JOB DESCRIPTION
Proficient with Microsoft and other related applicationsHelp evaluate business opportunities based on products on the market and supply-and-demand numbers.
Ensure Quality control testing compliance and clearance per task in the R&D Dept.
Tasked with analyzing data to verify that research has been completed and pharmaceutical development is on the right track
Ensure documentation is kept up to date
Set up the digital or automated documentation including SOP and all in the R&D Dept.
Readily available for special tasks such as training of Interns and Marketing people
Conduct qualitative and quantitative chemical analyses or experiments in laboratories for quality or process control or to develop new products or knowledge
Conduct and validate chemical and biological quality control assays and document statistical data from testing to confirm compliance with quality standards
Ensure R&D Dept. is compliant in terms of the cGMP standard in terms of documentation, SOP, etc.
Another task that may be assigned on top of the job responsibilities.
Ready to be assigned in other Dept. or Satellite affiliate company
JOB QUALIFICATION
Degree in Pharmacy, Biology, Chemistry, Chemical Engineering or any related courses
Professional license preferred but not required
Knowledgeable in documentation, Pharmaceutical Manufacturing and cGMP
Proficient with Microsoft and other related applications
OTHER JOB REQUIREMENTS
Education
Bachelor's/College Degree
Field of study
Biology, Chemistry, Engineering (Chemical), Pharmacy/Pharmacology
Specialization
Chemical Engineering, Pharmacy, Biotechnology
JOB BENEFITS
Documenation, Academic Research, Knowledge in MS Office
Proficient with Microsoft and other related applicationsHelp evaluate business opportunities based on products on the market and supply-and-demand numbers.
Ensure Quality control testing compliance and clearance per task in the R&D Dept.
Tasked with analyzing data to verify that research has been completed and pharmaceutical development is on the right track
Ensure documentation is kept up to date
Set up the digital or automated documentation including SOP and all in the R&D Dept.
Readily available for special tasks such as training of Interns and Marketing people
Conduct qualitative and quantitative chemical analyses or experiments in laboratories for quality or process control or to develop new products or knowledge
Conduct and validate chemical and biological quality control assays and document statistical data from testing to confirm compliance with quality standards
Ensure R&D Dept. is compliant in terms of the cGMP standard in terms of documentation, SOP, etc.
Another task that may be assigned on top of the job responsibilities.
Ready to be assigned in other Dept. or Satellite affiliate company
JOB QUALIFICATION
Degree in Pharmacy, Biology, Chemistry, Chemical Engineering or any related courses
Professional license preferred but not required
Knowledgeable in documentation, Pharmaceutical Manufacturing and cGMP
Proficient with Microsoft and other related applications
OTHER JOB REQUIREMENTS
Education
Bachelor's/College Degree
Field of study
Biology, Chemistry, Engineering (Chemical), Pharmacy/Pharmacology
Specialization
Chemical Engineering, Pharmacy, Biotechnology
JOB BENEFITS
Documenation, Academic Research, Knowledge in MS Office
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Compact Pharmaceuticals Corp
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Position Research and Development assistant recruited by the company Compact Pharmaceuticals Corp at , Joboko automatically collects the salary of , finds more jobs on Research and Development Assistant or Compact Pharmaceuticals Corp company in the links above
About the company
Compact Pharmaceuticals Corp jobs
17 Sta. Monica St. Malinta Valenzuela City