Johnson & Johnson is inviting applications for the position of Analyst II – Document Publishing under its Regulatory Affairs Group. This is an excellent opportunity for professionals with experience in Regulatory Document Publishing, eCTD publishing, Veeva, Adobe Acrobat, Microsoft Word templates, and document management systems.

The role is available in Hyderabad, Bangalore, and Mumbai with a Hybrid Work model. Professionals experienced in preparing regulatory submission-ready documents, electronic publishing, quality control, and document lifecycle management are encouraged to apply.

If you have 4–6+ years of pharmaceutical document publishing experience, this opportunity allows you to contribute to global regulatory submissions within one of the world’s leading healthcare companies.

Job Details

Key Responsibilities

The selected candidate will:

• Create submission-ready regulatory documents.
• Perform document formatting, hyperlinking, and bookmarking.
• Prepare complex regulatory publishing documents using industry-standard publishing software.
• Manage electronic document repositories, indexing, storage, and archiving.
• Perform technical Quality Control (QC) of Word, PDF, and other submission files.
• Support electronic submission publishing activities.
• Assist document authors in preparing submission-ready regulatory documents.
• Participate in validation and testing of publishing software.
• Follow SOPs, templates, and regulatory publishing best practices.
• Mentor junior document specialists when required.
• Resolve document processing issues independently.
• Utilize AI and digital tools to improve document publishing efficiency while complying with company policies.

Required Qualifications

Candidates should possess:

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related discipline.
• 4–6+ years of document publishing or regulatory document processing experience.
• Experience within the pharmaceutical or healthcare industry.
• Strong Microsoft Word and Adobe Acrobat skills.
• Experience with electronic document management systems.
• Knowledge of Veeva, Regulatory Information Systems, and publishing tools.
• Excellent communication and organizational skills.
• Ability to manage multiple projects simultaneously.

Preferred Skills

Johnson & Johnson is looking for professionals with expertise in:

• Regulatory Document Publishing
• eCTD Publishing
• Electronic Document Management Systems
• Veeva Vault
• Adobe Acrobat
• Microsoft Office
• Microsoft Word Templates
• Hyperlinking & Bookmarking
• Regulatory Compliance
• Quality Assurance (QA)
• Proofreading
• Project Management
• Regulatory Information Systems
• Analytical Reasoning
• Risk Assessment
• Process Improvement
• Problem Solving

Why Join Johnson & Johnson?

Employees can expect:

• Opportunity to work with a globally recognized healthcare leader.
• Hybrid work flexibility.
• Exposure to global Regulatory Affairs projects.
• Career development and mentoring opportunities.
• Collaborative international work environment.
• Competitive salary and employee benefits.
• Opportunity to work with advanced AI-enabled regulatory publishing processes.

Salary (Estimated)

Based on similar Regulatory Affairs Document Publishing positions in India, the estimated salary range is:

₹12,00,000 – ₹18,00,000 per annum (CTC)

Actual compensation may vary depending on experience, skills, and company policies.

How to Apply

Application Link