Global biosimilars leader Alvotech is inviting applications for the position of Regulatory Labeling Business Operational Associate. This partially remote opportunity is ideal for professionals with experience in regulatory affairs, labeling operations, documentation management, quality control, and Veeva Vault Regulatory Information Management (RIM) systems.
Candidates with at least two years of experience in regulatory labeling, proofreading, document review, and regulatory operations can apply for this exciting biotechnology industry role.
About Alvotech
Alvotech is a global biotechnology company focused on expanding access to affordable, high-quality biologic medicines worldwide. The company develops and manufactures biosimilars and operates across multiple international markets, supporting innovation in science, quality, manufacturing, and regulatory compliance.
Job Details
| Particulars | Details |
|---|---|
| Position | Regulatory Labeling Business Operational Associate |
| Company | Alvotech |
| Location | India (Home Office) |
| Work Mode | Partially Remote |
| Employment Type | Full-Time |
| Experience Required | Minimum 2 Years |
| Department | Regulatory Labeling |
| Application Deadline | 11 June 2026 |
Key Responsibilities
The selected candidate will support regulatory labeling implementation and lifecycle management activities across global regulatory projects.
Major Duties Include:
- Perform proofreading and quality control checks for labeling text and artwork.
- Support labeling development and lifecycle management activities.
- Generate labeling comparison reports using Microsoft Word and related tools.
- Review and verify regulatory labeling documents using text verification software.
- Provide proofreading verdicts within Veeva Vault RIM systems.
- Maintain labeling documentation and controlled records.
- Support tracker maintenance and operational reporting activities.
- Assist in data migration and documentation projects.
- Escalate regulatory or operational concerns appropriately.
- Follow SOPs, company policies, and regulatory procedures.
- Complete departmental training and compliance requirements.
- Contribute to a collaborative and innovative regulatory affairs environment.
Eligibility Criteria
Applicants should meet the following requirements:
Educational Qualification
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Regulatory Affairs, or a related field.
Experience
- Minimum 2 years of experience in:
- Regulatory Affairs
- Labeling Operations
- Documentation Management
- Quality Assurance Documentation
- Regulatory Compliance Operations
Technical Skills
Candidates should possess experience with:
- Regulatory labeling software
- Text comparison tools
- Proofreading applications
- Microsoft Word and Excel
- Veeva Vault Regulatory Information Management (RIM)
- Global Vision, Verify, or similar verification software
Preferred Skills
- Change control management experience
- Strong attention to detail
- Excellent documentation practices
- Project coordination skills
- Ability to manage multiple priorities
- Strong communication skills in English
Why Join Alvotech?
Working at Alvotech offers professionals an opportunity to contribute to the global biosimilars industry while building expertise in regulatory affairs and labeling compliance.
Benefits
- Remote work flexibility
- Global biotechnology exposure
- Career growth in regulatory affairs
- Experience with advanced regulatory technologies
- International project collaboration
- Learning and development opportunities
- Inclusive and innovation-driven work culture
Important Keywords for Job Seekers
- Regulatory Labeling Associate Jobs
- Regulatory Affairs Jobs in India
- Veeva Vault RIM Jobs
- Remote Regulatory Affairs Jobs
- Regulatory Documentation Jobs
- Labeling Compliance Jobs
- Biotechnology Regulatory Jobs
- Regulatory Operations Associate Jobs
- Global Vision Proofreading Jobs
- Pharma Regulatory Affairs Careers
How to Apply
