Chemist

4 days ago


Davao City, Davao, Philippines NCH Full time

Qualifications:

Candidate must possess a Bachelor/College Degree in Chemistry or related courseMust be a Registered/Licensed Chemist.Preferably with 1 year of experience in similar position in manufacturing setting.Have an excellent communication and good interpersonal skills.With background ORACLE/SAP/ERP.With background in ISO 9001 quality management system or ISO 14001 environmental management system.Willing to work in NCH Philippines Inc. #8 DBP Village, MA-A Road,, Talomo, Davao City Job Description:

Conducts in-house physical analyses, chemical analyses, and coordinates with an outside or third party analyses for the following:

Microbiological AnalysesHeavy Metals Analyses of ROHSEfficacy or Kill Rate Tests (as per request from Sales)Ambient Air Monitoring of the Plant Facilities (annually)Waste Water Analysis Sampling (quarterly)And other certifications from Government Agencies when necessary Conducts Lab Batch of the following to ensure its effectiveness and compatibility: New Product DevelopmentEnhanced ProductRaw Material ReplacementDevelops materials for Product Launching covering: MSDS, Technical Data Sheets, Labels Facilitates the preparation of the following documents for Sales and Export Use: Certification of Analysis of productsCertification on its uses, application, safety and others.Provides MSDS for each of the products as per requestCertification on its safety for transport by Air or Land Responsible in the preparation of Self Monitoring Report (SMR) on a quarterly basis for DENR and LLDA. And annual preparation of request for license renewal of PERMIT TO OPERATE (DENR), and DISCHARGE PERMIT (LLDA) . Responsible in the preparation of Plant for the Annual Audit conducted by FDA ( FOOD and DRUG AGENCY) relevant to our License to Operate as : HOUSEHOLD HAZARDOUS SUBSTANCES MANUFACTURER AND IMPORTERCOSMETICS MANUFACTURER Responsible in ensuring the ISO 9001:2015 Certification is maintained and pass the renewal audit every 3 years, as well as the yearly surveillance audit, by implementing regular ISO Meetings and Management Review. Responsible in the application for all products requiring Certificate of Product Registration under FDA, and its renewal as well. Troubleshoots complaints and identifies corrective and preventive actions for local and export concerns.

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