Bengaluru Karnataka Clinical specialist Jobs – 166 Open Jobs Today

Regulatory Affairs Specialist
ZEISS Group —Bengaluru, Karnataka
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
BC-Sector-Health Care-Clinical Consultant-Clinical Domain Specialist-Senior
EY —Bengaluru, Karnataka
- HIPAA
- EMR systems
- Epic
Clinical AI Data Specialist
PinnacleU —HSR Layout, Bengaluru, Karnataka
- ₹20,00,000 - ₹38,00,000 a year
- Full-time
- SQL
- AI
- Communication skills
Quick apply
Regulatory Affairs Specialist
Natus Sensory —Bengaluru, Karnataka
- Full-time
- Remote
- English
- Continuous improvement
- Health insurance
- Paid time off
SPE-Claims HC
Cognizant —Bengaluru, Karnataka
- Full-time
- Remote
- Nursing
- B.Sc
- Analysis skills
- Health insurance
- Work from home
Clinical Data Specialist
Fortrea —Bengaluru, Karnataka
- Weekend availability
- English
- Bachelor's degree
- Medical terminology
13h
Clinical Trial Implementation Specialist
DSG Inc —Hoodi, Bengaluru, Karnataka
- Call employer
- Health insurance
- Paid time off
Clinical Content Specialist (Payment Integrity - Drugs & Biological)
2070Health —Bengaluru, Karnataka
- Full-time
- Doctoral degree
- Research
- Communication skills
- Health insurance
Quick apply
Claims Manager (Healthcare)
CONNECT AND HEAL PRIMARY CARE PRIVATE LIMITED —Bangalore City, Bengaluru, Karnataka
- ₹9,00,000 - ₹11,00,000 a year
- Full-time
- Analysis skills
- Bachelor's degree
- Organisational skills
Quick apply
2h
Customer Care Representative
Workplace Options —Bengaluru, Karnataka
- ₹5,50,000 a year
- Overnight shift
- Hybrid work
- Microsoft Excel
- English
- Research
- Health insurance
Quick apply
7d
Veeva Vault Product Specialist Clinical
Bayer —Bengaluru, Karnataka
- English
- Research
- Master's degree
Nursing SME
orbitnext-tech.com —Bengaluru, Karnataka
- From ₹70,086 a month
- Full-time
- Nursing
- Master's degree
- Project management
Quick apply
1d
Regulatory Specialist – Medical Devices
Quest Global —Bengaluru, Karnataka
- Full-time
- B.Sc
- Microsoft Office
- Bachelor's degree
Quick apply
Medical Documentation Specialist (India)
Commure —Bengaluru, Karnataka
- Full-time
- AI
- Medical terminology
Manager - Cell & Gene Therapy - Lab Product
Thermo Fisher Scientific —Bengaluru, Karnataka
- Full-time
- Sales
- Master's degree
- Business development
Senior Clinical Specialist - Ultrasound
Siemens Healthineers —Bengaluru, Karnataka
- Full-time
- Research
- Master's degree
- Project management
8d
Talent Development Specialist
Clario —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Site Specialist
ICON Plc —Bengaluru, Karnataka
- Full-time
- Analysis skills
- Bachelor's degree
- Communication skills
- Health insurance
Medical Documentation Specialist - Entry Level (India)
Commure —Bengaluru, Karnataka
- Full-time
- AI
- Medical terminology
Study Startup Specialist II
PSI CRO —Bengaluru, Karnataka
- Full-time
- English
- Bachelor's degree
- Communication skills
Quick apply

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Regulatory Affairs Specialist

ZEISS Group -
Bengaluru, Karnataka

Apply Now

Job details

Full-time

Qualifications

Microsoft Office
Diagnostic evaluation
.NET
Master's degree
Bachelor's degree
FDA regulations

Full job description

ZEISS in India

ZEISS in India is headquartered in Bengaluru and present in the fields of Industrial Quality Solutions, Research Microscopy Solutions, Medical Technology, Vision Care and Sports & Cine Optics.

ZEISS India has 3 production facilities, R&D center, Global IT services and about 40 Sales & Service offices in almost all Tier I and Tier II cities in India. With 2200+ employees and continued investments over 25 years in India, ZEISS’ success story in India is continuing at a rapid pace.

Further information at ZEISS India .

Job purpose

To support the planning, execution, and management of regulatory activities for global medical devices (software and hardware), ensuring compliance with EU MDR, US FDA, and other country-specific regulations. The role focuses on preparing regulatory submissions, monitoring post-market commitments, and collaborating with cross-functional teams to meet program milestones.

Duties and responsibilities

Regulatory Support:

Assist in preparing technical documentation and submissions for Class I, IIa, and IIb medical devices in compliance with EU MDR and US FDA 510(k).
Support country-specific registration processes (e.g., China NMPA and other international markets).
Participate in the evaluation of regulatory impacts for design changes such as ECRs, PSM decisions, and updates to claims matrices.

Coordination and Collaboration:

Collaborate with Product Management, Clinical Affairs, QA, and Program Delivery teams to align regulatory timelines with project objectives.
Represent Regulatory Affairs in team meetings and provide regulatory input to support product development and market approvals.

Submission and Documentation Management:

Prepare and maintain documentation such as STED, GSPR, DoC, CER, and PMS reports.
Assist in monitoring timely country releases across various markets and manage change notifications.

Risk and Post-Market Oversight:

Identify potential regulatory risks and propose mitigation strategies.
Support post-market regulatory activities, including responses to regulatory authorities and tracking post-market surveillance.

Process Improvement:

Contribute to initiatives for process standardization and digitalization in regulatory activities (e.g., Signavio /CARA/Polarian /ADO tools).

Qualifications

Bachelor’s/Master’s degree in Life Sciences, Biomedical Engineering, Pharmacy, or a related field.
3–5 years of experience in Regulatory Affairs for medical devices.
Strong working knowledge of EU MDR and US FDA 510(k) requirements.
Exposure to multi-country registrations and clinical evaluation processes like CER and PMS is preferred.
RCC or equivalent certification is a plus.
Familiarity with technical documentation structure is an advantage.
Strong MS Office and documentation skills.

Other Attributes

Strong attention to detail and structured problem-solving skills.
Effective communication and collaboration abilities in global cross-functional teams.
Accountability and ownership of assigned tasks.
Ability to adapt to evolving regulatory landscapes and manage ambiguity effectively
Comfortable working across time zones.

Job purpose

Duties and responsibilities

Regulatory Support:

Assist in preparing technical documentation and submissions for Class I, IIa, and IIb medical devices in compliance with EU MDR and US FDA 510(k).
Support country-specific registration processes (e.g., China NMPA and other international markets).
Participate in the evaluation of regulatory impacts for design changes such as ECRs, PSM decisions, and updates to claims matrices.

Coordination and Collaboration:

Collaborate with Product Management, Clinical Affairs, QA, and Program Delivery teams to align regulatory timelines with project objectives.
Represent Regulatory Affairs in team meetings and provide regulatory input to support product development and market approvals.

Submission and Documentation Management:

Prepare and maintain documentation such as STED, GSPR, DoC, CER, and PMS reports.
Assist in monitoring timely country releases across various markets and manage change notifications.

Risk and Post-Market Oversight:

Identify potential regulatory risks and propose mitigation strategies.
Support post-market regulatory activities, including responses to regulatory authorities and tracking post-market surveillance.

Process Improvement:

Contribute to initiatives for process standardization and digitalization in regulatory activities (e.g., Signavio /CARA/Polarian /ADO tools).

Qualifications

Bachelor’s/Master’s degree in Life Sciences, Biomedical Engineering, Pharmacy, or a related field.
3–5 years of experience in Regulatory Affairs for medical devices.
Strong working knowledge of EU MDR and US FDA 510(k) requirements.
Exposure to multi-country registrations and clinical evaluation processes like CER and PMS is preferred.
RCC or equivalent certification is a plus.
Familiarity with technical documentation structure is an advantage.
Strong MS Office and documentation skills.

Other Attributes

Strong attention to detail and structured problem-solving skills.
Effective communication and collaboration abilities in global cross-functional teams.
Accountability and ownership of assigned tasks.
Ability to adapt to evolving regulatory landscapes and manage ambiguity effectively
Comfortable working across time zones.

Your ZEISS Recruiting Team:

Saptarshi Chowdhury

Apply Now

Refine Your Search

clinical specialist jobs in bengaluru karnataka

Regulatory Affairs Specialist

BC-Sector-Health Care-Clinical Consultant-Clinical Domain Specialist-Senior

Clinical AI Data Specialist

Regulatory Affairs Specialist

SPE-Claims HC

Clinical Data Specialist

Clinical Trial Implementation Specialist

Clinical Content Specialist (Payment Integrity - Drugs & Biological)

Claims Manager (Healthcare)

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Medical Documentation Specialist (India)

Manager - Cell & Gene Therapy - Lab Product

Senior Clinical Specialist - Ultrasound

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Site Specialist

Medical Documentation Specialist - Entry Level (India)

Study Startup Specialist II

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