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Weekend Mrp Controller Jobs in California (NOW HIRING)

Be available to work OT and Weekends as needed. Qualifications: Required Qualifications: * High ... This position requires access to export-controlled information. To conform to U.S. Government ...

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Description Role Summary The Master Scheduler is responsible for centrally controlling and ... Maintain ERP/MRP and planning data accuracy to support planning decisions and reporting. * Prepare ...

Description: Role Summary The Master Scheduler is responsible for centrally controlling and ... Maintain ERP/MRP and planning data accuracy to support planning decisions and reporting. * Prepare ...

... for centrally controlling and coordinating the end-to-end order processing and operational ... Maintain ERP/MRP and planning data accuracy to support planning decisions and reporting. * Prepare ...

Experience with MRP/ERP systems (SAP, Oracle, Warp Drive etc.) Nice to Have * Strong computer ... Must be able to work extended hours and/or weekends as needed Compensation and Benefits: * Hourly ...

Production Coordinator

Los Angeles, CA · On-site

$24 - $30/hr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Experience with MRP/ERP systems (SAP, Oracle, Warp Drive etc.) Nice to Have * Strong computer ... Must be able to work extended hours and/or weekends as needed Compensation and Benefits: * Hourly ...

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Weekend Mrp Controller information

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Production/Industrial - Lead Operator - Manufacturing

Niktor

Fremont, CA • On-site

$27.50 - $30/hr

Other

Posted 7 days ago


Job description

Job Description: Lead Operator, Manufacturing
Location: Fremont, CA - Niche Diagnostics Division (NDX)
Standard Shift: 6:00 AM - 2:45 PM, Monday through Friday, flexible to occasional swing shift
About the Role
The Lead Operator is a working leader on the Filling manufacturing floor, partnering with the Supervisor and Manager to keep production running, develop people, and build a team where every operator can perform at their best. This role operates in a cGMP environment and includes handling DEA-controlled substances (Schedules I-V) in strict accordance with DEA, FDA
What You'll Do
• Lead, coach, and motivate a diverse team of operators to meet daily production goals.
• Facilitate daily tier meetings and accountability boards, keeping Supervisors/Managers informed on performance, challenges, and team morale.
• Promote a culture of safety, quality, and accountability, consistently modeling and reinforcing 4i values.
• Support the development of operators through training and performance feedback in partnership with leadership.
• Execute manufacturing and/or testing of complex products in compliance with cGMP, ensuring accurate and complete documentation while addressing nonconformance issues.
• Collaborate with cross-functional teams to prioritize work, resolve issues, and remove operational barriers.
• Ensure materials are prepared for work orders and that team members are effectively organized for daily execution.
• Review batch records, execute MRP transactions, and maintain documentation in alignment with cGMP and Quality System requirements.
• Support inventory management activities to maintain accuracy and availability of materials.
• Track and trend employee performance and equipment productivity, while identifying potential improvements
• Engage in 5S and continuous improvement initiatives, collaborating across departments to enhance processes and procedures.
• Represent the department in required meetings and communicate key updates
• Perform additional duties as assigned by department and/or Management.
Schedule and Flexibility
• Standard shift is 6:00 AM to 2:45 PM, Monday through Friday.
• Leads must be flexible to support after-hours overtime, flexible to swing shift demand and occasional weekend overtime as production demand requires.
What You Bring
Leadership Mindset
• You take ownership without being asked, and you bring the team with you.
• You build trust across a diverse workforce and adapt your style to get the best out of each person.
• You can have direct conversations with respect, hold the line on standards, and give credit publicly.
Experience
• 3-4 years in direct manufacturing and leadership experience with 1+ year in a lead, trainer, or coaching role.
• Working knowledge of cGMP, Quality System Regulations, and ISO, with comfort handling nonconformances and CAPAs.
• Hands-on experience operating and troubleshooting production equipment.
Skills
• Clear communicator across operators, peers, and management.
• Strong attention to detail with batch records, SOPs, and inventory transactions.
• Comfortable using MRP systems, electronic document systems, and Microsoft Office (Word, Excel, PowerPoint).
Education
High school diploma or equivalent required. College Degree preferred.
Physical and Work Environment
• Ability to lift up to 40 lbs. without assistance.
• Work in compliance with all Good Manufacturing Practices (GMP) and safety standards, including exposure to cold room/freezer environments (as low as -20°C) and loud equipment.
• Required use of Personal Protective Equipment (PPE), including lab coat, gloves, safety glasses, steel-toed shoes, and hearing protection.
• Responsible for handling and overseeing DEA-controlled substances (Schedules I-V); must successfully complete a background check, including controlled substance screening.
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