Bengaluru Karnataka Clinical specialist Jobs – 168 Open Jobs Today

Regulatory Affairs Specialist
ZEISS Group —Bengaluru, Karnataka
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
Manager - Cell & Gene Therapy - Lab Product
Thermo Fisher Scientific —Bengaluru, Karnataka
- Full-time
- Sales
- Master's degree
- Business development
Sr External Data Specialist
eClinical Solutions —Bengaluru, Karnataka
- Computer literacy
- B.Sc
- English
1h
Pharmacovigilance Services Specialist
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
CMO Content Specialist
Labcorp —Bengaluru, Karnataka
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
9h
Medical Science Liaison
Healthminds Consulting —Bengaluru, Karnataka
- Full-time
- Nursing
- Medicine
- B.Sc
Lactation Consultant
Ooru Healthcare —Bengaluru, Karnataka
- ₹40,000 - ₹60,000 a month
- Full-time
- Nursing
- English
- In-person
Quick apply
10d
Specialist Global WFM
Sagility —Bengaluru, Karnataka
- Microsoft Excel
- Project management
- Bachelor's degree
MEDICAL OFFICER / DOCTOR – OCCUPATIONAL HEALTH CENTRE (OHC)
Bharath Home Medicare Private Limited —Sarjapura, Bengaluru, Karnataka
- ₹45,000 - ₹50,000 a month
- Full-time
- Medicine
- Bachelor's degree
- Computer skills
Quick apply
Early Intervention Specialist ((Speech Language Pathology)) - CAREADD Project
St. John’s National Academy of Health Sciences —Bengaluru, Karnataka
- ₹30,000 - ₹40,000 a month
- Email
- English
- Master's degree
- Bachelor's degree
Manager – Network Hospital Support
Azim Premji Foundation —Bengaluru, Karnataka
- Travel
- Communication skills
Marketing Automation Specialist
Norstella —Bengaluru, Karnataka
- Full-time
- Software troubleshooting
- Salesforce
- SQL
- Health insurance
1d
Embryologist – Application Specialist
Esco Lifesciences Group —Bengaluru, Karnataka
- Sales
- Bachelor's degree
- Travel
Early Intervention Specialist (Occupational Therapy) - CAREADD Project
St. John’s National Academy of Health Sciences —Bengaluru, Karnataka
- ₹30,000 - ₹40,000 a month
- Email
- English
- Master's degree
- Bachelor's degree
Senior Implant Specialist
Ridgetop Dental international —Bengaluru, Karnataka
- Full-time
- Master's degree
- In-person
- Paid time off
Quick apply
Sales Executive – Healthcare / Diagnostics / Pharma
MontezIT —HSR Layout, Bengaluru, Karnataka
- ₹6,00,000 - ₹7,00,000 a year
- Full-time
- Medicine
- Sales
- Business development
Quick apply
Consultant Orthodontist
Manya Dental Clinic —Bengaluru, Karnataka
- ₹18,010.69 - ₹77,381.86 a month
- Full-time
- Bachelor's degree
- In-person
- Communication skills
Quick apply
2d
HR Associate
Dezy —Bengaluru, Karnataka
- Bachelor's degree
- Human resources
- Computer networking
Quick apply
EEG Associate
MS CLINICAL —Bengaluru, Karnataka
- Full-time
RC-REGULATORY COMPLIANCE-PV-CA-Argus-Manager
EY —Bengaluru, Karnataka
- Oracle
- Master's degree
- SQL
- Flexible schedule

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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

Manager - Cell & Gene Therapy - Lab Product

Sr External Data Specialist

Pharmacovigilance Services Specialist

CMO Content Specialist

Medical Science Liaison

Lactation Consultant

Specialist Global WFM

MEDICAL OFFICER / DOCTOR – OCCUPATIONAL HEALTH CENTRE (OHC)

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Sales Executive – Healthcare / Diagnostics / Pharma

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HR Associate

EEG Associate

RC-REGULATORY COMPLIANCE-PV-CA-Argus-Manager

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