Regulatory Affairs Consultant- Small Molecules
Regulatory Affairs Consultant- Small Molecules
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Job Description
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
- Around 810 years of relevant experience in handling of pre approvals (INDNDA) and post approval life cycle management of drug products in various markets.
- Contribute to preparation (including authoring where relevant) and delivery of simple and with experience increasingly more complex regulatory maintenance submissions from a global and/or regional perspective.
- Working knowledge of EU and 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.
- Preparation and review of Marketing Authorization Applications & Variations for various 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 Worksharing 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 crossfunctional 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 with emphasis on Veeva Vault.
- Strong communications skills and ability to guide and mentorteam members.
- Ability to work independently and within stipulated time period.
- To drive first time quality and efficiency on allocated project assignments.
Required Experience:
Contract
Employment Type
Full Time
