Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist. The following applies: Key Responsibilities: Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines Demonstrable Cross Functional capability (Full role profile available on application) Apply to response "at" mvgrecruitment
for over 5000 clients Reporting to Regulatory Affairs Manager Job purpose: Support the Regulatory team stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist. The following applies: Key Responsibilities: Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines Demonstrable Cross Functional capability (Full role profile available on application) Apply to response "at" mvgrecruitment
Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical (no endorsements) Own reliable vehicle Must be available immediately (no notice applicable) (Advantageous) officer. Assist with marketing and regulatory affairs. Functions Assists QA Manager with overseeing that Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical (no endorsements) Own reliable vehicle Must be available immediately (no notice applicable) (Advantageous)
Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical (no endorsements) Own reliable vehicle Must be available immediately (no notice applicable) (Advantageous) officer. Assist with marketing and regulatory affairs. Functions Assists QA Manager with overseeing that Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical (no endorsements) Own reliable vehicle Must be available immediately (no notice applicable) (Advantageous)
proven experience in a pharmaceutical regulatory affairs environment including compilation and submission experience of working in several groups in regulatory affairs or experience at a health authority. Implement business priorities. License maintenance: Ensure all post-approval product maintenance activities including technical changes to the label or the packs, PBRERs, and post approval commitments are submitted and approved
proven experience in a pharmaceutical regulatory affairs environment including compilation and submission experience of working in several groups in regulatory affairs or experience at a health authority. Implement business priorities. License maintenance: Ensure all post-approval product maintenance activities including technical changes to the label or the packs, PBRERs, and post approval commitments are submitted and approved
Environmental Management is highly regarded. 6 – 8 years' post qualification experience in Environmental Management management and reduction, recycling, responsible water management, energy consumption and emission reduction implementation, measurement and verification of energy, water and waste efficiency projects. Anticipate and keep
Environmental Management is highly regarded. 6 – 8 years' post qualification experience in Environmental Management management and reduction, recycling, responsible water management, energy consumption and emission reduction implementation, measurement and verification of energy, water and waste efficiency projects. Anticipate and keep