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<h3>Job Description</h3>
Job DescriptionManufacturing Plant Maintenance Mechanic
Location: Avon, Massachusetts
Hours: First shift, 7:00am–3:30pm
Rate: $29.00–$34.00 hourly, depending on experience
 Your impact
Reliable equipment means reliable products. In this role, your technical mastery keeps our production lines running—and our customers supplied with the quality they trust. The work you do each day directly improves safety, uptime, and yield.
 Key responsibilities
<ul>
<li>Own routine care of assets: clean, lubricate, align/adjust, and calibrate equipment.</li>
<li>Test systems, troubleshoot faults, repair issues, and order/replace components.</li>
<li>Perform preventive maintenance and tackle unscheduled repairs across mechanical and electrical systems.</li>
<li>Evaluate chronic failures and propose upgrades that improve availability, capability, and output.</li>
<li>Root-cause and resolve equipment problems with a continuous-improvement mindset.</li>
<li>Write detailed technical reports covering modifications and maintenance procedures.</li>
</ul>
 Qualifications
<ul>
<li>Capable of lifting up to 50 lbs consistently during the shift.</li>
<li>Experience in manufacturing or warehouse environments preferred.</li>
</ul>
 Grow with PPG
We are builders, learners, and doers. At PPG, we strive to be better today than yesterday—every day.
PPG: WE PROTECT AND BEAUTIFY THE WORLD™
From industrial and transportation to consumer products and construction, PPG elevates surfaces everywhere. Discover more at <a href="http://www.ppg.com" target="_blank">www.ppg.com</a> and follow @PPG.
 How we show up (The PPG Way)
<ul>
<li>We create mutual value with customers.</li>
<li>We act as One PPG.</li>
<li>We trust our people—always.</li>
<li>We make it happen.</li>
<li>We run it like we own it.</li>
<li>We do better today than yesterday—every day.</li>
</ul>
 Compliance and equal opportunity
Disclaimer:
We ask that you have the use of, or access to, information subject to the International Traffic in Arms Regulations. Only U.S. Citizens, Green Card holders and political asylees or refugees are eligible to apply.
All applicants must provide one of the following forms of identification as part of their application:
(1) Passport, (2) Birth Certificate, (3) Certificate of Naturalization (USCIS Form N-550 or N-570), or (4) Permanent Resident Card (USCIS Form I-551.
PPG provides equal opportunity to all candidates and employees.
All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, color, creed, religion, national origin, age, disability status, marital status, veteran status, sexual orientation, gender identity or expression.
If you need assistance to complete your application due to a disability, please email <a href="mailto:recruiting@ppg.com" target="_blank">recruiting@ppg.com</a>.
 What to expect next
Benefits will be discussed with you by your recruiter during the hiring process.
Your feedback matters—visit Glassdoor.com to share your candidate experience so we can improve.

Manufacturing Plant Maintenance Mechanic

<h3>Job Description</h3>
Industry: Pharmaceuticals
Title: Quality Control Analyst II - Microbiology
Job ID: NORT000014
Location: Norton MA
Duration: 06+ months contract (+Possibility of extension)
 
*This position is onsite and will be primarily located in Norton, MA. There may be occasional responsibilities at a secondary location in Cambridge, MA.
 
Overview:
The Quality Control Microbiology Analyst II plays a role in supporting the department's efforts to maintain the highest standards of quality and compliance from development through to commercialization. In addition to executing routine and non-routine testing in support of development through commercial programs, the Analyst II may participate in data trending, investigations, and laboratory operations. By ensuring these critical activities are executed within project milestones and timelines, the Analyst II contributes to routine laboratory operations, thereby enhancing the overall efficiency and effectiveness of the QC functions .
 
 
Key Responsibilities (including but not limited to):
<ul>
<li>Perform routine and non-routine microbiological assays (bioburden, TOC, endotoxin, conductivity), with increasing complexity, to support critical utility samples, in-process samples, and product release, following established SOPs</li>
<li>Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics</li>
<li>Assist in the maintenance of laboratory equipment and inventory to ensure smooth laboratory operations</li>
<li>Ensure data is submitted timely; may qualify as a data reviewer to ensure timely and efficient data availability.</li>
<li>Perform role-specific operational assignments (e.g., critical utility sampling, environmental monitoring, product testing, etc.).</li>
<li>Contribute to the revision and updating of controlled documents, including SOPs, work instructions, and test methods, to ensure continuous improvement and compliance with requirements</li>
<li>Adhere to internal standards, policies, and SOPs, as well as regulatory and industry standards (e.g., GMP, GLP, ICH guidelines) to maintain the highest levels of quality and compliance.</li>
<li>Collaborate with QC and cross-functional teams to ensure seamless quality control operations and to support the collective company goals</li>
<li>Participate in inspection readiness activities as well as supporting onsite audits and inspections, as needed.</li>
<li>Support continuous improvement initiatives aimed at enhancing QC processes and procedures, increasing laboratory efficiency and effectiveness.</li>
<li>Collaborate with other organizational functions including Manufacturing, Materials Management, and Quality Assurance to ensure alignment with overall business goals.</li>
<li>Support various quality events as needed (i.e., investigations, deviations, CAPAs, change controls)</li>
</ul>
 
Qualifications
<ul>
<li>B.S. in biology, biochemistry, chemistry, or related scientific field ; Associate's degree, Biotech Certificate, or equivalent considered</li>
<li>Pharmaceutical/Biotech industry experience with 2 years in a regulated laboratory setting, Quality Control, or equivalent, relevant experience</li>
<li>Demonstrated prior experience/understanding of microbiology testing and EM/CU sampling</li>
<li>Experience with quality events preferred (i.e., investigations, deviations, CAPAs, change controls)</li>
<li>Data analysis experience preferred</li>
<li>Ability to work under direction, with attention to detail, in an environment where priorities shift</li>
<li>Good communication and teamwork abilities, capable of working effectively in a collaborative environment</li>
<li>Knowledge of LIMS, Excel, Word, and PowerPoint is helpful</li>
</ul>

Quality Control Analyst

<h3>Job Description</h3>
Job Description
Job Descriptions:
Manufacturing:
Corrugator&nbsp;positions available. For more details, please send resume or come in to fill out an application.
All Shifts available, M-F, $19.00 / hr. plus depending on position and qualifications.
Please apply at NewCorr Packaging 66 Lyman Street Northboro, MA. 01532'
Company DescriptionState of the art corrugator company looking to hire all shift. No skills needed. Will train. 
<h3>Company Description</h3>
State of the art corrugator company looking to hire all shift. No skills needed. Will train.

Manufacturing Corrugated

<h3>Job Description</h3>
ARN Process Operator &amp; Mechanical Maintenance Technician
 
Job Summary:
We are a growing, locally based company seeking skilled professionals to support production operations and equipment maintenance. This dual-role position involves operating manufacturing processes and performing mechanical maintenance to ensure the smooth operation of our systems and equipment. The job title and pay will be based on experience.
Shift Schedule:
<ul>
<li>Current: Monday–Friday, 8:00 AM to 4:30 PM</li>
<li>Extended hours and/or night shifts may be required as production expands.</li>
</ul>
 
Key Responsibilities:
Process Operation (70% of Role)
<ul>
<li>Operate and monitor machinery for manufacturing natural vitamin E and related products.</li>
<li>Set up and adjust equipment conditions based on testing feedback.</li>
<li>Monitor process parameters, such as flow rates, temperature, and pressure.</li>
<li>Perform controlled shutdowns, cleaning, and basic repairs of equipment.</li>
<li>Follow cGMP (current Good Manufacturing Practices) and food safety regulations.</li>
<li>Document production activities, maintain records, and update process flow diagrams.</li>
<li>Collaborate with team members to foster a productive and cooperative work environment.</li>
</ul>
 
Packaging, Staging, and Warehousing (20% of role)
<ul>
<li>Assist with packaging finished products according to specifications.</li>
<li>Prepare and stage products for storage or shipment.</li>
<li>Label, palletize, and wrap shipments to meet quality and safety standards.</li>
<li>Move materials and finished products to appropriate warehouse locations.</li>
<li>Maintain accurate inventory records and follow warehouse procedures.</li>
</ul>
 
Mechanical Maintenance (10% of Role)
<ul>
<li>Perform maintenance and minor repairs on production-related systems and equipment, including:</li>
<li>Chillers</li>
<li>Vacuum pumps</li>
<li>Liquid sanitary process pumps</li>
<li>Conduct routine inspections, adjustments, and cleaning of mechanical equipment.</li>
<li>Recommend additional repairs or equipment upgrades as needed.</li>
<li>Maintain inventory of parts and supplies, and assist with ordering.</li>
<li>Operate forklifts (training and certification provided).</li>
</ul>
 
Safety &amp; Compliance
<ul>
<li>Adhere to occupational safety and health regulations.</li>
<li>Make recommendations to improve worker safety and operational efficiency.</li>
</ul>
 
Required Qualifications:
<ul>
<li>Education:</li>
<li>High School Diploma or equivalent.</li>
<li>Preferred: Associate or Bachelor’s degree in a science-related field with 2+ years of production experience.</li>
<li>OR completion of an approved technical training program (e.g., automotive or motorcycle repair, pump maintenance).</li>
</ul>
 
Experience:
<ul>
<li>At least 3 years of experience operating industrial equipment, preferably in a chemical, food, or related processing environment.</li>
<li>Mechanical aptitude, with experience in pumps, chillers, and vacuum systems.</li>
<li>Familiarity with chemical or food processing, printing press operation, or applied chemical/food engineering is highly desirable.</li>
<li>cGMP Manufacturing Experience</li>
</ul>
 
Skills:
<ul>
<li>Ability to read engineering drawings and blueprints.</li>
<li>Proficient in using hand and power tools.</li>
<li>Basic computer skills, including Microsoft Office Suite (Word, Excel), Outlook, and other relevant programs.</li>
<li>Effective verbal and written communication skills.</li>
<li>Strong analytical and problem-solving abilities.</li>
</ul>
 
Additional Requirements:
<ul>
<li>Valid driver’s license and dependable transportation.</li>
<li>Ability to lift up to 50 lbs and work at various heights.</li>
<li>Willingness to undergo a pre-employment background check, drug screening, and workplace physical.</li>
</ul>
 
Preferred Qualifications:
<ul>
<li>OSHA-related safety training.</li>
<li>Previous experience in automotive or motorcycle repair, or familiarity with pumps and HVAC systems.</li>
</ul>

Process Operator & Mechanical Maintenance Technician

<h3>Job Description</h3>
Job Description
POWERED BY TEAMWORK. Are you ready to be part of a team that drives big ideas and even bigger wins? At Safran, we believe in the power of both collaboration, and individual contributions. We understand that it takes diverse perspectives, problem-solving skills, dependability, and trust to push each other forward and achieve great success. For us, working here is more than just a job; it's a passion. There's the unique opportunity to lead the way in aerospace and defense and contribute to creating a safer and more sustainable world.
We trust our employees to bring bold ideas to build the future of aerospace together, contributing to our ranking by TIME as the leading Aerospace &amp; Defense company on the 2023 World's Best Companies list (#59 on the full list). Join our team and become part of the group that's making amazing things happen on the ground and in the skies. Together, we'll proudly step back and say, "We did that."
Safran Aircraft Engines designs, produces, and sells, alone or in partnership, commercial and military aircraft engines offering world-class performance. Through CFM International*, Safran Aircraft Engines is the world's leading supplier of engines for single-aisle mainline commercial jets. Safran Aerospace Composites in Rochester, NH is dedicated to the production of 3D woven composite parts, made using the RTM (resin transfer molding) process. The first application of this technology is the production of blades and fan cases for the LEAP (registered trademark) engine, developed by CFM International, designed to power the next generation of single-aisle aircraft. This technology creates less noise and decreases fuel consumption for aircraft engines, thereby reducing greenhouse gas emissions. We do this with energy, passion, and curiosity, and we're backed by our rich heritage and culture of innovation. *CFM International is a 50/50 joint company between Safran Aircraft Engines and GE.
In addition to our generous paid time off, comprehensive health insurance, and exceptional 401(k) employer contributions, we offer:
•Four day work week, Mon-Thu (10 hour days) •Performance-based bonuses •Fitness reimbursements •Paid parental leave •Wellness programs
Position Summary: This position will be responsible to successfully perform all tasks associated with, and operate all equipment within, the bonding process (bond layup / de-flash / surface prep), in either the fan blade or fan case value streams. Standard work methods and safe work habits must be followed to ensure conformance to customer requirements. This position reports to a Value Stream Manager and works under the direction of a Team Lead.
This is a first shift position, Monday-Thursday, 5:15am-3:15pm.
Principal Duties and Responsibilities (*Essential Functions) •*Ability to successfully perform all tasks associated with the bonding process, including kitting, bond layup, vacuum bagging, autoclave setup, surface preparation and operation and de-flash with the appropriate level of supervision. •*Accurately follow step-by-step work instructions throughout the bonding process (using a variety of computer systems). •*Inspect all work in accordance with all applicable work instructions and shop procedures. •*Perform all prescribed preventive maintenance (PM) on applicable equipment and processes as required per the PM charts. •*Electronically record part parameters using measurement tools such as micrometers and calipers. •*Precisely use hand tools such as razor blades, scalpels, hand sanders, as well as air/pneumatic tools. •Document material and process deviations through the approved Material Review Report (MRR) process. •Actively participate in continuous improvement and corrective action processes. •Comply with all OSHA regulations related to these operations including but not limited to safety shoes, hearing and eye protection. •This individual also has responsibility for the safe handling and movement of hazardous materials, including waste. •Other duties as assigned
The starting salary for this position is $22 USD per hour. Actual compensation will be determined based on experience, education, and other factors permitted by law.
Job Specifications •High school diploma or high school equivalency required. •Prior experience in a manufacturing environment strongly preferred. •Successful completion of relevant coursework in an accredited advanced manufacturing program may be substituted for experience in a manufacturing setting. •Experience with composite materials preferred. •Basic mechanical aptitude; familiarity with metric system preferred. •Excellent hand eye coordination including the ability to manipulate small items with speed and accuracy. Capable of producing fine finish work and assembling components accurately •Requires good organization skills and attention to detail. •Capable of working with epoxy and adhesive materials. •Ability to participate effectively in a team environment. •Good written and verbal communication skills. •Basic computer skills including software data entry and keyboarding. •Knowledge of and compliance with AS9100C or ISO9001 standards preferred.
Working Conditions •The work is performed in a plant environment. Employee will be exposed to any number of elements but with none present to the extent of being disagreeable. •Lighting and temperature are adequate. •Eye protection must be worn in manufacturing areas, approximately 90% of a standard work day. •Ear protection must be worn during certain operations, approximately 10% of a standard work day. •Various moving parts and machinery common to manufacturing facilities. •Frequently required to reach with hands and arms. •Regularly required to stand and walk. •Occasionally lift and/or move up to 35 pounds. •Specific vision abilities required by this job include close vision.
Candidates for positions with Safran Aerospace Composites must be legally authorized to work in the United States. Employment eligibility verification will be required at the time of hire. Visa sponsorship is not available for this position now or in the future. Relocation assistance is not offered for this position.
Disclaimer The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.
All qualified applicants will receive consideration for employment without regard to race, color, ethnicity, religion, sex, national origin, disability, veteran status, genetic data, or other legally protected status.
 Job Posted by ApplicantPro

Composites Manufacturing Operator - 1st Shift

<h3>Job Description</h3>
Production Supervisor needed to lead a team of roughly 7-12 employees in Rochester, MA. Company is in growth mode looking for someone who desires long-term employment and career growth. 
Location: Rochester, MA (100% On-site)
Salary Range: $115K–$120K, health insurance with an HRA, dental, vision, LTD, and a 401(k) retirement plan with an employer match. 3 weeks PTO, 1 week sick. Generous relocation package offered. Qualified candidates are encouraged to apply.
Company Overview
A leading precast concrete supplier in MA and NH with 50+ years of experience, providing high-quality products such as septic tanks, manholes, drainage structures, curbing, steps, and retaining walls. Serves engineers, contractors, and homeowners with a focus on performance and customer service. 
Position Summary
<ul>
<li>Lead and supervise production operations in a precast concrete facility.</li>
<li>Support the Plant Manager in ensuring safety, quality, and compliance with regulations.</li>
<li>Coordinate work activities and resources for efficient, high-quality output.</li>
</ul>
Responsibilities
<ul>
<li>Oversee and participate in the production of concrete products.</li>
<li>Delegate tasks and ensure adherence to safety policies and quality standards.</li>
<li>Coordinate schedules and set production priorities with the Plant Manager.</li>
<li>Drive continuous improvement to boost efficiency and reduce costs.</li>
<li>Maintain and track equipment maintenance and requisitions for supplies.</li>
<li>Manage hiring, training, and evaluation of production staff.</li>
<li>Prepare incident reports and ensure a clean, safe work environment.</li>
<li>Attend management meetings and stay current with NPCA PQS courses.</li>
<li>Encourage employee engagement and improvement programs.</li>
</ul>
Minimum Qualifications
<ul>
<li>5+ years’ experience in precast manufacturing.</li>
<li>Strong self-starter with energy and results orientation.</li>
<li>Knowledge of quality systems, health &amp; safety compliance, and production tools.</li>
<li>Ability to read blueprints and apply math concepts.</li>
<li>Proficient in MS Word, Excel, and general computer skills.</li>
<li>Strong communication and leadership skills.</li>
<li>Valid driver’s license.</li>
<li>PQS1 and ACI certifications preferred.</li>
</ul>
Supervisory Responsibilities
<ul>
<li>Assist the Plant Manager in supervising production employees.</li>
<li>Serve as Acting Plant Manager in their absence.</li>
</ul>
Key Competencies
<ul>
<li>Teamwork and collaboration</li>
<li>Critical thinking and decision-making</li>
<li>Time management and organization</li>
<li>Delegation and coordination</li>
<li>Conflict resolution and stress tolerance</li>
</ul>
Work Environment &amp; Physical Demands
<ul>
<li>Industrial plant setting.</li>
<li>Frequent climbing, lifting, walking, and handling materials.</li>
<li>Ability to lift/carry up to 50 lbs and work at heights up to 10 ft.</li>
<li>Must wear proper PPE at all times.</li>
</ul>

Production Supervisor

<h3>Job Description</h3>
Title: Director of Manufacturing Operations
 
My client in the manufacturing industry is seeking a Director of Operations to oversee all day-to-day operations within manufacturing, installation, supply chain, distribution, and QA.
 
Candidates must have the following:
<ul>
<li>US Citizen or Green Card</li>
<li>Ability to travel as needed to New Hampshire location</li>
<li>Minimum Bachelor’s degree</li>
<li>Minimum 10 years of manufacturing/operations experience, including medical device industry experience</li>
<li>OEM (Original Equipment Manufacturing) experience</li>
</ul>
 
Compensation is up to $200K + 15% bonus + equity
 
Essential Duties and Responsibilities
<ul>
<li>Responsible for following procedures within the company’s quality system per ISO 13485 requirements and other applicable international standards.</li>
<li>Work with sales and marketing to meet anticipated sales forecasts.</li>
<li>Manage contract manufacturer and suppliers.</li>
<li>Create a flexible manufacturing environment for the production of Lifeward products through the establishment of a compliant supply-chain.</li>
<li>Through staff and third-party personnel, coordinate the installation, service and repairs of equipment at customer sites.</li>
<li>Build and maintain an organization to comply with ISO 13485 regulations, and GMP guidelines.</li>
<li>Identifies, recommends, and implements new processes, technologies, and systems to improve and streamline organizational processes and use of resources and materials.</li>
<li>Assures development of project plans and cost-effective systems in line with Lifeward’s business plan and vision.</li>
<li>Establishes and administers budgets for multiple projects, monitors and controls costs, and reviews and approves cost-control reports, cost estimates, and staffing requirements for projects.</li>
<li>Keeps up-to-date on emerging technologies and trends in operations management.</li>
<li>Performs additional duties as requested</li>
<li>Manage field service depot</li>
<li>Manage parts procurement</li>
<li>Warehouse management end to end</li>
</ul>

Director of Manufacturing Operations

<h3>Job Description</h3>
Top Skills: Lean manufacturing, Six Sigma, process development/design, equipment selection/integration, supply chain coordination, familiarity with industry standards (ie. AS9100, ITAR, and NADCAP), strong knowledge of manufacturing processes (ie. CNC machining, additive manufacturing, assembly, and testing

Manufacturing Engineer

<h3>Job Description</h3>
The Principal Electronics Engineer will be a part of the R&amp;D organization and an important contributor to the realization of the next generation robotic platform that will change the future of healthcare. 
You will be a technical lead in driving to resolve complex multi-disciplinary issues. Additionally, you will create, refine and implement technical processes and best practices for electrical engineering development. The result of your work will directly influence design iterations in a regulated medical device development environment. 
 
This is a role well suited to an ambitious professional, looking for the next step in their career. As a Principal Electrical Engineer, Robotics, you will be responsible for:
<ul>
<li>Responsible for leading multidisciplinary teams to debug and troubleshoot complex issues and to thoroughly document the investigation including recommendations to design</li>
<li>Responsible for electrical engineering planning and design for robustness and reliability for PCBs and cabling</li>
<li>Responsible for generating and implementing best practices and process documentation for electronics development</li>
<li>Project Management responsibilities may include vendor and supplier management, directing design and test technician resources.</li>
<li>May lead/conduct characterization or testing of PCBAs </li>
</ul>
 
This position may suit you best if you are familiar with what is below, and would like to do develop your career with Healthineers
<ul>
<li>You have technical systems understanding and interactions between electronics, controls/software and electromechanical disciplines</li>
<li>You have a solid understanding of determining system performance between cross disciplines</li>
<li>You have demonstrated successes in systematically determining root cause of electro-mechanical systems</li>
<li>You have strong electronics fundamentals for analog, digital and electromechanical design</li>
<li>You have strong presentation skills</li>
<li>You have strong technical collaboration skills including scheduling meetings/discussions, identifying discussion points and driving to obtain agreement on decisions for workstreams</li>
<li>You have experience developing Class II &amp; III medical devices in a regulatory environment, applying relevant standards such as ISO 13485 IEC 60601-1, 60601-1-2</li>
<li>You have demonstrated experience with electronic design for motor control and mixed-signal electronic design for precise sensing applications </li>
<li>You are highly proficient in the use of electrical CAD tools, Altium preferred</li>
<li>You possess working knowledge of EMC and electrical safety</li>
<li>You have exceptional analytical skills with proficiency in analytical tools such as MATLAB/Simulink and Spice required</li>
<li>You have exceptional data analysis skills; required </li>
<li>You have excellent communication, teamwork, interpersonal skills with the ability to self-direct and have some project management skills </li>
</ul>
 
Required skills to have for the success of this role
<ul>
<li>Bachelor’s degree in Electrical Engineering required, MS or PhD preferred</li>
<li>Minimum of 15 years of experience in R&amp;D or product development required</li>
<li>Willing to travel up to 10%</li>
</ul>

Principal R&D Electronic Engineer

<h3>Job Description</h3>
As a Principal Electrical Engineer, you will play a pivotal role in developing new products and sustaining existing production contracts. This challenging position requires a blend of technical expertise, strategic thinking, and hands-on experience in developing and sustaining products. You will be responsible for ensuring our electronics and software products deliver cutting edge performance, evaluating make-vs-buy decisions, and continuously improving our design, analysis and project planning processes. This role offers an exciting opportunity to work with cutting-edge technology and shape the company’s future products and capabilities.
\n
Specific Job Duties shall include but not be limited to:
\n
<ul>\n
<li>\nElectrical Engineering
<ul>
<li>Provide technical leadership and mentorship to fellow engineers, including guiding, reviewing and approving their design work.</li>
</ul>
\n</li>
\n
<li>Establish technical objectives, milestones, project timelines and budgets</li>
\n
<li>Building and sustaining a CMMI® capability level 3 (or equivalent) software development organization</li>
\n
<li>Lead the design of circuits, firmware and software for MCU, FPGA, DSP and CPU devices for new and existing products.</li>
\n
<li>Development of low power and low noise circuits, electromechanical devices and assemblies</li>
\n
<li>Development of sensor modules including real time processing of sensor data</li>
\n
<li>Design and development of robotic systems</li>
\n
<li>Design and development of power amplifiers </li>
\n
<li>Guide the team in the use of electronic CAD tools (Altium, Eagle etc.)</li>
\n
<li>Guide the team in state of the art utilization of version control tools (e.g. Github, JIRA)</li>
\n
<li>System design using standard interfaces such as Ethernet, CAN, I2C, SPI, PCIe, USB, etc.</li>
\n
<li>C++ or Rust or C programming</li>
\n
<li>Implementing computer vision, AI and control system algorithms</li>
\n
<li>support make vs buy decisions </li>
\n
<li>Work with contract manufacturers to develop and execute development as well as production and testing.</li>
\n
<li>\n</li>
\n
<li>\nCross functional
<ul>
<li>Working across engineering departments to deliver on project goals</li>
</ul>
\n</li>
\n
<li>Working knowledge of product development methodologies such as Failure Modes and Effects Analysis (FMEA), Risk management, Change Management, and Advanced Product Quality Planning (APQP)</li>
\n
<li>Work with the quality team to implement and oversee software and electronics related testing for product quality control</li>
\n
<li>Work with senior management to develop technology road maps, project plans and strategies </li>
\n
<li>\n</li>
\n</ul>
\n
Requirements and Education:
\n
Required Qualifications:
\n
<ul>\n
<li>Bachelors degree or higher in electrical engineering, software engineering or related field</li>
\n
<li>7+ years of experience with excellent working knowledge of microprocessor-based, mixed signal circuit design </li>
\n
<li>4+ years of relevant experience building complex electromechanical hardware/software systems</li>
\n
<li>4+ years of relevant experience developing API’s for low level devices</li>
\n
<li>3+ years experience in engineering, within the aerospace/defense, automotive, or medical device fields</li>
\n
<li>Working knowledge of product development methodologies such as Failure Modes and Effects Analysis (FMEA), Risk management, Change Management, and Advanced Product Quality Planning (APQP)</li>
\n
<li>Proficient with Microsoft suite</li>
\n
<li>Eligible to obtain and maintain an active U.S. Secret security clearance</li>
\n</ul>
\n
Preferred Qualifications:
\n
<ul>\n
<li>MS or higher in related field</li>
\n
<li>Exposure to ISO 9001/AS 9100 quality systems.</li>
\n
<li>Experience with high mix low volume manufacturing and suppliers</li>
\n
<li>Experience with electromechanical hardware</li>
\n
<li>Experience with Python / Matlab and experimental data collection</li>
\n</ul>
\n
Compensation and Benefits
\n
In addition to competitive wages, Massa offers an excellent benefits package, including health, dental, life, and disability insurance(s), along with a 401k plan with profit sharing opportunity! This package is offered to full-time hourly and salaried employees.
\n
When you join Massa, you’re not just joining a company; you’re joining a family. Applicants who are selected for this full-time position will be able to grow here by demonstrating their capability to do so. Being detail-oriented, having a strong work ethic, and taking pride in the company are essential for success!
\n
Employment with Massa Product Corporation may require an individual to obtain a U.S. Security Clearance. Cleared individuals must be U.S. Citizens, pass a background check successfully, and consent to a non-disclosure agreement. 
\n\n
Massa is an Equal Opportunity/Merit-Based/Affirmative Action Employer

8,469 Manufacturing Jobs