Supplier Quality Engineer jobs at Walmart - 285 jobs

A technology company in San Francisco seeks a Software Engineer for its Site Reliability team. This role involves defining and building reliability and scalability in an AI-driven infrastructure. Candidates should have over 5 years of experience in SRE/infrastructure, proficiency in AWS and Terraform, and a strong commitment to collaboration across teams. The position offers competitive benefits, including flexible PTO and medical coverage. #J-18808-Ljbffr

Job Purpose: Eliminate Losses in the supply chain, OEE, Waste, Quality, speed, brand and reduce Tobacco/NTM waste through structured root cause analysis & standardization. Results: Overall Equipment Efficiency improvement through reduction of quality defects, rate losses, process centerline deviations, minor stops, and changeover losses Product Quality Measures (consumer complaints, product and package defects) Waste minimization through scrap reduction and improved process stability Responsibilities: Organizes IOS workshops schedule and Agenda Plans and Schedule the training program Synchronizes resources: Training window-Trainers-Materials-Machine availability and apprentices Certification processes coordination Create operating principles for line training. Lead the Finished Product Quality (FPQ) Daily Management System for quality factors. Own process centerline compliance for all Q-Factor standards. Lead Startups and New Initiatives Qualification including IQ, OQ, and PQ. Coordinate resources to develop standards for new initiatives (SOPs, critical maintenance procedures, Q-Factor audits, troubleshooting guides, skills matrices, step-up cards). Lead chronic loss elimination across waste, scrap, quality incidents, and consumer claims. Build team capability in technical troubleshooting for process failures. Manage rapid changeover methodology for brand changes. Own standardized equipment and the change management system for the assigned process. Serve as engineering's primary point of contact for technology and platform-related topics. Provide structured feedback to design and engineering. Maintain a comprehensive Loss Map related to this role. Training provider management (Assessment, quotation, purchases, payments, agenda, etc.) Training / Skills - Category A: Machine Safety - Job Safety Analysis FPQ, Centerlines, Q-Factors Centerlines Daily Management System Tobacco and material waste reduction Chronic loss elimination, RCA, Focused Improvement Machine operating principles Validation: IQ / OQ / PQ Training / Skills - Category B: Ability to provide structured feedback to design Laser Focus Boards Reliability Engineering tools (FMEA) Autonomous Maintenance (AM) steps Skills and Education Required Skills: Ability to lead cross-functional teams Excellent communication and documentation skills Ability to prioritize effectively in a high-speed manufacturing environment Education and Experience: Associate's degree in Mechatronics Engineering, Electronic, Electromechanics, or equivalent experience. Recently graduated is an option. 1-5 years of experience in manufacturing, process engineering, quality engineering, or related fields Other Expectations Spend more than 70% of time on the production floor Become the designated process expert for assigned manufacturing area

KEY RESPONSIBILITIES * New Product Quality Conformance o Supports quality in new product processes by serving as member and/or resource on development teams. o Writes, executes and reports test plans based upon scientific methods to support the new product process and on-going testing. * Ongoing Quality Conformance o Provides receiving-inspection technical support and writing/reviewing receiving-inspection procedures. o Leads the material review board (MRB) and implements corrective actions internally and externally with suppliers. o Supports and or provides input for published monthly performance reports as well as identify areas for improvement. o Support engineering solutions to quality assurance. o Plans, controls and ensures process and product quality in accordance with quality principles, which include planning processes, material control, acceptance sampling, and measurement systems. * FEMA (Failure Mode Effects Analysis) o Understand issues through progression. o Testing and supplier interaction. o Internal CAR if needed for understanding of diagnosed issue. o Lead FEMA projects. * Environmental o Provides support in our efforts to continually make products greener by supporting our Environmental initiatives. * Vendor/supplier interaction o Plans, conducts and report audits of suppliers. o Interfaces with suppliers concerning quality issues and represent Johnson Outdoors' interests. o Evaluates defective parts returned from the field. o Ensures compliance to all company quality policies. SUPERVISORY/MANAGEMENT RESPONSIBILITIES * None EDUCATION AND EXPERIENCE REQUIRED Education: Engineering Degree, Mechanical or Electrical Degree Experience: Typically requires 2 or more years of experience in quality engineering within a similar industry. KNOWLEDGE, SKILLS AND ABILITIES * Ability to influence decision-making and build critical relationships in a manufacturing organization. * Strong business and financial acumen and possess a good working knowledge and understanding of business operations. * Demonstrated leadership skills and abilities. Ability to effectively manage a group of people across shifts and work under deadlines while maintaining positive employee relations. * Fundamental understanding of: quality philosophies, methods, tools, standards, organizational and team dynamics, customer expectations and satisfaction, supplier's relations and performance, interpersonal relationships, and professional ethics. * Understanding of quality systems and their development, documentation and implementation with respect to domestic and international standards or requirements. * Thorough understanding of problem-solving and quality improvement tools and techniques. This includes knowledge of management and planning tools, quality tools, preventative and corrective actions, and how to overcome barriers to quality improvements. * Ability to work across departmental lines within the organization. * Strong verbal and written communication skills to effectively develop and communicate quality policies, initiatives and problem solve. Ability to communicate effectively across departmental lines and externally as needed. * Proficient in MS Word, Excel spreadsheets and Power Point. * Ability to travel (Amount of time required varies by location). Qualifications EducationBachelors of Mathematics (preferred) ExperienceTypically requires 2 or more years of experience in quality engineering within a similar industry. (preferred) Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

About AkzoNobel Since 1792, we've been supplying the innovative paints and coatings that help to color people's lives and protect what matters most. Our world class portfolio of brands - including Dulux, International, Sikkens and Interpon - is trusted by customers around the globe. We're active in more than 150 countries and use our expertise to sustain and enhance the fabric of everyday life. Because we believe every surface is an opportunity. It's what you'd expect from a pioneering and long-established paints company that's dedicated to providing sustainable solutions and preserving the best of what we have today - while creating an even better tomorrow. Let's paint the future together. For more information please visit ***************** 2024 Akzo Nobel N.V. All rights reserved. Job Purpose The Quality Control Manager holds a strategic and critical role in ensuring the site meets customer expectations while driving cost control and waste reduction. This position exists to lead the Site Quality Control Department, manage customer complaint response, and oversee continuous improvement initiatives related to quality control. The role is responsible for the development, maintenance, and continuous improvement of the site Quality Management System (QMS). Through leadership of key quality activities, this position mentors employees, ensures compliance with quality standards, and supports operational excellence across the site. Key Responsibilities Quality Systems & Compliance * Ensure compliance with all established safety rules, procedures, and the company's Code of Conduct. * Lead and manage the site Quality Management System, including document control, customer complaint handling, corrective and preventive actions. * Monitor changes to management system standards and ensure timely integration into site business processes. * Manage internal and external audits, ensuring readiness, effectiveness, and implementation of corrective actions. Continuous Improvement & Problem Solving * Identify deficiencies in business processes; prioritize improvement initiatives and lead cross-functional teams to implement corrective and preventive actions. * Drive continuous improvement through the use of Lean principles (ALPS) to reduce waste and improve efficiency. * Promote fact-based, data-driven problem solving across the organization. Leadership & Communication * Promote quality system awareness through regular communication and training to ensure organization-wide understanding. * Develop and deliver training programs to strengthen quality knowledge and capability. * Prepare and present reports to site and regional leadership on the effectiveness and health of the Quality Management System. * Lead, direct, coach, and mentor quality team members to support growth and performance. Customer & Supplier Interface * Serve as the Site Management Team (SMT) representative for plant quality issues and customer quality interface. * Partner with Sales and Marketing to ensure customer quality issues are effectively managed and resolved. * Support supplier quality development in collaboration with Purchasing and cross-functional teams. * Collaborate with Regional ISC, Commercial, RDI, CI, and Quality teams to ensure alignment and consistency. Level of Autonomy * Acts independently as the Site Management Team (SMT) authority for plant quality issues. * Serves as the primary customer interface for quality-related matters. * Makes independent decisions related to quality system compliance, audit readiness, corrective actions, and continuous improvement priorities. Job Requirements Education & Experience * Bachelor's degree in Chemistry, Chemical Engineering, Engineering, or a related field (or equivalent combination of education and experience). * Minimum of 7 years of quality systems experience. * Experience with process mapping, quality system development, and statistical analysis tools. * Manufacturing experience required, preferably in a quality leadership role. * Strong working knowledge of Microsoft Word, Excel, PowerPoint, and Visio. * Proven experience leading cross-functional and large teams. * Working knowledge of business management systems and governing standards (e.g., ISO 9000, TS 16949). Essential Qualifications * Demonstrated commitment to safety leadership and compliance. * Strong analytical, problem-solving, and decision-making skills. * Ability to analyze and interpret data using statistical tools (Gage R&R, DOE, t-tests, multi-vari studies). * Ability to work independently while managing multiple priorities. * Strong coaching, leadership, and communication skills. * Excellent written and verbal communication skills in English, with the ability to communicate effectively at all organizational levels. Compensation/Rewards/Benefits The salary range for these skills is: $115,000 to $135,000. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range. This salary range may also be modified in the future. * Medical insurance with HSA * Dental, Vision, Life, AD&D benefits * Annual bonus * 401K retirement savings with 6% company match * Generous vacation, personal and holiday pay * Paid Parental leave * Hybrid work for most exempt roles * Active Diversity & Inclusion Networks * Career growth opportunities on a regional and global scale * Tuition Reimbursement * Employee referral bonus At AkzoNobel we are highly committed to ensuring an inclusive and respectful workplace where all employees can be their best self. We strive to embrace diversity in a context of tolerance. Our talent acquisition process plays an integral part in this journey, as setting the foundations for a diverse environment. For this reason we train and educate on the implications of our Unconscious Bias in order for our TA and hiring managers to be mindful of them and take corrective actions when applicable. In our organization, all qualified applicants receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age or disability. Requisition ID: 50424 #LI-KG1

Work is Sweet! 'Quality without Compromise' is not just a motto at See's Candies. It is the most important ingredient in our recipe for success. See's Candies has been in business since 1921 and maintains a reputation for producing the highest quality candy and providing superior customer service. See's is a leader in the confectionary industry with over 250 retail shops across the USA. We are seeking friendly, enthusiastic individuals who are passionate about providing great customer service. Summary: POSITION OBJECTIVE: The Supplier Quality Manager is responsible for ensuring that suppliers meet See's quality standards by developing and implementing quality assurance programs, conducting supplier audits, and resolving quality issues. Key duties include collaborating with internal teams, monitoring supplier performance, driving corrective actions, and supporting new product development to ensure a high-quality supply chain. The pay range for this position is expected to be $100,000k-$110,500k annually; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Job Description: POSITION RESPONSIBILITIES: * Quality program development: Create and implement supplier quality assurance programs that align with company goals and industry regulations. * Supplier evaluation and audits: Conduct audits to assess supplier capabilities, processes, and compliance with quality standards. This includes performing initial and surveillance audits and selecting suppliers based on quality standards. * Performance monitoring: Establish metrics to monitor supplier performance, such as defect rates, and use this data to report on performance and drive improvements. * Problem-solving and corrective actions: Lead the analysis of quality issues and coordinate corrective and preventive actions (CAPA) with suppliers to resolve defects and prevent recurrence. * Cross-functional collaboration: Work with internal departments like engineering, procurement, and production to identify and mitigate quality risks, define process parameters, and ensure alignment between supplier capabilities and company requirements. * New product development support: Participate in new product development teams to ensure suppliers are capable of meeting quality standards for new products. * Continuous improvement: Drive a culture of quality excellence and implement continuous improvement initiatives throughout the supply base. * Risk management: Identify and mitigate quality-related risks in the supply chain. MINIMUM QUALIFICATIONS: * A bachelor's degree in life sciences, quality management, or a related field. * Minimum of 2 years of experience in supplier quality management, and SQF experience. Food industry experience is required. * Strong understanding of quality management systems, auditing, and problem-solving methodologies. * Excellent communication, negotiation, and leadership skills are essential for managing supplier relationships and driving cross-functional teams. The total compensation package for this position may also include other elements, in addition to a full range of generous medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. See's is an EOE See's will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable local, state or federal law (including San Francisco Ordinance #131192 and Los Angeles Municipal Code 189.00).

The Quality Manager, will lead a dedicated multishift Quality department and play a key role in ensuring our personal care products meet the highest standards of safety, quality, and regulatory compliance. We are looking for a proactive, collaborative leader who excels at developing talent, solving problems and strengthening quality systems in a fast-moving manufacturing environment. Job Responsibilities: Lead the Quality department across two shifts, driving team development, building bench strength, and reinforcing a culture of accountability, continuous improvement and high operational standards. Interacts with customers and internally with UBP production, supply chain, marketing and the R&D groups. Create, revise and manage cGMP procedures and supporting documents and carry out additional duties as needed to uphold quality and regulatory standards. Exercise authority to accept, reject or quarantine raw materials and finished products in accordance with quality standards. Handles customer complaints, nonconformance and corrective actions. Ensure that actions and reports generated conform to regulations/requirements. Plan, schedule, conduct internal audits, analytical methods and validation as well as raw materials suppliers and contractor manufacturers. Coordinates FDA, EPA and third-party certification activities and responds to customer audits and inquiries to ensure compliance and transparency. Works with Customer Service, R&D, and Operation teams to resolve and assist with customer/consumer complaints, internal concerns and new product development and processing. Partners with the Operations team to communicate quality concerns and drive continuous improvement initiatives. Supports the R&D department in multiple aspects: Vendor qualifications, raw material testing, etc. Other duties as required by management. Requirements: At least 5 years of experience in Quality Management Continuous improvement mindset, with strong decision-making ability Effective communicator with ability to collaborate cross functionally Must have previous manufacturing industry experience (preferably in the Beauty Industry) Strong working knowledge of current Good Manufacturing Practices (cGMPs) Adaptable and flexible in a fast-paced environment with changing priorities

Job Description The Quality Manager, will lead a dedicated multishift Quality department and play a key role in ensuring our personal care products meet the highest standards of safety, quality, and regulatory compliance. We are looking for a proactive, collaborative leader who excels at developing talent, solving problems and strengthening quality systems in a fast-moving manufacturing environment. Job Responsibilities: Lead the Quality department across two shifts, driving team development, building bench strength, and reinforcing a culture of accountability, continuous improvement and high operational standards. Interacts with customers and internally with UBP production, supply chain, marketing and the R&D groups. Create, revise and manage cGMP procedures and supporting documents and carry out additional duties as needed to uphold quality and regulatory standards. Exercise authority to accept, reject or quarantine raw materials and finished products in accordance with quality standards. Handles customer complaints, nonconformance and corrective actions. Ensure that actions and reports generated conform to regulations/requirements. Plan, schedule, conduct internal audits, analytical methods and validation as well as raw materials suppliers and contractor manufacturers. Coordinates FDA, EPA and third-party certification activities and responds to customer audits and inquiries to ensure compliance and transparency. Works with Customer Service, R&D, and Operation teams to resolve and assist with customer/consumer complaints, internal concerns and new product development and processing. Partners with the Operations team to communicate quality concerns and drive continuous improvement initiatives. Supports the R&D department in multiple aspects: Vendor qualifications, raw material testing, etc. Other duties as required by management. Requirements: At least 5 years of experience in Quality Management Continuous improvement mindset, with strong decision-making ability Effective communicator with ability to collaborate cross functionally Must have previous manufacturing industry experience (preferably in the Beauty Industry) Strong working knowledge of current Good Manufacturing Practices (cGMPs) Adaptable and flexible in a fast-paced environment with changing priorities

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Sr Supplier Quality Engineer - Saxonburg, PA Sr. Supplier Quality Engineer - Saxonburg, PA PURPOSE The Sr. Supplier Quality Engineer provides support for audits, corrective actions, and qualifications of key suppliers. The position provides guidance and ownership to evaluate suppliers' technical capabilities while working in partnership with internal customers to assure a continuous supply of qualified parts to manufacturing. This position will be responsible for visiting assigned suppliers, as needed, to ensure all quality controls are in place and all regulatory requirements are met. This position will also work with Suppliers who are issued corrective actions to help improve operations quality controls to ensure uninterrupted supply of quality materials. This position also works closely with the Supply Center Manufacturing and Supply Chain to pro actively identify any issues. In addition, the standard BAYER Core Competencies and Role Competencies also apply in the evaluation of the incumbent s suitability for placement into this role classification. YOUR TASKS AND RESPONSIBILITIES The primary responsibilities of this role, Sr. Supplier Quality Engineer, are: Constantly working to improve our supplier base and this position leverages broad engineering knowledge to assess new suppliers; Identify process improvements and lead supplier process qualifications; Leads smaller stand alone projects, or larger sub projects in support of Supplier Quality departmental objectives; Guides suppliers' process validation approaches; Utilizes statistical analyses to reduce risk and enable success of projects; Becomes a trusted partner working with cross functional, internal stakeholders to lead project initiatives within Supplier Quality functional scope; Communicates technical matters in a manner that effectively conveys messages to diverse audiences; Creates, assigns, and tracks project tasks with the supplier and then aligns with the Bayer project teams on supplier's progress; Plans and manages own work activities of significant technical scope with minimal direction in order to meet objectives and deliver on needed deadlines; Leads teams on project activities of medium technical scope at the sub-module level; Able to provide advice and mentoring to less experienced engineers or technicians; Develops, qualifies and maintains supplier and partner relationships as directed; Performs ISO 9001 or ISO 13485 QMS audits at suppliers; Guides suppliers on proper 8D corrective action responses; Communicates comfortably at all levels of the organization. WHO YOU ARE Bayer seeks an Incumbent who possesses the following: REQUIRED QUALIFICATIONS • Bachelor's Degree in Engineering; • Experience using relevant quality, supplier management or medical device manufacturing knowledge across a breadth of technical disciplines; • 1-2 years technical leadership, which can include but not limited to, leading process improvements, performing audits, and 8D corrective actions. • Driven individual who seeks to identify and implement improvements in processes; • Collaborative and team oriented contributor; • 15% travel within the United States and potentially abroad. PREFERRED QUALIFICATIONS • 4-7 years using relevant quality, supplier management or medical device manufacturing knowledge across a breadth of technical disciplines. Employees can expect to be paid a salary between $73,964.00 to $110,946.00. Additional compensation may include a bonus or incentive compensation (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. This posting will be available for application until at least 1-5-2026. YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location: United States : Pennsylvania : Saxonburg Division: Pharmaceuticals Reference Code: 858919 Contact Us Email: hrop_*************

Safety is a core value at Voyant Beauty. We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel. If you're seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you. Come join us and be a part of our journey. A Brief OverviewThe Plant Quality Manager provides strategic and operational leadership for all quality functions at a high-volume OTC manufacturing facility. This role ensures GMP compliance, drives a quality culture, and leads quality system improvements to enhance overall site performance. As a critical leader, the Plant Quality Manager will strengthen the Quality organization, foster quality culture transformation, and optimize operational excellence across the facility. The ideal candidate is a hands-on, technically proficient leader with cGMP knowledge (21 CFR 210/211) and the ability to align cross-functional teams to elevate the site's quality systems and compliance.What you will do Lead QA, QC Labs, Document Control, Validation, and Complaint Management operations. Oversee implementation and improvement of site QMS in line with FDA and corporate standards. Serve as quality site lead for FDA and customer inspections. Ensures inspection readiness at all times. Address compliance issues and manage CAPAs effectively. Promote accountability, data integrity, and a right-first-time mindset. Collaborate with Ops, Eng, R&D, etc., on investigations, change management, validations, and continuous improvement. Supervise review of batch records, product release, deviations, and investigations. Work with customers, and other stakeholders to meet compliance expectations. Analyze metrics to drive performance and quality improvement. Coach and develop a High Performing Team. Ensure effective resourcing of quality teams. Represent site quality leadership in executive meetings. Contribute to corporate quality strategy alignment. Participate in strategic planning and facility expansion discussions. Some duties may vary slightly by location. Education Qualifications Bachelor's Degree in Chemistry, Pharmacy, Microbiology, Chemical Engineering, or similar. (Preferred) advanced degree (Preferred) Experience Qualifications 10+ years in FDA-regulated OTC, pharmaceutical, or personal care environments. (Preferred) 10+ years managing FDA inspections and remediation efforts. (Preferred) 10+ years background in aerosol manufacturing and topical formulations is a plus. (Preferred) Skills and Abilities Expertise in cGMPs, 21 CFR 210/211, ICH, USP (High proficiency) Leading FDA/customer audits and inspection readiness (High proficiency) Remediation planning and effectiveness verification (High proficiency) Working with Ops, Eng, and R&D on QMS topics (High proficiency) Team coaching, mentoring, and resourcing (High proficiency) Effective internal/external stakeholder communication (High proficiency) ERP (e.g., SAP), LIMS (e.g., MasterControl), TrackWise (High proficiency) Driving transformation in quality mindset and execution (High proficiency) Licenses and Certifications ASQ Certification (Preferred) Lean Six Sigma or OpEx training (Preferred) To Staffing and Recruiting Agencies: Our company does not accept unsolicited curriculum vitae's or applications from agencies. We are not responsible for any fees related to unsolicited curriculum vitae's or applications and explicitly reserve its right to contact candidates presented in such unsolicited curriculum vitae's or application. Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, color, national origin, sexual orientation, age, disability or veteran status. Voyant Beauty will consider requests for accommodations due to a disability impacting a qualified employee's ability to perform the essential functions of their position consistent with applicable laws. In addition to federal law requirements, Voyant Beauty complies with applicable provincial and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Voyant Beauty believes our people are more than just employees; they're the driving force behind everything we achieve. Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual's contribution is valued and celebrated. We invest in their growth, providing opportunities for development and advancement within our dynamic team. Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products. We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs. This can include skincare, haircare, bath and body products, fragrances, and more. Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life. Safety is a core value at Voyant Beauty. We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel. If you're seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you. Come join us and be a part of our journey. A Brief Overview The Plant Quality Manager provides strategic and operational leadership for all quality functions at a high-volume OTC manufacturing facility. This role ensures GMP compliance, drives a quality culture, and leads quality system improvements to enhance overall site performance. As a critical leader, the Plant Quality Manager will strengthen the Quality organization, foster quality culture transformation, and optimize operational excellence across the facility. The ideal candidate is a hands-on, technically proficient leader with cGMP knowledge (21 CFR 210/211) and the ability to align cross-functional teams to elevate the site's quality systems and compliance. What you will do Lead QA, QC Labs, Document Control, Validation, and Complaint Management operations. Oversee implementation and improvement of site QMS in line with FDA and corporate standards. Serve as quality site lead for FDA and customer inspections. Ensures inspection readiness at all times. Address compliance issues and manage CAPAs effectively. Promote accountability, data integrity, and a right-first-time mindset. Collaborate with Ops, Eng, R&D, etc., on investigations, change management, validations, and continuous improvement. Supervise review of batch records, product release, deviations, and investigations. Work with customers, and other stakeholders to meet compliance expectations. Analyze metrics to drive performance and quality improvement. Coach and develop a High Performing Team. Ensure effective resourcing of quality teams. Represent site quality leadership in executive meetings. Contribute to corporate quality strategy alignment. Participate in strategic planning and facility expansion discussions. Some duties may vary slightly by location. Education Qualifications Bachelor's Degree in Chemistry, Pharmacy, Microbiology, Chemical Engineering, or similar. (Preferred) advanced degree (Preferred) Experience Qualifications 10+ years in FDA-regulated OTC, pharmaceutical, or personal care environments. (Preferred) 10+ years managing FDA inspections and remediation efforts. (Preferred) 10+ years background in aerosol manufacturing and topical formulations is a plus. (Preferred) Skills and Abilities Expertise in cGMPs, 21 CFR 210/211, ICH, USP (High proficiency) Leading FDA/customer audits and inspection readiness (High proficiency) Remediation planning and effectiveness verification (High proficiency) Working with Ops, Eng, and R&D on QMS topics (High proficiency) Team coaching, mentoring, and resourcing (High proficiency) Effective internal/external stakeholder communication (High proficiency) ERP (e.g., SAP), LIMS (e.g., MasterControl), TrackWise (High proficiency) Driving transformation in quality mindset and execution (High proficiency) Licenses and Certifications ASQ Certification (Preferred) Lean Six Sigma or OpEx training (Preferred) To Staffing and Recruiting Agencies:Our company does not accept unsolicited curriculum vitae's or applications from agencies. We are not responsible for any fees related to unsolicited curriculum vitae's or applications and explicitly reserve its right to contact candidates presented in such unsolicited curriculum vitae's or application. Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, color, national origin, sexual orientation, age, disability or veteran status. Voyant Beauty will consider requests for accommodations due to a disability impacting a qualified employee's ability to perform the essential functions of their position consistent with applicable laws. In addition to federal law requirements, Voyant Beauty complies with applicable provincial and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Lead Supplier on site assessments (OSAs) and action planning to source selection. Lead supplier training and development activities. PPAP for new purchased components and major changes to existing components for commodities and/or product development programs as assigned. Proficient in APQP and PPAP processes and basic knowledge of ISO9001:2015 requirements. Identify and lead projects to drive external failure rates and internal defect rates down year over year for assigned commodities. Requires the following: Project Management, strong leadership, interpersonal skills, customer satisfaction focused, team oriented, and results driven. Strong computer skills in MS suite as well data management and quality management systems. Ability to work with multiple computer programs and systems to effectively interpret data which requires basic knowledge of SQL database, Excel Macros, Power BI, etc. **Responsibilities** + Serves as an active quality liaison and main point of contact between suppliers, supply chain, operations and design engineering when major quality problems exist that affect product quality. Works with suppliers to obtain and close Corrective Actions and to ensure that root causes have been properly identified and eliminated. + Responsible for addressing and resolving supplier issues and driving formal corrective action. Leads the tracking and root cause analysis of designated supplier's product/process non-conformances. Recommends resolution to non-conformances where appropriate. + Ability to lead and conduct Supplier Assessments in conjunction with Supply Chain to qualify potential new suppliers or evaluate existing suppliers. Works with existing supply base to meet quality standards. Works with the Supply Chain organization to develop new suppliers capable of meeting quality standards. + Drives the part approval (PPAP) and quality improvement processes using the appropriate tools (PFMEA's, process flow charts, control plans, capability studies, part layouts, Gage R & R, SPC, etc.) as required. + Works with Supply Chain management to identify strategic suppliers and uses the supplier scorecard system to monitor performance of those strategic suppliers. + Assists suppliers with statistical analysis of process potential (Ppk) and process capability (Cpk) where necessary to improve performance. + Works with key suppliers to develop and implement quality targets and plans. Assists with Supplier performance monitoring, including: PPM's, 8D, % On-time delivery, % PPAP completed on-time and first time; ECN's initiated at PPAP. + Supports and assists suppliers to improve quality and reduce total cost per part by eliminating waste in the supply chain process. Use 6 sigma and lean manufacturing/lean enterprise tools to drive the results. + Represents the company to all external parties (customer and supplier) in a professional and beneficial manner. + Responsible for establishing, reviewing, and approving all suppler requirements related to Quality Systems on assigned new product developments. + Supports suppliers (or participates where appropriate) in effective Process Failure Mode Analysis to ensure all failure modes are captured, all appropriate failure modes from the DFMEA are carried over into the process FMEA, all rankings are appropriately assigned, actions are taken against high RPN's, and historical lessons learned information is carried over into current PFMEA's. + Maintains effective and professional relationships with managers and personnel at both supplier and customer locations. **Qualifications** + Bachelor's Degree in a technical field + A minimum of 5 years quality related experience + Experience working in two or more functional areas: Engineering, Project Management, Quality, Manufacturing or Operations is preferred + Able to travel 10-20% of the time **Benefits & Perks - What's In It For You*** Hussmann is committed to supporting your total wellbeing through a wide variety of benefits and wellness programs to support your physical, emotional, financial, social, and environmental health. Here's what you can expect: + **Health Benefits** - Offering medical, dental, vision, prescription plans, plus Health Savings Account and Flexible Spending Account options. + **Voluntary Benefits** - Life, accident, critical illness, disability, legal, identity theft, and pet insurance. + **Hussmann Retirement Savings & Investment Plan** - 401(k) plan with company matching contributions and immediate vesting. + **Paid Time-Off Benefits** - Paid time off, stewardship and parental leave. + **Educational Assistance** - Tuition reimbursement for job-related courses after six months of service. + **Health Management and Wellbeing Programs** -EAP, virtual health management, chronic condition, and tobacco cessation. *Available to eligible employees starting the first day of the month following their start date. Eligibility for each benefit may vary based on employment status. **About Hussmann** For over a century, Hussmann Corporation has been a global leader in commercial refrigeration equipment - delivering solutions that meet the demands of the modern food retailing industry. Headquartered in St. Louis, MO, Hussmann offers a diverse range of products and connected solutions designed to enhance operational efficiency, optimize visibility of merchandise, and keep food fresh. With a nationwide network of skilled technicians, Hussmann goes beyond manufacturing - a trusted partner, relentlessly driving customer success. For more information about Hussmann, please visit **************** . Hussmann is a subsidiary of Panasonic USA. Hussmann is proudly committed to creating an inclusive environment. All qualified applicants will receive consideration for employment without regard to veteran status, disability, age, race, color, religion, sex, national origin, genetics, medical condition, or any other characteristic protected by law. \#LI-SM1 REQ-151576

Job Description Supplier Quality Engineer II SIG SAUER, Inc. is a leading provider and manufacturer of firearms, electro-optics, ammunition, airguns, suppressors, remote controlled weapons stations, and training. For over 250 years SIG SAUER, Inc. has evolved, and thrived, by blending American ingenuity, German engineering, and Swiss precision. Today, SIG SAUER is synonymous with industry-leading quality and innovation which has made it the brand of choice amongst the U.S. Military, the global defense community, law enforcement, competitive shooters, hunters, and responsible citizens. Additionally, SIG SAUER is the premier provider of elite firearms instruction and tactical training at the SIG SAUER Academy. Headquartered in Newington, New Hampshire, SIG SAUER has over 3,400 employees across sixteen U.S. locations in three states, and four additional global facilities. SIG SAUER is certified a Great Place to Work™. For more information about the company and product line visit: **************** Position Summary: The Supplier Quality Engineer II will ensure the overall quality of supplied manufactured products. They will investigate and disposition nonconforming product and work to prevent its reoccurrence at the source by way of SCAR's, implementing control plans, and utilizing R&R and biased gaging methods. They will also support production needs in a timely manner by organizing required scrap, sorts, and rework for supplied nonconforming material as necessary. Working in a team environment, the Supplier Quality Engineer II will collaborate with cross functional teams including Design Engineers, Manufacturing, internal Quality, Project Management, Production Planning, Incoming Inspection, Purchasing as well as outside manufacturing and OSP suppliers. FLSA: Exempt Job Duties and Responsibilities: Review and disposition non-compliant material of increased complexity utilizing provided and self-verified inspection data, and use quality methods such as statistics, or pareto to assess causes and priorities. Accurately & independently assess issue culpability. Accurately determine correct gaging methods to aid incoming inspection and when verifying inspection data. Collect data for Gage R&R and bias. Design and source custom gages for specific applications. Experienced in MRP, PPAP, and Microsoft programs including Access. Extensive knowledge of the supplier quality management systems and Vendor Evaluation systems. Highly proficient in print reading and able to interpret dimensional tolerances and apply them to components of enhanced complexity. Identify external specification referenced in technical documentation and apply to the inspection process. Understanding and working fluency of GD&T symbology assigned per ASME Y14.5. Review design drawings for completeness and correctness. Independently generate documentation required to maintain and support ISO compliance. Serve as a contributing member of ISO audit teams. Enhanced understanding of the ISO process. Proficient in ATF Compliance and recognizing when input from the compliance team is needed to resolve/clarify compliance related issues. Independently identify areas of need for SCARs to generate and drive to completion SCARs, and execute to meet business needs. Engage in continuous improvement projects and tasks. Participate in 5s workplace organizational activities and maintain work area in accordance with 5s standard. Must follow all required safety and ISO procedures. Miscellaneous duties as assigned. Education/Experience & Skills: Bachelor's degree in Engineering sciences, and 3-6 years of experience in a Manufacturing or Quality Engineering role. High level of mechanical technical expertise required. Must be proficient with inspection equipment such as calipers micrometers, dial indicators, microhites, and hardness tester. Proficient with Microsoft Outlook, Word, Excel, and PowerPoint applications. Must have experience with CAD software. Possess experience in evaluating and troubleshooting all steps from receiving inspection of raw material to final inspection of completed parts of the manufacturing processes at suppliers, and assist in implementing permanent corrective actions to the supplier's manufacturing process. Must be able to clearly, concisely, and accurately convey ideas and information to suppliers and internal customers, both verbally and in written form. Must know their audience to be able to communicate effectively. Ability to work independently as well as part of a team. Completes tasks as assigned in a timely manner. Requires little supervision to identify additional tasking. Able to organize and prioritize tasks with minimal assistance. Able to make decisions with minimal guidance on corrective actions for supplier quality problems that arise. Communicate effectively to leadership verbally and in written format regarding problems and corrective action. Analysis of supplier quality failures, particularly related to prevention of receipt & advancement of non-compliant material. Working Conditions: Prolonged periods of sitting at a desk and working at a computer using a keyboard and mouse performing repetitive tasks. The duties of this job normally require exposure to a typical manufacturing area where frequent standing, sitting, stooping/squatting, walking and stair climbing can be expected along with frequent lifting and/or moving of tooling, parts, containers, and materials up to 40 pounds. Must be able to reach with hands and arms, bend and kneel frequently at a minimum 50% of the shift, as well as undergo repetitive wrist, hand, elbow, shoulder, and ankle motions. Must demonstrate proficient fine motor skills, be able to grip, reach, pull, turn, and use tools to torque fixtures in various machinery. Specific vision abilities required may include close vision, distance vision, peripheral and depth perception and ability to focus. Must wear required Personal Protective Equipment (PPE) where required. Must comply with all work exposure EH&S training requirements and adhere to SIG SAUER Inc. Security Mandates. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by law.

SIG SAUER, Inc. is a leading provider and manufacturer of firearms, electro-optics, ammunition, airguns, suppressors, remote controlled weapons stations, and training. For over 250 years SIG SAUER, Inc. has evolved, and thrived, by blending American ingenuity, German engineering, and Swiss precision. Today, SIG SAUER is synonymous with industry-leading quality and innovation which has made it the brand of choice amongst the U.S. Military, the global defense community, law enforcement, competitive shooters, hunters, and responsible citizens. Additionally, SIG SAUER is the premier provider of elite firearms instruction and tactical training at the SIG SAUER Academy. Headquartered in Newington, New Hampshire, SIG SAUER has over 3,400 employees across sixteen U.S. locations in three states, and four additional global facilities. SIG SAUER is certified a Great Place to Work. For more information about the company and product line visit: **************** Position Summary: The Supplier Quality Engineer II will ensure the overall quality of supplied manufactured products. They will investigate and disposition nonconforming product and work to prevent its reoccurrence at the source by way of SCAR's, implementing control plans, and utilizing R&R and biased gaging methods. They will also support production needs in a timely manner by organizing required scrap, sorts, and rework for supplied nonconforming material as necessary. Working in a team environment, the Supplier Quality Engineer II will collaborate with cross functional teams including Design Engineers, Manufacturing, internal Quality, Project Management, Production Planning, Incoming Inspection, Purchasing as well as outside manufacturing and OSP suppliers. FLSA: Exempt Job Duties and Responsibilities: * Review and disposition non-compliant material of increased complexity utilizing provided and self-verified inspection data, and use quality methods such as statistics, or pareto to assess causes and priorities. Accurately & independently assess issue culpability. * Accurately determine correct gaging methods to aid incoming inspection and when verifying inspection data. Collect data for Gage R&R and bias. Design and source custom gages for specific applications. * Experienced in MRP, PPAP, and Microsoft programs including Access. Extensive knowledge of the supplier quality management systems and Vendor Evaluation systems. * Highly proficient in print reading and able to interpret dimensional tolerances and apply them to components of enhanced complexity. Identify external specification referenced in technical documentation and apply to the inspection process. * Understanding and working fluency of GD&T symbology assigned per ASME Y14.5. Review design drawings for completeness and correctness. * Independently generate documentation required to maintain and support ISO compliance. Serve as a contributing member of ISO audit teams. Enhanced understanding of the ISO process. * Proficient in ATF Compliance and recognizing when input from the compliance team is needed to resolve/clarify compliance related issues. * Independently identify areas of need for SCARs to generate and drive to completion SCARs, and execute to meet business needs. * Engage in continuous improvement projects and tasks. * Participate in 5s workplace organizational activities and maintain work area in accordance with 5s standard. * Must follow all required safety and ISO procedures. * Miscellaneous duties as assigned. Education/Experience & Skills: * Bachelor's degree in Engineering sciences, and 3-6 years of experience in a Manufacturing or Quality Engineering role. * High level of mechanical technical expertise required. Must be proficient with inspection equipment such as calipers micrometers, dial indicators, microhites, and hardness tester. * Proficient with Microsoft Outlook, Word, Excel, and PowerPoint applications. Must have experience with CAD software. * Possess experience in evaluating and troubleshooting all steps from receiving inspection of raw material to final inspection of completed parts of the manufacturing processes at suppliers, and assist in implementing permanent corrective actions to the supplier's manufacturing process. * Must be able to clearly, concisely, and accurately convey ideas and information to suppliers and internal customers, both verbally and in written form. Must know their audience to be able to communicate effectively. * Ability to work independently as well as part of a team. * Completes tasks as assigned in a timely manner. Requires little supervision to identify additional tasking. Able to organize and prioritize tasks with minimal assistance. * Able to make decisions with minimal guidance on corrective actions for supplier quality problems that arise. Communicate effectively to leadership verbally and in written format regarding problems and corrective action. Analysis of supplier quality failures, particularly related to prevention of receipt & advancement of non-compliant material. Working Conditions: * Prolonged periods of sitting at a desk and working at a computer using a keyboard and mouse performing repetitive tasks. * The duties of this job normally require exposure to a typical manufacturing area where frequent standing, sitting, stooping/squatting, walking and stair climbing can be expected along with frequent lifting and/or moving of tooling, parts, containers, and materials up to 40 pounds. * Must be able to reach with hands and arms, bend and kneel frequently at a minimum 50% of the shift, as well as undergo repetitive wrist, hand, elbow, shoulder, and ankle motions. * Must demonstrate proficient fine motor skills, be able to grip, reach, pull, turn, and use tools to torque fixtures in various machinery. * Specific vision abilities required may include close vision, distance vision, peripheral and depth perception and ability to focus. * Must wear required Personal Protective Equipment (PPE) where required. * Must comply with all work exposure EH&S training requirements and adhere to SIG SAUER Inc. Security Mandates. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by law.

SIG SAUER, Inc. is a leading provider and manufacturer of firearms, electro-optics, ammunition, airguns, suppressors, remote controlled weapons stations, and training. For over 250 years SIG SAUER, Inc. has evolved, and thrived, by blending American ingenuity, German engineering, and Swiss precision. Today, SIG SAUER is synonymous with industry-leading quality and innovation which has made it the brand of choice amongst the U.S. Military, the global defense community, law enforcement, competitive shooters, hunters, and responsible citizens. Additionally, SIG SAUER is the premier provider of elite firearms instruction and tactical training at the SIG SAUER Academy. Headquartered in Newington, New Hampshire, SIG SAUER has over 3,400 employees across sixteen U.S. locations in three states, and four additional global facilities. SIG SAUER is certified a Great Place to Work™. For more information about the company and product line visit: www.sigsauer.com Position Summary: The Supplier Quality Engineer II will ensure the overall quality of supplied manufactured products. They will investigate and disposition nonconforming product and work to prevent its reoccurrence at the source by way of SCAR's, implementing control plans, and utilizing R&R and biased gaging methods. They will also support production needs in a timely manner by organizing required scrap, sorts, and rework for supplied nonconforming material as necessary. Working in a team environment, the Supplier Quality Engineer II will collaborate with cross functional teams including Design Engineers, Manufacturing, internal Quality, Project Management, Production Planning, Incoming Inspection, Purchasing as well as outside manufacturing and OSP suppliers. FLSA: Exempt Job Duties and Responsibilities: Review and disposition non-compliant material of increased complexity utilizing provided and self-verified inspection data, and use quality methods such as statistics, or pareto to assess causes and priorities. Accurately & independently assess issue culpability. Accurately determine correct gaging methods to aid incoming inspection and when verifying inspection data. Collect data for Gage R&R and bias. Design and source custom gages for specific applications. Experienced in MRP, PPAP, and Microsoft programs including Access. Extensive knowledge of the supplier quality management systems and Vendor Evaluation systems. Highly proficient in print reading and able to interpret dimensional tolerances and apply them to components of enhanced complexity. Identify external specification referenced in technical documentation and apply to the inspection process. Understanding and working fluency of GD&T symbology assigned per ASME Y14.5. Review design drawings for completeness and correctness. Independently generate documentation required to maintain and support ISO compliance. Serve as a contributing member of ISO audit teams. Enhanced understanding of the ISO process. Proficient in ATF Compliance and recognizing when input from the compliance team is needed to resolve/clarify compliance related issues. Independently identify areas of need for SCARs to generate and drive to completion SCARs, and execute to meet business needs. Engage in continuous improvement projects and tasks. Participate in 5s workplace organizational activities and maintain work area in accordance with 5s standard. Must follow all required safety and ISO procedures. Miscellaneous duties as assigned. Education/Experience & Skills: Bachelor's degree in Engineering sciences, and 3-6 years of experience in a Manufacturing or Quality Engineering role. High level of mechanical technical expertise required. Must be proficient with inspection equipment such as calipers micrometers, dial indicators, microhites, and hardness tester. Proficient with Microsoft Outlook, Word, Excel, and PowerPoint applications. Must have experience with CAD software. Possess experience in evaluating and troubleshooting all steps from receiving inspection of raw material to final inspection of completed parts of the manufacturing processes at suppliers, and assist in implementing permanent corrective actions to the supplier's manufacturing process. Must be able to clearly, concisely, and accurately convey ideas and information to suppliers and internal customers, both verbally and in written form. Must know their audience to be able to communicate effectively. Ability to work independently as well as part of a team. Completes tasks as assigned in a timely manner. Requires little supervision to identify additional tasking. Able to organize and prioritize tasks with minimal assistance. Able to make decisions with minimal guidance on corrective actions for supplier quality problems that arise. Communicate effectively to leadership verbally and in written format regarding problems and corrective action. Analysis of supplier quality failures, particularly related to prevention of receipt & advancement of non-compliant material. Working Conditions: Prolonged periods of sitting at a desk and working at a computer using a keyboard and mouse performing repetitive tasks. The duties of this job normally require exposure to a typical manufacturing area where frequent standing, sitting, stooping/squatting, walking and stair climbing can be expected along with frequent lifting and/or moving of tooling, parts, containers, and materials up to 40 pounds. Must be able to reach with hands and arms, bend and kneel frequently at a minimum 50% of the shift, as well as undergo repetitive wrist, hand, elbow, shoulder, and ankle motions. Must demonstrate proficient fine motor skills, be able to grip, reach, pull, turn, and use tools to torque fixtures in various machinery. Specific vision abilities required may include close vision, distance vision, peripheral and depth perception and ability to focus. Must wear required Personal Protective Equipment (PPE) where required. Must comply with all work exposure EH&S training requirements and adhere to SIG SAUER Inc. Security Mandates. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by law.

Founded over 35 years ago, First Quality is a family-owned company that has grown from a small business in McElhattan, Pennsylvania into a group of companies, employing over 5,000 team members, while maintaining our family values and entrepreneurial spirit. With corporate offices in New York and Pennsylvania and 8 manufacturing campuses across the U.S. and Canada, the companies within the First Quality group produce high-quality personal care and household products for large retailers and healthcare organizations. Our personal care and household product portfolio includes baby diapers, wipes, feminine pads, paper towels, bath tissue, adult incontinence products, laundry detergents, fabric finishers, and dishwash solutions. In addition, we manufacture certain raw materials and components used in the manufacturing of these products, including flexible print and packaging solutions. Guided by our values of humility, unity, and integrity, we leverage advanced technology and innovation to drive growth and create new opportunities. At First Quality, you'll find a collaborative environment focused on continuous learning, professional development, and our mission to Make Things Better . We are seeking a Quality Manager for our First Quality Retail Services located in Lewistown, PA. This position will be responsible for the creation, implementation and monitoring of all corporate & site Quality practices within their site of operation. Leading a team of quality professionals and driving a culture of continual improvement. Play a pivotal role and work collaboratively within the site management team, and drive quality engagement through all levels of the organization. Primary responsibilities include: Provide leadership and planning to develop, implement and maintain quality systems to ensure compliance to regulatory, industry, and customer standards. Serves as the Management Representative for all site compliance and quality systems Supervises the activities of assigned staff and monitor the activities of QA/QC personnel within the QA Department. Assure that all resources utilized for the quality functions are procured, maintained, and perpetuated in a cost effective and timely manner within the goals of the strategic business plan. Take the leadership role in maintaining/changing the quality culture of the company - serve as the visible model of Quality. Educate team members in the quality philosophy and practices, including improvement strategies. Represents the company to vendors, customers, and appropriate regulatory officials in matters related to quality. Administers the quality audit program. Provides training to team members, as required, for implementing quality initiatives. Work with cross-functional teams to prioritize key site projects and determine appropriate resources and timing; integrate lean six sigma activities with quality system activities such as Corrective and Preventive Action (CAPA) and Quality Improvements to assure effectiveness and compliance to customer and regulatory requirements. Develops annual quality plans and recommendations for continual improvement in conjunction with the Quality Leader and Operations Manager Determines methods and implements plans for professional development of personnel within the QA Department. Proposes budgets and monitors budget activity for the QA Department. Provides statistical analysis for evaluation of processes, and issue KPI reports to site leadership and divisional leaders at determined frequencies. Conducts lab tours and explains quality system to visitors. Understands competitive product features in comparison to products. Completes required reports and summaries for regulatory & industry agencies. Assists and substitutes for the Divisional Quality Leader, as needed. Observes all safety rules and always uses the proper safety equipment. Performs other duties as necessary when directed to do so. Follows necessary GMP, FDA, and ISO regulations. Manage master validation plan. Implement, monitor and review online Quality systems, including vision QMS Software, and SPC systems. The ideal candidate should possess the following: Bachelor's degree in an Engineering, Technology, Mathematics, Business, or Science discipline. Three years minimum experience as a Quality Manager, Technical Manager, or QC Supervisor in a manufacturing environment (preferably FDA-regulated environment). Six sigma Green Belt certified, preferred. Supervisory experience. Auditing experience in GMP and/or ISO systems. ASQ Certification or equivalent training (CQE, CQA, CQT, or CQM). Advanced skills in oral and written communications. Standard skills in technical, business, and managerial fields. Standard skills in statistics, procedure implementation, and quality auditing. Competent in interactions with executive management, vendors, and customers. What We Offer You We believe that by continuously improving the quality of our benefits, we can help to raise the quality of life for our team members and their families. At First Quality you will receive: Competitive base salary and bonus opportunities Paid time off (three-week minimum) Medical, dental and vision starting day one 401(k) with employer match Paid parental leave Child and family care assistance (dependent care FSA with employer match up to $2500) Bundle of joy benefit (year's worth of free diapers to all team members with a new baby) Tuition assistance Wellness program with savings of up to $4,000 per year on insurance premiums ...and more! First Quality is committed to protecting information under the care of First Quality Enterprises commensurate with leading industry standards and applicable regulations. As such, First Quality provides at least annual training regarding data privacy and security to employees who, as a result of their role specifications, may come in to contact with sensitive data. First Quality is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identification, or protected Veteran status.

Job Ad Now that you've found the job description, what's next? At VF, we strive to foster a culture of belonging based on respect, connection, openness, and authenticity. As a purpose-led, performance-driven company, we are committed to inclusion, diversity, equity, and action. So, before we get to the job details, take a minute to learn a little more about us - our values and our culture - visit ************ Join VF Corporation as an Engineering Intern for a full-time, 6+ month opportunity at our warehouse in Fort Worth! This hands-on internship is designed for aspiring engineers eager to gain practical experience in a dynamic environment, where you'll collaborate with industry professionals, contribute to innovative projects, and help optimize our operations. If you're ready to make an impact and develop your skills in a supportive team, we want to hear from you! What will you do? As an Engineering Intern with us here at VF Corporation, you will Collaborate with operations and engineering to identify waste, validate existing SOPs, and conduct system testing, while also performing time studies to confirm standards. Additionally, you will ensure effective communication of any changes to associates through the Distribution Center leadership team. Let's break down that day-in-the-life a bit more. Work with operations / engineering to identify the waste in each department. Work with operations to validate the existing SOPs and revise them as needed. Work with engineering team to perform system testing. Work with operations / engineering to perform time study (MOST & stopwatch) to validate the existing standards. Work with Distribution Center leadership to communicate changes to associates. What do you need to succeed? We all have unique skills that we bring to work and celebrate every day. For this role, there are foundational skills you'll need to succeed and excel. The foundational skills and experience you will need in this internship are: Candidates must be currently enrolled in a program related to Industrial Engineering, Supply Chain Management, Procurement, or a related field, or have a recent degree in one of those areas. Excellent verbal and written communication skills. Able to work independently. Proficiency in Microsoft office (PowerPoint, Excel, Word & Outlook). Ability to work full-time (40 hours per week) for a 6+ month period. Preferred Skills: Experience in Power BI Greenbelt (lean/six sigma) certificate What do we offer you? Work with iconic brands like The North Face, Vans, Timberland, and Dickies! Gain valuable experience and join a company that values teamwork and excellence. Members of our Distribution team benefit from skill and career development, working in collaborative teams, and competitive industry wages. Free to Be, Inclusion & Diversity As a purpose-led, performance driven company, we strive to foster a culture of belonging based on respect, connection, openness, and authenticity. We are committed to building and maintaining a workplace that celebrates the diversity of our associates, allowing them to bring their authentic selves to work every day. We just have one question. Are you in? Hiring Range: $19.44 USD - $24.30 USD per hour Benefits at VF Corporation: You can review a general overview of each benefit program offered, including this year's medical plan rates on ******************** and by clicking Looking to Join VF? Detailed information on your benefits will be provided during the hiring process. P lease note, our hiring ranges are determined and built from market pay data. In determining the specific compensation for this position, we comply with all local, state, and federal laws. At VF, we value a diverse, inclusive workforce and we provide equal employment opportunity for all applicants and employees. All qualified applicants for employment will be considered without regard to an individual's race, color, sex, gender identity, gender expression, religion, age, national origin or ancestry, citizenship, physical or mental disability, medical condition, family care status, marital status, domestic partner status, sexual orientation, genetic information, military or veteran status, or any other basis protected by federal, state or local laws. If you require accommodations during the application process, please contact us at ********************** . VF will provide reasonable accommodations for qualified individuals to the extent required by applicable law. Pursuant to all applicable local Fair Chance Ordinance requirements, including but not limited to the San Francisco Fair Chance Ordinance, VF will consider for employment qualified applicants with arrest and conviction records.

Founded over 35 years ago, First Quality is a family-owned company that has grown from a small business in McElhattan, Pennsylvania into a group of companies, employing over 5,000 team members, while maintaining our family values and entrepreneurial spirit. With corporate offices in New York and Pennsylvania and 8 manufacturing campuses across the U.S. and Canada, the companies within the First Quality group produce high-quality personal care and household products for large retailers and healthcare organizations. Our personal care and household product portfolio includes baby diapers, wipes, feminine pads, paper towels, bath tissue, adult incontinence products, laundry detergents, fabric finishers, and dishwash solutions. In addition, we manufacture certain raw materials and components used in the manufacturing of these products, including flexible print and packaging solutions. Guided by our values of humility, unity, and integrity, we leverage advanced technology and innovation to drive growth and create new opportunities. At First Quality, you'll find a collaborative environment focused on continuous learning, professional development, and our mission to Make Things Better . We are seeking an experienced Warehouse Automation Engineer for our First Quality facility located in McElhattan, PA; Lewistown, PA; or Macon, GA. This position will be responsible for optimizing, managing, and improving the material flow within the warehouse ensuring that goods are stored, handled, and transported efficiently, safely, and cost-effectively. Expected to apply principles of engineering, technology and best in class logistics to improve current systems, devise layouts and enhancements for material handling solutions within current automation footprints and beyond. Principal Accountabilities/ Responsibilities: Optimize and develop layouts for warehouse systems that optimize space and streamline processes Analyze and recommend improvements in logistics operations, systems and processes Drive the selection, implementation, maintenance and improvements of automation technologies Collaborate with other departments to ensure that automation logistics or automation considerations are integrated into the overall operational strategy and business goals Manage relationships with current and future automation OEMs and partners Support and drive asset purchases and capital expense needs for warehouse ops ~50% travel is required Frequent standing/walking throughout facilities Possibility of travel to OEM/vendor locations Education and experience requirements: Bachelor's degree in engineering, supply chain, logistics or a related field. Strong project engineering background is crucial 5+ years' experience in manufacturing and/or warehousing Experience with robotics, material handling automation, warehouse automation preferred Lean/Six Sigma certification a plus Proficiency in process mapping, statistical analysis and data visualization tools Strong organizational skills Project leadership and management Analytical mind set Continuous improvement approach Critical thinking and problem solving skills a must Ability to work within a team and independently Strong written and communication skills Clear and logical thinker What We Offer You We believe that by continuously improving the quality of our benefits, we can help to raise the quality of life for our team members and their families. At First Quality you will receive: Competitive base salary and bonus opportunities Paid time off (three-week minimum) Medical, dental and vision starting day one 401(k) with employer match Paid parental leave Child and family care assistance (dependent care FSA with employer match up to $2500) Bundle of joy benefit (years' worth of free diapers to all team members with a new baby) Tuition assistance Wellness program with savings of up to $4,000 per year on insurance premiums ...and more! First Quality is committed to protecting information under the care of First Quality Enterprises commensurate with leading industry standards and applicable regulations. As such, First Quality provides at least annual training regarding data privacy and security to employees who, as a result of their role specifications, may come in to contact with sensitive data. First Quality is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identification, or protected Veteran status. For immediate consideration, please go to the Careers section at ******************** to complete our online application. First Quality is committed to protecting information under the care of First Quality Enterprises commensurate with leading industry standards and applicable regulations. As such, First Quality provides at least annual training regarding data privacy and security to employees who, as a result of their role specifications, may come in to contact with sensitive data. First Quality is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identification, or protected Veteran status.

Job Title: Quality Process Engineer Department: Operations Reports to: Plant Operations Manager FLSA Status: Exempt Quality Process Engineer position is responsible for continuous improvements activities across all domestic manufacturing locations within Rawlings Sporting Goods Company. Essential Duties & Responsibilities: Comply with all OSHA and company Environmental, Health, Safety, and Security policies. Develop product manufacturing specifications and quality standards based on new product requirements. Implement and train workers in new specifications and standards. Perform first article inspections and troubleshooting related manufacturing problems, documenting and maintaining product and manufacturing documentation. Investigate and recommend new manufacturing processes and procedures. Manage both large and small manufacturing projects. Determine operations required to produce products and develop processes to ensure quality, cost, and efficiency requirements are met. Research the purchase of equipment or upgrades to existing equipment. Participates and leads continuous improvement activities plant wide. Investigates and performs root cause analysis on production and customer issues. Understands and applies statistical processing analysis and controls (SPC) on critical quality parameters. Completes product, process and test audits at manufacturing sites. Implements and audits production specifications on newly designed products. Performs and maintains production measurement systems analysis on critical quality measurements such as gauge R&R and calibration records. Properly organizes and maintains QA inspection documents. Creates / Manages the work instructions for the plant Creates / Maintains the Bill of Materials / Routers for the production process. Performs time studies for the process. Works with the bat development team to make sure all materials needed are orders for sample/production runs. Knowledge, Skills, Abilities and Education Required: Bachelor's degree in engineering preferably Composite, Mechanical, Chemical, or Electrical Engineering. One to three years manufacturing engineering experience. Excellent verbal and written communication skills. Good organizational skills and recording keeping. Work independently as well as part of a team. PLC programming experience a plus. Computer skills - Microsoft Excel, Word, Chartrunner, Minitab or any other data acquisition software. Working knowledge of JDEdwards or an ERP system is a plus. Travel as needed. Working Conditions: General office and manufacturing working environment. Safety Hazards: Exposure to dust, airborne fibers, fumes, dirt, noise, vibrations, chemicals, and solvents. Walking between buildings year-round is required. Safety glasses, hearing protection, and gloves are required while performing certain tasks. LANGUAGE SKILLS Ability to read and interpret documents such as contracts, ability to write advertising, reports and correspondence. Ability to speak effectively before groups of customers or employees of organization. Must have proven exceptional written presentation and verbal communication skills. MATHEMATICAL SKILLS Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, and percentages. Ability to apply concepts of basic math and algebra. REASONING ABILITY Ability to apply common sense understanding and carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit and use hands requiring finger dexterity, and handling or working with equipment. The employee is frequently required to reach with hands and arms. The employee is regularly required to stand and walk. The employee will occasionally lift and/or move objects weighing 10-25 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision. Employee will be required to hear telephone. This does not list all the duties of the job. You may be asked to perform other instructions and/or duties. You will be evaluated in part based upon your performance of the task listed in this job description.

Job Title: Quality Process Engineer Department: Operations Reports to: Plant Operations Manager FLSA Status: Exempt G Quality Process Engineer position is responsible for continuous improvements activities across all domestic manufacturing locations within Rawlings Sporting Goods Company. Essential Duties & Responsibilities: Comply with all OSHA and company Environmental, Health, Safety, and Security policies. Develop product manufacturing specifications and quality standards based on new product requirements. Implement and train workers in new specifications and standards. Perform first article inspections and troubleshooting related manufacturing problems, documenting and maintaining product and manufacturing documentation. Investigate and recommend new manufacturing processes and procedures. Manage both large and small manufacturing projects. Determine operations required to produce products and develop processes to ensure quality, cost, and efficiency requirements are met. Research the purchase of equipment or upgrades to existing equipment. Participates and leads continuous improvement activities plant wide. Investigates and performs root cause analysis on production and customer issues. Understands and applies statistical processing analysis and controls (SPC) on critical quality parameters. Completes product, process and test audits at manufacturing sites. Implements and audits production specifications on newly designed products. Performs and maintains production measurement systems analysis on critical quality measurements such as gauge R&R and calibration records. Properly organizes and maintains QA inspection documents. Creates / Manages the work instructions for the plant Creates / Maintains the Bill of Materials / Routers for the production process. Performs time studies for the process. Works with the bat development team to make sure all materials needed are orders for sample/production runs. Knowledge, Skills, Abilities and Education Required: Bachelor's degree in engineering preferably Composite, Mechanical, Chemical, or Electrical Engineering. One to three years manufacturing engineering experience. Excellent verbal and written communication skills. Good organizational skills and recording keeping. Work independently as well as part of a team. PLC programming experience a plus. Computer skills - Microsoft Excel, Word, Chartrunner, Minitab or any other data acquisition software. Working knowledge of JDEdwards or an ERP system is a plus. Travel as needed. Working Conditions: General office and manufacturing working environment. Safety Hazards: Exposure to dust, airborne fibers, fumes, dirt, noise, vibrations, chemicals, and solvents. Walking between buildings year-round is required. Safety glasses, hearing protection, and gloves are required while performing certain tasks. LANGUAGE SKILLS Ability to read and interpret documents such as contracts, ability to write advertising, reports and correspondence. Ability to speak effectively before groups of customers or employees of organization. Must have proven exceptional written presentation and verbal communication skills. MATHEMATICAL SKILLS Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, and percentages. Ability to apply concepts of basic math and algebra. REASONING ABILITY Ability to apply common sense understanding and carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit and use hands requiring finger dexterity, and handling or working with equipment. The employee is frequently required to reach with hands and arms. The employee is regularly required to stand and walk. The employee will occasionally lift and/or move objects weighing 10-25 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision. Employee will be required to hear telephone. This does not list all the duties of the job. You may be asked to perform other instructions and/or duties. You will be evaluated in part based upon your performance of the task listed in this job description.