Pharma Regulatory Affairs
We have 97 ads for keyword pharma regulatory affairs
(0.001 seconds)Scientist packaging development
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Full-timeJob Family: Research & DevelopmentSub Job Family: R&D - GeneralPreferred type of working: On-PremiseYears of Experience: 3 - 5Business unit:
Regulatory Specialist
Department: RA CMC and Device Are you passionate about your work? Do you want to build excellence within processes in the most efficient way? Do you have an
Regulatory Professional
Department: RA CMC and Device Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you
Senior Regulatory Professional
Department: RA CMC and Device Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you
IPM Specialist
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Full-timeJob Family: Legal, Compliance & AuditSub Job Family: Intellectual Property ManagementPreferred type of working: On-PremiseYears of Experience: 10
Advanced Quality Advisor
Department: R and D Quality GBS Job Level: 6 Does your motivation come from challenges and working in a dynamic environment? Do you have an eye for detail and
(X758) - Regulatory Affairs Executive
Industry: Class A & B Medical Devices Qualification: Postgraduate or equivalent in Pharma/ Medical device Sector OR Biomedical Engineer Experience: Min. 2
Head Regulatory Affairs India
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A
Global medical advisor
Department : Rare Disease medical affairs GMA:GBS. Are you a postgraduate in medicine willing to be a credible and valued scientific expert of the organization
Senior Manager : R and D Quality GBS
Department: R and D Quality About the department R and D Quality is part of the Development Organisation and plays a vital role in supporting the drug and
[G353] | Senior Clinical Research Scientist
About the job Job Title: Department: R&D; Location: Bengaluru Years of Experience: 5 -7 years Employment Type: Full Time Employment About Qure.ai: Qure.ai is
Clinical Marketing Manager
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Full-timeShift: DayTravel Requirements: 50% of the timeEmployee Type: EmployeeGlobal Job Level (HCM): Professional 3 (9) Company DescriptionAt Intuitive, we
Regulatory Affairs Executive
To prepare and submit product registration dossiers of assigned products to targeted countries ROW as per CTD requirements, To respond to queries received from
Associate Director : RA CMC and Device
Department: RA CMC Do you aspire to accelerate your leadership career within a global pharmaceutical company built on life:changing innovations? Does leading a
Legal Counsel
Department: Global Legal Global Business Services (GL:GBS) Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a
Head Regulatory Affairs India
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A
Head Regulatory Affairs India
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A
Regulatory Executive
Position: Regulatory ExecutiveEligibility : M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory Affairs. Should have good knowledge of
Regulatory Affairs Executive
We are Urgently Looking for Regulatory Affairs Executive. Assisting Role in Ra Team and Responsible to Filings,Experience :2 - 4 Years No. of Openings :1
Regulatory Executive
Position: Regulatory ExecutiveJob Location: Vile Parle Mumbai: MaharashtraEligibility :M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory