Point your AI agent at freehire and let it find you a job. A CLI and an MCP server over the whole job API — no browser.
Perform quality checks and compliance tasks in a biotech manufacturing environment, reviewing documentation and supporting GMP processes during night shifts.
Perform quality assurance tasks in a biotech/pharma environment, reviewing documentation, ensuring GMP compliance, and supporting investigations to maintain product safety and regulatory standards.
Senior architect designing Salesforce Data Cloud and AI solutions for Life Sciences clients, including identity resolution, agentic AI workflows, and CRM integrations.
Alternant(e) en marketing digital pour concevoir et déployer des campagnes omnicanales dans le secteur pharmaceutique, en collaboration avec des équipes internes et partenaires externes.
At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise…
The Clinical Systems & Technology function provides operational leadership for the clinical business ownership of clinical technology, automation, and clinical reporting across the organisation. The role…
This is a hybrid role and will require frequent on-site presence at our Cambridge MA facility About This Role Biogen is seeking a strategic and analytically rigorous Senior Manager to join the US Commercial Insights…
Career Category Medical Services Job Description The Scientific Communications Operations Manager is accountable for driving development, execution, and implementation of a wide scope of projects and technology…
Regulatory Data Manager Location: Remote (U.S.) Department: Compliance & Data Management Reports To: SVP, Compliance & Data Management About Us We are a leading marketing and regulatory research organization…
About the Job: The Process Engineer is part of the Process Engineering team within the Strategic Operations department responsible for developing, installing and maintaining automated laboratory systems supporting the…
Maintain and optimize CRM systems for a biopharma company, ensuring accurate data and compliance with healthcare regulations.
Configures, implements, and supports enterprise systems (e.g., Veeva Vault, ERP, AWS/Azure) for a biotech company, ensuring compliance with GxP/SOX and aligning IT with business needs.
Job Purpose: The Change Control Continuous Improvement Manager is responsible for identifying, developing, and implementing process improvement initiatives within the Change Control and Document Revision functions.…
About the role The Senior Account Manager will be a driving force behind day-to-day activities on a client brand and is a key team member in leading the development of client projects. The Senior Account Manager is…
Build and secure AWS-based CI/CD pipelines for healthcare apps using Terraform, Ansible, Kubernetes, and security tools like Trivy and SonarQube.
QA specialist reviews GMP manufacturing records, batch dispositions, and lab data for a biopharma company, ensuring compliance with FDA/EU standards and overseeing external CDMO operations.
The Senior Quality Assurance Specialist is responsible for ensuring that computerized systems used in GxP-regulated environments are validated and maintained in compliance with applicable regulations. This role also…
Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to…
Lead QA for materials and supplier governance at a gene-therapy manufacturing site, ensuring regulatory compliance, supplier quality agreements, and warehouse operations meet GMP standards.
We couldn't check your fit for this role — add a CV to your profile to see it next time.