Manager Reg Consulting (CP/DCP/MRP - Submissions- EU market)

Syneos Health, Inc.; Pune District; On-site; INR 10,00,000 - 15,00,000; Full time

Job summary

A leading biopharmaceutical solutions organization is seeking a Manager Reg Consulting in Pune, India. This role requires expertise in regulatory strategy and end-to-end lifecycle management for global products. Candidates should possess strong communication skills and experience in submissions for the EU market. The position involves managing multiple projects, mentoring junior staff, and driving process efficiency initiatives. A collaborative approach and client-focused mindset are essential for success in this dynamic environment.

Benefits

Career development opportunities

Engaged line management

Qualifications

• Experience with regulatory submission processes and lifecycle management.
• Strong expertise in EU procedures for submissions.
• Ability to manage multiple global projects and drive successful outcomes.

Responsibilities

• Lead regulatory strategy across a portfolio of global products.
• Manage end-to-end regulatory lifecycle, including MAAs and renewals.
• Serve as primary liaison with clients and regulatory authorities.
• Oversee project teams and mentor junior staff.
• Drive quality improvement and process efficiency for client projects.
• Provide technical solutions to regulatory challenges.

Skills

Regulatory strategy

EU market knowledge

Project management

Excellent communication skills

Team leadership

Tools

Regulatory Information Management Systems (RIMS)

Veeva Vault

Electronic document management platforms

Job description

Manager Reg Consulting (CP/DCP/MRP - Submissions- EU market)

Updated: December 3, 2025
Location: Pune, MH, India
Job ID:25103788

Description

Manager Reg Consulting (CP/DCP/MRP - Submissions- EU market)

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

Job Responsibilities

• Portfolio Management - Lead regulatory strategy independently across a portfolio of global products.
• Manages end-to-end regulatory lifecycle: MAAs, renewals, variations, HAQs, annual reports, xEVMPD, GMP clearances, safety updates/PSUR/PSUSA/RMP
• Strong expertise in EU markets for procedural (CP/DCP/MRP/National) submissions, Worksharing, Supergrouping and global regulatory requirements.
• Acts as primary liaison with clients, regulatory authorities, and cross-functional teams.
• Leads and reports on client/regulatory agency meetings, providing strategic and operational regulatory guidance to client and internal team.
• Oversees project teams, mentor junior staff, and monitor utilization/performance.
• Drives quality improvement and process efficiency initiatives for client projects.
• Provides technical solutions to complex regulatory challenges and act as subject matter expert (SME)
• Proficient in Regulatory Information Management Systems (RIMS), Veeva Vault, and electronic document management platforms.
• Ensures accurate document management, version control, and tracking systems to maintain compliance and audit readiness.
• Delivers internal training and knowledge sharing across RA and other departments.
• Supports business development through proposals, builds regulatory systems and infrastructure to support GRAS initiatives.
• Represents the company at seminars, conferences, industry associations, authors articles for trade journals etc.
• Excellent written/verbal communication skills
• Flexible in managing multiple global projects, adapting to evolving regulations, and driving successful outcomes
• Ability to lead diverse teams, build strong client/regulator relationships, and influence cross‑functional stakeholders.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.