Ajay Gowda Email & Phone Number | Customer-centered Quality and Regulatory Specialist bringing broad background in project management, complaints handling, risk evaluations, Post Market Surveillance, customer relations and continuous improvement. Demonstrated skills in developing and deepening internal and external relationships. Practiced problem-solver with technologically savvy nature and expert in Medical Devices (Joint Replacements) and Combinational products (Inhalers, Prefilled Syringes, Growth Hormone Injectors) with 6+ years knowledge in Quality Control and Regulatory. Presently Working Novartis Pharmaceuticals as Technical Expert (Global MS&T) responsible for key responsibilities : • Review/Maintenance and contribute to the Novartis medical device's Technical documents including Design History Files (DHF), Post-Market Surveillance (PMS), Human Factors Engineering (HFE) /usability engineering documents • Risk management plan and report • Knowledge on software as medical devices

Ajay Gowda

Customer-centered Quality and Regulatory Specialist bringing broad background in project management,...
Hyderabad, Hyderabad, India

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Ajay Gowda’s Phone Numbers +1 212-830-****

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Ajay Gowda’s Location Hyderabad, Hyderabad, India

Ajay Gowda’s Current Industry

Ajay Gowda’s Prior Industry Pfizer | Gsk

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Technical Expert

Present

Assistant Manager

2020-04-01 00:00:00 - 2022-07-01 00:00:00

Specialist

2017-09-01 00:00:00 - 2020-03-01 00:00:00

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Ajay Gowda is a Customer-centered Quality and Regulatory Specialist bringing broad background in project management, complaints handling, risk evaluations, Post Market Surveillance, customer relations and continuous improvement. Demonstrated skills in developing and deepening internal and external relationships. Practiced problem-solver with technologically savvy nature and expert in Medical Devices (Joint Replacements) and Combinational products (Inhalers, Prefilled Syringes, Growth Hormone Injectors) with 6+ years knowledge in Quality Control and Regulatory. Presently Working Novartis Pharmaceuticals as Technical Expert (Global MS&T) responsible for key responsibilities : • Review/Maintenance and contribute to the Novartis medical device's Technical documents including Design History Files (DHF), Post-Market Surveillance (PMS), Human Factors Engineering (HFE) /usability engineering documents • Risk management plan and report • Knowledge on software as medical devices