Pharmavise Corporation

Quality Engineer I — Medical Device (Onsite — Arden Hills, MN) Possible Contract Extension

Job Purpose This 12-month contract role leads technical efforts at the Arden Hills Post Market Complaint Investigation Site (CIS), focusing on analyzing product performance data to investigate and escalate issues…

UX UI Designer — Medical Device (Hybrid — Spencer, IN) Contract-to-Hire

Agile API Bootstrap CSS Figma +11 skills

UX/UI Designer owning end-to-end design for internal business tools and data-heavy dashboards at a medical device company, using Figma and Bootstrap in a hybrid role in Spencer, IN.

Clinical Research Manager

Open 47d RemoteContract

This is a remote position. The Clinical Research Manager (CRM) is responsible for the strategic and operational oversight of clinical trials conducted across various phases. This role ensures that studies are executed…

CRM GCP

Open 47d RemoteFull-timeSenior

Business Development Manager – Life Sciences Consulting (US – Remote) Full-time

This is a remote position. We have an exciting opportunity for a Business Development Manager. Job Summary: We are seeking a motivated and results-driven Business Development Manager (BDM) to help Pharmavise expand its…

Business Development Cmos CRM Pre-sales

Clinical Data Manager

Data Quality GCP Oracle Veeva

This is a remote position. The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock. The CDM ensures that data is accurate,…

Open 47d RemoteNorth AmericaContract

Clinical Project Manager

Lead and manage clinical trials from initiation through closeout—overseeing timelines, budgets, vendors, and cross-functional coordination—while ensuring GCP/ICH compliance, using CTMS and MS Project in a fully remote role.

GCP PMP SAP

Quality Engineer

Corrective Action Iso 13485 Minitab Six Sigma Veeva

This is a remote position. We are seeking a talented and self-driven Quality Engineer to ensure all products, processes, and quality systems within the organization comply with applicable medical device regulations and…

Project Manager

ERP GCP Iso 13485 Jira PMP +4 skills

Experienced Project Manager for life sciences consulting in regulated GxP environments, leading cross-functional projects in pharmaceutical, biotechnology, and medical device organizations.

Learning Design Specialist — Medical Device (Hybrid — Maple Grove, MN) Possible Temp-to-Hire

Agile SharePoint Storyboarding Technical Writing

A Learning Design Specialist designs and develops learning materials for a medical device company's urology sales organization, collaborating with stakeholders to create engaging training experiences using eLearning tools like Articulate, ensuring quality and compliance.

Project Engineer

Agile Iso 13485 Smartsheet Stakeholder Management Vendor Management

This is a remote position. We are seeking a talented and self-driven Project Manager to lead cross-functional programs within the medical device industry, ensuring projects are executed on time, within scope, and in…

Open 47d HybridNorth AmericaContract

Associate Project Manager — Medical Device (Hybrid — Minnetonka, MN) Possible Contract Extension

As an Associate Project Manager, you lead sustaining projects on the Urology Project Management team, collaborating cross-functionally to drive business-critical projects and improve patient care.

PMP

Open 47d North AmericaContractSenior

Senior Software Engineer — Medical Device (Onsite — Irvine, CA) Possible Temp-to-Hire

Android Cybersecurity Embedded Systems Linux Reverse Engineering +2 skills

Senior Software Engineer for a medical device company, customizing and validating Android OS (v5) for a Class III device, focusing on cybersecurity, integration, and regulatory compliance. Core technologies include Android OS, AOSP, embedded systems, and medical device regulations (IEC 62304, ISO 14971).

Clinical Trials Manager – Patient Engagement (Direct Portfolio Project Manager) (Hybrid – Indianapolis, IN) Contract with Possible Extension

Manage clinical trial projects with a focus on developing and delivering patient recruitment and retention strategies for a Fortune 500 pharmaceutical client in a hybrid Indianapolis role.

UX UI Designer — Medical Device (Hybrid — Maple Grove, MN) Contract-to-Hire

Agile API Bootstrap CSS Figma +11 skills

Design intuitive internal business tools and dashboards for a medical device company using Figma and Bootstrap in a hybrid setting.

Open 47d North AmericaContractSenior

Senior Software Business Analyst — Medical Device (Hybrid — Maple Grove, MN) - Contract

Agile Azure Azure DevOps Confluence DevOps +7 skills

Bridges clinical users and dev teams to define requirements for medical device software, ensuring compliance with FDA, ISO 13485, and IEC 62304 standards using Jira and Agile methodologies.

Contract Lifecycle Management

Contract Administrator

Open 47d RemoteContract

This is a remote position. We are seeking an experienced Contract Administrator to support contract development, review, and negotiation activities for a leading organization in the medical device and life sciences…

Regulatory Affairs Biosimilars Per Diem Consultant

This is a remote position. From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our…

Regulatory Compliance

Open 47d HybridNorth AmericaContract

Legal Operations Specialist — Medical Device (Hybrid — Arden Hills, MN) Possible Temp-to-Hire

Our Fortune 500 Medical Device client has an exciting opportunity for a Legal Operations Specialist. Job Summary: Responsible for implementing and supporting project management processes. Candidate will establish and…

Process Engineer — Medical Device (Onsite — Maple Grove, MN) Contract

Process Improvement Six Sigma

Our F500 Medical Device client has an exciting opportunity for a Process Engineer. Job Summary: Leads clinical build line, own process development deliverables such as process validation documentation, characterize…