Pharma Job at Opella | Apply for Trainee Junior Specialist Position
Opella is hiring a Trainee Junior Specialist – Electronic Documentation in Hyderabad. This role offers an exciting opportunity to work with clinical and regulatory documents in the electronic Document Management System (eDMS). A Pharma Job at Opella means you’ll contribute to submission-ready documentation, collaborate with medical and regulatory teams, and gain hands-on experience in document management in the pharmaceutical and self-care space. Ideal candidates will have a background in Life Sciences, Pharmacy, or M Pharma with a keen interest in electronic documentation and regulatory submissions.
Job Details:
- Job Position: Trainee Junior Specialist – Electronic Documentation Specialist
- Location: Hyderabad, India
About the Company:
Opella is a global leader in self-care, offering the third-largest portfolio in OTC & VMS markets. Headquartered in France, Opella owns over 100 consumer-loved brands, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale, and Mucosolvan. With 11,000 employees, 13 world-class manufacturing sites, and four specialized science and innovation centers, Opella is committed to making self-care simple, effective, and accessible. As a certified B Corp, Opella is dedicated to promoting healthier people and a more sustainable planet. Pharma Job at Opella is more than a job; it’s part of this vision.
Job Description:
The Trainee Junior Specialist – eDS ensures submission-readiness and proper formatting of clinical and regulatory documents in the electronic Document Management System (eDMS). This includes documents such as CTD, PSMF, and clinical dossiers. A Pharma Job at Opella means you will assist with document compilation, publishing, and navigation for submission to Health Authorities, while collaborating with internal teams for accurate and timely delivery.
This role is suitable for M Pharma graduates or other life sciences postgraduates looking to start a career in document management and regulatory affairs
Key Responsibilities:
- Format and organize clinical and regulatory documents using tools like Microsoft Word and Adobe Acrobat.
- Collaborate with medical writers, regulatory teams, and project managers to ensure documents are complete and accurate.
- Assist in compiling submission packages, ensuring they meet all regulatory and internal standards.
- Learn and grow by getting trained on Opella systems, gradually taking on more responsibilities in document management and project coordination.
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Support smooth communication and coordination with external vendors when required.
Educational Qualification:
Graduate or Postgraduate in Pharmacy. This is a basic qualification for a Pharma Job at Opella.
Experience and Skills
- Basic knowledge of Microsoft Word and Adobe Acrobat.
- Strong communication and teamwork skills.
- Willingness to learn new tools, systems, and processes.
- Fluency in English (spoken and written).
