analytical, and organizational skills. Applicants must be Zambian nationals. How to Apply Send your CV and Cover Letter to hr@levantbiotech.com with the subject: Application – Regulatory Affairs Manager Only shortlisted candidates will be contacted.