Public Affair Manager - Mumbai City

We are looking for an experienced Manager – Regulatory Affairs to handle Regulated Markets (US,EU UK RoW Australia etc.) in the pharmaceutical industry. · The role involves managing product registrations regulatory submissions compliance activities authority interactions and lead ...

Job summary · We are seeking a skilled Regulatory Affairs professional with strong expertise in Indian regulatory frameworks to support regulatory compliance and ensure timely product approvals. · ResponsibilitiesPrepare and submit registration dossiers for certificates and licen ...

Developing and implementing strategic communication plans to enhance the company's reputation and relationships with stakeholders. · ...

Responsible for leading Regulatory Affairs individuals accountable for management of life cycle changes including change assessments and submissions all the way to approvals of PLCM (Product Life Cycle Management) projects to support regulatory compliance continued supply of Apot ...

This position involves managing product registrations/submissions and maintaining strong working relationships with regional product leads. · Actively lead product registrations by preparing/requesting documentation needed for complex filings. · Maintain awareness of legislation ...

The incumbent will be responsible for providing scientific inputs for new product development reviewing and approving product claims conducting claim substantiating studies conducting scientific training for marketing team responsible for co-ordinationg with third party manufactu ...

The incumbent will be responsible for providing scientific inputs for new product development, · reviewing and approving product claims, conducting claim substantiating studies, · conducting scientific training for marketing team, ...

Prepare regulatory dossiers for new products and submissions. · ...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures... · ...

Job Details · Responsibilities: · Expert in Regulatory submissions in India. Develop and maintain strong client relationships and help drive opportunities for increased service support to Line Manager. · Participation in regulatory processes to gain and maintain marketing authori ...

To manage and execute regulatory strategies, submissions, approvals, · and lifecycle management activities for pharmaceutical products across ROW markets. · ...

Manager Regulatory Affairs (EU/UK): Handle EU & UK MA filings, eCTD submissions, lifecycle management & variations. · 14+ yrs pharma regulatory exp. · ...

Handle regulatory affairs activities related to APIs and pharmaceutical intermediates)prepare submissions and updates. · ...

The role will involve expertise in D & C Act and Rules as well as FSSAI regulations with experience in FDA related activities. This profile will ensure timely and robust functional/cross-functional coordination (R&D, QC, Marketing, Legal, Production etc.) transparent execution an ...

This is a job in corporate affairs and legal department. · ...

Role Brief: · Responsible for survey, Rehabilitation of a cluster of slum dwellers through the process of tenant management. Responsible for managing the end to end process of tenant management for a cluster / project. · Roles and Responsibilities · Policy · Possess a thorough un ...

We look for people who focus on getting results, embrace learning and bring a positive energy. · ...

Description · You Lead the Way. We've Got Your Back. · With the right backing, people and businesses have the power to progress in incredible ways. When you join Team Amex, you become part of a global and diverse community of colleagues with an unwavering commitment to back our c ...

Responsible for leading Regulatory Affairs individuals accountable for management of life cycle changes including change assessments and submissions all the way to approvals of PLCM projects to support regulatory compliance continued supply of Apotex products. · ...

The Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. · Bachelor degree in Biological Sciences eg BioMedical, Biochemistry, Pharmac ...

NuVvaGen Bioscience is an export-focused manufacturing company renowned for its advanced automation and state-of-the-art infrastructure. The facility spans 100,000 square feet and is equipped with PLC/VFD-enabled machinery to ensure high production efficiency. · Preparation and f ...