Medical Writer Job at Opella | Healthcare Job in Hyderabad
Looking for a rewarding medical writer job with a leading global self-care company? Opella invites experienced professionals to join as a Senior Medical Regulatory Writer in Hyderabad, contributing to innovative healthcare solutions for millions worldwide. This is an exciting healthcare job opportunity for those passionate about medical communication, regulatory writing, and improving access to self-care.
- Job Position: Senior Medical Regulatory Writer
- Company: Opella (Self-Care Division)
- Location: Hyderabad, India
About the Company
Opella is a global self-care leader with one of the world’s largest portfolios in Over-The-Counter (OTC) and Vitamins, Minerals & Supplements (VMS) healthcare products. Headquartered in France, Opella’s mission is to make self-care simple and accessible to more than half a billion consumers worldwide. With over 11,000 employees, 13 manufacturing sites, and 4 innovation centers, Opella produces some of the most trusted names in healthcare, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale, and Mucosolvan. As a B Corp Certified organization, Opella is committed to improving global health and sustainability.
Medical Writer Job – Qualifications
- Degree in healthcare in a related scientific discipline preferred.
- Minimum 3–4 years of experience in the pharmaceutical or consumer healthcare industry.
- Proven expertise in technical and regulatory writing for healthcare authority submissions.
- Experience in a global or regional role is advantageous.
- Strong attention to detail, time management, and understanding of medical regulatory requirements.
Job Description
The Senior Medical Regulatory Writer at Opella will play a crucial role in creating, reviewing, and delivering regulatory and clinical documentation that supports product safety, efficacy, and compliance. This medical writer job is ideal for professionals who thrive in a global, science-driven environment and are eager to contribute to impactful healthcare innovation.
Medical Writer Job – Key Responsibilities
- Write, edit, and deliver high-quality regulatory and clinical documents such as CSRs, COs, SCEs, SCSs, SCPs, SBPs, PBRERs, RMPs, ACOs, and Clinical Evaluation Reports.
- Ensure content accuracy, compliance with regulatory standards, and timely delivery.
- Mentor junior writers and provide peer review support.
- Collaborate with cross-functional teams including regulatory, pharmacovigilance, and corporate affairs departments.
- Manage documentation for clinical trials, ensuring transparency and compliance with public disclosure regulations.
- Maintain therapeutic area knowledge and contribute to global submission strategies.
