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The Clinics Head will lead the offline business segment, focusing on expanding clinic operations across major cities in India while maximising profitability.
will be instrumental in providing regulatory expertise to licensing activities and guiding the wider team and selected partners on global regulatory process. The role will also lead the development and continuous improvement of the regulatory database for various healthcare products across low- and middle-income countries.
The role will act as a Subject Matter Expert for product development and related technical areas within the organization. The role involves offering technical insights to in-licensing and out-licensing processes, including providing technical guidance to licensees to accelerate product development, and ensuring effective alliance management. The position requires a solid understanding of the generic drug development process, regulatory requirements, and project management skills, with an emphasis on innovative approaches to public health and voluntary licensing projects. In addition, this role demands a high level of autonomy, cross functional collaboration and learning agility to respond to innovative projects.
Lead & spearhead global expansion: Drive revenue & market share growth in Rest of the World markets through strategic partnerships, marketing initiatives, and business development activitiesExpertise & leadership: Combine international business acumen with marketing savvy to build a thriving regional presence & achieve ambitious commercial goals.
Global Regulatory Affairs Head position is responsible for end-to-end regulatory activities, from pre-approval, fillings, to post-approval activities. The position is responsible for HA meetings across US & EU markets, ensuring adequecy in the dossier submissions for formulations.
This is an excellent opportunity in a team management role with a leading/global pharma giant to drive regulatory submissions for US/Europe geography.
The main responsibility of the incumbent will be to handle the sales distribution for our client in FMCG for either Karnataka or Telangana as a whole
This is an exciting role for the Shared Service Centre of a leading pharmaceutical company based out of Gurugram . The role provides you an excellent opportunity lead a team of regulatory affairs associates for preparation and filling of regulatory submissions for the Biopharma business Units and Market Units.
The incumbent would be leading consumer insights across all categories within the organisation and lead stakeholder management.
The job involves working in a global consulting organisation on various strategy consulting projects. It would involve working with different stakeholders, both internal and external, on multiple consulting assignments.
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