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    <title>restor3d Jobs</title>
    <link>http://j.brt.mv/CompanyPortal.do?companyGK=50693&amp;portalGK=41164</link>
    <description><![CDATA[Job Postings available for application.]]></description>
    <language>en-us</language>
    <pubDate>Fri, 12 Jun 2026 16:24:55 EDT</pubDate>
    <lastBuildDate>Fri, 12 Jun 2026 16:24:55 EDT</lastBuildDate>
    <generator>BrightMove ATS</generator>
    <item>
      <title><![CDATA[Manufacturing Engineer I - Wilmington, MA]]></title>
      <link>http://j.brt.mv/jb.do?reqGK=27779397&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>19be2da7-5405-42ae-8c48-be0eb9ff7172</guid>
      <description><![CDATA[Job Summary: The Manufacturing Engineer I will be responsible for the selection, development, qualification, and scale-up of production processes and equipment across different manufacturing departments. Process objectives are the high quality, high volume production of patient-tailored implants and associated instruments.
 
Duties and responsibilities: 
-       Develop and maintain strong, internal working relationships across restor3d.
-       Understand the objectives, responsibilities, and mission of the Operations department and works towards those goals.
-       Prioritize and plan work activities; adapt for changing conditions.
-       Initiation, execution, and documentation of IQ, OQ, & PQ activities
-       Optimization of manufacturing processes (5S) for Lean Manufacturing
-       Development of formal training programs for the production personnel
-       Day-to-day production support activities such as NCRs and CAPAs
-       Processing of engineering change orders from originator to final approval
-       Developing and updating preventative maintenance programs
-       Writing and executing process validation plans and reports, using sound, data/stats supported results.
-       Play a major role in the CNC process for the manufacturing of implants
-       Using Statistical tools for alternative material evaluations and validations projects
-       Support of material handling and control system
-       Conduct time studies and process flow mapping.
-       Assure compliance with the requirements set forth by US FDA QSR and ISO regulations
-       Documentation of manufacturing processes and inspection criteria within the company&rsquo;s documentation procedures.
-       Evaluate and recommend capital equipment to best suit needs of company&rsquo;s selected fabrication processes.
-       Participation on project teams as a key contributor bringing proactive solutions and execution.
-       Other responsibilities as assigned.
 
Required Education and Experience:
-       1-3 years of experience in manufacturing process support and development in the medical device industry.
-       Bachelor&rsquo;s Degree in Engineering required 
 
Preferred Education and Experience:
-       Previous experience in orthopedics strongly preferred
-       Previous experience working with CNC machines preferred 
-       Medical Device/GMP experience preferred
 
Required Skills:  
-       Excellent written and verbal communication skills.
-       Able to work accurately in medical device regulated environment with strong attention to detail.
-       Demonstrated ability to monitor own work to ensure quality, accuracy and thoroughness.
-       Strong organizational, analytical and time-management skills.
-       Able to self-motivate and work both independently and as part of a team.
-       Understanding of ISO 13485 and QSR regulations
-       Knowledge of statistical analysis (Green Belt preferred)
-       Experience working with CNC manufacturing processes
-       Knowledge of computer aided design (SolidWords preferred)
 
Physical Requirements: 
-       Working at a desk for prolonged periods of time.
-       Working with CNC machines/equipment.]]></description>
      <pubDate>Fri, 12 Jun 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Buyer/Planner - Wilmington, MA]]></title>
      <link>http://j.brt.mv/jb.do?reqGK=27779305&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>30bdbd9c-7b7a-4afc-a55b-5f12aba513f2</guid>
      <description><![CDATA[Job Summary
Buyer/Planner is responsible for procuring materials and equipment required to support production and meet the Company&rsquo;s Sales & Operations Plans and Quality Objectives. This role owns purchasing, planning, expediting, and scheduling activities, ensuring seamless logistical support of customer orders in a fast-paced, high-growth environment. The ideal candidate demonstrates strong problem-solving skills, a bias to action, and the ability to operate with urgency and accountability.

Essential Duties and Responsibilities

Develop and maintain strong cross-functional relationships across the organization.
Understand Production objectives and align daily activities to support business goals.
Prioritize and execute work in a fast-moving, dynamic environment with changing priorities.

Purchasing:

Plan and execute purchases for assigned commodities and projects; negotiate and implement optimal sourcing strategies.
Issue purchase orders, confirm deliveries, and proactively expedite as needed.
Resolve purchasing issues related to delivery, receiving, and invoicing.
Partner with Supplier Engineering to develop strategic supplier relationships, monitor performance, and mitigate supply chain risks.
Support supplier qualification and negotiate cost-effective solutions.
Drive supplier accountability through performance tracking and scorecards.
Participate in MRB activities and support corrective actions and recovery plans.
Maintain and continuously improve purchasing procedures and documentation.

Inventory Management:

Develop and communicate supplier forecasts using MRP and business plans.
Manage components and finished goods inventory, including consigned inventory.
Balance service levels, inventory accuracy, and inventory turns to meet business objectives.
Maintain and publish accurate tracking systems to proactively identify and communicate supply risks.
Take ownership of issues, drive root cause analysis, and implement timely solutions.
Perform other duties as assigned.


Qualifications

Bachelor&rsquo;s degree required.
APICS certification preferred.
3&ndash;5 years of experience in purchasing and planning, preferably in a regulated industry.
Hands-on experience with ERP/MRP systems, with strong preference for SAP ERP.
Advanced Microsoft Excel skills (data analysis, pivot tables, lookups, and reporting).
Experience in lean manufacturing environments is a plus.


Skills, Abilities, and Competencies

Strong problem-solving mindset with the ability to make data-driven decisions quickly.
Demonstrated bias to action with a sense of urgency and ownership.
Ability to thrive in a fast-paced, rapidly changing environment.
Excellent analytical, organizational, and time management skills.
Strong written and verbal communication skills.
Ability to influence internal and external stakeholders to mitigate supply chain risks.
High attention to detail and commitment to accuracy.
Self-motivated, with the ability to work independently and cross-functionally.
Knowledge of lean principles and continuous improvement methodologies.]]></description>
      <pubDate>Thu, 11 Jun 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Operations Coordinator (Planning & Warehouse) - Durham, NC]]></title>
      <link>http://j.brt.mv/jb.do?reqGK=27778014&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>edc9ab0a-d422-4542-8285-45e08c18de67</guid>
      <description><![CDATA[Job Summary: 
This role provides flexible support across both Planning and Warehouse operations to ensure smooth day-to-day execution. The position is critical to maintaining continuity during periods of high workload, employee absences, and peak demand. The Operations Coordinator acts as a cross-functional resource who helps bridge communication gaps, streamline material flow, ensure inventory accuracy, and align operational priorities across departments.
Schedule: M-F, 11:30am to 8pm
Duties and responsibilities:
&middot;      Crosstrain in both planning and warehouse functions to provide operational flexibility across departments 
&middot;      Support, order tracking, schedule updates, shipping, receiving, staging, and documentation as needed
&middot;      Coordinate with teams to ensure timely material flow and production readiness 
&middot;      Monitor backlogs, requests, NCRs, and urgent matters to help prevent production delays. 
&middot;      Support during PTO, staffing shortages, or busy operational times. 
&middot;      Work in identifying, recommending, and supporting enhancements to manual processes and operational inefficiencies.  
&middot;      Assist with inventory management, cycle counts, inventory reconciliation, and system accuracy. While performing system audits and investigating inventory discrepancies or transaction errors in ERP/WMS systems 
&middot;      Support the processing of transfer orders and material requests while ensuring FIFO practices and proper inventory rotation.   
&middot;      Verify accuracy of inventory transactions, labels, lot/batch information, and documentation 
&middot;      Communicate updates and priorities to cross-functional teams, including Customer Service, QC, Manufacturing, and Procurement  
&middot;      Support with daily operational meetings by delivering status updates on material availability, shipping priorities, and planning issues.  
&middot;      Assist in coordinating urgent or high-priority orders to guarantee timely shipment and ongoing production support.  
&middot;      Help in creating reports on inventory, shipping status, planning metrics, or operational performance.  
&middot;      Ensure adherence to company procedures, safety standards, and quality system expectations. 
&middot;      Support leadership in executing special projects, operational changes, and assigned implementation tasks. Engage in ongoing improvement initiatives and process standardization efforts.  
 
Required Education and Experience:
&middot;        High school diploma or equivalent required
&middot;       1&ndash;3 years of experience in warehouse, planning, logistics, manufacturing, or supply chain operations
Experience with ERP/WMS systems in an operational environment
&middot;       Experience supporting cross-functional teams in a fast-paced environment
Preferred Education and Experience:
&middot;       Associate degree in Supply Chain, Business, Operations, or related field preferred 
&middot;       Experience in medical devices, manufacturing, or regulated environments preferred 
&middot;       SAP experience preferred 
&middot;       Experience with inventory control, production planning, shipping, or warehouse coordination 
&middot;       Previous experience supporting continuous improvement initiatives or process optimization
Required Skills:  
&middot;       Strong organizational and multitasking abilities
&middot;       Ability to prioritize and manage changing operational demands
&middot;       Strong communication and interpersonal skills
&middot;       Detail-oriented with strong accuracy and follow-through
&middot;       Proficient in Microsoft Office, especially Excel and Outlook
&middot;       Ability to work independently and collaboratively across departments
&middot;       Basic analytical and problem-solving skills
&middot;       Comfortable learning and navigating ERP/WMS systems
&middot;       Ability to adapt quickly and support multiple operational functions
&middot;       Strong sense of urgency and accountability
Physical Requirements: 
&middot;       Able to stand and walk for extended periods throughout the workday
&middot;       Capable of lifting, moving, or carrying between 25 and 50 pounds as required.
&middot;       Ability to bend, reach, push, pull, and perform repetitive movements.
&middot;       Comfortable operating around warehouse equipment and material handling activities 
&middot;       Proficiency in using computers, scanners, and standard office equipment regularly
&middot;       Capability to work flexible hours to support during peak periods or staffing shortages when operational needs arise.]]></description>
      <pubDate>Thu, 21 May 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Advanced Inspection Programmer - Durham, NC]]></title>
      <link>http://j.brt.mv/jb.do?reqGK=27777664&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>c4ca1a1c-4b14-428e-8c3d-29b8c2ba1bf7</guid>
      <description><![CDATA[Job Summary: 


We are seeking a skilled Advanced Inspection Programmer to support quality and inspection activities. This role will be responsible for creating, maintaining, and executing programs to ensure products meet engineering specifications and surgeon requirements, on CMM, C-Vision  and Benchmark machines.  


The Programmer will work closely with Quality, Engineering, and Manufacturing teams. Along with focusing on development of additional inspectors programming skills. 


Duties and responsibilities: 




Develop and maintain strong internal working relationships across restor3d. 






Understand the objectives, responsibilities, and mission of restor3d and the Quality Control department and work towards those goals. 






Develop, program, and execute inspection programs for production and first article inspections utilizing CMM Manager, Zone 3 and C-vision software. 






Communication and training of additional team members for development of their programming abilities. 






Interpret engineering drawings, Geometric Dimensioning and Tolerancing (GD&T), CAD models, and implant specifications to develop accurate inspection routines. 






Further develop inspection processes.  






Perform first article inspections (FAI), in-process inspections, final inspections, and receiving inspections. 






Analyze inspection data and communicate results to quality and engineering teams. 






Identify nonconformances and support root cause and corrective action activities 






Maintain inspection documentation, reports, and records as well as Good Document Practices (GDP). 






Calibrate and verify inspection equipment as needed. 








Assist with audits and customer quality requirements as required. 






Support Measurement System Analysis (MSA) and SPC activities, and continuous improvement initiatives related to metrology and inspection. 






Support the development of Best Practices document and work instructions for the advanced inspection processes. 




Required Education and Experience: 




High School Diploma, GED, or equivalent work experience 






4+ years of experience performing technician-level inspection within a FDA regulated environment. 






5+ years working with CMM Manager or Zone-3, or equivalent   






Working knowledge of GxP procedures and requirements  






GD&T certification required. 




Preferred Education and Experience: 




CMM Manager experience is required  






Zone 3 experience highly desired 






Calypso, Measure X, and Smart Profile experience highly desired 




Required Skills: 




Excellent written and verbal communication skills 






Advanced knowledge of inspection/metrology. 






Experience writing quality procedures desired 








Ability to read and interpret engineering drawings including GD&T. 






Skilled in the use of computer software to include, but not limited to Microsoft products (Outlook, Word, and Excel), Adobe PDF, SolidWorks, in-spec metrology software. 






Must be able to work in a team environment, execute responsibilities with minimal direct supervision, and have high attention to detail. 




Physical Requirements: 




Extended periods of sitting]]></description>
      <pubDate>Fri, 15 May 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Polymers Post Processing Technician  - Durham, NC]]></title>
      <link>http://j.brt.mv/jb.do?reqGK=27776745&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>ab7a1074-1397-41ef-9819-28ab6b4b3e10</guid>
      <description><![CDATA[Job Summary:
The Polymers Post Processing Technician will be responsible for the post-processing of 3D printed polymer devices. Relevant processes include: part washing, UV curing, support removal, and surface finishing.
Shift: Tuesday -Saturday 11:00am - 7:00pm
Duties and responsibilities
&middot;       Develop and maintain strong internal working relationships across restor3d.
&middot;       Understand the objectives, responsibilities, and mission of the XXXX department and work towards those goals.
&middot;       Prioritize and plan work activities; adapt for changing conditions.
&middot;       Full operation of part washing and UV curing machines for polymer parts. Includes machine load and unload, operation, maintenance, general upkeep and troubleshooting.
&middot;       Using various tools for polymer model finishing. Includes support removal and surface sanding as needed.
&middot;       Following appropriate safety precautions, including usage of PPE and maintaining lab cleanliness.
&middot;       Visual inspection of manufactured goods as part of quality-controlled processes.
&middot;       Perform production activities for equipment set-up/line clearance, processing, labeling, and record completion while following quality system guidelines and Good Manufacturing Practices (GMP).
&middot;       Participate in continuous improvement projects.
&middot;       Compliance to safety (OSHA), GMP, GDP, GLP and 21 CFR 820.
&middot;       Performs other related duties as assigned.
&middot;       Other responsibilities as assigned.
Required Skills:  
&middot;       Excellent verbal and written communication skills
&middot;       Able to work accurately in a fast-paced, hectic, ever-changing environment with strong attention to detail.
&middot;       Demonstrated ability to monitor own work to ensure quality, accuracy, and thoroughness.
&middot;       Strong organizational, analytical, and time-management skills.
&middot;       Able to self-motivate and work both independently and as part of a team.
Education and Experience:
&middot;       High school diploma or GED required
&middot;       Associates or post-secondary education preferred
&middot;       Experience in the use of basic machine shop tools and equipment is required
Mechanically inclined
&middot;       Working knowledge of GMP, GLP, and GDP is required
&middot;       Experience in FDA 21 CFR 820 Quality system is preferred
Physical Requirements: 
&middot;       Position requires the ability to intermittently lift and carry up to 50 pounds
&middot;       PPE including eye protection, hearing protection, and gowning required depending on task performed
&middot;       May require extended periods of standing, extensive work with the operator&rsquo;s hands and tools, as well as occasional squatting, kneeling, and working with a ladder]]></description>
      <pubDate>Mon, 04 May 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Manufacturing Engineer II - Wilmington, MA]]></title>
      <link>http://j.brt.mv/jb.do?reqGK=27775264&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>f6889c3a-884a-4ee5-8bf5-672523bd0d4b</guid>
      <description><![CDATA[TITLE:  Manufacturing Engineer II
DEPARTMENT:  MFG Engineering
REPORTS TO: Principal Process Engineer
STATUS: Exempt
LOCATION:  Wilmington, MA
 
Job Summary:
The Manufacturing Engineer II will be responsible for the selection, development, qualification, and scale-up of production processes and equipment across different manufacturing departments.  Process objectives are the high quality, high volume production of patient-tailored implants and associated instruments.
 
Essential Duties and Responsibilities:

Develop and maintain strong internal working relationships across restor3d.
Understand the objectives, responsibilities, and mission of the Engineering department and work towards those goals.
Prioritize and plan work activities; adapt for changing conditions.
Initiation, execution, and documentation of IQ, OQ, & PQ activities.
Optimization of manufacturing processes (5S) for Lean Manufacturing.
Development of formal training programs for the production personnel.
Processing of engineering change orders from originator to final approval.
Writing and executing process validation plans and reports using sound, data/stats supported results.
Troubleshoot process failures and perform root cause analysis.
Using Statistical tools for alternative material evaluations and validations projects.
Conduct time studies and process flow mapping.
Assure compliance with the requirements set forth by US FDA QSR and ISO regulations.
Documentation of manufacturing processes and inspection criteria within the company&rsquo;s documentation procedures.
Evaluate and recommend capital equipment to best suit needs of company&rsquo;s selected fabrication processes.
Participation on project teams as a key contributor bring proactive solutions and execution.
Other responsibilities as assigned.
 

Qualifications:

3-5 years of experience in manufacturing process support and development in the medical device industry.
Previous experience in orthopedics strongly preferred.
Medical Device/GMP experience required.
Bachelor&rsquo;s Degree in Engineering required.

 
Skills, Abilities, Competencies Required:

Excellent written and verbal communication skills.
Understanding of ISO 13485 and QSR regulations.
Able to work accurately in medical device regulated environment with strong attention to detail.
Experience with ISO Class 7 cleanrooms, or equivalent.
Demonstrated ability to monitor own work to ensure quality, accuracy, and thoroughness.
Strong organizational, analytical, and time-management skills.
Able to self-motivate and work both independently and as part of a team.
Knowledge of statistical analysis.
Knowledge of computer added design (SolidWorks preferred).
Knowledge of C++, C#, and/or python programming language is a plus.]]></description>
      <pubDate>Mon, 13 Apr 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Additive Manufacturing Technician - Wilmington, MA]]></title>
      <link>http://j.brt.mv/jb.do?reqGK=27774631&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>dcac2de4-5455-422d-95ec-29659f7bb2b4</guid>
      <description><![CDATA[Job Summary
Temporary position through end of 2026 with potential to extend.
The Additive Manufacturing Technician will be responsible for the manufacturing and processing of restor3d jig components, as well as the handling and processing of nylon powder in accordance with engineering. 
Shift &ndash; Mon &ndash; Fri, 8:00 am &ndash; 4:30 pm
Essential Duties and Responsibilities:
&middot;      Prioritize and plan work activities; adapt for changing conditions.
&middot;      Execute daily start-up activities.
&middot;      Perform machine set-ups and turnovers; load and unload machines as required.
&middot;      Perform inspection of blended powder and components as required.
&middot;      Strict adherence to Good Documentation Practices when executing all assignments.
&middot;      Assist in performing required process capability studies, machine validation and process validation.
&middot;      Comply with all company policies and procedures including safety regulations, personal protective equipment requirements, Standard Operating Procedures, Work Instructions, and Good Manufacturing Procedures.
&middot;      Responsible for upkeep of manufacturing areas and provide a clean and safe work environment.
&middot;      Other duties as assigned.
 
Qualifications:
&middot;      High School Diploma, GED, or equivalent work experience.
&middot;      Prior experience working in a regulated environment preferred. 
&middot;      Familiarity with SAP (or equivalent) ERP systems and Microsoft Office Applications.
&middot;      Excellent verbal and written communication.
&middot;      Demonstrated English reading and writing skills.
&middot;      Ability to understand and follow comprehensive work instructions and guidance documents
&middot;      Demonstrated ability to be a team player and work well with others.
&middot;      Ability to work with team members to plan workload, set goals, and achieve team goals on a daily basis.
&middot;      Able to self-motivate and work both independently and as part of a team.
&middot;      Able to work accurately in a fast-paced, ever-changing environment with strong attention to detail.
&middot;      Demonstrated ability to monitor own work to ensure quality, accuracy, and thoroughness.
&middot;      Flexible to work overtime, extended hours, and weekends as business demands.
&middot;      Ability to receive and follow instructions and communicate with co-workers.
 
Working conditions:
&middot;      Ability to physically stand, bend, squat, and lift up to 40 pounds.
&middot;      Capable of working in material blending area with necessary personal safety equipment (eye protection, dust masks).
&middot;      Must be aware of hazards within the company; adhere to quality and safety standards established by FDA and other regulatory agencies.
&middot;      Able to work in changing environments (reduced lighting, increased noise, temperature variances, unpleasant odors, dust, etc.).]]></description>
      <pubDate>Tue, 31 Mar 2026 00:00:00 EDT</pubDate>
    </item>
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