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 Duties: Serve on the Academic Exco team. Manage the regulatory and student affairs team and budget. Lead 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
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 industry . Experience working with SAHPRA and other Regulatory Authorities in Africa. Excellent spoken and written
competent and experienced Regulatory Affairs Scientist for the Regulatory Affairs Department Key Job 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
for CAMs & Coismetics products, as opposed to pharma products Excellent references are a requirement
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
Knowledge & Attributes: Effective territory management Analyse Impact Rx data Ability to effectively pressure, to set priorities and to demonstrate time management skills Knowledge of basic financial calculations Specialists and Key Opinion Leaders Good territory management To target and segment HCPs The main purpose of business thereby building up a solid customer base Manage the territory to achieve service level requirements may be given to a Sales Consultants whereby the management of a Wholesaler/Shortliner will be facilitated
position will report to the QC (Quality Control) Manager. NOTE - For now, the positions are on an 18-month testing. And perhaps to stand in as Acting QC Manager from September too. Job functions: Lead validation submissions, new product development and during regulatory and customer inspections. Maintain temperature
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
of FMCG and/or OTC pharma products Marketing Manager experience to apply. Manage the OPEX (cost centers targets for the FMCG and pharmaceutical industries. Managing agency and business expectations; assisting in channel spend per commercial objectives Approval of regulatory compliance submissions Support channel in preparing preparing DOH submissions regarding product updates Manage channel strategy execution and customer conference such as those in sales, product development, regulatory affairs, and art, to guarantee alignment and
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