Medical Devices Regulatory Jobs

Kamet Consulting Group - Hyderabad, Telangana, India

creatively, take initiatives, and drive innovative solutions. We are looking for a Sr. Regulatory Affairs / Regulatory Intelligence Associate (Pharmaceutical and Medical Devices) specializing

from: linkedin.com - 4 days ago

Pharmaceutical Company - , , India

: B.Pharm / M.Pharm Work Experience: 3-5 years of experience in regulatory functions from pharmaceutical organizations. Knowledge of ROW market and regulatory experience in medical devices is preferred

from: linkedin.com - Yesterday

Global Technologies - Bangalore, Karnataka, IN

to independently own activities - (Preferred)Knowledge and understanding IEC 62304 and other relevant medical device regulatory standards highly preferred. - (Preferred) Experience with risk management activities

from: adzuna.in - 2 days ago

Aurolab - Madurai, Tamil Nadu, India

, testing, and optimizing hardware components and systems for medical devices, ensuring compliance with regulatory standards and industry best practices. Responsibilities: Collaborate with cross-functional

from: linkedin.com - 5 days ago

Staffing Support India - , , India

collaboratively in a team environment, as well as independently on projects. Creative thinker with a keen eye for detail and a passion for delivering high-quality work. Understanding of the medical device industry

from: linkedin.com - Yesterday

Global Technologies - Bangalore, Karnataka, IN

62304 and other relevant medical device regulatory standards highly preferred. - (Preferred) Experience with risk management activities compliant with IEC 14971. Responsibilities : - Developing new

from: adzuna.in - 4 days ago

Quanticate - , , India

with pharmaceutical, biotechnology, and medical device companies to support their regulatory and scientific communication needs. The Senior Medical Writer will be responsible for developing high-quality clinical study

from: linkedin.com - Yesterday

Indegene - Bengaluru, Karnataka, India

Must have: Bachelor’s or master's degree in engineering/life science; Overall experience: 7-10 years Minimum 3-year experience with Medical Devices Regulatory Affairs or Q&C/R&D Minimum 3-year experience

from: linkedin.com - 8 days ago

Antal International India - Others

to Europe and US markets. - Incumbent should be carrying strong knowledge of relevant regulations and guidelines for medical devices, including FDA 21 CFR, EU Medical Device Regulation (MDR), and ISO 13485. 1

from: iimjobs.com - 9 days ago

Fourth Frontier - Bengaluru, Karnataka, India

requirements for medical devices. Oversee, support, and ensure that an effective and efficient quality management system is built and maintained. Responsibility for ensuring that all applicable quality system

from: linkedin.com - Yesterday