Key Responsibilities:
i. Perform Laboratory testing on different health products and technologies in compliance
with relevant standards to determine their quality using applicable techniques.
ii. Document information associated with of laboratory testing using the Laboratory
Information Management System (LIMS) from sample preparation to the stage of review
of results.
iii. 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.
iv. 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.
v. 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.
vi. 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
vii. Prepare Standard Operating Procedures and Work Instructions to be used in performing
different tasks and duties in the laboratory
viii. Participate in self-inspections and external audits for continuous improvement and
compliance with relevant standards
ix. Ensure compliance to safety and regulatory requirements while working under Good
Laboratory Practices (GLP).
x. Conduct daily environmental monitoring of controlled areas within the laboratory to
ensure adherence to set limits of differential temperature and relative humidity as
established by international guidelines.
xi. Maintain safety at all times while working in the laboratory as a requirement of Good
Laboratory Practices (GLP).
xii. Maintain accurate records related to laboratory activities following Good record-keeping
Practices for compliance with requirements of the Quality Management System.

Candidate Profile:
i. Bachelor’s Degree in Analytical Chemistry from a recognized institution
ii. Minimum 5 years of relevant experience in a Pharmaceutical Quality Control Laboratory
iii. Technical Competencies; Knowledge of regulatory standards such as GMP (Good
Manufacturing Practice) and GLP (Good Laboratory Practice); Knowledge of 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
iv. Functional skills; Communication skills, problem-solving skills, analytical skills,
innovation skills, interpersonal skills, attention to detail and high level of integrity