Apply for Senior RA Specialist at Stryker Gurugram. Check eligibility, experience, responsibilities, salary details and apply online for regulatory affairs role now.
Introduction
Regulatory Affairs professionals looking to grow in the medical device and pharma sector have an excellent opportunity here. The Senior RA Specialist at Stryker role focuses on global regulatory submissions, compliance, and lifecycle management. This hybrid position offers exposure to international regulatory frameworks and cross-functional collaboration, making it ideal for experienced professionals aiming to advance their regulatory careers.
Job Overview
| Job Title | Senior RA Specialist |
|---|---|
| Company Name | Stryker |
| Location | Gurugram, India |
| Employment Type | Full-Time (Hybrid) |
| Department | Regulatory Affairs |
| Experience Required | 3–6 Years |
| Education | Bachelor’s in Life Sciences / Pharmacy / Engineering |
| Salary | As per company standards |
Company Overview
Stryker is a globally recognized leader in medical technologies, offering innovative products and services in orthopedics, medical devices, and surgical solutions. With a strong focus on improving patient outcomes, Stryker operates across multiple countries and provides excellent career growth opportunities, global exposure, and a collaborative work environment.
Job Location & Employment Type
- Location: Gurugram, India
- Work Mode: Hybrid (Office + Remote)
- Employment Type: Full-Time
Open Positions / Department Details
This role is part of the Regulatory Affairs team, responsible for ensuring product compliance with global regulatory requirements and supporting submission activities across multiple regions.
Key Roles & Responsibilities
Regulatory Strategy & Submissions
- Support development and execution of regulatory strategies
- Assist in identifying regulatory pathways for product changes
- Prepare and submit regulatory dossiers (FDA, EU MDR, and other markets)
- Ensure compliance with global regulatory standards
Documentation & Compliance
- Maintain regulatory documents, technical files, and audit-ready dossiers
- Ensure accuracy and completeness of submission documentation
- Support publishing activities (eCTD and non-eCTD formats)
Lifecycle Management
- Support regulatory requirements for product lifecycle changes
- Assist in labeling, design, and manufacturing change assessments
- Maintain Regulatory Information Management (RIM) systems
Cross-Functional Collaboration
- Work with R&D, Quality, Clinical, and Marketing teams
- Coordinate submission timelines and deliverables
- Support responses to regulatory authority queries
Process Improvement & Audits
- Contribute to SOP development and process improvements
- Support audits, inspections, and compliance activities
- Monitor regulatory updates and assess business impact
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or related field
- Advanced degree preferred
Experience
- 3 to 6 years of experience in Regulatory Affairs or related domain
Skills Required
- Strong knowledge of global regulatory frameworks (FDA, EU MDR, CDSCO, etc.)
- Experience in regulatory submissions and documentation
- Attention to detail and strong organizational skills
- Project management and coordination abilities
- Effective communication and stakeholder management
- Ability to work in a fast-paced, global environment
Salary & Benefits
- Salary: As per company standards
- Hybrid work flexibility
- Opportunity to work on global regulatory projects
- Career growth in regulatory affairs and compliance
- Exposure to international regulatory authorities
- Learning and development opportunities
Selection Process
The hiring process generally includes:
- Online application submission
- Resume screening
- Technical interview
- HR interview
- Final selection
How to Apply
Candidates interested in the Senior RA Specialist at Stryker role can apply through the official Stryker careers portal. Ensure your resume highlights regulatory experience and knowledge of global frameworks.
Important Dates
- Posted On: Recently
- Apply as soon as possible (no fixed deadline mentioned)
Why Apply for This Job?
- Work with a leading global medical technology company
- Gain exposure to international regulatory frameworks
- Build expertise in regulatory submissions and compliance
- Opportunity to collaborate with global teams
- Strong career growth in regulatory affairs and medical devices
- Hybrid work model for better work-life balance
FAQs
1. Who can apply for this job?
Candidates with 3–6 years of experience in regulatory affairs and a relevant degree can apply.
2. What is the salary for this role?
Salary is not disclosed but will be as per company standards.
3. Is experience in medical devices required?
Experience in medical devices or pharma regulatory affairs is preferred.
4. What are the key skills required?
Knowledge of regulatory frameworks, documentation skills, and project coordination are essential.
5. How can I apply?
You can apply online through the official Stryker careers website.
Conclusion
The Senior RA Specialist at Stryker role is a strong opportunity for regulatory professionals aiming to work in a global environment. With exposure to international regulations, cross-functional collaboration, and career advancement opportunities, this position can significantly enhance your professional journey. Apply now to take your regulatory career to the next level.
Disclaimer
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