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QA SPECIALIST (GMP OFFICER)12 HOUR SHIFTS DAYS & NIGHTS (S F BAY AREA)
Job Field: Legal Jobs
Location: San Carlos, CA
Salary: $Not stated
Location: San Carlos, CA
Salary: $Not stated
JOB SUMMARY:
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<tr><td valign="top" width="450"><b>value="Apply to job" id=button1 name=button1 onClick="javascript:ApplyNow();"> Job ID 96482BRPosting Title QA Specialist (GMP Officer)12 Hour Shifts Days & Nights (S F Bay Area)Division PharmaBusiness Unit Pharma - Global DevelopmentCountry USAWork Location San Carlos, CACompany/Legal Entity USA Novartis Pharmaceuticals Corporation, East Hanover, NJFunctional Area ProductionTherapeutic/Disease Area RespiratoryJob Type Full TimeEmployment Type RegularJob Description Supports day to day site compliance needs on the shop floor. Identifies and resolves compliance issues within the Process Unit unilaterally and cross-functionally. Works closely with the Process Units and Quality Organization to ensure compliance with current FDA regulations through operational oversight, internal audits, deviation management, and proactive process improvement initiatives. Assists with Regulatory Agency inspections/ activities, as needed.
</tr>
<tr><td valign="top" width="450"><b>value="Apply to job" id=button1 name=button1 onClick="javascript:ApplyNow();"> Job ID 96482BRPosting Title QA Specialist (GMP Officer)12 Hour Shifts Days & Nights (S F Bay Area)Division PharmaBusiness Unit Pharma - Global DevelopmentCountry USAWork Location San Carlos, CACompany/Legal Entity USA Novartis Pharmaceuticals Corporation, East Hanover, NJFunctional Area ProductionTherapeutic/Disease Area RespiratoryJob Type Full TimeEmployment Type RegularJob Description Supports day to day site compliance needs on the shop floor. Identifies and resolves compliance issues within the Process Unit unilaterally and cross-functionally. Works closely with the Process Units and Quality Organization to ensure compliance with current FDA regulations through operational oversight, internal audits, deviation management, and proactive process improvement initiatives. Assists with Regulatory Agency inspections/ activities, as needed.
KEY REQUIREMENTS:
Not stated
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