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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.
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.
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.
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.
Responsible for developing new and existing businesses within their territory. Meet sales objectives and satisfy customer needs by educating and selling the company product lines and services to research facilities.
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.
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.
Seeking a Regulatory Manager to join our team who will ensure compliance with all relevant regulations, standards and guidelines. This person will work closely with internal departments and provide guidence to ensure regulatory requirement are met.
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
The Senior Formulation Scientist position is responsible for business continuity activities that include qualifying new/alternate raw materials (fragrances, surfactants, dyes, preservatives etc.), new applicators and packaging components, developing new processing methods to aid scale up and Production, troubleshooting commercial batches and help in process development and cost-saving initiatives to support all products made.
Our client is looking for a Construction Project Manager - Interiors - New Jersey to join their team in the New Jersey market. This role will offer long term development and provide the successful candidate with exposure to high end interiors projects as well as life sciences, ground up commercial, and more divisions within the business.
As a Project Manager specializing in healthcare, life science or cGMP projects, you will play a key role in overseeing the planning, execution, and delivery of large-scale construction projects. You will be responsible for managing all aspects of the project lifecycle, from initial concept through to completion, ensuring that projects are delivered on time, within budget, and to the highest quality standards.
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