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Write and structure CMC process development reports for gene-editing lipid nanoparticles, turning raw lab data into regulatory-ready documentation while collaborating with cross-functional teams.
Lead QA testing for enterprise quality applications like StarLIMS and Veeva, ensuring compliance and reliability across Mattel’s global product quality and regulatory workflows.
As the Senior Specialist IT Support, you will report to the Manager IT Systems & Infrastructure and play a key role in delivering high-quality IT services across the region, combining hands-on technical expertise…
The Position At Maze Therapeutics, we believe precision medicine has the power to transform the lives of patients with both common and rare diseases. As Trial Master File (TMF) Senior Manager for Clinical Operations,…
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The Veeva Vault System Senior Specialist is responsible for…
About Fulcrum The $1.5 trillion insurance industry is powered by brokers. Every business needs insurance, and the brokerage industry is hamstrung by account management capacity. Account managers are constantly pulled…
Build and deploy GenAI and agentic AI systems for pharma clients using Microsoft Copilot Studio, ChatGPT Enterprise, and AWS Bedrock, integrating structured and unstructured data pipelines.
Work Schedule Second Shift (Afternoons) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed…
Build and refresh dashboards in PowerBI/SQL to deliver data-driven insights for Sanofi’s global commercial teams, using pharma datasets and advanced Excel.
Viatris Germany GmbH Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs…
Regulatory Affairs Responsible, External Manufacturing API Location: Budapest, Hungary You’ve built experience, now use it where bold ideas meet real impact. At Opella, we’re challenging how self-care works for…
Own and validate GxP-regulated business systems for GSK, ensuring compliance and driving adoption while balancing business needs and technical trade-offs.
Acts as a bridge between Biogen’s quality teams and IT, configuring Veeva Vault Quality to automate documentation, training, and QMS processes while ensuring regulatory compliance and smooth user adoption.
Develop and maintain Veeva Vault Quality solutions (Training, QualityDocs, QMS) for Biogen’s global biotech operations using Agile practices and Veeva APIs.
Techno-functional analyst bridges pharmacovigilance teams and IT to configure Veeva Vault Safety, document requirements, and lead validation and UAT for global biotech compliance.
Sales Director Rare Disease Commercial EU4+UK Region Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales…
Manager, Medical Affairs Operations, France Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Medical…
Designs electronic case report forms (eCRFs) for clinical trials using Oracle InForm/Central Designer or Veeva CDMS/Studio, ensuring data quality and compliance with protocols and standards.
Job Description The Position Organon is seeking an entrepreneurial and innovative Marketing Trainee Neurology for Northwest Europe (f/m/d). This marketing role within the newly established Northwest Europe cluster will…
Analyzes pharma sales data, maintains CRM systems (Veeva, Snowflake), and builds dashboards to optimize sales incentives and territory planning.
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