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<h3>Job Description</h3>
Job Description
Join a leading healthcare technology service provider as an Imaging Engineer supporting a critical client site in the Wauseon, OH area. This is a full-day, on-site position with the flexibility of starting your day from home before heading to the client location. Ideal for professionals passionate about maintaining and servicing diagnostic imaging equipment in a high-impact healthcare setting.
APPY NOW!!
Key Responsibilities:
<ul>
<li>
Troubleshoot, calibrate, and repair a wide range of imaging equipment including X-ray, CT, MRI, ultrasound, and mammography systems.
</li>
<li>
Perform preventive maintenance and electrical safety checks on imaging and biomedical devices.
</li>
<li>
Provide technical support and guidance to clinical staff on equipment use and best practices.
</li>
<li>
Ensure all documentation, compliance standards, and customer service benchmarks are consistently met.
</li>
</ul>
Qualifications:
<ul>
<li>
Hands-on experience with general radiography, fluoroscopy, portable units, X-Ray, CT, MRI and C-Arms is required.
</li>
<li>
Associate degree in Biomedical Technology or a related technical field preferred.
</li>
<li>
CBET certification a plus.
</li>
<li>
Strong communication, problem-solving, and customer service skills essential for success in a hospital environment.
</li>
</ul>
Location: Remote Field Role – Report daily to a client site in Wauseon, OH Schedule: Full-time, Day Shift M-F Hourly Rate: $40.86 - $63.99/hr (Depending on Experience) Benefits: Comprehensive benefits package available
APPLY NOW!!
 Pay Details: $40.86 to $63.99 per hour Search managed by: Deanna Murphy Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://www.lhh.com/us/en/candidate-privacy" target="_blank">https://www.lhh.com/us/en/candidate-privacy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>

Imaging Engineer

<h3>Job Description</h3>
Job DescriptionOur client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a “Process Development Engineer” in Santa Clara, CA Duration: Longterm Contract with possible Full Time Conversion Description 
The Process Development Engineer provides technical and operational support for consumable and cartridge manufacturing, bridging new product implementation with process optimization to ensure compliance, quality, and manufacturing robustness. Responsibilities include process troubleshooting, validation (IQ/OQ/PQ), process characterization, in-process controls (CTQs/IPCs), root cause investigations, statistical analysis (DOE/SPC), and continuous improvement initiatives using Lean Six Sigma. The role requires strong collaboration in a GMP/ISO 13485 regulated environment, authorship of technical documentation (ERP/SAP), and participation in audits, CAPAs, and technology transfer from R&amp;D to operations. 
Qualifications: 
<ul>
<li>
Bachelor’s or higher in Biomedical, Chemical, Mechanical Engineering, or related discipline 
</li>
<li>
Minimum 5 years’ experience in medical device, IVD, or regulated manufacturing 
</li>
<li>
Hands-on experience with process validation, technology transfer, and manufacturing support 
</li>
<li>
Proficiency in DOE, SPC, and statistical tools (JMP, Minitab) 
</li>
<li>
Familiarity with GMP, ISO 13485, FDA QSR (21 CFR 820) compliance 
</li>
<li>
Experience with microfluidics, surface chemistry, reagent formulation, cleanroom operations, or automated liquid handling (preferred) 
</li>
<li>
Lean Six Sigma Green Belt certification (preferred) 
</li>
</ul>
 Please respond with your updated resume and contact information to <a href="mailto:hr@dawarconsulting.com" target="_blank">hr@dawarconsulting.com</a>/<a href="mailto:kavitha@dawarconsulting.com" target="_blank">kavitha@dawarconsulting.com</a>

Process Development Engineer

<h3>Job Description</h3>
Job DescriptionJob Summary
We are seeking a hands-on Quality Engineer to join our team. This role is crucial for ensuring the highest quality, safety, and effectiveness of our medical devices. You will be instrumental in both executing key quality tasks and supporting the continuous development and adherence to our Quality Management System (QMS). This is an exciting opportunity to directly impact product quality and regulatory compliance in a growing, innovative company.
Responsibilities
<ul>
<li>Contribute to the development, implementation, and maintenance of our Quality Management System (QMS) and associated standards.</li>
<li>Plan and execute incoming inspections for components and materials.</li>
<li>Support and optimize production line testing of our devices to ensure consistent quality.</li>
<li>Actively support design and development activities, including design reviews, verification, validation, and maintaining the Design History File (DHF) for both new and existing products.</li>
<li>Participate in risk analysis and management activities in accordance with ISO 14971, ensuring product safety throughout the lifecycle.</li>
<li>Investigate product complaints, reported quality issues, and nonconformities.</li>
<li>Drive root cause analysis and implement effective corrective and preventive action plans (CAPAs) to prevent recurrence.</li>
<li>Support supplier qualification, monitoring, and corrective actions to ensure the quality of supplied components and services.</li>
<li>Develop, review, and approve essential QMS documentation, including SOPs, work instructions, test plans, protocols, and reports.</li>
<li>Ensure strict adherence to medical device regulations such as FDA 21 CFR Part 820, ISO 13485, IEC 60601-1, IEC 62304. Provide quality support for regulatory submissions, including 510(k) activities.</li>
<li>Prepare and maintain documentation to ensure audit readiness and support internal and external audits.</li>
<li>Identify and implement opportunities for process improvement within the QMS and across the product development and manufacturing lifecycles.</li>
<li>Work closely with R&amp;D, Engineering, Manufacturing, and Regulatory Affairs teams, serving as a hands-on quality resource to integrate quality requirements effectively.</li>
</ul>
Qualifications
<ul>
<li>Bachelor's degree in Biomedical Engineering, Electrical Engineering, Mechanical Engineering, or a related scientific discipline.</li>
<li>5+ years of direct experience as a Quality Engineer in the medical device industry.</li>
<li>Proven hands-on experience in developing and implementing quality systems and standards.</li>
<li>Solid understanding and practical experience with medical device regulations and standards, including FDA 21 CFR Part 820, ISO 13485, IEC 60601-1, IEC 62304, and IEC 60601-2-37.</li>
<li>Demonstrated experience in planning and executing incoming inspections and production line testing of products/components.</li>
<li>Experience investigating product complaints, quality issues, and nonconformities.</li>
<li>Track record of developing and implementing corrective and preventive action plans (CAPAs).</li>
<li>Familiarity with Design Controls, Risk Management (ISO 14971), and supporting regulatory submissions (e.g., 510(k)).</li>
<li>Experience with electronic Quality Management Systems.</li>
<li>Strong analytical, problem-solving, and critical thinking skills.</li>
<li>Excellent communication skills, both written and verbal, for effective documentation and cross-functional collaboration.</li>
<li>Highly detail-oriented with the ability to manage multiple tasks in a dynamic, fast-paced startup environment.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with ultrasound devices.</li>
<li>Experience with Enzyme eQMS</li>
<li>ASQ Certified Quality Engineer (CQE) or other relevant quality certifications.</li>
<li>Direct experience supporting a medical device product through initial manufacturing scale-up and commercial launch.</li>
</ul>
 Job Posted by ApplicantPro

Quality Engineer

<h3>Job Description</h3>
Job DescriptionCareers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the United States. We're proud to offer many development and advancement opportunities to our nearly 50,000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footprint. Facility: Sanford Med Ctr Fargo Location: Fargo, ND Address: 5225 23rd Ave S, Fargo, ND 58104, USA Shift: Day Job Schedule: Full time Weekly Hours: 40.00 Salary Range: $34.50 - $57.00 Job Summary Provides advanced technical support to physicians, advanced practice providers, and clinical staff on clinical technologies. Provides expert planning for clinical technology expansion. The Lead Clinical Engineer is a key member of the perioperative services team, responsible for the oversight, integration, and optimization of advanced clinical technologies within the procedural environment. This role ensures the safe, effective, and efficient operation of complex systems including surgical navigation, robotic-assisted surgery platforms, integrated operating room systems, and patient monitoring technologies. The engineer serves as the primary technical expert and liaison between clinical staff, biomedical engineering, IT, and external service providers, ensuring that all perioperative technologies support optimal patient outcomes and clinical workflows. This position requires a deep understanding of electromechanical systems, software interfaces, and networked medical devices. The Lead Clinical Engineer will lead efforts in technology planning, acquisition, and implementation, contributing to capital equipment decisions and long-term strategic planning. They will be responsible for troubleshooting and resolving technical issues in real-time, including during surgical procedures, and will conduct root cause analyses for adverse events involving clinical technologies. The role also includes supporting preventive maintenance schedules, performing minor repairs, and coordinating emergency service responses when necessary. In addition to technical responsibilities, the Lead Clinical Engineer will develop and deliver training programs for clinical staff, ensuring safe and proficient use of surgical technologies. They will also play a critical role in policy development, compliance with regulatory standards, and continuous quality improvement initiatives. The ideal candidate will possess strong leadership, communication, and problem-solving skills, and will thrive in a fast-paced, high-stakes environment where collaboration and adaptability are essential. This role is embedded within the surgical services department and may require direct support during patient care activities. The Lead Clinical Engineer is expected to be a proactive innovator, continuously seeking opportunities to enhance the integration and performance of clinical technologies in support of surgical excellence. Qualifications Bachelor’s degree required or Master’s degree preferred in mechanical engineering, biomedical engineering, industrial engineering or a similar engineering or scientific background. Two years’ experience working with medical equipment, and background in equipment testing and quality control/quality assurance preferred. Professional Engineer (PE) license preferred. If PE license is not obtained, background experience or Master’s degree is highly preferred. Benefits Sanford Health offers an attractive benefits package for qualifying full-time and part-time employees. Depending on eligibility, a variety of benefits include health insurance, dental insurance, vision insurance, life insurance, a 401(k) retirement plan, work/life balance benefits, and a generous time off package to maintain a healthy home-work balance. For more information about Total Rewards, visit <a href="https://sanfordcareers.com/benefits" target="_blank">https://sanfordcareers.com/benefits</a> . Sanford is an EEO/AA Employer M/F/Disability/Vet. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-877-673-0854 or send an email to <a href="mailto:talent@sanfordhealth.org" target="_blank">talent@sanfordhealth.org</a> . Sanford Health has a Drug Free Workplace Policy. An accepted offer will require a drug screen and pre-employment background screening as a condition of employment. Req Number: R-0236058 Job Function: Allied Health Featured: No

Lead Clinical Engineer - Surgical Services

<h3>Job Description</h3>
Job DescriptionSalary: $72,000-$93,000 
Injectech, LLC has been a trusted supplier of fluid-control components for over 20 years. Our current senior management team has been with Injectech since the very beginning, bringing extensive knowledge of the medical device industry to every project.
 
Our Employees are important to us! We want the best for our employees, not just at work, but through all aspects of their life. That is why we pay 100% of the employees share of health insurance cost and match up to 6% for our 401k plan and provide free financial advice about retirement, debt, and any future financial needs from a licensed Financial Advisor. We strongly believe that the only way for our company to be successful is to make sure our employees have healthcare, mental healthcare, retirement options and financial education available to them.
 
We work hard to create a culture that promotes open lines of communication, a flexible work-life balance, continuous improvement in every department, and a place where employees want to be every day. We strive to hire and retain the best people, because we know a company is only as good as its employees. We hope you will join our team as we continue to grow and improve! 
Job Summary:
We are seeking a highly skilled and detail-oriented Medical Injection Molding Process Engineer to lead the development, optimization, and validation of injection molding processes used to manufacture precision medical components. This role is responsible for ensuring robust, repeatable, and compliant manufacturing processes that meet regulatory requirements (ISO 13485) and support high-volume production in a cleanroom environment. The Process Engineer will play a key role in new product introductions, continuous improvement initiatives, and troubleshooting activities.
 
General Duties (includes but not limited to):
<ul>
<li>Develop, optimize, and validate injection molding processes for new and existing medical products.</li>
<li>Lead mold and material trials, establish robust process windows, and conduct Design of Experiments (DOE) to optimize quality and efficiency.</li>
<li>Collaborate with R&amp;D, tooling, quality, and manufacturing teams during product development and commercialization.</li>
<li>Author and execute validation protocols (IQ, OQ, PQ) in compliance with ISO 13485 requirements.</li>
<li>Troubleshoot molding and tooling issues; implement root cause analysis and corrective actions (CAPA).</li>
<li>Evaluate and approve mold designs, materials, and process control plans to ensure manufacturability and scalability.</li>
<li>Specify and support installation of new injection molding machines, robotics, and auxiliary equipment.</li>
<li>Analyze process data using risk-based (e.g., PFMEA) and statistical methods (e.g., SPC, SixmaXL); maintain documentation of process settings and changes.</li>
<li>Drive continuous improvement initiatives focused on yield, cycle time, scrap reduction, and cost savings.</li>
<li>Train technicians and operators on molding best practices, process control, and cleanroom requirements.</li>
<li>Ensure compliance with cleanroom protocols and current Good Manufacturing Practices (cGMP).</li>
</ul>
 
Qualifications:
Education &amp; Experience:
<ul>
<li>Bachelors degree in Plastics Engineering, Mechanical/Industrial Engineering, Biomedical Engineering, or related field.</li>
<li>37 years of experience in injection molding process development, with a focus on medical device manufacturing.</li>
<li>Experience in a regulated cleanroom environment (ISO Class 7/8) and with medical-grade and engineering materials (e.g., PC, PA, ABS, Acrylic, PP).</li>
</ul>
Skills &amp; Competencies:
<ul>
<li>Deep knowledge of injection molding principles, mold design, and thermoplastic materials.</li>
<li>Ability to learn and adhere to electronic Quality Management System (eQMS). </li>
<li>Proficient in scientific injection molding techniques and DOE methodology.</li>
<li>Familiarity with validation practices per ISO 13485 standards.</li>
<li>Experience with injection molding equipment (e.g., Fanuc, JSW) and related software (RJG, SigmaXL, etc.).</li>
<li>Strong analytical, troubleshooting, and project management skills.</li>
<li>Excellent written and verbal communication; ability to write technical reports and validation documentation.</li>
<li>Detail-oriented, quality-focused, and able to work independently or in cross-functional teams.</li>
</ul>
 
Working Conditions:
<ul>
<li>Work performed in both office and ISO Class 7/8 cleanroom manufacturing environments.</li>
<li>Occasional travel to suppliers or tooling vendors may be required.</li>
<li>Use of personal protective equipment (PPE) and adherence to cleanroom protocols is mandatory.</li>
</ul>
 
Benefits
<ul>
<li>401K Retirement Plan- Eligible to contribute starting the first of the month, 2 months after your hire date. Injectech matches up to 6% of your salary. Contributions are 100% invested immediately. Both Roth and Traditional options are available.</li>
<li>Health Insurance- Coverage begins the first of the month after 30 days of employment. Injectech covers 100% of the employees' premium. You may add a spouse, domestic partner, or dependents at your own cost via pre-tax payroll deductions. </li>
<li>Dental, Vision and Supplemental Insurance Plans- Offered at a group discount rate for employees, spouses, domestic partners, and dependents.</li>
<li>Employee Assistance Program- Available to all employees and their family members at no cost. </li>
</ul>
<ul>
<li>Sick Time- Accrues at 1 hour for every 30 hours worked, up to 48 hours per year.</li>
<li>Paid Time Off (PTO)
<ul>
<li>First 36 months: 6.66 hours per month (up to 80 hours per year).</li>
<li>After 36 months: 8 hours per month (up to 96 hours per year).</li>
<li>Accrual rates continue to increase with tenure.</li>
</ul>
</li>
<li>Holiday Pay- 10 paid holidays per year.</li>
<li>Voluntary Paid Time Off (VTO)- Up to 20 hours per year to volunteer at any 501(c)(3) nonprofit of your choice.</li>
<li>Life and AD&amp;D Insurance- Injectech provides a $50,000 policy at no cost to employees. Additional coverage is available for purchase.</li>
</ul>
Effective 6 Months After Hire Date:
<ul>
<li>Profit Share Program- Eligible to participate the month following 6 full months of employment.</li>
</ul>
 
Drug Testing Policy
Injectech is committed to maintaining a safe and productive workplace. As part of this commitment, all potential employees must pass a drug screening as a condition of employment. The drug test is a 5-panel screening and must be completed prior to your start date.
 
Injectech is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, or any other characteristic protected by law. We are committed to creating a diverse and inclusive workplace and encourage candidates from all backgrounds to apply.

Process Engineer

<h3>Job Description</h3>
Job Description
GenomOncology, a precision medicine software company, provides the healthcare community with data-driven insights to improve cancer care. Their cutting-edge solutions empower their clients' precision oncology workflows by transforming data into actionable treatment options and strategic insights, ultimately driving measurable results. With their expertise and innovative solutions, they aim to help revolutionize the field of oncology, empowering healthcare professionals to make data-driven decisions and elevate the standard of cancer care. They are currently seeking an Application Engineer to join their team and help to advance product development, client success, and solutions delivery. 
 
The Application Engineer position is focused on ensuring customer service and satisfaction with the use of GO applications and solutions. This role serves as a liaison between the Client and the GO Product Development/Development Operations teams. Specific activities for this position include facilitating client discussions and requirement gathering; designing, configuring and testing GO applications and solutions; collaborating with the GO Client Service, Product Development and Development Operations teams for application updates, configurations, deployments and troubleshooting; and contributing to the GO knowledge management repository in the form of documentation and process definition.
 
ESSENTIAL RESPONSIBILITIES:
<ul>
<li>Serve as liaison between Client Service / Product Development / Development Operations and GO clients.</li>
<li>Participate and/or facilitate client meetings to gather design requirements, answer questions on solution design and functionality, and report status on GO tasks and activities.</li>
<li>Collaborate with Account/Project Managers in the development of project plans, time estimates and general planning activities for client delivery.</li>
<li>Gather application configuration, feature/functionality specification and data requirements from client and document as JIRA design tickets.</li>
<li>Create UI, Report and Data Output mockups and wireframes to illustrate the desired functionality and output within the GO tool(s).</li>
<li>Collaborate with Product Development to ensure design tickets are fully understood and ready for development.</li>
<li>Participate in application feature and design reviews with the Product Development,</li>
<li>Application Engineering and Innovation teams.</li>
<li>Write validation test(s) in YAML and gherkin to test and validate the feature/functionality/configuration the design ticket specifies is met.</li>
<li>Execute both manual and automated testing of GO tools to ensure the design specifications are met.</li>
<li>Create JIRA tickets to specify deployment requirements for Application, Content and/or annotations, therapy and trial updates that are ready for deployment.</li>
<li>Support Development Operations (and/or Perform) in the deployment of Application,Content and/or Pipeline Rules updates to GO Internal, GO-hosted, and Client-hosted environments.</li>
<li>Respond to Client support requests and questions.</li>
<li>Perform application troubleshooting and/or coordinate troubleshooting activities amongst the Product Development / Development Operations teams. May include running troubleshooting scripts when necessary.</li>
</ul>
 
ANCILARY RESPONSIBILITIES:
<ul>
<li>Maintain individual tasks and activities list within Jira</li>
<li>Identify new feature/solution requests from clients to bring to the GO Innovation and Product Development teams for consideration.</li>
<li>Create application training guides and conduct training sessions with clients</li>
<li>Update Client Trackers to maintain current versioning of GO Tools, Datasets and Configurations.</li>
<li>Contribute to and maintain GO Knowledge Management on application and tool functionality and GO processes.</li>
<li>Attend and engage in Team and All Company meetings.</li>
</ul>
 
REQUIREMENTS:
<ul>
<li>Strong critical-thinking and analytical skills</li>
<li>Superior service orientation</li>
<li>Outstanding interpersonal and communication skills, both oral and written</li>
<li>Strong ability to translate client requirements into technical requirements for accurate development of application customization/enhancement</li>
<li>Understanding of the Standard Software Development Life Cycle process and/or experience with Jira is a plus.</li>
<li>Strong working knowledge of Google Workspace and MS Office Suite</li>
<li>Self-motivated and ability to work autonomously and as a collaborative team member </li>
<li>Strong multi-tasking and prioritizing capabilities and ability to be flexible and adaptable in a fast-paced work environment</li>
<li>High attention to detail</li>
<li>Continuous improvement oriented and ability to learn new technologies and subjects quickly</li>
</ul>
 
EDUCATION:
<ul>
<li>Bachelor’s Degree: Engineering (Mechanical, Biomedical, Software) preferred</li>
<li>1-3+ years application design or related experience; experience in solution design, quality assurance, technical support and client service within a Software Development</li>
<li>Life Cycle (SDLC) process is desired Previous experience in biomedical field is desired</li>
</ul>

Application Engineer

<h3>Job Description</h3>
Job Description
Our client in Fairfield, NJ is looking for a Senior&nbsp;Product Release Engineer for a Full time position. Pay is $110-125k annually DOE
Responsibilities:&nbsp;
<ul>
<li>Oversee all aspects of programs from concept definition through successful transfer to manufacturing, advocate for the customer and needs/requirements.</li>
<li>Provide leadership to cross-functional technical teams responsible for successful launch of multiple complex programs.</li>
<li>Responsible for overseeing the coordination and on-time/in-budget completion of all project tasks which may involve some or all of the following technologies: progressive stamping, insert molding, factory automation and other related tooling/processes.</li>
<li>Oversee the creation and distribution of project schedules. Ensure that project milestones and deadlines are met including assignment of responsibilities.</li>
<li>Facilitate design definition, design reviews, tooling kickoff, and project postmortem activities.</li>
<li>Understand and meet Regulatory (FDA) requirements and processes for development.</li>
<li>Advanced Product Quality Planning (APQP) including completion of related documentation, including but not limited to: DOE’s, FMEA’s, Process Flowcharts, Control Plans, Capability Studies and Gage R&amp;R’s.</li>
<li>Oversee the creation of BOMs and initiation of the change control process (ECO) relating to Engineering documentation.</li>
</ul>
Requirements:
<ul>
<li>Bachelor’s degree in mechanical engineering or biomedical engineering.</li>
<li>Minimum of 10 years of medical device experience.</li>
<li>Experience in developing and implementing procedures, methods, and tools for the manufacture or design and testing of medical products.&nbsp;</li>
<li>Experience in contributing to technical and cross-functional teams in accomplishing projects with notable impact on company objectives.&nbsp;</li>
<li>Experience in Regulatory (FDA) requirements and processes for development.</li>
</ul>
Benefits:&nbsp; The company offers a competitive benefits package that includes medical, dental, vision, 401k, pet insurance, etc...&nbsp;
Company DescriptionPrideStaff is a 16 time Best of Staffing Award Winning full-service staffing company. 
<h3>Company Description</h3>
PrideStaff is a 16 time Best of Staffing Award Winning full-service staffing company.

Senior Product Release Engineer

<h3>Job Description</h3>
Job Description
Position Summary:
We are seeking a detail-oriented and hands-on Secondary Operations Engineer / Process Engineer to join our medical tubing manufacturing team. This role is responsible for the development, validation, and continuous improvement of secondary operations processes to ensure high-quality, cost-effective production of medical-grade tubing products. The ideal candidate will bring strong technical skills, process engineering experience, and a deep understanding of quality standards within a regulated manufacturing environment.
Key Responsibilities:
<ul>
<li>Develop, implement, and optimize secondary operations for medical tubing, including cutting, hole punching, tipping, flaring, bonding, printing, molding and assembly.</li>
<li>Design and validate fixtures, tools, and equipment to support post-extrusion processes.</li>
<li>Collaborate with suppliers and equipment vendors for tooling design, maintenance, and upgrades.</li>
<li>Create, implement and maintain process documentation (work instructions, process flows, validation protocols, etc.).</li>
<li>Work with cross-functional teams (R&amp;D, Quality, Production) to support new product introductions and process scale-up.</li>
<li>Collaborate with Sales on evaluating and quoting new products, new product development and customer support. Participate in weekly review meetings to align capabilities with customer specifications.</li>
<li>Work with quality to conduct root cause analysis and lead corrective/preventive actions (CAPA) for process issues or non-conformances.</li>
<li>Train and support operators on new or revised secondary processes.</li>
<li>Follow and maintain a schedule of active projects and give necessary updates.</li>
<li>Drive continuous improvement and cost reduction initiatives using lean manufacturing and Six Sigma principles.</li>
<li>Facilitate project scale up activities including transferring manufacturing across multiple locations.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or related field.</li>
<li>5+ years of experience in medical device manufacturing or plastic tubing industry.</li>
<li>Hands-on experience with secondary operations processes and automation.</li>
<li>Familiarity with GMP, ISO 13485, and FDA regulations.</li>
<li>Strong troubleshooting skills and knowledge of statistical process control.</li>
<li>Experience with validation (IQ/OQ/PQ) and process documentation.</li>
<li>Excellent communication, documentation and project management skills.</li>
</ul>
Preferred Skills:
<ul>
<li>Experience with laser cutting, RF welding, or thermal bonding.</li>
<li>Proficient in CAD software (SolidWorks or similar) and Microsoft Office Suite.</li>
<li>Knowledge of polymer materials commonly used in medical devices (e.g., PVC, Pebax, Polyurethane).</li>
<li>Lean Six Sigma certification (Green Belt or higher).</li>
<li>Bilingual in Spanish, a plus</li>
<li>Prior Secondary Operations experience on molded or manufactured parts</li>
</ul>
Proterial Cable America, Inc. is a second chance employer. We believe in giving individuals who have made past mistakes an opportunity to rebuild their lives and contribute positively to society. People with criminal records are encouraged to apply.

Secondary Ops Engineer / Process Engineer

<h3>Job Description</h3>
Job Description
Location: Princeton, NJ
*This role will require full-time presence on-site at our client in Princeton, NJ* **This role is not eligible for relocation assistance**
The Zifo Lab Computing Engineer provides both consulting, analytical and technical laboratory services, including multivendor instrument, information technology as well as in-lab validation/compliance services when applicable. The individual will provide the consulting skills required to analyze customer needs and gaps to propose solutions for the desired state. He or she will work with business users and managers of customers in conjunction with the internal Zifo support team. 
Requirements
Required Skills:
<ul>
<li>Excellent customer service skills complemented by an ability to listen to and interpret client requests</li>
<li>Ability to troubleshoot complex instrument and technology issues</li>
<li>Strong oral and written communication skills</li>
<li>Ability to identify, track and complete tasks for multiple projects </li>
<li>Knowledge of laboratory safety practices as defined by the company and/or customer’s site safety code</li>
<li>Candidate must demonstrate in-depth understanding in one or more of the following areas of Bio/Pharma industry:</li>
<ul>
<li>Drug Discovery &amp; Development Processes</li>
<li>Clinical study planning &amp; Data management</li>
<li>Lab Workflows</li>
<li>Chemical &amp; Biologics material Management</li>
<li>Sample Management</li>
<li>Robotic Systems Integration &amp; Qualification</li>
</ul>
</ul>
Responsibilities:
<ul>
<li>Requirements Management and onsite Validation/Compliance support </li>
<li>IT Consulting</li>
<li>Customer Liaison</li>
<li>Onsite Lab IT Support </li>
</ul>
Requirements Management 
<ul>
<li>Understand problem statement/challenges</li>
<li>Define scope </li>
<li>Gather requirements.</li>
<li>Assist with Validation/Compliance activities (IOPQ) as required.</li>
<li>Analyze current state business processes and requirements.</li>
<li>Assist in building plans for process improvement</li>
</ul>
IT Consulting
<ul>
<li>Analyze gaps/opportunities for improvement based on industry Best Practice</li>
</ul>
<ul>
<li>Evaluate Industry trends to identify areas for optimization</li>
<li>Evaluate vendor solutions and facilitate demos of prototypes as Proofs of Concept</li>
<li>Recommend process improvements that fit business needs </li>
</ul>
Customer Liaison:
<ul>
<li>Meeting with internal/external service groups/leads</li>
<li>Liaise between System/Lab owners and third parties to coordinate best times for services</li>
<li>Provide weekly planning schedules for review at status meeting with customer leads</li>
<li>Monthly Operational review meetings/ Quarterly metrics reporting with department heads</li>
</ul>
On Site Lab IT Support: 
<ul>
<li>Perform break/fix support for all Instrument connected systems</li>
<li>Implement Windows based security policies as required</li>
<li>Ensure adherence to client’s corporate policies through periodic reporting &amp; compliance programs</li>
<li>Acts as the technical support contact for field service engineers and external vendors</li>
<li>Provide technical subject matter expertise for new system validation and change management</li>
<li>Create and maintain a physical inventory of lab equipment, PC’s, software, and any other information pertinent to the environment if applicable</li>
<li>Perform system preventative maintenances based on client’s schedule, if applicable</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s/Master’s degree or equivalent in Pharmaceutical, Bio-technology, Bio-medical, Chemical Engineering</li>
<li>Demonstrated domain area knowledge.</li>
<li>Candidate must possess excellent analytical and interpersonal skills along with a proven track record in system design, implementation, have demonstrated ability to guide the activities of colleagues, and have demonstrated ability to gain client’s confidence and trust.</li>
<li>Operations KPI and Metrics tracking</li>
<li>Optional requirement: Candidate needs to be familiar with the US and International Regulations and Standards governing the development of technical solutions such as GLP, GMP, 21 CFR Part 11, Part 210, Part 211, Part 820</li>
<li>Technical Skills:</li>
<li>Operating System familiarity with at least 1 of the following: Unix, Windows, MVS</li>
<li>Change Control Management and Risk Management </li>
<li>Office Tools proficiency required in : MS Word, Excel, PowerPoint</li>
<li>Office productivity tool proficiency in at least 1 of the following: Visio, MS Project, SharePoint</li>
</ul>
Benefits
About Zifo:
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&amp;D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.
We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Lab Computing Engineer

<h3>Job Description</h3>
Job Description
Join the Innovation Engine at Advanced Instruments, a part of Nova Biomedical
 
 At Advanced Instruments, now proudly part of Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. As a global leader in analytical technologies for the biopharmaceutical and clinical markets, our solutions are trusted in over 100 countries to accelerate drug development and enhance patient care.
Together, we are united by a bold vision: to improve the health of every patient through innovation and excellence. Our mission is to deliver smart, science-driven solutions that optimize processes, increase efficiency, and ensure confidence in results—ultimately leading to better outcomes for patients and providers alike.
Our integration brings together over 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. From FDA-registered, ISO-certified manufacturing to 125+ FDA approvals and industry-trusted diagnostics, we set the standard for quality and reliability. Advanced Instruments is also the global leader in osmolality testing, with a legacy of innovation that continues to shape the future of life sciences.
With headquarters in Norwood and Waltham, Massachusetts, and a growing global presence of 1,965 employees, we’re building an empowered, collaborative culture grounded in our shared values: Customer Centricity, Ingenuity, Ownership &amp; Accountability, Collaboration, and Integrity. We’re honoring our founder led legacies—and shaping a future defined by impact.
Explore what’s next with us at <a href="http://www.novabiomedical.com" target="_blank">http://www.novabiomedical.com</a> or <a href="https://www.aicompanies.com" target="_blank">https://www.aicompanies.com</a>
 
 
About the role
 
 As a Senior Software Engineer (UI), you’ll be at the forefront of crafting intuitive, high-performance interfaces for software platforms that power Osmometry instrumentation—spanning both new systems and legacy applications. You’ll collaborate closely with a multidisciplinary team of Software, Firmware, and Hardware Engineers to bring elegant, user-centric solutions to life.
In our fast-moving commercial environment, success hinges on decisive action and thoughtful execution. You’ll drive usability and innovation across our product suite by making informed technical decisions, engaging stakeholders for critical input, and proactively surfacing challenges. This role is ideal for someone who thrives on turning complexity into clarity and is passionate about delivering impactful user experiences.
 
What we are looking for in you: 
<ul>
<li>Commercial experience in C#/.NET Programming Experience in Visual Studio</li>
<li>Solid understanding of Object-Oriented Design and Principles</li>
<li>Commercial experience on an Agile team, with comfort in sprint planning, stand-ups, sprint review, retrospectives, and backlog refinement</li>
<li>Be accountable for development and delivery of assigned software features and/or applications within a cross functional team, from design through validation, within an Agile Software development team</li>
<li>Refactor existing code to proactively avoid roadblocks and avoid technical debt</li>
<li>Take part in group breakdown of new software features into actionable work items, and work with the team to estimate the time and complexity involved in them</li>
<li>Implement software design language and branding goals from Marketing</li>
<li>Support Software QA team automated UI test suite development</li>
<li>Able to work onsite in Norwood, MA</li>
<li>Degree in Computer Science, Engineering, or Science field </li>
</ul>
 
 
EEO Statement:
Advanced Instruments takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Advanced Instruments will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
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