Salary: 30,000 - 50,000Schedule starts at 8:30 AM - 11 AM and ends at 5:30 PM - 8 PM·Registration of products with the FDA, ensuring compliance with LTO and
Responsibilities:• Configuring and maintaining SAP QM modules.• Creating and managing quality inspection plans and performing quality inspections.•
- BACHELOR'S DEGREE IN PHARMACY- PREFERABLY LICENSED- NEW GRADUATES ARE WELCOME TO APPLY- ENSURE COMPANY COMPLIANCE WITH FDA REQUIREMENTS FOR TRADING PERSONAL
JOB DESCRIPTION:Ensure compliance with FDA regulationPreparations and submission of documents to regulatory agenciesReview and Evaluate all technical documents
Take your career to the next level at the Worldâs Largest Sports Retailer!Decathlon Philippines is opening more and more stores in the next 3 years, and we
DivisionQualityDepartmentQualityEmployment TypePermanentJob PurposeReview the compliance level of site for deficiency response, prepare master validation
DivisionQualityDepartmentQualityEmployment TypePermanentJob PurposeReview the compliance level of site for deficiency response, prepare master validation
Job DescriptionJoin our team as an Engineering Design Manager and play a crucial role in delivering successful projects in any portion of EPC projects.We are
Job Title: Regulatory Affairs OfficerQualifications: Licensed Pharmacist 3-4 years of relevant work experience Strong relationships with FDA
Description:Duties and Responsibilities:Performs evaluation of raw materials, packaging materials, in-process and finished products to ensure conformance with
JOB DESCRIPTION:•Ensure compliance with FDA regulation•Preparations and submission of documents to regulatory agencies•Review and Evaluate of all
JOB DESCRIPTION:? Ensure compliance with FDA regulation? Preparations and submission of documents to regulatory agencies? Review and Evaluate all technical
The Assistant Quality Assurance Manager is responsible for leading, directing, and managing the Quality Assurance operations to support the objectives of
Ensure compliance with FDA regulationPreparations and submission of documents to regulatory agenciesReview and Evaluate all technical documents for all new and
Salary: 30,000 - 50,000Schedule starts at 8:30 AM - 11 AM and ends at 5:30 PM - 8 PM·Registration of products with the FDA, ensuring compliance with LTO and
- Licensed pharmacist or graduate of any allied science or engineering course- With 5 years experience particularly in the medical device manufacturing
About DexcomFounded in 1999, Dexcom, Inc. (NASDAQ: DXCM), develops and markets Continuous Glucose Monitoring (CGM) systems for ambulatory use by people with
- Ensure compliance with FDA regulation- Preparations and submission of documents to regulatory agencies- Review and Evaluate all technical documents for all
Requirements:EXPERIENCE MUST BE FROM FOOD INDUSTRY /MANUFACTURE/IMPORT/RESTAURANTEducation: Bachelor's degree in relevant fields like regulatory affairs, life
Requirements:EXPERIENCE MUST BE FROM FOOD INDUSTRY /MANUFACTURE/IMPORT/RESTAURANTEducation: Bachelor's degree in relevant fields like regulatory affairs, life