Regulatory Affairs Associate

Regulatory Affairs Specialist">The Regulatory Affairs team is seeking a highly skilled and experienced specialist to support the management of regulatory submissions for healthcare products across diverse geographies.">Key Responsibilities:">Management and coordination with vendors of technical and legal requirements for obtaining marketing authorization...

Key Responsibilities:Lead and manage CMC regulatory activities for USFDA submissions including ANDA preparation, review, and filing.Oversee compilation and submission of Annual Reports, amendments, and deficiency responses.Interface with cross-functional teams including Quality Assurance, Production, and R&D to gather required documentation and data.Review...

Company DescriptionDr Reddy s Laboratories Ltd is a leading multinational pharmaceutical company based across global locations Each of our 24 000 plus employees comes to work every day for one collective purpose to accelerate access to affordable and innovative medicines because Good Health Can t Wait We started in 1984 with a modest investment 20...

Department Details Role Summary We are seeking a detail-oriented and proactive Regulatory Affairs Associate to join our Regulatory Publishing team In this role you will be responsible for preparing and submitting high-quality electronic submissions eCTD NeeS to global health authorities ensuring compliance with international regulatory standards ...

About Infodesk www.infodesk.comInfodesk is the leading enterprise intelligence management SaaS platform, serving the top 100 companies acrossglobal life sciences,government, professional, and investment services.Infodesk's proprietary "Smarter Data" technology gathers, normalizes, enriches, and summarizes content in real time from external and internal...

Job Summary:We are looking for an experienced Regulatory Business Analyst with strong hands-on experience in Veeva Vault RIM to support regulatory operations and digital transformation initiatives within the pharmaceutical domain. The ideal candidate should have a deep understanding of regulatory processes and documentation, and be capable of working closely...

Department - MEDICAL & REGULATORY AFFAIRS - Job posted on - Jun 09, 2025 - Employment type - P-P8-Probationer-HO Executive **Position: Medical Advisor** **Responsibilities**: - Presentingscientificmaterialclearlyandconcisely. - Negotiationskills,excellentinterpersonalandcommunicationskills. - Abilityandwillingnesstoacquireknowledgein...

Job Summary: We are looking for an experienced Regulatory Business Analyst with strong hands-on experience in Veeva Vault RIM to support regulatory operations and digital transformation initiatives within the pharmaceutical domain. The ideal candidate should have a deep understanding of regulatory processes and documentation, and be capable of...

The Compliance Associate is responsible in performing internal audit and produce audit report based on guidelines and procedures, develop compliance policies, provide support to Business Units in order to maintain internal control framework. Job Responsibilities: - Assist and support in audit testing, identify internal control issues/exceptions, report,...

About the jobAbout FreyrFreyr is a fast-growing, innovative company specializing in providing end-to-end regulatory solutions and services for the Life Sciences industry. With a commitment to excellence and innovation, we assist pharmaceutical, medical device, and biotech companies in navigating the complexities of regulatory compliance.Why Freyr?At Freyr,...