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Regulatory Affairs Labelling Manager

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Lead regulatory labelling strategy for medicinal products in Hertfordshire. Develop and maintain Core Data Sheets and EU/US product information, ensuring global compliance. Collaborate cross-functionally, providing strategic guidance throughout the product lifecycle. Requires strong regulatory af...
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United Kingdom , Hertfordshire
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Not provided
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Regulatory Program Manager

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Lead regulatory lifecycle management projects in Paris, driving pharmaceutical innovation. Coordinate cross-functional CMC, regulatory, and supply teams to advance a portfolio of products. Ideal candidates have strong project management and CMC expertise within the pharma industry.
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France , Paris
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EHS Project Manager

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Join our team as an EHS Project Manager in Lexington, MA. You will develop and implement critical safety programs for facilities and construction projects within biotech/pharma. This role requires strong EHS regulatory knowledge and experience with risk assessment and management systems. We seek ...
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United States , Lexington
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90.00 - 95.00 USD / Hour
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Automation Technician

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Join a global CMO as an Automation Technician in Neuchâtel. Provide vital technical support for OT infrastructure, cybersecurity, and process control systems (PCS). Utilize your expertise in GMP, SCADA, and industrial networks to ensure compliance and seamless operations. This role offers a colla...
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Switzerland , Neuchâtel
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Not provided
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Project Manager

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Lead the development of Companion Diagnostics (CDx) from concept to care as a Project Manager in Tucson. You will create integrated plans, manage budgets, and mitigate risks to drive project execution. This role requires strong PM expertise to guide cross-functional teams and ensure quality throu...
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United States , Tucson
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Not provided
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Assistant Scientist - QC Micro

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United States , Zebulon
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Not provided
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QA Validation, Senior Associate

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United States , Boston
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90.00 - 97.00 USD / Hour
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Senior Project Manager

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United States , San Diego
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75.00 - 90.00 USD / Hour
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QA Consultant

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United States , Durham
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Not provided
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Medical Director, Hematology

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United States , Boston
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Veeva Clinical Business Administration Specialist

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Join our Boston team as a Veeva Clinical Business Administration Specialist. You will optimize Veeva Vault Clinical systems, providing crucial user support and driving process improvements. The role requires expertise in eTMF/CTMS, system validation, and clinical trial processes. This is a key op...
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United States , Boston
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Medical Writing Operations Manager

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Lead document quality and submission readiness for a top pharmaceutical firm in Cambridge, US. Utilize your regulatory publishing expertise to manage and QC clinical documents like CSRs and IBs, ensuring eCTD compliance. This role demands sharp detail-orientation and proficiency in MS Office/Adob...
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United States , Cambridge
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70.00 - 77.00 USD / Hour
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Proclinical
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