Regulatory Affairs 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 ...

Job summary · Together, we're on a mission to make good health more affordable and accessible · ResponsibilitiesManagement of the submission and approval process for Teva products in APAC Region (Australia, New Zealand, Singapore, Malaysia etc) to support business opportunities f ...

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. · ...

Serve as a country or regional expert supporting the Medical Affairs function and project teams within a defined area of expertise Act as a senior technical authority and primary knowledge source within the therapeutic or functional specialty. · ...

+Supports the Medical Affairs function and project teams within area of expertise. · + · +Defines and delivers training for junior members of the team. · Contributes to establishing and implementing policies, procedures and standards for own work and work of others, ensuring comp ...

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

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. · ...

We look for people who focus on getting results, embrace learning and bring a positive energy. · Above all, they must be passionate about doing something meaningful for consumers, patients and the healthcare professionals we serve every day. · ...

The Medical Affairs Manager will devise strategies and planning for launch of new indication/products including KOL engagement and medical education. They will liaise with professional associations and KOLs to build and drive scientific advocacy for the product/therapy area. · ...

The Manager will coordinate and prepare regulatory submissions and provide strategic advice to cross-functional teams.As Manager, you will manage the coordination and preparation of regulatory submissions and provide strategic regulatory advice and operational regulatory support ...

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 ...

We are looking for an innovative Regulatory Affairs Manager to join our team in Mumbai, India. As a key member of our global leadership team, you will be responsible for ensuring compliance with regional and global regulatory requirements throughout the lifecycle of our chemical ...

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