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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.
The Quality Assurance Engineer at the client will be responsible for developing and qualifying tests, participating in design reviews, and ensuring compliance with Quality Management Systems. The role also involves risk assessment, statistical analysis, and guiding junior team members in the medical device industry.
You will be responsible for 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.
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.
The Director Finance will be the finance business partner to the US operations leaders and key liasion between them and the India Finance teams.
My client is looking to add a Senior Accountant to their team in order to continue the company's exciting acquisitive and organic growth! Working alongside the Controller and with the senior leadership team, this individual will help manage the month-end close and reporting processes and assist in other technical accounting processes, such as intercompany accounting, fixed assets, inventory, and more! As the Senior Accountant, you will also support the company in their finance and operation initiatives within their fast-paced entrepreneurial organization.
The Senior Manufacturing Engineer will champion improving manufacturing processes throughout the facility. By developing and maintaining processes, you will save costs, reduce scrap, and drive efficiency.
The Staff Manufacturing Engineer will be the lead technical individual while working with outside vendors through new and existing product lines.
As a Clinical Microbiology Sales Specialist, you will be responsible for driving sales of our capital equipment solutions into the clinical laboratory space across the United States. Leveraging your expertise in microbiology and laboratory operations, you will engage with key decision-makers to understand their needs, provide consultative guidance, and effectively demonstrate the value of our products.
Responsible for managing client expectations, queries and project information flow. Participate in developing best practices in project management and implement by leading by example.
Effectively and proactively source candidates through various online and networking channels for the clinical functions.
As Clinical/Healthcare Recruiter, under the direction of the Head of People, you will perform the full-cycle recruitment of all clinical requisitions to source and select highly qualified, and diverse candidates. You will be responsible for fully utilizing multiple recruiting resources to source, screen, qualify, and hire all senior clinical levels to advance clinical job requisitions.
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.
I'm partnered with the CFO at a $200M, entrepreneurial medical device company located near Hanover Park, IL. This client is a market leader in their space and is looking to double in size over the few years. With exciting new products set to launch in the near future, it is the perfect time to join as the Corporate Controller and capitalize on the growth!
Reporting directly to the CFO, you will be responsible for consolidating 5 entities and the overall accounting function for the US division, while leading a team of 3 individuals. You will also be involved in strategic finance initiatives alongside the CFO. This is a great opportunity to join a growing company and further your career!
I'm partnered with the CFO at a $200M, entrepreneurial medical device company located near Hoffman Estates, IL. This client is a market leader in their space and is looking to double in size over the few years. With exciting new products set to launch in the near future, it is the perfect time to join as the Corporate Controller and capitalize on the growth!
The Program Manager will be an essential piece in the development of new and existing products in their portfolio. They will oversee the entire development of from design concept to market release.
Reporting into the General manager, The Director of Quality & Regulatory will maintain and enhance the current ISO 13485, FDA cGMP and Canadian Medical Devices Conformity Assessment System (CMDCAS), Complaint system, and Quality Management System (QMS). The role is part of the Senior Management team and helps drive day-to-day activities as well as strategic initiatives.
At this publicly traded company you will be working directly with the Senior Manager of Accounting & Financial Reporting
Project Engineers will leverage their technical expertise, experience, and resourcefulness to enhance the delivery of our construction services. As the largest general contractor in the country, my client is a leader across all major market segments, including healthcare, education, commercial, sports, aviation, pharmaceutical, retail, and green building.
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