Technology Transfer Officer – Quality

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Quality Chemical Industries Limited is hiring a Technology Transfer Officer – Quality Control to do the following;

Key Responsibilities:

Carry out comparative dissolution studies for test products and reference comparator products to assure pharmaceutical equivalence

Carry out cleaning validation for new products that are developed at Formulation Development

Carry out analytical method validations and verifications and compile reports for the same to the Formulation Development to assure the consistency of the developed analytical method

Perform Analytical Method Transfer during transfer of the products from Formulation Development to Manufacturing

Carry out accelerated and long-term stability studies as well as compile reports of the same

Conduct impurity profiling of drug substances including the identification and quantification of impurities

Assist the Formulation Development Quality Chemical Officers in developing analytical methods, such as spectroscopy-based methods, chromatographic methods or dissolution methods amongst others

Assist the Formulation Development Officers in conducting experiments, analysing results and preparing reports for various pharmaceutical formulations developed

Execute and report experimental work related to biopharmaceutical characterization in support of drug product development

Participate in the evaluation of new analytical techniques in the area of pre-formulation sciences, automated workflows and biorelevant testing

Create and review specifications in the SAP system

Handle ERP System/ SAP for specification generations and Trackwise system for deviation and complaints

Prepare SOPs, FMECAs, protocols, and any other documents assigned by the line manager from time to time

Any other job responsibility/ assignment given by Supervisor/ Manager deemed fit within your jurisdiction

Qualifications and Experience Required

Bachelor’s Degree in Chemistry, Chemical Engineering, Industrial Chemistry, or Science Technology (Chemistry), or any other science related field

Minimum of 3 years’ experience in Quality Control in a manufacturing plant or standard recognized laboratory

Familiar with pharmaceutical regulations and guidelines, such as Good Manufacturing Practices (GMP) and International Council for Harmonization (ICH) guidelines

Certification in Quality Management or Quality Assurance is an added advantage

Good teamwork, interpersonal skills and adherence to Quality Management Systems

Self-starter, flexible and able to work well under pressure at work

Proficiency in Excel and its basic formulae, and in PowerPoint presentations

Familiar with the various analytical tools like the Pareto Chart, Waterfall, Pie Charts, Bar Charts and Line Charts

Be observant, creative and innovative in line with the business needs

Able to work Shifts program as per business needs

How to Apply

Applicants with the above requirements can post their applications, curriculum vitae, copies of relevant academic and professional qualifications, contact details for three (03) professional referees and a day-time telephone number to:

Sr. Human Resources Business Partner

Email:

recruitment@qcil.com

Deadline for receiving applications:

Wednesday 08

th

October 2025

Only short-listed candidates will be contacted. Qcil is an equal opportunity employer and therefore lobbying for the above position will lead to automatic disqualification.