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Manager Ramp Operations Jobs in Menifee, CA (NOW HIRING)

Yard Staff - Part-Time

Perris, CA

$16 - $20/hr

About the team - Yard Operations We conduct hundreds of live auctions each year around the world ... Manages keys for equipment. * Operates forklift to load/unload stationary row equipment. * Boosts ...

Yard Staff - Part-Time

Perris, CA · On-site

$16 - $20/hr

Manages keys for equipment. * Operates forklift to load/unload stationary row equipment. * Boosts ... Parks sold equipment on the ramp. * Perform other duties as assigned. Qualifications * Good ...

Yard Staff- Part-TIme

Perris, CA

$16 - $20/hr

SmartEquip, an innovative technology platform that supports customers' management of the equipment ... About the team - Yard Operations We conduct hundreds of live auctions each year around the world.

Yard Staff- Part-TIme

Perris, CA · On-site

$17.65 - $22.06/hr

Manages keys for equipment. * Operates forklift to load/unload stationary row equipment. * Boosts ... Parks sold equipment on the ramp. * Perform other duties as assigned. Qualifications * Good ...

Work in a multidisciplinary team with other professionals such as the DevOps team, Managers, and ... You will be expected, within a short ramp-up period, to make major contributions to the product ...

Site Trainer

Moreno Valley, CA · On-site

$72K - $82K/yr

... operation schedules * Assist with launch activities and workforce ramp-up initiatives What We're ... Strong organizational and time management skills * Proficiency with Microsoft Office programs

... operation schedules * Assist with launch activities and workforce ramp-up initiatives What We're ... Strong organizational and time management skills * Proficiency with Microsoft Office programs

... operation schedules * Assist with launch activities and workforce ramp-up initiatives What We're ... Strong organizational and time management skills * Proficiency with Microsoft Office programs

Be Seen First

In this role, you will work closely with R&D, Regulatory, Operations, and other cross-functional ... minimal ramp-up * Experience with risk management in accordance with ISO 14971 * Experience ...

... case management * Participate in startup readiness activities including process development, warehouse layout reviews, equipment safety evaluations, and operational ramp-up planning * Support ...

Safety Specialist

Moreno Valley, CA · On-site

$75K - $92.50K/yr

... case management * Participate in startup readiness activities including process development, warehouse layout reviews, equipment safety evaluations, and operational ramp-up planning * Support ...

... case management * Participate in startup readiness activities including process development, warehouse layout reviews, equipment safety evaluations, and operational ramp-up planning * Support ...

Sales Coordinator

Riverside, CA · On-site

$28 - $36/hr

Gateway Fleets is a fast-growing fleet solutions company with an ambitious revenue ramp ahead. We ... quotes, manage contracts, and ensure accurate billing. You will serve as a key operational ...

Hybrid HIS San Diego

Murrieta, CA · Hybrid

$39.80K - $54.60K/yr

Support the launch and ramp-up of four new clinic locations, ensuring each meets operational and ... Coordinate with front office staff on scheduling, inventory management, and patient flow ...

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Showing results 1-20

Manager Ramp Operations information

See Menifee, CA salary details

$34.9K

$61.2K

$134.4K

How much do manager ramp operations jobs pay per year?

As of May 30, 2026, the average yearly pay for manager ramp operations in Menifee, CA is $61,169.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,300.00 and $73,000.00 per year, depending on experience, location, and employer.
What cities near Menifee, CA are hiring for Manager Ramp Operations jobs? Cities near Menifee, CA with the most Manager Ramp Operations job openings:
Quality Engineer - Instrumentation Quality Engineer

Quality Engineer - Instrumentation Quality Engineer

Aequor

Lake Forest, CA • On-site

$75.90K - $98.10K/yr

Other

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Job Description:

About the Role

In this role, you will work closely with R&D, Regulatory, Operations, and other cross-functional stakeholders to provide hands-on quality engineering support across the product development lifecycle. You will contribute to key activities such as design controls, risk management, verification and validation, supplier-related quality support, change control, and product transfer. The ideal candidate brings strong technical judgment, demonstrated quality capability, and the ability to operate independently in a fast-paced environment.


Major Accountabilities:

  • Provide hands-on quality engineering support for new product development projects and design changes to existing instrumentation products
  • Ensure quality requirements are appropriately applied throughout development, documentation, verification, validation, and transfer activities
  • Partner with project teams to provide practical quality guidance, technical assessment, and risk-based decision support that helps keep development activities moving forward
  • Review and approve design control deliverables, including risk management files, verification and validation documentation, and related development records
  • Evaluate product and process changes for quality and regulatory impact, and support change control activities from assessment through implementation
  • Partner with cross-functional teams to investigate deviations, support root cause analysis, and drive corrective and preventive actions as needed
  • Maintain compliance with applicable GxP requirements, standard operating procedures, and documentation practices


Minimum Qualifications

  • Bachelor’s degree in engineering, life sciences, or a related technical field
  • 2+ years of quality engineering experience in the medical device industry, including direct support of instrumentation or electromechanical product development in an ISO 13485 environment
  • Experience with design controls, change control, and product impact assessments
  • Working knowledge of applicable medical device quality system and regulatory requirements, including ISO 13485, design controls and GxP principles
  • Ability to work effectively across global, cross-functional teams, communicate clearly with technical and non-technical stakeholders, and contribute with minimal ramp-up
  • Experience with risk management in accordance with ISO 14971
  • Experience reviewing or supporting verification and validation protocols, reports, and related documentation

Preferred Qualifications

  • Statistical knowledge to support sample size determination and the design of verification and validation studies
  • Working knowledge of applicable product and safety standards, such as the IEC 60601 series and ISO 14971
  • ASQ Certified Quality Engineer (CQE) certification
  • Six Sigma Green Belt or higher

Strong communication, organization, collaboration, and independent problem-solving skills.