Manufacturing Associate - Weekend Shift (Rancho Cucamonga, CA)

Cedent; Rancho Cucamonga (CA); On-site; USD 35,000 - 50,000; Full time

Job summary

A leading manufacturing company in Rancho Cucamonga seeks a Manufacturing Associate who will be responsible for operating production equipment, building product subassemblies, and ensuring quality through inspections using precise tools. The ideal candidate should possess at least a high school diploma, with a preference for an associate degree, and a minimum of 2 years of laboratory experience, preferably in medical devices. Strong communication skills and the ability to lift 25lbs are essential for this role.

Qualifications

• Minimum High School diploma, Associates degree preferred.
• 2+ years of laboratory experience, preferably in medical devices.
• Must have experience working in a cleanroom environment.

Responsibilities

• Operate production equipment according to good manufacturing practices.
• Build product subassemblies and perform final packaging tasks.
• Inspect materials and finished products for quality.

Skills

Communication

Record keeping

Team player

Flexibility

Ability to lift 25 lbs

Education

High School diploma

Associates degree

Lean manufacturing or Six Sigma certification

Laboratory experience

Tools

Microscope

Computer

Job description

The Manufacturing Associate’s responsibilities include but are not limited to: lifting 25lbs over 8 hours of continuous repetitive motion, using 10x microscope and magnifying glass for inspections, building product subassemblies, molding product subassemblies, final assemblies and final packaging, preparing and assembling material, setting up and operating production equipment in accordance with current good manufacturing practices and complying with regulatory and quality system procedures.

Essential Job Duties and Responsibilities

• Start up and shut down processing equipment
• Build product subassemblies and final assemblies
• Test products or subassemblies for functionality or quality
• Measure and record data associated with operating equipment
• Control machines and operate processes
• Set up and operate production equipment
• Assist engineering team in developing, building, or testing new product, processes or procedures
• Inspect subassemblies and finished products for quality using 10x microscope and magnifying glass
• Prepare materials for final packaging and package final product for delivery
• Plan and arrange work to meet production requirements
• Clean production equipment and/or work areas
• Provide information to supervisors and co-workers by telephone, in writing, email, or in person

Requirements

Knowledge, Skills and Abilities

• Ability to communicate in writing and orally with supervisors and co-workers
• Ability to read, write and understand information and ideas presented in writing
• Good record keeping and documentation skills
• Must adhere to all applicable regulations, and quality system procedures
• Able to work on a diverse team
• Ability to be cross‑trained
• Flexibility and a team player
• Able to lift 25lbs

Education and Experience

• Minimum High School diploma, Associates degree preferred
• 2+ years of laboratory experience, preferably in medical devices
• Must have experience working in cleanroom environment
• Lean manufacturing and/or Six Sigma certified, a plus
• Microscope experience, a plus

Physical Requirements

• Must be able to remain in a stationary position for a certain amount of time.
• Occasionally move about inside the cleanroom and travel to and from office buildings to access supply cabinets, setup and operate equipment, employee offices, office machinery, etc. This may include, but is not limited to, bending and walking.
• Must be able to operate a computer and other office productivity machinery, such as a computer printer, computer keyboard, calculator, etc.
• Ability to listen and speak with employees and vendors. Must be able to exchange accurate information in these situations.
• Occasionally lift up to 25 pounds and transport to other offices. This may be performed with reasonable accommodation.
• View and type on computer screens for a certain amount of time.
• Must be able to read and manually conduct inspection processes and procedures with provided tools.
• Role may require performing functions within a controlled environment under standard gowning requirements for an extended amount of time.