MEDICINE REGISTRATION OFFICERS - 3 months Contract

 

Recruiter:

Kgadi Staffing Solutions

Job Ref:

MEDICINE REGISTRATIO..

Date posted:

Friday, August 27, 2021

Location:

Pretoria, South Africa

Salary:

R48 000.00 per month


SUMMARY:
A 4 months contract for a Medicine Registration Officers exist at our client''''''''s office in Pretoria

POSITION INFO:

REQUIREMENTS:

  • Appropriate 4-year Bachelor of Pharmacy Degree, Registration with SAPC as a Pharmacist, and Proven relevant experience.
  • A relevant NQF 9 level qualification in the health sciences will be an added advantage.

EXPERIENCE:

  • Grade 2: B Pharm Degree - 8 years (Registration as Pharmacist required)
  • Grade 3: B Pharm degree – 16 years (Registration as a Pharmacist required).
 

COMPETENCIES, KNOWLEDGE AND SKILLS:

  • Sound and in-depth knowledge of the Medicines and Related Substances Act 101, 1965 as amended and the regulations pertaining to the Act.
  • Sound knowledge of regulatory scientific and technical requirement (in terms of quality, safety and efficacy aspect).
  • Knowledge of Good Pharmacovigilance Practice
  • Comprehensive knowledge and understanding of the international regulators.
  • Knowledge of MS Office.
  • Computer skills.
  • Planning and organising skills.
  • Drive and self-management skills.
  • Communication skills (verbal, written, conflict management, presentation).
  • Ability to work in a highly pressured environment and driven by a sense of urgency to meet deadlines.
  • Assertiveness.
  • Ethical behaviour.
  • Prepared to travel and work irregular hours.
  • A valid driver’s licence.
 

DUTIES

  • Evaluate safety related submissions and responses thereof.
  • Co-ordinate Pharmacovigilance activities and Committee meetings
  • Supervise administrative staff and attend to queries addressed to the Pharmacovigilance Unit.
  • Provide technical assistance and support to appropriate Advisory Committee/s and SAHPRA generally.
  • Develop Standard Operating Procedures (SOPs), related policies and guidelines pertaining to Pharmacovigilance activities.
  • Promote vigilance by collecting, managing and accessing ADR and medication error reports including post-marketing surveillance and research data.
  • Create and promote PV awareness and education amongst reporters regarding the significance/importance of reporting ADRs and the use of the reporting tools
  • Collaborate with different stakeholders to strengthen PV within the country
  • Evaluate and communicate vigilance related issues
  • Perform other functions that may arise from time to time.


 

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