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.
Our Fortune 500 Medical Device client has an exciting opportunity for a Manufacturing Engineer. Job Summary Responsible for sustaining and improving manufacturing processes and semi-automated equipment to support safe,…
Job Summary: The day-to-day responsibilities of this role center around supporting manufacturing operations. The Manufacturing Engineer I will provide daily manufacturing support by reviewing prior-day performance…
Our Fortune 500 global Pharmaceutical client is seeking an experienced Sr. Associate Manager CoDesign, Patient Engagement. Job Summary: The Sr. Associate Manager CoDesign, Patient Engagement, CDDA will provide…
This is a remote position. We have an exciting opportunity for a Business Development Representative. Job Summary: Pharmavise is seeking a highly driven and communication-focused Business Development professional with…
Leads sustaining projects on the Urology Project Management team, collaborating cross-functionally and internationally to drive business-critical projects.
Lead software integration projects for a medical device client using agile methodologies and MS Project.
Develops and performs software systems testing/validation for medical device R&D/manufacturing, using Python and tools like Github/Bitbucket; analyzes requirements, documents work, and maintains quality standards.
UX/UI Designer crafting intuitive, user-centered experiences for internal business tools and applications. Works end-to-end from concept to implementation, uses Figma, and designs for data-heavy environments with complex visualizations.
Leads design assurance for medical devices, ensuring ISO14971 risk management and V&V processes. Focuses on quality plans, hazard analysis, testing, and compliance for medical device clients.
Supplier Quality Assurance Engineer II for a Fortune 500 medical device client, driving supplier quality improvement, CAPA investigations, and quality systems compliance in a hybrid role in Arden Hills, MN.
Role involves leading clinical trial projects focused on patient recruitment and retention strategies. Requires managing cross-functional teams and using systems like SAP, Ariba, and Excel to ensure efficient trial delivery.
Manages cross-functional projects for a medical device Quality organization using Microsoft Project to support post-market surveillance, risk management, and manufacturing quality operations.
Design custom automated test equipment (ATE) including circuits and software for FDA-regulated medical devices, supporting R&D verification and production testing.
Job Summary: Facilitate and process the transition of pricing and contracting data between systems. Provide support to the Pricing and Contracting teams including customer set up, establishing contracting records, and…
Oversee process improvement and integration projects for a medical device company, driving adoption of project management best practices and technologies while collaborating across teams.
Job Summary: Develops, establishes and maintains software quality engineering methodologies, programs, systems, and practices which meet Client , customer, and regulatory requirements. Serves as a Quality…
Our F500 Medical Device client has an exciting opportunity for a Process Engineer III. Job Summary: Develops new technology , products, materials, processes, or equipment with minimal supervision . Independently, or as…
Sr. Project Manager for an F500 medical device client, implementing and standardizing project management processes, managing process improvement projects, and ensuring quality compliance using Microsoft Project and Office Suite — onsite in Arden Hills, MN.
This is a remote position. We have an exciting opportunity for a Talent Acquisition Specialist. Job Summary: Pharmavise is seeking a highly driven, communication-focused Talent Acquisition Specialist to support…
Remote UX/UI Designer creating compliant digital interfaces for medical device and life sciences applications, primarily using Figma while adhering to FDA, ISO 13485, and IEC 62366 standards.
We couldn't check your fit for this role — add a CV to your profile to see it next time.