Greenfield project experience preferred (lab setup,equipment qualification,method validation / transfer) Experience: 4 6 Years4 6 years of QC experience in a pharma OSD facility
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The ideal candidate should have experience in equipment / utility qualification documentation and QMS activities in a pharmaceutical setup. . Key Responsibilities: . 5 8 years of experience in QA Ph
6 10 years of experience in QC Pharma (OSD preferred) Experience: 610 Years
Preparation and approval of URS (User Requirement Specifications) for production equipment and systems. Experience: 3 10 Years (depending on level)
and prepare reports. . Support regulatory department for product documentation,filing,etc. . Should have knowledge about SAPExperience: 10- 14 years (Apart from the QA functions,working on new proje
. API Production: Execute and oversee the manufacturing processes of active pharmaceutical ingredients,following approved batch records and standard operating procedures (SOPs)Technology Transfer and
Hands-on experience in URS preparation,equipment qualification,SOP writing,and QMS . .
This includes completing the required coursework,projects,internships,and examinations and are verified through SCMs Student education verification: Verification of education documents of the passed-o
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