JOB TITLE: DIRECTOR- PRODUCT EVALUATION & REGISTRATION
REPORTS TO: Chief Regulatory Officer
JOB PURPOSE:
WE ARE STILL MAKING CVs FOR P100. COVER LETTERS FOR P50
Pay with FNB EWallet to 76981238 or Orange Money on number 76981238
Whatsapp us on +26776981238
JOIN US ON OUR WHATSAPP CHANNEL HERE
To oversee the management of human, financial and other resources allocated to the department to ensure efficient and effective regulation and control of human and veterinary medicines, medical devices, complementary medicines and cosmetics for protection and promotion of human and veterinary public health.
MAIN DUTIES
- To advise the CEO on matters pertaining to product evaluation and registration.
- Ensure that drug applications are assessed according to approved guidelines and regulations for registration.
- Actively participate in and coordinate the development of regulations and procedures of drug registration.
- Manage the development and maintenance of computerised software and database for registered drugs.
- To ensure all human and veterinary medicines, medicated feeds, medical devices, vaccines and biological products, complementary medicines and cosmetic products are correctly evaluated for quality, safety and efficacy.
- Ensure timely update of the registers with approved variations, new products, suspensions and deletions.
- Works closely with the necessary department heads to implement quality management systems in the department.
- Manage, assess and evaluate variation applications for registered products (human and veterinary drugs, complementary medicines and related products).
- Manage, motivate and coach employees in the department and manage their performance through regular communication and timely feedback annual performance appraisal and making provision for appropriate training and development options.
- Prepare, implement and monitor departmental budget and annual work plans to achieve the organisational strategic objectives.
- To foster cooperation with regional and international bodies on matters pertaining to the department.
- To ensure effective management of the Post Marketing Surveillance and Control of Clinical Trials unit in the MRA’s formative stage.
QUALIFICATIONS:
Academic Qualification:
- Holder of MSc or its equivalent in Pharmacy,
- Human Medicine, Veterinary Medicine or related field from recognized institution
Work experience: At least ten years’ experience in current regulatory affairs and six years in senior managerial position in a reputable organization
Essential skills: Ability to work independently, good interpersonal and communication skills; good working knowledge of ICT Applications. Desirable attributes: High degree of integrity and probity; Excellent organizational skills; Strong ability to follow detailed processes and procedures; Precision in execution of work with attention to detail; Initiative, diplomacy and good judgement; Good written and oral communication skills; Good interpersonal skills and team spirit; Tact and discretion in the handling of confidential files and information.
More Information
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JOB APPLICATION DETAILS
APPLICATION DETAILS
If you have the above capabilities, meet the minimum requirements and believe that you can grow with BOMRA, kindly send your application, latest CV and certified copies of certificates and two(2) current referee's details to: [email protected]
Closing Date for Submission: 28 March 2022.
Only short-listed candidates will be contacted
Please say that you got this job advertisement through Jobs Botswana
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