Medical Regulatory Affairs
We have 485 ads for keyword medical regulatory affairs
(0.002 seconds)Formulation Specialist - DF - BRaIN
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Full-timeJob Family: Research & DevelopmentSub Job Family: Formulation R&D - OSDPreferred type of working: On-PremiseYears of Experience: 6 -
Clinical Trial Associate
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Full-timeJob Family: Clinical DevelopmentSub Job Family: Clinical OperationBusiness unit: BiologicsYears of Experience: 1 - 3 Company Description Dr. Reddy’s
Clinical Research Associate
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Full-timeJob Family: Clinical DevelopmentSub Job Family: Clinical OperationPreferred type of working: HybridBusiness unit: BiologicsYears of Experience: 3 - 6
Senior Regulatory Professional
Department: RA Diabetes Are you passionate about driving regulatory strategy and life cycle management of product portfolio ensuring interactions with
Formulation Specialist - DF - BRaIN
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Full-timeJob Family: Research & DevelopmentSub Job Family: Formulation R&D - OSDPreferred type of working: On-PremiseYears of Experience: 6 -
Regulatory Professional II
Department: RA CMC Biotech and Rare Disease Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient
Global Medical Advisor
Department : Global Medical Affairs. Are you a proven leader who can set direction and drive team performance? Do you have expertise in driving medical affairs
Assistant Manager - Micro Catheters - (TD945)
We are hiring for a company that develops and manufactures advanced vascular medical devices, such as micro catheters, to improve patient care. Focused on
Formulation Scientist - BRaIN
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Full-timeJob Family: Research & DevelopmentSub Job Family: Formulation R&D - OSDPreferred type of working: On-PremiseYears of Experience: 3 - 6Business
Process Engineer (Active Pharmaceutical Ingredient)
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Process Engineer (Active Pharmaceutical Ingredient) Full-timeJob Family: Engineering & ScienceSub Job Family: Process Engineering - APIPreferred type of
Process Engineer API (Active Pharmaceutical Ingredient)
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Full-timeJob Family: Research & DevelopmentSub Job Family: R&D - GeneralBusiness unit: IPDOYears of Experience: 3 - 6 Company DescriptionDr. Reddy’s
Quality Management Associate (Quality Events & CAPAs)
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Quality Management Associate (Quality Events & CAPAs) Full-timeDepartment: PV QM Company DescriptionWe are PrimeVigilance (part of Ergomed Group), a
Regulatory Professional
Department: Regulatory Affairs Rare Blood Disorders Are you passionate about driving regulatory strategy and life cycle management of product portfolio
Global Medical Advisor
Department :Global Medical Affairs. Are you a proven leader who can set direction and drive team performance? Do you have expertise in driving medical affairs
Benefit/Risk Officer (Pharmacovigilance)
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Full-timeDepartment: Benefit-Risk Management Company DescriptionWe are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service
PV Associate/Literature
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Full-timeDepartment: Literature Company DescriptionWe are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider
Safety Systems Specialist
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Full-timeDepartment: Safety Information Systems Company DescriptionWe are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance
Medical Information System Administrator
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Full-timeDepartment: Safety Information Systems Company DescriptionWe are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance
Administrative Assistant - entry level
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Full-timeDepartment: ICSR Management Company DescriptionWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider
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