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 stakeholders Establish regulatory priorities and allocate resources and workloads Review regulatory agency submission accuracy, comprehensiveness, or compliance with regulatory standards Co-ordination and submission of new
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
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 and notify the Responsible Pharmacist (RP) of findings. Assist with QA batch release of Act 101 products products in the absence of QA Manager and RP/Deputy RP. Review and update SOPs and Technical Quality Agreements but not mandatory. Ability to work between RA and QA.
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
QA Post Basic Pharmacist Assistant Sector: Pharmaceutical Manufacturing Location: Johannesburg – onsite Full-Time Requirement: Qualified Post Basic Pharmacist Assistant with QA experience gained in pharmaceutical detail-oriented Quality Assurance Post Basic Pharmacist Assistant to contribute to their Quality Management Job Summary: The Quality Assurance Post Basic Pharmacist Assistant plays a pivotal role in supporting Qualification: Post Basic Pharmacist Assistant and SAPC registered Estimate of 3 - 5 years QA experience gained
for an experienced QA Pharmacist (batch release and general QA functions). General QA batch release - a degree required (Non-negotiable) 1 to 3 years of QA experience, preferably at a CAMS or Cosmetics company
involve general production pharmacist duties, as well as evolving into QA and QC functions. And perhaps
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
The position could suit an ambitious Senior RA Pharmacist too, who is ready to step up into an RA Manager