Quality Control Manager

Location:

Harare, Zimbabwe

Posted:

June 11, 2025

Contact this candidate

Resume:

CURRICULUM VITAE FOR :

MUNJANGANJA COLLINS TATENDA

** ********* ********, ********, ********

Cell: +263-*********, +263*********, +263********* Email: *************************@*****.*** or *************@*****.*** PROFILE

I am an extremely assertive, reliable, and committed young man seeking employment in your organisation. Due to my academic qualifications will be able to bring in new ideas to the best of your organisation.

I am a goal getter who is able to work under pressure producing outstanding results within my areas of responsibility.

PERSONAL INFORMATION

Name Collins Tatenda Munjanganja

Date of birth 05 March 1995

ID Number 22-2019658P27

Sex Male

Marital status single

Nationality Zimbabwean

Languages English

Drivers Licence class 4 (C36453AD)

PROFESSIONAL EXPERIENCE

1) Quality Control Manager, Datlabs Pharmaceuticals (NOVEMBER 2024 TO DATE)

Prepares the annual departmental budget.

Actively participate in the evaluation and approval of raw material and packaging suppliers by drawing up a procedure i.e. Approve or reject materials

Assure that all laboratory errors, product failures and any deviations from the expected results are investigated and that any corrective and preventive actions are carried out.

Ensures that all key laboratory processes are validated and any changes to these processes are done through the change control system.

Assure that all personnel are trained in all procedures that pertain to their specific job function(coordinating Analysts and Lab technicians proficiency test)

Ensures that all key equipment is calibrated and qualified

When necessary, holds meeting with staff as a means of communication

Reviews process improvements through interaction with other departments

Participating in external and vendor audits

Participating in root cause, risk assessment investigation

Ensure that the QC Chemistry and Microbiology Laboratory is complying with Medicines control authority of Zimbabwe

2) HEAD OF QUALITY CONTROL, PLUS FIVE PHARMACEUTICALS

(NOVEMBER 2022 TO NOVEMBER 2024)

Deputizing the HQA and Authorized in his or her absence

Security and storage of GMP documents, e. g. BMIs, BMRs, Validation protocols and reports, analysis reports, Calibration Certificates, reviewed SOPs.

Storage, security and maintenance of records for retained samples.

Approval and monitoring of contract manufacturers and analysis

Participation in external audit (vendor audit)

Supervision of the regular internal audits or self-inspections

Formulating departmental budgets

Monitoring and control of the manufacturing environment and plant hygiene

Approval and monitoring of supplier’s materials

Ensuring the correct labelling of containers of materials and products

Daily health checks of employees and staff entering the production areas 3) LABORATORY MANAGER PLUS FIVE PHARMACEUTICALS

MANUFACTURING DIVISIONS, BULAWAYO, ZIMBABWE (DECEMBER 2019 TO OCTOBER 2022.

Handling Customer complaints and recalls

Checking and/or approving Good Manufacturing Practise documents, Batch manufacturing Instructions and Standard operating procedures

Checking manufacturing and test procedures and records

Batch release for placement in the market.

To produce a Quality Policy and a Quality Manual, to maintain these documents and identify areas for improvement in quality management in the laboratory

Assists in maintaining a safe working environment by ensuring appropriate health and safety procedures are in place and adhered to.

Develop and implement a Corrective and Preventative Action (CAPA) system for the laboratory and Production Area

Monitoring maintenance, qualification and calibration of QC’s Laboratory equipment.

Writing down specifications for raw materials, packaging and labelling materials, in- process materials and finished products to ensure compliance with marketing authorization’s file and/or latest edition of either the United States Pharmacopeia, British Pharmacopeia, European Pharmacopeia.

Ensuring that all weighing and measuring instruments used at the plant are calibrated and records kept in accordance with relevant current Good laboratory Practice, current good manufacturing Practises and SOPs’ requirements.

Develop, implement and supervise a system of internal audit throughout the laboratory and to ensure that effective and immediate action is taken to resolve any issues identified

Ensuring that all products after completion of production are analysed and pass/comply with specifications before released for sale

Monitoring storage conditions for starting materials, samples, reference standards, retention samples, in-process materials and finished products.

Analysis of R & D products under stability studies and presenting the reports in a manner determined by the Development Manager

Performance appraisal of Quality control personnel.

Ordering Suppliers of reagents in the laboratory

Ensuring that laboratory equipment/instruments, reagents, materials, stationary, computers, utilities and any other company resources deployed in the laboratory are used for their intended purpose and are not abused or wasted.

Fulfilling obligations to report any changes, under areas of responsibility, which will materially affect the safety, quality and efficacy of the products manufactured at the premises to the Plant Manager.

Checking Analysts, Q.C Inspectors and other laboratory logbooks and notebooks for compliance and discrepancies identification and correction. 4) QUALITY CONTROL ANALYST, PLUS FIVE PHARMACEUTICALS MANUFACTURING DIVISION, BULAWAYO, ZIMBABWE (AUGUST 2018 TO NOVEMBER 2019)

Full analysis of all Pharmaceutical and non- Pharmaceutical Raw materials according Quality Control specifications.

Analysis of water samples and report compilation

Ensuring that all raw materials are placed in raw materials quarantine and are affixed with status stickers

Documentation of analytical results.

Analysis of intermediate and bulk products.

Analysis of finished products.

Analysis of stability samples and report compilation

Inspection of production and stores area for risk of cross contamination and mix ups

Ensuring that all work done is documented in personal logbook

Performing daily calibrations on the pH meters, Analytical balances and Moisture Analyser

Calibrations of secondary standards from primary standards

Documentation of all tests results and completeness of all analytical reports, running files and raw material files

Informing the Quality Control Manager on analysis problems and out of specification results

Adherence to laboratory safety standards and all quality control related standard operating procedures

Informing team leaders and production supervisors in production in –process results

Checking of Technicians and Quality control inspectors analytical work and logbooks 5) JUNIOUR QUALITY CONTROL ANALYST, INTERN PLUS FIVE PHARMACEUTICALS MANUFACTURING BULAWAYO, ZIMBABWE

(JULY2016-JUNE2017)

ACADEMIC QUALIFICATIONS

1) Bachelor of Science Honours degree in Chemistry (University of Zimbabwe 2014-2018): UPPER Second division-Degree class 2.1 2) Masters in Analytical Chemistry (2023- Ongoing) (National University Of Science and Technology)

KEY COMPETENCIES AND INTERESTS

Key skills:

Familiarisation of the High-Performance liquid Chromatography, Uv vis, Thin layer Chromat ography, FTIR (Fourier Transform Infra -Red), Gas Chromatography, Particle size Analyser Good interpersonal, numerical, analytical and time management skills Proficient in Microsoft Office package and Maestro package Interests

Sport: soccer and swimming

Networking

REFERENCES

Ms Amelia Antonio

Quality Assurance Pharmacist

Datlabs Pharmaceutical Manufacturing Division

Bulawayo Zimbabwe

Cell: +263*********

Email: ******.*******@*******.**.** or *********@*****.*** Mrs. M Chigavazira

Quality Assurance Manager

Plus, Five Pharmaceutical Manufacturing division Pvt Ltd Bulawayo

Cell: +263********* or +263***-***-***