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<h3>Job Description</h3>
Join the team building components that power America’s undersea strength. \n 
\n
Mace Machine is a precision CNC manufacturer specializing in complex, tight-tolerance parts for our nation's defense. We are seeking an experienced Swiss-style CNC Programmer/Machinist to take a leading role in production, continuous improvement, and workforce development as we expand our capabilities.
\nWhat You’ll Do\n
<ul>\n
<li>\n
Program, set up, and operate Citizen L20/L32/A20 Swiss-type lathes for precision, small-diameter components.
\n</li>
\n
<li>\n
Lead and mentor operators and apprentices to strengthen team capability and efficiency.
\n</li>
\n
<li>\n
Drive continuous improvement projects in setup reduction, tool life management, process documentation, and workflow optimization.
\n</li>
\n
<li>\n
Collaborate with Quality and Engineering teams to ensure conformance to AS9100 and defense manufacturing standards.
\n</li>
\n
<li>\n
Participate in training and process standardization initiatives that elevate the entire shop’s performance.
\n</li>
\n</ul>
\nWhat We’re Looking For\n
<ul>\n
<li>\n
Minimum 5 years’ experience programming and setting up Citizen, Star, or Tsugami Swiss machines.
\n</li>
\n
<li>\n
Proven supervisory or lead machinist experience in a high-mix, low-volume environment.
\n</li>
\n
<li>\n
Strong understanding of G-code, tooling, offsets, and process optimization.
\n</li>
\n
<li>\n
Comfort working from engineering drawings and military specifications.
\n</li>
\n
<li>\n
A hands-on leader with a passion for mentorship, precision, and progress.
\n</li>
\n</ul>
\nWhy Mace Machine\n
<ul>\n
<li>\n
Small-team environment where your ideas directly shape the future of our operation.
\n</li>
\n
<li>\n
Work on mission-critical parts supporting U.S. Navy and defense programs.
\n</li>
\n
<li>\n
Competitive pay, health insurance, and retirement plan.
\n</li>
\n
<li>\n
Opportunities to lead improvement initiatives and training programs.
\n</li>
\n</ul>
\n
Join a company where precision meets purpose.
\n

Swiss CNC Programmer / Machinist - Team Lead & Process Improvement

<h3>Job Description</h3>
Job Description We're seeking a Senior Process Engineer who's ready to be part of a company committed to formulating everyday success for every customer through innovative, reliable products used to adhere, seal, and protect at every level of the building envelope. ABOUT THE ROLE We are seeking an experienced and highly motivated Process Project Engineer to both manage capital improvement projects and provide direct technical support to our manufacturing operations. The ideal candidate is a hands-on engineer with a strong background in chemical process environments. In addition to managing the entire project lifecycle-from scope definition to commissioning-this role will be a key technical resource for the site, responsible for driving continuous improvement by analyzing workflows, identifying bottlenecks, and optimizing existing processes to enhance safety, quality, and efficiency. This position requires a unique blend of technical engineering acumen, project management discipline, and a practical, plant-floor perspective. We are hiring in Houston, TX, Rockland, MA, and Waukesha, WI. WHAT YOU'LL BE DOING Project Lifecycle Management: 
<ul>
<li>Lead capital projects from initial concept and feasibility studies through design, procurement, installation, commissioning, and final documentation.</li>
<li>Develop detailed project scopes, schedules, and cost estimates ($).</li>
<li>Manage multiple projects simultaneously, providing regular status updates to stakeholders.</li>
</ul>
 Process Optimization &amp; Plant Support: 
<ul>
<li>Analyze production data, workflows, and processes to identify bottlenecks, inefficiencies, and opportunities for improvement.</li>
<li>Develop and implement data-driven solutions to improve product quality, increase operational efficiency, and enhance process safety.</li>
<li>Lead and support continuous improvement initiatives and root cause analysis investigations for production and safety-related issues.</li>
<li>Provide daily technical support to Operations and Maintenance teams to troubleshoot process upsets and ensure stable, reliable production.</li>
</ul>
 Technical Design &amp; Equipment Specification: 
<ul>
<li>Read, interpret, and modify Piping &amp; Instrumentation Diagrams (P&amp;IDs).</li>
<li>Perform engineering calculations to properly size and specify process equipment, including pumps, piping, vessels, valves, and instrumentation.</li>
<li>Research and identify the best available equipment and technology for specific applications.</li>
<li>Ensure all designs comply with internal standards and relevant industry codes (e.g., ASME, API).</li>
</ul>
 Procurement &amp; Vendor Management: 
<ul>
<li>Develop comprehensive Request for Quotation (RFQ) packages for equipment and services.</li>
<li>Perform technical and commercial bid analyses to select suppliers and contractors.</li>
<li>Visit supplier sites to conduct equipment trials and Factory Acceptance Tests (FATs).</li>
<li>Perform Site Acceptance Tests (SATs) when equipment has arrived onsite.</li>
</ul>
 Construction &amp; Contractor Management: 
<ul>
<li>Vet, select, and manage on-site contractors for all installation and construction activities.</li>
<li>Lead safety orientations and ensure all on-site work is performed in strict adherence to company safety protocols (e.g., Lockout/Tagout, hot work permits).</li>
<li>Ensure that all local, state, and federal rules and regulations are followed during construction (building permits, modification of PSM or RMP, etc.).</li>
<li>Provide direct on-site supervision to ensure equipment is installed and erected according to engineering specifications and best practices.</li>
<li>Commission equipment and work directly with other functions such as operations, maintenance, and quality to ensure that equipment meets design standards.</li>
<li>Work in cross-functional teams to create Standard Operating Procedures (SOPs), follow Management of Change (MOC) protocol, and provide/create equipment documentation where necessary.</li>
</ul>
 Maintenance &amp; Reliability Integration: 
<ul>
<li>Apply a "Design for Maintainability" mindset to all projects, ensuring safe and efficient access for future maintenance and repairs.</li>
<li>Collaborate with the Maintenance and Reliability teams to identify critical spare parts, develop preventative maintenance plans, and ensure a smooth handover of project documentation.</li>
</ul>
 WHAT WE ARE LOOKING FOR Education: 
<ul>
<li>Bachelor of Science in Chemical Engineering (Required)</li>
<li>Master of Science in Chemical Engineering (Preferred)</li>
</ul>
 Experience: 
<ul>
<li>Minimum of 5-7 years of combined project and process engineering experience in a chemical manufacturing environment.</li>
<li>Proven track record of managing "cradle-to-grave" capital projects from $50K to $5M+.</li>
<li>Demonstrated experience in process optimization, troubleshooting, and continuous improvement in a manufacturing setting.</li>
<li>Direct, hands-on experience with the specification, installation, and startup of process equipment (pumps, piping, tanks, control systems).</li>
<li>Demonstrated experience in managing and directing contractors and skilled trades.</li>
<li>Experience in a maintenance or reliability role is a strong plus.</li>
<li>Experience working in a PSM and RMP regulated environment.</li>
</ul>
 Skills &amp; Abilities: 
<ul>
<li>High proficiency in reading and creating P&amp;IDs, Electrical Schematics, Construction Plans, and other technical drawings.</li>
<li>Strong analytical and problem-solving skills with a data-driven approach to decision- making.</li>
<li>Knowledge of continuous improvement methodologies (e.g., Lean, Six Sigma) and root cause analysis tools.</li>
<li>Strong understanding of process control fundamentals (DCS/PLC).</li>
<li>Excellent communication skills, with the ability to effectively interact with plant operators, maintenance technicians, and senior management.</li>
<li>A robust safety mindset and knowledge of OSHA and industry safety standards.</li>
<li>Proficiency with MS Project or similar project scheduling software.</li>
<li>Experience with AutoCAD or other CAD software is desirable.</li>
</ul>
 WHAT WE OFFER 
<ul>
<li>Competitive Compensation</li>
<li>Retirement Savings</li>
<li>Medical, Dental, Disability and Life Insurance Coverage</li>
<li>Holistic Health &amp; Well-Being Programs</li>
<li>Health Savings Accounts (HSA) &amp; Flexible Spending Accounts (FSA) for</li>
<li>Health and Dependent Care</li>
<li>Vision and other Voluntary Benefits and Discounts</li>
<li>Paid Time Off and Holidays</li>
<li>Paid Parental Leave (Maternity and Paternity)</li>
<li>Educational Assistance Program</li>
</ul>
 #BuildingEnvelope Amrize is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We thank all applicants for their interest; however, only those selected for an interview will be contacted. BUILDING INCLUSIVE WORKSPACES At Amrize, there is endless opportunity for you to play your part. Whether you're in a technical, managerial, or frontline role, you can shape a career that works for you. We're seeking builders, creative thinkers and innovators. Come put your expertise to work while developing the knowledge and skills to drive your career forward. With us you'll have the chance to build your ambition! Amrize North America Inc. takes pride in our hiring processes and our commitment that all qualified applicants will receive consideration for employment without regard to age, race, color, ethnicity, religion, creed, national origin, ancestry, gender, gender identity, gender expression, sex, sexual orientation, marital status, pregnancy, parental status, genetic information, citizenship, physical or mental disability, past, current, or prospective service in the uniformed services, or any other characteristic protected by applicable federal, state or local law. Amrize North America Inc, and its respective subsidiaries are Equal Opportunity Employers, deciding all employment on the basis of qualification, merit and business need. Amrize Canada Inc. is committed to the principles of employment equity and encourages the applications from women, visible minorities, and persons with disabilities. In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request accommodation in order to apply for a position with us, please email <a href="mailto:recruiting-accommodations@amrize.com" target="_blank">recruiting-accommodations@amrize.com</a>. This email address should only be used for accommodations and not general inquiries or resume submittals. In Ontario, our organization/business is committed to fulfilling our requirements under the Accessibility for Ontarians with Disabilities Act. Under the Act, accommodations are available on request for candidates taking part in all aspects of the selection process. While we sincerely appreciate all applications, only candidates selected for an interview will be contacted.]]&gt;

Senior Process Engineer

<h3>Job Description</h3>
Job Description
Nanobiosym is on the cusp of rewriting the rules of personalized medicine, novel technologies, and healthcare delivery. Founded by a renowned MIT and Harvard trained Physician and Physicist, Nanobiosym's innovative pipeline of products leverage novel advances in physics, biomedicine, and nanotechnology. Awarded the first ever X-PRIZE for healthcare, and a recipient of multiple other prestigious peer-reviewed funding awards, Nanobiosym is currently adding to its talented team as it expands into a global commercial enterprise.
 
DUTIES
<ul>
<li>Injection Molding Experience Strongly preferred</li>
<li>Coordinate a production and Engineering Team in a variety of manufacturing processes.</li>
<li>Collaborate with team members and management to develop and improve injection molded and assembled products and processing thru numerous manufacturing steps.</li>
<li>Develop and assist in the process and product monitoring, including the creation of a validation protocol (IQ, OQ, PQ) that comply with FDA regulations.</li>
<li>Provide troubleshooting focus and direction for the team with details of root cause analysis.</li>
<li>Utilizes DOE/DRM/COS/Lean principles and statistical process control to develop creative, thorough and practical technical solutions. </li>
<li>This is a hands-on position in a growing organization and an opportunity which will grow rapidly</li>
</ul>
QUALIFICATIONS
<ul>
<li>
<ul>
<li>S. or B.S. in Engineering (Plastics or Mechanical preferred)</li>
<li>Six Sigma Black Belt, a plus</li>
<li>5 years of experience in molding highly critical dimensional parts in manufacturing environment</li>
<li>5 years of experience in resins, and scientific mold process development</li>
<li>Demonstrated experience with viscosity analysis, ultrasonic and electric contact welding</li>
<li>Experience in statistical analysis and statistical process control</li>
<li>Recent experience with a ISO 13485 environment</li>
<li>Good Communication and Organizational Skills</li>
<li>Master molder certified preferred</li>
</ul>
</li>
</ul>
 Job Posted by ApplicantPro

Engineer: Process Improvement Engineer

<h3>Job Description</h3>
Job Description
**Manufacturing Operator (Contract 6
+ Months, potential for contract to hire)
**1st Shift (7:00am - 3:30pm), Mon-Fri
**2nd Shift (3pm-11:30pm), Mon-Fri
**
Location: Hopkinton, MAPay Rate: 
$25/hr Notes: 
<ul>
<li>They need people to start asap</li>
<li>**Location</li>
</ul>
**:
Onsite at Hopkinton, MA location – **candidates must be local to Hopkinton
**
<ul>
<li>**Contract Duration</li>
</ul>
**: 6 months
<ul>
<li>**Rate: </li>
</ul>
**$25/hour
<ul>
<li>**Interview process:</li>
</ul>
** 30 min for site tour and process walkthrough, then 30 min with the 3 line Leads all together
**Manufacturing Operator
**:The Manufacturing Operator reports to the Manufacturing Line Lead and helps in performing all tasks involved in the production of fluid management products including production tasks such as kitting of parts, cutting of tubing and polymer film, reading design drawings, performing basic and complex assembly techniques, executing detailed visual inspections, operating manual and automated machinery, and completing packaging and labeling activities. The successful candidate will play a key role in ensuring that the department’s safety, quality, and production goals are met.Responsibilities:• Conduct basic assembly techniques• Read manufacturing drawings and follow standard operating procedures of varying complexity• Perform detailed visual inspections on in-process and finished products• Package and label finished products• Work with a Team in a fast-paced ISO certified cleanroom environment for 8 hours a day• Perform daily housekeeping tasks as assigned• Cut tubing and polymer film to meet tolerances using both manual and automated tools.• Safely operate cleanroom machinery by closely following the standard operating procedures• Perform inventory counts and report any inaccuracies on in a timely manner• Complete documentation according to Good Documentation Practices (GDP)• Learn the Repligen Performance System and contribute to a culture of continuous improvementQualifications:• 0-2 years of relevant experience• HS Diploma or equivalent• Basic arithmetic skills• Strong attention to detail with an emphasis on quality standards• Ability to use hand tools, and equipment including repetitive forceful gripping, grasping, pushing, and pulling• Stand and move during shift, including reaching, bending, stooping, grasping• Ability to frequently lift up to 30 pounds and occasionally lift up to 50 pounds• Wear PPE (Personal Protective Equipment) and adhere to chemical hygiene• Follow all safety protocols

Manufacturing Clean Room Technician

<h3>Job Description</h3>
Job DescriptionDEKA R&amp;D has an immediate opening for a Quality Specialist to work in the Quality Department in a dynamic Medical Device Research and Development environment.&nbsp; The position reports to the Director of Quality.&nbsp; The Quality Specialist is actively involved with everyday quality assurance operational tasks for ongoing product development projects and commercially released products. How you will make an impact:
<ul>
<li>Review and Approve Quality System Records</li>
<li>Support updating procedures and processes to support the QMS</li>
<li>Support the site Corrective and Preventive Action program</li>
<li>Provide QA support relative to DHR Review/inspections and final acceptance of materials/products</li>
<li>Review labels for accuracy and precision</li>
<li>Initiate non-conforming materials reports and segregate / control non-conforming materials as required</li>
<li>Review and close complaint files per complaint requirements</li>
<li>File and maintain records manually and electronically</li>
<li>Support QMS collection and trending of quality data</li>
<li>Manage QMS databases for action items and implementation</li>
<li>Support vendor qualification and management</li>
<li>Support external and internal audits</li>
<li>Support as backup to Training Coordinator, CAPA Coordinator, and Calibration Coordinator</li>
<li>Provide training as required to DEKA personnel&nbsp;</li>
<li>Promote QMS awareness to non-QA departments throughout DEKA</li>
</ul>
Skills needed to be successful:&nbsp; &nbsp; &nbsp; &nbsp;&nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;
<ul>
<li>Preferred 2+ years’ experience in Quality Assurance in an FDA regulated environment – with QSR (21 CFR Part 820) and ISO 13485 experience if possible.</li>
<li>Experience with documentation in a regulated field such as medical device</li>
<li>Prior auditing experience is a plus</li>
<li>Strong written/verbal communication skills</li>
<li>Ability to:
<ul>
<li>Learn custom software programs</li>
<li>Multitask and carry tasks through to completion</li>
<li>Manage multiple sources of data and develop reports</li>
</ul>
</li>
</ul>
About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
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Quality Specialist

<h3>Job Description</h3>
Job Description
General Description:
The primary objective of the Maintenance Millwright is to maintain the mill and yard equipment in proper working order. PM work orders will be completed in a timely manner to ensure overall efficiency meets or exceeds the company standards. The daily activities of any maintenance personnel is subject to change due to the needs of the mill therefore, scheduled hours must be flexible. This position may also include running equipment as needed.
Responsibilities:
<ul>
<li>Work longer hours on short notice</li>
<li>Communicating with the purchaser and Sawmill Manager to further support cost effective ways to manage purchasing and inventory control facility wide:</li>
<li>Initiate purchasing of all consumable parts (with PM Parts Purchaser)</li>
<li>Working with the PM Parts Purchaser and Sawmill Manager to build a Preventive Maintenance program for each area that is easily maintained: </li>
<li>Sawmill Machinery</li>
<li>Waste Systems and dust collection systems</li>
<li>All outside yard equipment</li>
<li>Compressor PM and Service</li>
<li>Building Needs</li>
<li>Follow PM program per the instructions outlined:</li>
<li>Complete PM work orders as required</li>
<li>Complete training to complete HOT WORK Permits</li>
<li>Knowledge of cutting torches</li>
<li>Weld/Fabricate:</li>
<li>Mig &amp; Stick Welding</li>
<li>Assemble and install equipment using hand and power tools</li>
<li>Troubleshoot and replace / repair defective parts</li>
<li>Adjust clearances and align parts</li>
<li>Learn to operate all sawmill equipment efficiently</li>
<li>Problem Solving:</li>
<li>Analyze information and evaluate to choose the best solution to solve problem</li>
<li>Travel to all locations as needed </li>
<li>Work a minimum of 20% OFF production hours each week (when the facility is not running)</li>
<li>Perform other related duties as assigned</li>
</ul>
Qualifications / Requirements:
<ul>
<li>High School Diploma or Equivalent</li>
<li>Effective Written and Oral communication skills</li>
<li>Able to work well with minimal supervision</li>
<li>Ability to Prioritize tasks and follow specified procedures</li>
<li>5+ years relevant maintenance experience</li>
</ul>

Maintenance Millwright

<h3>Job Description</h3>
Job Description
General Description:
The Production Machine Operator/General Laborer shall work to ensure all actions reflect the company culture, work meets or exceeds company standards, and values and working environment reflects that as outlined by the Mill Manager. The Production Machine Operator /General Laborer will primarily stack, operate the stack track or drills, debarker, tag and strap lumber and will be responsible for keeping the machine areas clean at all times. The Production Machine Operator/ General Laborer will operate in a way that is efficient and productive while supporting the safety mission and standards as outlined at Kennebec Lumber Company. 
Responsibilities:
<ul>
<li>Operate designated machine per SOP guidelines.</li>
<li>Operate lug loaders and position lumber to optimize machine efficiency. </li>
<li>Overseeing machine operation and flow of various lumber handling systems</li>
<li>Operating Automatic Lumber Stacker and fixing Tags onto finished packs of lumber</li>
<li>Strapping packs/bundles of lumber with a strapping device</li>
<li>Maintaining facility in a clean professional condition</li>
<li>Maintain good working relationships with all co-workers and management and follow up as needed on recommendations and /or citations.</li>
<li>Participate, Motivate, Support, and Implement on site safety practices and culture.</li>
<li>Other Duties as Assigned</li>
</ul>
Safety Requirements:
Safety First – Personal Protective Equipment
<ul>
<li>Steel or Safety Toe footwear is required in all areas.</li>
<li>Gloves required in designated areas – per task.</li>
<li>Hearing Protection required in all areas (Exception being inside the cab of outside machine forklifts).</li>
<li>Eye Protection required in all areas</li>
<li>Report all near misses and unsafe acts to immediate supervisor.</li>
<li>Pedestrian awareness at all times.</li>
<li>Florescent vests and hard hats are required for all outside activity (Exception, pedestrian travel from one building to another).</li>
<li>Never walk through any overhead door that is controlled remotely (Always use access door next to overhead).</li>
<li>Familiarize yourself with the various work areas. Learn how to operate the conveyor belts and the emergency stop buttons.</li>
<li>Familiarize yourself with the various possible pinch points that are in your area.</li>
</ul>
Physical Requirements:
<ul>
<li>Bend, stretch &amp; twist multiple times daily.</li>
<li>Moderate to Heavy wrist / hand repetitions.</li>
<li>Stand for long periods of time.</li>
<li>Ability to work swiftly and accurately.</li>
<li>Ability to lift up to 50 lbs.</li>
<li>Ability to push &amp; pull up to 25 lbs.</li>
<li>Ability to climb and ascend and descend stairs frequently.</li>
<li>No allergies to sawdust, particles in the air (respiratory concerns).</li>
<li>Ability to work in all weather conditions (below 0 degrees temps to over 90-degree temps).</li>
</ul>

Production Machine Operator

<h3>Job Description</h3>
Job Description
Our client, a leader in the electronics industry, is seeking an Electronics Test Technician to join their team. As an Electronics Test Technician, you will be part of the technical support team, ensuring high-quality standards in product performance. The ideal candidate will have strong problem-solving skills, attention to detail, and a solid understanding of electronic systems, which will align successfully in the organization.
Job Title: Electronics Test Technician
Location: Peabody, MA (Relocating to Salem, NH)
Pay Range: $25-$32 (Based on skills and experience)
Shift: 9/80 schedule, Monday to Friday with every other Friday off.&nbsp;Flexible start time from 6-7am. What's the Job?
<ul>
<li>Conduct testing and troubleshooting of large electro-mechanical systems to ensure compliance with specifications.</li>
<li>Utilize diagnostic tools and software for effective problem resolution.</li>
<li>Perform root cause analysis and implement solutions for complex system issues.</li>
<li>Work with essential testing equipment including digital multimeters, oscilloscopes, and signal generators.</li>
<li>Follow technical documentation and schematics to diagnose and resolve issues at the component level.</li>
</ul>
What's Needed?
<ul>
<li>At least 3 years of relevant experience in electronics testing and troubleshooting.</li>
<li>Associates degree in a related field.</li>
<li>Familiarity with various testing methodologies and automated testing tools.</li>
<li>Ability to lift, carry, push, and pull up to 25 lbs.</li>
<li>Strong attention to detail and ability to interpret technical documentation.</li>
</ul>
What's in it for me?
<ul>
<li>Opportunity to work in a dynamic and innovative environment.</li>
<li>Flexible start times to accommodate your schedule.</li>
<li>Engagement in hands-on technical work with advanced electronic systems.</li>
<li>Collaborative team culture that values your input and expertise.</li>
<li>Potential for career growth and professional development.</li>
</ul>
Upon completion of waiting period associates are eligible for:
<ul>
<li>Medical and Prescription Drug Plans</li>
<li>Dental Plan</li>
<li>Supplemental Life Insurance</li>
<li>Short Term Disability Insurance</li>
<li>401(k)</li>
</ul>
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
About ManpowerGroup, Parent Company of: &nbsp;Manpower, Experis, Talent Solutions, and Jefferson Wells
ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells –&nbsp;creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.

Electronics Test Technician

<h3>Job Description</h3>
Job DescriptionCOMPANY OVERVIEW: Merrimack Manufacturing is a&nbsp;medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that&nbsp;will play a crucial part in bringing innovative and life changing products to life. POSITION OVERVIEW: This position will support manufacturing quality operations in a dynamic, fast-paced, medical device manufacturing environment. This environment includes the manufacture, inspection, and testing of devices for process validation and commercial production. RESPONSIBILITIES:
<ul>
<li>Working under the direction of Quality Engineers support, drive, and coordinate final inspection and acceptance of medical devices.</li>
<li>Support quality engineers in processing nonconformances, deviations, and rework authorizations by gathering data, updating logs, or drafting documentation.</li>
<li>Perform Device History Record (DHR) reviews for completeness, accuracy, and compliance to internal and regulatory requirements.</li>
<li>Identify and document errors or missing information in DHRs and coordinate with production or quality teams for timely correction. </li>
<li>Work cooperatively with team members on commercial production lines to support quality requirements and projects.</li>
<li>Provide administrative and technical support for change orders, training records, and CAPA follow-up as assigned.</li>
<li>May perform inspections for components, materials, devices and documents. </li>
<li>Position requires daily contact with members of Production, Engineering, Materials, and Quality departments and occasional contact with auditors and customers</li>
</ul>
 QUALIFICATIONS AND SKILLS:
<ul>
<li>2 + years of experience in occupation related to Manufacturing or Quality Control of medical devices.</li>
<li>Experience with compliance, with applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 is preferred. </li>
<li>Experience with Microsoft Office software (Word, Outlook, Excel) required.</li>
<li>Self-starter and independent individual with strong organizational, time management and communication skills.</li>
<li>Ability to drive assigned tasks to closure</li>
<li>Must be able to manage multiple priorities. </li>
<li>Use critical thinking and deductive reasoning to make risk based decisions.</li>
</ul>
 EDUCATION: Associate degree or equivalent experience in Manufacturing, Quality, Mechanical or related engineering / life sciences related discipline. &nbsp;
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