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.
Position Summary: The QA Manager/Sr. Manager manages a team of QA Specialists and the process for the QA oversight of Deviations and CAPAs. This team performs daily deviation triage (classification) and investigation…
At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to…
The Manufacturing Quality Assurance (MQA) Specialist II provides real-time guidance and support on the cleanroom floor to ensure GMP compliance in a biopharmaceutical manufacturing environment. Responsibilities include batch record review, deviation triage, facility walkthroughs, and mentoring team members.
This position is on 2-2-3 shifts, 7a-7p and 7p-7a. MFG Support Associate I/II is responsible for the execution of production activities of Media and Buffer preparation within a GMP environment. The Manufacturing…
This role serves as a client-facing Quality Assurance liaison, managing batch status, quality metrics, and regulatory compliance within a biopharmaceutical environment. The position involves overseeing deviation investigations, CAPA approvals, and ensuring adherence to cGMP standards for commercial programs.
Job summary Identifies, evaluates, develops and closes new customers and expands business at existing customers. Identifies and assists in progressing biopharmaceutical business opportunities including new scientific…
Build cloud-based data platforms and tools for biopharmaceutical R&D, using Python, JavaScript/TypeScript, React, AWS, and data stacks like Pandas and Airflow to accelerate drug development.
Job Summary The Senior Director, Warehouse Operations is responsible for strategic leadership, operational performance, and continuous improvement of all warehouses, inventory, logistics, warehouse purchases, warehouse…
JOB SUMMARY The Facilities Engineering Department is responsible for all aspects of maintaining the site infrastructure in an active reliable state to support cGMP operations. Facilities Engineering oversees the…
JOB SUMMARY *Dayshift, 7am-7pm, 2-2-3 rotating schedule The Manufacturing Support Associate I/II position is designed as an introduction to the environment of cGMP manufacturing. This position performs all…
JOB SUMMARY The Global Supply Chain Material Planning Manager will report to the Sr Manager of Global Supply Chain Planning. The Global Supply Chain Material Planning Manager will be client facing by participating…
Oversee quality assurance for raw materials in a biopharmaceutical manufacturing environment, reviewing documentation, releasing materials, and managing supplier quality to ensure cGMP compliance.
This is a remote role with preference for candidates located on the West Coast, USA. Position Summary: Identifies, evaluates, develops and closes new customers and expands business at existing customers. Identifies and…
JOB SUMMARY The SAP Enterprise Data Architect role provides expertise in SAP S/4HANA data architecture, enterprise data modeling, migration strategy, and data governance. This is a key role in designing scalable data…
Job Description Process Engineering is responsible for all Manufacturing process equipment and ensures the equipment and site infrastructure is in an active state to support cGMP operations. As a Process Engineer, you…
Position Summary: Identifies, evaluates, develops and closes new customers and expands business at existing customers. Identifies and assists in progressing biopharmaceutical business opportunities including new…
Job Description This individual will provide thought-leadership, expertise, and management of managed validation services to the IT Validation & Compliance infrastructure in a Contract Development and Manufacturing…
We couldn't check your fit for this role — add a CV to your profile to see it next time.