Job Overview
| Particulars | Details |
|---|---|
| Position | Scrum Master (Medical Device Domain) |
| Company | Rudhra Info Solutions |
| Location | Hyderabad, Telangana |
| Job Type | Full-Time |
| Experience | Fresher |
| Category / Department | General |
| Application Mode |
🏢 About Rudhra Info Solutions
Company Overview
Rudhra Info Solutions (RIS) is a technology consulting and IT services company with over 13 years of experience delivering digital transformation solutions across multiple industries. The company specializes in cloud technologies, enterprise platforms, data engineering, healthcare, life sciences, Salesforce, AWS, ServiceNow, Tableau, and Mulesoft solutions.
Company Mission
To accelerate business growth through innovative IT services, advanced technology products, and customer-focused digital transformation solutions that enable organizations to achieve long-term success.
Company Vision
To empower businesses worldwide through innovation, trusted partnerships, and transformative technology solutions that create meaningful digital experiences.
Core Values
• Customer Satisfaction
• Innovation
• Integrity
• Collaboration
• Quality Excellence
• Continuous Improvement
• Long-Term Partnerships
What Makes Them Different
• 13+ years of industry expertise.
• Strong presence in Healthcare and Life Sciences.
• Certified professionals across leading enterprise technologies.
• Customer-first approach with scalable digital solutions.
• Proven success delivering enterprise transformation initiatives.
Leadership / Company Philosophy
Rudhra Info Solutions believes technology should empower businesses through innovation, collaboration, and customer-centric solutions while maintaining the highest standards of quality and service.
📍 Rudhra Info Solutions
Plot No. 17, Gopal Nagar Extension,
Mannivakkam Extension, Mannivakkam,
Chennai, Tamil Nadu, India
💡 Editor's Note / Preparation Tip
📝 Resume Preparation Tips
• Highlight Scrum Master certifications and Agile transformation experience.
• Showcase Medical Device or Healthcare domain projects prominently.
• Include PI Planning, Release Management, and stakeholder management experience.
• Quantify Agile delivery improvements and team achievements.
• Keep your LinkedIn profile updated with certifications and accomplishments.
🎯 Interview Preparation
• Revise Scrum, SAFe Agile, and Agile scaling concepts thoroughly.
• Prepare examples of managing distributed teams and resolving dependencies.
• Review PI Planning, Sprint Planning, and Release Management processes.
• Be ready to discuss Agile metrics, team coaching, and stakeholder communication.
• Prepare real-world examples of overcoming delivery challenges.
🚀 Professional Tips
• Strengthen your SAFe Agile and Agile coaching expertise.
• Stay updated with Medical Device regulatory and compliance trends.
• Improve facilitation and conflict-resolution skills.
• Focus on servant leadership and continuous improvement practices.
• Demonstrate measurable Agile transformation success in interviews.
📝 Job Description
🚀 Hiring | Scrum Master (Medical Device Domain) | Rudhra Info Solutions
Are you an experienced Scrum Master with expertise in the Medical Device domain? 🏥 Rudhra Info Solutions is looking for a seasoned Agile professional to lead cross-functional teams, drive Agile excellence, and manage large-scale product delivery. If you have hands-on experience with SAFe Agile, Scrum, PI Planning, JIRA, and stakeholder management, this is a great opportunity to work on impactful healthcare technology projects.
Position Details ━━━━━━━━━━━━━━━━━━
📌 Position: Scrum Master (Medical Device Domain)
📍 Location: Hyderabad, Telangana
🏢 Work Mode: On-site (Work mode not specified in the original post)
💼 Experience: 9–12 Years
🎓 Qualification: B.E. / B.Tech / MCA (Mandatory)
📋 Employment Type: Full-Time
⚡ Joining Preference: Immediate to Short Notice Preferred
Preferred Skills ━━━━━━━━━━━━━━━━━━
✔ Agile Coaching & Mentoring
✔ Cross-Functional Team Leadership
✔ Risk & Issue Management
✔ Continuous Process Improvement
✔ Healthcare / Life Sciences Domain Exposure
✔ Excellent Communication & Facilitation Skills
Candidate Requirements ━━━━━━━━━━━━━━━━━━
• 9–12 years of overall professional experience.
• Proven experience as a Scrum Master.
• Strong experience in the Medical Device domain (Mandatory).
• Hands-on expertise with SAFe Agile and Scrum frameworks.
• Experience using JIRA and Atlassian tools.
• Strong knowledge of Product Management and Release Management.
• Experience managing stakeholders and cross-team dependencies.
• Prior experience collaborating with US-based distributed teams.
• Mandatory qualification: B.E., B.Tech, or MCA.
• Excellent communication, leadership, and facilitation skills.
Why Join Rudhra Info Solutions? ━━━━━━━━━━━━━━━━━━
⭐ Join an organization with over 13 years of IT industry expertise.
⭐ Work on cutting-edge healthcare and life sciences technology projects.
⭐ Collaborate with certified professionals across multiple technology domains.
⭐ Be part of a customer-centric organization focused on innovation.
⭐ Exposure to enterprise-scale Agile transformation initiatives.
⭐ Work with globally distributed teams and international clients.
⭐ Continuous learning, professional growth, and career advancement opportunities.
⭐ Contribute to impactful digital transformation projects across industries.
How to Apply ━━━━━━━━━━━━━━━━━━
📩 Interested candidates can apply here:
🌐 benazir.j@rudhrainfosolutions.com
💡 Know someone who would be a great fit? Tag them or share this opportunity with your network!
🎯 Key Responsibilities
- ✓ Facilitate Scrum ceremonies including Sprint Planning, Daily Stand-ups, Sprint Reviews, and Retrospectives.
- ✓ Drive Agile delivery following Scrum and SAFe Agile best practices.
- ✓ Coordinate PI Planning activities and release planning across multiple teams.
- ✓ Collaborate with Product Owners and stakeholders to prioritize work effectively.
- ✓ Identify, manage, and resolve project risks, blockers, and dependencies.
- ✓ Ensure successful execution of Agile projects within defined timelines.
- ✓ Monitor team performance and promote continuous improvement initiatives.
- ✓ Support product and release management activities throughout the development lifecycle.
- ✓ Work closely with globally distributed teams, including US-based stakeholders.
- ✓ Foster a collaborative, transparent, and high-performing Agile culture.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Scrum Master (Medical Device Domain) role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
Q1. Where is the job located?
➡ Hyderabad, Telangana.
Q2. What experience is required?
➡ 9–12 years of relevant professional experience.
Q3. Is Medical Device domain experience mandatory?
➡ Yes, prior Medical Device domain experience is mandatory.
Q4. Which Agile framework is required?
➡ Strong hands-on experience with Scrum and SAFe Agile.
Q5. Is experience with global teams required?
➡ Yes, experience working with US-based distributed teams is required.
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