Job Description
What You’ll Do:
- Prepare and submit registration documents in a timely manner to avoid lapses in approvals and ensure prompt submission of new dossiers.
- Submission of documents on as per the within the required time limit to NMRA.
- Maintain and regularly update the registration status; liaise with principals regarding documentation and regulatory requirements.
- Ensure all company stores and processes comply with NMRA rules and regulations.
What We’re Looking For:
- A bachelor’s degree or a professional qualification in Pharmaceutical Science, Biomedical Science, Regulatory Affair’s or a related field.
- 3-5 years of hands-on experience in regulatory affairs, preferably within the pharmaceutical industry.
- Strong attention to detail with a proactive and problem-solving mindset.
- Effective communication and interpersonal skills.
Send Your CV to: [email protected]
Please mention the position you are applying for as the subject when submitting your application.
More Information: 076 277 8792
