If you’re a life sciences graduate or experienced professional looking for your next career leap, MakroCare has just opened exciting opportunities in Hyderabad! With five diverse roles across research, writing, and regulatory domains, this is your chance to join a global leader in pharmaceutical and medical device development.
🔬 About MakroCare
MakroCare, part of the MakroGroup, is a globally recognized name in Strategic Development and Commercialization for the pharmaceutical, biotech, and medical device industries. The company is ISO certified in multiple categories:
- ISO 9001 (Quality Management)
- ISO 27001 (Information Security)
- ISO 20000 (IT Service Management)
- ISO 14155 (Clinical Investigation of Medical Devices)
MakroCare focuses on a broad range of services, including:
- Regulatory & Risk Planning
- Clinical Research & Medical Support
- Drug & Medical Device Development
- Emerging Market Expansion
Their work culture promotes innovation, work-life balance, and global exposure in a high-compliance environment.
🚀 5 Exciting Open Roles in Hyderabad
Here are the current job openings at MakroCare and what they involve:
1. Literature Search Analyst
- Experience: 2–6 Years
- Qualification: UG/PG in Life Sciences (Pharmacy preferred)
- Key Responsibilities:
- Conduct systematic and targeted literature searches
- Prepare Clinical Evaluation Reports (CERs)
- Extract, analyze, and summarize data for medical and regulatory use
- Ensure accuracy, completeness, and regulatory compliance
2. Medical Writer (CER)
- Experience: 4–6 Years
- Qualification: Bachelor’s/Master’s in Life Sciences
- Key Responsibilities:
- Write and review clinical and regulatory documents (e.g., CERs, protocols)
- Conduct systematic literature reviews for medical devices
- Prepare Clinical Overview and Non-Clinical Overview reports
- Follow ICH and other international writing guidelines
3. Research Analyst – I (Regulatory Bodies – Secondary Research)
- Experience: 1–3 Years
- Qualification: BSc/MSc in Life Sciences
- Key Responsibilities:
- Conduct detailed secondary research on regulatory authorities
- Study drug development pathways and approval timelines
- Track and analyze clinical trial data and regulatory frameworks
4. Clinical Quality Assurance (CQA) – Associate
- Experience: 2–3 Years
- Qualification: BSc/MSc in Life Sciences
- Key Responsibilities:
- Review SOPs and QMS documentation for ISO, ICH-GCP standards
- Conduct internal audits and staff training
- Prepare quality reports and trend analysis dashboards
5. Associate – Regulatory Affairs (Publishing)
- Experience: 1–3 Years
- Qualification: BSc in Life Sciences
- Key Responsibilities:
- Prepare and publish eCTD/aCTD submissions for global markets (US/EU/UK/ROW)
- Manage end-to-end regulatory documentation lifecycle
- Handle agency communications and compliance reporting
✅ Why Choose MakroCare?
- 🌐 Global Exposure: Work with international teams and regulatory bodies
- 💼 ISO-Certified Work Environment: Assured quality and standards
- 🎓 Learning Opportunities: Career growth and upskilling supported
- 🏠 Hyderabad-Based Roles: Centralized location for pharma talent
- ⏳ Work-Life Balance: Policies that support your professional and personal goals
🏢 Career Path and Growth Potential
MakroCare encourages long-term development and frequently promotes from within. Whether you’re starting as a regulatory associate or an analyst, you’ll have access to cross-functional training and internal job mobility across global offices.
🏆 Ideal Candidates
- Graduates from Pharmacy, Biotechnology, or Life Sciences
- Analytical thinkers and team players
- Strong command over regulatory writing, literature review, and compliance norms
- Familiarity with ICH-GCP, ISO guidelines, and global submission standards
📅 Application Timeline
As these are verified roles posted on April 29, 2025, interested candidates are encouraged to apply immediately to avoid missing out.
💼 Final Thoughts
MakroCare’s hiring drive is a golden opportunity for professionals who want to be part of meaningful global projects. The company’s commitment to compliance, innovation, and employee development makes it one of the most desirable places to work in the life sciences space.
Don’t wait—Hyderabad’s next big clinical career step could be just a click away.
Note: This blog is for informational purposes only. Always verify job details directly with the employer.
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