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Salary
$21k – $46k per year (Estimated)
Location
In office (Shanghai)
Seniority
Senior
Employment
Full-Time
Overview
Company
Impact
Profile match
Clario is a healthcare technology company headquartered in Philadelphia, Pennsylvania, with a history dating back to 1972. The organization provides clinical trial endpoint technology and services, including electronic clinical outcome assessments, medical imaging, cardiac safety monitoring, and respiratory solutions. It operates on a global scale, supporting pharmaceutical and biotechnology firms through all phases of clinical research to generate high-quality evidence for regulatory submissions.

Join Clario, a part of Thermo Fisher Scientific and play a critical role in preparing and managing the clinical trial devices that support research studies around the world. As a Senior Production Representative, you will be responsible for provisioning, configuring, quality checking, and preparing clinical trial equipment for deployment while ensuring compliance with established procedures, quality standards, and timelines. You will serve as a subject matter resource within the production environment, contribute to operational excellence, and help ensure that study equipment is delivered accurately and efficiently to support the successful execution of clinical trials.

What We Offer

  • Competitive compensation and incentives

  • Pension, social insurance, and housing fund

What You'll Be Doing

  • Configure, provision, and prepare clinical trial devices and equipment for deployment in accordance with study requirements and operational procedures.

  • Perform quality control reviews to verify the accuracy and completeness of device provisioning activities.

  • Ensure all equipment, materials, and study-related components are prepared and available to support project timelines.

  • Maintain accurate provisioning records and documentation in accordance with quality and regulatory requirements.

  • Utilize Enterprise Resource Planning (ERP) systems to track inventory, device status, and production activities.

  • Complete device provisioning activities across multiple Digital Physiology Solutions and clinical trial service lines.

  • Monitor daily production priorities and support achievement of operational metrics, quality goals, and delivery commitments.

  • Participate in daily operational meetings and communicate status updates, risks, and performance metrics related to assigned responsibilities.

  • Support continuous improvement initiatives that enhance efficiency, quality, and productivity within the production environment.

  • Train, mentor, and support onboarding activities for new team members while sharing best practices and operational knowledge.

  • Collaborate with cross-functional stakeholders to ensure equipment readiness and successful project execution.

  • Identify, escalate, and help resolve production, equipment, inventory, or process-related issues that may impact study delivery.

Additional Responsibilities

  • Perform inspection, troubleshooting, and repair of study devices returned from customers or field locations.

  • Conduct final testing and verification activities in accordance with applicable repair and quality procedures.

  • Maintain accurate repair documentation and ensure devices meet established quality standards before reissue.

  • Support inventory management, asset tracking, and operational readiness activities as required.

What We Look For

  • Bachelor's degree in Business Administration, Engineering, Supply Chain Management, Operations Management, or a related field preferred.

  • Equivalent experience in logistics, supply chain, manufacturing, engineering, production operations, or related environments will be considered.

  • Apprenticeship, vocational training, or professional experience in industrial, logistics, manufacturing, or operational environments is advantageous.

  • 0 to 3 years of experience in production operations, logistics, supply chain management, manufacturing support, or related fields.

  • Experience working in a fast-paced operational environment while managing multiple priorities and deadlines.

  • Strong attention to detail with a commitment to accuracy, quality, and process compliance.

  • Experience with Enterprise Resource Planning (ERP) systems strongly preferred.

  • Proficiency with Microsoft Office applications, including Excel, Word, Outlook, and Teams.

  • Strong organizational, communication, and problem-solving skills.

  • Ability to work independently while collaborating effectively across teams and departments.

  • Demonstrated ability to mentor or support less experienced team members.

  • Strong time management skills with the ability to prioritize competing responsibilities.

  • English language proficiency required; Mandarin language skills preferred for local operational support.

  • Professional presence with the ability to communicate effectively with leadership, internal stakeholders, and cross-functional teams.

At Clario, a part of Thermo Fisher Scientific, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work-and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

EEO Statement

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

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