Parexel Hiring for Regulatory Affairs Jobs walk-in drive in Bengaluru for experienced professionals across biologics, CMC, and labeling domains.
Parexel Regulatory Affairs Walk-In Drive 2025 – Bengaluru | Biologics, CMC & Labeling Hiring
Parexel, one of the most respected global clinical research organizations, has officially announced a major Walk-In Drive for Regulatory Affairs professionals in Bengaluru. This hiring initiative targets experienced candidates across Biologics, Small Molecules, CMC, Lifecycle Management, and Regulatory Labeling. The walk-in interview is scheduled for 20 December 2025 and is an excellent opportunity for professionals seeking career growth with a world-class CRO. Parexel Hiring for Regulatory Affairs Jobs
With a reputation built on scientific excellence, regulatory expertise, and ethical clinical research practices, Parexel continues to expand its regulatory operations in India. This walk-in drive is a strategic recruitment effort aimed at strengthening its regulatory affairs team in Bengaluru.
This opportunity is open for candidates holding degrees such as B.Pharm, M.Pharm, MSc, BSc, Life Sciences, or related qualifications, with 2 to 10 years of relevant experience. Parexel Hiring for Regulatory Affairs Jobs
Key Highlight Box
- Hiring Organization: Parexel
- Job Location: Bengaluru
- Event Type: Walk-In Interview
- Walk-In Date: 20 December 2025
- Reporting Time: 10 AM onwards
- Experience Required: 2 to 10 Years
- Education: B.Pharm, M.Pharm, MSc, BSc, Life Sciences
- Departments Hiring:
- Regulatory Affairs – Biologics & Small Molecules
- Regulatory CMC
- Lifecycle Management
- Regulatory Labeling
- Hiring Type: Permanent Roles
- Industry: Clinical Research Organization (CRO)
- Application Mode: Direct Walk-In
- Job Verification: Verified Job
About Parexel
Parexel is a globally recognized Contract Research Organization providing end-to-end clinical development, regulatory consulting, and commercialization services. Headquartered in the United States and operating in over 50 countries, Parexel partners with leading pharmaceutical, biotechnology, and medical device companies worldwide. Parexel Hiring for Regulatory Affairs Jobs
The organization plays a critical role in accelerating new drug development and ensuring regulatory compliance across major global markets such as the United States, Europe, Asia-Pacific, and emerging regions. Known for its strong ethical standards, innovation-driven culture, and scientific excellence, Parexel continues to be one of the most desirable employers in the regulatory and clinical research sectors.
Why This Walk-In Drive Is a Major Opportunity
Regulatory Affairs professionals with expertise in global CMC strategy, biologics submissions, vaccines, monoclonal antibodies, labeling, and post-approval lifecycle management are currently in high demand. Parexel’s hiring drive aims to onboard skilled professionals who can support complex regulatory programs across multiple therapeutic areas. Parexel Hiring for Regulatory Affairs Jobs
Candidates attending this walk-in drive will have the opportunity to work on:
- Global regulatory strategy development
- High-impact submissions such as IND, NDA, BLA, IMPD, and MAA
- Biologics, vaccines, and monoclonal antibody projects
- Global labeling compliance and artwork management
- Advanced regulatory systems such as Veeva Vault RIMS
This makes the walk-in drive highly suitable for professionals looking to be part of large-scale, international regulatory operations. Parexel Hiring for Regulatory Affairs Jobs
Walk-In Drive Details
- Walk-In Date: 20 December 2025
- Interview Time: From 10 AM onwards
- Job Location: Parexel Bengaluru Office
- Interview Type: Direct Walk-In
- Experience Range: 2 to 10 Years
- Hiring Domains: Regulatory Affairs, CMC, Labeling, Lifecycle Management
Open Positions at Parexel – Bengaluru
1. Regulatory Affairs Consultant – Biologics / Small Molecules
Experience Required: 7 to 10 Years
This senior-level role is designed for experienced regulatory professionals with strong global exposure and leadership capability. Parexel Hiring for Regulatory Affairs Jobs
Key Responsibilities
- Lead and author global and regional regulatory maintenance submissions across US, EU, and Rest of the World markets
- Manage full lifecycle management for small molecules and biologics, including vaccines and monoclonal antibodies
- Handle CMC-related agency queries and health authority responses
- Prepare and review critical regulatory documents such as IND, IMPD, DMF, BLA, NDA, and MAA gap analyses
- Review and manage CMC sections for regulatory variations (Type IA, IB, II), renewals, and annual reports
- Evaluate change controls and assess regulatory strategy impact
- Oversee artwork and labeling updates and post-approval CMC submissions
- Work extensively on RIMS platforms such as Veeva Vault
Qualifications & Skills
- Strong understanding of US, EU, and global regulatory frameworks
- Hands-on experience in global CMC authoring and health authority interactions
- Ability to lead, mentor, and guide regulatory teams
- Proficiency in regulatory databases and document management systems
2. Senior Regulatory Affairs Associate – Biologics / Small Molecules
Experience Required: 2 to 6 Years
This role is suitable for early-to-mid-level RA professionals who are actively involved in submissions and regulatory strategy execution. Parexel Hiring for Regulatory Affairs Jobs
Key Responsibilities
- Prepare and author CMC modules, regulatory variations, renewals, and annual reports
- Manage EU procedures including DCP, MRP, and National submissions
- Evaluate regulatory impacts of change controls and deviations
- Plan and deliver submission content for global markets
- Review DMFs, stability data, and product specifications
- Support safety variations and post-approval updates
- Utilize Veeva Vault RIMS for submission tracking and documentation
Qualifications & Skills
- Experience across US, EU, Canada, and Australia regulatory submissions
- Strong understanding of global CMC regulations
- Ability to handle lifecycle management submissions independently
- Knowledge of post-approval regulatory activities
3. Senior Regulatory Affairs Associate – Labelling
Experience Required: 2 to 6 Years
This specialized role focuses on global labeling compliance, packaging components, and artwork management. Parexel Hiring for Regulatory Affairs Jobs
Key Responsibilities
- Develop and maintain CCDS and USPI documents
- Manage global packaging and labeling artwork approvals for US, EU, Switzerland, Canada, and Australia
- Handle SPL creation, troubleshooting, and lifecycle maintenance
- Execute post-approval labeling submissions and PSUR updates
- Maintain artwork trackers and compliance documentation
- Coordinate with quality, supply chain, and technical operations teams
Qualifications & Skills
- Strong understanding of global labeling regulations and guidance
- Experience with Veeva, TVT, Docubridge, and document control systems
- Knowledge of CMC components used in annual reports
- Excellent coordination and regulatory governance skills
Who Should Attend This Walk-In Drive
This walk-in interview is ideal for candidates with experience in: Parexel Hiring for Regulatory Affairs Jobs
- Global CMC regulatory submissions
- Biologics and vaccine regulatory strategy
- Small molecule regulatory operations
- Lifecycle management
- Global labeling and post-approval compliance
- Health authority communications
- Regulatory intelligence and documentation management
Freshers are not eligible for this drive as all roles require prior hands-on experience in Regulatory Affairs. Parexel Hiring for Regulatory Affairs Jobs
Why Join Parexel
Parexel offers one of the most stable, growth-oriented, and scientifically driven work environments in the CRO industry.
Benefits of Working at Parexel
- Opportunity to work with global clients and regulatory agencies
- Exposure to high-value submissions across multiple regions
- Strong learning and development programs
- Consistent growth in biologics, vaccines, and advanced therapeutics
- Supportive and inclusive corporate culture
- Robust internal mobility and career advancement programs
- Access to industry-leading regulatory tools and platforms
Work Location – Bengaluru Regulatory Hub
Parexel’s Bengaluru office acts as a major regulatory operations center supporting global markets. The office is equipped with state-of-the-art regulatory infrastructure, collaborative workspaces, and international regulatory project exposure. Parexel Hiring for Regulatory Affairs Jobs
How to Apply – Walk-In Interview Process
Step 1: Attend the Walk-In Directly
Candidates meeting the eligibility criteria can directly attend the walk-in interview on: Parexel Hiring for Regulatory Affairs Jobs
- Date: 20 December 2025
- Time: 10 AM onwards
Step 2: Walk-In Venue Address
Arliga Ecoworld, Building No. 5B, 3rd Floor
Sarjapur – Marathahalli Outer Ring Road
Devarabeesanahalli Village, Varthur Hobli
Bangalore East Taluk
Bengaluru – 560103
Step 3: Documents to Carry
- Updated Resume (Multiple Copies)
- Government Photo ID Proof
- Education Certificates
- Experience Letters
- Latest Salary Slips
Step 4: Experience Requirement
Only candidates with 2 to 10 years of Regulatory Affairs or Labeling experience should attend the interview.
Final Words
This Parexel Regulatory Affairs Walk-In Drive 2025 in Bengaluru is one of the most significant hiring events for experienced RA professionals this year. With opportunities spanning biologics, small molecules, lifecycle management, and global labeling, this drive opens doors to long-term global regulatory careers. Parexel Hiring for Regulatory Affairs Jobs
If you have the relevant experience and expertise, attending this walk-in could be a decisive step toward working with one of the world’s most trusted clinical research organizations. Parexel Hiring for Regulatory Affairs Jobs
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Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
