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Lead the development, purification, and production of ADCs. Support the completion of the new facility and laboratory with design, build out, and start-up.
Are you an EHS Manager in the Pharma/Biotech industry looking for your next opportunity? Do you have managerial experience and feel comfortable managing a team of 8 direct reports? Do you have cGMP experience? Do you have your CSP or QEP? Are you local to Syracuse or willing to relocate? If so, please read on and apply to the Senior EHS Manager - Pharma opening located in Syracuse, NY.
This role involves leading and executing Internal audits across various settings to ensure adherence to regulatory standards and internal policies, contributing to the advancement of healthcare innovation and quality within the company.
The HR Generalist will be responsible for all benefits and payroll related support, employee relations and policies and procedures.
As Human Resources Generalist, you will be responsible for supporting efforts regarding recruiting, associate relations, performance management, compensation & benefits administration, policy administration, and execution of special programs.
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.
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.
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.
At this publicly traded company you will be working directly with the Senior Manager of Accounting & Financial Reporting
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