Norbrook Laboratories Limited is one of the world’s leading pharmaceutical companies.
The following vacancy has arisen at our facility in Karuri, Kenya.
Reporting to the Quality & Compliance Director
Duties & Responsibilities:
To ensure full compliance of the facility and operation with the cGMP, GDP and GLP and continuous improvement of the Company Quality Control Systems.
Manage quality analysis and documentation process for all raw material, packaging and finished goods
Oversee all activities of the quality control laboratory
Ensure all documents appertaining to cGMP are in place for all processes in the facility, co-ordinate and develop cGMP training on site.
To convene self—inspections and supplier quality audits and follow up of CAPA
Responsible for hosting and managing audits from VMD, NDA, TFDA , other regulatory bodies and third party consumer audits.
Other duties in line with the position.
Qualifications and Experience:
Minimum: Bachelor’s degree in Pharmacy from a recognized University.
Registered by Pharmacy and Poisons Board with a current practice license
Comprehensive understanding of pharmaceutical manufacturing for finished dosage forms with 5+ years’ experience post internship in Quality control in manufacturing facility/es.
Proactive, able to work independently, have previous team management and supervisory experience.
Thorough knowledge of regulatory requirements and quality guidelines, attention to detail with good analytical skills
Strong leadership skills and ability to work well under pressure
Adequate knowledge of relevant computer packages
