Senior Regulatory Pharmacist. Job Purpose: Support the Regulatory team to provide superior Regulatory services To ensure legal and regulatory compliance with the relevant medicine Regulatory Authorities (Country Pharmacy Council, ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work of products: Assisting with internal product queries from relevant departments Assisting with external stakeholders Establish regulatory priorities and allocate resources and workloads Review regulatory agency submission
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE 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
is looking for an experienced Regulatory and Quality Assurance Pharmacist to join their company Job Requirements 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:
/>Vet industry experience
Knowledge of regulatory submissions in Botswana, Nambia, Zambia, Zimbabwe
Duties
Regulatory Affairs Duties
Regulatory Affairs Pharmacist (POS24192)
Area; Aeroton
Salary R750 800k
Purpose the role:
Support the Regulatory team to provide superior Regulatory services to relevant departments ensure legal compliance with the relevant medicine Regulatory Authorities (Country Specific where applicable) Pharmacy Council, ensuring timeous processing of regulatory applications.
Qualifications &
Pharmacy Council
looking for a Regulatory Affairs/Quality Assurance Pharmacist to join their team. Regulatory Affairs (RA): including database maintenance. Quality Assurance (QA): Assist QA Manager with artwork review and quality management logs, and notify the Responsible Pharmacist (RP) of findings. Assist with QA batch release of Act 101 required. Prepare for inspections, renew licenses, and assist with GMP in-house training. Act as an authorized
company has an opportunity for an experienced RA Pharmacist (2 years of RA dossier compilation experience) relationships effectively and provide required regulatory support. Reviewing artwork relating to products 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
Regulatory Affairs Pharmacist OTC POS24203
Based: Midrand Pharmacy Council
the compliance of pharmaceutical products with regulatory requirements in South Africa and other designated designated markets. This role involves managing regulatory submissions, writing and reviewing Chemistry, Manufacturing up-to-date knowledge of regulatory guidelines. Key Responsibilities: 1. Regulatory Submissions: Prepare Prepare, compile, and submit regulatory dossiers for new product registrations, renewals, and variations to Products Regulatory Authority (SAHPRA) and other relevant authorities. Manage timelines for regulatory submissions
different territories. The position will suit an RA Pharmacist with at least 2 to 3 years of solid RA dossier products is preferred, but not required (RA pharmacists with a desire to learn about RA for CAMS and welcome to apply). B.Pharm degree 2 - 4 years of RA Pharmacist experience compiling dossiers on Extedo, docuBridge