Customs Affairs Manager Jobs in Gauteng
- Johannesburg (2,619)
- South Africa (1,362)
- Gauteng (392)
- Sandton (202)
- Pretoria (199)
- Central Johannesburg (192)
- Ekurhuleni (160)
- Centurion (153)
- Midrand (151)
- Kempton Park (111)
- Accounting / Finance (1,228)
- Sales (1,142)
- IT / Computing / Software (1,043)
- Engineering (531)
- Transport / logistics / warehouse (331)
- Admin / clerical / secretarial (318)
- Marketing / advertising / PR (249)
- Construction / trades (146)
- Retail / wholesale (144)
- Freerecruit (324)
- Isanqa (77)
- Job Crystal (68)
- Professional Career Services - Gauteng (66)
- Hire Resolve (58)
- Restaurant Staff (57)
- University Of Johannesburg (50)
- Insphired Recruitment Solutions (44)
- E-merge It Recruitment (42)
- Agc Recruitment (40)
Regulatory Affairs Manager Johannesburg
Mvg Recruitment Specialists
Johannesburg
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
share this job on whatsappRegulatory Affairs Scientist (customer And Regulatory Support) Market Related
Vela PersonnelSouth Africa
competent and experienced Regulatory Affairs Scientist for the Regulatory Affairs Department Key Job Outputs: Pharmaceutical Ingredients (APIs) Responding to customer (both internal and external) and regulatory authority ability to interact well with internal and external customers Minimum of 3years experience in pharmaceutical
Regulatory Affairs Pharmacist Gauteng
Mna RecruitmentGauteng
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
Regulatory Affairs Pharmacist Midrand
Mvg Recruitment SpecialistsMidrand
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 Johannesburg
Mvg Recruitment SpecialistsJohannesburg
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
Head Of Medical Affairs Gauteng
Mna RecruitmentGauteng
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 clinical research an advantage. Candidate should be customer and patient oriented while having the ability
Regulatory Affairs Pharmacist Centurion
Futurelink Global RecruitmentCenturion
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 close findings via CAPA. Log and follow up on customer complaints, deviations, CAPAs, and change controls release of Act 101 products in the absence of QA Manager and RP/Deputy RP. Review and update SOPs and Technical
Head Of Regulatory Affairs
Johannesburg
Monthly
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
Regulatory Affairs Pharmacist Midrand
Specialist Search RecruitmentSouth Africa
R800k to R1 mil, negotiable based on experience 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
Regulatory Affairs Manager (jhb) Market Related
Mvg Recruitment SpecialistsJohannesburg
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
Share on Facebook
Share on Twitter
Share on Linkedin