Drug Regulatory Affairs
We have 103 ads for keyword drug regulatory affairs
(0.001 seconds)PV Medical Writer II/III (strong aggregate report writing experience required)- homebased in India
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Full-timeDepartment: Medical Writing Company DescriptionWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider
Medical Writer II/III (strong aggregate report writing experience required)- homebased in India
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Full-timeDepartment: Medical Writing Company DescriptionWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider
Team Member ASAT
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Full-timeJob Family: Research & DevelopmentSub Job Family: Structure Elucidation LabPreferred type of working: On-PremiseYears of Experience: 3 - 6Business
Team Member ASAT
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Full-timeJob Family: Research & DevelopmentSub Job Family: Structure Elucidation LabPreferred type of working: On-PremiseYears of Experience: 3 - 6Business
Clinical Medical Manager (x8 positions)
Location: Delhi/Mumbai/Hyderabad Business Unit: CMR (Clinical, Medical, Regulatory and Pharmacovigilance) Are you passionate about what you are doing? Do you
PV Specialist-Safety Data Exchange Agreements (SDEA)
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Full-timeJob Family: Medical Affairs & PharmacovigilanceSub Job Family: PharmacovigilancePreferred type of working: On-PremiseBusiness unit: GMO Company
(KYU-705) QA- Document Coordinator
ZTMP TEMPLATE FORMAT TO SHARE REQUIREMENTS Basic Details: - Position title (if any) : QA - Document Coordinator Designation : Executive Reports to : Head of
Pharmacovigilance Associate
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Full-timeJob Family: Medical Affairs & PharmacovigilanceSub Job Family: PharmacovigilanceBusiness unit: NAG Company DescriptionDr. Reddy’s Laboratories
PV Specialist - IT and Digitalization
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Full-timeJob Family: Medical Affairs & PharmacovigilanceSub Job Family: PharmacovigilancePreferred type of working: On-PremiseYears of Experience: 6 -
Manager BD In-Licensing
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Full-timeJob Family: General ManagementSub Job Family: Business Development & AlliancesBusiness unit: GG EMYears of Experience: 6 - 12 Company
Lead-PMO
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Full-timeJob Family: Supply Chain ManagementSub Job Family: Supply Chain PlanningPreferred type of working: On-PremiseYears of Experience: 12 - 20Business
Regulatory Professional
. Department: Regulatory Affairs Rare Blood Disorders Are you passionate about driving regulatory strategy and life cycle management of product portfolio
Regulatory Professional I
. Department: Regulatory Affairs CMC and Device Are you passionate about what you are doing? Do you want to build excellence within processes in the most
Biopharmaceutics Scientist
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Full-timeJob Family: Clinical DevelopmentSub Job Family: Biopharmaceutics & Bio AnalyticalPreferred type of working: On-PremiseYears of Experience: 6 -
Senior Regulatory Professional
Department: Regulatory Affairs Rare Blood Disorders Are you passionate about driving regulatory strategy and life cycle management of product portfolio
[BZ-409] - Project Coordinator
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis,
Lead-PMO
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Full-timeJob Family: Supply Chain ManagementSub Job Family: Supply Chain PlanningPreferred type of working: On-PremiseYears of Experience: 12 - 20Business
Team Member Packaging Development
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Full-timeJob Family: Innovation & DesignPreferred type of working: On-PremiseYears of Experience: 6 - 12Business unit: Biologics Company DescriptionDr.
Senior Regulatory Professional
.Department: Regulatory Affairs Rare Blood Disorders Are you passionate about driving regulatory strategy and life cycle management of product portfolio
Team Member - QA CTO
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Full-timeJob Family: QualitySub Job Family: Quality AssurancePreferred type of working: On-PremiseYears of Experience: 6 - 12Business unit: GMO Company