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Remote Medical Device Project Manager Jobs in Ladera Ranch, CA

Stryker

Manager, Clinical Data Research (Remote)

Irvine, CA · On-site +1

$116K - $193K/yr

Remote or Hybrid or Onsite The Manager, Clinical Data Research will oversee the end-to-end ... Minimum 8 years of experience in Clinical Data Management within the medical device, pharmaceutical ...

Stryker

Manager, Clinical Data Research (Remote)

Irvine, CA · On-site +1

$116K - $193K/yr

Remote or Hybrid or Onsite The Manager, Clinical Data Research will oversee the end-to-end ... Minimum 8 years of experience in Clinical Data Management within the medical device, pharmaceutical ...

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

This position plays a key role in supporting research projects at Diality, combing responsibilities ... device-specific regulatory pathways. * Experience with managing remote monitoring activities or ...

Socotec

Project Environmental Professional

Irvine, CA · On-site +1

Manage project schedules, budgets, deliverables, and client expectations. * Serve as a primary ... day remote/ hybrid schedule SOCOTEC is an Equal Opportunity Employer. SOCOTEC is an Equal ...

Socotec

Project Environmental Professional

Irvine, CA · On-site +1

$130K - $150K/yr

Manage project schedules, budgets, deliverables, and client expectations. * Serve as a primary ... day remote/ hybrid schedule SOCOTEC is an Equal Opportunity Employer. SOCOTEC is an Equal ...

PM2CM

Cost Engineer Hybrid-Remote

Anaheim, CA · On-site +1

PM2CM, Inc., (Project Management to Construction Management) is a professional services company ... Hybrid-Remote (Tuesday and Wednesday in the office/field) JOB OPPORTUNITY: WE ARE HIRING JUNIOR ...

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All JobsMedical Device Project JobsRemote Medical Device Project Manager JobsRemote Medical Device Project Manager Jobs in Ladera Ranch, CA

Remote Medical Device Project Manager information

See Ladera Ranch, CA salary details

$40.9K

$109.2K

$172.2K

How much do remote medical device project manager jobs pay per year?

As of Aug 8, 2026, the average yearly pay for remote medical device project manager in Ladera Ranch, CA is $109,154.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,400.00 and $130,800.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a remote medical device project manager?

To thrive as a Remote Medical Device Project Manager, you need strong project management skills, a background in engineering or life sciences, and knowledge of medical device regulations, often supported by a PMP certification or similar credential. Familiarity with project management tools like Microsoft Project, collaboration platforms, and regulatory submission systems (such as FDA eCTD) is commonly required. Exceptional communication, leadership, and problem-solving abilities help in leading cross-functional remote teams and managing stakeholders. These skills are crucial for ensuring regulatory compliance, timely product development, and effective coordination in a dispersed work environment.

What are some common challenges faced by remote medical device project managers, and how can they be addressed?

Remote Medical Device Project Managers often face challenges such as coordinating cross-functional teams across different time zones, maintaining clear communication with stakeholders, and ensuring regulatory compliance from a distance. These challenges can be addressed by establishing regular virtual meetings, using project management tools to track progress, and implementing standardized documentation practices. Building strong relationships with team members and fostering an open communication culture are also key to overcoming these hurdles and ensuring project success.

What does a remote medical device project manager do?

A Remote Medical Device Project Manager oversees the planning, execution, and completion of projects related to medical devices, all while working remotely. They coordinate cross-functional teams, manage timelines and budgets, ensure regulatory compliance, and communicate with stakeholders to keep projects on track. Their role is crucial for ensuring that new medical devices are developed efficiently and safely, meeting both company goals and industry standards.

What is the difference between Remote Medical Device Project Manager vs Remote Medical Device Quality Assurance Specialist?

AspectRemote Medical Device Project ManagerRemote Medical Device Quality Assurance Specialist
CertificationsPMP, CAPM, or equivalent project management certificationsISO 13485 Lead Auditor, CQE, or similar quality assurance certifications
Work EnvironmentOversees project timelines, teams, and deliverables remotely within medical device companiesEnsures compliance, audits, and quality processes remotely in medical device manufacturing or development
Employer & Industry UsageUsed by medical device firms managing product development projects remotelyCommon in companies focusing on quality standards and regulatory compliance remotely

The Remote Medical Device Project Manager focuses on managing project timelines, teams, and deliverables remotely, ensuring successful product development. In contrast, the Remote Medical Device Quality Assurance Specialist concentrates on maintaining quality standards, conducting audits, and ensuring regulatory compliance remotely. Both roles require specialized certifications and are vital in the medical device industry, often working in similar remote environments but with distinct responsibilities.

What job categories do people searching Remote Medical Device Project Manager jobs in Ladera Ranch, CA look for? The top searched job categories for Remote Medical Device Project Manager jobs in Ladera Ranch, CA are:
What cities near Ladera Ranch, CA are hiring for Remote Medical Device Project Manager jobs? Cities near Ladera Ranch, CA with the most Remote Medical Device Project Manager job openings:
Remote Medical Device Project Manager jobs near you

LabWare 8 LIMS Configuration & Integration Specialist

Stark Pharma Solutions Inc

Irvine, CA • Remote

Contractor

Re-posted 5 days ago

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Role: LabWare 8 LIMS Configuration & Integration Specialist

Location: Remote (California-Based Project)

Duration: Through March 2027 (Potential Extension)

Position Overview

We are seeking an experienced LabWare 8 LIMS Configuration & Integration Specialist to support a large-scale LabWare 8 upgrade initiative within a GMP-regulated pharmaceutical laboratory environment. This role will lead critical workstreams focused on configuring raw material and commercial product testing workflows, master data management, equipment integration, and validation support.

The ideal candidate will have extensive hands-on experience with LabWare 8 configuration, laboratory system integrations, and GMP laboratory operations, with the ability to deliver compliant and scalable LIMS solutions.

Key Responsibilities

  • Configure and implement LabWare 8 LIMS workflows supporting raw material and commercial product testing processes.
  • Lead master data configuration and management activities to support laboratory operations.
  • Design, configure, and optimize laboratory workflows while ensuring compliance with GMP and regulatory requirements.
  • Support integration of LabWare 8 with laboratory instrumentation and enterprise systems.
  • Collaborate with Quality, Validation, Laboratory Operations, and IT teams to ensure successful project execution.
  • Translate business, quality, and regulatory requirements into compliant LIMS configurations.
  • Support system validation activities, ensuring complete requirements-to-configuration-to-validation traceability.
  • Troubleshoot configuration, workflow, and integration issues while driving timely resolution.
  • Assist with user acceptance testing (UAT), system testing, and deployment activities.
  • Support inspection readiness efforts and ensure compliance with regulatory expectations for computerized systems.
  • Provide technical guidance and documentation throughout the project lifecycle.

Required Qualifications

  • 8+ years of experience working with Laboratory Information Management Systems (LIMS).
  • Strong hands-on experience configuring and implementing LabWare 8 LIMS.
  • Proven experience supporting LabWare upgrades, implementations, or enhancement projects.

Experience configuring workflows for:

  • Raw Material Testing
  • Commercial Product Testing
  • Laboratory Equipment and Instrument Workflows
  • Demonstrated experience supporting GMP-regulated laboratory environments.
  • Experience integrating LabWare with laboratory instruments and enterprise systems.
  • Strong understanding of computerized system validation (CSV) principles and documentation requirements.
  • Experience supporting validation deliverables with end-to-end traceability.
  • Excellent communication and stakeholder management skills within regulated environments.