Quest Pharmaceuticals is a WHO-GMP certified science-based healthcare company, providing excellence in pharmaceutical solutions, since 2001. We are among the most trusted pharmaceutical manufacturers in Nepal, and are recognized as one of the finest. Driven by a vision of securing Nepal’s healthcare needs, Quest Pharmaceuticals produces international standard effective medications at affordable prices. Since establishment, Quest has helped millions lead healthier lives, with a range of general solutions, and specialized drugs for cardiovascular, dermatological, diabetic, and hypolipidemic ailments.
We are looking for a highly enthusiastic, result-oriented, dynamic, and self-motivated QA Officer for the Quality Assurance Department who has a strong desire to join and grow with us.
Position: Quality Assurance Officer
Department: Quality Assurance
Project Location(s):Chhatapipara, Bara
Participate in preparation, distribution, review, revision, retrieval, archiving, disposal and other control procedure of various documents like SOPs, guidelines, protocols, specifications, MFPI, BPPR, artwork, etc as desired by the company policy and regulatory compliance.
Monitor assessment and control over GxP Practices like Good Manufacturing Practices, Good Laboratory Practices, Good Storage and Distribution Practices, Good Engineering Practices, Good Documentation Practices etc, for continual regulatory compliance.
Participate in various validations, qualifications and calibration activities ranging from protocol preparation, scheduling, execution, reports etc, as defined in Validation Master Plan.
Maintain current knowledge and updates of relevant GMP regulations, including proposed and final rules & guidelines.
Assure all the practices/procedures and specifications defined in relevant documents are strictly followed accordingly. Report any discrepancy or deviation from standard.
Report any change or involve in assessment of any change reported in the system, process or procedure as per standard change control procedure.
Manage risks to quality of products through out the product life cycle in line with principles of Quality Risk Management.
Report and record any observation, incident, non-conformity or deviation in the process or system as per the defined procedure and assure proper investigation is done to find the root cause and appropriate CAPA is taken.
BPharm/ MPharm or equivalent degree. Registration in Nepal Pharmacy Council is a must.
Candidates having prior experience in related field will be preferred
Skills and Competencies
Must have knowledge and updates of relevant GMP regulations
Must have good knowledge of good documentation practices, knowledge of BPPR and COA
Knowledge of In-Process Control, Sampling of Bulk and Intermediates, Line Clearance, Dispensing etc.
Good leadership Skills along with ability to work in a team
Excellent knowledge of MS Office
Excellent verbal and written communication skills, as well as outstanding aptitude for time management
Proficient in English language
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