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Regulatory Consultant (Eu Mkt, Module 3)

Syneos Health
Syneos Health
4-5 years
Not Disclosed
India
10 Feb. 12, 2026
Job Description
Job Type: Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Regulatory Consultant (EU Market, Module 3 – CMC)
Location: India (Remote)
Job ID: 25105260
Company: Syneos Health
Industry: Regulatory Affairs / Pharmaceutical / Clinical Research
Employment Type: Full-Time
Experience Required: 4–5 Years (Regulatory Affairs – EU Market, CMC Module 3)
Updated: February 3, 2026

Job Overview
Syneos Health is hiring an experienced Regulatory Consultant specializing in EU market submissions and CMC Module 3 documentation. This remote role involves managing regulatory activities across product lifecycle management, post-approval variations, and global regulatory submissions. The ideal candidate will have strong expertise in regulatory affairs, Chemistry, Manufacturing, and Controls (CMC), and European regulatory frameworks.

Syneos Health is a globally recognized biopharmaceutical solutions organization that integrates clinical, medical affairs, and commercial expertise to accelerate therapy development and deliver improved patient outcomes worldwide.

Key Responsibilities

  • Author and manage CMC Module 3 documentation and regulatory submissions

  • Prepare and review CMC sections for post-approval variations and lifecycle management activities

  • Conduct gap analysis of existing product data against global and regional regulatory requirements

  • Prepare and support administrative and technical components of regulatory submissions including IND, product registrations, and pre-approval documentation

  • Develop briefing packages for regulatory agency meetings and scientific advice interactions

  • Manage day-to-day regulatory project activities within defined timelines, scope, and budget

  • Provide regulatory support throughout product development lifecycle in cross-functional teams

  • Act as subject matter expert and support troubleshooting and resolution of regulatory issues

  • Prepare cost estimates for regulatory services and contribute to proposal development

  • Support client meetings, project updates, and business development initiatives

  • Ensure compliance with global regulatory requirements and company policies

  • Participate in project audits and regulatory inspections as required

  • Develop training materials and share regulatory best practices internally and externally

  • Contribute to standard operating procedures (SOPs) and process improvement initiatives

  • Provide guidance and oversight to team members on project execution

  • Maintain individual training records and complete required compliance training

Eligibility Criteria and Qualifications

  • M.Pharm degree required; BS, PhD, or equivalent qualification in a science-related field preferred

  • Minimum 4–5 years of experience in regulatory affairs within pharmaceutical or medical device industry

  • Proven experience in CMC Module 3 authoring and lifecycle management activities

  • Experience in EU and GCC regulatory markets

  • Experience in regulatory submissions such as IND, NDA, MAA, PMA, CTD, and electronic submissions

  • Strong understanding of global regulatory frameworks and submission requirements

  • Excellent written and verbal communication skills in English

  • Strong analytical and problem-solving abilities with attention to detail

  • Ability to manage multiple projects simultaneously with varying requirements

  • Strong interpersonal and stakeholder management skills

  • Advanced proficiency in Microsoft Office applications

  • Knowledge of quality management systems and regulatory compliance standards

  • Ability to work independently and within cross-functional teams

Skills and Competencies

  • Expertise in Chemistry, Manufacturing, and Controls (CMC) documentation

  • Knowledge of product lifecycle management and post-approval regulatory processes

  • Strong project management and organizational skills

  • Customer-focused approach with strong service orientation

  • Adaptability, initiative, and proactive decision-making capabilities

About Syneos Health
Syneos Health is a leading fully integrated biopharmaceutical solutions organization with more than 29,000 employees across 110 countries. The company combines clinical development, medical affairs, and commercial capabilities to help customers accelerate therapy delivery and address modern healthcare challenges. Over the past five years, Syneos Health has supported 94 percent of novel FDA-approved drugs and 95 percent of EMA-authorized products, contributing to more than 200 studies across 73,000 sites and over 675,000 clinical trial patients globally.

The organization promotes professional development, diversity, and a collaborative work culture focused on innovation and employee growth.