Quality Engineer
Quality manager job in Gulfport, MS
Senior Quality Engineer - Automotive - QE / QA
Salary $85,000 - $115,000 + Benefits & Paid Relocation to the Southern USA where the charming neighborhoods give this locality a small-town feel, but you have all the amenities of the Big City with restaurants, events, festivals, art exhibits, & museums from the traditional to the funky. There is great shopping & eating - from groovy little cafes to microbreweries.
Automotive client is recruiting a Senior Quality Engineer who will provide quality support to production operations to ensure integrity of products. You'll be instrumental in driving quality improvement with the goal of zero defects! Team focused company that takes pride in their quality image, product performance, and customer service.
As the Senior Quality Engineer, you'll proactively lead all product development and launch activities which include design reviews, DFMA reviews, DCP reviews, customer visits, supplier visits and DV and PV testing. You'll manage the processes and system quality requirements, new product development, & launch or process changes. You'll supervise quality technicians and auditors. You'll also develop Process Control plans and will work on cycle time improvements, inventory reduction, scrap reduction, MRO costs, and labor costs.
As the Senior Quality Engineer, you'll identify improvement opportunities, develop proposals, provide and implement training for mistake-proofing throughout the manufacturing process. You'll spearhead Continuous Improvement opportunities.
Minimum requirements for this Senior Quality Engineer:
Degree in Engineering or similar discipline
At least 5 years of experience in a Quality role in the automotive industry
Proficient with automotive Quality tools such as QS-9000 and TS-16949, FMEA, APQP, PPAP, MSA, Process Flow and Corrective Actions
Experience with Problem Solving methodologies such as 5 Why, 8-D, etc.
Experience and knowledge of advanced quality planning, inspection and techniques
Experience with Supplier relationships
Excellent Verbal and Written communication skills
Proficient at MS Office & typical QA softwares.
Quality Program Manager
Quality manager job in Columbus, MS
At Aurora Flight Sciences, we design, build, and fly advanced aircraft and enabling technologies from concept to reality. We are searching for a talented and self-motivated Quality Program Manager to help us create the future of flight. Responsibilities will include but not be limited to the following:
Responsibilities
The role of the Quality Program Manager (QPM) is to act as the primary point of contact (POC) for all customer/program specific quality management activities within the assigned program office. The QPM proactively manages actions required to ensure 100% Quality while maintaining 100% on-time delivery performance on behalf of the program.
Minimum Requirements
* Education/experience typically acquired through advanced education (e.g. Bachelor) and typically 6 or more years' related work experience or an equivalent combination of education and experience (e.g. Master+4 years' related work experience, 10 years' related work experience, etc.).
* Knowledge and experience in AS9100 QMS environment.
* Composite and/or metallic aircraft manufacturing and assembly experience.
* Proficient with MS Office suite.
* Must be a US Person.
Preferred Requirements
* 10+ years in program management role in Quality and/or Quality Engineering.
* Minitab or equivalent statistical data analysis experience ASQ certifications in Quality Management, Quality Engineering, Continuous Improvement, or Auditing.
* Experience with FAA conformity processes and documents (e.g., 8130).
Physical Requirements
* Ability to work in a manufacturing environment and wear proper PPE.
* Ability to transport objects up to 35 pounds as well as consistently stoop, crawl, bend, crouch, climb and kneel.
* Must be able to work alternate shifts and/or extended hours if required.
* Work onsite in Columbus, MS.
Salary Range (Annualized USD)
* Minimum Range: $68,000.00 to $122,000.00
* Maximum Range: $84,000.00 to $149,000.00
Fuels Quality Control Manager
Quality manager job in Meridian, MS
Description JOB DESCRIPTION/SUMMARY The CQC Manager will be assigned to Department of Defense (DoD) construction project(s) located in various regions. This individual will be responsible for all aspects of quality control (QC) and must be onsite during all phases of the construction work. While at the jobsite, the CQC Manager works with the customer and other contractor staff to ensure QC objectives are met in accordance with the contract requirements and high standards of service delivery are maintained. DUTIES AND RESPONSIBILITIES · Prepare and update the QC Plan.· Attend coordination meetings with the Client, subcontractors, and vendors.· Implement the “Three Phases of Control” for all definable features of work.· Perform inspections to ensure work is completed in compliance with contract requirements.· Stop work that does not comply with the contract plans and specifications and direct the removal and replacement of any defective work.· Prepare and submit daily quality control reports.· Conduct weekly QC meetings at the jobsite. • Oversee the review and approval of design and construction submittals.· Ensure As-Built drawings are updated daily.· Coordinate onsite and offsite testing. Maintain a testing log.· Review invoices prior to approval to ensure all relevant work has been completed in accordance with the contract requirements.· Perform punch-list and pre-final inspections.· Perform other duties as requested by supervisors and senior level managers in support of successful performance on all projects.MINIMUM QUALIFICATIONS, SKILLS, AND EDUCATIONAL REQUIREMENTS
A Bachelor's of Science degree from an accredited school in engineering or sciences with a minimum of seven (7) years' experience (within the last ten (10) years), as a Superintendent, Project Manager, or Project Engineer and at least five (5) years field experience as a CQC Manager with repairs to DoD petroleum, oil, and lubricants (POL) facilities, tank rehabilitation, tank cleaning and repairs and emergency inspection
Familiar with requirements of USACE EM-385-1-1, and experience in the areas of hazard identification, safety compliance, and sustainability
Knowledge and experience with POL industry standards including API Std 650, API Std 653, API RP 2016, and API Std 2015 and procedures an applicable DoD criterion
Completion of course entitled Construction Quality Management for Contractors must be completed prior to fieldwork
INTER-PERSONAL RELATIONSHIPS Must work effectively with employees, subcontractors, and clients at all levels. WORKING CONDITIONS The position requires working at the construction job site for extended periods of time. The position may require working during weekends and extended hours in order to meet deadlines.
We are committed to a merit-based hiring process that values individual skills, qualifications, and performance. Our hiring practices comply with all applicable federal, state, and executive orders, including the recent Executive Order on Equal Opportunity Hiring.
Auto-ApplyDirector, Quality - Life Sciences
Quality manager job in Jackson, MS
Datavant is a data platform company and the world's leader in health data exchange. Our vision is that every healthcare decision is powered by the right data, at the right time, in the right format. Our platform is powered by the largest, most diverse health data network in the U.S., enabling data to be secure, accessible and usable to inform better health decisions. Datavant is trusted by the world's leading life sciences companies, government agencies, and those who deliver and pay for care.
By joining Datavant today, you're stepping onto a high-performing, values-driven team. Together, we're rising to the challenge of tackling some of healthcare's most complex problems with technology-forward solutions. Datavanters bring a diversity of professional, educational and life experiences to realize our bold vision for healthcare.
Datavant is seeking a strategic and hands-on **Director of Quality** to lead product and supplier quality assurance efforts within our **Life Sciences business unit** , which includes the **Datavant Connect** and **Aetion Evidence Platform** . These platforms deliver regulatory-grade real-world data (RWD) solutions through tokenization, data linkage, and privacy-preserving analytics.
As Director of Quality, you will own the implementation and evolution of GxP-aligned quality practices that support regulated data services and software. This includes oversight of software validation, privacy compliance, supplier qualification, and audit readiness. You will also lead a team of quality specialists and partner cross-functionally with Product, Engineering, Security, Privacy, and Customer Assurance to ensure that we meet or exceed regulatory expectations and customer trust standards.
This role is essential to operationalizing Datavant's **Quality Management System (QMS)** across internal and external stakeholders and enabling continued growth in regulated RWD and evidence generation environments.
**What You Will Do**
+ Lead the development and continuous improvement of Datavant's QMS across Life Sciences products and supplier relationships, ensuring GxP and privacy compliance.
+ Manage and mentor a team of quality specialists responsible for core functions such as CAPA, internal audits, validation, and supplier monitoring.
+ Serve as the primary quality liaison to product development teams (Connect and Aetion), providing guidance on SDLC quality controls, validation strategies (GAMP 5, Part 11), and regulatory risk mitigation.
+ Oversee supplier qualification and re-evaluation processes, including risk-based assessments, audit coordination, and performance monitoring.
+ Establish and maintain quality metrics (e.g., CAPA closure, audit readiness scores, supplier performance) and drive continuous improvement initiatives.
+ Support readiness for and participation in customer audits and external assessments (e.g., pharma clients, CROs, regulatory partners).
+ Partner with Security and Privacy teams to align product and supplier practices with frameworks like HIPAA, GDPR, and FedRAMP.
+ Lead or support periodic management reviews of the QMS and contribute to strategic quality planning and resource allocation.
+ Ensure clear documentation and traceability across all quality activities, systems, and changes in compliance with FDA 21 CFR Part 11 and ICH E6(R3).
+ Represent Datavant's quality program in external communications, including client onboarding, RFIs, and quality-related escalations.
**What You Need to Succeed**
+ 8+ years of experience in quality, compliance, or regulatory roles within life sciences, digital health, or regulated software organizations.
+ Strong working knowledge of relevant regulations and frameworks, including **FDA 21 CFR Part 11, GAMP 5, ISO 9001, ICH E6(R3), HIPAA** , and **GDPR** .
+ Proven leadership in scaling and operationalizing a **QMS in a SaaS, RWD, or GxP context** .
+ Experience managing and mentoring cross-functional teams.
+ Demonstrated success overseeing **validation, supplier oversight, internal audits, and CAPA management** .
+ Deep understanding of **data governance, privacy, and security** best practices.
+ Experience interacting with external auditors, customer compliance teams, or regulatory agencies.
+ Strong communication skills-capable of explaining complex quality topics to product, legal, technical, and customer-facing stakeholders.
**What Helps You Stand Out**
+ Prior experience supporting real-world data (RWD) platforms or evidence generation technologies used in regulatory submissions.
+ Background working in or with tokenization, health data linkage, or privacy-enhancing technologies.
+ Experience interfacing directly with pharmaceutical, biotech, or CRO quality teams.
+ Training or certification in Six Sigma, ISO Auditing, or software validation methodologies.
+ Familiarity with supplier portals, quality dashboards, or eQMS platforms (e.g., Veeva, MasterControl).
+ Experience contributing to industry working groups on quality, data integrity, or health data compliance.
\#LI-BC1
We are committed to building a diverse team of Datavanters who are all responsible for stewarding a high-performance culture in which all Datavanters belong and thrive. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status.
At Datavant our total rewards strategy powers a high-growth, high-performance, health technology company that rewards our employees for transforming health care through creating industry-defining data logistics products and services.
The range posted is for a given job title, which can include multiple levels. Individual rates for the same job title may differ based on their level, responsibilities, skills, and experience for a specific job. This role is eligible for additional variable compensation.
The estimated base salary range (not including variable pay) for this role is:
$165,000-$230,000 USD
To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case-by-case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy-related medical conditions, and/or religion.
This job is not eligible for employment sponsorship.
Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. To learn more about our commitment, please review our EEO Commitment Statement here (************************************************** . Know Your Rights (*********************************************************************** , explore the resources available through the EEOC for more information regarding your legal rights and protections. In addition, Datavant does not and will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay.
At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. (We can only see aggregate responses, not individual ones. In fact, we aren't even able to see whether you've responded.) Responding is entirely optional and will not affect your application or hiring process in any way.
Datavant is committed to working with and providing reasonable accommodations to individuals with physical and mental disabilities. If you need an accommodation while seeking employment, please request it here, (************************************************************** Id=**********48790029&layout Id=**********48795462) by selecting the 'Interview Accommodation Request' category. You will need your requisition ID when submitting your request, you can find instructions for locating it here (******************************************************************************************************* . Requests for reasonable accommodations will be reviewed on a case-by-case basis.
For more information about how we collect and use your data, please review our Privacy Policy (**************************************** .
Site Quality Manager
Quality manager job in Jackson, MS
Gray Construction is looking to add a Site Quality Manager to their Field Operations Team. This is a field/project based position.
Responsibilities
Why Gray?
Gray is a fully integrated, global service provider deeply rooted in engineering, design, and construction, along with smart manufacturing and equipment manufacturing services. Consistently ranked as a leader in the industry, we focus on the following markets for domestic and international customers: Food & Beverage, Manufacturing, Data Centers, Distribution, and Advanced Technology.
Founded in 1960, Gray's robust offering enables us to create one-of-a-kind solutions at the highest levels of customization, delivering unmatched precision and partnership to some of the world's most sophisticated organizations. Still, these areas do not define Gray-our people do. Passion, commitment, and a great team spirit all speak to the team members at Gray.
Manage daily activities of the quality control program.
Attend project pre-construction meetings to discuss the QMS Program and review Lessons Learned in the presence of subcontractors and manufacturers.
Train team members in the use of the quality control program and support question resolution pertaining to the program use.
Perform administrative set up of projects within the quality program database, assist in the support and maintenance of database program and assist in the implementation and audits the effectiveness of the quality program.
Ensure the quality program provides a fair and effective monitoring of the overall quality of the organization on a regular and timely basis.
Accumulate data from the quality control program for company utilization (for marketing, training, and areas of improvement/best practices).
Conduct jobsite inspections/audits to ensure that quality controls are in place and report findings to the Project Team and Leadership.
Perform quality control inspections of installations as they are being put in place to ensure strict compliance and coordination with the contract documents.
Work with the Service Team Manager for incorporating checklist items into QMS System based on warranty callback items.
Inspect products, materials, and equipment as they arrive at the jobsite to ensure compliance with the contract documents and approved submittals.
Ensure manufacturer, fabricator and installer qualifications are current and applicable based on the contract requirements.
Coordinate required sampling of work in a timely manner with sufficient time for testing and analyzing results to prevent delaying work.
Coordinate and maintain jobsite test and inspection plan and subsequent logs ensuring all documentation is current including any changes to the work or design criteria.
Create and maintain an approved Project Specific Quality Control Plan.
Qualifications
Associate's degree or equivalent from two-year college or technical school AND a minimum of five years of construction experience OR a minimum seven years related construction experience with increasing responsibility in lieu of a degree.
Experience within the light/heavy industrial sector highly desired.
Excellent leadership, organizational, communication, and problem solving skills.
The selected candidate will have excellent communication and organization skills and will be required to travel up to 100% of the time.
Visa Sponsorship: This role is not eligible for visa sponsorship.
This position requires travel as our projects are scattered throughout the United States and, in some cases outside of the U.S.. The selected candidate can live anywhere in the USA, but would be required to travel to the project site per Gray's travel policy.
If you are a high achiever striving to exceed expectations in a fast-paced innovative company, then Gray is the place for you.
The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Physical Demands & Work Environment
The physical demands described here are representative of those that must be met by a team member to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this position, the team member is frequently required to stand, walk, sit, use hands, reach with hands or arms and talk or hear. They may occasionally be required to climb or balance, stoop, kneel, or crouch. Must occasionally lift and/or move up to 50 pounds. Specific vision abilities required include close vision.
Generally, normal office environment where noise level is moderate and temperature/humidity is controlled. Overtime may be required.
Supervisory Responsibilities
This position will indirectly manage subcontractors and has authority of overall quality on projects.
Gray is proud to be an Equal Opportunity Employer and welcomes everyone to apply. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
#LI-GA1
Auto-ApplyQuality Manager
Quality manager job in Flowood, MS
Precision Aviation Group (PAG) is a leading provider of products and value-added services to the aerospace and defense industries worldwide. With over 1.1 million square-feet of sales and services facilities in the United States, Canada, Australia, Singapore, Brazil - PAG's 27 locations and customer-focused business model serve aviation customers through Supply Chain and Inventory Supported Maintenance, Repair and Overhaul (ISMRO) services.
JOB PURPOSE
The Quality Manager is responsible for overseeing the Quality Assurance program of the FAA-certified Part 145 repair station. This role ensures that all maintenance and repair activities are performed in compliance with FAA regulations, customer requirements, and internal procedures. The QA Manager will lead all internal audits, managing corrective actions, maintaining quality documentation, and work closely with the Chief Inspector, Accountable Manager, maintenance teams, and regulatory bodies to uphold the highest standards of safety and airworthiness.
JOB DUTIES AND RESPONSIBILITIES
Essential Job Functions:
Develop, implement, and maintain the repair station's Quality Assurance program in compliance with FAA regulations (14 CFR Part 145), OEM requirements, and company policies.
Conduct internal audits, surveillance, and inspection programs to monitor compliance with quality standards.
Ensure timely and effective resolution of non-conformities, discrepancies, and customer findings, including root cause analysis and corrective/preventive actions (CAPA).
Manage quality control documentation, including procedures, manuals, training records, and inspection checklists.
Interface with regulatory authorities (FAA, EASA, etc.) and coordinate external audits and inspections.
Provide guidance and support to maintenance and inspection staff to ensure proper documentation, tool control, parts traceability, and technical data usage.
Oversee training programs related to quality and compliance to ensure personnel qualifications are current and documented.
Monitor supplier and vendor performance and conduct audits as required.
Analyze quality trends and metrics to drive continuous improvement and ensure a high level of customer satisfaction.
Participate in customer quality reviews and respond to audit reports or corrective action requests.
Maintain awareness of regulatory and industry changes and assist with updating internal systems accordingly.
Other various duties, as directed by the BU Leader.
Marginal Job Functions:
Knowledge of general office clerical procedures.
Strong computer skills with expertise in Microsoft Word, Excel, and PowerPoint.
Ability to regularly exercise sound judgment.
SAFETY REQUIREMENTS
Will participate in and support safety initiatives, safe work practices and compliance.
Will participate in safety activities including the following: immediately reporting hazards, unsafe work practices and accidents/injuries.
Will follow all safety rules, FAA regulations, PPE compliance and equipment operation requirements.
WORKING CONDITIONS
Physical Demands: 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. This position may require walking primarily on a level surface for periods of time as well as reaching above shoulder heights or below the waist or lifting as required to file documents or store materials throughout the workday
Equipment Operated: Ability to operate office machines and equipment and troubleshoot problems with equipment.
Work Location: Trace Aviation 1014 N. Flowood Dr., Flowood, MS 39232
Protective Equipment Required: None
Potential Hazards: Exposure to materials identified on Material Safety Data Sheets.
JOB SPECIFICATIONS
Knowledge, Skills and Abilities: Must have a minimum of 5 years' experience.
Must be Highly Motivated individual
Must possess Excellent Organizational and Communication Skills
Must have Data Entry Skills / computer literate
Must be able to read, write and understand English
Must be available to work Fulltime, M-F, Hours ranging from 7am- 5pm
Must pass FAA/DOT Pre-Employment drug test and background screen, also will be subjected to random drug and alcohol testing.
Education/Training: Bachelor's degree in Aviation Maintenance, Quality Management, Engineering, or a related field preferred.
Experience:
Minimum of 5 years' experience in a Part 145 repair station environment.
Knowledge of FAA regulations (Part 145, Part 43, Part 65), EASA, and AS9100/ISO 9001 standards.
Experience with internal auditing, root cause analysis, and corrective action systems.
Strong organizational, communication, and leadership skills.
Proficiency in Microsoft Office and quality management systems (e.g., Quantum, CAMP, Corridor & Pentagon).
Certificates/Licenses: FAA Airframe & Powerplant (A&P) Certificate preferred or equivalent aviation quality experience.
We offer competitive pay along with a comprehensive benefits package. Full-time associates become eligible for health benefits on the first of the month following 30 days of employment. Available options include medical and dental plans, vision coverage, company-paid basic life insurance, voluntary life insurance, short- and long-term disability, flexible spending accounts, and telemedicine. Other benefits include vacation and PTO time accrued with each pay cycle with a vacation carryover/payout option at year-end, 9 paid holidays, 401k with company match contributions.
Qualified candidates with strong drive, work ethic and commitment to quality are invited to apply at www.precisionaviationgroup.com using the Careers tab.
AA/EOE/M/F/D/V
Director-Quality
Quality manager job in Meridian, MS
Case Management Director-RN oversees a staff of case management RNs, LPNs, Social Workers, and/or Case Management Assistants responsible for patient care coordination, discharge planning, utilization review, and social services. The director ensures alignment of objectives and initiative to support organizational goals. A Case Management Director-RN evaluates patient care data to ensure that care is provided in accordance with clinical guideline and organizational standards.
Job Responsibilities
* Oversees transition management and discharge planning to promote length of stay, care coordination, and patient flow.
* Ensures consistency in workflows, documentation, quality, and outcomes of the department.
* Participates and supports readmission reduction strategies
. • Contributes to overall quality, patient satisfaction, and financial goals.
* Works with medical staff, nursing, administration, and other disciplines to improve care, reduce waste, increase efficiency, and achieve optimal outcomes.
* Supports revenue cycle activities supporting utilization review, medical necessity, payor requirements, and denial prevention.
* Ensures compliance with state and federal regulatory requirements, TJC accreditation standards, and CMS requirements.
* Accountable for budgeting and financial performance of the department.
* Interviews, hires, trains, and supervises of all employees of the department.
* Provides opportunity for professional growth through continued education and training.
* Performs other duties as assigned while supporting the mission, vision, and values to enhance quality, utilization, service delivery, and customer satisfaction.
Experience
Minimum Required : 5 years acute care nursing; 2 years of case management
Preferred/Desired : Management experience
Licensure
Current RN Licenses in state which practicing
Quality Manager
Quality manager job in Columbus, MS
Quality ManagerLocation: Columbus, MS
We are seeking a highly experienced Quality Manager to lead and oversee our quality management processes in an aerospace manufacturing environment. The ideal candidate will drive compliance with industry standards, foster a culture of continuous improvement, and ensure the highest level of product reliability and customer satisfaction.
Key Responsibilities Leadership & Team Management
Lead, mentor, and develop the quality management team, ensuring alignment with company goals and quality performance metrics.
Foster a culture of accountability, continuous improvement, and cross-functional collaboration.
Quality Assurance & Compliance
Develop, implement, and maintain the Quality Management System (QMS) in compliance with AS9100, ISO 9001, and other industry/customer requirements.
Oversee the creation and execution of inspection plans, work instructions, and quality documentation.
Ensure compliance with all regulatory, customer, and internal standards.
Continuous Improvement & Problem Solving
Drive quality improvement initiatives, focusing on defect reduction, product reliability, and process optimization.
Lead root cause analysis (RCA), corrective and preventive actions (CAPA), and non-conformance resolution.
Implement and oversee statistical process control (SPC), failure mode and effects analysis (FMEA), and other quality tools.
Customer & Supplier Relations
Act as the primary liaison for quality-related concerns, ensuring prompt resolution of issues and maintaining strong customer relationships.
Collaborate with suppliers to ensure adherence to quality expectations and drive continuous improvements.
Auditing & Performance Monitoring
Manage internal and external audits, customer inspections, and compliance reviews.
Track and analyze key performance indicators (KPIs), presenting insights and improvement opportunities to senior leadership.
Training & Development
Provide ongoing quality training to employees, equipping teams with the necessary skills to uphold industry-leading standards.
Qualifications Experience & Education
8-10 years of quality management experience in aerospace manufacturing, with a proven track record of leading teams and driving quality initiatives.
Bachelor's degree in Engineering, Manufacturing, or a related field (Master's degree preferred).
Certifications & Skills
ASQ Certified Quality Manager (CMQ/OE), Six Sigma, or equivalent certifications preferred.
Expertise in AS9100, ISO 9001, and other aerospace quality standards.
Strong analytical, problem-solving, and decision-making skills.
Proficiency in SPC, FMEA, RCA, CAPA, and quality management tools.
Excellent communication skills with the ability to interact effectively with customers, suppliers, and internal teams.
Ability to perform effectively in a fast-paced, high-pressure environment.
Additional Requirements
Experience with aerospace-specific certifications and regulatory compliance.
Demonstrated ability to drive quality performance improvements within complex manufacturing processes.
Strong attention to detail and commitment to process excellence.
Ability to travel occasionally to supplier sites or customer locations as needed.
Manufacturing Quality Manager
Quality manager job in Gulfport, MS
Job Description
The Manufacturing Quality Manager is responsible for overseeing quality assurance within manufacturing and packaging operations to ensure compliance with regulatory requirements, internal standards, and customer expectations. This role plays a key part in maintaining a compliant, efficient, and continuously improving production environment, with an emphasis on operational excellence and regulatory readiness.
Key Responsibilities
Provide quality oversight for all on-site manufacturing and packaging activities.
Lead and supervise QA personnel responsible for line release, batch record review, and validation support.
Manage inspection and testing of raw materials and packaging components.
Oversee the lifecycle of standard operating procedures (SOPs), including review, approval, and updates.
Support investigations and resolution of product quality issues and deviations.
Approve batch records, specifications, and related documentation.
Oversee product disposition, recall activities, and pest control programs.
Conduct internal audits to ensure compliance and inspection readiness.
Manage environmental monitoring of facilities and equipment.
Support product stability studies and cross-functional quality initiatives.
Partner with senior quality leadership on compliance and process improvement strategies.
Qualifications
Bachelors degree in Chemistry, Biology, or a related scientific field.
At least 8 years of quality assurance experience in a regulated manufacturing environment.
Experience with multiple dosage forms, including liquids and solids.
Proven leadership experience managing QA teams or quality staff.
Strong knowledge of cGMPs and applicable regulatory requirements.
Skilled in quality systems, including change control, deviations, and CAPA.
Experience with audits and regulatory inspections.
Proficiency with Microsoft Office and quality management systems.
Additional Requirements
Strong organizational and communication skills.
Ability to manage multiple priorities under time-sensitive conditions.
Comfortable working in plant and production environments, with the ability to stand, walk, and sit for extended periods.
Plant Quality Manager
Quality manager job in Olive Branch, MS
Under the direction of the Plant Manager, the Quality Manager is accountable for overseeing and improving overall plant quality through the implementation of process quality systems, while ensuring all quality related issues are addressed to achieve maximum efficiency. Works in collaboration with Metal North America Quality Systems, Operating strategy and Personnel.
Key Responsibilities:
* Responsible for maintenance of plant quality systems including but not limited to inspection and test method, work instructions, procedures, plant specs, GMP's, Food Safety Compliance and Best Practices.
* Develop and drive continuous improvement initiatives in plant quality.
* Support continuous improvement initiatives in supplier quality.
* Responsible for ensuring quality system adherence and all aspects of product integrity is maintained.
* Responsible for appropriate disposition of finished product through data driven analysis, while assuring compliance to all specifications.
* Maintain established and new customer contact to maintain strong relationships, resolving quality issues and ensuring technical and quality support.
* Responsible for leading plant root cause and corrective action investigations for customer complaints and internal quality nonconformance's.
* Audit implementation of correction actions implementation for customer complaints and internal quality nonconformance's.
* Coordinate with Metal North America Commercial, Product Development, Quality and Engineering regarding new business and product trials.
* Responsible for accurate and timely resolution of all supplier defective material claims.
* Responsible for tracking the HFI system including balance, disposition, re-work and inventory levels.
* Ensure that plant quality procedures are up to date, in alignment with Metal North America Quality requirements and followed.
* Ensure quality objectives (KPI's) are communicated with floor personnel and develop processes to promote compliance.
* Responsible for educating and instructing plant department leads and supervisors in HACCP, internal auditing and other food safety quality (BRC) programs.
* Prepare quality reviews and submit them to management.
* Assist in the development of special plant projects and work in conjunction with Metal North America Personnel.
* Maintain continuous communication and interaction with all Ardagh Metal Packaging plants.
* Work closely with Human Resources to address and resolve personnel issues.
* Direct supervision of plant personnel; may vary by location.
* Other responsibilities as assigned.
Requirements:
* Must possess strong analytical, computer and communication skills
* Ability to solve complex problems outside of normal processes
* Driven and energetic
* Ability to work with all levels of personnel
* Bachelor's degree in technical or relevant discipline
* Minimum eight (8) years' experience in manufacturing
* Four (4) years quality experience
* Excellent management/leadership aptitude
* Black or Green Belt Certification (preferred)
* Food Safety (BRC/SQF) and HACCP certification (preferred)
Experience with can manufacturing improvement methods implementation (preferred)
About Ardagh Metal Packaging
Ardagh Metal Packaging (AMP) is a leading supplier of sustainable, infinitely recyclable metal beverage cans to brand owners globally. An operating business of sustainable packaging business Ardagh Group, AMP is a leading industry player across Europe and the Americas, with innovative production capabilities, 23 production facilities, more than 6,000 employees and recorded revenues of $4.8 billion in 2023.
AMP is 76%-owned by Ardagh Group and is listed on the New York Stock Exchange under the ticker AMBP.
About Ardagh Group
Ardagh Group is a global supplier of infinitely recyclable metal and glass packaging solutions, producing packaging for brand owners around the world. We have grown to a team of approximately 20,000 people with revenues of more than $9 billion. Today we have a presence across the Americas, Europe and Africa.
* Ardagh produces many of the beverage cans and bottles that contain your favourite beverages.
* Our packaging is manufactured from metal and glass - permanent materials that can be infinitely recycled without any loss of quality.
* Ardagh produces more than 60 billion containers per year (more than 160 million containers per day).
The future we're creating for Ardagh is built around our four Core Values of Inclusion, Trust, Teamwork and Excellence. We offer exciting and rewarding opportunities for talented and creative people. If you have ambition and want to make an impact with your career, come and join our team - you'll enjoy the journey!
Nearest Major Market: Memphis
Fabrication QC Manager
Quality manager job in Long Beach, MS
About Us
At ENFRA, we blend a rich history with a forward-looking vision. With over 100 years of experience, we are a pillar of stability in the energy infrastructure industry and a leader in innovative energy solutions. Our commitment to leveraging emerging technologies ensures that we remain at the forefront of the Energy-as-a-Service sector.
We believe in growth-not just for our business, but for our people. Our team members have the opportunity to advance their careers in a supportive environment that values continuous learning and development. We embrace innovation and encourage creative problem solving to tackle the energy infrastructure and energy challenges of tomorrow.
Inclusion is at the heart of our culture. We strive to create a workplace where every voice is heard and valued, fostering a collaborative environment where diverse perspectives drive our success.
Join us to be part of a legacy of excellence and a future of groundbreaking advancements. At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success.
Overview
As the Fabrication QC Manager, this role encompasses overseeing and managing all aspects of the operations quality control and assurance processes. This position typically involves strategic leadership and technical expertise to ensure a safe and compliant work environment while the products meet established industry and project quality standards.
Responsible for assisting in the overall supervision and administration of quality for the Fabrication Business Units to maintain a safe and healthy work environment for all employees.
Responsibilities
• Developing, Implementing and maintaining Quality Standards
• Daily inspection of machinery, equipment, and working conditions to ensure compliance with regulatory requirements as applicable to quality and code standards
• Prepares daily report of findings with recommendations for corrective action.
• Assisting in development of standardized job inspection instructions per client and code requirements
• Conduct and maintain related training records
• Testing and certifying welders and welding procedures
• Maintaining welder continuity logs per applicable codes
• Scheduling contract NDE as needed
• Regulatory Compliance: Ensuring that all quality control activities comply with relevant regulatory requirements, standards and codes. The individual needs to stay informed about regulatory changes within the industry and communicate changes to the organization.
• Quality Improvement Initiative: This individual will be required to identify opportunities for process improvement, defect reduction, and enhanced efficiency through data analysis, root cause analysis, and statistical techniques. They will be responsible to Lead or support cross-functional quality improvement projects to achieve measurable quality objectives.
• Data Analysis and Reporting: Analyzing quality data, trends, and metrics to identify opportunities for improvement, predict potential issues and make data-driven decisions. Preparing comprehensive reports and presentations for management review and strategic planning.
• Establishing and maintaining quality control standards and procedures that align with industry regulations, customer requirements, and organizational goals. This includes developing quality assurance policies, quality manuals to obtain ISO 9001 - 2015 certification and ASME S stamp
• Managing and
• Cross-functional Collaboration: Collaborating closely with other departments such as estimating, engineering, project planning, and fabrication shop to resolve quality issues, implement corrective actions, and support new product solutions.
• Review RFQ's assisting estimating in bid requirements
• Mentoring and Training: Provide training, coaching and mentorship to junior quality control professionals on quality control principles, techniques and best practices. Promoting a culture of quality, excellence and continuous improvement throughout the organization.
• Perform and document in process verifications/inspection, for piping, plumbing and sheet metal fabrication to ensure products meet project, client, code and design specifications
• Inspects and collates documentation as required
• Prepares project turnover packages as required
• Detail-oriented and willing to tackle various ongoing projects in a fast-paced environment.
Qualifications
Preferred Education, Experience, and Qualifications
• CWI preferred but not required for the right candidate
• ASNT Level 2 in ASME B31 piping
Travel Requirements
• 0-5% of time will be spent traveling to job site(s)/office location.
Physical/Work Environment Requirements
• Prolonged periods of sitting at a desk and working on a computer.
• Climbing stairs.
• Requires kneeling, standing or sitting for prolonged periods.
• Repeating motions that may include the wrists, hands and/or fingers.
• Light work that includes adjusting and/or moving objects up to 20 pounds.
#LI-CG1
Pay Range USD $88,380.00 - USD $117,970.00 /Yr.
ENFRA is proud to be an Equal Opportunity Employer of Minorities, Women, Protected Veterans, and Individuals with Disabilities, and participates in the e-Verify program. All qualified applicants will receive consideration for employment without regard to race, creed, color, religion, sex, age, sexual orientation, gender identity, national origin, veteran status, disability, or any other classification protected by law.
Auto-ApplyQuality Control Manager (QCM)
Quality manager job in Vicksburg, MS
Job Description
Arrowhead Contracting, Inc. is on a mission to find experienced and qualified people to join our team as we provide maintenance, construction, and renovation services on military bases throughout the US southeast. We're hiring for a full-time Quality Control Manager (QCM) to join us and help support our successful job completion.
Your expertise is reflected in your competitive salary of $80,000 - $120,000/year. We support earning licenses and offer terrific benefits like:
PTO
Bonus structure
Health insurance
401(k)
Growth opportunities
Company shirts
Per diem
QUALIFICATIONS
5+ years of experience as a quality control manager (QCM) for federal construction projects
USACE CQM certification
OSHA 30-hour class
This position requires travel. Candidates with flexibility and willingness to travel may be given preference during the hiring process.
7+ years of experience or experience as a site safety and health officer (SSHO) for federal construction projects would be preferred.
YOUR IMPACT
Normal hours of onsite operations are Monday - Friday, 7:00 am - 4:00 pm.
As a Quality Control Manager (QCM), your work is critical to our successful project completion and job site safety. You will be onsite, closely inspecting the field crew's work to ensure it meets our quality standards and client expectations. First on this job site and then on future job sites throughout the region, you check safety standards and ensure all workers adhere to company standards and job site requirements. You will complete safety reports, monitor job progress, hold weekly progress meetings, prepare 3-week look aheads, and serve as a government site liaison. You will also hold daily site safety meetings and prepare safety presentations based on the elements of work being performed that day. Other duties include:
Overseeing and making decisions related to the performance of work related to scheduling, delivery, logistics, and quality control
Overseeing work among assigned trades to promote a coordinated project operation
Resolving local area problems regarding procedures, precedence, design clarifications, adequate labor and equipment, schedule, and all other appropriate matters
Managing the overall site safety program as required and ensuring subcontractor compliance with company standards and all applicable safety codes and regulations
Creating schedules and determining sequencing of work. Developing and implementing recovery strategies to maintain the project schedule
Communicating with owners and architects/engineers in connection with field issues. Investigating and resolving such issues
Managing the work to ensure that it is installed in compliance with and conforms to the approved contract documents
WHO WE ARE
Headquartered in Florida, Arrowhead Contracting, Inc. is focused on completing comprehensive construction services in the public and private sectors. From site utilities and building maintenance to earthwork and disaster relief, we provide a diverse range of services to meet our clients' needs. We have a rich history and a proven track record of delivering exceptional results, and we're hiring results-driven, customer-oriented people to help us reach even greater heights! If you're looking for a position where you can grow professionally and make a tangible impact on others, come build your career with us!
HOW TO APPLY
Please complete our initial application to be considered for this position.
Must be able to pass a background check to get on military bases.
Job Posted by ApplicantPro
Quality Control Laboratory Manager
Quality manager job in Gulfport, MS
Allen Spolden is actively recruiting for a Quality Control Laboratory Manager. This is a perm (Direct Hire) opportunity. Relocation assistance will be provided. Work Schedule: M-F, flexible start (4am up to 11am).
Salary: Dependent on experience.
Job Summary:
The Quality Control Manager is responsible for managing laboratory personnel and maintaining the laboratory to ensure all products and procedures meet the requirements of 21CFR210, 21CFR211, Regulatory Agencies, and customer expectations.
Supervisory Responsibilities:
Maintain the laboratory quality management system to ensure compliance with cGMP.
Audit the Quality Control Laboratory to ensure compliance to SOP's.
Investigate, assess, and troubleshoot test and/or equipment problems.
Review Out-of-trend/Out-of-specification results and participate in investigations to determine root cause and CAPA.
Ensure analytical equipment is calibrated and well maintained at all times.
Ensure that laboratory personnel training requirements are met and that training records are current.
Interview, hire, and train new staff.
Provide constructive feedback and retraining as needed.
Handles discipline of employees in accordance with company policy.
Duties/Responsibilities:
Maintain the laboratory quality management system to ensure compliance with cGMP.
Establish product test methods and specifications. This includes raw materials, in-process product, finished products and stability samples.
Audit the Quality Control Laboratory to ensure compliance to SOP's.
Maintain appropriate laboratory inventory to ensure timely release of materials.
Participate in method qualifications, validations, and transfers.
Other duties as assigned.
Required Skills/Abilities:
Excellent verbal and written communication skills in English.
Excellent management and teamwork skills.
Excellent organizational skills and attention to detail.
Excellent time management skills with a proven ability to meet deadlines.
Ability to function well in a high-paced and at times stressful environment.
Ability to understand and follow all Standard Operating Procedures and current Good Manufacturing Practices provided by the Company.
Knowledge and control of analytical equipment including calibration and maintenance.
Understanding of quality systems including change control, deviations and CAPAs.
Ability to handle multiple tasks concurrently and complete them in a timely manner.
Experience:
Pharmaceutical Labatory Manager: 5 years (Required)
Chemistry/Pharmaceutical: 5 years (Required)
CGMP: 5 years (Required)
FDA regulations: 5 years (Required)
Requirements
Education and Experience
B.S. in Chemistry, Biology, or a related discipline.
Experience in computer software, such as Microsoft applications.
Good knowledge and understanding of quality control, SOPs, cGMPs, OSHA, and FDA policies and regulations.
10+ years of management experience in a pharmaceutical laboratory setting.
Pharmaceutical experience required.
Physical Requirements:
Ability to walk, stand, or sit 8 or more hours a day.
Ability to lift heavy items up to 40 lbs. or more.
Job Type: Full-time
Pay: $80,000 or more depending on experience
Benefits
Benefits:
Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance
QA / QC Manager - Critical Facilities
Quality manager job in Decatur, MS
Job DescriptionData Center QA / QC Manager - Decatur, MS
client is a Engineering Design and Commissioning Company that is a leader in the Data Center space. This role will be onsite at a the Customer's Data Center. They provide design, commissioning consulting and management expertise in Data Center / Mission Critical Facilities Space with the mindset to provide reliability, energy efficiency, sustainable design and LEED expertise when providing these consulting services for Enterprise, Colocation, and Hyperscale Data Center Projects. This career-growth minded opportunity offers exciting projects with leading-edge technology and innovation as well as competitive salaries and benefits.
We are looking for an experienced Data Center QA/QC Manager to support multiple critical facility data centers. The QA/QC Manager will be responsible for managing the overall quality assurance and quality control of the commissioning and testing of the equipment prior to going live with the data center in accordance with company's policies and procedures. These Data Centers are a 7x24x365 a year operation. Responsibilities include the delivery of quality and consistent services and support as established by the Corporation while satisfying unique site requirements, managing issue resolution and ensuring proper performance reporting of key metrics for the region, establishing goals and objectives for the region based on strategic and business plans of the corporation. The successful candidate will have demonstrated experience in creating and implementing multi-facility, standards based Operations & Maintenance programs. Must have experience analyzing processes, creating process documentation, developing operational procedures and communicating effectively with both business and operations managers. The Subject Matter expert supports the development and implementation of Mission Critical O&M initiatives, based on company's best practices.
Responsibilities:
Performing periodic site walk-throughs in order to ensure Company's procedures (SOPS and MOPS) and standards are followed. This includes assisting the Facilities Manager, Technicians and any other contracted vendors
Communicating the status of the operation process with senior management
Site acceptance and commissioning of the facility to ensure the site meets the superior and dynamic standards of Company Standards
Assisting in the development of procedures/Method of Procedures (MOPs) for the DC build in addition to approving MOPs for data hall work
Provide coverage for onsite data center manager with both routine and emergency service on a variety of state of the art critical systems such as: medium voltage switchgear, diesel generators, UPS systems, power distribution equipment, chillers, cooling towers, computer room air handlers, fire detection / suppression; building monitoring systems; etc.
Supervise the on-site testing coordination with the facility manager, facility technicians, sub-contractors and vendors, ensuring that all work is performed according to established practices and procedures
Manage at a high level - the client relationship and act as escalation point of contact for testing and commissioning issues
Manage the establishment of performance benchmarks, conduct analyses and prepare reports on all aspects of the critical facility operations and maintenance
Review MOPs and SOPs for all work on critical data center facility equipment
Ensure that a constant state of readiness in support of the mission goal of 99.999% uptime
Conduct critical facilities Operations and Maintenance (O&M) program analysis and reporting
Coordinate with Design/Construction Team
Assess, recommend and implement industry best practices into new and existing Critical Environment Programs
Provide feedback to senior management for the continuous improvement of the Critical Environments program
Develop process documentation and training materials
Qualifications:
10+ years of data center facility operations and maintenance experience
Data Center Commissioning and Testing Experience
5 years leadership experience in data center facility operations
Solid Understanding of Critical Electrical and Mechanical / HVAC equipment in a data center environment
Navy Nuke Experience - Navy Nuke Trained / Naval Nuclear Training - EMN - Electricians Mate (Nuclear Trained) ; ETN - Electrical Technician (Nuclear Trained) ; MMN - Machinist Mate (Nuclear Trained)
Strong verbal and written communications skills; Good presentation skills
Bachelor's Degree in Electrical Engineering / Mechanical Engineering a plus
Superior analytical, planning and problem resolution skills
Highly organized with proved project management abilities
Strong organizational skills and detail oriented
Strong customer service skills
Strong verbal and written communications skills; proficient in Microsoft Office
Submittal Instructions:
Please apply directly by clicking the link below, alternatively you can forward your resume directly to: **************************************
After applying, if you have further questions, you may call ************ and ask for Iggy. You can also submit via our career portal and take a look at other Critical Facility openings we are working on at, ***************************
If this job is not for you, feel free to forward this along. WE PAY FOR REFERRALS!!
Company offers competitive salaries and benefits package including medical insurance, a 401(k) plan
EOE/AA Employer M/F/D/V
Pkaza LLC is a third-party employment firm. All fees assessed by Pkaza LLC will be paid by our employer that we represent and not by the candidate
Easy ApplyQuality Engineer
Quality manager job in Southaven, MS
Senior Quality Engineer - Automotive - QE / QA
Salary $85,000 - $115,000 + Benefits & Paid Relocation to the Southern USA where the charming neighborhoods give this locality a small-town feel, but you have all the amenities of the Big City with restaurants, events, festivals, art exhibits, & museums from the traditional to the funky. There is great shopping & eating - from groovy little cafes to microbreweries.
Automotive client is recruiting a Senior Quality Engineer who will provide quality support to production operations to ensure integrity of products. You'll be instrumental in driving quality improvement with the goal of zero defects! Team focused company that takes pride in their quality image, product performance, and customer service.
As the Senior Quality Engineer, you'll proactively lead all product development and launch activities which include design reviews, DFMA reviews, DCP reviews, customer visits, supplier visits and DV and PV testing. You'll manage the processes and system quality requirements, new product development, & launch or process changes. You'll supervise quality technicians and auditors. You'll also develop Process Control plans and will work on cycle time improvements, inventory reduction, scrap reduction, MRO costs, and labor costs.
As the Senior Quality Engineer, you'll identify improvement opportunities, develop proposals, provide and implement training for mistake-proofing throughout the manufacturing process. You'll spearhead Continuous Improvement opportunities.
Minimum requirements for this Senior Quality Engineer:
Degree in Engineering or similar discipline
At least 5 years of experience in a Quality role in the automotive industry
Proficient with automotive Quality tools such as QS-9000 and TS-16949, FMEA, APQP, PPAP, MSA, Process Flow and Corrective Actions
Experience with Problem Solving methodologies such as 5 Why, 8-D, etc.
Experience and knowledge of advanced quality planning, inspection and techniques
Experience with Supplier relationships
Excellent Verbal and Written communication skills
Proficient at MS Office & typical QA softwares.
Director-Quality & Compliance
Quality manager job in New Albany, MS
This position is responsible for all quality, compliance, patient safety, and medical staff credentialing activities within the hospital. It has primary responsibility for interfacing with the medical staff in matters pertaining to the above, and for managing the relationship with the corporate departments responsible for these functions at the system level.
* Develops and implements strategy relating to matters of quality, outcomes and experience, and for identifying and mitigating risks to the patient and/or staff. Creates and manages major elements of the Strategic A3s relating to Right Care
* Oversees all activities relating to complying with the requirements for hospital accreditation and licensure. Interfaces directly with JCAHO, the Mississippi Department of Health, and CMS as necessary.
* Oversees the hospital's benchmarking programs. Is the hospital's point of contact and manages the hospital's engagement with Leapfrog, Premier, Quest, and Vizient.
* Designs programs and oversees the orientation and education of staff in matters of quality, regulatory compliance, patient safety, and patient experience.
* Is the primary liaison with the medical staff in matters of quality, regulatory compliance, investigation of claims and actions, and patient experience. Is the hospital's representative to the Peer Review, and Quality Committees.
* Assists the medical staff office in matters relating to credentialing, the delineation of privileges, the medical staff bylaws and rules and regulations, and the disciplinary process.
* Is the primary interface with the corporate departments responsible for quality, compliance, and patient safety at the system level.
* Participates in community health activities including mortality review, planning for events impacting the health status of the citizenry, and in the adoption and administration of regulations affecting the hospital.
* Prepares and oversees the budget for the assigned areas of responsibility. Recommends programs and expenditures that can influence outcomes, experience, and/or the mitigation of risk.
* Develops and administers policy relating to quality, compliance, and patient safety.
Specifications
Experience
Description Minimum Required Preferred/Desired
Five (5) years of clinical experience as a registered nurse or healthcare management with previous experience in Quality, Risk and/or Compliance
5 years experience in quality, risk or compliance; baccalaureate, associate or diploma degree in a health-related field, nursing preferred; Certified Professional in Healthcare Quality (CPHQ)
Education
Description Minimum Required Preferred/Desired
Completion of a baccalaureate, associate or diploma degree in health-related field
Baccalaureate degree - Nursing preferred
Training
Description Minimum Required Preferred/Desired
Special Skills
Description Minimum Required Preferred/Desired
Knowledge of licensure and accrediting requirements; ability to communicate and work effectively with medical staff, department heads and administration; excellent organizational skills and problem solving abilities
Licensure
Manufacturing Quality Manager
Quality manager job in Gulfport, MS
The Manufacturing Quality Manager is responsible for overseeing quality assurance within manufacturing and packaging operations to ensure compliance with regulatory requirements, internal standards, and customer expectations. This role plays a key part in maintaining a compliant, efficient, and continuously improving production environment, with an emphasis on operational excellence and regulatory readiness.
Key Responsibilities
Provide quality oversight for all on-site manufacturing and packaging activities.
Lead and supervise QA personnel responsible for line release, batch record review, and validation support.
Manage inspection and testing of raw materials and packaging components.
Oversee the lifecycle of standard operating procedures (SOPs), including review, approval, and updates.
Support investigations and resolution of product quality issues and deviations.
Approve batch records, specifications, and related documentation.
Oversee product disposition, recall activities, and pest control programs.
Conduct internal audits to ensure compliance and inspection readiness.
Manage environmental monitoring of facilities and equipment.
Support product stability studies and cross-functional quality initiatives.
Partner with senior quality leadership on compliance and process improvement strategies.
Qualifications
Bachelors degree in Chemistry, Biology, or a related scientific field.
At least 8 years of quality assurance experience in a regulated manufacturing environment.
Experience with multiple dosage forms, including liquids and solids.
Proven leadership experience managing QA teams or quality staff.
Strong knowledge of cGMPs and applicable regulatory requirements.
Skilled in quality systems, including change control, deviations, and CAPA.
Experience with audits and regulatory inspections.
Proficiency with Microsoft Office and quality management systems.
Additional Requirements
Strong organizational and communication skills.
Ability to manage multiple priorities under time-sensitive conditions.
Comfortable working in plant and production environments, with the ability to stand, walk, and sit for extended periods.
Plant Quality Manager
Quality manager job in Olive Branch, MS
Under the direction of the Plant Manager, the Quality Manager is accountable for overseeing and improving overall plant quality through the implementation of process quality systems, while ensuring all quality related issues are addressed to achieve maximum efficiency. Works in collaboration with Metal North America Quality Systems, Operating strategy and Personnel.
Key Responsibilities:
Responsible for maintenance of plant quality systems including but not limited to inspection and test method, work instructions, procedures, plant specs, GMP's, Food Safety Compliance and Best Practices.
Develop and drive continuous improvement initiatives in plant quality.
Support continuous improvement initiatives in supplier quality.
Responsible for ensuring quality system adherence and all aspects of product integrity is maintained.
Responsible for appropriate disposition of finished product through data driven analysis, while assuring compliance to all specifications.
Maintain established and new customer contact to maintain strong relationships, resolving quality issues and ensuring technical and quality support.
Responsible for leading plant root cause and corrective action investigations for customer complaints and internal quality nonconformance's.
Audit implementation of correction actions implementation for customer complaints and internal quality nonconformance's.
Coordinate with Metal North America Commercial, Product Development, Quality and Engineering regarding new business and product trials.
Responsible for accurate and timely resolution of all supplier defective material claims.
Responsible for tracking the HFI system including balance, disposition, re-work and inventory levels.
Ensure that plant quality procedures are up to date, in alignment with Metal North America Quality requirements and followed.
Ensure quality objectives (KPI's) are communicated with floor personnel and develop processes to promote compliance.
Responsible for educating and instructing plant department leads and supervisors in HACCP, internal auditing and other food safety quality (BRC) programs.
Prepare quality reviews and submit them to management.
Assist in the development of special plant projects and work in conjunction with Metal North America Personnel.
Maintain continuous communication and interaction with all Ardagh Metal Packaging plants.
Work closely with Human Resources to address and resolve personnel issues.
Direct supervision of plant personnel; may vary by location.
Other responsibilities as assigned.
Requirements:
Must possess strong analytical, computer and communication skills
Ability to solve complex problems outside of normal processes
Driven and energetic
Ability to work with all levels of personnel
Bachelor's degree in technical or relevant discipline
Minimum eight (8) years' experience in manufacturing
Four (4) years quality experience
Excellent management/leadership aptitude
Black or Green Belt Certification (preferred)
Food Safety (BRC/SQF) and HACCP certification (preferred)
Experience with can manufacturing improvement methods implementation (preferred)
About Ardagh Metal Packaging
Ardagh Metal Packaging (AMP) is a leading supplier of sustainable, infinitely recyclable metal beverage cans to brand owners globally. An operating business of sustainable packaging business Ardagh Group, AMP is a leading industry player across Europe and the Americas, with innovative production capabilities, 23 production facilities, more than 6,000 employees and recorded revenues of $4.8 billion in 2023.
AMP is 76%-owned by Ardagh Group and is listed on the New York Stock Exchange under the ticker AMBP.
About Ardagh Group
Ardagh Group is a global supplier of infinitely recyclable metal and glass packaging solutions, producing packaging for brand owners around the world. We have grown to a team of approximately 20,000 people with revenues of more than $9 billion. Today we have a presence across the Americas, Europe and Africa.
· Ardagh produces many of the beverage cans and bottles that contain your favourite beverages.
· Our packaging is manufactured from metal and glass - permanent materials that can be infinitely recycled without any loss of quality.
· Ardagh produces more than 60 billion containers per year (more than 160 million containers per day).
The future we're creating for Ardagh is built around our four Core Values of Inclusion, Trust, Teamwork and Excellence. We offer exciting and rewarding opportunities for talented and creative people. If you have ambition and want to make an impact with your career, come and join our team - you'll enjoy the journey!
Fabrication QC Manager
Quality manager job in Long Beach, MS
**About Us** At ENFRA, we blend a rich history with a forward-looking vision. With over 100 years of experience, we are a pillar of stability in the energy infrastructure industry and a leader in innovative energy solutions. Our commitment to leveraging emerging technologies ensures that we remain at the forefront of the Energy-as-a-Service sector.
We believe in growth-not just for our business, but for our people. Our team members have the opportunity to advance their careers in a supportive environment that values continuous learning and development. We embrace innovation and encourage creative problem solving to tackle the energy infrastructure and energy challenges of tomorrow.
Inclusion is at the heart of our culture. We strive to create a workplace where every voice is heard and valued, fostering a collaborative environment where diverse perspectives drive our success.
Join us to be part of a legacy of excellence and a future of groundbreaking advancements. At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success.
**Overview**
As the Fabrication QC Manager, this role encompasses overseeing and managing all aspects of the operations quality control and assurance processes. This position typically involves strategic leadership and technical expertise to ensure a safe and compliant work environment while the products meet established industry and project quality standards.
Responsible for assisting in the overall supervision and administration of quality for the Fabrication Business Units to maintain a safe and healthy work environment for all employees.
**Responsibilities**
- Developing, Implementing and maintaining Quality Standards
- Daily inspection of machinery, equipment, and working conditions to ensure compliance with regulatory requirements as applicable to quality and code standards
- Prepares daily report of findings with recommendations for corrective action.
- Assisting in development of standardized job inspection instructions per client and code requirements
- Conduct and maintain related training records
- Testing and certifying welders and welding procedures
- Maintaining welder continuity logs per applicable codes
- Scheduling contract NDE as needed
- Regulatory Compliance: Ensuring that all quality control activities comply with relevant regulatory requirements, standards and codes. The individual needs to stay informed about regulatory changes within the industry and communicate changes to the organization.
- Quality Improvement Initiative: This individual will be required to identify opportunities for process improvement, defect reduction, and enhanced efficiency through data analysis, root cause analysis, and statistical techniques. They will be responsible to Lead or support cross-functional quality improvement projects to achieve measurable quality objectives.
- Data Analysis and Reporting: Analyzing quality data, trends, and metrics to identify opportunities for improvement, predict potential issues and make data-driven decisions. Preparing comprehensive reports and presentations for management review and strategic planning.
- Establishing and maintaining quality control standards and procedures that align with industry regulations, customer requirements, and organizational goals. This includes developing quality assurance policies, quality manuals to obtain ISO 9001 - 2015 certification and ASME S stamp
- Managing and
- Cross-functional Collaboration: Collaborating closely with other departments such as estimating, engineering, project planning, and fabrication shop to resolve quality issues, implement corrective actions, and support new product solutions.
- Review RFQ's assisting estimating in bid requirements
- Mentoring and Training: Provide training, coaching and mentorship to junior quality control professionals on quality control principles, techniques and best practices. Promoting a culture of quality, excellence and continuous improvement throughout the organization.
- Perform and document in process verifications/inspection, for piping, plumbing and sheet metal fabrication to ensure products meet project, client, code and design specifications
- Inspects and collates documentation as required
- Prepares project turnover packages as required
- Detail-oriented and willing to tackle various ongoing projects in a fast-paced environment.
**Qualifications**
**Preferred Education, Experience, and Qualifications**
- CWI preferred but not required for the right candidate
- ASNT Level 2 in ASME B31 piping
**Travel Requirements**
- 0-5% of time will be spent traveling to job site(s)/office location.
**Physical/Work Environment Requirements**
- Prolonged periods of sitting at a desk and working on a computer.
- Climbing stairs.
- Requires kneeling, standing or sitting for prolonged periods.
- Repeating motions that may include the wrists, hands and/or fingers.
- Light work that includes adjusting and/or moving objects up to 20 pounds.
\#LI-CG1
**Pay Range**
USD $88,380.00 - USD $117,970.00 /Yr.
ENFRA is proud to be an Equal Opportunity Employer of Minorities, Women, Protected Veterans, and Individuals with Disabilities, and participates in the e-Verify program. All qualified applicants will receive consideration for employment without regard to race, creed, color, religion, sex, age, sexual orientation, gender identity, national origin, veteran status, disability, or any other classification protected by law.
Submit a Referral (**************************************************************************************************************************
**Job Locations** _US-MS-Long Beach_
**ID** _2025-8578_
**Category** _Quality Control/Purchasing_
**Position Type** _Full-Time_
**Remote** _No_
QA / QC Manager - Critical Facilities
Quality manager job in Decatur, MS
Data Center QA / QC Manager - Decatur, MS
client is a Engineering Design and Commissioning Company that is a leader in the Data Center space. This role will be onsite at a the Customer's Data Center. They provide design, commissioning consulting and management expertise in Data Center / Mission Critical Facilities Space with the mindset to provide reliability, energy efficiency, sustainable design and LEED expertise when providing these consulting services for Enterprise, Colocation, and Hyperscale Data Center Projects. This career-growth minded opportunity offers exciting projects with leading-edge technology and innovation as well as competitive salaries and benefits.
We are looking for an experienced Data Center QA/QC Manager to support multiple critical facility data centers. The QA/QC Manager will be responsible for managing the overall quality assurance and quality control of the commissioning and testing of the equipment prior to going live with the data center in accordance with company's policies and procedures. These Data Centers are a 7x24x365 a year operation. Responsibilities include the delivery of quality and consistent services and support as established by the Corporation while satisfying unique site requirements, managing issue resolution and ensuring proper performance reporting of key metrics for the region, establishing goals and objectives for the region based on strategic and business plans of the corporation. The successful candidate will have demonstrated experience in creating and implementing multi-facility, standards based Operations & Maintenance programs. Must have experience analyzing processes, creating process documentation, developing operational procedures and communicating effectively with both business and operations managers. The Subject Matter expert supports the development and implementation of Mission Critical O&M initiatives, based on company's best practices.
Responsibilities:
Performing periodic site walk-throughs in order to ensure Company's procedures (SOPS and MOPS) and standards are followed. This includes assisting the Facilities Manager, Technicians and any other contracted vendors
Communicating the status of the operation process with senior management
Site acceptance and commissioning of the facility to ensure the site meets the superior and dynamic standards of Company Standards
Assisting in the development of procedures/Method of Procedures (MOPs) for the DC build in addition to approving MOPs for data hall work
Provide coverage for onsite data center manager with both routine and emergency service on a variety of state of the art critical systems such as: medium voltage switchgear, diesel generators, UPS systems, power distribution equipment, chillers, cooling towers, computer room air handlers, fire detection / suppression; building monitoring systems; etc.
Supervise the on-site testing coordination with the facility manager, facility technicians, sub-contractors and vendors, ensuring that all work is performed according to established practices and procedures
Manage at a high level - the client relationship and act as escalation point of contact for testing and commissioning issues
Manage the establishment of performance benchmarks, conduct analyses and prepare reports on all aspects of the critical facility operations and maintenance
Review MOPs and SOPs for all work on critical data center facility equipment
Ensure that a constant state of readiness in support of the mission goal of 99.999% uptime
Conduct critical facilities Operations and Maintenance (O&M) program analysis and reporting
Coordinate with Design/Construction Team
Assess, recommend and implement industry best practices into new and existing Critical Environment Programs
Provide feedback to senior management for the continuous improvement of the Critical Environments program
Develop process documentation and training materials
Qualifications:
10+ years of data center facility operations and maintenance experience
Data Center Commissioning and Testing Experience
5 years leadership experience in data center facility operations
Solid Understanding of Critical Electrical and Mechanical / HVAC equipment in a data center environment
Navy Nuke Experience - Navy Nuke Trained / Naval Nuclear Training - EMN - Electricians Mate (Nuclear Trained) ; ETN - Electrical Technician (Nuclear Trained) ; MMN - Machinist Mate (Nuclear Trained)
Strong verbal and written communications skills; Good presentation skills
Bachelor's Degree in Electrical Engineering / Mechanical Engineering a plus
Superior analytical, planning and problem resolution skills
Highly organized with proved project management abilities
Strong organizational skills and detail oriented
Strong customer service skills
Strong verbal and written communications skills; proficient in Microsoft Office
Submittal Instructions:
Please apply directly by clicking the link below, alternatively you can forward your resume directly to: **************************************
After applying, if you have further questions, you may call ************ and ask for Iggy. You can also submit via our career portal and take a look at other Critical Facility openings we are working on at, ***************************
If this job is not for you, feel free to forward this along. WE PAY FOR REFERRALS!!
Company offers competitive salaries and benefits package including medical insurance, a 401(k) plan
EOE/AA Employer M/F/D/V
Pkaza LLC is a third-party employment firm. All fees assessed by Pkaza LLC will be paid by our employer that we represent and not by the candidate
Easy Apply