Vacancy
Job Description
A Quality Control Manager is required by a pharmaceutical manufacturing company, in
Bulawayo, to be responsible of ensuring the quality of the company’s products and to oversee
the overall quality control function within the manufacturing plant.
Duties and Responsibilities
Oversee the overall quality control operations
Setting quality control objectives
Developing and implementing quality control procedures including manuals,
standard operating procedures
Ensuring compliance with WHO’s GMP, GLP and NMRA standards and
requirements
Supervising team of analysts, inspectors, and environmental team
CAPA implementation
Training and developing staff to ensure that they are knowledgeable and skilled for
their responsibilities
Conducting routine and non-routine analyses and testing of raw materials, in-process
materials, environmental samples, finished product, stability samples, real-time
samples, R&D samples and water samples among others.
Ensuring that all analytical methods are validated
Ensuring calibration and validation of all measuring, analytical and QC instruments.
Real-time stability testing and monitoring to ensure compliance with shelf-life of
products, APIs and excipients
Quality inspection of production processes, storage and dispensing of materials and
finished goods,
Inspect all product returns, analyze the defect, and document the results and
implement CAPA
Maintaining and improving product quality by completing product and company systems,
compliance and surveillance audits; investigating customer complaints; collaborating with
other members of management to develop a new product, and manufacturing and training
methods.
Systematically examining and testing pharmaceutical products at various stages of production
to identify and rectify defects or variations. Ensuring that each product meets the specified
quality standard before reaching the market and safeguarding patient safety.
Qualifications and Experience
At least a bachelor’s degree in: Chemistry or Applied; Pharmacy; Pharmaceutical
Chemistry; Microbiology; Chemical Engineering or related areas
Minimum 3 years’ experience
Expert knowledge of WHO’s GMP and GLP standards, MASCA and NMRA
regulations
Strong verbal and written communication skills
Good analytical, problem solving, supervisory, teamwork and leadership skills
Pronounced sense of personal responsibility and high level of personal integrity
Willingness to work beyond normal hours including weekends and holidays
Track record of achievement and traceable references
Job Summary
More Information
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Job Application Details
APPLICATION DETAILS
Prospective candidates in possession of the above should send applications together with currently detailed CVs to [email protected] on or before 10 February 2025
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