Principal Supplier Quality Engineer
Quality manager job in Alpharetta, GA
Job Title: Principal Supplier Quality Engineer
Job Country: United States (US)
Here at Avanos Medical, we passionately believe in three things:
Making a difference in our products, services and offers, never ceasing to fight for groundbreaking solutions in everything we do;
Making a difference in how we work and collaborate, constantly nurturing our nimble culture of innovation;
Having an impact on the healthcare challenges we all face, and the lives of people and communities around the world.
At Avanos you will find an environment that strives to be independent and different, one that supports and inspires you to excel and to help change what medical devices can deliver, now and in the future.
Avanos is a medical device company focused on delivering clinically superior breakthrough solutions that will help patients get back to the things that matter. We are committed to creating the next generation of innovative healthcare solutions which will address our most important healthcare needs, such as reducing the use of opioids while helping patients move from surgery to recovery. Headquartered in Alpharetta, Georgia, we develop, manufacture and market recognized brands in more than 90 countries. Avanos Medical is traded on the New York Stock Exchange under the ticker symbol AVNS. For more information, visit ***************
Essential Duties and Responsibilities:
Ensure conformance to industry practices, domestic and international regulatory requirements and established company procedures.This position provides technical leadership for Supplier Quality Management processes and activities. The primary purpose of this position is to implement, coordinate, support, and monitor activities related to the Global Supplier Quality Management (SQM) activities across Avanos. This position may also train R&D, Technical Quality, Operations, and other functions on the established processes and any enhancements as needed and perform other additional duties as assigned..
Key Responsibilities:
Provide global technical leadership in the development and implementation of quality and regulatory compliance strategies and best practices to ensure the manufacturing and distribution of products comply with applicable regulatory requirements.
Lead cross-functional collaboration with Procurement, R&D/Operations, Technical Quality, and Logistics teams to address quality issues at contract manufacturers and suppliers.
Establish and administer the supplier audit program for quality/regulatory compliance.
Maintain the Approved Supplier List (ASL).
Support the Global Supplier Review Board, including providing metrics for
supplier assessments.
Actively engage with suppliers in the event of a supplier issue requiring corrective action or upcoming external audits.
Provide guidance as needed for corrective action required because of assessment findings.
Execute supplier audits in accordance with approved schedules.
Support documentation of supplier changes through the supplier notification, change management, QNC, or CAPA processes.
Contribute to the supplier qualification vetting process and perform supplier evaluations to ensure appropriate suppliers are being selected.
Continuously improve existing Supplier Quality Management Process to ensure compliance with regulatory requirements.
Develop, implement, and execute a system for conducting due diligence evaluations for supplier qualifications and acquisitions.
Provide auditing support during due diligence and integration activities as needed.
External Interface:
This role will primary interface externally with suppliers and with external auditors from Notify Bodies and Regulatory Agencies
Your qualifications
Required:
Personnel performing work affecting product quality shall be competent based on appropriate education, training, skills and experience.
Preferred:
B.S. in Engineering, Science, Business, or another relevant field
Minimum of 10 years of collective experience in a Research, Manufacturing, Quality and/or Regulatory Affairs function within a medical device, pharmaceutical, biologic, or other highly regulated industry.
Supplier Quality Engineering experience in the Medical Device industry
Strong understanding of Risk Management principles and techniques.
Knowledge of Statistical Techniques
Experience in root cause analysis and failure investigation tools
Working knowledge of the MDSAP Single Audit program including the regulations for US, Japan, Canada, Australia, and Brazil
Working knowledge of the key medical device compliance related standards such as ISO 13485, ISO 14971, ISO 19011, ISO 10993, etc.
Certification as CQA, CBA, MDA, or ISO 13485 Lead Auditor
Strong project management skills
Ability to make reasonable decisions and be able to effectively justify them
Strong collaborative skills and customer service approach
Exceptional written, verbal, and presentation communication skills
The statements above are intended to describe the general nature and level of work performed by employees assigned to this classification. Statements are not intended to be construed as an exhaustive list of all duties, responsibilities and skills required for this position.
Avanos Medical is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity or any other characteristic protected by law.
IMPORTANT: If you are a current employee of Avanos or a current Avanos Contractor, please apply here.
Join us at Avanos
Join us and you can make a difference in our products, solutions and our culture. Most of all, you can make a difference in the lives, people, and communities around the world.
Make your career count
Our commitment to improving the health and wellbeing of others begins with our employees - through a comprehensive and competitive range of benefits. We provide more than just a salary - our Total Rewards package encompasses everything you receive as an employee; your pay, health care benefits, retirement plans and work/life benefits.
Avanos offers a generous 401(k) employer match of 100% of each pretax dollar you contribute on the first 4% and 50% of the next 2% of pay contributed with immediate vesting.
Avanos also offers the following:
benefits on day 1
free onsite gym
onsite cafeteria
HQ region voted 'best place to live' by USA Today
uncapped sales commissions
Quality Supervisor
Quality manager job in Columbus, GA
Quality Supervisor!
Shift: 2nd Shift (4:00 PM - Midnight), with required overlap for dayshift coordination.
Are you a proven leader with a strong quality and regulatory background? Do you thrive in a dynamic, hands-on environment and believe in leading by example? We are looking for a Quality Supervisor to manage our critical second-shift operations in Columbus, GA.
What You'll Be Doing:
This role is about much more than oversight-it's about leadership, development, and ensuring excellence. You will:
Lead the Team: Oversee all 2nd shift quality activities, manage the daily workflow, and provide problem-solving guidance. You will directly manage a team of 5-7 Quality Leads and have an overall team of approximately 20 people reporting into you for the second shift.
Drive Quality: Be the final line of defence. You'll need to stand your ground-if something isn't correct, it simply cannot leave the door.
Mentor and Develop: Be a coach and a trainer. You will be responsible for helping the team grow, ensuring effective cross-training, and expecting them to learn the product and assist in the process. A background in training is ideal.
Supervise Operations: Manage scheduling, approve time off, and perform candidate interviews for new team members.
Be Flexible: Be willing to work overtime as needed. Flexibility is a must to meet our operational needs. Our standard work week is Monday to Friday, but you must be available to work some Saturdays.
What You'll Bring:
Proven experience in a quality role, preferably in a supervisory or leadership capacity.
A strong Quality Background and experience with Regulation.
Excellent people skills with a demonstrated ability to lead, motivate, and interact effectively with all levels of staff.
A "lead by example" approach to management and a decisive nature.
Opportunity for Growth:
For high-performing candidates seeking a higher salary, there is the possibility of managing both sites in the future.
If you are ready to take ownership of a vital second-shift operation and ensure a standard of quality that is second to none, we encourage you to apply today!
Quality Control Manager
Quality manager job in Fort Stewart, GA
CONSTRUCTION QUALITY CONTROL MANAGER
The Construction Quality Control (CQC) Manager is responsible for implementing and managing the Quality Control Program for federal construction projects, ensuring compliance with contract specifications, applicable regulations, and the U.S. Army Corps of Engineers (USACE) or other federal agency standards. The CQC Manager acts as the primary point of contact with government quality assurance representatives and ensures that all construction activities are executed with the highest quality and safety standards.
Key Responsibilities:
Develop, implement, and manage the Contractor Quality Control (CQC) Plan in accordance with project specifications and federal guidelines.
Serve as the main liaison between the company and government inspectors, including representatives from USACE, NAVFAC, or other federal entities.
Conduct daily quality control inspections and coordinate with field teams to verify that work complies with all contract documents, safety standards, and codes.
Manage the Three Phases of Control: Preparatory, Initial, and Follow-Up Meetings and Inspections.
Ensure all subcontractors and vendors meet quality control standards and understand contract specifications.
Prepare and maintain documentation including daily QC reports, submittal logs, test records, deficiency tracking, and punch lists.
Coordinate testing and inspections by third-party agencies as required.
Lead and document weekly QC and safety meetings with subcontractors and project team members.
Monitor subcontractor performance and enforce corrective actions when necessary.
Support the project team in identifying and mitigating risks to quality and schedule.
Ensure materials delivered to the site conform to approved submittals and specifications.
Qualifications:
Education: Bachelor's degree in Construction Management, Engineering, or related field preferred. Equivalent work experience may be considered.
Experience: Minimum 5 years of experience in construction quality control on federal government projects.
Certifications:
USACE/NAVFAC Construction Quality Management (CQM-C) Certification - Required
OSHA 30-Hour Construction Safety Certification - Preferred
First Aid/CPR Certification - Preferred
Strong knowledge of federal construction standards, EM 385-1-1, and applicable codes and regulations.
Excellent communication, documentation, and organizational skills.
Proficiency in Microsoft Office Suite, Procore, or similar project management software.
Preferred Attributes:
Ability to work independently and proactively manage quality processes.
Strong leadership and conflict resolution skills.
Detail-oriented with a focus on problem-solving and continuous improvement.
Experience with LEED or sustainability requirements (optional depending on project).
Electrical Quality Control Manager
Quality manager job in Savannah, GA
The ideal candidate is a critical thinker who will proactively improve the quality systems of the company through internal audits, participation in process improvement programs, and interaction with key partners to obtain constructive feedback.
Responsibilities
Develop standardized production, quality, and customer-service standards
Identify potential risks before they become a problem, focusing on root cause analysis and preventive action
Perform internal and external quality audits and compile detailed reports of findings
Build a strong team through coaching, mentoring, specific training and performance evaluations
Qualifications
Bachelor's degree or equivalent experience in Engineering
5+ years' relevant work experience
Highly organized with excellent attention to detail
Toxicology Laboratory Manager
Quality manager job in Atlanta, GA
Supervise laboratory personnel, including recruitment, training, scheduling, and performance evaluations.
Foster a collaborative and efficient work environment to promote team productivity.
Manage and prioritize toxicology testing workflows to meet turnaround times and maintain high-quality output.
Oversee equipment maintenance, inventory control, and supply procurement to ensure uninterrupted laboratory operations.
Implement and monitor quality control and assurance programs to maintain compliance with ASCP, CAP, CLIA, and other regulatory standards.
Address nonconformance and implement corrective actions to ensure accuracy and reliability in testing.
Ensure adherence to all relevant regulatory and accreditation requirements, including CLIA and CAP guidelines.
Prepare the laboratory for inspections and audits and maintain all necessary documentation.
Evaluate and integrate new toxicology instruments, assays, and technologies to enhance laboratory capabilities.
Collaborate with the leadership team on strategic decisions for laboratory growth and service expansion.
Oversee the interpretation of toxicology results and preparation of comprehensive reports.
Analyze laboratory performance data and implement process improvements where needed.
Director, Quality Assurance - Medical Manufacturing (On-site Savannah, GA)
Quality manager job in Savannah, GA
Don't just work somewhere, join Brasseler and be a valued team member of a world-class health care organization!
Our Culture: Provides a safe and welcoming environment where team members can balance their lives and develop their careers. All people and experiences are valued and respected. Different perspectives are encouraged and lead to better results. This makes us who we are and enables us to be a world-class healthcare organization. All who join us are accountable to this charge.
Our Philosophy:
Quality products sold with integrity has been the hallmark of Brasseler USA from the beginning. Brasseler USA's strong reputation of providing high quality, clinician endorsed and innovative dental and medical instrumentation nationally has spanned over 40 years. We have been offering a full-range of products made in the USA since 1976. Many of our products are manufactured at our headquarters in Savannah, GA.
Explore our career opportunities below to learn more.
JOB OVERVIEW:
This position is responsible to develop, implement and direct the company's quality assurance policies, procedures and methods to evaluate and improve the quality of complex products, materials, components and/or operations using standard procedures (e.g. 9001:2015, ISO 13485:2016, QMSR, etc.), and may take all reasonable and prudent steps necessary to maintain compliance with company and product registration requirements, with appropriate notification to, and/or direction from their direct supervisor.
KEY RESPONSIBILITIES:
Direct all phases of highly technical quality assurance audit activities.
Oversee the Quality Management Systems of multiple entities ensuring compliance with global MDSAP requirements as applicable.
Oversee the preparation, documentation and conduction of Quality Assurance audits of Distribution Centers, joint Ventures, X-Ray Centers, private label manufacturers, non-manufacturing suppliers of Medical Devices and Pharmaceuticals
Direct and oversee Quality Assurance audits to ensure the effective and timely facilitation of suppliers and internal quality audits and follows-up on CAPAs/Observations.
Oversee suppliers to assure the quality of their products, materials, components and/or operations.
Lead in the monitoring of supplier performance efforts and recommend changes to improve the production process.
Stay current with new or potential business opportunities, and prepare for all QA activities.
Direct and oversee the research for applicable FDA, ISO and ASTM/ANSI standards to ensure the company's ongoing compliance with U.S. and International Regulatory Requirements (Medical Devices Directives, Medical Device Regulations, and FDA QS requirements).
Serve as FDA Official Correspondent for US Facilities and US Agent for foreign HS entities.
Serve as the Management Representative for the site for interaction with regulatory agencies.
Serve as Person Responsible for Regulatory Compliance (PRRC) at manufacturing locations for Corporate Brand products, under the European Medical Device Regulation.
Assist with due diligence and follow-up surveillance audits as required and serve as SME for some manufacturing partners.
Assess the effectiveness of existing policies, guidelines and procedures and recommend changes.
Consult and direct process and product transfer projects compliant to the applicable regulations, directives, and standards.Provide ongoing direction and guidance to the team and provide guidance and development opportunities as needed.
Select, develop, and evaluate TSMs to ensure the efficient operation of the department.
SPECIFIC KNOWLEDGE & SKILLS:
Knowledge of ISO 9000 certification and maintenance.
Knowledge of ISO 13485 certification and maintenance.
Knowledge of the European Medical Device Regulation 2017/745.
Knowledge of US FDA Quality Management System Regulation
Knowledge of MDSAP country specific regulatory requirements
GENERAL SKILLS & COMPETENCIES:
Attract, retain, motivate, coach and develop team members for high performance.
Excellent writing and communication skills.
Excellent analysis and problem solving skills.
Excellent decision making skills.
Understand, interpret and act on financial information that contributes to business profitability.
Ability to plan and manage complex projects, manage risks, costs, time and project teams.
Excellent planning/ organizational skills and techniques.
Communicate effectively with senior management and key stakeholders.
Excellent negotiating skills.
Uses skills to lead teams to achieve company goals in effective ways.
Ability to Influence, build relationships, navigate politics and manage conflicts.
Broad and wide-range of professional and managerial skills with a full understanding of industry practices and company policies and procedures.
Ability to lead and develop virtual teams.
Strategic planning skills.
Budget development and monitoring skills
WORK EXPERIENCE:
Typically 10 or more years of increasing responsibility and complexity in terms of any applicable professional experience; 5 or more years of management experience. Experience managing the quality management systems of multiple manufacturing locations is preferred.
PREFERRED EDUCATION:
Bachelor's Degree or global equivalent in Engineering , Science or related technical discipline. Master's degree preferred. RAPS and ASQ or other equivalent Certifications preferred.
TRAVEL/ PHYSICAL DEMANDS:
Typically 25% or more
Office environment. No special physical demands required.
Additional Job Description
JOB COMPLEXITY:
Work on complex issues where analysis of situations or data requires an in-depth knowledge of the company. Participate in corporate development of methods, techniques and evaluation criteria for projects, programs, and people. Establish and assure adherence to budgets, schedules, work plans, and performance requirements. Provide managers with departmental goals and objectives and ensure adherence to established goals and objectives.
DISCRETION:
Erroneous decisions will have a serious impact on the success of functional, division, or company operations. Accountability generally resides with or is shared with supervisor.
SUPERVISION:
Direct and control the activities of a functional area through several department managers or senior professionals within the company. Control of planning, staffing, budgeting, managing expense priorities, and recommending changes to methods.
INTERACTION:
Regularly interact with executives and/or major customers. Require the ability to change the thinking of, or gain acceptance from, others in sensitive situations, without damage to the relationship. Manage vendor relationships.
PERFORMANCE REQUIREMENTS:
Typically, to advance to a new grade, TSMs must demonstrate professional behavior and should consistently be at the high-end of meets expectations or consistently exceed expectations.
Benefits available include: Medical, Dental and Vision Coverage, 401K Plan with Company Match, Generous Time Off, Paid Parental Leave, Income Protection, Work Life Assistance Program, Flexible Spending Accounts, Educational Benefits, Worldwide Scholarship Program and Volunteer Opportunities.
*Benefits may vary by location or status.
Henry Schein is an Equal Employment Opportunity Employer and does not discriminate against applicants or employees on the basis of race, color, religion, creed, national origin, ancestry, disability that can be reasonably accommodated without undue hardship, sex, sexual orientation, gender identity, age, citizenship, marital or veteran status, or any other legally protected status.
Auto-ApplyDirector, Food Safety and Quality Assurance
Quality manager job in College Park, GA
Schweid & Sons is a family-owned and operated premium ground beef company with a proud heritage spanning four generations. We supply top-quality beef to Retail, Foodservice, and National Account customers across the U.S. and are committed to quality, customer service, and innovation in protein manufacturing.
Summary:
Schweid and Sons is looking for a Director of Food Safety and Quality Assurance (FSQA) to add to our team. Reporting to the VP of Operations, you will lead the continued development and implementation of a comprehensive, best-in-class approach to food safety, sanitation, quality, and regulatory compliance. As the leader of food safety, QA, and regulatory, your goal will be to provide high-level strategy and guidance to take the company into the future. To be successful in this role, you must have a strong food safety and quality background and knowledge of regulatory requirements. In addition to that, you must be a strategic problem solver and have an eye for identifying areas of improvement. This is an incredible opportunity to join a well-established food manufacturing company that prides itself on putting its team members first by providing an incredible culture, amazing benefits, and unparalleled employee retention.
Job Functions /Responsibilities:
Provide advice regarding culture, growth, planning, talent, and legal issues.
Lead two QA managers in a two-site operation
Advise the Senior Leadership Team on food safety, quality, and regulatory compliance matters
Articulate activities and needs of the QA and Food Safety
Collaborate with leadership on major organizational initiatives
Ensure all initiatives align with the company's desired culture, mission, and strategic plan
Support the food safety management system through adherence to policies
Continuously work to increase knowledge, solve problems, and develop new technologies
Develop food safety and quality strategy roadmaps and lead its execution enterprise-wide
Communicate with Sales, customer service, and customers on regular basis
Lead all SQF audits
Develop food safety plans
Develop food safety training programs
Qualifications / Experience:
Bachelor's Degree required
Exceptional leadership required
HACCP and SQF certified
Exceptional communication skills
8 + years of Food Safety, Quality, and USDA Regulatory experience required
5 + years of QA management and/or 3+ years Director level experience required in protein producing industries
5 + years related protein experience required, strong preference for beef experience, ideally with ground beef.
Food/nutrition manufacturing experience required
SQF audit leadership experience required
Quality Management System experience required
Experience developing food safety and training plans required
Able to effectively analyze data to develop presentations and reports
Must be proficient in the use of Microsoft Office (Excel, Outlook, Word, and PowerPoint)
What We Offer
Time Off: PTO, Safe & Sick Time, and Paid Holidays.
Health Benefits: Medical, vision, dental, HRA and voluntary disability benefits.
Financial Benefits: 401(k) + employer match and life insurance.
Location: This is an on-site role located in College Park, GA.
Environment: Our facility is refrigerated. In this role you will be exposed to < 40 degrees for multiple hours of the day.
Auto-ApplyManager, Quality
Quality manager job in Fairburn, GA
DP World in Fairburn, GA is searching for a sharp, driven, and quality-obsessed Quality Manager ready to take ownership of our standards and elevate them to the next level. In this role, you'll be the champion of quality performance, leading key initiatives that ensure our operations run flawlessly. You'll design, implement, and refine quality procedures, analyze performance trends, and work side-by-side with leadership to drive continuous improvement across the site.
This isn't a behind-the-scenes role - this is your chance to influence major decisions, strengthen customer satisfaction, and build a best-in-class quality culture that sets the tone for the entire facility.
If you're passionate about operational excellence, thrive in fast-paced environments, and are ready to create real impact - we want to see what you can bring to the table.
About the Role
How you will contribute
* Manage and analyze data from customers and internal sources as input for problem solving and communicate/report to appropriate personnel. Interacts with staff within the location and within the Company and all customer and prospective customer representatives.
* Directly supervises Quality functions and staff across all shifts and provides consistent direction of the company's quality plans.
* Administer all projects and documentation relative to assigned processes (i.e. operator instructions, PFMEA's and process control plans).
* Develop and design irreversible corrective actions for known problems. Use established problem solving techniques to reduce process variation.
* Manage quality processes and reports - 3rd party sorts, suspect material, damage material etc. - Suspect Material - maintain relationships with suppliers to deal with suspect material.
* Champion Lean engineering goals. Includes being an aid in developing, implementing and maintaining a Lean culture within the organization using a hands-on approach in order to provide input on processes from a quality perspective.
* Responsible for the development, implementation and monitoring of the Quality System. Reports to Management on effectiveness of the Quality System.
* Generate, interpret, analyze, and communicate results using management tools, graphs, and reports; actively coach the organization concerning quality with tools and reports.
* Provide input on document enhancement and retention; Maintain ISO documentation and controls, administer activities required to maintain ISO certification, and actively coach the organization for maintaining ISO system.
* Other duties as assigned
Your Key Qualifications
* Bachelor's degree in business, engineering, or related field preferred.
* Progressive experience performing professional level quality management duties; preferably in automotive or logistics industry.
* Additional education, training and/or work experience in area of specialization inherent to the position may be required.
* Knowledge of principles and procedures used in logistics operations and practice.
Compensation
DP World offers exciting and challenging roles within a growing international organization. We strive to hire and develop the right people, locally and globally, stimulating personal growth and self-development within an informal atmosphere. We offer a market competitive compensation package.
About DP World
Trade is the lifeblood of the global economy, creating opportunities and improving the quality of life for people around the world. DP World exists to make the world's trade flow better, changing what's possible for the customers and communities we serve globally.
With a dedicated, diverse and professional team of more than 111,000 employees from 159 nationalities, spanning 77 countries on six continents, DP World is pushing trade further and faster towards a seamless supply chain that's fit for the future.
We're rapidly transforming and integrating our businesses -- Ports and Terminals, Marine Services, Logistics and Technology - and uniting our global infrastructure with local expertise to create stronger, more efficient end-to-end supply chain solutions that can change the way the world trades.
What's more, we're reshaping the future by investing in innovation. From intelligent delivery systems to automated warehouse stacking, we're at the cutting edge of disruptive technology, pushing the sector towards better ways to trade, minimising disruptions from the factory floor to the customer's door.
DP World is on a mission to transcend boundaries and bridge the gap between all nations and cultures - not just in what we do but also in how we behave.
We are dedicated to creating a culture where everyone feels respected, supported, and empowered to reach their full potential. We believe that embracing inclusion and diversity, drives innovation and growth and helps us connect people, businesses, and societies. Free minds and different perspectives are changing our world, and together we can change what's possible.
The DP World family comprises of syncreon, Imperial and P&O.
WE MAKE TRADE FLOW
TO CHANGE WHAT'S POSSIBLE FOR EVERYONE.
Nearest Major Market: Atlanta
Job Segment: Logistics, Supply Chain Manager, Supply Chain, Quality Manager, Facilities, Operations, Quality
Quality Manager
Quality manager job in Acworth, GA
Full-time Description
Quality Manager
The Quality and Operations Manager will be responsible for overseeing and managing the quality control and food safety systems at our Acworth location to ensure that all products meet the required food safety, quality, and regulatory standards. This role will involve leading a quality and food safety team, managing audits and certifications, ensuring compliance with internal and external standards, and driving continuous improvement across the production process.
Responsibilities:
Develop, implement, and maintain comprehensive quality assurance programs to ensure food safety and regulatory compliance (including SQF, HACCP, GMP, and FSMA)
Establish, update, and enforce policies and procedures to meet federal, state, and local regulations (FDA, USDA, and other applicable food safety laws), industry standards, and customer requirements.
Lead internal and external audits, including third-party certification audits (SQF), customer audits, and regulatory inspections.
Ensure the facilities are consistently audit-ready by monitoring programs, records, and floor operations.
Manage and ensure timely completion of corrective and preventive actions from audit findings.
Investigate quality and food safety related issues, conduct root cause analysis, and develop corrective and preventive actions.
Lead initiatives for continuous improvement in product quality, efficiency, and food safety, using data analysis, customer feedback, and internal performance metrics.
Supervise, train, and mentor a team of QA professionals across multiple buildings - food and non-food secondary packaging. Ensure the team is equipped with the necessary skills and knowledge to perform their roles effectively and remain compliant with food safety and quality standards. Conduct performance evaluations, set team objectives, and support career development.
Collaborate with cross-functional teams on new project launches, ensuring all food safety and quality requirements are met.
Perform all other duties as assigned.
Requirements
Qualifications:
Fluent English writing/speaking required. Bi-lingual (Spanish) preferred.
BS Degree in Food Technology, Food Science, Engineering, or related business degree required. Master's Degree Preferred.
Minimum 10+ years of experience in quality and food safety, including 7+ years in a leadership role within a food manufacturing environment (co-manufacturing, Fast Moving Consumer Goods - FMCG.)
Deep understanding of food safety regulations, GMP, HACCP, and SQF standards. Familiarity with FDA, USDA, and other relevant regulatory bodies.
Strong leadership, communication, and organizational skills. Ability to work cross-functionally, manage projects, and lead a team to drive continuous improvement.
Previous experience with GFSI (SQF) audits.
Certified in HACCP, PCQI, and SQF Practitioner.
Quality Manager
Quality manager job in Thomasville, GA
Job Description
Check-Mate Manufacturing LLC located in Thomasville, GA is a subsidiary of Check-Mate Industries based in West Babylon, New York. Over the past 40 years, Check-Mate has proven to be the winning move for hundreds of customers in a diverse range of industries. The company has been recognized as an innovator and leader in tool & die, stampings and assemblies. Whether producing high-precision tools and progressive dies, stamping, or assemblies for everything from healthcare to personal security products, Check-Mate
out-thinks
,
out-maneuvers
, and
out
-performs
its competition.
QUALITY MANAGER
Check-Mate Industries has an immediate opening for a Quality Manager at its Thomasville, GA facility.
SUMMARY OF POSITION:
The Quality Manager is responsible for ensuring manufactured products at Check-Mate Industries meet set standards of quality, reliability and performance. Sets and implements both internal and external quality requirements to ensure that company products and services meet customer expectations. Develops quality management system for Check-Mate Industries utilizing ISO/TS 16949 standards. Manages quality engineers and quality inspectors.
Quality Management System (QMS)
Quality Manager maintains the Quality Management System to ensure compliance to QMS Standards.
Quality Manager supports External QMS audits.
Process Planning
Quality Manager conducts assessments of company production processes to develop in-house quality policies, procedures and specifications.
Quality Manager collaborates with an organization's purchasing, materials, warehouse and production departments to ensure raw materials from external suppliers meet quality requirements.
Quality Manager evaluates customer requirements to ensure their needs are met by set customer service standards.
Quality Manager specifies quality requirements for raw materials obtained from vendors and suppliers.
Quality Manager implements and monitors quality assurance standards to ensure consistent product quality.
Quality Manager establishes procedures and processes for sampling, recording and reporting of quality data.
Quality Manager conducts and monitors the analysis/inspection of raw materials and final products to ensure compliance with set specifications.
Quality Manager conducts tests to verify the quality of raw materials and finished products.
Material Review Board
Quality Manager carries out research to identify ways to reduce waste and maximize resources.
Quality Manager collects, compiles, and analyzes relevant quality statistical data to obtain information regarding quality performance.
Quality Manager approves compliant products and reject defective ones.
Quality Manager collects and compiles relevant quality statistical data is also part of the quality manager description.
Corrective and Prevention Action (CAPA)
Quality Manager reviews existing process and product specification to identify the need for improvement or upgrade.
Quality Manager addresses both internal and external quality issues in order to bring to resolution.
Quality Manager analyzes data for trends in order to prevent issues from occurring.
Audits
Quality Manager conducts surveys to identify customer requirements and ensure they are being met by established quality standards.
Quality Manager ensures manufacturing processes comply with local and global standards of production.
Quality Manager conducts quality audits to make sure set quality policies and procedures are being adhered to.
Quality Manager monitors product development processes to identify deviations from quality policies.
Quality Manager assists external quality auditors in coordinating on-site audits.
Calibration
Quality Manager maintains proper records of quality test, procedures and standards.
Quality Manager maintains records and documentation of quality tests and other quality-related activities.
Supervisory
Quality Manager oversees the recruitment and training of quality assurance personnel to ensure an effective work unit.
Quality Manager organizes training for quality assurance staff to enhance their skill and knowledge of product quality requirements.
Quality Manager supervises quality engineers, technicians, inspectors, and other company staff to ensure they perform their duties in line with established quality procedures.
Quality Manager offers recommendations to company management on ways to improve on existing quality processes.
Quality Manager collaborates with quality personnel to implement procedures, systems, and standards of operation.
Quality Manager prepares and presents reports to update upper management on quality activities.
Quality Manager prepares and presents to senior management reports of quality operations.
Minimum Requirements:
Bachelor's degree in business administration, management, engineering, or in other related discipline.
5+ years' experience with PFMEA, PPAP/FAI, SPC and control plans
Experience working with quality/safety standards ITAR, RoHS and OSHA
Ability to use precise measuring equipment such as micrometers, calipers, gauge blocks, dial indicators, attribute gauges, height gauges, CMM and methodologies including Gage R&R
Certified Quality Inspector/Auditor preferred
5+ years' experience in Metals manufacturing (stamping, forming & welding) and quality assurance
Experience with ISO 9001, 140001/ IATF16949 etc. implementation
1-3 years' experience with Plex ERP, SAP, MRP or other manufacturing-wide resource systems
5+ years' experience with SME Root Cause and Failure Analysis (CAPA), ASQ Design of Experiments, Lean and Total Quality Systems
Experience with lean manufacturing principles (Six Sigma)
Proficiency using Microsoft Suite (Excel, Access)
EOE/AA/M/F/VET/D
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Program Manager, Product Quality and Readiness
Quality manager job in Atlanta, GA
About Rivian Rivian is on a mission to keep the world adventurous forever. This goes for the emissions-free Electric Adventure Vehicles we build, and the curious, courageous souls we seek to attract. As a company, we constantly challenge what's possible, never simply accepting what has always been done. We reframe old problems, seek new solutions and operate comfortably in areas that are unknown. Our backgrounds are diverse, but our team shares a love of the outdoors and a desire to protect it for future generations. Role Summary At Rivian, handing over the keys isn't just a transaction; it is the start of an adventure. As the Program Manager, Product Quality & Readiness, you are the guardian of that standard. You are a strategic operator and systems thinker obsessed with defining the technical frameworks and quality gates that ensure every vehicle delivered to a customer is flawless in both function and form. You operate at the critical junction where the factory ends and the customer journey begins. Your mission is to architect the intelligent, scalable operating system that performs the final validation of our vehicles before they ever reach a customer's driveway. You ensure that the first moment of ownership is pure joy, unmarred by technical oversight or cosmetic imperfection. More critically, you will transform this validation phase into the ultimate feedback loop. You will capture high-fidelity data to drive systemic improvements in the factory, while simultaneously driving rigorous operational execution in the field to ensure vehicle presentation is immaculate. You are the operational bridge ensuring quality is a closed-loop system that centers the customer at every stage. Responsibilities The Customer Advocate: You never lose sight of the human being waiting for their keys. You view every defect-whether a software bug or a smudge on the glass-as a potential friction point in a customer's adventure, and you fight relentlessly to eliminate them. The Clarity Creator: You are an expert at simplifying complex quality challenges into structured, measurable technical programs. The Data Architect: You use data to diagnose systemic issues, build compelling business cases, and ensure every requirement is backed by measurable field impact. The Strategic Partner: You excel at translating field reality into actionable HQ plans, fostering alignment and shared success with central teams, especially Manufacturing. A Long-Term Builder: You are focused on building sustainable, scalable systems that will power our quality standards for years to come. Qualifications 8+ years of experience in Technical Program Management, Product, Process/Industrial Engineering, or Operations within a complex hardware-intensive industry (Automotive, Aerospace, or similar). This requirement is reduced to 5 years for candidates with a Master's degree. Customer Obsession: A demonstrated ability to connect technical processes to customer outcomes. You understand that "Quality" is defined by the user experience, not just the spec sheet. Operational Rigor: Experience defining Standard Operating Procedures (SOPs) for field or factory teams. You understand that while the factory builds the product, the field team delivers the experience, and you know how to drive compliance in product presentation, quality, and cleanliness. Proven experience in defining, deploying, and owning technical systems and data pipelines, specifically around quality control, manufacturing execution (MES), or diagnostic tooling. Exceptional ability to synthesize high-volume data (telemetry, manufacturing data) into clear, strategic narratives for both executive and engineering audiences. The Operator-Engineer Mindset: You are equal parts operator (focused on execution, logistics, and people) and engineer (focused on systems, optimization, and tools). Applied Ingenuity: A degree in a hands-on technical field is preferred. However, we value applied ingenuity above all; a demonstrated track record of solving complex problems in rigorous environments may be accepted in lieu of specific academic credentials. Pay Disclosure Salary Range/Hourly Rate for California Based Applicants: $121,800 - $161,450 (actual compensation will be determined based on experience, location, and other factors permitted by law). Benefits Summary: Rivian provides robust medical/Rx, dental and vision insurance packages for full-time and part-time employees, their spouse or domestic partner, and children up to age 26. Full Time Employee coverage is effective on the first day of employment. Part-Time employee coverage is effective the first of the month following 90 days of employment. Salary Range/Hourly Rate for Illinois Based Applicants: $102,300 - $135,580 (actual compensation will be determined based on experience, location, and other factors permitted by law). Benefits Summary: Rivian provides robust medical/Rx, dental and vision insurance packages for full-time and part-time employees, their spouse or domestic partner, and children up to age 26. Full Time Employee coverage is effective on the first day of employment. Part-Time employee coverage is effective the first of the month following 90 days of employment. Equal Opportunity Rivian is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices laws. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, ancestry, sex, sexual orientation, gender, gender expression, gender identity, genetic information or characteristics, physical or mental disability, marital/domestic partner status, age, military/veteran status, medical condition, or any other characteristic protected by law. Rivian is committed to ensuring that our hiring process is accessible for persons with disabilities. If you have a disability or limitation, such as those covered by the Americans with Disabilities Act, that requires accommodations to assist you in the search and application process, please email us at candidateaccommodations@rivian.com. Candidate Data Privacy Rivian may collect, use and disclose your personal information or personal data (within the meaning of the applicable data protection laws) when you apply for employment and/or participate in our recruitment processes ("Candidate Personal Data"). This data includes contact, demographic, communications, educational, professional, employment, social media/website, network/device, recruiting system usage/interaction, security and preference information. Rivian may use your Candidate Personal Data for the purposes of (i) tracking interactions with our recruiting system; (ii) carrying out, analyzing and improving our application and recruitment process, including assessing you and your application and conducting employment, background and reference checks; (iii) establishing an employment relationship or entering into an employment contract with you; (iv) complying with our legal, regulatory and corporate governance obligations; (v) recordkeeping; (vi) ensuring network and information security and preventing fraud; and (vii) as otherwise required or permitted by applicable law. Rivian may share your Candidate Personal Data with (i) internal personnel who have a need to know such information in order to perform their duties, including individuals on our People Team, Finance, Legal, and the team(s) with the position(s) for which you are applying; (ii) Rivian affiliates; and (iii) Rivian's service providers, including providers of background checks, staffing services, and cloud services. Rivian may transfer or store internationally your Candidate Personal Data, including to or in the United States, Canada, the United Kingdom, and the European Union and in the cloud, and this data may be subject to the laws and accessible to the courts, law enforcement and national security authorities of such jurisdictions. Please note that we are currently not accepting applications from third party application services.
8+ years of experience in Technical Program Management, Product, Process/Industrial Engineering, or Operations within a complex hardware-intensive industry (Automotive, Aerospace, or similar). This requirement is reduced to 5 years for candidates with a Master's degree. Customer Obsession: A demonstrated ability to connect technical processes to customer outcomes. You understand that "Quality" is defined by the user experience, not just the spec sheet. Operational Rigor: Experience defining Standard Operating Procedures (SOPs) for field or factory teams. You understand that while the factory builds the product, the field team delivers the experience, and you know how to drive compliance in product presentation, quality, and cleanliness. Proven experience in defining, deploying, and owning technical systems and data pipelines, specifically around quality control, manufacturing execution (MES), or diagnostic tooling. Exceptional ability to synthesize high-volume data (telemetry, manufacturing data) into clear, strategic narratives for both executive and engineering audiences. The Operator-Engineer Mindset: You are equal parts operator (focused on execution, logistics, and people) and engineer (focused on systems, optimization, and tools). Applied Ingenuity: A degree in a hands-on technical field is preferred. However, we value applied ingenuity above all; a demonstrated track record of solving complex problems in rigorous environments may be accepted in lieu of specific academic credentials.
The Customer Advocate: You never lose sight of the human being waiting for their keys. You view every defect-whether a software bug or a smudge on the glass-as a potential friction point in a customer's adventure, and you fight relentlessly to eliminate them. The Clarity Creator: You are an expert at simplifying complex quality challenges into structured, measurable technical programs. The Data Architect: You use data to diagnose systemic issues, build compelling business cases, and ensure every requirement is backed by measurable field impact. The Strategic Partner: You excel at translating field reality into actionable HQ plans, fostering alignment and shared success with central teams, especially Manufacturing. A Long-Term Builder: You are focused on building sustainable, scalable systems that will power our quality standards for years to come.
Manufacturing Quality Manager
Quality manager job in Thomasville, GA
Any salary estimation specified in this job board may or may not be aligned with our organization's pay philosophy. Apply to connect with a Talent Acquisition Partner who can provide you more details!
Job Title: Manufacturing Quality Manager
Position Overview
The Manufacturing Quality Manager is responsible for leading, developing, and administering the plant's Quality Management System (QMS) to ensure products meet strict customer, regulatory, and industry requirements. This role oversees ISO 9000/9001 and other third-party accreditations (e.g., ASME), drives continuous improvement, and leads a team of quality professionals in a high-volume manufacturing environment ($25-$50M). The position requires strong leadership, independent judgment, technical expertise, and the ability to improve both product quality and customer satisfaction.
Essential Duties & Responsibilities
Quality Management System (QMS) & Certifications
Develop, implement, and maintain a robust ISO 9000/9001-compliant QMS, ensuring ongoing certification.
Achieve and maintain all third-party accreditations (ISO 9000/9001, ASME, customer-specific standards).
Manage internal and external audits; ensure timely corrective and preventive actions (CAPA).
Maintain and control QMS documentation, including manuals, procedures, work instructions, records, and reports.
Quality Assurance & Control
Oversee all inspection and testing activities: incoming materials, in-process, and final product.
Develop inspection plans, test methods, and quality standards for welding, machining, fabrication, and assembly operations.
Identify quality trends and root causes using statistical tools (SPC, Pareto, 5-Why, Ishikawa).
Ensure calibration of measurement instruments and compliance with metrology standards.
Develop and maintain quality performance metrics (KPIs) to improve the cost of poor quality.
Leadership & Team Management
Lead and manage the Quality Assurance department, including exempt, non-exempt, and hourly personnel.
Provide coaching, direction, and development for the team, promoting accountability and engagement.
Foster a culture of continuous improvement and employee involvement.
Serve as a key member of the Plant Operating Management Team, contributing to strategic plans and operational decisions.
Customer & Internal Collaboration
Act as the primary point of contact for customer quality issues, complaints, and audits.
Resolve issues requiring interpretation of quality standards in situations with ambiguity or controversy.
Work cross-functionally with production, engineering, supply chain, and corporate quality to support business and customer requirements.
Improve the overall customer experience through enhanced quality systems and communication.
Continuous Improvement & Lean Initiatives
Promote and lead Lean and continuous improvement initiatives to enhance product quality, reduce defects, and eliminate waste.
Drive CAPA, FMEA, and problem-solving activities to ensure sustained improvements.
Support cross-functional Kaizen events and improvement projects.
Training & Development
Develop and conduct training programs on quality procedures, inspection techniques, auditing, and QMS requirements.
Train employees in Lean, SPC, and other quality tools to strengthen plant-wide quality awareness.
Decision-Making & Independence
Operate with a high degree of autonomy and professional judgment.
Make data-driven decisions regarding quality issues, process deviations, supplier concerns, and customer escalations.
Handle complex or controversial situations requiring diplomacy and clear communication.
Qualifications
Education & Experience
Bachelor's degree in Engineering, Quality, Manufacturing, or equivalent experience.
8+ years of quality experience in manufacturing, including 3+ years in a supervisory or management role.
Experience working in welding, machining, fabrication, or similar heavy manufacturing environments strongly preferred.
Technical Skills
Knowledge of ISO 9000/9001 QMS requirements and maintaining certifications.
Strong proficiency in SPC, statistical analysis, and root cause tools.
Experience with audits, CAPA, FMEAs, control plans, and process validation.
Ability to interpret mechanical blueprints, electrical diagrams, and technical specifications.
Familiarity with ERP/MES systems and digital quality tools.
Leadership & Professional Skills
Proven leadership skills with the ability to motivate, develop, and guide diverse teams.
Excellent communication, interpersonal, and problem-solving abilities.
Ability to work independently, handle ambiguity, and make sound decisions.
Strong organizational, analytical, and strategic thinking skills.
Working Conditions
Work performed in both office and manufacturing floor environments, including exposure to welding, machining, and fabrication operations.
Occasional exposure to moderately disagreeable conditions or minor hazards; proper PPE required.
Limited physical demands; involves routine movement and light handling of materials.
Other Information
This job description reflects the general nature and responsibilities of the role and is not intended to be an exhaustive list of duties. Management reserves the right to change or modify job responsibilities as needed.
Benefits of Being a Cleaver-Brooks Employee:
We offer a competitive salary and comprehensive benefits package, including medical, dental, vision, maternity support program, discounted virtual physician visits, voluntary medical benefits (Critical Illness, Hospital Care, and Accidental Injury), FSA, HSA, life insurance, short term and long term disability, cash matching 401(k) plan, employee assistance program (EAP), pet insurance, employee discount program, generous vacation and 11 paid holidays.
Who is Cleaver-Brooks:
Cleaver-Brooks is the market leader in providing fully integrated boiler and burner systems. We lead the boiler/burner industry due to our unmatched distribution network's ability to deliver the knowledge, service, training and support that are essential to long-term performance. Our customers will tell you that we're the only equipment provider that manufactures boilers, burners, controls, and a full array of ancillary and aftermarket products. They'll also mention that our unique single-source capability means that we can deliver fully integrated boiler room solutions that reduce overall costs and optimize space. It is our focus on products that deliver the most efficient, reliable, safe and environmentally sustainable solutions that differentiate us in the marketplace. Cleaver-Brooks continues a 90+ year legacy of providing the customers we serve with extraordinary products designed to deliver unsurpassed performance through the power of commitment.
This description indicates the general nature of the tasks and responsibilities required of position given this classification. It is not intended as a complete list of specific duties and responsibilities. Nor is it intended to limit or modify the right of management to assign, direct, and control the specific duties of individuals performing this function. The Company reserves the right to change, modify, amend, add to or delete from any section of this document as it deems, in its judgment, to be proper. This description supersedes any previous descriptions for this position
.
By applying for this job and providing your mobile number, you consent to receive an initial text message from a Cleaver-Brooks Talent Team member. You will have the option to opt out upon receiving the message. Messages may include updates on your application, scheduling initial screenings or interviews, and similar communications. Standard message and data rates may apply, and message frequency may vary.
QC Manager
Quality manager job in Gainesville, GA
The Quality Control Manager is responsible for establishing and overseeing quality control processes to ensure the safe and consistent production of bakery products, including bread and cake. This role includes managing inspections from raw material intake to production and finished product shipping, while addressing any quality or food safety issues. The role also encompasses supplier management, food regulatory compliance, labeling, and the inspection of materials and products.
ESSENTIAL JOB FUNCTIONS:
The Quality Control Manager will be responsible for, but not limited to, the following:
Respond to food safety and quality issues related to the production of 50100 types of bakery products (bread and cake).
Manage and oversee process controls to ensure that quality inspectors can record and analyze inspection results in the SAP system.
Develop and maintain food safety programs such as SQF and HACCP to proactively prevent food safety incidents.
Establish and maintain infrastructure for microbiological analysis and baking test labs for bakery items.
Lead internal, customer, and government responses in the event of a food safety issue.
QUALIFICATIONS:
BA/BS degree in Food Science, Food Engineering, or a related field; equivalent experience may be considered.
Minimum of 7 years of hands-on experience in quality control within the food or bakery industry.
Strong communication and reporting skills, both verbal and written.
Demonstrated passion for quality control and bakery product excellence.
Bilingual in English and Korean strongly preferred.
Experience with SAP or similar ERP systems is a plus.
Familiarity with food safety regulations and global standards (e.g., HACCP, GMP, FSMA)
EMPLOYEE BENEFITS:
Health Insurance options: PPO Medical, Dental, Vision covered (Company 100% paid) *insurance starts on the very 1st date.
Life Insurance (Company 100% paid)
Flexible Time (starting time can vary everyday)
Short Term and Long-Term Disability Leave (short term 100% covered)
Lifestyle Allowance (up to net $70 per Month)
Cellphone reimbursement eligible
Employee Discounts (40% off company's products & services)
401(k) 5% Match (no vesting period!) from Day 1
Paid Time Off (generous and increases by tier!): Max ceiling of 180 hours PTO (15 days) the 1st year and increases by tier.
Wellness Day: 40 Hours (Use it or Lose it System)
Paid Maternity Leave (paid 100% for 12 weeks)
Paid Secondary Caregiver Leave (up to 2 weeks)
Paid Creative Leave
Paid Holidays (11 days)
Educational Benefit
Employee Club Activities
& Much More!
Manufacturing Quality Manager
Quality manager job in Thomasville, GA
Any salary estimation specified in this job board may or may not be aligned with our organization's pay philosophy. Apply to connect with a Talent Acquisition Partner who can provide you more details!
Job Title: Manufacturing Quality Manager
Position Overview
The Manufacturing Quality Manager is responsible for leading, developing, and administering the plant's Quality Management System (QMS) to ensure products meet strict customer, regulatory, and industry requirements. This role oversees ISO 9000/9001 and other third-party accreditations (e.g., ASME), drives continuous improvement, and leads a team of quality professionals in a high-volume manufacturing environment ($25-$50M). The position requires strong leadership, independent judgment, technical expertise, and the ability to improve both product quality and customer satisfaction.
Essential Duties & Responsibilities
Quality Management System (QMS) & Certifications
Develop, implement, and maintain a robust ISO 9000/9001-compliant QMS, ensuring ongoing certification.
Achieve and maintain all third-party accreditations (ISO 9000/9001, ASME, customer-specific standards).
Manage internal and external audits; ensure timely corrective and preventive actions (CAPA).
Maintain and control QMS documentation, including manuals, procedures, work instructions, records, and reports.
Quality Assurance & Control
Oversee all inspection and testing activities: incoming materials, in-process, and final product.
Develop inspection plans, test methods, and quality standards for welding, machining, fabrication, and assembly operations.
Identify quality trends and root causes using statistical tools (SPC, Pareto, 5-Why, Ishikawa).
Ensure calibration of measurement instruments and compliance with metrology standards.
Develop and maintain quality performance metrics (KPIs) to improve the cost of poor quality.
Leadership & Team Management
Lead and manage the Quality Assurance department, including exempt, non-exempt, and hourly personnel.
Provide coaching, direction, and development for the team, promoting accountability and engagement.
Foster a culture of continuous improvement and employee involvement.
Serve as a key member of the Plant Operating Management Team, contributing to strategic plans and operational decisions.
Customer & Internal Collaboration
Act as the primary point of contact for customer quality issues, complaints, and audits.
Resolve issues requiring interpretation of quality standards in situations with ambiguity or controversy.
Work cross-functionally with production, engineering, supply chain, and corporate quality to support business and customer requirements.
Improve the overall customer experience through enhanced quality systems and communication.
Continuous Improvement & Lean Initiatives
Promote and lead Lean and continuous improvement initiatives to enhance product quality, reduce defects, and eliminate waste.
Drive CAPA, FMEA, and problem-solving activities to ensure sustained improvements.
Support cross-functional Kaizen events and improvement projects.
Training & Development
Develop and conduct training programs on quality procedures, inspection techniques, auditing, and QMS requirements.
Train employees in Lean, SPC, and other quality tools to strengthen plant-wide quality awareness.
Decision-Making & Independence
Operate with a high degree of autonomy and professional judgment.
Make data-driven decisions regarding quality issues, process deviations, supplier concerns, and customer escalations.
Handle complex or controversial situations requiring diplomacy and clear communication.
Qualifications
Education & Experience
Bachelor's degree in Engineering, Quality, Manufacturing, or equivalent experience.
8+ years of quality experience in manufacturing, including 3+ years in a supervisory or management role.
Experience working in welding, machining, fabrication, or similar heavy manufacturing environments strongly preferred.
Technical Skills
Knowledge of ISO 9000/9001 QMS requirements and maintaining certifications.
Strong proficiency in SPC, statistical analysis, and root cause tools.
Experience with audits, CAPA, FMEAs, control plans, and process validation.
Ability to interpret mechanical blueprints, electrical diagrams, and technical specifications.
Familiarity with ERP/MES systems and digital quality tools.
Leadership & Professional Skills
Proven leadership skills with the ability to motivate, develop, and guide diverse teams.
Excellent communication, interpersonal, and problem-solving abilities.
Ability to work independently, handle ambiguity, and make sound decisions.
Strong organizational, analytical, and strategic thinking skills.
Working Conditions
Work performed in both office and manufacturing floor environments, including exposure to welding, machining, and fabrication operations.
Occasional exposure to moderately disagreeable conditions or minor hazards; proper PPE required.
Limited physical demands; involves routine movement and light handling of materials.
Other Information
This job description reflects the general nature and responsibilities of the role and is not intended to be an exhaustive list of duties. Management reserves the right to change or modify job responsibilities as needed.
Benefits of Being a Cleaver-Brooks Employee:
We offer a competitive salary and comprehensive benefits package, including medical, dental, vision, maternity support program, discounted virtual physician visits, voluntary medical benefits (Critical Illness, Hospital Care, and Accidental Injury), FSA, HSA, life insurance, short term and long term disability, cash matching 401(k) plan, employee assistance program (EAP), pet insurance, employee discount program, generous vacation and 11 paid holidays.
Who is Cleaver-Brooks:
Cleaver-Brooks is the market leader in providing fully integrated boiler and burner systems. We lead the boiler/burner industry due to our unmatched distribution network's ability to deliver the knowledge, service, training and support that are essential to long-term performance. Our customers will tell you that we're the only equipment provider that manufactures boilers, burners, controls, and a full array of ancillary and aftermarket products. They'll also mention that our unique single-source capability means that we can deliver fully integrated boiler room solutions that reduce overall costs and optimize space. It is our focus on products that deliver the most efficient, reliable, safe and environmentally sustainable solutions that differentiate us in the marketplace. Cleaver-Brooks continues a 90+ year legacy of providing the customers we serve with extraordinary products designed to deliver unsurpassed performance through the power of commitment.
This description indicates the general nature of the tasks and responsibilities required of position given this classification. It is not intended as a complete list of specific duties and responsibilities. Nor is it intended to limit or modify the right of management to assign, direct, and control the specific duties of individuals performing this function. The Company reserves the right to change, modify, amend, add to or delete from any section of this document as it deems, in its judgment, to be proper. This description supersedes any previous descriptions for this position
.
By applying for this job and providing your mobile number, you consent to receive an initial text message from a Cleaver-Brooks Talent Team member. You will have the option to opt out upon receiving the message. Messages may include updates on your application, scheduling initial screenings or interviews, and similar communications. Standard message and data rates may apply, and message frequency may vary.
Quality Control Manager
Quality manager job in Fort Stewart, GA
The Quality Control Manager entails planning, designing, implementing, and overseeing quality control initiatives. Additionally, this position manages quality assurance processes, procedures, and documentation related to deliverable preparation and tracking. This role conducts reviews of construction and demolition projects.
Bristol Alliance of Companies (Bristol) is committed to building lasting relationships that reflect our hard work, ingenuity, and dedication to safety. Every employee has an impact on our success, which benefits the Native Culture, land, and people of the Bristol Bay region.
Our values: People, Communities, Reputation, Teamwork, Trust, and Truth.
Essential Functions
Assist with preparing proposal technical approach and cost related to quality program implementation.
Prepare Quality Control Project Plans, including Definable Features of Work, inspection requirements, and testing plan.
Prepare appropriate, targeted field forms associated with this plan.
Ensure compliance with Submittal requirements, including maintaining submittal logs, tracking review/approval/resubmittal, and review of technical submittals as required based on subject matter expertise.
Assist project team in preparing RFIs as necessary.
Implementation field 3-phase quality control processes in accordance with USACE Construction Quality Management for Contractors training.
Document field quality deficiencies, and track via Deficiency Log through closeout.
Build the lead a QC team of subject team matter experts to execute successful job-specific QC programs.
Work with the field team to understand the timing and rationale for quality “hold points' for inspection and testing.
Plan with the field team to effectively implement the inspection and testing plan.
Complete targeted Daily Quality Control Reports, notes of Preparatory and Initial Phase meetings, and reports of deficiencies. The focus must be on the features of the work inspected and tested and the results of those inspections/testing, not field productivity.
Report on the status of quality program implementation to the Program Quality Control Manager, with copies to PM and Site Superintendent.
Assist the project team in resolving outstanding quality concerns.
Troubleshoot and problem-solve as required on all projects.
Other duties as assigned.
Competencies
Ability to track records of meeting production, quality, and customer services standards in a fast-paced construction environment.
Skilled in written and oral communication.
Knowledge of management for contractors, and appropriate experience and expertise in implementing inspection and testing programs for remediation and construction projects.
Ability to be a detail-oriented problem solver.
Ability to gather and analyze data, reason logically and creatively, draw conclusions and make appropriate recommendations.
Ability to handle multiple projects and tasks, prioritize and organize, and work well under stress in a fast-paced environment.
Ability to be flexible and adapt to constant change.
Ability to work flexible hours as required to meet deadlines.
Skilled in interpersonal communication with staff and clients.
Skilled with Microsoft Excel and Word.
Knowledge of mentoring field quality technicians.
Skilled with USACE-RMS (resident management system).
Ability to clearly speak, write, read, and understand English language.
Required Education and Experience
High school diploma or GED.
Bachelor's degree in engineering, architecture, or construction management. Equivalent years of experience may be substituted for a degree.
Minimum 5 years construction quality control experience on construction similar to this contract.
Required to have completed the Construction Quality Management (CQM) for the contractor's course. If CQM does not have a current certification, obtain the CQM for contractor's course certification within 90 days of award.
Must be a U.S. Citizen.
Experience with projects ranging from $1MM - 30MM.
Direct experience with and/or established relationships with Federal clients.
Valid driver's license.
Preferred Education and Experience
OSHA 30
Broad experience in a wide range of civil, vertical construction, demolition, and environmental remediation.
Experience with updating corporate quality plans and developing project-specific quality control inspection/testing plans and field forms for a wide range of projects.
Experience reading plans and specifications.
Work Environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
Position may be subject to both inside and outside environmental conditions, noise sufficient to cause the worker to shout.
Position may be subject to a variety of physical conditions - proximity to moving mechanical parts, moving vehicles, electric current, working on scaffolding and high places, exposure to high heat or exposure to chemicals.
Position may be subject to atmospheric conditions - fumes, odors, dusts, mist, gases, or poor ventilation.
Position may be subject to close visual acuity to perform activities such as viewing a computer terminal and extensive reading.
Physical Qualifications
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.
Mobility: must be able to stoop, kneel, reach, walk, lift, grasp, feel, talk, hear, and perform repetitive motions.
Hearing: must be able to hear audible safety alarms.
Visual Acuity: must be adequate to perform the above listed tasks in a safe manner and perform activities such as viewing a computer terminal and extensive reading.
Lifting: must be able to exert up to 50 pounds of force occasionally and up to 20 pounds of force frequently, and/or a negligible amount of force constantly to lift, carry, push, pull or otherwise move objects, including the human body.
Benefits
Excellent salary and benefits package to include paid time off, paid holidays, comprehensive health plan including medical, dental, vision, life, short-term disability insurance, and 401(k) plan with employer match.
Equal Opportunity Employer Statement
Bristol companies are equal opportunity employers and offer any available positions to all, without regard to race, color, religion, sex, national origin, age, disability, veteran status, parenthood, pregnancy, marital status, or changes in marital status, in accordance with applicable state and federal laws. This applies to recruitment, placement, pay, benefits, training, employment status changes, social and recreational programs, and other conditions and benefits of employment.
Bristol grants employment preference first to BBNC and Choggiung shareholders, their spouses, or descendants, and second to Alaska Native Corporation shareholders in accordance with P.L. 93-638.
Disclaimer
This is not intended to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee. Other duties, responsibilities, and activities may change or be assigned at any time with or without notice.
This job description is not a contract or employment. It does not promise or guarantee any particular benefit or specific action. All employment with Bristol is “at-will” which means that Bristol or employee can terminate the employment relationship at any time with or without cause.
Construction QC Manager
Quality manager job in Augusta, GA
Perini Management Services Inc., a Tutor Perini Company, is seeking a Quality Control Manager for our office located in Fort Gordon, Augusta, GA. As a Quality Control Manager at Perini Management Services, reporting to Project Manager, you will have the opportunity to:
Implement and maintain the approved Contractor Quality Control Plan including responsibility for all required preparatory meetings, initial inspections and follow up inspections.
Develop understanding/working knowledge of company quality control program, industry standards, procedures, etc. required to perform assigned work.
Manage and review shop drawings and product submittal process.
Plan, schedule and run Preparatory Meetings.
Perform quality control inspections and witness tests to determine acceptability of work.
Schedule and coordinate QA inspectors with Owner's Rep.
Assist in maintaining work performance records, inspection records and other related items; assure correctness of all documents.
Assist in preparation/implementation of quality control procedures, i.e., inspection instructions, control measuring and test equipment, etc.
Participate in internal/external quality control audits.
Prepare and submit daily activity and work-force reports.
Inspect and inventory material shipments for compliance.
Insure progress by proactively addressing Q.C. issues
Coordinate and schedule third-party inspectors/inspections.
Requirements:
Experience as QC/QA on multiple Design-Build Projects
Four (4) year engineering degree or equivalent, or 5 or more years of construction QC, Supervision, and/or Management Experience
Temporary relocation to project required.
Experience with Federal Government Clients preferred.
NAVFAC/USACE QCM Certification Required
EM385 certification a plus.
Experience with RMS software preferred.
Field experiences inspecting/installing MEP systems preferred.
About Perini Management Services, Inc.
At home or abroad, our focus is on client satisfaction
Our client-centered approach and competitive, enterprising spirit has yielded many longstanding partnerships throughout the country and the world. We are a close-knit team of construction professionals eager to take on new challenges suited to our expertise. We are committed to working with clients to deliver the projects they need in the time they need it.
When U.S. federal agencies need a construction partner to respond to critical situations, they can count on Perini Management Services, Inc. We've provided construction services to U.S. federal agencies for more than four decades, responding to disasters and supporting military operations throughout the country and around the globe. U.S. federal agencies include the Army Corps of Engineers, Air Force, Navy, Coast Guard, National Park Service, Federal Law Enforcement Training Center, Customs and Border Protection, Fish and Wildlife Service and the Department of State.
At Perini Management Services you will have the opportunity to work on a variety of large, high-profile, projects that impact our national and global communities.
Extraordinary Projects need Exceptional Talent
Perini Management Services builds extraordinary projects, and we need exceptional talent.
Join us and realize your full potential.
Equal Opportunities Employer
Perini Management Services, Inc is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national origin, gender, sexual orientation, gender identity, age, physical or mental disability, genetic factors, military/veteran status or other characteristics protected by law.
Auto-ApplyConstruction Quality Control Manager
Quality manager job in Kings Bay Base, GA
Since 1996, RQC, LLC. has been a leading player in Southern California's robust commercial and governmental Design-Build economy. Headquartered in beautiful Carlsbad, CA, we are a full-service Design-Build company. We offer management of projects throughout the United States, with our field operations team members who work on location for each of our projects. We specialize in fast-track projects in new commercial construction for both public and private clients, with a primary focus on the Department of Defense market.
We are looking for a Construction Quality Control Manager candidate to join our Field Operations team. Project assignment is located at Naval Base King's Bay, GA, an active military base.
QC Managers are responsible for planning, coordinating, and implementing a project-specific quality control program, executing its performance according to contract requirements, completing administrative documentation on time, and cultivating customer satisfaction with the client, all in alignment with RQ's Mission, Vision, and Values. Local candidates will be given preference depending on the location of the project, though relocation or travel to on-site management will be required for the QC Manager position. The QC Manager position must work on-site.
Pay: $110K-145k per year, depending on experience
Benefits: Medical, Dental, Vision, 401k with Match, vehicle allowance
Ideal Candidates will have the following experience:
* A BA/BS degree in Industrial/Construction/Electrical/ Mechanical/Civil Engineering, Construction Management, Architecture, or a related field is the minimum formal education preferred for this position. A combination of equivalent work experience and training in the field may be qualifying.
* Ten or more years combined experience (or equivalent) in the commercial construction industry as a Superintendent, QC Manager, Project Manager, or Project Engineer required, as well as two years' experience as a QC Manager required.
* A current USACE CQM for Contractors Certificate is required and RMS/QCS training is preferred (training is available).
* Specialty inspection training and licenses/certs highly desired.
* LEED AP, AP+, or Green Associate (GA) Certificate preferred.
* Level 1 EM 385-1-1, CRP, First Aid, OSHA 30-hour certifications required. Training can be provided.
* Computer literacy (Microsoft Office, Outlook, Internet, etc.) required.
* Specific software literacy (Procore, Autodesk Build, RMS/QCS) preferred.
COMPANY PROFILE: RQC, LLC is a full-service contracting and design firm that specializes in Design/Build projects for both public and private clients, with a primary focus on the Department of Defense. Our mission is "to provide our customers the best-built environment while being the first choice of all stakeholders."
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, creed, gender (including gender identity and gender expression), religion (all aspects of religious beliefs, observance or practice, including religious dress or grooming practices) marital status, registered domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition (including cancer or a record or history of cancer, and genetic characteristics), sex (including pregnancy, childbirth, breastfeeding or related medical condition), genetic information, sexual orientation, veteran status, or any other basis or status protected by federal, state, or local law or ordinance or regulation.
All candidates considered for hire must provide evidence of identity and U.S. work authorization at the time of hire. Additionally, all candidates must successfully pass a drug screening and commercial criminal background check, including a stricter Department of Defense background check, for access to job site at military base (if applicable for position being hired for).
Quality Program Manager
Quality manager job in Atlanta, GA
The first 3 letters in workplace safety are Y-O-U! TK Elevator is currently seeking a Quality Program Manager located in Atlanta, GA. Responsible for assimilating into the field organization to deliver consistent processes into field operations leveraging current field best practices, processes recommended by the design team, and harmonizing the production activities to align with the field needs and practices.
ESSENTIAL JOB FUNCTIONS:
* Lead and coordinate remediation of field product. Partner with engineering, manufacturing, and field functions along with suppliers to drive timely execution of Service Bulletin and PCI (Product Corrective Instruction).
* Leveraging data from across the organization identify best practices currently in place in the field for key tasks, including but not limited to installation and modernization.
* Implement best practices identified to initially pilot branches and eventually to all North America branches
* Use available data systems to ensure that the identified standard of work is consistently executed
* Partnering with engineering identify corrections to be completed on fielded units, coordinate with manufacturing operations to compile an effected units list, and coordinate with procurement to verify that any necessary materials are available for the field to complete the correction.
* Partner with the field organization to complete identified field corrections in a timely and systemic manner
* Leveraging available data systems monitor the execution of the field corrections and report to the business leadership team during standard operating mechanisms
* Partner with Quality team members to provide ad hoc and scheduled training for field personnel on the quality processes including but not limited to defect reporting.
* Using lessons learned and available data drive process improvement with the field organization to resolve identified systemic issues.
EDUCATION & EXPERIENCE:
* Bachelor's degree
* 8-10 years of experience in elevator service / installation / modernization and associated certification and training.
* Quality/Technical Skills - Certified elevator constructor including ability to trouble shoot reported defects. Understanding of processes both technical and procedural at TK Elevator.
* Problem Solving - Skilled at evaluating data from multiple sources, including field personnel, to identify and develop solutions for systemic technical and procedural issues
* Effective Communications - Ability to communicate across the spectrum of the business with credibility while being concise, clear, and accurate.
* Flexibility and Adaptability - Must be able to identify best practices from all data source including those that may not be systemically documented or known.
* Managing Multiple Priorities - Ability to manage multiple concurrent objectives, projects, groups, or activities, making effective judgments as to prioritizing and time allocation.
* Lean Six Sigma Certification, preferred
* Black belt certification, preferred
* Project Management Certification, preferred
Provided they meet all eligibility requirement under the applicable plan documents, employees will be offered
* Medical, dental, and vision coverage
* Flexible spending accounts (FSA)
* Health savings account (HSA)
* Supplemental medical plans
* Company-paid short- and long-term disability insurance
* Company-paid basic life insurance and AD&D
* Optional life and AD&D coverage
* Optional spouse and dependent life insurance
* Identity theft monitoring
* Pet insurance
* Company-paid Employee Assistance Program (EAP)
* Tuition reimbursement
* 401(k) Retirement Savings Plan with company match: Employees can contribute a portion of their pay on a pre-tax or Roth basis. The company provides a dollar-for-dollar match on the first 5% contributed.
Additional benefits include:
* 15 days of vacation per year
* 11 paid holidays each calendar year (10 fixed, 1 floating)
* Paid sick leave, per company policy
* Up to six weeks of paid parental leave (available after successful completion of 90 days of full-time employment)
Eligibility requirements for these benefits will be controlled by applicable plan documents. This is intended to provide a general description of benefits and other compensation and is not a substitute for applicable plan documents or company policies.
Supplier Quality Manager
Quality manager job in Athens, GA
Energy, it defines LanceSoft. Consider our unique ‘keep apace' operational culture, the spirited lot of hand-picked professionals, our ‘up-to-the-minute' knowledge base, together they form a dynamic mix of value-generating characteristics that help us delve into the heart of a problem to deliver precise services and solutions - repeatedly.
In business since 2000, LanceSoft is a reputed and credible Contingent Workforce Management Services firm that has established itself as a pioneer in providing highly scalable workforce solutions and exceptionally competent global Pharmaceutical & IT services to a diverse set of customers across various industries around the globe. LanceSoft is headquartered out of the Washington DC Metropolitan (Herndon, VA) and operates out of various locations in the US, Canada and India.
LanceSoft specializes in recruiting and retaining top clinical research & scientific talent for leading pharmaceutical and biotech companies. Our staff maintains a commitment to excellence by developing lasting and professional relationships with both hiring managers and job seekers throughout the industry. Our dedicated & professional Account Management and experienced delivery team is well versed in industry specific requirements and market trends.
We provide staffing solutions specializing in all areas of the clinical development process for the Pharmaceutical, Biotechnology, and Medical Device industries. We understand the clinical trial process from Phase I through Phase IV. We provide the most experienced, highly screened candidates on a contract, contract to hire, or permanent hire basis.
Our Clientele: Johnson & Johnson, Merck, Pfizer, Novartis, Purdue, Eisai, Aetna, Becton & Dickinson, Actavis Pharmaceutical, Shire Pharmaceutical.
Follow up on LinkedIn and keep up to date with our newest and hottest openings.
Job Title: Supplier Quality Manager
Detailed Job Description:
• Coordinate completion of Specification Agreements with suppliers.
• Coordinate completion of Quality Agreements with suppliers.
• Perform actions associated with Change Control documents and Corrective/Preventive Acton's (CAPA); including ownership of these records.
• Provide updates to Supplier Records on behalf of account owners.
• Complete Supplier data for metrics and risk management documents.
• Manage low risk (low criticality) supplier accounts as needed.
• Support Supplier Quality projects as needed.
• Establish information for supplier updates in SAP.
• Perform supplier risk assessments (paper-based).
• Support documentation activities for delisting of suppliers.
• Perform assessments for leveraging of existing audits.
• Assist in audit preparation to enable a Third Party Auditor to perform supplier audits.
Qualifications
Requirements:
• cGMP (Current Good Manufacturing Practices) knowledge and experience.
• Supplier Quality experience preferred.
• Computer skills - database entry, MS Office applications (Word/Excel), general electronic application use.
• Self-motivated.
• Works both individually and in a team.
• Effective communication; capable to coordinate with suppliers and internal departments.
Additional Information
• Full-time: 40 hours per week/(5 days/8 hours)
• Periodically accessible to either Athens, GA, Horsham, PA, or Raritan, NJ office locations.
All your information will be kept confidential according to EEO guidelines.
Quality Control Manager - Aerosol Manufacturing
Quality manager job in Orchard Hill, GA
Orchard Hill, GA Are you looking to join a company where you're more than just a number? At ARI, a family-owned aerosol manufacturer, we believe people come first. If you're ready to be part of a growing team that values hard work, supports each other, and builds something great every day, this is your opportunity!
We are seeking an experienced and knowledgeable
Quality Control Manager
to oversee all quality, regulatory, and compliance functions for our aerosol manufacturing facility producing flammable, pressurized, and consumer-facing products. This position will ensure full compliance with FDA regulations, OSHA standards, DOT hazardous materials rules, and all federal and state labeling requirements. The QCM provides strategic quality leadership, manages the QC/QA function, establishes testing and inspection standards, and ensures products consistently meet specifications, safety standards, and customer expectations.
Job Responsibilities
Quality Leadership & Management
Lead the Quality Control and Quality Assurance initiative ensuring compliance with GMP standards
Develop, implement, and maintain the Quality Management System (QMS) tailored to aerosol manufacturing requirements.
Establish quality objectives and KPIs to support operational efficiency and product safety.
Serve as the primary point of contact for regulatory agencies, certification bodies, and customer audits.
Regulatory Compliance (Aerosol Focus)
Ensure full compliance with FDA, OSHA, EPA, DOT, CPSC, and state regulatory requirements.
Oversee adherence to CFR regulations for any OTC, drug, or therapeutic aerosol products.
Maintain compliance with OSHA Process Safety Management (PSM), hazardous chemical handling, LOTO, and safety protocols involving flammable propellants.
Ensure all hazardous materials handling complies with DOT and HMIS/GHS classification and shipping standards.
Labeling, Documentation & Claims
Ensure all product labels meet federal and state requirements, including:
FDA labeling standards for OTC or regulated aerosol products
CPSC guidelines
DOT hazard communication
GHS/OSHA labeling for chemicals
Review and approve product claims, ingredient disclosures, warnings, and safety statements.
Maintain documentation required for regulatory inspections, batch records, COAs, SDSs, and production specifications.
Quality Control & Testing
Oversee all laboratory testing procedures, including flammability tests, pressure checks, fill weight validation, crimp testing, and stability testing.
Ensure proper calibration, validation, and maintenance of testing equipment.
Create and enforce QC sampling standards for raw materials, in-process checks, and finished products.
Approve final release of finished aerosol products.
Continuous Improvement & Risk Reduction
Lead root cause analysis, CAPA, and non-conformance investigations.
Identify and implement process improvements using Lean, Six Sigma, or similar methodologies.
Support initiatives related to reducing risk associated with flammable propellants, compressed gases, and high-pressure filling operations.
Audits, Inspections & Safety
Lead internal audits and coordinate external audits from customers, certification bodies, and regulatory agencies.
Maintain inspection readiness for FDA and OSHA.
Oversee compliance with facility safety programs, including hazard analysis, HAZCOM, PPE, and emergency response procedures.
Qualifications
Education & Experience
Bachelor's degree in Chemistry, Engineering, Manufacturing, or related scientific field.
5+ years of quality experience in manufacturing, with at least 3+ years in aerosol, pressurized packaging, or chemical production preferred.
Demonstrated experience with FDA, OSHA, labeling regulations, and hazardous materials compliance.
Experience managing plant-wide quality initiatives.
ASQ certifications (CQE, CQM, Six Sigma) preferred.
Skills & Competencies
Strong understanding of aerosol filling processes, valve/crimp standards, propellant behavior, and quality hazards unique to aerosol production.
Knowledge of GMPs, GLPs, risk assessments, HACCP principles, and process validation.
Ability to interpret and enforce federal and state labeling laws.
Exceptional problem-solving, decision-making, and leadership skills.
Excellent communication skills with the ability to collaborate across all levels of the organization.
Why ARI?
We are a family-owned and operated company known for innovation, teamwork, and a strong commitment to employee development. We offer a competitive salary and PTO allowance, professional development opportunities, and a supportive work environment. Don't miss out on this opportunity, apply TODAY!
Employment Eligibility Verification
ARI is a participant in the U.S. Department of Homeland Security's E-Verify program. All newly hired employees are required to complete the Form I-9 and have their employment eligibility verified through the E-Verify system. This process ensures that all employees are legally authorized to work in the United States in accordance with federal law.
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