Production Specialist (On-Site)

Clario is a 50+ year old company that delivers industry leading clinical trial endpoint technology solutions. The future of clinical trials is vibrant, with new technologies revolutionizing what's possible. From new trial modes to faster and integrated evidence and findings, our innovative clinical trial solutions mean we can unlock better evidence.

What we offer:

• Competitive compensation

• Medical, dental, and vision insurance beginning Day 1 of employment

• Flexible work schedules

• Attractive PTO plan

• Engaging employee programs

ESSENTIAL DUTIES AND RESPONSIBILITIES

Core Production Responsibilities:

• Assemble, solder, and configure electronic or mechanical devices for use in clinical trials or medical applications.

• Perform device-level inspections and quality control checks to ensure functionality and compliance with standards.

• Use handheld test equipment (e.g., voltmeters) to verify device integrity.

• Prepare and organize materials, tools, and workstations required for production.

• Accurately record production data and complete documentation in accordance with internal SOPs.

• Use applicable ERP system(s) to track inventory, record production steps, and close work orders.

• Attend and participate in daily production team meetings, sharing relevant area metrics and feedback.

• Respond professionally to internal requests related to production and device preparation.

Team Support and Training:

• Assist with onboarding and training of new hires within the production team.

• Lead product-specific training sessions in coordination with Product Management.

• Coordinate and conduct briefings or floor meetings, sharing updates and addressing production priorities.

QUALIFICATIONS AND SKILLS NEEDED

What we look for:

Work Location Requirement:

This position requires full-time, on-site work from our office, Monday through Friday (100% in-office). Candidates must have the availability and commitment to work from the office during standard business hours.

Mandatory Requirements:

Education:

High school diploma or GED equivalent.

Experience:

• Minimum of 2-5 years of hands-on experience in a production or manufacturing environment, ideally involving precision tasks.

• Proficiency in manual assembly, including soldering, component installation, and electronic device testing.

• Experience working in a fast-paced, detail-oriented production setting.

• Ability to operate standard electronic testing tools, such as handheld voltmeters.

• Demonstrated reliability and flexibility to work additional hours as needed.

• Ability to work independently and as part of a team, with minimal supervision.

• Strong organizational skills, excellent attention to detail, and a commitment to quality.

• Good time management and the ability to prioritize tasks effectively.

• Fluent in English (written and verbal).

Technical Skills:

• Proficient in Microsoft Office Suite, particularly Excel.

• Experience using Enterprise Resource Planning (ERP) systems in a production environment.

Nice to Have Qualifications:

• Experience with ISO-compliant documentation procedures, preferably ISO 9001 and/or ISO 13485.

• Previous experience in logistics, supply chain, or inventory control.

• Ability to train and onboard new employees, including preparation and presentation of materials.

• Experience in medical device assembly or regulated manufacturing environments.

• Basic knowledge of quality assurance standards and manufacturing best practices.

The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. The Company reserves the right to amend or change this job description to meet the needs of the Company. This job description and any attachments do not constitute or represent a contract.

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.