HEAD CHEMISTRY – Medicines Control Authority of Zimbabwe 355 views

VACANCY: HEAD CHEMISTRY, GRADE E2 (CHEMISTRY DIVISION)
The Medicines Control Authority of Zimbabwe (MCAZ) is inviting qualified, honest, self-motivated and experienced applicants for the following post:
Head Chemistry -1 Post

1.0 Duties and Responsibilities

Reporting to the Director-General, the incumbent will be responsible for the following, among other duties:
1 Lead, manage, supervise, authorize and implement Chemistry division activities in the chemical analysis of medicines and other medical products for quality, efficacy and safety, and ensure compliance with required specifications and MASCA Act;
2 Plan, implement and review Chemistry laboratory strategic goals and annual work plans in line with the MCAZ corporate strategy;
3 Manage and adhere to the approved budget;
4 Lead in resource mobilization for project activities;
5 Manage and monitor projects performance and fund utilization for defined budget projects to meet timelines;
6 Advise and consult MCAZ Committees on relevant technical issues pertaining to Chemistry laboratory;
7 Facilitate timeous procurement of laboratory equipment, reagents, chemicals and consumables;
8 Manage and ensures proper equipment management including maintenance, service, calibration and internal qualifications are performed timeously;
9 Develop, Implement and maintain the Chemistry laboratory Regulatory Centre of Excellence (RCORE) status in Quality Assurance of medicines;
10 Provide strategic leadership in the implementation and retention of chemistry accreditation and certification status in IS017025, ISO 9001, WHO Prequalification and WHO GBT laboratory review and testing function;
11 Plan and implement analytical methods validations, transfer and verification of compendia methods for use in the laboratory and provide expert advice in all analytical problems and challenges;

2.0 Requirements

2.1 Bachelor of Science Honours degree in either Chemistry, Applied Chemistry, Chemical Technology or equivalent.
2.2 MBA/MBL/MSc in Strategic Management degree will be an added advantage.
2.3 At least three (3) years experience in a managerial capacity in a pharmaceutical manufacturing Quality Control or Regulatory Quality Control Laboratory.
2.4 At least five (5) years’ postqualifying experience in Quality Control and/or Quality Assurance of medicines in pharmaceutical manufacturing or regulatory environment.
2.5 Expert practical knowledge in Laboratory QMS implementation in ISO 17025,9001 and WHO

Prequalification programme.

2.6 Expert knowledge in Quality Control and Quality Assurance of medicines.
2.7 Expert knowledge in analytical instrumentation and equipment management and excellent analytical skills.
2.8 Good people management skills and a team player.
2.9 Business-minded and strategic thinker.
2.10 Excellent communication and report writing skills.