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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 the architectural design of electrical and electronics systems, including schematic design, component selection, and system integration. Collaborate with hardware and software teams to define system requirements and specifications, ensuring alignment with project objectives and constraints. Develop and maintain detailed project plans, schedules, and budgets, tracking progress and ensuring timely delivery of milestones.
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.
As Head - Quality Control, you would be responsible for all QC related checkpoints, providing leadership & technical expertise as per SOPs, supporting clinical studies, leading regulatory audits, ensuring product quality & implementing digitalised systems for improved technical proficiency.
The job involves leading the sales for the life care solutions business unit of a leading medical devices player. The main responsibility will be to build the retail channel and develop capabilities in the retail space for the organisation.
The incumbent will be responsible for developing the roadpmap for product SKU strategy in channels such as GT, MT and e-commerce with te help of customer, product, pricing and channel insights
Drive commercial success by developing and executing market-winning strategies, optimising sales force effectiveness, and maximising market access for pharmaceutical products.Utilise market research, data analysis, and strategic thinking to identify and capitalise on growth opportunities, ensuring alignment with overall corporate objectives.
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