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Production Control Manager Jobs in Racine, WI (NOW HIRING)

Inventory Control Lead Department: Supporting Quality Employment Type: Full Time Location: SMC ... management for returned products throughout the repair process. Once a part of the team, you will ...

... management for returned products throughout the repair process. Once a part of the team, you will ... The Inventory Control Lead will coordinate inventory operations, provide guidance to inventory ...

Provides direction to the workforce in executing the schedule as worked out with Production Control. * Provide appropriate leadership and successful individualized communication. * Provide effective ...

Bachelor's degree in operations management, production control, or a related field. * 2-4 years of experience in production planning, with a strong understanding of MRP and ERP systems (preferably ...

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Production Control Manager information

See Racine, WI salary details

$29.1K

$80.7K

$129.9K

How much do production control manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for production control manager in Racine, WI is $80,694.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,800.00 and $96,100.00 per year, depending on experience, location, and employer.

What is a production control manager?

A Production Control Manager is responsible for overseeing and coordinating the scheduling, planning, and flow of production activities within a manufacturing facility. They ensure that production targets are met efficiently, materials and resources are properly allocated, and any potential delays or issues are addressed quickly. This role often involves working closely with other departments such as purchasing, inventory, and quality control to optimize production processes. Their goal is to maintain smooth operations and meet delivery deadlines while minimizing costs and waste.

What does a production control manager do?

A production control manager oversees day-to-day production activities and works to boost sales, efficiency, and labor productivity. As a production control manager, your duties involve managing production staff, coordinating machine repairs and maintenance, ensuring the project budget is met, and developing safety programs. Positions are most common with manufacturing and supply chain companies. A career as a production control manager typically requires at least an associate degree in engineering, business administration, or a related field, along with extensive experience in a factory setting. Some employers prefer a bachelor’s degree and prior management experience. Additional qualifications include strong interpersonal and managerial skills, as well as knowledge of the industry.

What are the key skills and qualifications needed to thrive as a production control manager, and why are they important?

To thrive as a Production Control Manager, you need expertise in production planning, inventory management, and supply chain logistics, usually supported by a bachelor’s degree in business, engineering, or a related field. Familiarity with ERP/MRP systems, Lean manufacturing tools, and production scheduling software is typically required. Strong analytical, leadership, and communication skills enable effective coordination across departments and quick problem-solving. These skills ensure efficient workflow, cost control, and timely delivery in fast-paced manufacturing environments.

How does a production control manager typically collaborate with other departments to ensure smooth workflow?

A Production Control Manager works closely with various departments such as procurement, manufacturing, logistics, and quality assurance to coordinate production schedules and resolve bottlenecks. They regularly communicate with team leads and supervisors to monitor progress, adjust plans in response to unforeseen challenges, and ensure that materials and resources are available when needed. This collaborative approach helps maintain efficient operations, minimize downtime, and meet delivery deadlines. Effective cross-department communication is key to success in this role.

What are the most commonly searched types of Production Control jobs in Racine, WI?

The most popular types of Production Control jobs in Racine, WI are:

What job categories do people searching Production Control Manager jobs in Racine, WI look for?

The top searched job categories for Production Control Manager jobs in Racine, WI are:

What cities near Racine, WI are hiring for Production Control Manager jobs?

Cities near Racine, WI with the most Production Control Manager job openings:

Infographic showing various Production Control Manager job openings in Racine, WI as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $80,694 per year, or $38.8 per hour.

Associate Manager, Document Control

Merz North America

Racine, WI • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago


Job description

About Us

Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history. As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine. Our purpose is to fuel confidence by helping people look better, feel better, and live better. We believe you do not have to choose between living life and making a living. Live your best life with Merz Aesthetics.

A Brief Overview

The Associate Manager, Document Control is responsible for providing tactical and strategic leadership for the Document Control Specialists and the process for the review and approval for Merz QMS Documents. Day-to-day activities include coordination, management and review of the document control team and their activities. Perform and/or assist with tasks required to oversee the proper creation, revision, approval and release of documents in accordance with the Merz QMS, regulations and standards. Oversee and/or assist with tasks related to the activities associated with operation of Merz North America Inc. Quality System and as directed. Provide direct support to Quality Management/Quality Assurance personnel regarding operation of the department and Quality System. Provide support to other departmental activities as directed.

What You Will Do

  • Management Manage Document Control department and personnel. Leverage the Document Control team to ensure that business goals, deadlines and performance standards are met.
  • Document Control Ensure all aspects of the Document Control Function effectively and efficiently meet global standards and regulations.
  • Adherence to Regulations and Standards Maintain awareness of changes to global regulatory requirements and relevant standards related to Quality Systems and support the appropriate requirement or standard owner to ensure effective implementation. Support Training activities. Support Training activities including: maintaining training records, supporting Department Training Coordinator (DTC) program, conducting organization wide training (as needed), assists with on-time training goals, conducts orientation for new personnel (iMERZion), and reviewing DCN training plans.
  • Process Improvement Initiatives Drive continuous improvement initiatives / projects for the Quality Systems Department
  • Supports Internal, External and Vendor Audit Functions Supports Internal, External and Vendor Audit Functions as needed

Minimum Requirements

  • Bachelor's Degree
  • 3-5 years Quality experience in Medical Device, Pharmaceutical and/or equivalent regulated industry
  • 2+ years Supervisor or Lead Experience

Preferred Qualifications

  • ASQ CQA or CMQ/OE

Technical & Functional Skills

  • Knowledge of regulatory requirements for medical device / pharmaceutical organization required.
  • Strong technical and general problem-solving skills; experience with NCR/CAPA processes
  • Medical and/or scientific terminology
  • Professional phone etiquette plus careful handling of sensitive information
  • Computer skills in Microsoft Word, Excel, PowerPoint, Visio and Access; Adobe; and Quality System Management Software.
  • Familiar with ISO 13485 Quality System Standards, FDA Quality System Regulations, GMPs, and/or other international medical device regulations
  • Organized, attention to detail
  • Highly effective communication skills. Ability to work with company staff and communicate effectively throughout the organization.
  • Manage multiple priorities and work with interruptions.

Benefits

  • Comprehensive Medical, Dental, and Vision plans
  • 20 days of Paid Time Off
  • 15 paid holidays
  • Paid Sick Leave
  • Paid Parental Leave
  • 401(k)
  • Employee bonuses
  • And more!

Your benefits and PTO start the date you're hired with no waiting period!

This position is not eligible for employer-sponsored work authorization. Applicants must be legally authorized to work in the United States without the need for current or future employer-sponsored work authorization.