Stryker has announced an opening for a Regulatory Affairs Specialist in Bengaluru, India, within its Ortho Tech Division. The full-time, hybrid position focuses on regulatory compliance, submission support, regulatory intelligence, and coordination with cross-functional teams.
The official Stryker careers page confirms the position is based in Bangalore, Karnataka, India, with requisition ID R569389, and requires approximately 10% travel.
Stryker Regulatory Affairs Specialist – Job Overview
| Particular | Details |
|---|---|
| Company | Stryker |
| Position | Regulatory Affairs Specialist |
| Department | Regulatory Affairs / RAQA |
| Division | Ortho Tech |
| Location | Bengaluru, India |
| Job Type | Full Time |
| Work Mode | Hybrid |
| Experience | 3–7 years preferred with the required technical degree |
| Qualification | Bachelor’s degree in Engineering, Science, Regulatory Science or related field |
| Travel | 10% |
| Job ID | R569389 |
The official listing describes the role as an opportunity to build foundational regulatory affairs expertise while working in a highly regulated medical technology environment.
Roles and Responsibilities
The selected candidate will support regulatory activities for products across Stryker’s orthopedic instruments portfolio. Key responsibilities include:
- Monitoring regulatory requirements, guidance documents, and applicable industry standards across global markets.
- Researching regulatory requirements, approval pathways, and compliance information for products and programs.
- Maintaining regulatory intelligence files, submission documentation, and supporting records.
- Assisting with regulatory dossiers, pre-submission packages, and agency submission materials.
- Tracking regulatory submissions and applications under review and communicating status updates to stakeholders.
- Maintaining records of communications, regulatory commitments, and outcomes involving authorities and stakeholders.
- Coordinating meetings and preparing supporting materials for regulatory discussions.
- Supporting reviews of preclinical, clinical, quality, and technical documentation required for regulatory purposes.
Eligibility and Qualifications
Required Qualification
Candidates should have:
- A Bachelor’s degree in Engineering, Science, Regulatory Science, or a related technical field.
- 3–7 years of work experience is specified with the preferred technical degree.
- Demonstrated experience working with technical, scientific, or regulated documentation through academic, internship, co-op, or professional experience.
Preferred Qualifications
Stryker additionally prefers candidates who have:
- A Master’s degree in Regulatory Science or a related field.
- Experience in regulatory affairs, quality, clinical, research, or compliance activities.
- Familiarity with regulations and standards associated with medical devices, pharmaceuticals, biotechnology, or other regulated industries.
Salary and Benefits
Salary: Stryker has not published a specific salary range for this vacancy. For informational purposes only, a realistic market estimate for a Bengaluru Regulatory Affairs Specialist with the stated experience level may be around ₹8–14 lakh per annum; this is not an official Stryker salary figure.
Stryker’s official careers information states that its total rewards package can include bonuses, healthcare and insurance benefits, retirement programs, wellness programs, and service/performance awards, with benefits varying by location.
How to Apply for Stryker Regulatory Affairs Specialist
Eligible candidates can apply online through the official Stryker careers portal.
Application Mode: Online
Official Apply Link:
https://stryker.wd1.myworkdayjobs.com/en-US/StrykerCareers/job/Bengaluru-India/Regulatory-Affairs-Specialist_R569389
The official Stryker posting currently identifies the job as full-time, hybrid, located in Bengaluru/Bangalore, India.
