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Senior Regulatory Affairs Associate (Labelling)

Bengaluru, India Additional Locations Hyderabad,Telangana,India Job ID R0000025181 Category Regulatory / Consulting Date Posted 09/18/2024
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Overview

As part of Parexel Consulting, you will play a vital role in helping biopharmaceutical and medical device companies navigate the complex and ever-changing regulatory landscape. Drawing on your scientific, technical, and regulatory expertise, you will work closely with clients to develop and implement regulatory strategies that bring their products to market faster and keep them there.

We value collaboration, innovation, and continuous learning. As a member of our team, you will partner with a diverse group of clients, and be exposed to various product types and therapeutic areas. You will also develop your skills through challenging assignments and mentorship from experienced regulatory professionals. Plus, you will enjoy the flexibility of working remotely while still being part of a supportive and dynamic team.

Success Profile

Do you have these soft skills and interpersonal traits to succeed at Parexel?

  • Communicator
  • Detail-oriented
  • Problem-solver
  • Relationship-builder
  • Results-driven
  • Strategic

About This Role

Key Accountabilities:

Project Execution:

Regulatory Affairs Labeling 

  • Must have  4+ years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality. 
  • Good working knowledge of key labeling regulations/guidance and past experience in label development (CCDS, USPI, packaging) 
  • The ability to research and create comparator labeling documents. 
  • Strong understanding and experience creating annual reports. 
  • The ability to collaborate with Tech Ops for artwork implementation. 
  • Proficiency in SPL (all aspects, types, and troubleshooting) and the ability to manage the review and approval of labeling in a document management system. 
  • Electronic document management systems use and / or electronic submission experience. 
  • Life Cycle Management, Post Approval Labeling submissions including PSUR submissions. 

PAREXEL-related Activities:

  • Meets established metrics as specified in scorecard on an annual basis
  • Completes basic job-related responsibilities, including timesheets, expense reports, maintenance of CVs, training compliance, project deliverable archiving, participation in internal initiatives/projects as requested by management
  • Defines self-development activities in order to keep current within the industry (i.e. maintain membership in a relevant industry and/or scientific/technical association)

Skills:

  • Project management knowledge
  • Client-focused approach to work
  • Results orientation
  • Teamwork and collaboration skills
  • Excellent interpersonal and intercultural communication skills, both written and verbal
  • Critical thinking and problem-solving skills
  • Proficiency in local language and extensive working knowledge of the English language

Business Development:

  • Continue to build a network of industry colleagues through relationships formed during project engagements or through other industry experience
  • Communicates potential new business leads to PC management and account managers
  • May participate in project scoping calls and/or proposal preparation with the support of senior colleagues

Knowledge and Experience:

  • 4+ years of experience in an industry-related environment

Education:

  • Minimum of a Bachelor’s Degree in a Scientific or Technical Discipline

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