- JOB PURPOSE
Monitors and control materials passing through the compression section in compliance with current Good Manufacturing Practices (cGMP) thereby ensuring timely delivery of high-quality finished products.
SUMMARY OF DUTIES & RESPONSIBILITIES
¨ Checks and ensures that all operational rooms, equipment, and machinery are cleaned to current Good Manufacturing Practises (cGMP) and other international standards.
¨ Checks and ensures that rooms, equipment, and containers are properly assembled during the start-up of all production processes.
¨ Checks and ensures logbooks are accurately and promptly.
¨ Ensures that all operations are done according to the Standard Operating Procedures (SOPs).
¨ Ensures that all materials are accurately and properly labeled and checked to prevent mix-ups.
¨ Assists in co-ordinating activates in other sections with colleagues to ensure efficiency in the production processes to achieve targets set by production Management.
¨ Ensures that all technicians are adequately trained on the operation of equipment/machines to avoid errors in production processes.
¨ Assist in Co-ordinating safety and housekeeping activities to ensure compliance with Food and Drug Board and Company Policies.
¨ Provides any additional technical advice to ensure the efficient running of all equipment/machines in the packaging section.
¨ Performs other duties that may be assigned by the Managers.
REQUIREMENTS:
Bachelor Degree in Pharmacy (B. Pharm. /B.Sc. Plus 1-2 years’ experience in a pharmaceutical or related industry.
OR HND with five (5) years’ experience in a pharmaceutical or related industry.
OR City and Guilds Part lll with 10 years’ experience in a pharmaceutical or related industry.
MODE OF APPLICATION
All interested applicants with the requisite qualification should send their CV to hr@phyo-rikergh.com
