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    <title>restor3d Jobs</title>
    <link>http://portal.brightmove.com/CompanyPortal.do?companyGK=50693&amp;portalGK=41164</link>
    <description><![CDATA[Job Postings available for application.]]></description>
    <language>en-us</language>
    <pubDate>Tue, 21 Apr 2026 00:00:05 EDT</pubDate>
    <lastBuildDate>Tue, 21 Apr 2026 00:00:05 EDT</lastBuildDate>
    <generator>BrightMove ATS</generator>
    <item>
      <title><![CDATA[Manufacturing Engineer II - Wilmington, MA]]></title>
      <link>http://portal.brightmove.com/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[Metals Post Processing Technician, 2nd Shift - Durham, NC]]></title>
      <link>http://portal.brightmove.com/jb.do?reqGK=27774640&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>910b641f-4304-4e8c-99cf-7d1282e21468</guid>
      <description><![CDATA[Job overview
The Manufacturing technician will be responsible for production and post-processing of medical devices. Common secondary processes include deburring, Mirror Polishing, media blasting, filing, cleaning, and packaging.

Monday - Friday, 2:00 pm - 10:30 pm

Duties and responsibilities

Perform production activities for equipment set-up/line clearance, processing, labeling, and record completion while following quality system guidelines and Good Manufacturing Practices (GMP)
Support equipment maintenance activities as needed
Participate in continuous improvement projects
Perform inspections for components and product at all stages of manufacturing process
Compliance to safety (OSHA), GMP, GDP, GLP and 21 CFR 820.


Qualifications and experience

High school diploma or GED required
Associates or post-secondary education preferred
Experience in the use Rotary tools, Die Grinders, is required
Experience in the use of basic machine shop tools and equipment is required
Mechanically inclined
Working knowledge of GMP, GLP, and GDP is required
Strong verbal and written communication
Experience in FDA 21 CFR 820 Quality system is preferred
Tools and Equipment


Position may involve the use of:

Basic hand tools
Rotary tools
Media blasting cabinet
Cleaning and inspection equipment
Sealing and packaging equipment
Respirator, protective clothing, eye protection, and hearing protection


Materials Handling/Exposure

Position may involve handling of or exposure to metallic powders and other powered materials, mill coolant, tapping fluid, polymeric resins, cleaning solutions, inert gases, and acids.
Position requires the ability to intermittently lift and carry up to 50 pounds
PPE including eye protection, hearing protection, and gowning required depending on task performed
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


Working Conditions

Working conditions include standard conditions of a machine shop. Machine shop conditions may include noise, dust, and temperature extremes.
Working conditions may also include working in a clean room environment. Clean room environment will require wearing PPE &ndash; Gown, hair net, shoe covers and nitrile gloves.]]></description>
      <pubDate>Tue, 31 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Additive Manufacturing Technician - Wilmington, MA]]></title>
      <link>http://portal.brightmove.com/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>
    <item>
      <title><![CDATA[Manufacturing Technician, Clean and Pack, 2nd Shift - Durham, NC]]></title>
      <link>http://portal.brightmove.com/jb.do?reqGK=27774536&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>4a0ada73-4322-4fe7-9377-b13cc5f7ca72</guid>
      <description><![CDATA[Job Summary:
The Manufacturing Technician position is responsible for operating production equipment in a productive manner while maintaining a high level of quality in the manufacturing of restor3d implants and components.
2nd Shift - Monday - Fri, 2:00 pm - 10:30 pm

Essential Duties and Responsibilities:

Develop and maintain strong, internal working relationships across restor3d.
Understand the objectives, responsibilities, and mission of the Manufacturing department and works towards those goals.
Prioritize and plan work activities; adapt for changing conditions.
Execute daily maintenance and start-up activities.
Perform machine set-ups.
Operate machinery and processing equipment, including but not limited to clean line and pouch sealers, Perform inspection of components and assembly as required.
Perform cleaning, pouching/sealing and labeling
Strict adherence to Good Documentation Practices when executing all assignments.
Perform timely and accurate transactions of workflow in ERP system.
Participate in inventory cycle counts, variance investigation and reconciliation.
Assist in the investigation and implementation of corrective actions on product and process failures.
Comply with all company policies and procedures including safety regulations, personal protective equipment requirements, Standard Operating Procedures, Work Instructions and Good Manufacturing Procedures.
Responsible for upkeep of manufacturing areas and provide a clean and safe work environment.
Review all manufacturing documentation, assembly, inspection, test, packaging procedures and provide feedback.
Other duties as assigned.

Qualifications:

High School Diploma, GED, or equivalent work experience; work experience in a medical device and/or regulated environment preferred
Familiarity with Oracle (or equivalent) ERP systems and Microsoft Office Applications
Familiar with ISO Standards and Good Manufacturing Practices
Good verbal and written communication
Demonstrated English reading and writing skills
Shipping/receiving/stockroom experience a plus.

Skills, Abilities, Competencies Required:

Good written and verbal communication skills.
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.
Manual dexterity to handle tools, inspection gauges and equipment of different sizes.
Demonstrated organizational skills.
Ability to work in a fast-paced environment and multitask. Comfortable with change.
Ability to work as part of a team as well as independently.

Working conditions:

Ability to lift, pull and push up to 40 lbs
Ability to stand for prolonged periods of time
Ability to work in a Class 10,000 or ISO class VII clean room environment for prolonged periods of time
Busy work environment with frequent interruptions
Flexible to work overtime, extended hours and weekends as business demands
Must be aware of hazards within the company; adhere to quality and safety standards established by FDA and other regulatory agencies
Able to work in changing environments (reduced lighting, increased noise, temperature variances, unpleasant odors, dust etc.).]]></description>
      <pubDate>Mon, 30 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Quality Inspector, 2nd shift - Wilmington, MA]]></title>
      <link>http://portal.brightmove.com/jb.do?reqGK=27773682&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>851a61c0-0de7-4361-bc8f-80a07a10a525</guid>
      <description><![CDATA[Job Summary:
The Quality Inspector will be responsible for quality inspection/quality assurance activities. This includes interpretation and implementation of quality standards to routine inspection/testing and manufacturing activities. This individual will be focused on receiving inspections and would ideally have some exposure to supplier receiving, conformance reviews, sampling plans, and communicating with vendors.
Shift: 2nd Shift (3pm - 11:30pm)
Duties and responsibilities:
&middot;         Understand the objectives, responsibilities, and mission of the Quality Control department and work towards those goals.
&middot;         Ability to read and interpret prints and apply Geometric Dimensioning and Tolerancing (GD&T) as defined on the print.
&middot;         Inspect incoming, in-process, finished parts, and materials for conformance to quality control standards.
&middot;         Must be able to perform 100% inspections of non-conformance reports (NCR&rsquo;s).
&middot;         Other responsibilities as assigned.
Qualifications and experience:
&middot;         High School Diploma, GED, or equivalent work experience.
&middot;         3+ years&rsquo; experience performing inspection within an FDA or other regulated environment.
&middot;         Proficient in the use of hand measuring tools such as calipers, micrometers, dial indicators, etc.
&middot;         Ability to read and interpret engineering drawings
&middot;        Working knowledge of optical comparators and CMM for inspection.
&middot;         Understanding of calibration requirements for inspection equipment.
Skills:
&middot;         SAP experience a plus.
&middot;         GD&T certification a plus.
&middot;         Advanced metrology experience a plus.
&middot;         Contribute towards continuous improvement with regards to Quality, efficiency, and customer focused results.
&middot;         Proficient in the use of hand measuring tools such as calipers, micrometers, dial indicators, etc.
&middot;         Willingness and ability to embrace new inspection tools and methodologies.]]></description>
      <pubDate>Tue, 17 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Poly Post Processing Tech, 2nd shift - Wilmington, MA]]></title>
      <link>http://portal.brightmove.com/jb.do?reqGK=27772900&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>5aaf5020-97cb-45c4-96da-3829e030283e</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, surface finishing, and maintenance on desktop auxiliary machines.
Essential Duties and Responsibilities:

Develop and maintain strong internal working relationships across restor3d.
Understand the objectives, responsibilities, and mission of the Polymers Additive Manufacturing department and work towards those goals.
Prioritize and plan work activities; adapt for changing conditions
Full operation of part washing and UV curing machines for polymer parts. Includes machine load and unload, operation, maintenance, general upkeep and troubleshooting.
Using various tools for polymer model finishing. Includes support removal and surface sanding as needed.
Following appropriate safety precautions, including usage of PPE and maintaining lab cleanliness.
Visual inspection of manufactured goods as part of quality-controlled processes.
Perform production activities for equipment set-up/line clearance, processing, labeling, and record completion while following quality system guidelines and Good Manufacturing Practices (GMP).
Participate in continuous improvement projects.
Compliance to safety (OSHA), GMP, GDP, GLP and 21 CFR 820.
Performs other duties as assigned.

Qualifications:

High school diploma or GED required
Associates or post-secondary education preferred
Experience in the use of basic machine shop tools and equipment is preferred
Mechanically inclined
Working knowledge of GMP, GLP, and GDP is preferred
Strong verbal and written communication
Experience in FDA 21 CFR 820 Quality system is preferred

Skills, Abilities, Competencies Required:

Excellent written and verbal communication skills.
Able to work accurately in a fast-paced, hectic, ever-changing 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.
Position requires the ability to intermittently lift and carry up to 50 pounds
PPE including eye protection, hearing protection, and gowning required depending on task performed
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>Fri, 06 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Quality Control - DHR Reviewer (Quality Technician) - Wilmington, MA]]></title>
      <link>http://portal.brightmove.com/jb.do?reqGK=27771388&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>5d27002c-5b80-46e5-951a-9ac1fd22757e</guid>
      <description><![CDATA[Job Summary:
The DHR Reviewer/ Inspector will be responsible for product quality assurance activities. This includes interpretation and implementation of quality standards to routine manufacturing and product release activities. 
 
Duties and responsibilities:
&middot;       Develop and maintain strong internal working relationships across restor3d. 
&middot;       Understand the objectives, responsibilities, and mission of the Sterility & Lot Release department and work towards those goals. 
&middot;       Prioritize and plan work activities; adapt for changing conditions. 
&middot;       Review labels for accuracy and precision. 
&middot;       Review of Device History Records to perform release of sub-assemblies and finished goods. 
&middot;       Inspect finished parts, and materials for conformance to quality control standards. 
&middot;       Initiate and participate in resolution of non-conforming materials. 
&middot;       Responsible for final product release sign-off. 
&middot;       Other responsibilities as assigned. 
&middot;       Qualifications and experience 
 
Qualifications and Experience:
&middot;       Excellent written and verbal 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 be self-motivated and work both independently and as part of a team. 
&middot;       Must be able to work in a team environment, execute responsibilities with minimal direct supervision, and have high attention to detail. 
&middot;       Knowledge of FDA and ISO standards for Medical Devices is a plus. 
&middot;       Ability to multi-task, perform efficiently, and independently.]]></description>
      <pubDate>Fri, 13 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Customer Support Specialist - Wilmington, MA]]></title>
      <link>http://portal.brightmove.com/jb.do?reqGK=27770547&amp;companyGK=50693&amp;portalGK=41164</link>
      <guid>ef8272f3-7058-457b-ada0-909fbd33da39</guid>
      <description><![CDATA[Job Summary:
The Customer Support Specialist is responsible for providing effective customer support across all aspects of the business for both internal and external customers by using excellent, in-depth knowledge of company products, programs and systems.  This role will work closely with Sales, Product Marketing, Planning and Quality teams.
Essential Duties and Responsibilities:

Develop and maintain strong internal working relationships across Restor3d.
Understand the objectives, responsibilities, and mission of the Customer Support and Sales departments and work towards those goals.
Provide timely and accurate information to incoming customer order status and product knowledge requests.
Professionally handle incoming requests from customers and ensure that issues are resolved both promptly and thoroughly.
Verify customer, image, and patient records to ensure the information is current and accurate.
Track and meet the deadlines for incoming requests and existing orders requiring further resolution.
Manage the processing of various sales orders types.
Coordinate field inventory requests via Oracle and within the Millstone vendor portal. Monitor field inventory returns, including excess, damaged, expired or soon to expire items on a monthly basis and arrange for the return or destruction of that product according to active SOPs.
Continuously evaluate and identify opportunities to drive process improvements that positively impact the customer&rsquo;s experience
Support Customer Support and Sales teams in assigned project-based work
Other responsibilities as assigned.

 Qualifications:

Associates degree in Business Administration or related field is preferred.
3+ years work experience in one of the following areas is required: Customer Service, Medical office/field, Medical device or pharmaceutical experience. 
Advanced computer skills including Microsoft Office: Word, Outlook, Excel and Teams
Ability to analyze and review data, provide reports as needed.
Ability to solve complex problems within an established protocol of procedures and determine possible solutions.
Experience in database entry, CRM or other prospect tracking systems strongly desired e.g. Oracle, SAP, PACS, Agile).
Excellent telephone etiquette skills. 

Skills, Abilities, Competencies Required:

Excellent written and verbal communication skills.
Able to work accurately in a fast-paced, hectic, ever-changing environment with strong attention to detail.
Demonstrated ability to monitor own work to ensure quality, accuracy, and thoroughness.
Able to self-motivate and work both independently and as part of a team.
Ability to interact effectively with a large number of individuals both within and outside the organization.
Knowledge of customer services practices.
Exceptional time management, analytical and organizational skills, ability to prioritize work, meet deadlines and work under pressure.
Ability to manage and develop organized systems for filing, communications, and follow-up.
Ability to manage multiple, simultaneous projects and priorities effectively.
Ability to sense urgency and respond accordingly.
Use of discretion in confidential matters.
Flexibility and ability to adapt to changing pace and environment with frequent interruptions.
Willingness to learn needed skills on the job in order to enhance performance.]]></description>
      <pubDate>Mon, 02 Feb 2026 00:00:00 EST</pubDate>
    </item>
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