Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE and report on the assigned portfolio of products Conduct dossier due diligence to ensure all data gaps are with Regulatory Authorities, internal and external stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that regulatory compliance is maintained or enhanced. Key Requirements: Pharmacy Council 3 to 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable
supplier based in Midrand requires a Group Marketing Specialist. QUALIFICATIONS: A Grade 12 certificate as a Marketing degree / diploma. a formal qualification in Graphic Design in digital marketing will be latest trends and best practices in online health marketing and measurement Previous experience in a medical would be an advantage DIGITAL MARKETING Plan and execute all digital marketing, including Search engine optimisation optimisation / Search engine marketing (SEO), marketing database, email, social media and display advertising
certificate is the minimum requirement, as well as a Marketing degree / diploma.
a formal qualification
qualification in Graphic Design in digital marketing will be a definite advantage
Highly creative with experience
latest trends and best practices in online health marketing and measurement
Previous experience in a
advantage
DIGITAL MARKETING
Plan and execute all digital marketing, including Search engine
engine optimisation / Search engine marketing
(SEO), marketing database, email, social media and display
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE and report on the assigned portfolio of products Conduct dossier due diligence to ensure all data gaps are with Regulatory Authorities, internal and external stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that regulatory compliance is maintained or enhanced. Key Requirements: Pharmacy Council 3 to 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable
PE000998-CP-1 Our client is looking for an experienced Regulatory and Quality Assurance Pharmacist to join their experience Vet industry experience Knowledge of regulatory submissions in Botswana, Nambia, Zambia, Zimbabwe Job Duties Regulatory Affairs Duties Regulatory Submissions: Prepare and submit regulatory documents to comply with regulatory guidelines and requirements. Compliance: Monitor and interpret regulatory requirements registration of existing products. Coordinate with regulatory bodies for product approvals. Labeling and Advertising:
relationships effectively and provide required regulatory support. Reviewing artwork relating to products codes of conduct and regulations. Keeping abreast of developments and changes in the local regulatory environment 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 with Business Managers, Quality Assurance & Marketing departments Knowledge of Acts , Regulations and
Regulatory Affairs Pharmacist OTC POS24203
Based: Midrand Pharmacy Council
A long-established leader in the pharmaceutical sector has an opportunity for an RA Manager to lead their team. You need 5 years of RA experience in the dossier compilation of registered medicines. The position could suit an ambitious Senior RA Pharmacist too, who is ready to step up into an RA Mana
Senior Regulatory Affairs Pharmacist: OTC -POS24206
Area : Pharmacy Council
Key Job Outpu
tablish regulatory priorities and allocate resources and workloads
PE000998-CP-1 Our client is looking for an experienced Regulatory and Quality Assurance Pharmacist to join their experience Vet industry experience Knowledge of regulatory submissions in Botswana, Nambia, Zambia, Zimbabwe Job Duties Regulatory Affairs Duties Regulatory Submissions: Prepare and submit regulatory documents to comply with regulatory guidelines and requirements. Compliance: Monitor and interpret regulatory requirements registration of existing products. Coordinate with regulatory bodies for product approvals. Labeling and Advertising: