Trainee Junior Specialist Job in Hyderabad at Opella | Life Science Graduates Apply
Looking for a Trainee Junior Specialist Job in the pharmaceutical industry? Opella, a global leader in self-care and OTC products, is offering exciting Opella Jobs in Hyderabad. This entry-level role provides hands-on experience in electronic document management, regulatory submissions, and collaboration with cross-functional teams, making it ideal for Life Sciences graduates seeking to advance their careers.
Job Details
- Job Title: Trainee Junior Specialist – Electronic Documentation Specialist
- Location: Hyderabad, India
About the Company
Opella is a self-care challenger with the third-largest OTC & VMS portfolio globally. With 100 loved brands, 11,000 employees, 13 manufacturing sites, and 4 innovation centers, Opella’s mission is to bring health into people’s hands. Headquartered in France, the company proudly manufactures world-renowned brands such as Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale, and Mucosolvan. Explore more about Opella’s global impact through these Opella Jobs in Hyderabad.
Qualifications:
- Graduate or Postgraduate in Life Sciences (Biotechnology, etc.)
- Basic knowledge of Microsoft Word and Adobe Acrobat
- Good communication and teamwork skills
- Willingness to learn new tools and processes
- Fluent in English (spoken and written)
Job Description:
This Trainee Junior Specialist Job focuses on ensuring the format and submission-readiness of documents in the electronic Document Management System (eDMS), including clinical documents, CTD, and PSMF. The role involves compiling, publishing, and navigating documents required for Health Authority submissions. The eDS collaborates closely with Opella teams to ensure smooth operational delivery of high-quality papers.
Key Responsibilities:
- Format and organize clinical and regulatory documents using Microsoft Word and Adobe Acrobat.
- Collaborate with medical writers, regulatory teams, and other departments to ensure accuracy and completeness.
- Assist in compiling documents into submission packages meeting regulatory standards.
- Receive training on Opella’s systems and tools and gradually take on more responsibilities in document management and project coordination.
Who You’ll Work With:
- Medical writers
- Regulatory and clinical teams
- Project managers
- External vendors (if needed)
