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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 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 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.
The person in this role will be responsible for heading Sales for Nueroscience division for TIMEA region (Turkey, India, Middle East & Africa). The person in this role will be supporting sales with technical knowledge.
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.
As the Chief Business Officer (CBO) of our multi-specialty hospital, he will be a key member of the executive leadership team, responsible for driving the hospital's business strategy, growth, and overall financial performance. This role requires a dynamic and strategic leader with a deep understanding of the healthcare industry in India, excellent business acumen, and the ability to foster collaborative relationships both internally and externally.
As the Clinical Head of our multi-specialty hospital, he will play a pivotal role in leading and managing the clinical operations to ensure the delivery of high-quality patient care. This position requires a dynamic and experienced healthcare professional with a strong clinical background, leadership skills, and a commitment to excellence in healthcare delivery.
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.
Provide strategic direction and leadership for the Groups overall operations and growth .Develop and implement operational policies and procedures to ensure smooth functioning of all departments t business. Improve upon it and in all the hospitals. Collaborate with department heads to optimise work flows and enhance overall efficiency. Drive the current business and improve upon it. To set up and kick off new hospitals
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.
As the Head of RCM the candidate will initially be responsible for setting up, scaling and growing the business over a period of time. Their charter will overlook every process that comes within the RCM cycle along with the P&L ownership of the Business Unit.
This is an excellent opportunity to create a strong impact in the non-profit industry through designing, implementing and leading the growth and expansion plans of the organisation
Reporting into the Chairman/Founder you will leading the entire finance function for a fast growing healthcare organisation
1. CEO managing a P&L of 100 million $ and above and diversifying the current business into multiple revenue streams2. Growing the business by 3x-5x
This is an excellent opportunity in a team management role with a leading/global pharma giant to drive regulatory submissions for US/Europe geography.
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.
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.
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