Executive - Regulatory Affairs - Navi Mumbai

We are looking for a highly skilled and experienced Regulatory Affairs Associate to join our team at a reputed Pharma Company. · The ideal candidate will have a strong background in regulatory affairs and a minimum of 2 to 5 years of experience.Develop and implement regulatory st ...

We are inviting applications for the role of · Regulatory Consultant.The person will be responsible for Regulatory consulting services at the firm. · ...

+Job summary · We are inviting applications for the role of Regulatory Consultant and are looking for dynamic, driven individuals with strong initiative who can thrive in the entrepreneurial environment at our firm. · +ResponsibilitiesThe person will be responsible for Regulatory ...

We're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. · We are looking for a Director of Regulatory Affairs - Post-Approval (US Generics) who will be responsible for independently setting the strategic dire ...

+We're Teva, a leading innovative biopharmaceutical company. · +The Director, Regulatory Affairs – Post-Approval (US Generics) is responsible for setting strategic direction and ensuring successful execution of post-approval regulatory activities. · ...

We are inviting applications for the role of Regulatory Consultant and are looking for dynamic driven individuals with strong initiative who can thrive in the entrepreneurial environment at our firm. · ...

We're on a mission to make good health more affordable and accessible. The Director, Regulatory Affairs – Post-Approval (US Generics) leads the global regulatory strategy for post-approval lifecycle management of U.S. FDA-approved ANDAs/NDAs. · Define and lead the global regulato ...

JOB PURPOSE: · The Manager – Regulatory Affairs will be responsible for overseeing, managing, and ensuring end‑to‑end compliance with all statutory, regulatory, and accreditation requirements applicable to a Maharashtra State Private University. This includes liaison with bodies ...

The role involves maintaining regulatory databases, supporting document compilation and coordinating required documentation for regulatory submissions, amendments and license applications with FDA and CDSCO.The position also includes preparing Letters of Access and performing oth ...

+Job summary+We are looking for a RA-Executive to join our team. The role will be responsible the role also includes participation in investigations such as deviations, OOS/OOT,+ · +Key Responsibilities+To prepare, review and update SOP, Specification, Method of analysis, Report ...

We are looking for a RA-Executive to join our team. The role will be responsible the role also includes participation in investigations such as deviations, OOS/OOT, and supporting departmental responsibilities in the absence of the reporting authority, along with any duties assig ...

Ensure regulatory compliance throughout product lifecycle. · Manage medical device submissions to US FDA ...

Regulatory Affairs Officer performs daily tasks assisting AGM - Vet. Div., including BDM & Cust. queries to orders, shipment, Regd etc. · ...

The role involves managing quality management systems to ensure compliance with national and international medical device regulations. Key responsibilities include establishing regulatory strategies, implementing quality assurance measures, sterilization processes validation moni ...

To establish and maintain a world-class Quality Management System (QMS) that ensures 100% compliance with national and international medical device regulations. · Liaise with CDSCO/State FDA for manufacturing licenses and product registrations. · Prepare and submit technical doss ...

· Job Description: · works to help a company or organization meet all state, local, federal, international, and industrial regulations that apply to their products. · They must have excellent organizational, analytical, project management, and communication skills. · They work f ...

The Regulatory Affairs Manager will oversee all functions of the department including scheduling activities, dossier preparation and review, regulatory submissions and approvals, task management and timeliness, compliance assurance, team leadership and development. · ...

Develop and implement regulatory strategies to ensure compliance with EU regulations. · Collaborate with cross-functional teams to prepare and submit regulatory documents. · Conduct thorough reviews of regulatory submissions to ensure accuracy and completeness. · Build and mainta ...

This is a Regulatory Specialist role in the Global Regulatory Affairs Service Center Team in Mumbai (GRASC – Team). The person will be reporting to the Manager Regulatory Affairs. · Author Safety Data Sheets for multiple geographies across the globe as per applicable hazard commu ...

Executive - Regulatory Affairs · Roles and Responsibilities · To prepare dossiers as per CTD/ACTD guidelines for product registration, renewal & variation applications to submit in regulated / semi regulated countries. · To arrange administrative documents required for dossier su ...