submissions . Activities relating to product lifecycle management. Maintain and develop working relationships effectively effectively and provide required regulatory support. Reviewing artwork relating to products ensuring abreast of developments and changes in the local regulatory environment which directly impacts on the product Council (SAPC) is essential Minimum of 2 years Regulatory Affairs experience in pharmaceutical industry . Experience Experience working with SAHPRA and other Regulatory Authorities in Africa. Excellent spoken and written
an experienced and open-minded Student Regulatory Affairs Manager to join our esteemed campus in Cape Town in higher education and management to ensure compliance with all regulatory requirements and standards Serve on the Academic Exco team. Manage the regulatory and student affairs team and budget. Lead a small issues. Maintain the Internal Quality Assurance Management system and quality assurance processes. Serve like the Student Information System and Learner Management System. Oversee the production of academic transcripts
The company is an established leader in the pharmaceutical sector, with over 90 products, many of them 'famous-brand' and 'Blockbuster' products in the CAMS, cosmetics, and medical devices sector. They export to over 60 countries. In particular, this position will require input into RA requirements
pharmaceutical sector has an opportunity for an RA Manager to lead their team. You need 5 years of RA experience to step up into an RA Manager role. This role is more about project management. Ensure that the RA team monthly work output targets. Primarily you will be managing the RA team, rather than compiling dossiers. Although
competent and experienced Regulatory Affairs Scientist for the Regulatory Affairs Department Key Job Outputs: Compilation and update of documents to be submitted to regulatory authorities, this includes the compilation of to customer (both internal and external) and regulatory authority queries Ensuring that annual product according to internal procedures and in line with regulatory expectations Compilation of process qualification
experienced Regulatory Affairs Scientist (Development and Technical Support) for the Regulatory Affairs Department according to internal procedures and in line with regulatory expectations Performing risk assessments to evaluate nitrosamine impurities according to relevant regulatory guidelines Compilation of process qualification Compilation and update of documents to be submitted to regulatory authorities, this includes compilation of common
directives to maximise sales for the allocated department. K KEY RESPONSIBILITIES: Plan and implement visual the commercial departments Communicate marketing material for promotions to department staff Create visual area Manage the distribution and implementation of ticketing and décor in allocated area Manage and maintain implement accordingly People management - staffing, performance management, training & development
The company is an established leader in the pharmaceutical sector, with over 90 products, many of them 'famous-brand' and 'Blockbuster' products in the CAMS, cosmetics, and medical devices sector. They export to over 60 countries. In particular, this position will require input into RA requirements
Chemical and Regulatory Compliance Officer to join the regulatory team. This role focuses on managing the environmental product stewardship initiatives, and provide regulatory guidance to internal and external stakeholders Chemistry and minimum 2 years experience in chemical regulatory compliance required. Requirements: Bachelor's degree in Chemistry Proven experience in chemical regulatory compliance (min 2 years) Prior experience in skills and attention to detail Proficiency in regulatory tracking and compliance software. Strong communication
submissions . Activities relating to product lifecycle management. Maintain and develop working relationships effectively effectively and provide required regulatory support. Reviewing artwork relating to products ensuring abreast of developments and changes in the local regulatory environment which directly impacts on the product Council (SAPC) is essential Minimum of 2 years Regulatory Affairs experience in pharmaceutical industry . Experience Experience working with SAHPRA and other Regulatory Authorities in Africa. Excellent spoken and written