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Responsible to lead the business, the strategy, business planning, marketing, and sales of this portfolio. Working closely with the leadership team, you will be accountable for formulating all strategic goals in relation to oncology public channel portfolio and provide a strong platform for continued growth of the area. Emphasis will be placed on the growth of business revenue, profits, quality of sales and marketing in India and developing talent for leadership positions.
Lead business across India for Medical Devices in the Orthopaedics space
Develop and implement comprehensive strategies to enter and expand the Brand and Therapy presence in emerging markets.
Leading and strategizing the overall operations of the organisation, overseeing business development and client relationships, and ensuring the successful execution of projects within agreed timelines and quality standards, while driving profitability and growth in the competitive pharmaceutical industry.
This is an excellent opportunity to lead the business portfolio of a leading medical devices/services provider in the urology segment.
This is an excellent opportunity to join a budding organisation in the in vitro diagnostics industry having a directly visibility with the management of the company. This person will be responsible for setting up the base of client portfolio for the company and create a foundation for generating business.
This is an excellent opportunity to lead the marketing function for one of the leading health care brand that has a portfolio of both products & services towards community health and development. They are known for their exclusive health care centres and a range of OTC products within the health care industry
An excellent career opportunity to be a part of Healthcare & Lifesciences team at Michael Page. The role will provide you a chance to foray into a 360 degree role starting with Business Development, Account Management and closing recruitment mandates for key clients within Healthcare & Lifesciences practice.
An excellent opportunity to lead Business Development function for one of the leading CDMO for domestic market. The incumbent in this role will be responsible for overall sales and profitability for CDMO vertical.
Own the complete P&L of southern India and manage sales end to end while working with a global giant in medical devices space.
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.
The Quality Performance & Master Data Lead defines and implements the requirements for processes of
in the CHC Quality Management System.
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.
Leads successful and timely operational execution of global insourced or outsourced, Non-Registrational Data Generating or Registrational Data Generating interventional clinical trials from concept to final clinical study report.
Responsible for leading the global portfolio with focus on scientific & clinical research.
To drive and oversee R&D programs for Human and animal health, integrate innovation, quality and business into every aspect of the R&D operations. This senior management role is to ensure that human and Animal health R&D stays ahead of market trend in innovation, product development and launch in full compliance with sound scientific practice, GxP and regulatory expectations.
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 exciting opportunity to drive new initiatives, set up businesses, increase consumer research and focus on business planning alongside the leaders of the organisation.
My client is looking for someone to work as a cross-functional leader who has either contributed to or directly managed partnerships (specifically license transactions, collaborations, alliances, and/or joint ventures) and has experience with the drug discovery/development process, technology transfer, clinical development, regulatory processes, reimbursement, and global commercial dynamics in the pharmaceutical industry.
This is an excellent opportunity in a team management role with a leading/global pharma giant to drive regulatory submissions for US/Europe geography.
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