Specialist – Regulatory Informatics and Operations at Cencora, Noida
A rare chance has emerged for qualified professionals as Cencora invites applications for the position of Specialist – Regulatory Informatics and Operations in Noida, India. Among current Cencora Regulatory Jobs, this full-time role is ideal for candidates with a B.Pharm, M.Pharm, or a relevant Science degree and a minimum of three years of experience in regulatory operations.
About the Company
Cencora is a global organization specializing in regulatory affairs and operations within the pharmaceutical sector. The company is dedicated to supporting clients through complex regulatory environments, ensuring compliance with health authority requirements across various regions. Cencora operates in multiple countries, providing innovative solutions to enhance regulatory submission processes.
- Company: Cencora
- Affiliated Company: PharmaLex India Private Limited
- Job Role: Specialist – Regulatory Informatics and Operations
- Job Location: Noida, India
- Employment Type: Full-time
- Qualification: B.Pharm / Science Degree; M.Pharm Preferred
- Experience: Minimum 3 Years
- Job Requisition ID: R265000
- Shift Requirement: CET/US shifts may be required
Cencora Regulatory Jobs: Role Overview
The Specialist – Regulatory Informatics and Operations role supports regulatory submission activities across different Health Authority regions. This Cencora Regulatory Jobs listing involves regulatory processes covering dossier Modules 1 to 5, applicable document types, and submission activities. The role includes participation in pre-publishing, dossier compilation, dossier publishing, and post-publishing operations. A strong understanding of US and EU eCTD submissions is important for this position.
Key Responsibilities
- Developing and maintaining client relationships.
- Identifying opportunities for increased service support and communicating them to the respective lead.
- Supporting Regulatory Informatics and Operations processes.
- Providing support for regulatory dossier activities across Modules 1 to 5.
- Working with applicable regulatory document types and Health Authority regions.
- Supporting pre-publishing activities.
- Assisting with dossier compilation and performing dossier publishing activities.
- Participating in informatics-related Health Authority initiatives.
Eligibility Criteria
- B.Pharm or another relevant Science degree.
- Preferred Qualification: M.Pharm.
- Minimum 3 years of relevant experience in regulatory operations, regulatory publishing, eCTD submissions, or dossier management.
Required Skills
- Mandatory Skill: Submission Publishing.
- US Publishing Experience.
- Preferred Skills: Veeva Tool experience, Veeva Publishing experience.
- Technical Knowledge: Understanding of regulatory processes, dossier management, and regulatory submission processes.
How to Apply
Interested candidates can apply through the following link:
Why Consider This Cencora Regulatory Jobs Role?
The Cencora Regulatory Informatics and Operations job offers an opportunity to work in an international regulatory environment supporting regulatory submission and publishing processes. Professionals in this role may gain exposure to global regulatory submission processes, US and EU eCTD submissions, dossier publishing, and Health Authority requirements, making it a significant step in their careers in Regulatory Affairs.
Conclusion
For professionals exploring Cencora Regulatory Jobs, this opportunity for the Specialist – Regulatory Informatics and Operations role is an excellent fit for qualified candidates looking to advance their careers in regulatory affairs. Interested individuals are encouraged to apply before the deadline to seize this chance to contribute to a vital sector.
