Executive - Regulatory Affairs - Navi Mumbai, Maharashtra

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 ...

+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 ...

Head Regulatory Affairs Role & responsibilities ROW /EU Dossier Preparation Regulatory Strategy CTD ROW Regulatory Submissions Global Regulatory Compliance Regulatory Operations Pharmaceutical Lifecycle Management · ...

+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 per ...

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

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 ...

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'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. · ...

The company is looking for a Regulatory Affairs Manager to manage the submission and approval process for Teva products in the APAC Region. The successful candidate will have experience in regulatory affairs, particularly in generics, biosimilars, or innovative medicines. · ...

Management of the submission and approval process for Teva products in APAC Region (Australia, New Zealand, Singapore, Malaysia etc) to support business opportunities for the company.Ensure full compliance of marketed products according to local regulations by proactively managin ...

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 ...

The Manager Regulatory Affairs will prepare and review CTD and ACTD dossier. · ...

Prepare and review CTD and ACTD dossiers. · Coordinate with Plant and R&D for Regulatory Submission inputs. · Maintain regulatory compliance with plant. · ...

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 ...

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

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 ...

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. · ...