Engineering Structures Impact Factor Jobs in Airmont, NY

130 positions found

Electro Mechanical Assembler
✦ New
Salary not disclosed
Spring valley, NY 4 hours ago
Be visionary
Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins.
Job Description
Teledyne LeCroy is a leading manufacturer of high-performance electronic test and measurement equipment located in Chestnut Ridge, NY (Rockland County, NY). Our team consists of passionate and experienced engineers, technicians, and assemblers who work on a wide range of problems in a highly collaborative work environment.
We are currently looking for an Electro-Mechanical Assembler to support the manufacturing team in the production of oscilloscopes, probes, and cables.
Responsibilities:

  • Execute documented assembly procedures, both electrical and mechanical:

    • Product assembly by using a microscope and/or hand tools.
    • Hand soldering assembly of high precision small components.


  • Perform data entry into the manufacturing database.
  • Attend cell meetings:

    • Participate in cost reduction and process improvement initiatives.
    • Communicate issues, concerns, and questions to manufacturing engineering.



Education and Experience:
  • High school diploma or equivalent.

Job Knowledge and Skills:

  • Good eye/hand coordination.
  • Must be able to perform repetitive assembly work.
  • Ability to work in a fast-paced environment.
  • Must be able to read and understand English.
  • Clear communication skills, both verbal and written.
  • Must be able to work well in a team environment and independently.
  • Must be able to maneuver 25 lb. equipment.
  • Things that are a plus and will help you stand out.

    • Soldering experience
    • Microscope experience
    • Genuine interest in manufacturing as a career path
    • IPC J-Std-001 and/or IPC-A-610
    • Experience with UV glue or epoxy
    • Above average computer skills (Microsoft Office)
    • Ability to read and understand PCBA documents, diagrams, and schematics



Salary Range:
$32,300.00-$43,100.000
Pay Transparency
The anticipated salary range listed for this role is only an estimate. Actual compensation for successful candidates is carefully determined based on several factors including, but not limited to, location, education/training, work experience, key skills, and type of position.
Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions.
Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws.
Not Specified
Molding Process Technician
✦ New
🏢 Aptar
Salary not disclosed
Congers, NY 1 day ago

Join our team and Be You Be Aptar


Aptar is seeking a Molding Process Technician based in Congers, NY. The primary function of the Molding Process Technician is to operate injection molding equipment in order to successfully meet production demands and quality standards.


As a Molding Process Technician, you will:

  • Utilize your mechanical skills to install, remove and adjust Injection Molding machinery and equipment
  • Troubleshoot Injection Molding machines, follow process to resolve failures, other problems
  • Perform set-up of molds for all mold changes
  • Assist in preventative maintenance and repair of molding machines, molds and peripherals (robots)
  • Coordinates and sets up machines, robots and other equipment performing necessary tests to ensure company compliance. Trains employees in the correct procedures for operation as needed.
  • Perform cleaning and general maintenance tasks
  • Maintain a safe work environment following Company’s safety, ISO standards
  • Achieve adequate production levels while maintaining the expected product quality
  • Ensure molded components meet all product quality criteria including dimensional criteria
  • Communicate to supervisor and other technicians and document all technical information and issues
  • Participate in reducing the rate of scrap
  • Assist in training of employees in proper work methods for safe and efficient performance of job duties.
  • Maintain records, files and other documentation pertinent to assignments.



Who we are looking for:


Required Skills:

  • 1-3 years of experience working with injection molding equipment including machine adjustment, troubleshooting and mold installation and removal
  • Strong mechanical aptitude and mechanical skills.
  • Familiarity with automation 6/3 robotics
  • General knowledge of plastic materials and processes
  • Detail oriented
  • Ability to implement and tune all peripherals (6 axis robot, grinder)
  • Strong verbal and written communication skills
  • Strong Mathematical aptitude
  • Ability to read blueprints, use precision measuring/inspection tools
  • Effective computer skills, documentation, reporting, file management and web skills
  • Ability to work different work shifts
  • Continual improvement mindset. Self-Learner, trend of continuous learning
  • Ability to work and operate machinery in a Clean Room Environment.
  • Physically capable of the required work including but not limited to: Extensive use of manual dexterity, ability to grip, firmly hold, turn and practice strong hand coordination in order to troubleshoot, service and repair industrial equipment and use hand tools to perform the same.
  • Ability to regularly stand, walk, and bend during performance of essential job duties. Ability to lift up to 50 pounds.
  • Understands and practices safe working procedures. Observes safety rules and policies; brings to managements’ attention any unsafe acts or conditions



Who We are


At Aptar, we leverage insights, design, engineering and science to develop drug and consumer product dosing, dispensing and protection technologies for many of the world’s leading brands. Aptar in turn makes a meaningful difference in the lives, looks, health and homes of millions of patients and consumers around the world. Our innovations nasal drug delivery for emergency medicines, precise fragrance applications, mess-free ketchup dispensing for kids, connected technologies that support patients in adhering to their treatments and much more


With manufacturing facilities across North America, Europe, Asia and South America, and a dedicated team of over 13,000 employees in about 20 countries, Aptar is committed to creating impactful innovations for our customers and their consumers.


Our Culture

At Aptar, our success is driven by the individuals who contribute their unique talents and perspectives every day. We believe that when you bring your authentic self to work, we all thrive.


How We Support Our Employees

  • An exciting, inclusive and value based working environment
  • Award-winning corporate university offering personal development and training opportunities.
  • Competitive base salary and performance-based bonus plan.
  • Contribute to the communities where we reside.
  • Innovative benefits plan which includes: 401k & Retirement Savings plan, vacation, medical, dental, vision, life, disability, pet insurance, wellness plan, and generous paid maternity/paternity leave.


Compensation and Base Annual Pay

In compliance with pay transparency requirements, the salary range for this role is USD $36.00 to USD $45.00 per hour. This is not a guarantee of compensation or salary, as final offer amount may vary based on factors including but not limited to experience and geographic location. Aptar also offers a variety of benefits, including health, life, and disability insurance, 401(k) match and employer retirement savings contribution, flexible spending accounts, EAP, education assistance, parental leave, paid time off, company-paid holidays, and more. The specific programs and options available to an employee may vary depending on location, pay class, or other factors.


Aptar is an equal opportunities employer. We believe that a diverse workforce is key to our success. We welcome applications from all members of society irrespective of age, sex, disability, sexual orientation, race, religion or belief.


Stay updated on career opportunities by following us on LinkedIn!

Not Specified
2502 - RandD Scientist II
✦ New
Salary not disclosed
Franklin Lakes 1 day ago
Stellar Consulting Solutions is a boutique business and technology consulting company headquartered in Atlanta, GA.

We deliver high quality, agile, and experienced workforce for niche technology projects of any scale.

We help forward thinking clients to solve specific problems by understanding their needs and align talent that can move fluidly to match skill supply and demand on a real-time basis.

Stellar Consulting has a unique combination of technical and digital skills to recruit, engage, and retain qualified talent.

We have a stellar reputation for striving to achieve high ethical standards.

Our use of Innovative techniques and industry best practices has made us one of the fastest growing boutique firms delivering to enterprise business.

Role: RandD Scientist II Location: Franklin Lakes, NJ Duration: 12 Months(Contract#W2 With Medical Benefits) Client: Medical Device Job Summary: The RandD Scientist II works in the Specimen Management RandD team and helps develop and improve products used in clinical diagnostic testing.

The role involves conducting experiments, preparing samples, analyzing results, and supporting product development activities.

The scientist will also help investigate issues, maintain lab equipment, and work with different teams such as engineering, manufacturing, quality, and regulatory.

Key Responsibilities: Support product development and research projects within the RandD team.

Design and run experiments to test materials, chemicals, or biological samples.

Prepare samples or prototypes for testing and analysis.

Document test results and technical findings.

Help perform root cause analysis when product or process issues occur.

Work with cross-functional teams (Engineering, Manufacturing, Quality, Regulatory, Marketing).

Support design verification and product transfer to manufacturing.

Maintain laboratory equipment and facilities.

Follow Good Laboratory Practices (GLP) and lab procedures.

Required Skills / Knowledge: Knowledge of materials science, chemistry, or biological sciences.

Experience with materials characterization techniques such as: FTIR, TGA, DSC Experience with clinical samples (especially blood) is preferred.

Good skills in MS Office (Excel, Word, PowerPoint).

Ability to learn quickly and work hands-on in the lab.

Education and Experience: Bachelor's degree in fields such as: B.S.

degree in Materials Engineering, Mechanical Engineering, Chemical Engineering, Chemistry, Biomedical Engineering, Cell/Molecular Biology, Biochemistry, Materials Science, Chemistry, or related disciplines.

Minimum 2 years of laboratory experience
Not Specified
R&D Scientist II
✦ New
Salary not disclosed
Franklin Lakes 1 day ago
A-Line Staffing is now hiring R&D Scientist II (Chemistry Scientist II) in Franklin Lakes (07417).

The R&D Scientist II would be working for a Major Fortune 500 Company and has career growth potential.

R&D Scientist II Highlights: ??? Schedule: Monday???Friday, Day Shift (40 hours/week, 8 hours/day) ??? Pay Range: $38.81???$41.67 hourly R&D Scientist II Responsibilities: ??? Represent the R&D function as an Extended Team member supporting large technology and product development programs ??? Design and execute experiments supporting development, verification, and evidence generation efforts ??? Prepare samples/prototypes for internal and external analysis ??? Develop and execute test protocols; document results with guidance from senior staff ??? Conduct root cause analysis for product development and sustaining engineering activities ??? Support product development work streams including Requirements Management, Design Verification, and Design Transfer ??? Collaborate cross-functionally with Engineering, Marketing, Medical Affairs, Manufacturing, Quality, and Regulatory Affairs ??? Contribute to intellectual property growth, including patent applications and invention disclosures ??? Maintain laboratory equipment and ensure adherence to Good Laboratory Practices (GLP) ??? Mentor junior team members and foster a collaborative team environment ??? Travel as required (conferences, manufacturing sites, customer visits) R&D Scientist II Qualifications: ??? Bachelor???s degree in Materials Engineering, Mechanical Engineering, Chemical Engineering, Chemistry, Biomedical Engineering, Cell/Molecular Biology, Biochemistry, Materials Science, or related field ??? Minimum 2 years of direct laboratory experience ??? Proficiency with Microsoft Office ??? Regulatory experience in medical device or pharmaceutical industry ??? Materials testing experience (polymers, hydrogels, TCA lab, Environmental Stress Cracking testing) Preferred Qualifications: ??? Master???s or PhD degree ??? Experience with statistical analysis tools ??? Experience handling clinical specimens (especially human blood); bloodborne pathogen training will be provided If you are interested in this R&D Scientist II position, please apply to this posting with Luke H.

at A-Line!
Not Specified
Director, Drainage Agency (Department of Highways)
✦ New
Salary not disclosed
Chestnut Ridge, NY 1 day ago

The Rockland County Department of Highways, Drainage Division, is seeking a Director of the Drainage Agency. The work is specialized diverse, and complex in nature.

This is administrative and managerial work of a complex nature that involves responsibility for developing and implementing policies and procedures to implement safe, efficient and modern stream maintenance and drainage programs. The work is performed under the general direction of the Superintendent of Highways and in accordance with Federal and New York State applicable laws and regulations and Rockland County objectives and policies. Supervision is exercised over professional and technical employees. Develops policies and procedures with respect to drainage programs and makes recommendations to the Superintendent of Highways regarding same. Arranges for the engineering, construction, improvement, repair and maintenance of County streams, water courses, drainage courses, and tributaries and ensures that services are in compliance with policies and regulations. Oversees the administration of drainage-related capital projects, including but not limited to monitoring funding, supervising contract bid processes, ensuring compliance with regulations and project requirement. Responds to emergencies (e.g. severe flooding) by inspecting and monitoring flooding and related conditions, acting as liaison with County officials and first responders to exchange information and resolve problems, preparing reports regarding flood damage and related conditions in order to obtain New York State and Federal funding. Completes applications and prepares documents to secure New York State Department of Environmental Conservation (DEC) permits, as needed, regarding dam safety, streams, aquatic habitats, wetland programs, etc. Acts as liaison to a variety of governmental agencies and units of government, as needed, including but not limited to the Army Corp of Engineers, the New York State Department of Environmental Conservation, towns and village, etc. Approves plans, specifications and estimates for construction, maintenance and repair of stream watercourses and tributaries. Directs the control of trees, brush and weeds within the bounds of County streams. Plans and directs a program to inform residents about the programs and functions of the Drainage Agency. Oversees the Drainage Agency’s permit application process and ensures compliance with the Rockland County Stream Control Act as it applies to activities within areas under the jurisdiction of the Drainage Agency. Plans and directs a Stream Maintenance program, maintains records and makes reports. Acts for and in place of the Superintendent of Highways with respect to drainage matters, as needed. May provide legal opinions regarding Federal, New York State, and Rockland County laws that pertain to drainage matters. May inventory and purchase machinery, equipment and materials.

Thorough knowledge of New York State Department of Environmental Conservation requirements and regulations, thorough knowledge of general practices and regulations regarding stream maintenance and general construction procedures. Good knowledge of administrative procedures and techniques, especially as they pertain to a comprehensive modern stream maintenance and drainage programs, ability to plan, develop and implement general policies and procedures for a modern and efficient stream and drainage system, including stream maintenance and construction. Ability to establish and maintain cooperative relationships with others, including elected officials and Federal and New York representatives. Have the ability to understand and interpret laws and regulations that pertain to drainage-related matters. Ability to effectively communicate, both orally and in writing Also does related work as required.

Minimum Qualifications:

  • A Bachelor’s degree or higher in Civil Engineering, Civil Engineering Technology, Environmental Engineering, or comparable curriculum or;
  • A New York State license to practice law and
  • Four (4) years of post-degree supervisory, administrative or management experience that substantially involved responsibility for drainage and/or environmental programs and projects (e.g., development of policies and procedures, supervision of staff, enforcement, providing legal opinions and/or litigating related matters, overseeing the implementation of programs and projects, etc.).

Other Requirements and Information:

  • Must be a Resident of Rockland County.
  • This is a competitive position in Civil Service and reachability on an eligible list following a civil service examination would be a requirement for permanent appointment.

Salary and Benefits:

Salary and benefits are competitive with the public sector market including but not limited to the following:

  • $122,000.00 Annual Salary (as of January 1, 2026)
  • 40 Hour work week
  • Medical, Dental and Vision
  • Time off including vacation, personal and holiday time
  • New York State Pension eligibility
  • Other benefits, including, but not limited to deferred compensation, tuition reimbursement, leadership and other professional development training

How to Apply:

Interested candidates should email a completed Rockland County employment application, to


Click here to access the online application.

Position open until filled.

Not Specified
R&D Scientist II – Materials / Polymer Focus
✦ New
Salary not disclosed
Franklin Lakes, NJ 4 hours ago

R&D Scientist II – Materials / Polymer Focus (Lab-Based) - 626501

Location: Franklin Lakes, NJ (Onsite – 5 days/week)

Duration: 12-month contract (W2)

Pay Rate: ~$35.75 - $37.75/hr.


Overview

We are seeking a junior-level R&D Scientist II to join a Specimen Management R&D team, supporting the development of blood collection devices (e.g., tubes, needles, plastic components).

This role is highly lab-focused (≈50%+ hands-on testing) and ideal for candidates with a background in materials science, polymer chemistry, or chemical engineering who enjoy bench work and experimental testing.


Key Responsibilities

  • Conduct material characterization and testing, including:
  • FTIR, DSC, TGA, rheology, and mechanical testing
  • Environmental Stress Cracking (ESC) and Thermal Cycle Analysis (TCA)
  • Design and execute lab experiments and test protocols
  • Perform root cause investigations related to material and product failures
  • Support material selection, qualification, and vendor/material changes
  • Prepare samples and prototypes for internal and external testing
  • Document results and provide data-driven recommendations
  • Assist with small-scale material assessments and innovation efforts
  • Maintain lab equipment and follow Good Laboratory Practices (GLP)
  • Collaborate with cross-functional teams (R&D, Manufacturing, Quality, etc.)
  • Support testing involving human blood samples (training and PPE provided)


Required Qualifications

  • Bachelor’s or Master’s degree in: Materials Science, Polymer Chemistry, Chemical Engineering, Mechanical Engineering, or related field
  • 2+ years of laboratory experience (industry or academic)
  • Hands-on experience with materials testing and characterization
  • Strong interest in polymer/material science (non-metal/ceramic focus)
  • Comfortable working in a lab-heavy, hands-on role
  • Basic knowledge of statistical tools (Excel, Minitab, etc.)
  • Ability to conduct independent research and literature reviews


Preferred Qualifications

  • Polymers or plastic materials (especially for medical devices)
  • Material formulation or modification
  • ESC, TCA, or similar testing methods
  • Exposure to analytical chemistry techniques
  • Experience working with biological materials or blood samples
  • Background in tissue engineering or DNA-related work (nice-to-have)


Work Environment & Expectations

  • 50%+ lab-based work (testing, characterization, experimentation)
  • Remaining time focused on analysis, reporting, and innovation projects
  • Fully onsite role (no remote option)
  • No travel required
  • Dynamic, fast-paced R&D environment
  • Opportunity for long-term growth


Interview Process

  • Initial screening with Hiring Manager
  • Follow-up panel interview with project team (virtual via Teams)


Ideal Candidate Profile

  • Early-career scientist with a strong materials/polymer background
  • Curious, hands-on, and eager to learn
  • Comfortable working independently in a lab setting
  • Interested in medical device R&D and material innovation
Not Specified
Technical Project Manager
✦ New
Salary not disclosed
Mahwah, NJ 4 hours ago

We are looking for a skilled Technical Project Manager to lead product development initiatives from initial concept through launch. This role serves as the central connector between engineering, design, and business teams—ensuring clarity, alignment, and smooth execution throughout the full development cycle.


Responsibilities

  • Define what the product must deliver and ensure requirements are clearly communicated across technical and non-technical teams.
  • Guide projects from early concept through final launch, ensuring products meet quality, performance, and timing expectations.
  • Translate complex technical challenges into clear direction for cross-functional partners while supporting select hands-on technical activities when needed.
  • Develop and maintain detailed project schedules, ensuring milestones stay on track with internal goals and retailer timelines.
  • Facilitate strong communication and alignment across global teams, providing ongoing visibility into project status, risks, and decision points.
  • Prepare and deliver project updates to senior stakeholders, including recommendations, trade-offs, and key risks.
  • Collaborate with engineering and project teams to ensure solutions meet both technical feasibility and business needs.
  • Work in a fast-paced environment that values flexibility, problem-solving, and cross-functional collaboration.


Qualifications

  • 3+ years of experience in project management or engineering, ideally within consumer products, plastics, or hardware development.
  • Proven success managing full product lifecycles—from concept through production and launch.
  • Strong technical foundation with an understanding of engineering principles, manufacturing processes, and product constraints.
  • Ability to clearly communicate complex technical information to diverse stakeholders.
  • Proficiency in Microsoft Office; familiarity with CAD tools such as SolidWorks or CREO is a plus.
  • Experience presenting to senior leadership; exposure to executive-level communication is beneficial.
  • A proactive, hands-on approach with the ability to adapt quickly and work collaboratively across teams.


Salary Range (commensurate with experience)

$130,000 - $135,000 USD


Not Specified
Assembler - Manufacturing
✦ New
Salary not disclosed
Monsey, NY 4 hours ago
Mechanical Assembler
At Curtiss Wright we specialize in in the design, engineering and manufacturing of components/systems for the aerospace and defense sectors. Our facility in Monsey, NY has a focus on electrical units and housings for navy applications.
The Mechanical Assembler is responsible for assembling ruggedized mechanical enclosures, sub-assemblies, and system cabinets for defense applications. This role supports the assembly of integrated subsystems and products in accordance with established blueprints, engineering drawings, and quality standards. The position requires attention to detail, precision, and adherence to production schedules to ensure all products meet Curtiss-Wright's high standards of quality and reliability.
Location: Monsey, NY
hourly rate: $22.00 - $26.00
Please note that the salary range information provided is a general guideline only, reflecting a position based in New York. Criteria such as the candidate's qualifications and relevant experience, the scope of the specific position, as well as market and business considerations will be evaluated when extending an offer.
We Take Care of Our People
Paid Time Off I 401K with Employer Match and Profit Sharing I Health and Wellness Benefits I Learning and Development Opportunities I Referral Program I Competitive Pay I Recognition I Employee Stock Purchase Plan I Inclusive & Supportive Culture *
Your Challenge

  • Perform assembly-type functions using hand and power tools.

  • Read and interpret mechanical drawings, blueprints, and work instructions.

  • Operate press brake, fastener machine, and index machine as required.

  • Install wiring, lights, and hardware assemblies.

  • Operate forklifts, cranes, and other shop equipment.

  • Conduct visual inspections and ensure compliance with quality standards.

  • Train and oversee assemblers (Lead level).

  • Coordinate workflow and safety (Lead level).

  • Perform other related duties as assigned by the supervisor.

  • Ability to use measuring devices accurately.

  • Strong math aptitude, including fractions and decimals.

  • Basic computer navigation and documentation skills.

  • Strong attention to detail and organizational ability.

  • Critical thinking and problem-solving ability.

  • Commitment to following company safety and operational procedures.

  • Ability to lead, train, and evaluate other employees in assembly techniques (Lead level).


What You Bring

  • Associate Level: 1-2 years of related mechanical assembly experience.

  • Staff Level: 2-4 years of professional mechanical assembly or fabrication experience.

  • Lead Level: 5+ years of progressive experience in mechanical assembly, including supervisory or lead responsibilities in a manufacturing or defense environment.

  • High School Diploma or GED required.

  • Technical or vocational training in Mechanical Engineering or Manufacturing preferred.

  • Associate's Degree in Mechanical Engineering from an accredited institution is a plus.


901D is a Defense Contractor; U.S. Citizenship or U.S. Person status is required for this position.
This position may require exposure to information subject to U.S. export control regulations under the International Traffic in Arms Regulations (ITAR) or the Export Administration Regulations (EAR). All applicants must be U.S. persons within the meaning of U.S. regulations.
#LI-TS1
No unsolicited agency submittals please. Agency partners must be invited to participate in a search by our Talent Acquisition Team and have signed terms in place prior to any submittal. Resumes submitted directly to any Curtiss-Wright employee or affiliate will not qualify for fee payment, and therefore become the property of Curtiss-Wright.
Compliance Statement
This position may require exposure to export-controlled information and subject to additional security screening. In the event information provided during the security screening reveals ineligibility to access export-controlled information, any offer of employment may be reconsidered or withdrawn.
Curtiss-Wright is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, sexual orientation, gender identity, physical or mental disability, age, ancestry, legally protected medical condition, family care status, marital status, religion, veteran status, national origin, or any other legally protected status. If you require accommodation during the recruitment process, please contact Talent Acquisition.
For US Applicants: EEO is The Law - click here for more information.
If you require accommodation due to a disability at any time during the recruitment and/or assessment process, please contact Talent Acquisition and we will make all reasonable efforts to accommodate your request.
Not Specified
Manufacturing Engineer
✦ New
Salary not disclosed
Congers, NY 1 day ago

About the Company

At MetroWall, we hold our values close to heart, with respect being the cornerstone of our interactions. We believe that fostering a respectful environment not only enhances collaboration but also drives innovation. Overcoming obstacles is part of our journey, and we view challenges as opportunities to grow and improve. By embracing these challenges, we consistently strive to exceed expectations, delivering exceptional results and setting new standards in our industry. Together, these values create a culture of excellence and continuous improvement. Alignment with these values is critical to the success of any employee at MetroWall.


About the Role

The Manufacturing Engineer acts as the bridge between Engineering and Production, owning all aspects of process definition, manufacturability, and continuous improvement for MetroWall’s glass partition, door, and framing systems.


RELOCATION ASSISTANCE NOT AVAILABLE.


Responsibilities

Process Design & Standardization:

  • Develop, document, and maintain manufacturing processes for aluminum and door assembly operations
  • Create Standard Operating Procedures (SOPs), setup sheets, visual work instructions, and tool/fixture lists
  • Define operation sequences, routing steps, and cycle times in ERP (Epicor/Kinetic)
  • Establish and maintain machine capability matrices, ensuring processes align with equipment limitations

Design for Manufacturability (DFM):

  • Participate in NPI and R&D project reviews to ensure designs are manufacturable within MetroWall’s equipment and process constraints
  • Collaborate with Product Design Engineers to optimize part geometry, tolerances, and hardware selection
  • Approve manufacturability sign-offs prior to product release (NPI Phase Gate)

Process Improvement & Cost Reduction:

  • Analyze production performance data to identify waste, bottlenecks, and rework causes
  • Implement Kaizen and lean initiatives
  • Lead trials to validate improved processes, new jigs, or revised toolpaths

Collaboration & Support:

  • Work closely with Production Managers to ensure practical implementation of processes
  • Support Production Engineers during complex custom projects or prototypes
  • Serve as a technical escalation point for production issues

Document & Revision Control:

  • Maintain all process documentation under version control (aligned with Engineering ECO system)
  • Link controlled documents to Epicor Work Orders and routings
  • Audit shop floor adherence to latest revision

Safety & Compliance:

  • Ensure compliance with OSHA and internal safety standards
  • Integrate safety instructions directly into work procedures


Qualifications:

  • Bachelor’s degree in Mechanical, Industrial, or Manufacturing Engineering.
  • 3+ years of manufacturing experience (preferably architectural aluminum/glass or similar fabrication).
  • Hands-on understanding of CNC machining, cutting, drilling, and assembly operations.
  • Familiarity with Epicor/Kinetic, AutoCAD/Inventor, and Lean manufacturing tools.
  • Strong documentation and communication skills.
  • Ability to work cross-functionally between Engineering and Production.
  • Strong organizational abilities to manage multiple tasks and projects simultaneously. Skilled in identifying issues, analyzing options, and implementing effective solutions in a timely manner.
  • Keen attention to detail with a commitment to producing high-quality work, ensuring accuracy and precision in all tasks.


Work Environment

  • Office & Field


Additional Responsibilities:

  • Work with all members of the MetroWall team to deliver a level of customer service that exceeds the expectations of our customers
  • Assist sales team personnel in selecting solutions for clients
  • Continuously improve existing/new internal processes and deliverables
  • Obtain thorough understanding of MetroWall products and their capabilities in order to provide support to other teams/team members
Not Specified
Manager, Operations (Collagen)
✦ New
🏢 Getinge
Salary not disclosed
Mahwah, NJ 1 day ago


With a passion for life



Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.



Are you looking for an inspiring career? You just found it.



Job Overview


The Manager, Collagen Operations serves as the sole site leader for the Mahwah, NJ Collagen facility and carries full responsibility for all site personnel decisions, site performance, and operational escalations. This role ensures the safe, compliant, and efficient operation of the site while driving a strong culture of quality, engagement, and continuous improvement.


This position is accountable for the implementation of operational strategy as defined by the Getinge France (La Ciotat) leadership team. The Manager must ensure that all production activities adhere to U.S. regulatory protocols, including FDA, ISO, GMP, ESD, and Medical Device requirements, while also ensuring that all U.S. people practices (HR, safety, compliance, labor standards) are fully adopted and consistently upheld.


The Manager leads the site in achieving production, safety, quality, and delivery objectives while ensuring strong communication, alignment, and reporting back to the Getinge France entity.



Key Responsibilities


Site Leadership & Escalations


Serve as the highest-ranking leader on-site, responsible for daily operational oversight.


Act as the primary escalation point for all personnel, safety, compliance, and operational matters.


Maintain a proactive presence on the production floor; ensure alignment between site activities and La Ciotat leadership direction.


Lead all site-level communication, engagement efforts, and leadership routines.



Safety, Quality & Compliance


Serve as the site owner for safety, quality, and environmental compliance.


Ensure strict adherence to all U.S. regulatory requirements, including FDA, ISO, GMP, ESD, environmental, and medical device standards.


Ensure all U.S. people practices-including investigations, corrective action processes, documentation, training standards, and HR compliance-are consistently applied.


Guarantee timely and effective management of nonconformances, CAPAs, and deviations; lead site-level reviews and escalations.



Operations Management


Lead the execution of the annual production plan and ensure on-time delivery in alignment with customer needs and La Ciotat directives.


Oversee production scheduling, resource planning, inventory management, and staffing decisions.


Ensure production equipment, cleanroom environments, and facilities are properly maintained and audit-ready.


Manage manufacturing engineering and support functions to drive continuous improvement, cost savings, and process optimization.


Ensure documentation accuracy and compliance, including SOPs, controlled documents, training records, and batch documentation.



People Leadership



Full responsibility for all site personnel management, including hiring, onboarding, development, coaching, performance management, and employee relations.


Drive a culture of engagement, teamwork, and accountability consistent with Getinge values and U.S. people practices.


Set clear objectives, oversee workload planning, conduct performance reviews, and support career development.



Cross-Functional & Global Collaboration


Collaborate closely with the La Ciotat Production Director and France-based teams to ensure alignment on operational execution, reporting, and strategy.


Partner with U.S.-based HR, Quality, EHS, Engineering, and Supply Chain teams to ensure compliance and best practices across all site functions.


Coordinate validation, feasibility builds, technical projects, and operational readiness with sustaining engineering and global partners.



Essential Duties


Organize and manage site production resources to meet daily, weekly, and annual plans.


Anticipate operational needs and align staffing with forecasts.


Define short-term production plans compatible with demand and capacity.


Lead investigations into deviations, failures, or operational issues and implement corrective actions.


Oversee preventive and corrective maintenance and technical shutdowns.


Submit and manage investment requests to support operational goals.


Ensure all personnel comply with safety rules, gowning, cleanroom regulations, and quality protocols.


Maintain readiness for internal and external audits at all times.



Minimum Requirements


High school diploma required; advanced education preferred.


3-5 years of experience as a production manager in medical device or similarly regulated environment.


Experience in cleanroom or controlled environment operations preferred.


Demonstrated ability to lead teams and run a manufacturing site with a high level of autonomy.


Strong computer skills; SAP experience a plus.



Targeted salary range: $138,000- $145,000, depending upon experience and location +15% bonus target



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About us



With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.



Benefits at Getinge:



At Getinge, we offer a comprehensive benefits package, which includes:




  • Health, Dental, and Vision insurance benefits
  • 401k plan with company match
  • Paid Time Off
  • Wellness initiative & Health Assistance Resources
  • Life Insurance
  • Short and Long Term Disability Benefits
  • Health and Dependent Care Flexible Spending Accounts
  • Commuter Benefits
  • Parental and Caregiver Leave
  • Tuition Reimbursement


Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law.Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

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