Equipment Validation Engineer - On‑Site Medical Devices
TRIPLECOM
Start your journey of growth and success with us, making your mark and creating a lasting impact on your career. At TRIPLECOM, we believe that our success is driven by the talent, dedication, and passion of our team members. We are always on the lookout for exceptional individuals who share our vision and are eager to make a positive impact in the industry we operate in. Working at TRIPLECOM means being part of a dynamic and innovative team that is committed to excellence. We foster a collaborative and inclusive work environment that values diversity and encourages personal and professional growth. As a member of our team, you will have the opportunity to work on exciting projects and contribute to cutting‑edge advancements in industry. We believe in providing our employees with the tools, resources, and support they need to thrive and succeed. Your ideas and contributions will be valued, and you will have the autonomy to make a meaningful difference. At TRIPLECOM, we are committed to fostering a culture of continuous learning and development. We provide ongoing training opportunities, mentorship programs, and access to the latest industry trends and technologies. We believe in empowering our employees to reach their full potential and achieve their career goals. If you are a talented professional with expertise in the respective fields and a passion for creating innovative solutions, we invite you to apply for these exciting positions. Join our dynamic team at TRIPLECOM as we strive to make a significant impact in the industry with new technology and services. If you are passionate and want to be part of a dynamic team that is making a difference, we invite you to explore our current career opportunities. Whether you are an experienced professional or just starting your career journey, we have positions that may be the perfect fit for you. Job Listing Azure Data Engineer – Eatontown, NJ Build Data Ingestion Pipelines for Data Migration using Azure Data Factory or Synapse Pipelines to orchestrate migration from various sources to a target location. Perform ETL or ELT based on data requirements. Sources include Relational Databases such as Oracle, MS SQL Server, PostgreSQL or files (CSV, JSON, XML) and REST APIs. Build a Data Warehouse Solution on Microsoft Fabric Platform and migrate all objects and data. Choose a Synapse Distribution Strategy based on tables categorized as facts or dimensions. Build processes to support both batch and streaming data using Synapse Real Time Analytics for streams and ADF for batch loads. Build data processing flows (ad‑hoc processes) to ensure data validation across systems, data quality, and data governance for proper access. Build reports and dashboards for business insights, KPIs and performance reporting. Work with cross‑platform teams, Data Architects, Technical Managers and stakeholders. Support downstream applications. Resolve production issues. Gather updated requirements, design, develop, and deploy solutions recursively under the supervision of architects or technical managers. Qualifications: Bachelor’s Degree required in Computer Science, Computer Engineering, Information Technology or a related field. Database Administrator – Eatontown, NJ Lead data migration activities including mapping, transformation and validation in Oracle Fusion Cloud. Provide techno‑functional support for Oracle Fusion applications, addressing both technical configurations and business process requirements. Design and build custom reports using Oracle BI Publisher, OTBI and other reporting tools. Integrate Oracle Fusion with other systems using Oracle Integration Cloud or other middleware. Gather, analyze and document requirements. Conduct UAT, data validation and system testing. Maintain documentation of data conversion processes, configuration settings and reporting standards. Other related duties as assigned. Bachelor’s Degree required in Computer Science, Applied Computer Science, Information Technology or Information Systems. Systems Engineer – Eatontown, NJ Design and develop solutions to complex application problems, system administration issues, or network concerns. Develop BI solutions using Microsoft Power Platform (Power BI, Power Apps, Power Automate). Develop Azure‑based reports, dataflows, dashboards and datasets. Assist in systems planning, business information analysis and process improvement initiatives. Automate report deployment to SharePoint using PowerShell. Debug and resolve data warehousing issues ensuring compliance with data quality standards. Develop and implement data security protocols. Perform systems management and provide technical leadership in fully integrated technology solutions. Document and communicate technical details and test procedures. Develop reusable components and services. Conduct data analysis to translate business needs into optimized database designs. Plan, test, integrate, deploy and sustain technical solutions. Establish metadata management covering unified data catalog, lineage and classification. Process reports and monitor system performance. Maintain excellent communication and vendor experience. Proficient in SDLC, Agile, DevOps and QA lifecycle. Implement data quality procedures and validation. Establish and document quality control procedures. Manage schedules, processing and distribution of reports. Troubleshoot systems and applications. Ensure compliance with regulatory reporting requirements such as GDPR and CCPA. Implement AI tools such as Copilot into BI and governance. Bachelor's Degree required in Computer Science, Computer Engineering, Computer Information Systems or Applied Computer Science. Quality Assurance Engineer – Eatontown, NJ Establish and maintain a master validation program, including site and individual product and process master validations. Create, review, support validation protocols and reports to aid process and reliability improvements. Support complaint handling program including analysis, investigation and follow‑up. Lead or support reliability and process improvement projects from a quality perspective. Establish and maintain process controls and SPC for specific production processes. Support corrective and preventive action (CAPA) program. Review and modify product designs and process documentation for quality characteristics such as manufacturability, serviceability, testability, reliability and conformance to product and quality system requirements. Demonstrate product compliance for sterilization, biocompatibility, package integrity, shelf life, reliability and electrical safety. Review and provide feedback on protocols and reports, vendor qualification and testing management. Assist with development and maintenance of product risk management files. Recommend requirements for first article inspection, incoming and in‑process inspections, and lot release testing, including sampling strategy and test methods. Participate in failure investigations to analyze internal system or process failures and implement corrective and preventive action. Participate in component and service new supplier evaluation and ensure appropriate quality controls by suppliers. Audit Design History Files and resolve documentation issues with cross‑functional teams. Identify and implement good quality engineering practices, including statistical methods and root cause analysis tools. Participate in supplier material‑related processes including coordination of MRB activities. Support continuous product and process improvement through detailed failure analysis for non‑conformances and implement effective, compliant solutions. Demonstrate the ability to implement ISO 14971 and other risk evaluation techniques. Equipment Validation Engineer – Norwood, MA Work will be 100% on‑site. Responsibilities include re‑qualification and re‑validation of equipment, IQ, OQ and PQ process support, protocol writing, protocol reporting, and execution. Must be well‑versed in IQ, OQ, and PQ, and have medical device experience; catheter experience is a plus. Duration: 3‑4 months contract. Interview: telephonic and Webex. Contractor Engineer – Pleasanton, CA Project work for combination medical devices. Activities include contributing to product design documentation, conducting laboratory studies of product performance, and supporting product development, manufacturing transfers, investigations and product enhancements. Work conducted in compliance with device design controls (FDA 21CFR820.30 and/or ISO 13485). Requires mechanical design and drawing proficiency, CAD (Creo or SolidWorks), and plastic design experience. Preference for candidates with Masters and mechanical engineering background. Responsibilities include CAD data model generation, prototype building, laboratory work, data analysis, and reporting. Compliance with regulatory reporting requirements including GDPR and CCPA. The role is a six‑month contract. Qualifications: Bachelor's Degree or equivalent in Mechanical or related field with 5+ years of experience. Other Skills: CAD experience (Creo or SolidWorks) and plastic design. Tolerance analysis, product design prototyping and testing experience. #J-18808-Ljbffr TRIPLECOM
- ...Syner-G is seeking a Validation Engineer to assist with the development and... ..., utilities, systems, equipment, and processes for (re)qualification... ...or manufacturing site issues. Execute periodic reviews... ...biotech, pharmaceutical, or medical device industry. Knowledge and...WebsiteMedical deviceWork at officeRemote workFlexible hours
- ...integrated architecture, engineering, construction, system... ...****Job Summary**The Validation Engineer III will... ...support to ensure facility equipment, utilities, processes... ..., biotechnology, or medical device manufacturing... ...Working Conditions* On-site presence required; may...WebsiteMedical deviceFor contractorsWork at office
- ...commissioning and qualification of process equipment such as centrifuges, filter presses,... ...job walks at the construction site with engineering teams to monitor progress and compliance... ...Press, Centrifuge, and Cleaning Validation as needed. Maintain high safety standards...WebsiteLocal areaFlexible hours
- ...production line of various medical devices as required by clients. Requires... ...work As required, work with Engineering personnel to assist and develop process and equipment validation/qualification plans and... ...have transportation to work on-site in Mansfield, MA. Desired...WebsiteMedical deviceHourly payLocal areaMonday to FridayDay shift
- ...OVERVIEW: Syner-G is seeking a Validation Engineer to assist with the... ...facilities, utilities, systems, equipment, and processes for (re)... ...observations or manufacturing site issues. Execute periodic... ..., pharmaceutical, or medical device industry. ~ Knowledge and...WebsiteMedical deviceWork at officeRemote workWork visaFlexible hours
$109.25k - $149.5k
Summary The Staff Engineer, Quality is responsible for providing... ...), Process/Test Method/Equipment Validations, Deviations, Control of Nonconforming... ...experience in a regulated medical device, life sciences, or pharma... ...veteran status. This site is governed solely by applicable...WebsiteMedical deviceTemporary work$94.3k - $129.95k
...the following areas of validation and be considered a... ...read and understand engineering P&ID’s and turnover documentation... ...qualification, equipment qualification,... ...Assurance role for a medical device or pharmaceutical environment... ...veteran status.This site is governed solely by...WebsiteMedical deviceContract workTemporary work$65k - $75k
...teams including Manufacturing, Engineering, R&D, and Quality to ensure... ...material priorities with site representatives from Manufacturing... ...regulatory requirements and validates the labels. Continually... ...we are looking for in you Medical device or regulated industry experience...WebsiteMedical deviceWork at officeImmediate startFlexible hours- ...existing). Authoring and reviewing Equipment Requirements Specifications. Document... ...~ A minimum of bachelor's degree in engineering or Technical field ~3+ years of prior... .... ~ Regulated industry experience, medical device or pharmaceutical experience preferred...Medical device
$25 per hour
...scientific, administrative role consisting of medical research and file maintenance. There is a... ...Consultant serving clients with medical devices, drugs and or biologics. Numerous ongoing... ...desirable. All work to be performed on site. Ideal candidate has strong attention to...WebsiteMedical devicePermanent employmentTemporary workWork at office$85k - $100k
Validation & Engineering Group, Inc. (V&EG) is a leading service supplier that... ..., Chemical, Food, and Medical Devices industries in Laboratory,... ...biotechnology manufacturing site in Norwood, MA. This role... ...activities for utilities, equipment, automation, and process systems...WebsiteMedical deviceFull timeFor contractors- ...Senior Manufacturing Engineer for an exciting and growing... ...taking complex medical device products from development... ...including embedded on-site work during critical builds... ..., with controls and validation rigor commensurate... ...procedures, change orders, equipment specifications, pFMEAs...WebsiteMedical devicePermanent employmentFull timeContract workWork at office
- Real Staffing in Boston is seeking a Software Verification & Validation Engineer for a critical Tool Validation Project within a leading medical device organization. This high-impact role involves leading validation activities for over 100 tools, ensuring compliance within...Medical deviceRemote work
- Integra LifeSciences Corporation in Braintree, MA is hiring a Senior Engineer II for Quality Validation. The role focuses on leading validation projects ensuring compliance with cGMP and managing cross-functional team interactions. Successful candidates will have a Bachelor...Medical device
$72.8k - $80.1k
...verification) Develop summary reports at client sites 2. Areas of Focus Pharmaceutical facilities Utilities Equipment 3. Project & Team Management Plan... ...- Bachelor's degree in a science or engineering field (or equivalent experience) - 0 - 4...WebsiteWorldwide$137k - $235.75k
Senior Robotics Verification & Validation (V&V) Engineering Manager Locations: Raynham, MA; Boston... ...master system test plans for complex medical devices, including system verification... ...test lab facilities, ensuring all equipment and infrastructure are properly calibrated...Medical deviceLocal areaImmediate start- ...Incorporated in Boston is seeking a Product Development Engineering Scientist focused on combination product development... ..., with at least 2 years of experience in the medical device sector. The position is on-site with additional benefits including bonuses and educational...WebsiteMedical device
- ...(US) is seeking a Product Development Engineering Scientist to focus on combination product... ...should have a solid background in medical device development, risk management, and a degree... ...comprehensive benefits and is primarily on-site, with some flexibility. #J-18808-...WebsiteMedical device
- Redbock - an NES Fircroft company is seeking a Senior Medical Device Engineer in Boston, Massachusetts. This role focuses on developing drug delivery... ...controls, and proficiency with SolidWorks. This is an on-site position, collaborating with cross-functional teams to...WebsiteMedical device
- ...Overview: The Manufacturing Engineer will work with other personnel to... ...and Line Layouts, Process Routers, Equipment Qualification and Process Validation Protocols, Standard Operation Procedures... ...: • 5 to 8 years of medical device manufacturing experience. • Knowledge...Medical deviceTemporary workWork at office
$28.7 per hour
...specifications and usage, and make medical device deliveries. Inspect... ...and maintain supplies, tools, equipment, and storage areas to ensure... ...Deliver equipment to customer sites and arrange merchandise for transport... ...work experience Possess a valid driver's license with no...WebsiteMedical deviceHourly payWork experience placementFlexible hoursDay shiftAfternoon shift- ...servicing Boston Scientific medical systems and devices. This is a hands-on,... ...to support optimal equipment performance, user... ...: Provide on-site service including... ...Electronics, Biomedical Engineering, Life Sciences, or a... ...supervision ~ Valid driver's license, clean...WebsiteMedical deviceWork experience placementWork at officeRemote work
$145.6k - $218.4k
...establishment of new research sites in Boston and Providence... ...possible. As the Product Lifecycle Engineering Principal Scientist, you will... ...activity with drug delivery devices and combination products. You... ...for commercialized medical devices and drug delivery combination...WebsiteMedical deviceSummer workFlexible hours- A leading life sciences company based in Boston is seeking a Life Science Engineer III to oversee calibration and validation processes in compliance with GxP and ISO standards. This role requires extensive experience in chromatography systems and involves mentoring staff...
$32.59 - $42.67 per hour
...Biomedical Equipment Engineer I MA-Boston - Boston, MA Overview Salary... ...portfolio includes: On-site technical field support and... ..., specialized, and high-tech medical equipment and systems. Utilize... ...Requirements Valid driver's license in good standing...WebsiteHourly payFull timeRemote work- A leading medical device firm in Massachusetts is seeking candidates for a role focused on coordinating... ...the remediation work at their site. The position requires extensive... ...Candidates should have a BS in science or engineering along with 5-7 years of relevant experience...WebsiteMedical device
- ...archival: design CRFs/eCRFs, create Data Validation Specifications, Data Management Plans,... ...the clinical team and partnering sites with professional demeanor Make decisions... ...for clinical development programs with medical devices leading toward FDA filing / approvals...WebsiteMedical device
$78k - $117k
...bringing innovative medical devices to life? Join our Global... ...Manufacturing Engineering team and play a critical... ...processes, including equipment specification, acquisition... ...global manufacturing sites to achieve project... ...executing and documenting validation activities, including...WebsiteMedical deviceFlexible hours- NextPhase Medical Devices LLC is hiring a Production Supervisor in Mansfield, MA. In this role, you will oversee production assembly tasks to ensure quality and schedule adherence while mentoring a high-performing team. The ideal candidate has over 5 years of experience...WebsiteMedical device
$96.75k - $145k
Senior Design Quality Engineer - Mansfield, MA We are seeking a Senior... ..., including test method validation, measurement systems... ...cross‑functional and multi‑site collaboration. Provide training... ...experience in the pharmaceutical/medical device industry or a related regulated...WebsiteMedical device
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