Top 12 Quality assurance manager Jobs in Springfield, Mo

Senior Quality Manager
Zimmer Biomet —Springfield, MO
- $130,000 - $160,000 a year
- Full-time
- 5 years
- Bachelor's degree
- Mentoring
- Wellness program
1d
Quality Assurance Manager, MT
LinkOne Ingredient Solutions —Springfield, MO
- $70,000 - $82,000 a year
- Weekends as needed
- Microsoft Excel
- Up to 50% travel
- 5 years
Quick Apply
ASME Code & Quality Manager
G2 Material Handling, Inc —Springfield, MO
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
- Health insurance
- Dental insurance
Quick Apply
19h
Manufacturing Quality Supervisor
Central States Industrial —Springfield, MO
- $29 - $34 an hour
- Full-time
- Mid-level
- US work authorization
- Leadership
- Health insurance
- Paid time off
Quality Manager - Springfield Remanufacturing Corp
SRC Holdings Corp. —Springfield, MO
- Management
- 5 years
- Engineering
- Paid holidays
- Health insurance
Quick Apply
Construction Quality Control Manager- USACE
Thalle Construction Company —United States
- Full-time
- Construction site
- In-person
- Senior level
- Paid holidays
- Disability insurance
Quick Apply
Quality Control Manager- Dam Project
Thalle Construction Company —United States
- Full-time
- Construction site
- In-person
- Senior level
- Paid holidays
- Disability insurance
Quick Apply
Project Manager - Air Quality
SWCA Environmental Consultants —United States
- $102,047.40 - $134,152.20 a year
- Online Application
- Remote
- 7 years
- Bachelor of Science
- Engineering
- Profit sharing
- Health insurance

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For positions that require any amount of travel: Valid driver's license, auto insurance (at least state minimum- more might be required), acceptable driving…
Senior Quality Manager
Zimmer Biomet —Springfield, MO
A Bachelor’s Degree in a technical field is required. Demonstrated independent decision-making ability applying regulations and standards related to the…
$130,000 - $160,000 a year
1d

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Senior Quality Manager

Zimmer Biomet -
Springfield, MO

Apply Now

Job Details

Full-time
$130,000 - $160,000 a year
1 day ago

Benefits

Wellness program

Qualifications

Organization design
ISO standards
Talent management
GMP
Team development
Bachelor's degree
Medical device manufacturing facility experience
Regulatory/legal compliance standards in production
Biomedical regulatory compliance
Legal compliance
Cross-functional communication
Senior leadership

Full Job Description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging.

What You Can Expect

This is an onsite role at our site in Norfolk, Virginia

Site Quality leader and Management Representative responsible for directing the quality function a medical device design and manufacturing site. Utilizes quality statistics to develop effective strategies to maintain and improve the performance of products and the quality system. Develops relationships with key development and manufacturing peers to identify emerging needs. Resolves complex problems that have implications beyond own area. Requires professional expertise and interpersonal skills to manage multiple projects and interface with personnel from all company disciplines and business units. Takes accountability, achieves results and develops self and others.

How You'll Create Impact

Develop and implement site-wide quality strategy aligned with corporate objectives and regulatory requirements (QMSR, GMP, ISO, and other global standards) including objectives, and planning to support the strategy.
Establish and refine key quality metrics, ensuring data-driven decision-making to enhance product integrity and regulatory compliance.
Partner with R&D, supply chain, manufacturing, and distribution teams to enhance quality processes across the product lifecycle and drive cross-functional teamwork to improve operational efficiencies, ensuring seamless integration of quality in all aspects of pharmaceutical production.
Serve as the primary quality representative during regulatory inspections and audits, ensuring adherence to industry and corporate standards.
Build, mentor, and lead a high-performing quality assurance and quality control (QA/QC) team, fostering a culture of collaboration and accountability.
Empower team to lead investigations into deviations, CAPA (Corrective and Preventive Actions), and change control processes to improve operational resilience and ensure timely product release and market supply by resolving quality-related issues effectively

What Makes You Stand Out

Must have a thorough knowledge of QMSR, GMP, ISO and other relevant regulatory requirements as applied to medical device development, manufacturing and distribution.
Demonstrated independent decision-making ability applying regulations and standards related to the manufacturing and distribution of medical device products.
Demonstrated management ability including organizational design and employee selection, development, motivation and performance.
Demonstrated ability to achieve productivity goals collaboratively without sacrificing quality in a manufacturing environment.
Demonstrated understanding of interactions and interdependency of elements within the quality system in a pharmaceutical manufacturing organization.
Must be able to work with all levels of employees, including hourly production employees through senior management.
Must possess excellent written and oral communication skills and the demonstrated ability to communicate with individuals of varying backgrounds.

Your Background

A Bachelor’s Degree in a technical field is required
7-10 years of work experience in medical device quality, preferably in manufacturing environments
5 years’ experience with direct management responsibility
CQE/CQM preferred

Expected Compensation: $130,000- $160,000 base salary. Role also comes with a comprehensive bonus.

EOE

Apply Now

Refine Your Search

quality assurance manager jobs in springfield, mo

Senior Quality Manager

Quality Assurance Manager, MT

ASME Code & Quality Manager

Manufacturing Quality Supervisor

Quality Manager - Springfield Remanufacturing Corp

Construction Quality Control Manager- USACE

Quality Control Manager- Dam Project

Project Manager - Air Quality

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