Post job

Quality manager jobs in Springfield, MO

- 22 jobs
All
Quality Manager
Quality Control Supervisor
Quality Assurance Manager
Quality Engineer
Quality Program Manager
Director Of Quality Management
Senior Quality Engineer
Quality Specialist
  • Quality Manager

    Vital Farms 4.5company rating

    Quality manager job in Springfield, MO

    Finding the right place to grow your career isn't (over) easy, so we're here to help by sharing a few reasons why the grass is greener at Vital Farms. We think you'll appreciate our focus on Conscious Capitalism, which drives business decisions that benefit all our stakeholders (leading to even better business results). You might be drawn to our innovative approach and refusal to settle for the “way things have always been done.” Or you could find it exciting to grow your skills while working for an industry-leading brand. Whether you're into our values, our brand, or our egg-cellent puns, we hope you'll join our Crew and help us change the world 108 square feet at a time! At Vital Farms, we're proud of the diverse communities we serve and the stakeholders who help bring our purpose to life. We're committed to fostering an inclusive and collaborative environment where every crew member feels valued. We see this as one of our greatest strengths - and your role is key to helping us build on it. Your Role: As the Vital Farms Quality Manager, you are passionate about food safety, quality, compliance, and training others. You are the designated plant champion to instill training and expectations to crew members that promote the production of safe, quality products in a sanitary environment. You care for people and love to create a good process. You feel rewarded by creating a culture of compliance, where crew members are trained and empowered to keep themselves and others working with the best systems and processes. You are a natural leader willing to step in to hold people accountable. You're not afraid to speak up when you see something that either doesn't seem right, or you know could be done better. You collaborate with leaders to find the best possible ways to teach our crew, support the needs of the business and stay aware of all best practices regarding food safety, quality assurance, sanitation and regulatory compliance, while behaving as a brand ambassador of Vital Farms' core values. What You'll Do: Champion Food Safety & Quality - Serve as the primary crew member responsible for Food Safety, Quality, Sanitation, and Regulatory Compliance at Egg Central Station, ensuring every egg that leaves our facility reflects the Vital Farms promise. Lead with Collaboration - As a key member of the ECS Leadership Team, partner closely with Operations, Maintenance, and SRW to foster a culture of teamwork, Food Safety, and efficiency, all while supporting the broader vision of Vital Farms. Design & Maintain Best-in-Class Programs - Develop, implement, and continuously improve Food Safety and Quality programs, policies, and procedures that meet regulatory and customer requirements while embracing industry best practices, with support from the Director of FSQA. Coach & Grow the Quality and Sanitation Teams - Lead, mentor, and work alongside our crew in the lab and on the plant floor, building a strong, engaged team that takes pride in protecting our brand and delighting our customers. Educate & Empower Crew Members - Create and deliver training on Food Safety and Quality topics (e.g., GMPs, HACCP, Food Defense, Allergens), equipping all crew with the knowledge and skills to carry out their work with excellence. Own Audit & Compliance Leadership - Serve as the SQF Practitioner and Internal Audit Team Leader, ensuring readiness for internal and external audits and representing Vital Farms with regulators, customers, and vendors. Protect Product Integrity - Oversee the final disposition of all products at ECS, ensuring materials that do not meet specifications are properly identified, reported, and resolved in alignment with company policy. Drive Continuous Improvement - Monitor data, review production paperwork, and analyze customer feedback to identify trends, resolve issues, and recommend improvements that strengthen our Food Safety culture and systems. Ensure Operational Excellence - Confirm all audits, inspections, and corrective actions are completed on time and to standard; oversee the maintenance of lab equipment and supplies to support reliable testing. Support Growth & Innovation - Partner with cross-functional teams to ensure Food Safety and Quality considerations are actively integrated into new business opportunities and innovations. What You Bring to the Table: This role is based onsite in Springfield, Missouri. Candidates must reside within a reasonable daily commuting distance. Bachelor of Science degree, preferably in Food Science, microbiology, or chemistry and/or equivalent work experience 5+ years of relevant experience, with a focus on compliance and regulatory requirements and industry standards and best practices. Minimum 2 years in a leadership or supervisory capacity required, with a proven ability to develop and mentor quality team members Ability to travel 10-20% travel for company events, team meetings, company onboarding and other business needs Comprehensive knowledge of Food Safety and Quality programs including HACCP Technical knowledge of analytical test methods. Knowledge of quality tools, quality trend reporting, advanced computer and writing skills, regulatory and compliance guidelines. Be FSMA PCQI, SQF Practitioner and HACCP Certified. Ideally will have developed and implemented all paperwork and training as it relates to FSMA Regulations and SQF Code Certification. Ability for strategic innovation thinking and strong communication skills required. Bilingual (Spanish) is a plus. Have a positive can-do attitude, good organizational skills, and the ability to work well both independently and as a member of a team. Proficient Microsoft Office skills Strong troubleshooting and problem resolution skills Ability to communicate with others in an effective and concise manner Ability to work well under pressure and meet deadlines through prioritization of tasks Consistent and punctual attendance is an essential function of the position You're no hero - You know the power of teamwork and celebrate the work of others before your own. You give a sh*t - You believe in acting like an owner and making Vital Farms a place to be proud of. You raise the standards - You know growth can be hard, but you strive to improve yourself and others each day. You can walk in someone else's boots - You seek to understand other's viewpoints and think that you get to better answers by sitting on the same side of the table. You don't walk on eggshells - You're not afraid to leave the bullsh*t behind and have honest conversations. We recognize that talent comes in many forms. Even if you don't meet every requirement, we encourage you to apply. You may have strengths we haven't yet considered! What We Bring to the Table: A fast-paced, energetic environment with passionate people who are leading a movement to bring ethically produced food to the table. Competitive pay and benefits (Medical, Dental, Vision, and Paid Parental Leave, just to name a few). Generous retirement contributions: 401(k) + 3% Contribution from Day 1. Free eggs and butter (yes, really!), along with friends and family discounts. Fun team SWAG that will make you the talk of the town. Professional development opportunities and an amazing team dedicated to your growth. At Vital Farms, compensation decisions are dependent upon a variety of factors, which may include, but are not limited to, skill level, experience, education, training, market demands, and business needs. A reasonable estimate of the current starting annual base salary for this position is $115,000 - $130,000. Please keep in mind that hiring at the maximum end of the range would not be typical in order to allow for potential continued future salary growth. Who We Are: Vital Farms, a Certified B Corporation, offers a range of ethically produced foods nationwide. Started on a single farm in Austin, Texas, in 2007, Vital Farms became a national consumer brand that works with 350 family farms and is the leading U.S. brand of pasture-raised eggs by retail dollar sales. Vital Farms' products, including shell eggs, butter, hard-boiled eggs, and liquid whole eggs, are sold in over 24,000 stores nationwide. Vital Farms' ethics are exemplified by its focus on the humane treatment of farm animals and sustainable farming practices. In addition, as a Delaware Public Benefit Corporation, Vital Farms prioritizes the long-term benefits of each of its stakeholders, including farmers and suppliers, customers and consumers, communities and the environment, crew members, and stockholders. In short, we exist to improve the lives of people, animals, and our planet through food. Commitment to Equal Opportunity To fulfill Vital Farms mission of bringing ethically produced food to the table, we're committed to building teams that reflect diverse perspectives and lived experiences. We believe that when all crew members feel valued and respected, they bring their best ideas forward - fueling innovation, belonging, and shared success. We strive to create a welcoming environment rooted in equal opportunity and encourage individuals from all backgrounds and experiences to apply. To that end, we make employment decisions based on qualifications, merit, and business need. Vital Farms does not discriminate on the basis of race, color, religion, gender and gender identity, sex (including pregnancy, childbirth, lactation and related medical conditions), sexual orientation, marital status, age, national origin, citizenship status, military or veteran status, physical or mental disability, genetic information or any other characteristic protected by applicable law. Ready to Join Us? Together, we're cultivating an environment where every Crew member can thrive, grow, and know they're part of something bigger - improving lives through ethical food. If this role sounds like the right fit for you, we'd love to hear from you! Even if you don't meet every qualification, we encourage you to apply - you might be exactly what we need! Next Steps: Shortly after you complete your application, you'll receive a follow-up email elaborating on any potential next steps in our process. If you don't immediately receive said follow-up email, we would highly encourage you to check your spam filter! In order to fulfill Vital Farms mission to “bring ethically produced food to the table,” we seek to build teams that leverage diverse perspectives to create a welcoming and innovative environment that is committed to the principles of equal employment opportunities. To that end, we make employment decisions based on qualifications, merit, and business need. Vital Farms does not discriminate on the basis of race, color, religion, gender and gender identity, sex (including pregnancy, childbirth, lactation and related medical conditions), sexual orientation, marital status, age, national origin, citizenship status, military or veteran status, physical or mental disability, genetic information or any other characteristic protected by applicable law. Notification to Agencies: **Vital Farms is not accepting unsolicited third-party recruitment agencies in the hiring process for this role. If you are a potential candidate interested in a role with Vital Farms, please submit an application directly. California Applicants: Please see our California Employment Candidate Privacy Statement for more information about how we collect, use, retain, and disclose personal information as part of our recruitment and hiring process.
    $115k-130k yearly Auto-Apply 60d+ ago
  • Mgr - Quality

    All Realtruck Career

    Quality manager job in Springfield, MO

    The Manager of Quality will develop, implement, maintain, and lead the Quality Management System for multiple manufacturing plants and/or distribution facilities. The Manager will function as a part of the plant senior leadership team who sets short and long-term strategy as it relates to the Quality Management System. The manager will be responsible for continuous improvement initiatives for all aspects of the functional area. This position will manage a staff of quality supervisors and inspectors. CORE FUNCTIONS · Develop and maintain strong relationships with operations management, engineering, sales, and dealer-based customers to understand business, quality, and customer needs. · Manage the staff of Quality Supervisors and Inspectors. Provide performance feedback, guide, mentor, and manage workload activities. · Communicate and collaborate with Operations management on the implementation of quality objectives and corporate objectives to maximize product quality and minimize cost. · Responsible for all aspects of maintaining ISO and/or IATF certification for all manufacturing facilities and implementing any additional quality related business certifications. · Identify recurring quality defects and conduct root-cause analysis and implementation of corrective action for process and quality system related concerns. · Establish and drive quality objectives for the business and strategic initiatives related to the quality system. · Lead continuous improvement activities to enhance the quality system. Conduct audits, including closing out audit findings, creating audit finding reports, and determining proper corrective and preventative actions. · Resolve all customer quality complaints, assigns corrective actions and provides feedback to customers on a resolution. · Ensure timely resolution of supplier failure, corrective actions and preventative actions. · Manage, facilitate, and/or implement automotive Quality Core Tools including APQP, Control Plans, PPAP, FMEA, SPC, and MSA as needed. · Manage key metrics and report to the leadership team. QUALIFICATIONS & REQUIREMENTS Education and Experience · Bachelor's degree in Quality Engineering, other engineering, or a related field is preferred. In lieu of degree 10+ years of quality in a manufacturing field required. · 7+ years of quality systems experience required, including 1-3+ years of leadership experience required, preferably in a manufacturing and assembly environment. · Previous ISO 9000:2015 / IATF 16949 experience is required Required Licenses · CQU (Certified Quality Engineer) or other ASQ certification preferred. · SPC and/or Lean Six Sigma certification is desired. Skills, Abilities, and Knowledge · Ability to communicate with and interact with production team members. · Ability to present and provide data to top management. · Ability to identify issues and inefficiencies and to implement and drive changes. · Proficient in quality database systems and Microsoft Office suite. · Ability to compute rate, ratio, and percent, and to draw and interpret graphs. Availability · Flexibility to support a 2-shift operation, which may include occasional Saturdays. Travel · Occasional Travel as needed for training and corporate events. COMPETENCIES · Adapts to changes in the work environment; Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events. · Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data; Designs work flows and procedures. · Responds promptly to customer needs; Responds to requests for service and assistance; Meets commitments. · Displays willingness to make decisions; Exhibits sound and accurate judgment; Supports and explains reasoning for decisions; Includes appropriate people in decision-making process; Makes timely decisions. · Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations; Uses reason even when dealing with emotional topics. · Looks for ways to improve and promote quality; Demonstrates accuracy and thoroughness. · Balances team and individual responsibilities; Exhibits objectivity and openness to others views; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed. SUPERVISOR RESPONSIBILITIES · This position plans, staffs, evaluates, and directs the work of employees of a work unit. This position will have direct reports. PHYSICAL REQUIREMENTS · This position may be required to exert up to 20 pounds of force occasionally and/or a negligible amount of force constantly to move objects. The use of arm and/or leg controls require exertion of force greater than that for sedentary work. Physical Activities · This position is subject to the following activities: stooping, kneeling, crouching, reaching, standing, walking, lifting, grasping, feeling, talking, hearing and repetitive motions of the wrists, hands, and/or fingers. Visual Acuity · This position is required to have close visual acuity to perform activities such as preparing and analyzing data and figures, transcribing, viewing a computer terminal; expansive reading; visual inspection involving small defects, small parts and/or operation of machines (including inspection); using measurement devices; and/or assembly of fabrication of parts at distances close to the eyes. Working Conditions · This position may be subject to a variety of physical conditions, such as exposure to atmospheric conditions that affect the respiratory system of the skin.
    $52k-86k yearly est. 18d ago
  • Quality Manager

    Hikinex

    Quality manager job in Springfield, MO

    / TITLE: Quality Systems Manager Drive activities concerned with the development, application, maintenance, and improvement of the company's Quality Management System (QMS), presently IATF 16949. This role directs supplier quality personnel to ensure the conformance of inbound materials and directs production quality personnel to ensure the conformance of outbound products. The position provides functional leadership for the IATF Program Manager in the successful execution of audits and certifications. A key responsibility is to work collaboratively with the Manufacturing Engineering team on continuous improvement initiatives and to provide leadership in transforming the quality management system and product quality across the entire organization. Essential Duties & Responsibilities: Partner with the IATF Team to develop and improve procedures and forms for all supporting Quality Management System processes. Utilize root cause analysis methodologies (e.g., Practical Problem Solving, 8D) to address all gaps discovered during internal and external quality management audits. Participate in and support root cause analysis to address external and internal quality-related problems. Use dFMEA and pFMEA tools to identify risks and actively lead initiatives to mitigate those risks, protecting the company from field exposure associated with non-conformance. Establish and maintain quality control plans. Using dFMEA and pFMEA, identify critical control points requiring error-proofing (poka-yoke) and/or data collection. Identify and execute appropriate sampling plans. Proactively reduce the frequency and costs of control plans as risk levels are lowered. Lead team members engaged in measuring, testing, and tabulating data concerning materials, product, or process quality and reliability. Manage the gauge system and actively pursue cost reduction related to gauge acquisition, maintenance, and calibration. Ensure compliance with all policies and procedures to meet quality standards. Provide leadership and training for Quality auditors. Address product/process-related quality concerns with customers and customer service, ensuring practices are consistent with documented procedures. Collaborate closely with production operators, manufacturing engineering, maintenance, sales, engineering, warranty/service, and supply chain. Champion quality improvement as part of everyday efforts. Qualifications / Training / Skill Requirements: Experience in a fabrication, machining, or assembly facility. Demonstrated problem-solving skills and experience. Direct experience with IATF or ISO quality management systems. Strong statistical background. Demonstrated Lean Manufacturing experience. Proven continuous improvement experience. Strong customer orientation. Six Sigma Green or Black Belt certification strongly preferred. Certified Quality Engineer (CQE) certification preferred. Education Requirements: Bachelor's degree in Quality Engineering or a related field. Experience Requirements Experience working in an IATF 16949 or ISO 9001 certified facility. Prior hands-on experience with process improvement, error proofing, dFMEA, pFMEA, APQP, control plans, process flow diagrams, and lean manufacturing principles.
    $52k-86k yearly est. 28d ago
  • Mgr - Quality

    Undercover Inc.

    Quality manager job in Springfield, MO

    Job Description The Manager of Quality will develop, implement, maintain, and lead the Quality Management System for multiple manufacturing plants and/or distribution facilities. The Manager will function as a part of the plant senior leadership team who sets short and long-term strategy as it relates to the Quality Management System. The manager will be responsible for continuous improvement initiatives for all aspects of the functional area. This position will manage a staff of quality supervisors and inspectors. CORE FUNCTIONS · Develop and maintain strong relationships with operations management, engineering, sales, and dealer-based customers to understand business, quality, and customer needs. · Manage the staff of Quality Supervisors and Inspectors. Provide performance feedback, guide, mentor, and manage workload activities. · Communicate and collaborate with Operations management on the implementation of quality objectives and corporate objectives to maximize product quality and minimize cost. · Responsible for all aspects of maintaining ISO and/or IATF certification for all manufacturing facilities and implementing any additional quality related business certifications. · Identify recurring quality defects and conduct root-cause analysis and implementation of corrective action for process and quality system related concerns. · Establish and drive quality objectives for the business and strategic initiatives related to the quality system. · Lead continuous improvement activities to enhance the quality system. Conduct audits, including closing out audit findings, creating audit finding reports, and determining proper corrective and preventative actions. · Resolve all customer quality complaints, assigns corrective actions and provides feedback to customers on a resolution. · Ensure timely resolution of supplier failure, corrective actions and preventative actions. · Manage, facilitate, and/or implement automotive Quality Core Tools including APQP, Control Plans, PPAP, FMEA, SPC, and MSA as needed. · Manage key metrics and report to the leadership team. QUALIFICATIONS & REQUIREMENTS Education and Experience · Bachelor's degree in Quality Engineering, other engineering, or a related field is preferred. In lieu of degree 10+ years of quality in a manufacturing field required. · 7+ years of quality systems experience required, including 1-3+ years of leadership experience required, preferably in a manufacturing and assembly environment. · Previous ISO 9000:2015 / IATF 16949 experience is required Required Licenses · CQU (Certified Quality Engineer) or other ASQ certification preferred. · SPC and/or Lean Six Sigma certification is desired. Skills, Abilities, and Knowledge · Ability to communicate with and interact with production team members. · Ability to present and provide data to top management. · Ability to identify issues and inefficiencies and to implement and drive changes. · Proficient in quality database systems and Microsoft Office suite. · Ability to compute rate, ratio, and percent, and to draw and interpret graphs. Availability · Flexibility to support a 2-shift operation, which may include occasional Saturdays. Travel · Occasional Travel as needed for training and corporate events. COMPETENCIES · Adapts to changes in the work environment; Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events. · Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data; Designs work flows and procedures. · Responds promptly to customer needs; Responds to requests for service and assistance; Meets commitments. · Displays willingness to make decisions; Exhibits sound and accurate judgment; Supports and explains reasoning for decisions; Includes appropriate people in decision-making process; Makes timely decisions. · Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations; Uses reason even when dealing with emotional topics. · Looks for ways to improve and promote quality; Demonstrates accuracy and thoroughness. · Balances team and individual responsibilities; Exhibits objectivity and openness to others views; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed. SUPERVISOR RESPONSIBILITIES · This position plans, staffs, evaluates, and directs the work of employees of a work unit. This position will have direct reports. PHYSICAL REQUIREMENTS · This position may be required to exert up to 20 pounds of force occasionally and/or a negligible amount of force constantly to move objects. The use of arm and/or leg controls require exertion of force greater than that for sedentary work. Physical Activities · This position is subject to the following activities: stooping, kneeling, crouching, reaching, standing, walking, lifting, grasping, feeling, talking, hearing and repetitive motions of the wrists, hands, and/or fingers. Visual Acuity · This position is required to have close visual acuity to perform activities such as preparing and analyzing data and figures, transcribing, viewing a computer terminal; expansive reading; visual inspection involving small defects, small parts and/or operation of machines (including inspection); using measurement devices; and/or assembly of fabrication of parts at distances close to the eyes. Working Conditions · This position may be subject to a variety of physical conditions, such as exposure to atmospheric conditions that affect the respiratory system of the skin.
    $52k-86k yearly est. 23d ago
  • Manager, Quality Assurance

    Curia

    Quality manager job in Springfield, MO

    Manager, Quality Assurance in Springfield, MO Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Quality Assurance Manager is responsible for oversight of the conditions and activities in the API manufacturing areas to ensure continual compliance with cGMP. This position requires expertise in all aspects of manufacturing of APIs, ability to work hands on, strong leadership skills, and the ability to collaborate in a cross-functional environment. The individual will work closely with all departments in the manufacturing environment and will report metrics to site management on a regular basis. Join our talented workforce, where a commitment to excellence and a customer-focused attitude is everything. We pursue excellence because our work has the power to improve patients' lives with the pharmaceuticals we develop and manufacture. We proudly offer Generous benefit options (eligible first day of employment) Paid training, vacation and holidays (vacation accrual begins on first day of employment) Career advancement opportunities Education reimbursement 401k program Learning platform And more! Responsibilities Assist the Site Quality Head with the development, implementation, and strict adherence to the quality assurance program Develop and/or review standards, policies, and procedures for all functions and departments involved with or related to the production and testing of all materials Oversee and assist with the site training and auditing programs, changes, investigations, validations, approval of specifications and methods, review of data and manufacturing records, and vendor qualifications Ensure immediate action is taken when non-compliance and/or undesired behavior by personnel in the facility is observed Make recommendations regarding facilities, equipment, personnel, procedures, and systems to carry out the quality function Ensure that the data integrity principles are understood and implemented consistently throughout the site Lead process improvement program including collaboration with Operations, Quality, and/or Training Leadership to make recommendations for enhancements to quality processes, teaching/coaching, and implementation of procedures Coordinate corrective action training based on both immediate and long-term feedback gathered from observations and evaluations Assist Site Quality Head during inspections by regulatory authorities, including implementing inspection-readiness programs and ensuring that proper CAPAs are prepared and completed on time Partner with site stakeholders to achieve and maintain operational excellence, site quality compliance and a strong, site-wide quality culture while achieving the site business goals. This includes also leading and supporting site-wide cGMP training activities Communicate effectively with internal and external customers making sure that the Curia values and business goals are consistently achieved Ensure daily inspections are carried out Qualifications Bachelor's Degree in Microbiology, Chemistry or related field Minimum 5 years of related industrial GMP experience in an FDA-regulated pharmaceutical environment, including 2 years' supervisory experience, OR Master's Degree in Microbiology, Chemistry or related field with minimum 3 years of related industrial GMP experience in an FDA-regulated pharmaceutical environment, including 2 years' supervisory experience Preferred Advanced degree in related field Prior work experience in a CMO Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer. #LI-KD1
    $59k-94k yearly est. Auto-Apply 60d+ ago
  • Manager, Quality Assurance

    Lake Pharma 3.8company rating

    Quality manager job in Springfield, MO

    Manager, Quality Assurance in Springfield, MO Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Quality Assurance Manager is responsible for oversight of the conditions and activities in the API manufacturing areas to ensure continual compliance with cGMP. This position requires expertise in all aspects of manufacturing of APIs, ability to work hands on, strong leadership skills, and the ability to collaborate in a cross-functional environment. The individual will work closely with all departments in the manufacturing environment and will report metrics to site management on a regular basis. Join our talented workforce, where a commitment to excellence and a customer-focused attitude is everything. We pursue excellence because our work has the power to improve patients' lives with the pharmaceuticals we develop and manufacture. We proudly offer * Generous benefit options (eligible first day of employment) * Paid training, vacation and holidays (vacation accrual begins on first day of employment) * Career advancement opportunities * Education reimbursement * 401k program * Learning platform * And more! Responsibilities * Assist the Site Quality Head with the development, implementation, and strict adherence to the quality assurance program * Develop and/or review standards, policies, and procedures for all functions and departments involved with or related to the production and testing of all materials * Oversee and assist with the site training and auditing programs, changes, investigations, validations, approval of specifications and methods, review of data and manufacturing records, and vendor qualifications * Ensure immediate action is taken when non-compliance and/or undesired behavior by personnel in the facility is observed * Make recommendations regarding facilities, equipment, personnel, procedures, and systems to carry out the quality function * Ensure that the data integrity principles are understood and implemented consistently throughout the site * Lead process improvement program including collaboration with Operations, Quality, and/or Training Leadership to make recommendations for enhancements to quality processes, teaching/coaching, and implementation of procedures * Coordinate corrective action training based on both immediate and long-term feedback gathered from observations and evaluations * Assist Site Quality Head during inspections by regulatory authorities, including implementing inspection-readiness programs and ensuring that proper CAPAs are prepared and completed on time * Partner with site stakeholders to achieve and maintain operational excellence, site quality compliance and a strong, site-wide quality culture while achieving the site business goals. This includes also leading and supporting site-wide cGMP training activities * Communicate effectively with internal and external customers making sure that the Curia values and business goals are consistently achieved * Ensure daily inspections are carried out Qualifications * Bachelor's Degree in Microbiology, Chemistry or related field * Minimum 5 years of related industrial GMP experience in an FDA-regulated pharmaceutical environment, including 2 years' supervisory experience, OR * Master's Degree in Microbiology, Chemistry or related field with minimum 3 years of related industrial GMP experience in an FDA-regulated pharmaceutical environment, including 2 years' supervisory experience Other Qualifications * Must pass a background check * Must pass a drug screen * May be required to pass Occupational Health Screening Preferred * Advanced degree in related field * Prior work experience in a CMO Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer. #LI-KD1
    $60k-90k yearly est. 60d+ ago
  • Deputy Director of Quality Management

    The Agency 4.1company rating

    Quality manager job in Springfield, MO

    Class Title: SENIOR PUBLIC SERVICE ADMINISTR - 40070 Skill Option: Health and Human Services Bilingual Option: None Salary: Anticipated Salary: $10,219 - $12,219 per month ($122,628 - $146,628 per year) Job Type: Salaried Category: Full Time County: Sangamon Number of Vacancies: 1 Bargaining Unit Code: None Merit Comp Code: Term Appointment/ Gubernatorial (Management Bill) A resume is highly encouraged to evaluate your qualifications and skills as part of your application. Please attach a DETAILED Resume/Curriculum Vitae (CV) to the MY DOCUMENTS section of your application if you decide to provide one. When applicable, titles that require specific coursework, professional license or certification will include a notation requesting the appropriate document(s) be uploaded in the Additional Documents section of your application. Failure to upload requested transcripts, license and/or proof of certification when specified may result in ineligibility. Please note that the Department of Human Services must verify proof of higher education for any degree earned (if applicable) regardless of vacancy title before any offer can be extended. Posting Identification Number 50920 Why Work for Illinois? Working with the State of Illinois is a testament to the values of compassion, equity, and dedication that define our state. Whether you're helping to improve schools, protect our natural resources, or support families in need, you're part of something bigger-something that touches the lives of every person who calls Illinois home. No matter what state career you're looking for, we offer jobs that fit your life and your schedule-flexible jobs that provide the gold standard of benefits. Our employees can take advantage of various avenues to advance their careers and realize their dreams. Our top-tier benefits and great retirement packages can help you build a rewarding career and lasting future with the State of Illinois. Position Overview The Division of Behavioral Health and Recovery is seeking to hire an energetic, self-motivated professional to fill the Deputy Director of Quality Management position. This position will organize, plan, execute, control and evaluate the ongoing monitoring of the quality of life and quality of care outcomes of individuals receiving services at State-Operated Psychiatric Hospitals (SOPHs), Develops the structure and productivity indicators for staff who will provide quality monitoring. Essential Functions Serves as Deputy Director of Quality Management. Organizes, plans, executes, controls, and evaluates the ongoing monitoring of all systems and processes concerning the quality of life and quality of care outcomes of individuals receiving services at State-Operated Psychiatric Hospitals (SOPHs). Serves as policy-making official. Serves as the DHS point of contact to assist in addressing concerns between DBHR (Division of Behavioral Health and Recovery) hospitals and OIG (Office of Inspector General), Equip for Equality, Guardianship and Advocacy, Human Rights Authority, Accreditation and Certification agencies, community partners, Office of the Auditor General. Receives, reviews and approves all OIG written responses for all DBHR hospitals. Designs data collection systems to collect specific quality indicators to determine consumer outcomes, report outcomes, analyze trends, collects and reviews critical incidents, and monitor corrective processes. Serves as full-line supervisor. Monitors SOPH problem-solving strategies when situational challenges impede or interfere with patient safety. Provides administrative direction and supervision to professional staff engaged in the formulation and implementation of the quality improvement policies, procedures, and strategies for the department. Performs other duties as required or assigned which are reasonably within the scope of the duties enumerated above. Minimum Qualifications Requires knowledge, skill and mental development equivalent to completion of four (4) years college. Requires four (4) years of clinical/administrative experience in a mental health service organization relative to quality management/improvement functions for a health or human services organization. Preferred Qualifications Five (5) years of professional experience working with accreditation and certification bodies such as The Joint Commission (TJC) or Commission on Accreditation of Rehabilitation Facilities (CARF). Five (5) years of professional experience developing, maintaining and managing quality assurance methods and processes by determining objectives, setting specifications and assessing results. Five (5) years of professional experience organizing, administering and evaluating ongoing services in a multi-disciplinary operation. Five (5) years of professional experience formulating and implementing policy and procedures for individuals being transitioned into community settings for a public or private organization. Five (5) years of professional experience developing and evaluating systems to collect and organize data for measuring performance indicators related to services or community provider services for a public or private organization. Five (5) years of professional supervisory experience, including assigning work, providing guidance to subordinates, recommending counseling and/or discipline following collective bargaining agreements, training staff and approving time off. Conditions of Employment Requires ability to pass the IDHS background check. Requires ability to pass a drug screen for drugs prohibited from recreational use under Illinois Law. Requires the ability to travel in the performance of job duties. Certain provisions of the revolving door restrictions contained in 5 ILCS 430/5-45 apply to this position. As a result, the employee should be aware that if offered non-State employment during state employment or within one year immediately after ending State employment, the employee shall, prior to accepting any such non-State employment offer, notify the Office of the Executive Inspector General for the Agencies of the Illinois Governor (OEIG) or may be subject to a fine. This position has been found to meet the requirements in section 4A-101 of the Illinois Governmental Ethics Act requiring the occupant/employee to file a Statement of Economic Interest. The Illinois Governmental Ethics Act (5 ILCS 420/4A et seq.) requires certain state officials and employees to file annual Statements of Economic Interest with the Office of the Secretary of State that will be made available for examination and copying by the public. All employees required to file a Statement of Economic Interest are also required to file the Supplemental Statement of Economic Interest with the Executive Ethics Commission. (See Executive Order 15-09) Fines and penalties apply to untimely filings. *The conditions of employment listed here are incorporated and related to any of the job duties as listed in the job description. Work Hours: 8:30am - 5:00pm, Monday - Friday; 1-hour unpaid lunch Work Location: 901 E Southwind Rd Springfield, IL 62703-5125 Division of Behavioral Health & Recovery Programmatic Development Quality Management Agency Contact: *************************** Posting Group: Leadership & Management; Social Services About the Agency: The Illinois Department of Human Services uplifts individuals and communities across Illinois. Our mission is to respond to the needs of all people in Illinois so they can lead healthy, safe, and enriched lives. Our vision is the future we are shaping with dignity and the well-being for everyone in Illinois. Our values are the principles that guide us as we work to remove systemic barriers and create lasting opportunities with Compassion, Accessibility, Responsibility, and Equity. Term Appointment: Candidates hired into a term position shall be appointed for a term of 4 years and are subject to a probationary period. The term may be renewed for successive four-year terms at the Director of the Department of Human Services's discretion. As a State of Illinois Employee, you will receive a robust benefit package that includes the following: A Pension Program Competitive Group Insurance Benefits including Health, Life, Dental and Vision Insurance 3 Paid Personal Business Days annually 12 Paid Sick Days annually (Sick days carry over from year to year) 10-25 Days of Paid Vacation time annually - (10 days in year one of employment) Personal, Sick, & Vacation rates modified for 12-hour & part-time work schedules (as applicable) 13 Paid Holidays annually, 14 on even numbered years Flexible Work Schedules (when available dependent upon position) 12 Weeks Paid Parental Leave Deferred Compensation Program - A supplemental retirement plan Optional Pre-Tax Programs such as Medical Care Assistance Plan (MCAP), Dependent Care Assistance Plan (DCAP) Federal Public Service Loan Forgiveness Program eligibility GI Bill Training/Apprenticeship Benefits eligibility for qualifying Veterans 5% Salary Differential for Bilingual Positions Commuter Savings Program (Chicago only) For more information about our benefits please follow this link: **************************************************** APPLICATION INSTRUCTIONS Use the “Apply” button at the top right or bottom right of this posting to begin the application process. If you are not already signed in, you will be prompted to do so. State employees should sign in to the career portal for State of Illinois employees - a link is available at the top left of the Illinois.jobs2web.com homepage in the blue ribbon. Non-State employees should log in on the using the “View Profile” link in the top right of the Illinois.jobs2web.com homepage in the blue ribbon. If you have never before signed in, you will be prompted to create an account. If you have questions about how to apply, please see the following resources: State employees: Log in to the career portal for State employees and review the Internal Candidate Application Job Aid Non-State employees: on Illinois.jobs2web.com - click “Application Procedures” in the footer of every page of the website. State employees should include temporary assignment in the application profile. Temporary assignment verification forms can be uploaded to the Additional Documents section. The main form of communication will be through email. Please check your “junk mail”, “spam”, or “other” folder for communication(s) regarding any submitted application(s). You may receive emails from the following addresses: ****************************** ***************************
    $122.6k-146.6k yearly Easy Apply 11d ago
  • Quality Manager

    SRC Industrial Corp 4.6company rating

    Quality manager job in Springfield, MO

    Job DescriptionWhat you will do: As an employee-owner, you will report to the General Manager. As the Quality Manager you would lead our quality assurance and continuous improvement initiatives within a dynamic manufacturing environment. This role oversees the quality and warranty teams, ensuring that all products meet internal, customer, and regulatory standards. The Quality Manager will leverage data-driven decision-making to drive corrective actions, improve customer satisfaction, and lead the organization toward operational excellence. Some Essential Duties: Lead and develop the Quality and Warranty teams, setting goals, providing training, and fostering a culture of continuous improvement. Oversee product quality control processes, ensuring all products meet specifications and regulatory requirements prior to shipment. Analyze nonconformance, warranty, customer complaint, and field failure data to identify trends and implement corrective/preventive actions. Conduct and manage internal audits, calibration programs, and measurement system analyses (MSA). Collaborate with engineering, operations, and production teams to resolve quality issues and enhance process capability. Coordinate and participate in customer audits, manage follow-up activities, and ensure timely resolution of findings. Lead root cause analysis initiatives for product and process issues. Lead the team that will develop and maintain documentation for the Quality Management System (QMS) in alignment with ISO standards. Monitor warranty claims and drive improvements that reduce failure rates and cost of poor quality. Report key quality metrics, performance trends, and customer satisfaction measures to leadership. Qualifications: Five years' experience in quality, engineering, or warranty in a manufacturing facility. Degree in a qualified field preferrable. Experience supervising and leading teams. Familiarity with ISO 9001 and Automotive OE Requirements (AIAG-FMEA, PPAP, APQP, etc.) or similar quality system requirements. What we do: We are an employee owned company that manufactures and remanufactures Air Compressors, Diesel & Gas Generators, Pumps, and IPUs. We are driven each day by our safety standards, quality product, employee morale, and customer satisfaction. We continue to push ourselves to be the number best remanufacturing option to our strategic partners. Rewards for you: Exceptional health benefits Vacation & Holiday Pay 5% 401(k) Match 100% Employee Owned Training and Advancement Opportunities 100% Tuition Reimbursement Quarterly Bonus Program Outstanding Company Culture How we do it: Through a culture of ownership! We're committed to creating a business of business-people through teaching Financial Literacy and playing The Great Game of Business. Our company is 100% Employee Owned and associates share in the wealth they help create. SRC Industrial Corp, a subsidiary of SRC Holdings Corporation (SRC), is headquartered in Springfield, Missouri. SRC was founded in 1983 by Jack Stack, renowned author, lecturer, and CEO who created the business literacy and open book management program “The Great Game of Business”. Click here to find out more about The Great Game of Business Location: 2801 N. Mulroy Rd, Springfield MO 65803
    $55k-88k yearly est. 12d ago
  • Director of Quality and Risk Management

    Perimeter Healthcare

    Quality manager job in Springfield, MO

    About the Role We are seeking a highly skilled Director of Quality & Risk Management to lead our behavioral health facility's quality, safety, regulatory compliance, and risk mitigation efforts. This leader will be responsible for ensuring coordinated, high-quality patient care in alignment with established clinical standards, mental health best practices, and organizational goals. This is a key leadership role that partners closely with Nursing, Clinical Services, Case Management, and Executive Leadership to drive excellence in Performance Improvement (PI), patient safety, regulatory readiness, and risk management activities across the facility. Director of Quality and Risk Mgt Key Responsibilities Quality & Performance Improvement * Lead the facility's Quality and Performance Improvement (QAPI) initiatives, ensuring continuous improvement of patient care and safety. * Monitor, evaluate, and report monthly PI and National Patient Safety Goals (NPSG) data to the CNO and CEO. * Assess program effectiveness and implement improvement strategies. * Support organization-wide quality goals and maintain confidentiality of sensitive information. Director of Quality and Risk Mgt Risk Management & Patient Safety * Ensure compliance with Joint Commission (TJC), CMS, HCFA, and State regulations. * Oversee safety and risk-management policies; investigate incidents and support corrective action plans. * Process unusual occurrence reports and lead investigations, documentation, and follow-up. * Coordinate legal processes and ensure accurate records regarding patient rights and safety. Director of Quality and Risk Mgt Leadership & Collaboration * Serve as a resource to clinical and nursing staff to ensure compliance with Standards of Care. * Participate in Nurse Staffing and Nurse Managers meetings to promote safe, effective care delivery. * Collaborate with Case Management to ensure timely and quality services for all patients. * Participate in Administrator-on-Call rotation. Regulatory Readiness & Compliance * Maintain thorough knowledge of Joint Commission standards and support accreditation activities. * Ensure adherence to facility policies, procedures, and professional standards. Qualifications * Education: Bachelor's degree in Nursing required; Master's in Psychiatric Nursing or related field preferred. * Licensure: Valid RN license (State or Compact). * Experience: Minimum 1 year in Nursing Administration or Nursing Leadership; behavioral health experience strongly preferred. * Skills: * Strong knowledge of psychiatric and medical nursing practices. * Proficiency in Microsoft Office. * Familiarity with Joint Commission standards. * Excellent organizational, communication, and leadership skills. * Ability to remain calm in emergencies and manage multiple priorities in a fast-paced environment. Director of Quality and Risk Mgt #INDSF
    $65k-100k yearly est. 2d ago
  • Quality Assurance Manager

    Provision People

    Quality manager job in Republic, MO

    Our award-winning client is seeking a Quality Assurance Manager to join their team. Lead oversight of the Quality Management System, ensuring compliance with 21 CFR Part 820, validating electronic records per 21 CFR Part 11, implementing robust Process and Quality Controls, managing Quality Data, and providing leadership to a team of Quality Assurance and Control Technicians. Responsibilities: Lead oversight of the Quality Management System with a focus on Quality Management System (QMS) Compliance: Establish and maintain a QMS compliant with 21 CFR Part 820. Review and approve quality system documents, reports, and records. Record Keeping: Ensure Quality Records are established and accessible per 21 CFR Part 820 and Quality System requirements. Validate electronic records and signatures for compliance with 21 CFR Part 11. Process and Quality Controls: Guarantee the definition and implementation of adequate Process Controls and Quality Controls throughout the production process. Ensure alignment with customer and regulatory requirements. Quality Data Management: Collect, analyze, and trend quality data. Provide quality performance data for reports and offer evidence-based recommendations for continuous process improvements. Supervision and Leadership: Supervise a team of Quality Assurance Technicians and Quality Control Technicians. Required Qualifications: Education: Preferably holds a BA/BS in sciences, with a preference for engineering backgrounds. Experience: Demonstrates a minimum of 5 years of proven expertise in the medical device industry. Possesses a minimum of 2 years of experience in a supervisory or management role.
    $59k-94k yearly est. 60d+ ago
  • Food Safety & Quality Program Manager

    Dairy Farmers of America 4.7company rating

    Quality manager job in Springfield, MO

    Function as a key member of the Retort Solutions (RS) team reporting to the Director, Quality Assurance supporting RS Divisional Leadership and manufacturing plants in the development, implementation, and sustainability of Food Safety and Quality Programs. Oversee the ongoing maintenance and continuous improvement of QMS programs and plant enabling tools. Support the build-out and growth of a winning food safety culture aligned with the Retort Solutions Divisional strategic master plan. JOB DUTIES AND RESPONSIBILITIES * Ensure alignment with Divisional and DFA Corporate FSQR governance as required. Partner with Retort Solutions Divisional business unit stakeholders to identify, design, and implement improvements and enhancements to the existing programs, to improve plant food safety and quality engagement. Support management of change initiatives as warranted. * Identify key issue trends and monitor plant CAPAs and complaints with cross-plant divisional impact and track to closure. Maintain Divisional level NC/CAPA database in a manner allowing for trend analysis, continuous improvement, and verification of effectiveness. Collaborate with others to align on problem solving tools and support training with plant teams to enhance skill set for an effective NC/CAPA program. * Partner with stakeholders to build and execute on tactical plan(s) that move FSQ programs/projects from current state to future state while ensuring continued momentum and minimizing disruption to the business. * Trend and report results from Regulatory, customer and third party audits and inspection reports at a Divisional level in alignment with FSQ governance where applicable. Manage relationship with SQF certifying body and support plant quality teams to manage audit schedule and reporting. Partner with cross functional stakeholders to identify, design, and implement process and system improvements to facilitate sharing of key learnings, best practices, and drive continuous improvement from audit findings to support the Quality Management System and Programs. * Develop and support a cross-functional Divisional internal audit program. Provide training and audit program materials as warranted. Trend internal audit results to develop continuous improvement plan. * Partner with Divisional resources to improve Customer Supplier Quality. Define and maintain data collection process that ensures manufacturing sites receive high quality materials every day. Leverage trend analysis and audit findings to close gaps in packaging quality, drive continuous improvement, and maintain compliance to DFA and customer requirements. * Work with Retort Solutions Division Continuous Improvement, Quality Systems and other business cross-functional representatives to deliver value by trend analysis and KPI reporting to drive continuous improvements on leading key indicator measures. Prioritize and drive focused FSQ improvement efforts, according to business risks identified by SWOT analysis and other assessments, such as external and internal audits. * Plant Quality Program Development and Improvement (ex. EMP, Sanitation) and RS Divisional Document Owner. Develop and deliver plant level Retort Solutions Division FSQ program training as directed * Promote harmonization and compliance to DFA Corporate policy/procedure with RS Divisional policy/procedure. * Adhoc site back-up to Plant Quality Managers to support the business as needed * The requirements herein are intended to describe the general nature and level of work performed by employee, but is not a complete list of responsibilities, duties, and skills required. Other duties may be assigned as required EDUCATION AND EXPERIENCE * Undergraduate degree in biological sciences, chemistry, food science, or related curriculum (or equivalent combination of education and experience) * 8 or more years of experience in FSQ within the food and beverage industry, preferable within the dairy or retort LACF category, including experience with QMS IT platforms (e.g., SAP, Ignition, SharePoint) * Demonstrated technical writing skills * Familiarity with GFSI certification standards (BRC, FSSC, SQF, etc.) * Certification and/or License - PCQI, Food Defense, Internal Auditor, Sanitation, other training certification (ex. Better Process Control School) may be required during course of employment An Equal Opportunity Employer including Disabled/Veterans
    $97k-118k yearly est. 8d ago
  • Associate Quality Engineer

    McCormick & Company 4.8company rating

    Quality manager job in Springfield, MO

    You may know McCormick as a leader in herbs, spices, seasonings, and condiments - and we're only getting started. At McCormick, we're always looking for new people to bring their unique flavor to our team. McCormick employees - all 14,000 of us across the world - are what makes this company a great place to work. We are looking to hire an Associate Quality Engineer immediately at our French's Manufacturing Plant in Springfield, Missouri. What We Bring To The Table: The best people deserve the best rewards. In addition to the benefits you'd expect from a global leader (401k, health insurance, paid time off, etc.) we also offer: • Competitive compensation • Career growth opportunities • Flexibility and Support for Diverse Life Stages and Choices • We prioritize our communities and the planet we share. We are proud to be awarded as a Diversity Inc. Top 50 company for Diversity and have multiple Sustainability awards (ranking #22 in the World and #1 in Food Products) • Wellbeing programs including Physical, Mental and Financial wellness • Tuition assistance POSITION OVERVIEW: Under the direction of the Quality Manager, the Quality Engineer (QE) develops and maintains documentation that captures best operating practices in the plant with a focus on Quality. The key objective of the QE is to reduce variation in operating methods thereby improving the reliability and repeatability of processes and eliminating defects. RESPONSIBILITIES: Leads management, disposition and system improvements for out of specification, defective materials (Raw, WIP, and Finished goods), and complaints using TPM process (e.g., FMEA, QC Matrix, SPC, 5 Why, 12 Step, DMAIC, Risk Assessments, etc.) to support the RCCA program Critically analyzes processes, systems and practices to identify current gaps and opportunities for improvement Drives process capability improvements through variation reduction, error-proofing, and implementation of statistics; this includes collecting and analyzing data to identify and prioritize Identifies opportunities and delivers improvement of product and process quality Provides Quality technical leadership for start-up of processes, equipment design, and formulation Develops capabilities of Operations, Warehouse and QA Teams to understand and implement quality standards and best practices Performs daily maintenance of Quality Programs (e.g., Infinity, Print Systems, checkweighers, x-rays, metal detectors, operational procedure review / update, Inspection Plans) Conducts internal audits and participates in external audits Participates on the Food Safety Team REQUIRED QUALIFICATIONS: Bachelor's degree in Chemistry, Food Science, Chemical Engineering, or a relevant technical field Minimum one (1) year of QA experience in manufacturing plant(s) - NOTE: internships and co-ops will be considered Knowledge and basic experience with statistical and focused improvement tools for process improvements such as SPC, Capability studies, FMEA, DOE, etc. Experience leading cross functional teams in the work place, school, or through extra-curricular activities Project management experience Demonstrated ability building and sustaining relationships at all levels, promoting a high-performance organization Experience working collaboratively to resolve issues with strong influencing, diplomacy, and partnering Excellent verbal and written communication skills Excellent organizational skills and ability to handle multiple projects and activities to ensure timely completion Ability to recognize problems and analyze and develop solutions using a logical thought process Ability to work through complex, time sensitive, multi-disciplinary and ambiguous problems Proficiency with Microsoft Word, Excel, and PowerPoint Willingness and ability to work flexible hours to support the needs of a multi shift operation Willingness to relocate for future assignments PREFERRED QUALIFICATIONS: Experience in the food, beverage, flavor, ingredient, and/or medical device manufacturing industry Experience working in a High-Performance Work Systems (HPWS) and/or Self Directed Work Team environment Experience working in a TPM environment SAP experience French's is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. French's does not offer employment visa sponsorships upon hire or in the future. You must be lawfully authorized to commence work upon being offered employment. #LI-SZ1 McCormick & Company is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. As a general policy, McCormick does not offer employment visa sponsorships upon hire or in the future.
    $60k-72k yearly est. 60d+ ago
  • Perishable Quality Control Supervisor

    AWG Enterprises

    Quality manager job in Springfield, MO

    . 6pm-4am, 5 days per week, rotating schedule ESSENTIAL FUNCTIONS: 1. Ensure only quality product is received and shipped by AWG by inspecting inbound loads regarding questionable quality or condition and determine proper handling. 2. Provide reasonable assurance that all incoming products conform to written and approved quality and weight specifications by conducting random audits. 3. Inspect quality in slot to confirm optimum quality for retail. 4. Monitor stock in perishable coolers/freezers verifying that proper rotation procedures have been observed, reporting any rotation or date problems. 5. Examine returned merchandise and damaged cases to determine disposition of product. 6. Ripen bananas to the optimum color for member stores. 7. Observe that bananas pulled for order selecting are pulled from the proper banana rooms and properly covered. 8. Report inventory levels, shelf life, shrinkage, and other quality related areas on a timely basis to Buyers and Sales Managers. 9. Be actively involved in identifying and correcting any problem areas in the distribution center which may impact the quality of perishable products such as temperatures, method of loading, product rotation, etc. 10. Inspect all loads of inbound meat products for proper temperature control, Country of Origin and HACCP. Documenting all pertinent information as required for proper governmental compliance. IMPORTANT FUNCTIONS: 1. Evaluate damaged cases and repair if possible. 2. Use computer to monitor inbound trucks, query product location and dating. Make any necessary adjustments to inventory. 3. Check and monitor temperatures of inbound product and perishable zones where meat and produce products are stored/received/shipped and that they are properly maintained. 4. Turn in weekly/daily reports to the Buyers and Sales Manager regarding product aging. 5. Provide the Sales Managers information concerning billbacks to ensure proper deductions are made when appropriate. 6. Perform other duties as requested by the Sales Manager or Fresh Director. 7. Collect and return temperature recorders to appropriate vendors. 8. Maintain QA tools and supplies (inventory on hand/needed) and calibrate temperature recorders. QUALIFICATIONS REQUIRED: Any combination of education, training and experience providing the following knowledge, skills, and abilities: Knowledge: Knowledge of meat and produce items, warehouse functions, billing, receiving procedures, accounting principles. Abilities: Communicate effectively verbally and in writing; read and understand pertinent data; perform mathematical calculations. Experience, Education and Training: High school diploma and 2-4 years' experience in grocery retail or wholesale. Physical Requirements: Perform lifting (up to 90 pounds), bending, squatting, kneeling, reaching from a floor level to six feet in height, walking, writing, sitting and climbing. Working in a cold environment (-20 to 40 degrees). Working Environment: Indoors, warehouse environment and inside meat freezer and cooler. Temperature ranges from 40 to -20 degrees Fahrenheit. Safety hazards possible maneuvering in the warehouse. Licensing/Certification: HACCP (Hazard Analysis Critical Control Point) certified preferred, but not required.
    $45k-71k yearly est. Auto-Apply 60d+ ago
  • Supervisor, Quality Control

    Curia Inc.

    Quality manager job in Springfield, MO

    To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives. We proudly offer * Generous benefit options * Paid training, vacation and holidays * Career advancement opportunities * Education reimbursement * 401k program * And more! Essential job duties * Manage the Quality Control Team Performance of analytical testing for various samples and incoming, in process, final products, and stability * Ensure that the analytical chemistry functions are completed in accordance with the Company and governmental standards of safety and quality, and that all experimental documentation is complete and timely * Supervise a team of scientists including, but not limited to, the motivation, education, efficiency, performance management and productivity of these individuals * Ensure that laboratory operations are conducted in a safe manner. Remain familiar with the contents of the Chemical Hygiene Plan. Follow safety rules fully * Maintain compliance with regulations at all levels as well as strict adherence to standard operating procedures and cGMPs as necessary * Communicate effectively in both verbal and written form on results, issues and plans. This may involve and include close interactions with other departments and/or customers * Organize workloads and coordinate activities in order to carry out multiple projects concurrently and in accordance with established objectives, timelines and deadlines * Assist with the maintenance, calibration, and validation of QC lab analytical instrumentation * Conduct investigations of OOS, Deviations, Change Control Management, and CAPAs * Supervise and perform pharmaceutical analysis to support API manufacturing * Authoring and revision of Quality Control SOPs and test procedures Quality Expectations of this Position: * Perform all documentation in compliance with good documentation practices as defined by site SOP's. * Strict compliance with all cGMP document * SOP's, Batch records, protocols, Change controls, controlled forms * Ensure all cGMP applicable training is kept current * Oversee and monitor performance of staff to ensure compliance with all cGMP SOP's. * Provide training and guidance to staff as needed on site SOP's, Batch records, protocols, change controls, controlled forms, etc. * Ensure staff have appropriate training documented prior to assigning work * Escalate any quality concerns to quality department. Education, experience, certification and licensures Required * Bachelor's degree in Chemistry or a scientific discipline with relevant coursework or work experience in analytical chemistry * Minimum 5 years' experience in a GMP or GLP environment working with Chromatography (HPLC/UPLC/GC), and other common analytical instrumentation Knowledge, skills and abilities * Ability to recognize what needs to be done, take action, and accomplish results * Strong oral and written communication skills, including effective listening * Demonstrated ability to effectively utilize team resources * Expert in cGMP, USP, EP and FDA regulations * Technical competence including the understanding of theory and interpretation of all lab techniques * Proficient use of computer software, including Microsoft Office Suite (excel, word) and other required software * Strong organizational skills with the ability to multi-task * Proficient in HPLC and GC operation with experience with multiple other analytical techniques and analytical equipment * Prior experience and knowledge in FDA GMPs (21 CFR, 211, 820, and/or 600); Physical requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand; walk; and sit; use hands to finger, handle, or feel; and talk or hear. The employee frequently is required to reach with hands and arms. The employee is occasionally required to climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. Work environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee has the potential of being exposed to fumes or airborne particles and toxic or caustic chemicals (wearing proper Personal Protective Equipment will be required in these situations). The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; outside weather conditions; and risk of electrical shock (always being aware of one's environment and taking proper precautions is required). The noise level in the work environment is usually moderate. Employee will be responsible for generating hazardous waste for treatment, storage and disposal. Affected employee will need to be familiar with the applicable training requirements included in the Resources, Conservation and Recovery Act. Employee will understand waste labeling, secondary containment, chemical compatibility, storage time limits, container size and quantity limits, container integrity when waste is left unattended and improper disposal of hazardous materials. The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel as classified. Management reserves the right to revise or amend duties at any time. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer. #LI-DR1
    $45k-71k yearly est. Auto-Apply 9d ago
  • Perishable Quality Control Supervisor

    AWG Ambassador 4.3company rating

    Quality manager job in Springfield, MO

    . 6pm-4am, 5 days per week, rotating schedule ESSENTIAL FUNCTIONS: 1. Ensure only quality product is received and shipped by AWG by inspecting inbound loads regarding questionable quality or condition and determine proper handling. 2. Provide reasonable assurance that all incoming products conform to written and approved quality and weight specifications by conducting random audits. 3. Inspect quality in slot to confirm optimum quality for retail. 4. Monitor stock in perishable coolers/freezers verifying that proper rotation procedures have been observed, reporting any rotation or date problems. 5. Examine returned merchandise and damaged cases to determine disposition of product. 6. Ripen bananas to the optimum color for member stores. 7. Observe that bananas pulled for order selecting are pulled from the proper banana rooms and properly covered. 8. Report inventory levels, shelf life, shrinkage, and other quality related areas on a timely basis to Buyers and Sales Managers. 9. Be actively involved in identifying and correcting any problem areas in the distribution center which may impact the quality of perishable products such as temperatures, method of loading, product rotation, etc. 10. Inspect all loads of inbound meat products for proper temperature control, Country of Origin and HACCP. Documenting all pertinent information as required for proper governmental compliance. IMPORTANT FUNCTIONS: 1. Evaluate damaged cases and repair if possible. 2. Use computer to monitor inbound trucks, query product location and dating. Make any necessary adjustments to inventory. 3. Check and monitor temperatures of inbound product and perishable zones where meat and produce products are stored/received/shipped and that they are properly maintained. 4. Turn in weekly/daily reports to the Buyers and Sales Manager regarding product aging. 5. Provide the Sales Managers information concerning billbacks to ensure proper deductions are made when appropriate. 6. Perform other duties as requested by the Sales Manager or Fresh Director. 7. Collect and return temperature recorders to appropriate vendors. 8. Maintain QA tools and supplies (inventory on hand/needed) and calibrate temperature recorders. QUALIFICATIONS REQUIRED: Any combination of education, training and experience providing the following knowledge, skills, and abilities: Knowledge: Knowledge of meat and produce items, warehouse functions, billing, receiving procedures, accounting principles. Abilities: Communicate effectively verbally and in writing; read and understand pertinent data; perform mathematical calculations. Experience, Education and Training: High school diploma and 2-4 years' experience in grocery retail or wholesale. Physical Requirements: Perform lifting (up to 90 pounds), bending, squatting, kneeling, reaching from a floor level to six feet in height, walking, writing, sitting and climbing. Working in a cold environment (-20 to 40 degrees). Working Environment: Indoors, warehouse environment and inside meat freezer and cooler. Temperature ranges from 40 to -20 degrees Fahrenheit. Safety hazards possible maneuvering in the warehouse. Licensing/Certification: HACCP (Hazard Analysis Critical Control Point) certified preferred, but not required.
    $44k-66k yearly est. Auto-Apply 60d+ ago
  • Senior Quality Engineer (Springfield, Missouri, United States, 65807)

    Timken Co. (The 4.6company rating

    Quality manager job in Springfield, MO

    What Timken makes possible begins with you. Those who came before us helped land a man on the moon, create the world's infrastructure, and introduce renewable energy alternatives. Now you can join the Timken team to write your own unique story and help drive what's next. A career at Timken means you can have an immediate impact doing Work That Matters to the world- improving the efficiency of today's industrial equipment and preparing for the future of motion on our planet and beyond. New employees can start contributing right away, and there are many opportunities to advance your career at your own pace. Join our global team of 19,000 people in 45 countries, and start helping our customers push the limits of what's possible in their world of motion. The Senior Quality Engineer plays a crucial role in identifying and recommending quality improvement parameters through the application of statistical methods pertinent to manufacturing processes. This position collaborates with cross-functional teams to identify areas of improvement and implement quality assurance processes. Essential Job Duties: * Data Analysis and Reporting: * Complete reports by collecting, analyzing, and summarizing data, making recommendations as necessary. * Support the gathering of product-related Quality metrics and reports. * Analyze information and report findings to the corresponding departments and leadership. * Customer Resolution: * Respond to customer complaints and initiate corrective actions in the customer or internal complaint system. * Receive, prepare, and gather PPAP documents for customer submission. * Project and Change Management: * Plan and suggest projects to reduce manufacturing costs, improve processes, enhance product quality and reliability, and increase process capability. * Uphold and suggest improvements for change management processes. * Review and approve engineering change notices as necessary. * Utilize manufacturing quality methods and procedures to enhance departmental processes. * Perform risk assessments and failure mode and effects analysis (FMEA). * Process Improvement and Standardization: * Promote, support, and create process improvements within the quality department. * Create standards for audit requirements. * Participate in process validation and qualification activities. * Ensure compliance with ISO standards and industry regulations. * Conduct inspections, audits, and tests to assess product quality. * Team Contribution: * Contribute to team efforts to achieve related results as needed. * Provide training to employees on quality processes and best practices. * Perform additional duties as assigned. Qualifications: * Required: * Associate's degree in a related engineering field with a minimum of 7 years of experience in a manufacturing quality role. * Demonstrated experience with ISO compliance, audit preparation, and document control. * Proficient in statistical quality tools including Statistical Process Control (SPC), Root Cause Analysis (RCA), and Design of Experiments (DOE). * Proven ability to manage quality-related projects independently. * Experience reviewing and approving engineering change notices and supporting change management processes. * Experience using quality management systems (QMS) and data reporting tools. * Ability to produce clear, concise reports and communicate findings to cross-functional teams. * Experience providing training or guidance on quality processes to team members. * Proficient in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook). * Preferred: * Bachelor's degree in a related engineering field with at least 4 years of experience in a manufacturing quality role. * Certification as a Quality Engineer (CQE), Six Sigma Green Belt, or equivalent credential. All qualified applicants shall be treated equally according to their individual qualifications, abilities, experiences and other employment standards. There will be no discrimination due to gender or gender identity, race, religion, color, national origin, ancestry, age, disability, sexual orientation, veteran/military status or any other basis protected by applicable law.
    $83k-101k yearly est. 9d ago
  • Quality Specialist On-Site: Springfield, MO.

    BPS Direct 4.3company rating

    Quality manager job in Springfield, MO

    The Quality Specialist will be responsible for the following: Serve as the leader in Quality issue management. Manage reporting to clearly outline and regularly communicate status of all current quality issues, inventory position, financial risk, corrective action, and anticipated resolution date. Work with product development, merchant business partners, distribution centers, supply chain, and compliance to determine scope of issues received and the business impact, e.g., amount produced, amount on hand/on order, inspection plan, and rejection rates. Track, receive, setup, and lead quality product reviews with associated product development and merchant teams. Define and document repair and/or inspection timing with outside repair facilities as well as the distribution centers. Provide dispositions for global quality failures. Collect and analyze quality failures, return rates, and VOC data. Provide insights for product design improvement to product development teams. Partner with product teams, to ensure all corporate, brand, regulatory and legal requirements are met. Provide suggestions for production risk control during development stage. Interface with compliance department to ensure that all product safety and regulatory requirements are met for importation and sale of products. Initiate quality product reviews to update protocols, standards, or procedures to prevent future quality issues. Maintain and distribute the Quality Assurance Manual to ensure an understanding and adherence at all sources with a focus on continuous improvement procedures. Ensure QA reporting tools provide efficient and user-friendly QA reports, forms, trackers, Standard Operating Procedures (SOPs) for both historical and future quality reporting. Serve as key contact for brands on product performance, product testing related issues, and requests pertaining to Bass Pro Shops brand standards and merchandise. Perform training in all aspects of quality management systems This position requires the minimum of a Bachelor's degree or equivalent in Quality Assurance, Engineering, Design, or a related field and 5 years related (progressive, post-baccalaureate) experience. Must also have knowledge of each of the following: (1) Textiles and apparel product manufacturing; (2) Quality systems and processes; (3) Product and materials testing; (4) Product Lifecycle Management (PLM) and use of PLM software; (5) Continuous improvement principles; (6) Quality Assurance tools and techniques including Lean, Six Sigma, and Total Quality Management (TQM); (7) Ability to identify and define problems, collect data, establish facts, and draw valid conclusions with a global perspective in a Quality Assurance or Product Development environment; (8) Instituting process improvements to ensure that design and production meet regulations; (9) Working with international suppliers; and (10) Working with product teams and cross-functional work groups. Background check and drug test required. Full-time, position located in Springfield, MO. Travel domestic and/or international, including overnight, as required; maximum 15%. EOE. Full Time Benefits Summary: Enjoy discounts on retail merchandise, our restaurants, world-class resorts and conservation attractions! Medical Dental Vision Health Savings Account Flexible Spending Account Voluntary benefits 401k Retirement Savings Paid holidays Paid vacation Paid sick time Bass Pro Cares Fund And more! Bass Pro Shops is an equal opportunity employer. Hiring decisions are administered without regard to race, color, creed, religion, sex, pregnancy, sexual orientation, gender identity, age, national origin, ancestry, citizenship status, disability, veteran status, genetic information, or any other basis protected by applicable federal, state or local law. Reasonable Accommodations Qualified individuals with known disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act and certain state or local laws. If you need a reasonable accommodation for any part of the application process, please visit your nearest location or contact us at ************************. Bass Pro Shops
    $25k-33k yearly est. Auto-Apply 4d ago
  • Quality Engineer-Lowe Boats

    Brunswick Boat Group

    Quality manager job in Lebanon, MO

    Are you ready for what's next? Come explore opportunities within Brunswick, a global marine leader committed to challenging conventions and innovating next-generation technologies that transform experiences on the water and beyond. Brunswick believes “Next Never Rests™,” and we offer a variety of exciting careers and growth opportunities within united teams defining the future of marine recreation. Innovation is the heart of Brunswick. See how your contributions will help transform vision into reality: Position Overview: As part of the talented Lowe team, the role of Quality Engineer is to develop, deploy, and monitor quality processes while influencing improvement opportunities across the Brunswick Value Streams. The Quality Engineer oversees Verification, Validation, and Non-Conformance systems ensuring compliance to Brunswick drawings, applicable standards and customer value while optimizing the cost of Quality. At Brunswick, we have passion for our work and a distinct ability to deliver. Essential Functions: · Develop and deploy Built In Quality across the value stream. · Develop and implement Quality Plans for new products as part of the HPPD process. · Serve as a consultative resource and collaborative partner to both customers and internal suppliers to ensure all needs and expectations are understood and addressed · Process PPAP/FAI submissions to enable timely new product shipments · Handle tactical quality issues both within the operation and external customers. · Review Corrective Action submissions to verify root cause analysis is complete and measures are taken to eliminate future reoccurrence · Conduct quality performance analysis and proactively provide insightful information to Operations and Customer Service. · Provide quality performance data as required to enable the assessment of past performance, ensure continued efficiency and identify continuous improvement opportunities · Document materials rejected due to quality issue to maintain inventory accuracy in MRB · Interpret engineering drawings, schematic diagrams, or formulas and confers with management or engineering staff to determine quality and reliability standards relative to warranty agreements · Work directly with Operations. Support internal audits against standards and provide analysis and development plans to improve. · Handle tactical quality issues (spills, PPAP, etc) to assure containment and RCCA. · Manage projects necessary to execute continuous improvement plans in accordance with the commodity strategy, and site Quality Goals. · This position may require occasional day and/or overnight travel by auto or airplane, up to 10%. Diversity of thought and experiences is fundamental when imagining the unimaginable. Certain skillsets/experiences are necessary; however, others can be developed along the way. Required Qualifications: · Quality concepts: basic quality tools and problem-solving techniques · Demonstrated knowledge regarding data models and data mining · Exposure to reporting packages (Business Objects etc), databases (SQL, etc) · High competency in Excel, Word, Powerpoint and Minitab. · Project management skills: training and demonstrated successful use of tools · Demonstrated strong attention to detail ensuring records and data systems are current and accurate · NMMA Certification within 1 year of employment. · Growing analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy · Requires excellent communication skills Education: · BS/BA in Engineering or a related technical field is preferred. · ASQ certified Quality Manager, Engineer, or Auditor is preferred · Lean six sigma Green or Black Belt certification with project experience is preferred · 1+ years of experience in a manufacturing, operations, quality engineering environment co-op/intern role is preferred Work Environment: While performing the duties of this job, the employee is occasionally exposed to high sound levels, welding processes, moving forklifts, elevated loads, and close quarters. The successful candidate will demonstrate a safety mindset to other employees. The anticipated pay range for this position is $57,700-$92,600 annually. The actual base pay offered will vary depending on multiple factors including job- related knowledge/skills, relevant experience, business needs, and geographic location. In addition to base pay, this position is eligible for an annual discretionary bonus. At Brunswick, it is not typical for an individual to be hired at or near the top end of the salary range for their role. Compensation decisions are dependent upon the specifics of the candidate's qualifications and the business context. This position is eligible to participate in Brunswick's comprehensive and high-quality benefits offerings, including medical, dental, vision, paid vacation, 401k (up to 4% match), Health Savings Account (with company contribution), well-being program, product purchase discounts and much more. Details about our benefits can be found here. Why Brunswick: Whatever tomorrow brings, we'll be at the leading edge. As the clear leader in the marine industry, we're committed to our values and supporting our exceptional people. We offer and encourage growth opportunities within and across our many brands. In addition, we're proud of being recognized for making a splash with numerous awards! About Brunswick Boat Group Brunswick Boat Group is home to a diverse portfolio of iconic marine brands, including Bayliner, Boston Whaler, Crestliner, Cypress Cay, Harris, Heyday, Lowe, Lund, Navan, Princecraft, Protector, Quicksilver, Rayglass, Sea Ray, Spartan, Thunder Jet, and Uttern. Each brand carries a legacy of innovation, craftsmanship, and performance that has shaped the boating industry worldwide. Across our fiberglass and aluminum manufacturing facilities, our team members are the driving force behind our success. We foster a culture rooted in safety, integrity, continuous improvement, and personal growth. Whether you're building unsinkable legends, pioneering wake sports, or crafting fishing and pontoon boats trusted for generations, you'll be part of a united team committed to delivering exceptional experiences on the water. Next is Now! We value growth and development, recognizing that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. Brunswick is an Equal Opportunity Employer and considers all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status or any other characteristic protected by federal, state, or local law. Diversity of experience and skills combined with passion is key to innovation and inspiration and we encourage individuals from all backgrounds to apply. If you require accommodation during the application or interview process, please contact ****************************** for support. For more information about EEO laws, - click here Brunswick and Workday Privacy Policies Brunswick does not accept applications, inquiries or solicitations from unapproved staffing agencies or vendors. For help, please contact our support team at: ****************************** or ************. All job offers will come to you via the candidate portal you create when applying through a posted position through https:///************************** If you are ever unsure about what is being required of you during the application process or its source, please contact HR Shared Services at ************ or ******************************. #Brunswick Corporation
    $57.7k-92.6k yearly Auto-Apply 58d ago
  • Quality Engineer-Lowe Boats

    Brunswick 4.5company rating

    Quality manager job in Lebanon, MO

    **_Are you ready for what's next?_** _Come explore opportunities within Brunswick, a global marine leader (******************************* Q6B2j\_mA) committed to challenging conventions and innovating next-generation technologies that transform experiences on the water and beyond. Brunswick believes "Next Never Rests," and we offer a variety of exciting careers and growth opportunities within united teams defining the future of marine recreation._ **Innovation is the heart of Brunswick. See how your contributions will help transform vision into reality:** Position Overview: As part of the talented Lowe team, the role of Quality Engineer is to develop, deploy, and monitor quality processes while influencing improvement opportunities across the Brunswick Value Streams. The Quality Engineer oversees Verification, Validation, and Non-Conformance systems ensuring compliance to Brunswick drawings, applicable standards and customer value while optimizing the cost of Quality. **At Brunswick, we have passion for our work and a distinct ability to deliver.** Essential Functions: · Develop and deploy Built In Quality across the value stream. · Develop and implement Quality Plans for new products as part of the HPPD process. · Serve as a consultative resource and collaborative partner to both customers and internal suppliers to ensure all needs and expectations are understood and addressed · Process PPAP/FAI submissions to enable timely new product shipments · Handle tactical quality issues both within the operation and external customers. · Review Corrective Action submissions to verify root cause analysis is complete and measures are taken to eliminate future reoccurrence · Conduct quality performance analysis and proactively provide insightful information to Operations and Customer Service. · Provide quality performance data as required to enable the assessment of past performance, ensure continued efficiency and identify continuous improvement opportunities · Document materials rejected due to quality issue to maintain inventory accuracy in MRB · Interpret engineering drawings, schematic diagrams, or formulas and confers with management or engineering staff to determine quality and reliability standards relative to warranty agreements · Work directly with Operations. Support internal audits against standards and provide analysis and development plans to improve. · Handle tactical quality issues (spills, PPAP, etc) to assure containment and RCCA. · Manage projects necessary to execute continuous improvement plans in accordance with the commodity strategy, and site Quality Goals. · This position may require occasional day and/or overnight travel by auto or airplane, up to 10%. **Diversity of thought and experiences is fundamental when imagining the unimaginable. Certain skillsets/experiences are necessary; however, others can be developed along the way.** Required Qualifications: · Quality concepts: basic quality tools and problem-solving techniques · Demonstrated knowledge regarding data models and data mining · Exposure to reporting packages (Business Objects etc), databases (SQL, etc) · High competency in Excel, Word, Powerpoint and Minitab. · Project management skills: training and demonstrated successful use of tools · Demonstrated strong attention to detail ensuring records and data systems are current and accurate · NMMA Certification within 1 year of employment. · Growing analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy · Requires excellent communication skills Education: · BS/BA in Engineering or a related technical field is preferred. · ASQ certified Quality Manager, Engineer, or Auditor is preferred · Lean six sigma Green or Black Belt certification with project experience is preferred · 1+ years of experience in a manufacturing, operations, quality engineering environment co-op/intern role is preferred Work Environment: While performing the duties of this job, the employee is occasionally exposed to high sound levels, welding processes, moving forklifts, elevated loads, and close quarters. The successful candidate will demonstrate a safety mindset to other employees. The anticipated pay range for this position is $57,700-$92,600 annually. The actual base pay offered will vary depending on multiple factors including job- related knowledge/skills, relevant experience, business needs, and geographic location. In addition to base pay, this position is eligible for an annual discretionary bonus. At Brunswick, it is not typical for an individual to be hired at or near the top end of the salary range for their role. Compensation decisions are dependent upon the specifics of the candidate's qualifications and the business context. This position is eligible to participate in Brunswick's comprehensive and high-quality benefits offerings, including medical, dental, vision, paid vacation, 401k (up to 4% match), Health Savings Account (with company contribution), well-being program, product purchase discounts and much more. Details about our benefits can be found here (************************************************************ . **Why Brunswick:** Whatever tomorrow brings, we'll be at the leading edge. As the clear leader in the marine industry, we're committed to our values and supporting our exceptional people. We offer and encourage growth opportunities within and across our many brands. In addition, we're proud of being recognized for making a splash with numerous awards (********************************** ! **About Brunswick Boat Group** Brunswick Boat Group is home to a diverse portfolio of iconic marine brands, including **Bayliner, Boston Whaler, Crestliner, Cypress Cay, Harris, Heyday, Lowe, Lund, Navan, Princecraft, Protector, Quicksilver, Rayglass, Sea Ray, Spartan, Thunder Jet, and Uttern.** Each brand carries a legacy of innovation, craftsmanship, and performance that has shaped the boating industry worldwide. Across our fiberglass and aluminum manufacturing facilities, our team members are the driving force behind our success. We foster a culture rooted in **safety, integrity, continuous improvement, and personal growth.** Whether you're building unsinkable legends, pioneering wake sports, or crafting fishing and pontoon boats trusted for generations, you'll be part of a united team committed to delivering exceptional experiences on the water. _Next is Now!_ _We value growth and development, recognizing that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying._ Brunswick is an Equal Opportunity Employer and considers all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status or any other characteristic protected by federal, state, or local law. Diversity of experience and skills combined with passion is key to innovation and inspiration and we encourage individuals from all backgrounds to apply. If you require accommodation during the application or interview process, please contact ****************************** for support. For more information about EEO laws, - click here (********************************************** Brunswick and Workday (**************************************************************************************** Privacy Policies Brunswick does not accept applications, inquiries or solicitations from unapproved staffing agencies or vendors. For help, please contact our support team at: ****************************** or ************. All job offers will come to you via the candidate portal you create when applying through a posted position through https:///************************* . If you are ever unsure about what is being required of you during the application process or its source, please contact HR Shared Services at ************ or ****************************** . \#Brunswick Corporation
    $57.7k-92.6k yearly 59d ago
  • Food Safety & Quality Program Manager

    Dairy Farmers of America 4.7company rating

    Quality manager job in Springfield, MO

    Function as a key member of the Retort Solutions (RS) team reporting to the Director, Quality Assurance supporting RS Divisional Leadership and manufacturing plants in the development, implementation, and sustainability of Food Safety and Quality Programs. Oversee the ongoing maintenance and continuous improvement of QMS programs and plant enabling tools. Support the build-out and growth of a winning food safety culture aligned with the Retort Solutions Divisional strategic master plan. JOB DUTIES AND RESPONSIBILITIES Ensure alignment with Divisional and DFA Corporate FSQR governance as required. Partner with Retort Solutions Divisional business unit stakeholders to identify, design, and implement improvements and enhancements to the existing programs, to improve plant food safety and quality engagement. Support management of change initiatives as warranted. Identify key issue trends and monitor plant CAPAs and complaints with cross-plant divisional impact and track to closure. Maintain Divisional level NC/CAPA database in a manner allowing for trend analysis, continuous improvement, and verification of effectiveness. Collaborate with others to align on problem solving tools and support training with plant teams to enhance skill set for an effective NC/CAPA program. Partner with stakeholders to build and execute on tactical plan(s) that move FSQ programs/projects from current state to future state while ensuring continued momentum and minimizing disruption to the business. Trend and report results from Regulatory, customer and third party audits and inspection reports at a Divisional level in alignment with FSQ governance where applicable. Manage relationship with SQF certifying body and support plant quality teams to manage audit schedule and reporting. Partner with cross functional stakeholders to identify, design, and implement process and system improvements to facilitate sharing of key learnings, best practices, and drive continuous improvement from audit findings to support the Quality Management System and Programs. Develop and support a cross-functional Divisional internal audit program. Provide training and audit program materials as warranted. Trend internal audit results to develop continuous improvement plan. Partner with Divisional resources to improve Customer Supplier Quality. Define and maintain data collection process that ensures manufacturing sites receive high quality materials every day. Leverage trend analysis and audit findings to close gaps in packaging quality, drive continuous improvement, and maintain compliance to DFA and customer requirements. Work with Retort Solutions Division Continuous Improvement, Quality Systems and other business cross-functional representatives to deliver value by trend analysis and KPI reporting to drive continuous improvements on leading key indicator measures. Prioritize and drive focused FSQ improvement efforts, according to business risks identified by SWOT analysis and other assessments, such as external and internal audits. Plant Quality Program Development and Improvement (ex. EMP, Sanitation) and RS Divisional Document Owner. Develop and deliver plant level Retort Solutions Division FSQ program training as directed Promote harmonization and compliance to DFA Corporate policy/procedure with RS Divisional policy/procedure. Adhoc site back-up to Plant Quality Managers to support the business as needed The requirements herein are intended to describe the general nature and level of work performed by employee, but is not a complete list of responsibilities, duties, and skills required. Other duties may be assigned as required
    $97k-118k yearly est. 9h ago

Learn more about quality manager jobs

How much does a quality manager earn in Springfield, MO?

The average quality manager in Springfield, MO earns between $42,000 and $107,000 annually. This compares to the national average quality manager range of $64,000 to $128,000.

Average quality manager salary in Springfield, MO

$67,000

What are the biggest employers of Quality Managers in Springfield, MO?

The biggest employers of Quality Managers in Springfield, MO are:
  1. Vital Farms
  2. SRC
  3. All Realtruck Career
  4. Hikinex
  5. Undercover Inc.
Job type you want
Full Time
Part Time
Internship
Temporary