Join Parexel as a Regulatory Affairs Associate – B. Pharma/ M. Pharm can Apply

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Unlock your career potential with Parexel! We’re excited to announce that we’re actively seeking talented individuals with a background in B. Pharma or M. Pharma to join our dynamic team as Regulatory Affairs Associates. If you’re passionate about regulatory compliance and eager to make a difference in the pharmaceutical industry, we invite you to explore this opportunity with us. Join Parexel and embark on a rewarding journey where your skills and expertise will thrive, contributing to impactful global healthcare solutions.

Skills

• Good understanding of regulatory framework, including regional trends, for various types of applications and procedures
• Contribute to preparation (including authoring where relevant) and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from either a global and/or regional perspective.
• Working knowledge of EU/US regulatory procedures including post approval requirements. Knowledge of ROW markets regulatory legislations would be an added advantage
• Experience in handling CMC related health authority queries
• Good understanding of regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions as well as knowledge of global pharmaceutical legislation and guidance specifically linked to regulatory CMC aspects in the ICH countries.

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Roles & Responsibility

• Preparation and review of Marketing Authorization Applications & Variations forvarious types of medicinal products (Orals & Parenterals) for filing in EU through different types of procedures (DCP/MRP/National Procedures).
• Preparation of documentation for different types of Variation procedures like Super grouping,
• Grouping and Work-sharing to the Marketing Authorizations.
• Regulatory review of DMFs, batch records, specifications, and stability data to ensure their compliance with the regulatory requirements.
• Providing regulatory impact assessment for change proposals and identification of required documentation for EU submissions
• Liaise closely with cross-functional members with aligned product responsibilities.
• Execute and maintain submission delivery plans, submission content plans, and proactively provide status updates to designated stakeholders.
• To prepare, review and submit safety variations to Health Authorities and perform post
• Approval CMC related updates.
• Working experience in Regulatory Information Management Systems like Veeva Vault.
• Strong communications skills and ability to guide and mentor team members.

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