Regulatory & Quality Control Specialist
5 months ago
**Job Number**
- 70885
**Job Type**
- Permanent
**Job Title**
- Regulatory & Quality Control Specialist
**Computer Skills**
- Intermediate to Advanced MS Word, Excel, PowerPoint
**Industry**
- Pharmaceutical
**City**
- Johannesburg
**Province**
- Gauteng
- This person will also be the Deputy Responsible Pharmacist of the Company.**Summary of position**:
**Regulatory**:
- Responsible for:
- preparation of good quality dossiers and submissions according to specified timelines, in designated countries, to ensure earliest registrations and approvals.
- preparation, review, and approval of product labeling.
- review and approval of product promotional materials.
- management of local pharmacovigilance activities
**Quality**:
- Responsible for:
- quality oversight of activities in a defined scope (manufacturing, warehousing, and distribution.
- QC checks and release of locally manufactured products (Act 36/1947) and imported products (Act 36/1947 and Act 101/1965).
- quality documentation e.g., SOPs, Annual Product Reviews, and Batch Manufacturing Documents.
- self-inspections and external audits
- assisting QA Manager in complex and external audits as required
**Main Accountabilities**:
**Regulatory**:
- Act as Deputy Responsible Pharmacist for the entity.
- Execute Regulatory Strategy
- Agency contact
- Preparation and submission of dossiers
- Maintenance & Lifecycle Management of product dossiers
- Project Management
- Regulatory due diligence on potential opportunities
- Management of local Pharmacovigilance activities
**Quality**:
- Operate at the appropriate level of quality requirements
- QMS & Documentation
- Conduct training on quality activities
- Audits & inspections.**Inherent Requirements**
**Requirements**:
- Must have Matric / Grade 12
- Must have a B. Pharm degree
- Registered with The South African Pharmacy Council
- Minimum 2 years of Quality Assurance Management experience
- Minimum 2 years experience as a Responsible Pharmacist
- Minimum 2 years experience in compilation and submission of Act 101 (SAHPRA)and Act 36 (DALRRD) dossiers
- CTD dossier format submission experience
- Thorough understanding of GDP/GMP/GWP
- MS Word, Excel, and PowerPoint - intermediate to advanced skills required.
- High accuracy and attention to detail skills
- Strong work ethic
**The following would enhance your position**:
- GDP/GMP/GWP Training / Certificate
- Animal Health industry experience
- Knowledge of regulatory submissions in Botswana, Namibia, Zambia and Zimbabwe
- Pharmaceutical Production knowledge
**What Qualification**
- B. Pharm degree, Registered with the SA Pharmacy Council
**Minimum Qualification**
- Bachelors
**Status**
- Available
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