Medical Writer Jobs at OrciMed Life Science Hyderabad for experienced pharmacovigilance professionals in signal management and regulatory safety writing roles.
Medical Writer Jobs at OrciMed Life Science – Apply Now
Job Role: Medical Writer – Signal Management, PSUR/PBRER, PADER & RMP
Company: OrciMed Life Sciences
Location: Hyderabad
Experience Required: Minimum 3+ Years
Qualification: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences
Job Type: Full-Time
Application Mode: Email Application
Job Status: Verified
🔷 Key Highlights
- Verified Medical Writer Job in Hyderabad
- Specialized Role in Pharmacovigilance & Safety Writing
- 3+ Years Experience Required
- Strong Exposure to Global Regulatory Submissions
- Opportunity to Work on PSUR, PBRER, PADER, and RMP
- Career Growth in a Leading Life Sciences Company
- Competitive Industry-Standard Salary
- Direct Email Application
📌 About OrciMed Life Science
OrciMed Life Science is a rapidly growing life sciences and healthcare services organization recognized for its strong focus on pharmacovigilance, regulatory compliance, drug safety, and medical writing solutions. The company supports pharmaceutical, biotechnology, and medical device organizations across global markets with high-quality documentation, regulatory safety reporting, and risk management support.
With a growing footprint in India and international markets, OrciMed Life Science has built a reputation for accuracy, compliance, scientific excellence, and client-focused service delivery. The organization is committed to fostering professional excellence, offering stable career growth, and providing exposure to high-value global safety and regulatory projects.
Joining OrciMed Life Science means working in a challenging, compliance-driven environment with experienced professionals, safety physicians, regulatory experts, and global stakeholders.
🧬 About the Role – Medical Writer (Pharmacovigilance & Safety Writing)
The Medical Writer role at OrciMed Life Science is a specialized opportunity for experienced pharmacovigilance and regulatory writing professionals. This position focuses on safety aggregate data analysis, regulatory documentation, and signal management in accordance with international drug safety regulations.
This role is ideal for medical writers who have hands-on experience with PSURs, PBRERs, PADERs, Risk Management Plans (RMPs), and signal detection activities. The selected candidate will play an essential role in ensuring regulatory compliance, patient safety, and accurate scientific communication.
This opportunity is best suited for professionals seeking stability, long-term growth, and exposure to high-impact regulatory safety projects.
📝 Detailed Job Responsibilities
As a Medical Writer at OrciMed Life Science, you will be responsible for the following core functions:
- Preparation of high-quality aggregate safety reports including PSURs, PBRERs, and PADERs
- Execution of signal detection, signal validation, signal prioritization, and signal management activities
- Authoring, reviewing, and updating Risk Management Plans (RMPs)
- Performing detailed literature review and safety data interpretation
- Working closely with safety physicians, pharmacovigilance teams, and regulatory professionals
- Supporting regulatory submissions to global health authorities
- Ensuring full compliance with EMA, FDA, ICH, and GVP guidelines
- Maintaining data accuracy, document consistency, and regulatory integrity
- Participating in quality review checks and regulatory audits
- Contributing to SOP development, writing templates, and process improvements
- Responding to regulatory queries related to safety documents
- Managing parallel projects while ensuring strict adherence to timelines
This role requires a deep understanding of pharmacovigilance operations and safety writing standards.
🎓 Educational Qualifications
Candidates must possess one of the following educational qualifications:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- Doctor of Pharmacy (Pharm.D)
- Master of Science (MSc)
- Bachelor of Science (BSc)
- Degree in Life Sciences, Biomedical Sciences, or Related Disciplines
Candidates from pharmacy, medical, biotechnology, and biomedical backgrounds are highly preferred.
✅ Experience & Skill Requirements
To be eligible for this position, candidates must meet the following skill and experience criteria:
- Minimum of 3 years of hands-on experience in medical writing, pharmacovigilance, or safety writing
- Proven expertise in PSUR, PBRER, PADER, and RMP preparation
- Strong understanding of signal management processes
- In-depth knowledge of ICH-GVP, EMA, and FDA regulations
- Ability to analyze safety data and prepare structured regulatory documents
- Excellent written and verbal communication skills
- Strong scientific interpretation skills
- High level of accuracy and attention to detail
- Ability to meet strict regulatory timelines
- Capability to work independently and in cross-functional teams
Experience working with global regulatory submissions is a major advantage.
🏙️ Job Location – Hyderabad
This is a full-time, office-based opportunity located in Hyderabad, one of India’s leading pharmaceutical and life sciences hubs. Hyderabad offers excellent career exposure in pharmacovigilance, regulatory affairs, clinical research, and drug safety operations.
Candidates seeking long-term growth in regulatory safety documentation will find Hyderabad to be a strong career destination.
📈 Career Growth & Learning Exposure
Working as a Medical Writer at OrciMed Life Science offers extensive learning and career development opportunities including:
- Exposure to global pharmacovigilance projects
- Hands-on experience with international regulatory submissions
- Skill development in advanced safety reporting
- Collaboration with experienced medical reviewers and safety physicians
- Long-term career growth in regulatory writing and drug safety
- Opportunities to move into lead and subject matter expert roles
This role is ideal for professionals aiming to build a long-lasting career in medical writing and pharmacovigilance.
💼 Why Choose OrciMed Life Science?
OrciMed Life Science offers a professional environment focused on scientific integrity, compliance, and employee development. Benefits include:
- Competitive salary aligned with industry standards
- Exposure to international regulatory markets
- Stable long-term projects
- Supportive team culture
- Continuous professional learning
- Clear growth pathway for experienced medical writers
- High-value regulatory documentation experience
This makes it a strong career option for professionals in pharmacovigilance and safety writing domains.
📊 Medical Writer Job Summary
| Category | Details |
|---|---|
| Job Title | Medical Writer |
| Specialization | Signal Management, PSUR, PBRER, PADER, RMP |
| Company | OrciMed Life Science |
| Job Location | Hyderabad |
| Experience | 3+ Years |
| Qualification | B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences |
| Job Type | Full-Time |
| Application Mode | |
| Industry | Pharmacovigilance, Drug Safety, Medical Writing |
| Job Status | Verified |
🔍 Who Should Apply for This Job?
This opportunity is highly suitable for:
- Experienced medical writers
- Pharmacovigilance professionals
- Drug safety scientists
- Regulatory documentation specialists
- Signal management experts
- Aggregate report writers
- Professionals with PSUR and RMP expertise
- Candidates seeking stable regulatory careers
If your background aligns with pharmacovigilance and safety writing, this job offers strong professional value.
⚠️ Important Instructions for Candidates
- Only candidates with relevant experience in safety writing should apply
- Freshers are not eligible for this role
- Applications without relevant experience may not be reviewed
- Only shortlisted candidates will be contacted by the company
- Ensure accurate information in your resume
📝 How to Apply (Final Section)
Eligible and interested candidates can apply for the Medical Writer position at OrciMed Life Science by following the steps below:
- Update your resume with relevant pharmacovigilance and safety writing experience
- Highlight your expertise in PSUR, PBRER, PADER, RMP, and signal management
- Mention your total years of experience clearly
- Add details of regulatory exposure (EMA, FDA, ICH, GVP)
- Email your updated resume to the official recruitment email ID
- Use the subject line exactly as instructed
📧 Application Email ID: careers@orcimedlifesciences.com
📝 Subject Line: Application for Medical Writer – OrciMed
✅ Shortlisted candidates will be contacted for further assessment and interview process.
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