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The Quality Assurance Assistant supports site quality systems by reviewing manufacturing records, managing documentation, and ensuring compliance with cGMP standards. They collaborate with production and supply chain teams to facilitate timely batch releases and maintain quality documentation.
Designs and oversees the architecture for an AI-driven field experience platform integrating CRM, intelligence, and agentic workflows for healthcare professionals, ensuring seamless pre-call, interaction, and post-call workflows while adhering to regulatory and security standards.
Job Description General/Position Summary The Pain Regional Account Manager is a field-based role responsible for delivering flexible, high-impact coverage across the Pain Business Unit to address territory vacancies,…
Valeris is a fully integrated life sciences commercialization partner that provides comprehensive solutions that span the entire healthcare value chain. Formed by the merger of PharmaCord and Mercalis, Valeris™…
Conduct GMP/GDP audits of contract manufacturers, labs, and distribution partners for a rare-disease biopharma company, ensuring FDA/EU/ICH compliance using Veeva Vault Quality Suite.
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice…
Configures and validates clinical trial management systems (CTMS) for research sites, provides user support, and generates operational reports to ensure study readiness and compliance.
Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of…
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed…
Czym będziesz się zajmować? Responsibilities: Design and maintain Robot Framework and additional automated test scripts for Veeva Vault and MuleSoft integrations. Automate functional, regression, UI, API and data…
Ensures clinical trials comply with GCP standards by managing audits, quality events, and regulatory inspections for a biopharma company developing RNAi-based therapies.
OVERVIEW As a Service Manager at eClinical Solutions, you will be the operational backbone of client engagements ensuring every aspect of the elluminate® platform service runs smoothly, reliably, and to the highest…
Pulmovant is a Roivant-backed clinical-stage biotechnology company developing innovative therapies for patients suffering from pulmonary diseases. Pulmovant’s first program, mosliciguat is designed to provide an…
About Sequel Sequel, headquartered in Manchester, New Hampshire, is a company developing the next generation of transformative drug-delivery advancements starting with diabetes. Sequel’s approach is to look at diabetes…
Oversees QA processes for cell/gene therapy manufacturing, ensuring cGMP compliance and documentation (SOPs, batch records) while collaborating with manufacturing, supply chain, and labs to maintain quality standards and foster a quality culture.
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