Quality Jobs

company About Forterra At Forterra, we are unleashing autonomy at scale to transform the battlefield. Our mission is to build the foundational platforms that enable an intelligent ecosystem to coordinate, adapt, and execute with speed and precision even in the uncertainty and disruption of modern conflict. In an era marked by rapid technological change and evolving threats, we design for flexibility, survivability, and operational dominance. Forterra delivers weapons, sensors, and battlefield effects through integrated autonomous networks reaching operational areas faster, safer, and without placing human lives at risk. Our systems operate with distributed control, dynamic routing, and real-time responsiveness, enabling sustained advantage across complex mission environments. role About the role Forterra is looking for a Senior Quality Manager to support a large autonomous research client in the Clarksburg, MD area. Key responsibilities will be to work closely with design and production teams to solve problems. The Senior Quality Manager will also own and manage all assigned CAPAs to ensure timely closure and that appropriate corrective actions are established and adhered to. The Senior Quality Manager will act as a key participant of the configuration management process where applicable. They will also help by responding to questions about how to achieve quality goals and implement changes to reduce the instance of human or machine errors. When working on a new project, the Senior Quality Manager will meet with customers (Internal/External) to discuss their quality expectations, including details about expected performance and visual appearance. They will also help design documents, processes, and procedures that clearly outline these specifications and communicate them to all responsible teams. As a leader of continuous improvement, the Senior Quality Manager will also observe the production process and identify how to implement cost effective improvements that drive consistent quality and improve efficiency. Lastly, the Senior Quality Manager will act as the escalation point for and support the Non-Conformance Management Review process. What you'll do Understand and analyze complex problems and derive solutions. Effectively communicate technical issues, solutions, ideas, and concepts to a diverse audience including Managers, Customers, and Executive Management. Drives continuous improvement and defect reduction using data analysis. Support nonconformance/noncompliance investigations to analyze and determine root cause, define corrective actions, and ensure corrective action implementation is effective. Lead program and quality assurance reviews. Monitor and ensures completion of monthly quality performance metrics. Understand design intent, requirements, and specifications and drives reviews of customer and Forterra requirements to ensure all are consumed into product/process requirements. Review quality documentation including policies, procedures, processes, to ensure compliance with internal and external requirements. Maintain, enforce, and measure quality assurance processes. Drive counter measures for Quality processes not achieving prescribed KPI/PPI targets. Monitor and control the overall activities of the team and identifies problem areas requiring support. Assign duties and monitor quality of work; assure that staff conforms to government regulations and organizational policies and procedures. Support representation of Quality processes during internal and external third-party audits. Conduct internal audits of products, processes and procedures to drive compliance. Provide support in development and growth of the APQP process. Provide support on occasion to conduct supplier evaluations, assessments, and audits. Monitor and manages the Quality department budget. Develop talent within the team to increase performance. Proactively addresses performance issues on the team. Perform other duties as assigned by management. Role may require up to 20% travel What We're Looking For Mission-First Mindset - We put the needs of the mission and our customers first and understand that the US and its allies have no preordained right to victory in any future conflict. Ownership Mentality - We’re looking for owners; those who have a natural bias to assume responsibility, a healthy dose of skepticism, and contribute to a culture of performance. Technical Aptitude and Intellectual Curiosity - We are first and foremost a technology company, working at the leading edge of capabilities like machine learning, autonomy, distributed networking, and multi-modal sensor fusion. Structured Thinker and Problem Solver - Leading technical programs requires clear communication and well-thought-out plans. A solution-driven approach, the ability to distill complexity into its essential, digestible components, and the ability to supervise execution are critical to ensure mission success. 360 Degree Leader - We are a non-hierarchical organization with a matrix structure that is dynamic and evolving. We expect you to be self-aware enough to recognize your position of unstated leadership within the company. You should have a demonstrated ability to lead and influence people through both formal and informal constructs and in situations where there is lack of clarity across teams What We Need Bachelor’s Degree in Science, Technology, Engineering, or Math (STEM) 6+ years of Quality Management work experience in Defense, Aerospace, Medical or Automotive manufacturing. 6+ years of direct Quality Management supervisory experience in Defense, Aerospace, Medical or Automotive manufacturing. Excellent oral and written communication skills. Self-guided and ability to work independently. Auditing experience within the ISO9001:2015 quality management standard. Proven track record of understanding and managing First Article Inspection / PPAPs. Working knowledge of Material Review Board (MRB) standards, practices, and customer engagement. Experience facilitating effective Root Cause Corrective Action (RCCA). Experience with Dimensional Inspection Techniques and demonstrated ability to read and interpret drawing and technical specifications. Experience with Advanced Product Quality Processes (PPAP, APQP, PFMEA, 8D, A3 Problem Solving) Strong interpersonal skills with the ability to interface with different functions at all levels. Excellent problem-solving skills and ability to organize and prioritize multiple tasks. Demonstrated work ethic, professional maturity, and strong attention to detail. AS9100, ISO 9001:2015, TS16949 or other quality management system equivalent. Experience in new program launch. Proficiency in utilizing Microsoft Excel, Word, PowerPoint, and in NetSuite or similar ERPs. (SAP, Plex, Etc.) Experience in Configuration Management Ability to travel up to 20%. What We Love to See Master’s Degree in Science, Technology, Engineering, or Math (STEM) 8+ years of Quality Management experience in Defense, Aerospace, Medical or Automotive manufacturing quality. 8+ years of direct Quality Management supervisory experience in Defense, Aerospace, Medical or Automotive manufacturing quality. ASQ Certification – Considered a strong plus. (CQE/CQA) Familiarity with IPC standards (IPC-620, IPC J-STD-001, IPC-A-610) Considered a plus. Geometric Dimensioning and Tolerancing (GD&T) Trained. Lead Auditor certification. ISO9001:2015 or equivalent standard. Lean or Six Sigma experience is a strong plus. Compliance and Regulatory experience. Understanding and ability to use the DMAIC Process: Define, Measure, Analyze, Improve and Control. Skilled in customer interaction and presentation. US Salary Range $135,000—$175,000 The salary range for this role is an estimate and is based on a wide variety of compensation factors. The salary offered to candidates will vary based on a variety of factors including (but not limited to) relevant work experience, education, specialized training, critical expertise, training, and more. Equity in Forterra is included in most of our full-time, high-demand roles and is therefore considered part of Forterra’s overall compensation package. In addition to base salary and equity, Forterra offers competitive benefits for full-time employees including: Premium Healthcare Benefits: Three plan options, including an HSA-eligible plan, with Forterra covering 80% of the plan premium for you and your dependents. Basic Life/AD&D, short and long-term disability insurance plans 100% covered by Forterra, plus the option to purchase additional life insurance for you and your dependents. Extremely generous company holiday calendar including a winter break in December. Competitive paid time off (PTO) offering 20 days accrued per year. A minimum of 7 weeks fully paid parental leave for birth/adoption. A $9k annual tuition reimbursement or professional development stipend. Fully stocked beverage refrigerators with all the Celsius your little heart desires. 401(k) retirement savings plan, including traditional, Roth 401(k), and after-tax deferral with company match up to 4%. Your recruiter will be able to share more information about our salary and benefits offering during the hiring process. CLEARANCE ELIGIBILITY - This position may require eligibility to obtain and maintain a U.S. security clearance. For more information about U.S. Security Clearances:  click here . Forterra is an equal-opportunity employer, providing and promoting equal employment opportunity in all personnel practices. Forterrans are unique, talented individuals who are united through a shared passion to deliver autonomous systems that enable national resilience and a robust supply chain. All qualified applicants will receive consideration for employment without regard to any factor, including veteran and disability status, and criminal history, in accordance with applicable local, state, and federal laws. Forterra is also committed to working with and providing reasonable accommodations to individuals with disabilities. Please let your recruiter know if you need an accommodation at any point during the interview process. To see Forterra’s candidate data privacy policy, please visit Forterra Legal | Job Applicant Privacy Notice .

QA, Quality

Sunstar Americas, Inc. is a global leader in the oral care industry and the manufacturer and distributor of GUM oral care products and solutions. We serve dental professionals and consumers in 90 countries worldwide and are driven by a mission: to enhance the health and well-being of people everywhere through high-quality, innovative oral care products and solutions.

With sales of €700m and 3,300 employees worldwide, Nemera is one of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices, injection devices, nasal and dermal pumps and ophthalmic delivery devices. Nemera has built very long lasting, strong relationships with the leading global pharmaceutical companies globally by providing high quality development, industrialization and manufacturing services. Nemera develops and manufactures its own IP product platforms but also offers also fully custom developments and contract manufacturing. Nemera’s manufacturing sites are located in the US, France, Germany, Brazil and Poland. The headquarters and Innovation Center for early device design and development are located in France (Lyon). We have big ambitions at Nemera! We are growing our franchises and strengthening our capabilities. Position Purpose : The Quality Project Manager’s role is to assure high quality products and services that satisfy both internal and external requirements including meeting and exceeding customer expectations in compliance with regulatory requirements. KEY RESPONSIBILITIES/ESSENTIAL FUNCTIONS: • Assists Associate Director of Quality in coordinating and executing goals and objectivess throughout the company to improve product quality and operating system efficiency. • Direct and coordinate the activities of Quality Department employees. • Establish and maintain sound relationships with production, technology, supply chain, quality teams and cross functional personnel to identify system and compliance gaps with proposed resolutions. • Act as liaison with metrology, QC and compliance team • Ensure adherence to project and company standards, while maintaining quality systems that meet customer, internal, and regulatory requirements (ISO, cGMP, FDA, Health & Safety). • Manage claims non-conformities, investigations, problem solving, root cause analysis, champion creation of effective and sustainable corrective actions. • Manage process and equipment Validations for new product and existing business. • Change control process owner • Define and implement quality initiatives to meet KPI’s and objectives. • Identify opportunities for improvement through data trending and analysis, as well as develop and implement quality and inspection processes. Engage in risk assessment process; data integrity, control and management utilizing risk assessment tools such as FMEA. • Review and approve technical protocols, reports, and specifications, as appropriate. • Participate and lead CAPA activities as required, utilizing problem solving techniques to reduce internal and external failures. • Employ necessary tools/resources and perspectives, treating all co-workers with respect/dignity and valuing feedback. • Responsible for the coordination and evaluation of the Quality department. • Supervises staff in line with company policies and laws, including hiring, training, task management, performance evaluation, discipline, and conflict resolution. • Make hiring decisions for their direct reports. • Represent the Quality Department in support of customer, ISO and third-party audits. • Other duties as assigned • WORK ENVIRONMENT: • Office and clean room environment that may include moderate noise levels and required appropriate PPE and cleanroom apparel • Ability to travel between office and production departments as well as company buildings required POSITION REQUIREMENTS: • Bachelor’s degree in Engineering or related field • 4+ years of relevant working experience in Quality in a manufacturing environment with 1+ year experience in a supervisory role • Excellent communication skill with the ability to understand, read, write, and speak English • Ability to apply advanced mathematical concepts and intermediate statistical (SPC) knowledge • Strong understanding of injection molding, Automation and FMEA. • Knowledgeable to equipment/process/product validation practices and principles. • Excellent interpersonal, organizational and communication skills. • Demonstrated leadership and the ability to motivate and influence others. • Able to lift up to 30 lbs. • Ability to push and pull items • Ability to sit, stand, walk 80% of shift required PREFERRED KNOWLEDGE/SKILLS: • Self-directed and possess knowledge of business and management principles involved in strategic planning, resource allocation and coordination of people and resources. • Knowledge of inspection tools, including their design, use, repair and maintenance • Medical device and/or Pharmaceutical Industry experience preferred • Six sigma training and/or certifications preferred. • Demonstrated organizational skills and general knowledge of PC applications such as Microsoft Word, Excel and Database software such as SAP Why Join Nemera? At Nemera, we prioritize patients when creating drug delivery devices, understanding that accurate dosing and ergonomics are crucial for treatment adherence. Joining Nemera means becoming part of a team that enjoys working together and consistently delivers on its commitments. We take pride in our work because it improves patients’ lives. We look forward to receiving your application (resume submitted in English is appreciated). We offer varied jobs job in an international group, if you want to discover more about Nemera, please look at our website www.nemera.netKnow someone at Nemera? We have a Referral Program so, be sure to have them submit you as a referral prior to applying for this position POSITION RANGE : $120,000 - $140,000 USD Salaried  (This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.) For US Benefits, CLICK HERE . Nemera is an equal opportunity employer and does not discriminate against any person on the basis of race, religion, color, gender, gender identity, sexual orientation, age, national origin, disability, veteran status, or any other protected class indication. This company is required by federal law to hire only persons who can establish they are eligible to work in the United States.

Assists in Developing, applying, and maintaining quality requirements and standards for the development and manufacture of quality products. Main processor of Engineering Changes from BTD’s customers. Understands and as needed, provides PPAP requirements to BTD customers. Must be capable of creating and updating quality control tools to be used in the production process. In regard to part acceptability works directly with production, sales and engineering to meet customer expectations. While working with QA Manager and leadership, assists BTD departments in problem solving, corrective actions and internal and external quality audits.

We are committed to our culture that values Customer Focus, Flexibility, Knowledge, Speed and Integrity. Joining our team means you will work in a high performing global company where employees collaborate and strive for excellence. Quality Data & Analysis Analyze quality data across production, inspection, test, and repairs to prioritize continuous improvement activities Run process capability (Cpk/Ppk) and correlation studies against defined qualification criteria Convert subjective inspection criteria into measurable, verifiable requirements Deploy and maintain SPC on critical product and test parameters Maintain quality KPIs: first pass yield, RMA rate, scrap and rework cost, supplier PPM, etc. Support product qualification between manufacturing sites, including site-to-site correlation Problem Solving & Corrective Action Lead root cause analysis on various quality issues using 8D, fishbone, and 5-Why methods Drive corrective actions to closure across departments and verify effectiveness Disposition nonconforming material through MRB Issue and close supplier corrective action requests (SCARs) with Supply Chain Process & Documentation Own PFMEAs and control plans for assigned product families Define inspection methods, sampling plans, and incoming inspection requirements Write and revise inspection criteria, process documentation, and work instructions Lead continuous improvement projects targeting yield, scrap, and rework Quality System & Audits Participate in internal audits as an auditor and support audit findings to closure Support external registrar and customer audits, including hosting assigned process areas Participate in supplier and site assessments alongside Supply Chain and Quality leadership Supply data and analysis for management review Required Bachelor's degree in Engineering or a related technical field 3+ years in a quality role with an electronics manufacturer Working knowledge of process capability, SPC, Gauge R&R, and sampling plans Hands-on root cause and corrective action experience (8D, fishbone, 5-Why) Electronics manufacturing background: PCBA, wire harness, and electromechanical assembly Advanced Excel including pivot tables; comfortable pulling and analyzing data from an ERP system Preferred IPC-A-610, J-STD-001, etc. High-voltage or power electronics products, including dielectric/hipot testing and encapsulation ASQ CQE or Six Sigma Green Belt+ Statistical software experience (Minitab, JMP, or equivalent) Multi-site or offshore manufacturing transfer experience XP Power provides a safe and healthy working environment that is stimulating and collaborative, where employees are empowered to make a real difference. We place our people at the heart of everything we do. We understand that if we provide our people with the ultimate experience, they will provide the ultimate experience to our customers. We also offer a comprehensive benefits package including: 100% Employer Paid Medical, Dental and Vision Insurance for full-time Employee-only coverage; you share the cost of coverage for your dependents Company Paid Bonus ( Percentage dependent on Company profitability and individual performance ) Company 401(k) Match ( up to 6% ) Mental Health Benefits Paid Time Off ( Accrued per pay period starting at 3 weeks per year ) 13 Company Paid Holidays  Paid Time Off for Volunteer Work ( up to 8 hours per year ) Employer Paid Supplemental Short-Term and Long-Term Disability Insurance  Veterinary Pet Insurance Company Social Events held throughout the year A Friendly Culture Where People Collaborate and Strive for Excellence

The QC Inspector 2 is responsible for ensuring raw materials, components, sub-assemblies, and finished products meet the required quality standards and specifications as defined by the Quality Management System (QMS). This position plays a critical role in upholding Dexter's commitment to delivering high-quality products by conducting thorough inspections and collaborating to address quality concerns.

The Quality Control Manager at Acero Precision is responsible for continually checking the precision machined parts to the blueprint to verify all part features, specifications and tolerances. Monitoring operations to ensure they meet production and quality standards is an ongoing process.

The Quality Control Manager at Acero Precision is responsible for continually checking the precision machined parts to the blueprint to verify all part features, specifications and tolerances. Monitoring operations to ensure they meet production and quality standards is an ongoing process.

The QA FINAL INSPECTOR is responsible for maintaining the company’s high production standards through continuously improving methods of inspection and standard operating procedures. The incumbent ensures that manufacturing errors are caught and corrected before shipment and that high quality products are sent to the customer on time.

The QA FINAL INSPECTOR is responsible for maintaining the company’s high production standards through continuously improving methods of inspection and standard operating procedures. The incumbent ensures that manufacturing errors are caught and corrected before shipment and that high quality products are sent to the customer on time.