O1 Assembly Operator - Entry Level - Hardware

TechDigital Group; Loveland (CO); Vor Ort; USD 30.000 - 40.000; Vollzeit

Zusammenfassung

An established industry player is looking for an entry-level Assembly Operator to join their Hardware Manufacturing Team. In this dynamic role, you'll align, calibrate, and execute test methods while working closely with a team to ensure quality and efficiency. You'll follow established procedures, maintain training records, and contribute to a safe work environment. Ideal candidates will thrive in a goal-focused setting and have a passion for quality improvement. This position offers a unique opportunity to grow within a company that values teamwork and operational excellence.

Qualifikationen

• Must have 0-2 years' relevant experience, preferably in a regulated industry.
• Ability to read and follow standard operating procedures.

Aufgaben

• Align, calibrate, and execute test methods according to operational plans.
• Maintain a safe and clean working environment by complying with procedures.

Kenntnisse

Fluent English

Proficiency with Microsoft applications

Experience with hand tools

Troubleshooting

Ausbildung

High school degree or equivalent

Jobbeschreibung

O1 Assembly Operator - Entry Level - Hardware

Description: Our company is seeking a team member to join our Hardware Manufacturing Team. In this role you will align, calibrate and execute test methods of varied complexity according to operational plans and customer demand. Weâ€TMre looking for associates whom thrive in a team-oriented, goal focused environment. We operate using Daily Management principles, providing immediate guidance and feedback to our associates and focusing on daily, monthly, and quarterly objectives. Youâ€TMll be responsible for following established operation procedures, maintaining appropriate training records for your role, sustaining a smooth flow of material and the execution of work orders to on-time completion. Beckman Coulter, an operating company within Danaher, is a growing organization looking for associates who meet the qualifications below. Our work delivers both instruments and reagents to customers in hospital and laboratory environments, supporting patient health. KEY RESPONSIBILITIES: MUST read, write and speak fluent English to understand the SOP/work instructions provided. Proficiency with Microsoft applications. Experience with hand tools is a plus for some departments. Able to execute assembly tasks following standard operating procedures with supervision. Troubleshoot issues as they arise, escalating as necessary, Assure compliance with FDA Quality System Regulations (QSR). Good Manufacturing Practices (GMP), and ISO regulatory requirements; Learn and participate in the company's lean manufacturing principles. Work directly and cooperatively with cross-functional team members to troubleshoot issues and ensure emphasis on quality. Identify and recommend quality improvements including but not limited to production methods, equipment performance, product quality and efficiencies. Maintain a safe and clean working environment by complying with procedures, rules, and regulations. Train new team members on equipment operations and work procedures as needed. Ability to complete appropriate paperwork, maintain accurate records of production and report status of work. PHYSICAL DEMANDS: While performing the duties of this job, the associate is regularly required to stand for prolonged period of time. The employee is frequently required to talk and hear; use hands to handle or feel; and reach with hands and arms above shoulder height and below the waist. The associate must be able to read and speak English. Using proper lifting techniques, the employee must be able to lift up to 30 lbs. Ability to maneuvers assembly components by hand in a repetitive manner conducive to efficiency, job specifications, safety, and quality goals. Ability to frequently stand (80%), bend, kneel, lift and sit to accomplish assembly production goals. EDUCATION/EXPERIENCE: High school degree (or equivalent degree). Must have 0-2 years' relevant experience. Experience in a regulated industry preferred (e.g. FDA, ISO).