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Production specialist
Contract: Irvine, California, US
Salary Range: 29.00 - 33.00 | Per Hour
Job Code: 361311
End Date: 2025-05-23
Days Left: 12 days, 12 hours left
To discuss more about this job opportunity, please reach out to Deepak Arya (LinkedIn URL - www.linkedin.com/in/deepak-arya-8a79aa22a/), email your updated resume at Email - deepak.arya@collabera.com or give me a call at (425)-298-1474. Thank you!
Pay rate: 29 - $33/hr.
Industry: Medical Devices
Shift Timing: 3 PM to 11.30 PM
Key Responsibilities:
- Assists in coordinating production activity in assigned work areas, ensuring that product is continuously processed in accordance with build schedules
- Coordinates communication of work instructions to personnel in designated areas in accordance with supervisory objectives
- Ensures that quality and production goals are met
- Performs regular process and quality performance audits of personnel, tooling, and equipment in assigned areas
- Advises supervisor or other appropriate contacts in the event of equipment failure
- Accumulates information for assigned areas regarding work in process inventory status and daily output quantities
- Provides feedback on defects encountered, and provides re-training support as necessary
- Provides assistance in expediting priority products and tasks in assigned areas
- Performs inspection and determines the disposition of rejected components per required documentation, as directed
- Resolves and/or facilitates resolution of problems, including identifying causes to prevent re-occurrence
- Daily meeting with manufacturing operators for better communication and continuous improvement
- Ensures PM (preventive maintenance) and Calibration stickers are up to date 5S audit and weekly meetings with other area value stream group leads in an organization
- Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
- Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments
- Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors
- Performs other related duties and responsibilities, on occasion, as assigned
Required Qualifications
- 1-3 years of experience as a group-lead in a manufacturing environment
- Associate degree in Electrical/Mechanical Technology, or other comparable specialized training in and working knowledge of the manufacture of medical devices or their equivalent
- 4 or more years of progressively more responsible assembly experience, including the ability to provide work/lead direction to a team
- Desired demonstrated knowledge of LEAN manufacturing, assembly, and production technical skills and quality practices
- Prior experience working in a clean room manufacturing environment
- Demonstrated organizational skills, attentiveness to detail, and the ability to work under minimal supervision are required
Job Requirement
- Assembler
- Production
- Manufacturing
- QMS
- FDA
- EMS
- Inspection
Reach Out to a Recruiter
- Recruiter
- Phone
- Deepak Arya
- deepak.arya@collabera.com
Apply Now
Apply Now
