Manage all aspects of QC laboratory, including sample analysis, data review, & release of raw material, in-process material, & finished product Ensure compliance with GMP regulations, USP/EP/JP pharmacopeia standard, & internal quality procedure
Required Candidate profile
Conduct investigation for Out-of-Specification (OOS) and Out-of-Trend (OOT) results, implement corrective & preventative action Review & approve all QC documentation Expertise in Sterile Formulation
QA / QC Manager,
Pharmaceutical & Life Sciences,
Quality Assurance,
Full Time, Permanent
Production & Manufacturing
Education
Any Graduate
Key Skills
Skills highlighted with ‘ class="ni-icon-jd-save">‘ are preferred keyskills
class="ni-icon-jd-save">API class="ni-icon-jd-save">Communication Skill target="_blank" class="styles_chip__7YCfG styles_non-clickable__RM_KJ"> class="ni-icon-jd-save">Sterile Formulation class="ni-icon-jd-save">Quality Control
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