Apply for QARA Associate pharma jobs for freshers in Pune. Check eligibility, salary, regulatory affairs role details and apply online.
Introduction
Starting a career in regulatory affairs and quality assurance can open doors to long-term growth in the pharmaceutical and medical device sectors. The QARA Associate job at SmartQR Technologies Pvt Ltd offers a valuable entry-level opportunity for freshers and early-career professionals. This role is designed for candidates who want to build expertise in compliance standards, documentation, and regulatory processes within a structured industry environment.
Job Overview
| Details | Information |
|---|---|
| Job Title | QARA Associate |
| Company Name | SmartQR Technologies Pvt Ltd |
| Location | Pune, Maharashtra, India |
| Employment Type | Full-Time |
| Department | Quality Assurance & Regulatory Affairs |
| Experience Required | 0–1 Year |
| Education | Pharmacy, Life Sciences, Biomedical Engineering |
| Salary | ₹2.5 – ₹4 LPA (Approx.) |
Company Overview
SmartQR Technologies Pvt Ltd operates in the medical device and healthcare technology space, focusing on compliance-driven solutions and innovation. The company works within highly regulated frameworks, ensuring adherence to national and international standards such as ISO and CDSCO guidelines. It provides a professional environment where freshers can gain hands-on experience in regulatory systems and quality management practices.
Job Location & Employment Type
The role is based in Pune, Maharashtra, one of India’s growing hubs for pharmaceutical and medical device industries. This is a full-time on-site opportunity, offering direct exposure to quality systems and regulatory operations.
Open Positions / Department Details
The opening is within the Quality Assurance and Regulatory Affairs (QARA) department. This team is responsible for ensuring that products meet regulatory standards and maintain compliance throughout their lifecycle.
Key Roles & Responsibilities
As a QARA Associate, your day-to-day responsibilities will include:
- Assisting in implementation and maintenance of Quality Management Systems (QMS) as per ISO 13485:2016
- Managing controlled documents and ensuring proper traceability
- Supporting regulatory submissions and compliance activities with CDSCO
- Participating in risk management processes aligned with ISO 14971
- Assisting in preparation of Design History File (DHF) and Verification & Validation (V&V) documents
- Supporting internal and external audits and CAPA processes
- Contributing to compliance with IEC 62304 software lifecycle standards
- Coordinating with internal teams for documentation and regulatory updates
Eligibility Criteria
Education
- Bachelor’s degree in Pharmacy, Life Sciences, Biomedical Engineering, or related field
Experience
- 0 to 1 year of experience (Freshers can apply)
Skills Required
- Basic understanding of Quality Assurance and Regulatory Affairs
- Knowledge of ISO 13485, CDSCO regulations, and CAPA systems
- Strong documentation and organizational skills
- High attention to detail and compliance mindset
- Good communication and coordination abilities
- Analytical thinking and problem-solving skills
Salary & Benefits
- Salary: ₹2.5 LPA – ₹4 LPA (based on industry standards)
- Opportunity to work in a regulated medical device environment
- Hands-on experience with ISO standards and CDSCO guidelines
- Exposure to audits, CAPA systems, and compliance processes
- Strong career growth potential in regulatory affairs and QA
Selection Process
The hiring process typically includes:
- Resume screening
- Initial HR interaction
- Technical or functional interview
- Final selection
How to Apply
Candidates interested in this opportunity can apply via email application.
Apply by sending your resume to:
📧 hr@smartqr.co.in
Make sure your resume highlights your knowledge of QA, regulatory affairs, and compliance standards.
Important Dates
- Application Deadline: Not specified (Apply early for better chances)
Why Apply for This Job?
The QARA Associate job at SmartQR Technologies Pvt Ltd is a strong starting point for candidates aiming to build a career in regulatory affairs and quality assurance. Here’s why this role is worth considering:
- Entry-level opportunity in the fast-growing medical device sector
- Hands-on exposure to ISO standards and regulatory frameworks
- Practical experience in audits, documentation, and CAPA systems
- High demand career path with long-term growth potential
- Opportunity to develop expertise in compliance and quality systems
This role is especially beneficial for candidates targeting careers in regulatory affairs, quality management, or compliance within pharma and medical devices.
FAQs
1. Who can apply for the QARA Associate role?
Candidates with a degree in Pharmacy, Life Sciences, Biomedical Engineering, or related fields can apply.
2. Is this job suitable for freshers?
Yes, this is an entry-level role open to freshers and candidates with up to 1 year of experience.
3. What is the salary for this role?
The estimated salary ranges between ₹2.5 LPA and ₹4 LPA depending on skills and qualifications.
4. What skills are required for QARA roles?
Knowledge of ISO standards, CDSCO regulations, documentation skills, and attention to detail are essential.
5. How can I apply for this job?
You can apply by sending your updated resume to the provided email ID.
Conclusion
The QARA Associate position at SmartQR Technologies Pvt Ltd offers a valuable opportunity for freshers to enter the regulatory affairs and quality assurance domain. With hands-on experience, exposure to global standards, and strong career growth potential, this role is ideal for candidates looking to build a future in compliance-driven industries. Apply as soon as possible to take advantage of this opportunity.
Disclaimer
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