Are you an experienced Safety Medical Writer looking for the next big step in your career? Apcer Lifesciences, a global leader in pharmacovigilance and regulatory services, is hiring for the role of Safety Medical Writer – Risk Management Plan (RMP) at its Noida and Ahmedabad offices. This is a fantastic opportunity for professionals with 3+ years of relevant experience in safety writing, regulatory documents, and pharmacovigilance to join a growing and dynamic team.
If you’re passionate about patient safety, regulatory compliance, and scientific writing, this role could be the perfect fit for you.
Key Responsibilities
As a Safety Medical Writer – RMP at Apcer Lifesciences, your role will involve:
- Preparing, reviewing, and updating Risk Management Plans (RMPs) in compliance with EMA/FDA guidelines.
- Writing and editing high-quality safety and regulatory documents.
- Collaborating with cross-functional teams including pharmacovigilance, regulatory affairs, and clinical research.
- Ensuring accuracy, consistency, and compliance with company standards and global regulations.
- Monitoring changes in regulatory requirements and updating documents accordingly.
Qualifications & Requirements
- Minimum 3 years of relevant experience in medical writing (safety & regulatory focus).
- Strong knowledge of pharmacovigilance regulations and RMP requirements.
- Excellent written and verbal communication skills.
- Advanced degree in Pharmacy, Life Sciences, Medicine, or related field preferred.
- Ability to manage timelines and deliver high-quality work under pressure.
Benefits of Working at Apcer Lifesciences
- Competitive salary package with growth opportunities.
- Exposure to global regulatory practices.
- Collaborative and innovative work environment.
- Learning and development programs for career advancement.
- Employee-centric culture with work-life balance.
How to Apply
Interested candidates can send their updated profiles to tanya.saini@apcerls.com.
