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Document Specialist

Propharma
Propharma
3+ years
Not Disclosed
10 March 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills:

Document Specialist

Company: ProPharma
Location: India
Job Type: Full-Time
Experience: Typically 3+ Years (Document Publishing / Regulatory Documentation)
Qualification: Not Specified
Salary Range: Not Specified

Job Overview

ProPharma is hiring a Document Specialist responsible for formatting, reviewing, compiling, and publishing regulatory documents for electronic submissions.

The role involves supporting end-to-end document publishing activities including preparation of Word and PDF documents, ensuring compliance with regulatory guidelines, and delivering high-quality outputs within timelines. The specialist will work closely with clients and internal teams to manage publishing workflows and maintain accuracy and consistency in regulatory submissions.

Key Responsibilities

  1. Document Formatting & Publishing

Format and review Word documents according to client and regulatory guidelines.

Convert and format documents into PDF ensuring eCTD compliance.

Prepare regulatory submissions including IND, CTA, NDA, BLA, and MAA.

  1. Document Compilation & Processing

Compile regulatory documents and ensure completeness for submission.

Manage document preparation, routing, and approval workflows.

Support electronic publishing activities across multiple projects.

  1. Quality Control & Compliance

Perform pre- and post-publishing quality checks.

Ensure adherence to regulatory standards such as ICH E3, E6(R2), M4, EU MDR, and IVDR.

Conduct peer review of documents processed by team members.

  1. Project & Timeline Management

Manage multiple publishing projects simultaneously.

Ensure timely completion of all assigned tasks.

Escalate issues impacting timelines or quality.

  1. Client & Stakeholder Interaction

Communicate directly with clients to manage expectations and deliverables.

Collaborate with internal teams during submission preparation.

Maintain alignment with client specifications and requirements.

  1. Process Improvement & Knowledge Management

Stay updated with industry practices and regulatory requirements.

Participate in process improvement initiatives and team activities.

Identify and communicate potential risks or concerns proactively.

Required Skills

Technical Skills

Advanced expertise in Microsoft Word formatting.

Strong knowledge of Adobe Acrobat and PDF tools.

Experience with eCTD publishing systems (e.g., ISI Toolbox, Core Dossier).

Regulatory Knowledge

Understanding of regulatory submission types (IND, NDA, BLA, MAA).

Knowledge of ICH guidelines and document publishing standards.

Familiarity with regulatory document workflows and compliance.

Analytical & Problem Solving

Strong attention to detail and quality.

Ability to troubleshoot document and formatting issues.

Communication & Collaboration

Fluency in English (written and verbal).

Strong interpersonal and stakeholder communication skills.

Ability to work effectively in a team environment.

Project Management

Ability to manage multiple tasks and deadlines.

Strong organizational and planning skills.

Basic Qualifications

Minimum 3 years of experience in document publishing or formatting

Experience in pharmaceutical or biotech industry preferred

Proficiency in document management and publishing tools

Preferred Competencies

Experience with regulatory submissions (IND, CTA, NDA, BLA, MAA)

Strong project management and communication skills

Ability to work independently and proactively

Key Competencies

Regulatory document publishing and formatting

eCTD submission and compliance

Quality control and document review

Project and timeline management

Client and stakeholder coordination

About the Company

ProPharma is a global consulting organization providing regulatory, clinical, quality, pharmacovigilance, and R&D technology solutions to pharmaceutical, biotechnology, and medical device companies. The company supports clients across the product lifecycle, helping accelerate development and ensure compliance with global regulatory standards