Hire Resolve's client is actively seeking a Regulatory Affairs Manager to join their team in Midrand, Gauteng. As a Regulatory Affairs Manager, you will be responsible for ensuring a thorough and seamless product registration process and dossier maintenance. You will ensure that the company complies with all regulations and maintains pharmacovigilance requirements. Responsibilities Lead, manage, and execute strategic direction as the regulatory affairs manager. Ensure and supervise that regulatory documentation meets relevant regulatory requirements and specifications. Provide input to the regulatory strategy in line with business objectives. Manage and implement safety updates where required. Manage Chemistry Manufacturing and Controls (CMC / P&A) updates and variations. Handle license renewals with service providers such as SAHPRA and the South African Pharmacy Council (SAPC) Write and develop SOPs in line with Global SOPs. Manage internal and external audits (e.g., Global & SAHPRA) Responsible for updates of dossiers, PI/PIL to ensure compliance with current legislation. Manage product complaints and deviations. Maintain regulatory documentation filing system. Ensure regulatory compliance and quality-related records are available and retained. Coordinate product recall or market withdrawal when necessary. Obtain and distribute updated information on domestic and international laws. Report ADR to Global Safety and SAHPRA and follow up on Adverse Drug Reactions (ADRs). Conduct pharmacovigilance training for local staff14. Answer requests from the Regulatory Authority in cooperation with Global Safety Oversee the implementation and maintenance of QMS to ensure compliance with industry standards and regulations. Identify areas for improvement within the quality system and implement corrective and preventive actions. Provide training to staff on quality standards, regulatory requirements, and best practices. Identify areas for improvement within the quality system and implement corrective measures. Maintain and manage quality related documentation, including standard operating procedures (SOPs), work instructions, and quality records. Ensure compliance with environmental regulations and standards at local, national, and international levels. The manager will also manage releases of finished products, customer complaints etc. Requirements B. Pharm (Bachelor of Pharmacy). Registration with the South African Pharmacy Council (SAPC). Minimum 10 years experience in Regulatory Affairs with human medicine and biologicals experience. Product registration and dossier maintenance. Pharmacovigilance experience and knowledge of SAHPRA submission portals. Launch procedures for new products. QA processes, APQRs, customer complaints. Knowledge of Regulations, Acts, and Guidelines for South Africa and East Africa. Microsoft Office Suite proficiency. Familiarity with ZAZIBONA processes and eCTD submissions Systems knowledge. Microsoft office suite including Word, Excel, Power Point at an Intermediate level. Familiar with ZAZIBONA processes. Competent and experienced in eCTD submissions. Benefits Contact Hire Resolve for your next career-changing move. Salary: negotiable. Apply for this role today contact Rebecca Grylls, Ashley Feldtmann, Thomas Stacey, Miné Roux at Hire Resolve or on LinkedIn You can also visit the Hire Resolve website: hireresolve.us or email us your CV: manufacturinghireresolve.za.com We will contact you telephonically in 3 days should you be suitable for this vacancy. If you are not suitable, we will put your CV on file and contact you regarding any future vacancies that arise.
