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Lead the development of the Bioprocess Filtration Portfolio, leveraging both new and existing assets to meet market demands and industry trends. Serve as the subject matter expert on bioprocess filtration, providing technical support and guidance to internal teams and external stakeholders.
Looking for a dynamic and hands-on General Manager to lead the innovation business, aligning with their values and growth plans.Location : Open ( preference is Australia, visa support provided )
Responsible for driving our business development activities, expanding our client base, and providing strategic input to enhance our service offerings. Provide strategic input and innovative solutions to enhance our service offerings and differentiate us in the market.
Take charge of advancing ADC process development and production. Contribute to shaping and launching the facility and lab through design, build-out, and startup support.
Provides scientific expertise in the development of methods and method validations. Maintain laboratory equipment, including troubleshooting and repair of LC-MS/MS and GC-MS/MS instruments.
Create and pioneer innovative synthetic pathways for pharmaceutical APIs within our cutting-edge laboratory, then seamlessly scale up these processes to kilogram-level production within our internal facilities. Uphold meticulous record-keeping practices in compliance with company policies, ensuring the traceability and transparency of experiments.
Lead the process development and production of ADCs. Support the development of the facility and laboratory design, build out, and start-up.
Identify and pursue new business opportunities in the pharmaceutical and biotechnology sectors related to preclinical discovery and development. Leverage a strong technical background in preclinical research, with a focus on immuno-oncology, oncology, degenerative disorders, or related areas to effectively communicate with clients and internal teams.
As a vital member of the team, the Process Engineer leads the design, installation, and implementation of processes and equipment to ensure the safe, compliant, and efficient production of small molecule active pharmaceutical ingredients (APIs) in a GMP environment.
You will be responsible for leading analytical development activities, implementing cGMP principles, and ensuring the successful execution of analytical projects. Your expertise in LC-MS and HPLC/UPLC techniques will be crucial in developing robust methods for characterizing and analyzing small molecules and late-stage APIs.
Responsible for driving sales of their CDMO/CRO Discovery and Process Chemistry services to biotech and pharmaceutical companies in the United States. Play a key role in identifying new business opportunities, building relationships with clients, and expanding their market presence.
Design and develop novel synthetic routes to pharmaceutical APIs in the laboratory and implementing the processes at kilogram-scale in internal facilities. Maintain clear and accurate records of experiments in laboratory notebooks in accordance with company policy.
Play a crucial role in their clinical development team, providing strategic medical leadership in the development of novel drugs and therapies. Responsible for US Clinical development and will offer medical guidance to discovery projects, ensuring the highest standards of clinical research.
My client is seeking a highly skilled and motivated Field Service Engineer to provide technical support, installation, repair and maintenance of our analytical instruments at customer sites. The Field Service Engineer will be responsible for ensuring that our customers receive exceptional service and support, in order to maximize their satisfaction and the performance of our products.
The Director of Regulatory Affairs is a department head who oversees regulatory strategy, operations, and intelligence. They are responsible for developing and implementing regulatory plans throughout the entire product lifecycle. The RA Director has a deep understanding of US, EU, and international regulations for Medical Device products, and works within a cross-functional team to ensure efficient commercialization.
The Lead Automation will integrate new practices throughout the ongoing and new product launches for the organization.
The Sustaining Engineering Manager will be responsible for ensuring that all technical aspects of product design and manufacturing are managed with internal and external members and partners.
As a Field Clinical Account Specialist you will be providing educational, clinical, and procedural direction to help achieve patient care, customer support, and service objectives. You will interface with and help our customers by being the resident expert on our Hepatic Arterial Infusion (HAI) pump and accessories
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