Quality

We are looking for an experienced and motivated Senior Quality Inspector to join our team in Rotherham. Reporting to the Quality Manager, you will take ownership of inspection activities and play a key role in ensuring products meet customer specifications and industry standards including ISO9001:2015 and AS9100.

This is a hands-on leadership role, where you will manage, mentor, and develop a team of 3 Inspectors, driving a high-performance, quality-focused culture across the department.

Key Responsibilities

Leadership & Team Management

• Lead, supervise, and motivate a team of 3 Inspectors to achieve daily production and quality targets
• Set clear expectations, monitor performance, and provide regular feedback and coaching
• Develop team capability through training, mentoring, and skills development
• Foster a positive, engaged, and accountable team culture
• Promote strong communication and collaboration across departments
• Encourage a continuous improvement mindset within the team

Quality & Inspection Activities

• Perform dimensional, visual, and functional inspections on components and assemblies
• Ensure compliance with engineering drawings, specifications, and aerospace standards
• Use inspection equipment such as CMM, gauges, and micrometers, maintaining calibration records
• Complete inspection documentation including FAIRs, ISIRs, and PAPS (Production Approval Process documentation) accurately
• Maintain traceability and audit-ready quality records

Quality Management & Continuous Improvement

• Identify non-conformances and raise NCRs in a timely manner
• Support root cause analysis and corrective / preventive actions
• Manage quality documentation and training matrices
• Contribute to internal and external audits
• Recommend and implement improvements to inspection processes and methodologies
• Support new project quality development, including PAPS submissions and approvals
• Maintain high standards of supplier quality

Stakeholder Collaboration

• Work closely with Production, Engineering, and Quality teams
• Support customer queries and ensure timely resolution of quality issues
• Collaborate with suppliers and external stakeholders where required

About You

Experience & Qualifications

• Proven experience in a quality inspection role within engineering, aerospace, or manufacturing
• Previous experience of people management or team leadership
• Strong understanding of ISO9001 / AS9100 quality systems
• Experience of completing or supporting PAPS (Production Approval Process) submissions
• Ability to read and interpret technical drawings
• Experience with CMM and inspection equipment
• Quality qualification (desirable but not essential)
• Experience producing FAIRs / inspection documentation (desirable)

Leadership & Behavioural Competencies

We’re looking for a leader who can inspire and engage others. You will demonstrate:

• Strong people leadership and team development skills
• Ability to engage, motivate, and influence at all levels
• A coaching mindset with a passion for developing others
• Excellent communication and interpersonal skills
• A proactive, solution-focused approach to problem solving
• Confidence in decision-making and driving accountability
• High attention to detail with a “right first time” mindset
• Ability to lead change and drive continuous improvement
• Self-motivation with the ability to work independently

What We Offer

• Opportunity to lead and shape a small, high-impact inspection team
• A role with strong visibility across the business
• Ongoing training and development opportunities
• A collaborative and quality-driven working environment

If you’re an experienced Quality Inspector ready to take the next step into leadership—or an established leader looking for a fresh challenge—we’d love to hear from you.

Trelleborg is looking to add a Quality Inspector to our team!

The Quality Inspector plays a critical role in ensuring that all incoming and outgoing materials meet established customer specifications, company standards, and regulatory requirements. This position is responsible for conducting thorough inspections, verifying product quality, and maintaining accurate documentation to support compliance and operational excellence. The ideal candidate is detail-oriented, reliable, and capable of working both independently and collaboratively in a fast-paced environment.

Tasks and Responsibilities: 

• Inbound Inspection
• Outbound inspection
• Acquire supporting documentation for orders
• Other duties as assigned

Education and Experience: 

• Associates degree preferred, HS diploma or GED required.
• Minimum 1 year experience in Quality inspection required.
• Basic blueprint reading skills required

 Competencies:  

• Strong interpersonal and communication skills.
• Basic computer skills
• Basic reading skills
• Basic arithmetic skills
• Time management skills including meeting deadlines for OTD.
• Ability to successfully work independently

 Travel: 

• Local coverage
• Travel for offsite training when required, 5%

Compensation range: $24.00-28.00/hour

Benefits:

• 401(k) matching
• Dental insurance
• Disability insurance
• Employee assistance program
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Tuition reimbursement
• Vision insurance

Apply here!

As an EEO/Affirmative Action Employer all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status.

This position requires the use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR.  ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. Green Card Holder), Political Asylee or Refugee. 

We are looking for a Quality Assurance Assistant to work in the Quality Department.

Overall Responsibilities:

• Testing of product characteristics according to customer specifications.
• Correct handling and operation of all equipment that is necessary to perform the required tests.
• Completion of all Quality Assurance documentation as per customer requirements, internal company procedures and AIAG manuals.
• Retention of all appropriate records according to the internal company procedures.
• In case of any deviations from any customer or internal specifications, the necessary actions have to be taken as per internal company procedures and guidelines.
• Printing and issuing of the relevant reports to other departments and customers.
• Filing and maintaining of relevant records in an orderly manner.
• Carry out any Quality Assurance-related tasks and projects.
• Compliance with the requirements of the ISO14001 environment management system and the ISO45001 occupational health and safety management system.
• Responsible for reporting any hazards / near misses / incidents immediately to the area management.

What we are looking for: 

We are seeking a detail-oriented and proactive individual with experience in operating machines. The ideal candidate will have:

• Have a minimum of O’ Level Standard of education;
• Have good communication skills in both Maltese and English language;
• Be Computer literate preferably with ECDL qualifications;
• Have a strong organisational and interpersonal skills;
• Be a team player;
• Be flexible to change and open to constructive feedback.

Work Place Culture: 

At Trelleborg Malta, we believe in creating a vibrant and inclusive workplace where your voice matters. You'll be recognized for your contributions and have plenty of opportunities for growth and development. Join us and be part of a team that supports and celebrates each other!

What we offer: 

Trelleborg Training: Enhance your skills by training while you work!

Career Development: Explore dynamic career paths and learn from our experienced employees.

Comprehensive Health Coverage: Benefit from health insurance cover.

Study Leave: Take advantage of study leave to further your education.

Convenient Parking: Enjoy easy, hassle-free parking facilities.

Social and Well-Being initiatives: Doctor on site, and frequent social activities

Salary: First six (6) months – €349.68 per week

            After six (6) months – €388.53 per week

Trelleborg is an equal opportunity employer. Join us and experience a rewarding, balanced work environment!  

Trelleborg Medical Solutions is seeking a VP Global Quality and Regulatory, based from their Minneapolis MN headquarters. 

As a valued team member with Trelleborg, you will enjoy:

• Competitive compensation: $220,0000-225,000 + bonus opportunities!
• Generous benefits package: Includes health, dental, vision, STD, LTD, life, 401k, paid time off, tuition reimbursement, and more!
• Clean work environment: Enjoy working in a very clean and climate-controlled environment every day!
• Greater opportunity for impact: You will have the autonomy and support to lead the production team and impact the production of life-saving devices.
• Growth and advancement: Join a global company that loves to promote from within and allows for advancement into one of their many other U.S. locations!

This position is a strategic business partner to the BA President in managing Global Regulatory and Quality functions throughout the BA.

This position drives the strategy for the BA to comply with the requirements of the global landscape for class I, II & III productions, in a cost effective and pragmatic manner.   The position takes a holistic approach to include manufacturing, services and 3rd party purchase for resale products into scope, and other business models as the business develops.   Stressing global in approach, inclusive of sales and logistic centers.

Tasks and Responsibilities

• Aligns the quality strategy to fulfill the business area strategy.
• Owns global Quality and Regulatory budget and cost-of-quality performance
• Drive quality as a competitive advantage enabling growth and commercial success
• Defines and tracks KPI’s aligned to business outcomes
• Champion of global culture of quality, accountability and continuous improvement
• Deploys Lean/Six Sigma or equivalent methodologies across the organization
• Lead implementation and optimization of eQMS and digital regulatory tools
• Utilizes data analytics and predictive insights to proactively manage quality risks
• Owns strategy with corporate objectives and manage product registrations in existing and emerging markets. Inclusive of material regulatory.
• Represents the company with regulators, industry bodies and external stakeholders

Oversees the remainder with delegation to their team.

• Oversee FDA listings, EU conformity declarations, etc., to ensure clearance to distribute products.
• Oversee product listings, declarations and regulatory approvals (ie 510(k), ISO, CE, CMDCAS) are submitted in accordance with all applicable regulations and are kept up to date. Responsibilities include: determining the type of listing, registration, and/or approval needed (by country); classifying the device appropriately per 21CFR, CE, CMDR, etc.; preparing & filing listings, 510(k)’s, Declarations of Conformity, etc. to all applicable countries.
• Oversee the Vigilance/Medical Device Reporting System including preparing and submitting reports and maintaining records/files of incidents including any remedial actions taken. Coordinate Recall & Field Action situations to comply with US & international regulations and company policies/procedures.
• Responsible for assuring products, labeling/packaging and advertising are in compliance with all applicable regulations.
• Coordinate FDA/EU or any other country required inspections and audits, respond to findings and maintain records of all activities. Assure that any product detentions are promptly resolved; provide interface with FDA field offices as needed.

Education and Experience

• 15 years plus of experience in a global organization within a regulatory or quality function
• Minimum of 4 Year College degree in a technical field
• Masters is plus
• Ability to work in a fast paced, global environment with matrix organization

Competencies

• American Society for Quality (ASQ) certification and/or Regulatory Affairs Certification (RAC) preferred
• Core competency as demonstrated by previous compliance responsibility for ISO 13485 and 14971; MDD; MDR; FDA cGMPs; FDA QSRs; UL; CE; and IEC Standards
• Subject Expert in US FDA Regulations, Standards, Documentation, Labeling
• Knowledge of laws, legal codes, court procedures, precedents, government regulations, executive orders, agency rules, and the democratic political process
• Knowledge of 21 CFR 801, 803, 806, 807, 820
• Knowledge of FDA guidelines and ISO standards for Medical Devices
• Knowledge in IEC 60601-1 and foreign regulations for medical devices
• Working knowledge of Medical Device Regulations, Quality Systems Regulations, and other US and Intl regulations and standards that apply to the Class II and Class I medical device industry
• Working knowledge of and ability to assist in the creation/review of technical sections in support of regulatory submissions for assigned projects including 510(k) and device combination products.
• Knowledge of FDA and FTC labeling, MSDS standards, CPSC, and EPA requirements
• Knowledge of technical standards and GMP

Travel requirements as needed by the BA to fulfill the obligations of the position

About the Company:

Trelleborg Medical Solutions partners with the world’s leading medical device and biopharmaceutical companies, collaborating from concept to commercialization to bring to market impactful solutions that improve patient quality of life. It leverages decades of design and manufacturing experience, in-depth knowledge of polymer materials and a deep understanding of customer applications and end-use environments to deliver pioneering, engineered solutions for transformative health technologies. Utilizing its global quality system and engineering and manufacturing network, the company is a production partner of choice for medical devices and biopharmaceutical companies.

#TMS

All qualified applicants will receive consideration for employment without regard to the individual's race, color, sex, national origin, religion, age, disability, genetic information, status as a military veteran or any other characteristic protected by applicable law.

Apply here!

Imagine leveraging your expertise while working for one of the leading contract manufacturers in the world. Seize this rare opportunity to be part of a healthcare and medical business unit with the support and stability of an organization that has been in business for over 100 years

Trelleborg Medical Solutions is seeking a Quality Assurance and Regulatory Director - Americas, based from their Minneapolis MN headquarters. 

As a valued team member with Trelleborg, you will enjoy:

• Competitive compensation: $160-180,000 DOE + bonus opportunities!
• Generous benefits package: Includes health, dental, vision, STD, LTD, life, 401k, paid time off, tuition reimbursement, and more!
• Clean work environment: Enjoy working in a very clean and climate-controlled environment every day!
• Greater opportunity for impact: You will have the autonomy and support to lead the production team and impact the production of life-saving devices.
• Growth and advancement: Join a global company that loves to promote from within and allows for advancement into one of their many other U.S. locations!

Tasks and Responsibilities

• Own and govern the effectiveness of the Americas Quality Management System in compliance with ISO 13485, FDA QSR, and applicable international standards.
• Serve as delegated ISO 13485 Management Representative and report on QMS effectiveness to executive management.
• Define and execute regional regulatory strategy aligned with global business objectives.
• Oversee product/material registrations, listings, certifications, and technical documentation throughout the product lifecycle.
• Lead inspection readiness and act as primary interface with FDA, Notified Bodies, and international regulatory authorities.
• Oversee vigilance, medical device reporting, recalls, and field actions across the Americas.
• Drive operational quality excellence through CAPA, nonconformance management, and continuous improvement initiatives.
• Serve as senior quality interface for key customers, supporting audits and quality agreements.
• Lead, develop, and mentor a regional team of quality and regulatory professionals.
• Ensure training and competency development for quality systems across regional operations.
• Maintain regulatory intelligence and proactively assess impact of regulatory changes.
• Periodically benchmark cost of quality operations with industry peers.

Education and Experience

• Bachelor’s degree in engineering, Life Science, or related technical field; Master’s preferred.
• 10+ years of progressive experience in Quality Assurance and/or Regulatory Affairs; 5 years within the medical device industry.
• Demonstrated leadership experience in a global, matrixed organization.

Competencies

• Expert knowledge of FDA QSR, 21 CFR (801, 803, 806, 807, 820), ISO 13485, ISO 14971, MDR/MDD.
• Strong regulatory intelligence and risk-based decision making skills.
• Ability to manage multiple priorities and lead through influence.
• Excellent written, verbal, and executive communication skills.

Geography and Travel Requirements

• Regional to the Americas (North, South and Central)
• Must be accessible to a major airport
• Travel expected up to 50%

#TMS

About the Company:

Trelleborg Medical Solutions partners with the world’s leading medical device and biopharmaceutical companies, collaborating from concept to commercialization to bring to market impactful solutions that improve patient quality of life. It leverages decades of design and manufacturing experience, in-depth knowledge of polymer materials and a deep understanding of customer applications and end-use environments to deliver pioneering, engineered solutions for transformative health technologies. Utilizing its global quality system and engineering and manufacturing network, the company is a production partner of choice for medical devices and biopharmaceutical companies.

Apply here!

What you´ll do: 

Imagine working for one of the leading contract manufacturers in the world. Trelleborg Medical Solutions is located 30 miles from California’s pristine Central Coast. As a premier manufacturer for life-saving medical components, Trelleborg Medical Solutions is a forward-thinking company. We have been active in our lean manufacturing journey for many years and are advancing towards making our business a showcase of excellence in the medical industry.

Seize this rare opportunity to be part of a healthcare and medical business unit that has been in business for over 100 years, all while enjoying the benefits of living in one of California’s most desired locations!

About the Job

Trelleborg Medical Solutions is seeking a Quality Engineer. In this role, you will be responsible for the development and administration of a Quality System compliant to FDA and ISO requirements, including the utilization of optimal, cost-effective lean manufacturing processes and methods for new and existing projects including inspection, test and label control operations.  

Quality Engineer Expectations:

• Supports internal audit program as necessary.
• Supports customer complaint (CC) and RMA system per procedures. Performs investigations, supports determination of the disposition of returned goods, determines re-inspection requirements, determines corrective and preventive actions (CAPA), issues complaint reports, supports completion of customer CAPAs, and approves to close.  Looks for trends to determine actions to decrease number of CCs
• Maintains Non-Conforming (NC) system per procedures. Performs investigations, participates in MRB (Material Review Board) activities, supports determination of the disposition, determines re-inspection requirement, supports determination of corrections/corrective actions and approves to close. Looks for trends to decrease number of NCs and provide feedback to management
• Maintains corrective and preventive action (CAPA) system per procedures. Initiates and performs root cause analysis. Uses statistical and capability analysis to solve problems. Implements and verifies CAPAs
• Performs trend analysis of CAPA, NCM, Complaint/Customer Feedback, Risk Management activities, Audits, etc. and presents periodic reports for management review. Assesses Design and any associated activities for manufacturability.
• Adheres to the company’s Quality System (QS), writes and approves QS documents
• Authors and executes Quality Plans for Quality Management Systems and Organizational Objectives projects.
• Support Engineering, Manufacturing, and Inspection personnel in design, methods, tooling, validations, and other areas related to the control of product quality.

Education and Experience: 

• 4 year degree in quality, engineering or any related field

Desired:

• 2+ years in a manufacturing environment in a technical support role
• ASQ Certified Quality Engineer
• Formal Six Sigma Yellow/ Green belt training

As a valued Trelleborg team member, you will enjoy:

• Greater opportunity for impact;
• Competitive compensation;
• Outstanding benefits package: Health, Dental, Vision, STD, LTD, Life, 401k;
• Generous paid time off;
• Bonus potential

#TMS

Salary range:  $87,000-$100,000

APPLY HERE!

Summary of the Role: 

Quality Engineers have the technical ability and expertise to solve complex problems. Problems can be either technical, with regards to product quality, or commercial, regarding processes. Both types of problems need specialized abilities to determine the root cause so that they can be resolved. Many quality functions, such as auditing or PPAP/FAIR need technical training and understanding of the applicable standards.

Tasks and Responsibilities: 

Summary of the Role: 

Quality Engineers have the technical ability and expertise to solve complex problems. Problems can be either technical, with regards to product quality, or commercial, regarding processes. Both types of problems need specialized abilities to determine the root cause so that they can be resolved. Many quality functions, such as auditing or PPAP/FAIR need technical training and understanding of the applicable standards. 

Tasks and Responsibilities:  

Do you approach new challenges with passion and take responsibility for your actions?

Be the change you want to see and start shaping industry from the inside.

About us

Trelleborg is a world leader in engineered polymer solutions for almost every industry in the world. And we are where we are because our talents brought us here.

At Trelleborg Marine & Infrastructure, we go beyond service, building lasting partnerships with engineers, contractors, and owners to deliver long-term solutions that make a real impact.

About the role

As the Quality Manager you will be responsible for defining, maintaining, and independently verifying product, process, and system quality across the organization. You will own the Quality Management System (QMS), ensure compliance with customer, regulatory, and internal requirements, and provide objective oversight of manufacturing activities. You will operate independently of production priorities and has authority over audits, nonconformance management, corrective actions, and product acceptance decision.

Your Responsibilities

• Own and maintain the Quality Management System (QMS) and related documentation
• Define quality standards, inspection criteria, control plans, and acceptance requirements
• Lead internal, external, customer, and regulatory audits
• Own the nonconformance, CAPA, and preventive action processes, including effectiveness verification
• Perform and validate root cause analysis for quality issues
• Oversee inspection, testing, and quality data analysis
• Manage supplier quality requirements, audits, and escalations
• Drive quality-focused continuous improvement initiatives
• Train employees on quality standards, procedures, and compliance expectations

What you bring

• Bachelor’s degree in Quality, Engineering, Manufacturing, or related discipline
• 5–10 years of experience in quality management within a manufacturing environment
• Experience with ISO or equivalent quality systems and customer audits
• Prior leadership or supervisory experience preferred.
• Chemistry or Chemical industry experience preferred.

Desired Competencies

• Quality management systems expertise
• Root cause analysis and problem-solving
• Audit leadership and regulatory knowledge
• Data analysis and risk-based thinking
• Clear, assertive communication
• Ability to operate independently and objectively

Traits we value

• High integrity and independence
• Detail-oriented and analytical
• Confident in escalation and decision-making
• Structured, methodical, and disciplined
• Collaborative while maintaining objectivity

Our Offer and Benefits

• A responsible and results-oriented task in an internationally active industrial company
• We provide an encouraging environment offering growth within the company while investing in your training/education
• Family and congenial working atmosphere with modern equipment
• Very attractive competitive compensation package
• Generous annual leave 

Application Process

Sound like the ideal environment for you?

Don't delay, apply now to shape your career at Trelleborg.

Trelleborg is an Equal Opportunity Employer, and we take pride in the diversity of our employees, valuing the special experience and expertise that people from different backgrounds bring to our business. The ability to develop ground-breaking technologies is one of our key assets and our people make it happen. 

We provide an encouraging environment which offers growth within the company while investing in employee training/education. Our facility is a close and friendly community which allows you to brainstorm your ideas with other colleagues.

We encourage applications from people of all nationalities, religions, genders, sexual identities, different ages and people with disabilities.

At Trelleborg our people are #shapingindustryfromtheinside

The Quality & HSE Manager is responsible for all activities related to quality and occupational safety within the site, as well as for developing, implementing, and continuously improving the company’s Quality Management System and Health, Safety & Environment programs. This role ensures compliance with all relevant standards, regulations, and corporate policies, while fostering a culture of continuous improvement, operational excellence, and safe working practices across the organization.

📍 Location: ITA – Torino (Pianezza).

Key Responsibilities

Quality Management

• Develop, maintain, and improve the Quality Management System in accordance with applicable standards (ISO 9001, IATF 16949, EN9100).
• Lead internal and external audits, manage corrective and preventive actions, and ensure timely closure of findings.
• Monitor quality performance metrics and drive continuous improvement initiatives.
• Manage product non-conformities, root-cause analysis, and cross-functional problem solving. Liaise with internal and external customers.
• Oversee supplier quality performance and coordinate supplier audits and evaluations.
• Ensure documentation control, versioning, and compliance across the organization.

Health, Safety & Environment (HSE) / RSPP

• Nominated RSPP
• Develop and implement HSE policies, standards, and procedures aligned with legal requirements and in accordance with applicable standards (ISO 45001, ISO 14001).
• Conduct risk assessments, safety inspections, incident investigations, and safety drills.
• Promote a strong safety culture and ensure engagement of all employees.
• Monitor and report HSE KPIs, ensuring compliance with applicable regulations.
• Manage waste disposal, environmental monitoring, and sustainability initiatives.
• Liaise with regulatory bodies, certification authorities, and external stakeholders.
• Coordinate training on safety practices, emergency response, and environmental awareness.

Leadership & Cross-Functional Collaboration

• Lead and mentor the Quality & HSE team, ensure adequate training.
• Work closely with other company departments to ensure integrated compliance.
• Drive continuous improvement programs.
• Act as the key point of contact for all quality and HSE communication internally and externally.

Qualifications & Experience

Education

• Bachelor’s or Master’s degree in Engineering.

Professional Experience

• 3-5 years in a Quality and HSE role, ideally in manufacturing, industrial, or technical environments.
• Experience with ISO management systems (ISO 9001, IATF16949, ISO 14001, ISO 45001).
• Proven record of conducting audits and managing certification processes.
• RSPP Certification already available is a plus

Skills & Competencies

• Strong knowledge of automotive quality tools and methodologies (FMEA, PPAP, SPC, APQP, MSA, root cause analysis, problem solving/8D).
• Good understanding of occupational safety laws and environmental regulations.
• Excellent communication, leadership, and training abilities.
• Fluent in Italian and English.
• Analytical, detail-oriented, and proactive mindset.
• Ability to manage multiple priorities and influence cross-functional teams.
• Certifications such as VDA6.3 Auditor and Six Sigma are a plus.

Our benefits for You:

• A modern multicultural work environment.
• Several weeks of induction training for your new tasks, where you will get to know our company, your contacts, and our structures.
• An exciting, multifaceted, and interdisciplinary field of activity.
• Extensive product training.
• Flexible office hours with remote work opportunities.

Why join Us?

• Opportunity to drive real impact in a fast-paced manufacturing environment.
• Work in an innovative and encouraging team.
• Career growth and professional development opportunities.
• Be part of a company that values continuous improvement and sustainability.

Ready to take the next step in your career?

Send us your CV in English and become a key player in crafting our production excellence! You will be contacted by our HR Team in Germany. 

Summary of the Role: 

Quality Engineers have the technical ability and expertise to solve complex problems. Problems can be either technical, with regards to product quality, or commercial, regarding processes. Both types of problems need specialized abilities to determine the root cause so that they can be resolved. Many quality functions, such as auditing or PPAP/FAIR need technical training and understanding of the applicable standards.

Tasks and Responsibilities: 

• Partner with customers to understand their QA needs and provide solutions
• Complete customer complaints with customer and suppliers
• Complete plans for standard products and provide to customers and suppliers
• Lead and create internal and external trainings as subject matter expert
• Collaborate with cross-functional teams to ensure customer satisfaction
• Review FAIS from factory and send to customers
• Manage customer portals
• Perform and support internal AS9100 audits
• Partner with suppliers as needed to support inspection gaps
• Experience completing PPAP/FAI required

Education and Experience: 

• Bachelor’s degree in engineering or other technical discipline
• 3 years’ experience in an engineering role, preferably in a manufacturing role
• Master’s degree counts towards 2 years’ experience
• 2 years’ experience in quality including experience with complex surfaces and assemblies
• Knowledge of aerospace processes, such as AS9100
• Proficiency in Microsoft Word and PowerPoint

Competencies: 

• Strong analytical, decision making and problem-solving skills
• Strong mechanical and technical aptitude
• Ability to self-manage and successfully work without supervision
• Ability to handle and prioritize dynamic workload
• Strong oral and written communication skills
• Excellent organization skills
• Proven proficiency with presentations and public speaking

The final compensation offered to the candidate may be based on geographical location, work experience and/or skill level. Additions to the compensation packing, including but not limited to paid time off, insurance benefits and 401(k) eligibility, will be outlined at the time of the job offer.

Compensation range: $75,000-$95,000

401(k) matching
Dental insurance
Disability insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Tuition reimbursement
Vision insurance

Application: 

Apply here!

Last Application Date 7/18/2026

As an EEO/Affirmative Action Employer all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status.

This position requires the use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR.  ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. Green Card Holder), Political Asylee or Refugee.