Key responsibilities:

• Perform Laboratory testing on different health products and technologies in compliance with relevant standards to determine their quality using applicable techniques.
• Document information associated with of laboratory testing using the Laboratory Information Management System (LIMS) from sample preparation to the stage of review of results.
• Perform training on behalf of MEDS for both internal and external stakeholders as subject matter experts for purposes of induction, client education and revenue generation as a service.
• Maintain Laboratory equipment through proper operation, cleaning and basic maintenance and perform defined verification tests on different equipment and instrument in the laboratory to confirm their suitability for use.
• Perform successful transfer of validated analytical testing methods from donor institutions e.g. manufacturers and laboratories to MEDS laboratory for use in analysis of samples from clients to determine their quality.
• Take part in Proficiency and inter-laboratory testing on behalf of the MEDS laboratory to demonstrate competence of the laboratory against peer laboratories and for compliance with relevant standards
• Prepare Standard Operating Procedures and Work Instructions to be used in performing different tasks and duties in the laboratory
• Participate in self-inspections and external audits for continuous improvement and compliance with relevant standards
• Ensure compliance to safety and regulatory requirements while working under Good Laboratory Practices (GLP).
• Conduct daily environmental monitoring of controlled areas within the laboratory to ensure adherence to set limits of differential pressure, microbial counts, particulate counts, temperature and relative humidity as established by international guidelines.
• Maintain safety at all times while working in the laboratory as a requirement of Good Laboratory Practices (GLP).
• Maintain accurate records related to laboratory activities following Good record-keeping Practices for compliance with requirements of the Quality Management System.

Job requirements:

• Bachelor’s Degree in Biological Science or any other related course.
• Minimum of two (2) years of relevant experience in a Pharmaceutical Quality Control Laboratory
• Technical competencies: Knowledge of regulatory standards such as GMP (Good Manufacturing Practice) and GLP (Good Laboratory Practice); Knowledge ISO/IEC 17025 :2017 standard; Knowledge of Laboratory Information Management System (LIMS); Safety and Compliance; Laboratory Equipment Maintenance and servicing; MS Office Suite Proficiency; Data Analysis
• Behavioural competencies: Communication skills; Problem-solving skills; Analytical skills; Innovation skills; Team Player; Integrity; Attention to detail; Interpersonal

• Perform Laboratory testing on different health products and technologies in compliance with relevant standards to determine their quality using applicable techniques.
• Document information associated with of laboratory testing using the Laboratory Information Management System (LIMS) from sample preparation to the stage of review of results.
• Perform training on behalf of MEDS for both internal and external stakeholders as subject matter experts for purposes of induction, client education and revenue generation as a service.
• Maintain Laboratory equipment through proper operation, cleaning and basic maintenance and perform defined verification tests on different equipment and instrument in the laboratory to confirm their suitability for use.
• Perform successful transfer of validated analytical testing methods from donor institutions e.g. manufacturers and laboratories to MEDS laboratory for use in analysis of samples from clients to determine their quality.
• Take part in Proficiency and inter-laboratory testing on behalf of the MEDS laboratory to demonstrate competence of the laboratory against peer laboratories and for compliance with relevant standards
• Prepare Standard Operating Procedures and Work Instructions to be used in performing different tasks and duties in the laboratory
• Participate in self-inspections and external audits for continuous improvement and compliance with relevant standards
• Ensure compliance to safety and regulatory requirements while working under Good Laboratory Practices (GLP).
• Conduct daily environmental monitoring of controlled areas within the laboratory to ensure adherence to set limits of differential pressure, microbial counts, particulate counts, temperature and relative humidity as established by international guidelines.
• Maintain safety at all times while working in the laboratory as a requirement of Good Laboratory Practices (GLP).
• Maintain accurate records related to laboratory activities following Good record-keeping Practices for compliance with requirements of the Quality Management System.

• Knowledge of regulatory standards such as GMP (Good Manufacturing Practice) and GLP (Good Laboratory Practice)
• Knowledge ISO/IEC 17025 :2017 standard
• Knowledge of Laboratory Information Management System (LIMS)
• Safety and Compliance
• Laboratory Equipment Maintenance and servicing
• MS Office Suite Proficiency
• Data Analysis
• Communication skills
• Problem-solving skills
• Analytical skills
• Innovation skills
• Team Player
• Integrity
• Attention to detail
• Interpersonal

• Bachelor’s Degree in Biological Science or any other related course.
• Minimum of two (2) years of relevant experience in a Pharmaceutical Quality Control Laboratory