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The Manager of Quality Assurance/Quality Control has a keen eye for detail and extensive experience in quality system development and control. This position is responsible for ensuring all external and internal quality assurance standards are met before our product reaches our customers. This candidate will continue to define the division’s QC/QA initiative and implement best practices with the purpose of identifying non-conformity issues and improving overall customer satisfaction.

Essential Duties and Responsibilities

• Design, deploy, and maintain the business unit’s quality management processes.
• Develop best practices for in-line and final inspections, product testing, and reporting.
• Evaluate and improve all processes that impact product quality and customer satisfaction.
• Prepare and communicate quality performance reports to suppliers, internal teams, and executive management.
• Establish and maintain QA audit standards for new and existing suppliers—domestic and international.
• Collaborate cross-functionally with internal teams, agents, and vendors to implement effective QA/QC protocols.
• Manage third-party lab testing programs (e.g., with Bureau Veritas), including test protocol development and execution.
• Advise internal and external stakeholders on product improvements and technical solutions.
• Oversee quality review during new vendor onboarding, ensuring completion of audits, certifications, and corrective action plans (CAPs ).
• Demonstrates high level of quality work, attendance and appearance.
• Demonstrates high degree of professionalism in communication, attitude and teamwork with customers, peers and management.
• Adhere to all local, federal and state laws in addition to Company policies, procedures, and practices.
• Performs any other duties that may be assigned by management.
• Demonstrates high level of quality work, attendance and appearance.
• Demonstrates high degree of professionalism in communication, attitude and teamwork with customers, peers and management.
• Adhere to all local, federal and state laws in addition to Company policies, procedures, and practices.
• Performs any other duties that may be assigned by management.

Qualifications

• Bachelor’s degree in Supply Chain, Business, or related field.
• 7–10+ years of experience in QA/QC within apparel or footwear.
• Strong knowledge of global audit protocols.
• Working knowledge of ISO, ASTM, AATCC standards and test methods.
• Experience working with global factories.
• Ability to manage third-party audit firms.
• Strong communication and negotiation skills.
• Analytical and data-driven decision making.
• Ability to influence cross-functional teams.
• High integrity and cultural sensitivity.
• Willingness to travel internationally as required.
• Thorough knowledge of manufacturing related quality assurance methodologies and standards.
• Experience working with ANSI or other sampling tables.

Competencies

• Ensure Effective Communication - Listens carefully and attentively to others' opinions and ideas. Communicates information clearly, concisely, and professionally.
• Establish Trust - Follows through on commitments. Is honest and direct with others. Promotes a culture of respect for, commitment to, and compliance with Company values, beliefs, and standards. Ensures the protection of confidential information.

Boot Barn Benefits & Additional Compensation Opportunities

• Competitive salary.
• Merchandise discount: 50% off of Exclusive Brands and 40% off of third-party brands.
• Paid Time Off plan for year-round Boot Barn Partners.**
• Medical, Dental, Vision and Life Insurance.**
• 401(k) plan with generous company matching.
• Flexible schedules and work/life balance.
• Opportunities for growth at every level – we are opening 50+ new stores each year.

**For eligible Boot Barn Partners

PAY RANGE: $80,000.00-$90,000.00/yr*

*compensation varies based on geography, skills, experience, and tenure

Physical Demands

In general, the following physical demands are representative of those that must be met by a Partner to successfully perform the essential functions of this job. Reasonable accommodations may be made to allow differently abled individuals to perform the essential functions of the job.

• Standing, walking and squatting less than fifty percent of the work shift.
• Required to lift, move and carry up to 40 pounds.
• Ability to read, count and write to accurately complete all documentation and reports.
• Must be able to see, hear and speak in order to communicate with partners and customers.
• Specific vision abilities include close vision, distance vision, peripheral vision, depth perception and ability to adjust focus.
• Manual dexterity required using hands to finger; handle, feel and type; reach with hands and arms.

[ ] Sedentary: Limited activity, no lifting, limited walking

[ X ] Light: Office work, some lifting, bending, stooping or kneeling, walking

[ ] Moderate: Mostly standing, walking, bending, frequent lifting

[ ] Arduous: Heavy lifting, bending, crawling, climbing

Work Environment

In general, the following conditions of the work environment are representative of those that a Partner encounters while performing the essential functions of this job. Reasonable accommodations may be made to allow differently abled individuals to perform the essential functions of the job within the environment.

• The workspace is clean, orderly, properly lighted and ventilated with the proper safety compliance.
• Noise levels are considered moderate.

Boot Barn, Inc. reserves the right to make exceptions to modify or eliminate this document or its content. This document supersedes all previous policies, procedures or guidelines pertaining to this subject.

Our core value of community bands us together in supportive and inclusive ways to drive our collective success. Boot Barn provides equal employment opportunity to all applicants and employees without regard to race, color, religion, sex, sexual orientation, age, national or ethnic origin, veteran or military status, disability, as well as any other protected status under the law.

Americans with Disabilities Act (ADA) - Boot Barn will provide reasonable accommodations (such as a qualified sign language interpreter or other personal assistance) with the application process upon your request as required by applicable laws. If you have a disability and require assistance in this application process, please visit your nearest Boot Barn Store or Distribution Center or reach out to Human Resources at 1-949-453-4400, Option 4.

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Quality Control Manager

The Company

Heico has a history of success. Since its founding over 40 years ago, The Heico Companies has grown from a single business to over 78 separate companies through a strategic acquisition policy, and by reinvesting its earnings into internal growth and new prospects. Historically talented at restoring distressed companies, Heico strategically targets acquisitions that will complement its ever-growing portfolio of companies in manufacturing, construction, and industrial services.

These four core operations are organized into groups: Applied Solutions Group, Construction Solutions Group, Industrial Technologies Group, and Metal Processing Group. Once acquired, new Heico companies are assigned to a group and run on a stand-alone basis, allowing for great independence as well as the opportunity to share knowledge about markets, production processes, and management practices across other Heico groups and companies.

Heico continues to seek out new opportunities and maintain its standard of success. The Heico Companies has remained a privately held company since its creation and maintains a majority ownership in each of its operations, which generates more than $3.3 billion dollars in revenues. Many of our businesses are certified Woman-owned Business Enterprises (WBE).

More information about the overall organization can be found at Strand is part of the Metals Processing Group which produces steel wire and cable/wire-related products that serve many industries and is wholly owned by The Heico Companies, LLC. The independent business model fosters entrepreneurship and growth and allows professional development at all levels.

The Position

The Quality ControlManager will develop, implement, manage and maintain effective Quality and Safety policies and procedures that meet or exceeds the criteria of federal, state, and business requirements.

This role is onsite in Baytown, TX and offers relocation assistance.

Job Details

• Conducts quality assurance audits of National Strand production assuring company standards are maintained and product integrity is preserved.
• Develop and implement best practices to ensure consistency in the quality of the product.
• Be a point of contact for customers when discussing technical specifications or complaints.
• Act as the focal point for all quality-related issues and report to management as needed.
• Schedule and coordinate all internal and external audit activities, address non-conformities, and maintain audit history.
• Provide weekly reports on quality performance and identify areas of improvement.
• Consults with management to resolve quality, production, and efficiency problems.
• Functions as an information source to departments when special and critical quality issues occur.
• Determine overall plant product quality by conducting and evaluating various product tests and tests related to steel wire making and processing.
• Consult with plant management and personnel on better operational procedures to improve overall efficiency and product yields.
• Discuss plant evaluation with plant management, make appropriate recommendations, and set a timetable for improvement and corrections.
• Work with accounting to ensure scrap and reject reporting is accurate and timely.
• Performs other duties as assigned.

Job Requirements

Experience: Minimum 3+ years of experience in a manufacturing environment. ISO 9000 experience preferred or similar.

Education: Bachelor’s degree in engineering or related field from an accredited University. Master’s degree is preferred. Metallurgical knowledge is highly desirable.

Communication: Excellent communication skills, both written and verbal communication. Proven capability to collaborate with non-professional as well as professional stakeholders at all levels. Excellent business communication and leadership; ability to manage multiple demands.

Technology: Strong working knowledge of MS Office and other support software. Knowledge of MS SharePoint is highly desirable.

Position Type and Expected Hours of Work - This is a full-time position. Typical work hours are Monday through Friday, 8:00 AM to 5:00 PM. Occasional evening and weekend work may be required as job duties demand.

Travel - This position might require occasional travel.

Work Environment - The position operates in a professional office environment using standard office equipment such as computers, iPads, phones, copiers, and filing cabinets. The employee is occasionally exposed to fumes or airborne particles, distracting noise levels and moving mechanical parts.

Physical Requirements - The physical demands described here are representative of those that must be met by the QC Manager position 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 talk or hear.The employee is frequently required to stand and walk. The employee is occasionally required to use hands to finger, handle or feel and reach with hands and arms, lift and/or carry up to 50 pounds, balance, bend, stoop or kneel, climb, push/pull and squat, or crouch.

Disclaimer: This position description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

About RevoGen Biologics LLC

RevoGen Biologics is committed to making lives better through cutting-edge biologics. Following time-tested rigorous guidelines, delivering quality products and services to our clients is our number one goal. We created RevoGen® Biologics with a client-centric mission in mind. Built on a solid foundation of best-practices and trust-driven relationships, we aim to improve the lives of everyone who uses our products. From doctors and surgeons to patients and distributors, we strive to deliver the most optimal experience for every person who interacts with RevoGen Biologics. Following rigorous, time-tested guidelines and conducting stringent donor screenings, we’re revolutionizing the field of bioregeneration to offer physicians and their patients quality biologics. 

Job Title: Tissue Bank Director

Location: San Antonio, Texas, USA

Department: Medical Affairs

Reports To: Medical Director

FLSA Status: Exempt

Position Summary

The Tissue Bank Director serves as the clinical expert for donor suitability, tissue recovery, processing criteria, supply requirements, quality metrics, and tissue training for the organization. The Tissue Bank Director provides leadership and oversight for all ocular, wound care, and bone filler tissue banking operations, including the recovery, processing, preservation, storage, and distribution of human ocular tissues and skin/amniotic or bone filler grafts used in transplantation, ophthalmic surgery, and advanced wound care. The Tissue Bank Director is responsible for creating an annual budget, forecasting tissue projections and revenue, and maintaining fiscal accountability within the department. In addition, the Tissue Bank Director is responsible for negotiating, executing, and adhering to processor and supplier agreements, including defined monthly, quarterly, and annual tissue allocation caps. The Tissue Bank Director is accountable for the tissue recovery staff’s adherence to all regulatory and accrediting agency standards, including, but not limited to CMS, FDA, and AATB, as well as all internal organizational policies, procedures, and guidelines. The Tissue Bank Director is responsible for strategic planning as it relates to departmental, tissue program, and donor network growth, and investigating business opportunities that lead to an increase in tissue donation and/or improvement in clinical outcomes.

 The Director ensures compliance with applicable regulations, including FDA 21 CFR Part 1271, AATB Standards, EBAA Standards, and state tissue banking requirements.

This role oversees supplier relationships, donor screening, validation, labeling, and release to maintain the highest standards of safety, sterility assurance, and ethical integrity.

Essential Duties and Responsibilities

·     Provide strategic leadership for ocular and wound graft tissue bank operations, including donor recovery, processing, packaging, labeling, and distribution.

·     Ensure full compliance with FDA 21 CFR 1271, AATB, and EBAA accreditation standards.

·     Develop, implement, and maintain Quality Management Systems (QMS) consistent with cGMP, cGTP, and ISO 13485.

·     Oversee donor eligibility determinations, donor records, and traceability of grafts.

·     Ensure sterile technique, aseptic processing, and validated preservation procedures for ocular and wound grafts (e.g., amniotic membrane, dermal tissue).

·     Manage staff training, competency assessments, and annual evaluations in compliance with AATB/EBAA standards.

·     Coordinate audits, inspections, and accreditation site visits; ensure timely response and corrective actions.

·     Review and approve all SOPs, validation studies, and change controls related to tissue processing and distribution.

·     Monitor product release, labeling, and final distribution for compliance with regulatory and internal quality standards.

·     Implement systems for product recall, deviation investigation, and complaint management.

·     Ensure donor and recipient adverse event tracking and regulatory reporting as required.

·     Foster collaboration with clinical partners, surgeons, and hospitals to ensure tissue quality and availability.

·     Lead initiatives in process improvement, cryopreservation, and innovative wound care product development.

·     Oversee documentation practices aligned with ALCOA+ data integrity principles.

·     Promote a culture of compliance, safety, and continuous improvement throughout all tissue bank operations.

Required Qualifications

·     Bachelor’s degree in Life Sciences, Biomedical Engineering, or related field required.

·     Advanced degree (MS, MPH, MBA, or PhD) preferred; CTBS certification strongly encouraged.

·     Certified Tissue Bank Specialist (CTBS) certification preferred.

·     Demonstrated experience and favorable outcomes with FDA inspections, notified body audits, and supplier quality programs.

• Expertise in QMS software platforms and document control systems.
• Strong analytical, problem-solving, and decision-making skills.

Competencies

·     Strong understanding of ocular tissue recovery, amniotic membrane processing, and aseptic wound graft techniques.

·     Proven ability to lead regulatory inspections and maintain accreditation.

·     Excellent leadership, communication, and analytical skills.

·     Proficiency in Quality Management Systems (QMS), document control, and risk management principles.

·     Ability to interface effectively with surgeons, clinicians, and regulatory professionals.

Work Environment & Physical Requirements

• This role operates within a combination of office, laboratory, and controlled cleanroom environments.
• Regular use of computers, phones, and office equipment.
• May require occasional lifting of materials up to 25 pounds.
• Exposure to manufacturing floor environments.
• May require standing for extended periods and occasional travel for audits or site visits.
• Compliance with biosafety and infection control protocols required.

Travel Requirements

• Occasional domestic travel may be required (approximately 10–20%) to support supplier evaluations and supplier business meetings.

Compensation & Benefits

• Competitive base salary commensurate with experience.
• Performance-based annual bonus eligibility.
• Comprehensive benefits package, including medical, dental, vision and 401(k) with company match.
• Paid time off, sick leave, and company holidays.
• Professional development opportunities and continuing education support.

Critical Process Filtration (CPF), a TCPA Company, is a leading manufacturer of high-quality filtration solutions serving the pharmaceutical, electronics, process water, and gas filtration markets. For more than 25 years, CPF has designed and manufactured advanced filtration products and proprietary equipment with the goal of becoming a premier provider of process filtration solutions.

Our ISO 9001–certified manufacturing facility in Nashua, New Hampshire assembles and packages all products in a controlled clean-room environment. CPF cartridge, capsule, and laboratory products are trusted by leading organizations across the life sciences, food and beverage, healthcare, water purification, and technology industries. We are seeking a motivated Outside Sales Representative to support continued growth and customer engagement.

Benefits

Our comprehensive benefits package includes Paid Time Off (PTO), Medical, Dental, 401(k), Life Insurance, and other voluntary benefit options.

Summary

The Outside Sales Representative is responsible for generating new business, managing assigned customer accounts, and driving revenue growth through direct customer engagement. This role requires frequent travel to customer sites and close collaboration with internal teams to deliver effective filtration solutions, particularly within life sciences environments.

Responsibilities

• Develop and manage a territory sales plan to achieve revenue and growth objectives.
• Identify, qualify, and pursue new business opportunities within assigned markets, with a focus on life sciences customers.
• Maintain and expand relationships with existing customers through regular in-person visits.
• Conduct product presentations, demonstrations, and technical discussions with customers and prospects in regulated life sciences environments.
• Prepare and present quotations, proposals, and sales documentation in accordance with company policies and customer requirements.
• Collaborate with Marketing, Customer Service, and Operations to ensure customer satisfaction and timely order fulfillment.
• Monitor customer needs, industry trends, and competitive activity; provide feedback to management.
• Attend trade shows, industry events, and customer meetings as required.
• Maintain accurate and timely records of sales activities, forecasts, and customer interactions in the CRM system.
• Travel up to 50% of the time, including visits to customer sites and industry events.
• Perform additional duties as assigned to meet business needs.

Qualifications

• Bachelor’s degree (B.A.) or equivalent in Business, Marketing, Life Sciences, or a related field, or equivalent sales experience.
• Three or more years of outside or field sales experience, preferably supporting life sciences, pharmaceutical, biotechnology, or medical device customers.
• Familiarity with regulated environments, including GMP practices and quality requirements, is strongly preferred.
• Proven ability to develop new business and manage customer relationships.
• Strong interpersonal, presentation, and communication skills.
• Excellent organizational, time-management, and problem-solving abilities.
• Ability to work independently while managing a travel-based schedule.
• Willingness and ability to travel up to 50%.
• Strong customer focus, professionalism, and results-driven mindset.
• Self-motivated, adaptable, and collaborative team player.

Equal Opportunity Employer Statement

Critical Process Filtration is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by applicable law.

Company Description

ANEUVO is a platform and therapy development company focused on treating disabling diseases and conditions that are not curable through traditional pharmaceutical approaches. The ANEUVO ExaStim® Stimulation System is a non-invasive neuromodulation system that has received CE Mark approval and FDA Breakthrough Device Designation for treating spinal cord injury. ExaStim® is currently cleared for use only in Europe, and its use is limited by United States law to investigational purposes.

Key Responsibilities:

1)    Process Development (In-House)

a.     Design, develop, and validate in-house manufacturing processes, including assembly, labeling,

packaging, and testing.

b.     Create process documentation such as work instructions, manufacturing travelers, and

validation protocols (IQ/OQ/PQ).

c.      Identify and implement process improvements to enhance quality, efficiency, and yield.

d.     Support setup and qualification of new equipment, tooling, and fixtures.

2)    Contract Manufacturer (CM) Support

a.     Collaborate with contract manufacturers to transfer processes, troubleshoot production issues, and ensure alignment with company quality and performance standards.

b.     Review and approve CM process documentation, validations, and change controls.

c.     Serve as the technical liaison between internal engineering and external manufacturing partners.

3)    New Product Introduction (NPI)

a.     Participate in design reviews to ensure manufacturability and scalability of new designs.

b.     Support pilot builds, process qualifications, and ramp-up to full production.

c.     Coordinate process transfer from development to manufacturing.

4)    Continuous Improvement & Quality

a.     Drive continuous improvement through Lean and Six Sigma methodologies.

b.     Investigate root causes of non-conformances and lead corrective/preventive action

implementation.

c.     Ensure compliance with applicable quality system regulations (e.g., FDA 21 CFR Part 820, ISO

13485).

5)    Documentation & Compliance

a.     Maintain accurate and complete process documentation.

b.     Support audits and regulatory inspections by providing technical documentation and process

evidence.

c.     Ensure processes meet safety and environmental standards.

Qualifications

1)    Education:

• Bachelor’s degree in Electrical, Mechanical, Manufacturing, Industrial, or Biomedical Engineering (or equivalent).

2)    Experience:

•  7+ years of experience in manufacturing engineering, preferably within a regulated industry (medical device, pharma, or aerospace).
• Hands-on experience with process development, validation, and supplier/CM management.

3)    Skills:

• Strong problem-solving and analytical skills.
•  Experience with statistical analysis tools (e.g., Minitab, JMP) and validation methodologies.
• Proficient in CAD tools and solid understanding of GD&T and design documentation.
• Excellent communication and project management skills.

Maxonic maintains a close and long-term relationship with our direct client. In support of their needs, we are looking for a Component Engineer 3.

Job Description:

Job Title: Component Engineer 3

Job Type: Contract

Job Location: Sunnyvale, CA

Work Schedule: On-site

Pay Rate: $ 75, Based on experience

Description:

Primary Function of the Position:

Responsible for ensuring suppliers meet ISI requirements for quality, service, delivery, and cost. Drive suppliers to continuously improve business and manufacturing processes specifically related to wire harness and cable assembly Evaluate and select suppliers within copper cables/harness industry. Guide Engineering in choosing suppliers for new products and provide DFM input to new designs. Supports both NPI and on-going production, monitors and works with suppliers to improve supplier performance. Executes detailed projects with suppliers to implement changes and improvements affecting quality, cost, capacity, risk, and sub-supplier management.

Essential Job Duties:

• Work with NPD to procure custom cables ensuring DFM to achieve quality and cost targets
• Support NPD with proto builds and track material readiness at Supplier
• Drive supplier rootcause analysis for cable harness failures
• Mitigate risks and ensure supply continuity by evaluating capacity, lead times and quality issues
• Develop and maintain harness standards, specifications, and design guidelines.
• Work with Strategic sourcing to evaluate new suppliers and new supplier manufacturing sites
• Complete project/ part qualification deliverables including Supplier pFMEA, Process Validations (IQ/OQ/PQ), Inspection Reports, Gage R&R, and Process Capability Analysis
• Work with suppliers to execute cost reductions, capacity improvements, and risk mitigation.
• Select the right process and supplier for the part, considering long-term fit and total cost of ownership.
• Manage supplier changes including manufacturing process changes, production optimization, facility changes, new equipment qualification, and new line validations.
• Drive changes to ISI requirements as necessary by initiating and managing changes to specifications and drawings through the engineering change order process.
• Own and drive to closure supplier variances from symptom through root cause analysis to corrective action, including careful CAPA documentation.
• Effectively prioritize and advance multiple concurrent projects and tasks
• Clearly communicate project status to key stakeholders
• Build, own, and relentlessly pursue a vision for developing suppliers.
• Understand proper level of documentation detail for tracking of actions and justification of decisions.
• Generate key metrics for the team and suppliers, and continually drive for timely achievement of those metrics.
• Drive suppliers to continually improve their business and manufacturing process performance to meet Company's requirements for supplier excellence using a collection of best practices in project management, Six Sigma, Lean, SPC and negotiation. Lead these efforts without managerial guidance at several suppliers simultaneously.
• Implement corrective and preventive actions for supplier process by driving supplier’s investigations and root cause analysis.
• Provide effective and timely supply base health information and recommendation to management by creating and delivering data-driven supply base information to any level of management at ISI with little or no guidance.
• Prepare and deliver supplier communications as required by independently working with suppliers on scorecard creation.

Work with suppliers and ISI engineering for the new product introduction to:

• Create product supplier landscapes to determine launch readiness and report to management.
• Develop supplier ramp readiness plans by judging business risk based on forecast, supplier capacity, quality performance, and process capability.
• DFM by engaging suppliers early in development cycle to feedback manufacturability improvements in the designs prior to production.
• Influence and guide Engineering in choosing suppliers by determining selection criteria for preferred suppliers and leading the team effort to evaluate preferred suppliers.
• Review, analyze and close customer complaints, manufacturing variance requests, and first article inspections by judging risk analyses and justifications.

Required Skills and Experience

• Minimum 3 years related experience with an BS Engineering degree or 1
• years’ experience with MS in Engineering.
• Excellent written and verbal communication skills including presentations to executive level management.
• Excellent Interpersonal skills and team building skills.
• A proven history of implementing Lean/6 Sigma/SPC Programs at suppliers.
• Excellent Project Management skills.
• Excellent analytical and problem-solving skills along with good judgment.
• Demonstrable knowledge in evaluating and challenging supplier technical,
• quality, and business capabilities.
• Demonstrable knowledge of a wide range of manufacturing processes
• including understanding of key input variables for quality, cost, and capacity (specialization can be in cable assembly, wire cutting , termination, crimping, Soldering, overmold )

Working Conditions

• Ability to travel to suppliers on an as-needed basis – domestic and international.

Preferred Skills and Experience

1-3 years of engineering experience in cable assembly, wire harness production, or electromechanical manufacturing.

The ideal Candidate possesses broad and deep hands-on cable assembly experience along with wire cutting, stripping, crimping , soldering, connector termination ,overmold ,potting and heat shrink application. Familiarity with either IPC-WHMA-A-620, NASA-STD-8739.4, or IPC J- STD-01 or ISO 14572 Understanding of electrical schematics, wiring designs, and harness acceptance testing

About Maxonic:

Since 2002 Maxonic has been at the forefront of connecting candidate strengths to client challenges. Our award winning, dedicated team of recruiting professionals are specialized by technology, are great listeners, and will seek to find a position that meets the long-term career needs of our candidates. We take pride in the over 10,000 candidates that we have placed, and the repeat business that we earn from our satisfied clients.

Interested in Applying?

Please apply with your most current resume. Feel free to contact Manish Rajput ( / (4 for more details.

ProSearch is partnering with a confidential client in the manufacturing space to hire a Senior Project Manager experienced in New Product Development (NPD) and New Product Introduction (NPI). This role leads complex electronics and embedded systems projects from concept through manufacturing transfer, ensuring on-time delivery, quality excellence, and regulatory compliance.

This is a career-defining opportunity for project leaders who thrive in technically rigorous, regulated industries and are passionate about cross-functional collaboration, structured execution, and team mentorship.

Responsibilities

• Deliver high-complexity NPD/NPI projects on scope, schedule, budget, and quality objectives.
• Serve as the primary customer interface, managing expectations and aligning deliverables with strategic goals.
• Lead cross-functional teams to define scope, schedules, cost estimates, and resources.
• Plan and manage all project phases, from design and verification to validation and manufacturing transfer.
• Maintain detailed project plans, risk registers, and status reports for stakeholders.
• Track milestones, manage dependencies, and proactively mitigate risks.
• Manage scope changes with PMO leadership and account managers.
• Drive continuous improvement by developing PMO processes, templates, and tools.
• Foster a collaborative, results-driven culture emphasizing quality, efficiency, and technical rigor.

Requirements

• 5–10 years managing complex technical projects in electronics product development, engineering services, or manufacturing.
• Proven ability to lead multidisciplinary teams and deliver large-scale, technically complex projects.
• Technical expertise in electronics, embedded systems, and manufacturing/NPI principles (DFM/DFT, verification/validation, production transfer).
• Knowledge of regulatory frameworks (FDA, ISO 13485) and experience applying them in project execution.
• Proficiency with project planning, scheduling, and resource management tools (Microsoft Project preferred).
• Strong organizational, analytical, and problem-solving skills, with attention to cost, schedule, and quality.
• Excellent communication, leadership, and mentoring abilities.
• Experience in regulated industries preferred (medical devices, automotive, defense).

Preferred

• PMP or equivalent certification.
• Lean/Six Sigma, or continuous improvement experience

Benefits

• Health wellness program with cash incentives
• Health insurance with low deductibles
• Disability, dental, and life insurance
• 401K retirement plan
• Tuition reimbursement
• Flexible medical and dependent care spending accounts
• On-site fitness gym

Why Join Us

At ProSearch and our client, your contributions directly impact product innovation, regulatory compliance, and operational excellence. You’ll join a collaborative, inclusive culture that values growth, mentorship, and measurable results.

Take the Next Step

If you are a results-driven Senior Project Manager ready to lead high-impact NPD and NPI projects in electronics, embedded systems, and manufacturing, we want to hear from you. Bring your expertise, leadership, and passion for structured execution to a team that values innovation, regulatory excellence, and measurable results.Apply now to make an impact.

Company Description

Tendon Manufacturing, established in 1988, is a full-service metal fabrication and manufacturing company with three locations in Warrensville Heights, Ohio. Tendon’s diverse offerings include laser cutting, welding, machining, assembling and powder coating. Our commitment to excellence and innovation has made Tendon Manufacturing a trusted name in the industry.

Role Description

The Director of Quality Control will oversee all quality management processes and practices at Tendon Manufacturing's three facilities. This is a full-time, on-site role where the Director will lead a team of quality professionals in ensuring compliance with industry standards and internal requirements. Responsibilities include developing and implementing quality control systems, conducting audits, analyzing quality data, and collaborating with customers & production teams to maintain and improve quality standards.

Qualifications

• Strong expertise in Quality Control and Quality Assurance practices
• Proficiency of Quality Management systems, such as ISO 9001
• Demonstrated leadership skills with experience managing quality teams
• Strong problem-solving abilities and analytical thinking
• Ability to ensure compliance with regulations, standards, and customer requirements
• Prior experience in metal fabrication or manufacturing industries

Responsibilities :

• Research, design, develop and implement control specifications based on customers’ requirements.
• Define performance level requirements of systems (machine level) and subsystems (component level) including sensors.
• Derive dynamic models, select appropriate control algorithms, simulate, rapid prototyping, and tuning of controls.
• Use design tools for controls development and data analysis to troubleshoot problems.
• Work with cross functional hardware, software, and product validation teams as well as suppliers for development of new sensors.
• Work across multiple engineering disciplines and development teams to coordinate system definition, design, and integration.
• Responsible for individual product design alignment with multi-product architectural strategy.
• Work with product verification and validation, and/ or customers to ensure system and components perform as needed.
• Maintain a clean and safe work area. Follow established safety and ergonomic standards.
• Learning, understanding, continuously improving, and promoting the quality management system in accordance with ISO standards.

Requirements:

• Minimum of a bachelor’s degree in engineering.
• Specific skills, proficiencies, and knowledge in field related to position listed above in the mandatory needs section.
• Experience in programming languages, such as C or C++ or related technologies.
• Experience with developing algorithms and simulations and creating models.
• Working knowledge of electrical theory, control components, robotics, and automation.
• Ability to apply design theory and methodology.
• Well-developed problem analysis and problem-solving techniques.
• Proficiency with a computer, including use of Microsoft Word and Excel.

If you are aerospace operations leader with strong CNC machining experience who thrives on being on the shop floor, solving production challenges, and driving measurable performance improvements and are looking to progress in your career this would be an excellent next step for you.

You will get to further develop your hands-on execution across complex machining and assembly operations, using your Six Sigma and Lean skills to optimize flow, quality, and delivery.

In this highly visible position you will work closely with senior leaders and have a clear pathway to progress within the organization.

About the Company

A leading aerospace manufacturer delivering high-reliability components and systems for defense and commercial platforms is seeking an Operations Leader to drive execution excellence. The organization partners with OEMs and Tier 1 suppliers and operates in a highly regulated, AS9100-certified environment, with a strong culture of continuous improvement and operational excellence.

This is a hands-on leadership role with direct accountability for day-to-day operational execution. You will spend significant time on the shop floor, addressing production bottlenecks, improving process reliability, and ensuring delivery, quality, and safety targets are consistently met.

While execution is the initial focus, this role offers a highly visible career pathway into the VP of Operations, giving you the opportunity to shape operations strategy across multiple facilities over time.

Key Responsibilities

• Lead daily manufacturing and assembly operations, with a strong presence on the shop floor.
• Identify, troubleshoot, and resolve production, quality, and workflow issues using Lean manufacturing and Six Sigma methodologies.
• Drive continuous improvement initiatives to reduce cycle time, scrap, and waste while improving throughput and yield.
• Partner with Engineering on new product introductions, ensuring Design for Manufacturing (DFM) principles are applied.
• Monitor and act on operational KPIs including safety, quality, delivery, cost, and productivity.
• Oversee material flow, production planning, and inventory control to maintain schedule adherence.
• Ensure compliance with AS9100, FAA, ITAR, ISO, and customer-specific manufacturing requirements.
• Support capital investment planning and productivity programs.
• Build, mentor, and develop high-performing teams, strengthening problem-solving capability across the operation.

What You Bring

• 8–12+ years of hands-on operations leadership within aerospace or a highly regulated manufacturing environment.
• Strong experience with CNC machining and precision assembly operations.
• Proven track record applying Lean, Six Sigma, and continuous improvement tools to real production challenges.
• Background in aerospace manufacturing, MRO, or complex electromechanical / systems integration environments.
• Comfortable collaborating across functions including Engineering, Quality, Supply Chain, and Program Management.
• Bachelor’s degree in Engineering, Manufacturing, Operations, or related field (MBA or advanced degree a plus).
• Ambition and capability to grow into a VP-level operations role over time.
• U.S. work authorization and willingness to travel across facilities as required.