Regulatory Affairs Labeling

Parexel; India; Remote; INR 1,200,000 - 2,200,000; Full time

Job summary

Parexel is hiring a Regulatory Labeling Specialist to join our team in a remote capacity. The role focuses on maintaining accurate, compliant product labeling throughout the lifecycle, supporting regulatory impact assessments, and Health Authority submissions.

You will collaborate with cross-functional teams to drive post-approval activities and CCDS updates. You will work with TrackWise and Veeva RIMS, coordinating with stakeholders to ensure timely submissions while upholding quality and

Qualifications

• Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or related field.
• 6+ years of experience in regulatory affairs or regulatory labeling.
• Knowledge of regulatory requirements for medicinal product labeling and Health Authority submissions.
• Fluent English; strong communication and planning skills.

Responsibilities

• Perform regulatory impact assessments for change controls and labeling updates.
• Manage CCDS creation and updates, ensuring accuracy and compliance.
• Prepare and submit variations, notifications, and renewals to Health Authorities.
• Respond to Health Authority questions on submissions.
• Coordinate labeling updates, including translations, with cross-functional teams.
• Manage post-approval activities in Veeva RIMS and track artwork updates.

Skills

Regulatory labeling knowledge

Project coordination

Planning & organization

Clear communication

Education

Bachelor's degree in Life Sciences/Pharmacy/Chemistry

Tools

Veeva RIMS

TrackWise

Job description

About Parexel

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart.

About the Role

We are seeking a Regulatory Labeling Specialist to join our team in a remote capacity. As a Regulatory Labeling Specialist, you will ensure that medicinal product information remains accurate, compliant, and current throughout its lifecycle. Accurate labeling helps patients and healthcare professionals get the information they need about medicines. This position plays a key role in regulatory impact assessment, product information management, Health Authority submissions, and post-approval compliance. You will collaborate with cross-functional teams and client stakeholders, follow industry-standard processes, and contribute to regulatory and labeling operations from planning through post-approval activities.

Responsibilities include assessing the regulatory impact of change controls, managing product information and labeling updates, preparing Health Authority submissions, and driving post-approval activities in Veeva RIMS, with opportunities to deepen your expertise and influence regulatory outcomes.

You will join a fast-paced, growth-oriented environment focused on making a meaningful impact through regulatory impact assessment, product information management, and Health Authority submissions. With diverse teams and continuous learning opportunities, the Regulatory Labeling Specialist can explore career paths and expand skills across regulatory affairs.

Key Responsibilities

• Perform regulatory impact assessments for change controls raised in TrackWise for medicinal products registered via the Centralized Procedure (CP), Mutual Recognition Procedure (MRP), Decentralized Procedure (DCP), or National Procedure (NP)
• Manage product information updates, including creation and updates of the Company Core Data Sheet (CCDS), applying clinical expertise
• Prepare and submit variations, notifications, and renewals to Health Authorities
• Respond to Health Authority questions on submissions
• Coordinate labeling updates, including translations, with team members and client stakeholders
• Manage all required post-approval activities in Veeva Regulatory Information Management System (RIMS), including artwork updates

You'll thrive in this role if you bring:

• Strong coordination skills and the ability to work effectively with team members and client stakeholders
• Strong planning skills, including planning variation submissions so they are completed on time and to the required quality to meet KPIs
• Clear communication skills and a collaborative, team-oriented approach
• Experience working in clinical research, healthcare, or a regulated environment
• A patient-focused mindset and strong attention to detail
• Comfort working with Veeva RIMS and TrackWise

Required Qualifications

• Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or related field, or equivalent professional experience

• 6 +years of experience in regulatory affairs or regulatory labeling
• Knowledge of regulatory requirements and Health Authority submission processes for medicinal product labeling
• Clinical expertise to support product information and CCDS updates
• Knowledge of Veeva RIMS
• Fluent in English
• Strong communication, organization, and planning skills

Preferred Qualifications

• Experience with xEVMPD

We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.

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