Regulatory Affairs Manager Industry: Pharmaceutical Location: JHB Equity Requirement: EE Lead the Regulatory regulatory applications. Key Responsibilities: Manage work streams for- and report on the assigned group new products Formulate or implement regulatory affairs systems, policies and procedures to ensure that Council Minimum of 5 years' experience in Regulatory Affairs, preferably in human medicines. Demonstrated experience application will be an advantage. Sound project management capabilities Proven ability to consistently deliver
Gauteng is looking for a Corporate Sales Manager (New Vehicles) to join their Sales least 3 years experience in a Dealership Sales Manager position
BMW Corporate Sales Manager R Negotiable, around R40000 - R45000 / Johannesburg
An experienced experienced corporate sales manager with BMW experience is required. Sales & marketing experience is preferable
external Partners and Principals, and to control and manage a portfolio of product outputs. To ensure legal regulatory applications. Key Responsibilities: Manage work streams for- and report on the assigned portfolio stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that Pharmacy Council -5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable experience commercialization and maintenance lifecycle Sound project management capabilities Proven ability to consistently deliver
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE EE Key Responsibilities: Manage work streams for- and report on the assigned portfolio of products Conduct stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that Council 3 to 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable experience commercialization and maintenance lifecycle Sound project management capabilities Proven ability to consistently deliver
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical employ a Regulatory Affairs Scientist. The following applies: Key Responsibilities: Managing and coordinating compilation and submission of new product applications. Managing and coordinating response to the regulatory authority registration process is required. Effectively managing, auditing and implementation of Regulatory systems Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines Demonstrable
pharmaceutical company has a vacancy for a Head of Medical Affairs. Job Purpose: Develop and maintain in depth knowledge and accepted standards of best practice. KOLs Management and development Develop & maintain professional
a Regulatory Affairs/Quality Assurance Pharmacist to join their team. Regulatory Affairs (RA): Submit Assurance (QA): Assist QA Manager with artwork review and quality management system for Act 101 products release of Act 101 products in the absence of QA Manager and RP/Deputy RP. Review and update SOPs and Technical
maintenance
Proven successful leadership and project management experience.
Fosters an environment that
experience of working in several groups in regulatory affairs or experience at a health authority
Knowledge
development, commercialisation and life cycle management of the assigned product(s) in product teams.
/>Responsible for the management of a skill group such as CMC, Regulatory affairs project management, etc.
Responsible
/>Responsible for skill development, performance management, and resource allocation
Provides
submissions . Activities relating to product lifecycle management. Maintain and develop working relationships effectively (SAPC) is essential Minimum of 2 years Regulatory Affairs experience in pharmaceutical industry . Experience required. Hard working – able to multi task and manage multiple projects simultaneously. Strong communication skills – experience in liaising with Business Managers, Quality Assurance & Marketing departments the business . Good Understanding of Quality Management Systems, SAHPRA Guidelines and Policies, Medicines