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.
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
Airoli | Ambernath | Amravati | Aurangabad | Dhule | Dombivali | Jalgaon | Kolhapur | Kurkumbh | Kurla | Madhapur | Mumbai | Nagpur | Nashik | Navi Mumbai | Pune | Pune city | Shirpur | Tandalja | Tarapur | Thane | Vikhroli | Yerawada |Haryana :
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Baddi | Solan |Rajasthan :
Banasthali | Bhiwadi | Jaipur | Pilani | Udaipur |Karnataka :
Bangalore | Belgaum | Bengaluru | B.G Nagara | Bommasandra | Colorado | Czech Republic | Karnataka | Mangaluru | Mysore | Udupi |Punjab :
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Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Kyiv |Lima Region :
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