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<h3>Job Description</h3>
Job Description
About DeepSight Technology 
DeepSight Technology is a leading innovator in medical device technology, specializing in advanced ultrasound solutions like enhanced needle guidance with NeedleVue™, high-resolution imaging from the tip of a needle with OnPoint™ Imaging, and superior diagnostic capability with the EchoLux™ Ultrasound system. Our mission is to revolutionize patient care through state-of-the-art systems, oIering unprecedented precision and accuracy for healthcare providers. 
Job Summary 
The Instrument Engineer will lead the design, prototyping, and optimization of DeepSight's interventional instruments. This role takes concepts from ideation to prototype, ensuring seamless integration into clinical applications. The ideal candidate excels in medical device development, rapid prototyping, and regulatory compliance, working cross-functionally with R&amp;D, clinical, and manufacturing teams. 
Key Responsibilities 
<ul>
<li> Develop interventional devices such as catheters, guidewires, venous access tools, biopsy instruments, and therapy delivery systems. </li>
<li> Design, prototype, and test instruments, fixtures, and assemblies. </li>
<li> Build and iterate proof-of-concept devices for pre-clinical testing. </li>
<li> Initiate and maintain the Device Master Record through development, including:</li>
</ul>
<ul>
<li>Drawings, specifications, and BOMs </li>
<li>Process instructions, test methods, and specifications </li>
<li>Fixtures, tooling, and material selection </li>
</ul>
<ul>
<li> Identify and collaborate with contract manufacturers and suppliers for sub-assemblies and production. </li>
<li> Work with clinical experts to ensure procedural requirements and constraints are incorporated into the instrument design. </li>
<li> Apply expertise in Advanced Manufacturing Techniques: </li>
</ul>
<ul>
<li>Lamination, extrusions, coiling, and braiding </li>
<li>Steering and bending sections </li>
<li>Bonding, adhesion technologies, and techniques </li>
<li>Laser cutting, welding of fine structures, EDM, and water jet machining </li>
</ul>
<ul>
<li> Ensure compliance with ISO 13485, ISO 60601, ASTM, and other relevant standards. </li>
<li> Develop and refine work instructions for designs, ensuring eIective communication with technicians. </li>
</ul>
Qualifications
<ul>
<li> B.S. or M.S. in Mechanical or Biomedical Engineering or related field. </li>
<li> 10+ years of experience in instrument engineering or medical device development. </li>
<li> Proficiency in CAD for device design and documentation. </li>
<li> Experience with medical device fabrication techniques (lamination, laser cutting, bonding, etc.). </li>
<li> Knowledge of interventional devices (catheters, guidewires, biopsy tools, etc.). </li>
<li> Familiarity with regulatory standards (ISO 13485, ISO 60601, ASTM). </li>
<li> Strong hands-on prototyping skills and ability to rapidly iterate designs. </li>
<li> Experience collaborating with contract manufacturers and suppliers. </li>
<li> Excellent problem-solving and cross-functional collaboration skills. </li>
</ul>
Why Join DeepSight? 
At DeepSight Technology, you'll be part of a team that's pushing the boundaries of ultrasound imaging and medical device innovation. This is an opportunity to develop groundbreaking instrumentation, collaborate with top engineers and clinicians, and impact the future of healthcare.
 Job Posted by ApplicantPro

Instrument Engineer

<h3>Job Description</h3>
Job Description
POSITION: QUALITY ENGINEER
DESCRIPTION SUMMARY
Responsible for sustaining and improving the processes required to manufacture a medical device under the guidance of an ISO 13485 Quality Management System, FDA requirements, and other international standards. Quality Engineer will be a member of the engineering team and report to the Manufacturing Engineering Manager.

PRIMARY RESPONSIBILITIES
<ul>
<li>Lead technical resource for Quality, RMA and Technical Support.</li>
<li>Plan, execute and oversee component inspection and testing process to verify conformance with specifications.</li>
<li>Create and revise incoming inspection documentation.</li>
<li>Work collaboratively with Quality team members to manage the NCR process including documentation, supplier communication, product returns and rework, SCAR root cause investigations and issue resolution.</li>
<li>Initiate and rationalize engineering changes from nonconforming component issues, suggest changes for approval or rejection.</li>
<li>Develop design recommendations to improve product reliability and performance.</li>
<li>Develop, test, and implement design changes as well as coordinate with suppliers and manufacturers to ensure smooth implementation.</li>
<li>Provide technical resource regarding equivalency in value engineering and analysis for current components and future product development projects.</li>
<li>Manage Bill of Materials across multiple product lines.</li>
<li>Prepare and review documentation with a high degree of accuracy, completeness, and effectiveness.</li>
</ul>
KNOWLEDGE AND SKILL REQUIREMENTS 
<ul>
<li>5+ years of experience in a manufacturing environment required.</li>
<li>Bachelor’s degree in Engineering (Mechanical, Manufacturing or Biomedical) required.</li>
<li>Working knowledge of AS 9100, ISO 9001 and/or ISO 13485 preferred</li>
<li>Proficient In CAD with SolidWorks expertise preferred.</li>
<li>Knowledge of manufacturing operations, process verification and validation, geometric dimensioning and tolerancing (GD&amp;T) including the ability to create and understand prints and specifications.</li>
<li>Ability to organize and prioritize workflow across multiple projects to meet established time frames and schedules.</li>
<li>Mechanically inclined with an affinity for tools and measuring equipment.</li>
<li>Proficient in Microsoft Office, a good working knowledge of Excel a must.</li>
<li>Excellent communication and organizational skills working in cross-functional teams.</li>
</ul>
This is an exempt; full time position. Compensation is dependent on experience and education. Benefits include a matching 401K, health, dental, vision and paid time off.

QUALITY ENGINEER

<h3>Job Description</h3>
Job Description
IRIDEX Corporation is a medical device manufacturer and operates in a global regulated environment (e.g. FDA). Regulations include (but are not limited to) FDA 21 CFR 820, EN ISO 13485, and the European Medical Device Regulation (MDR). Based on the position, experience in a regulated environment and the extent of working knowledge of appropriate regulations may vary. 
PURPOSE OF JOB:
The Quality Assurance (QA) department is committed to ensuring that all products are safe, reliable, and effective, consistently exceeding the expectations of patients, physicians, and healthcare providers. QA plays a critical role in maintaining product and process quality throughout the commercial production of Iridex’s portfolio, including laser consoles, delivery devices, and accessories.
In this role, the Quality Engineer will assist with the identification and resolution of product and process quality issues. Responsibilities include supporting root cause investigations, tracking corrective actions, evaluating nonconforming materials, and helping maintain compliance with FDA and ISO 13485 requirements. The position offers hands-on experience in a regulated manufacturing environment with exposure to electromechanical and software-integrated medical devices.
MAJOR DUTIES AND RESPONSIBILITIES:
<ul>
<li>Support investigations for product quality issues across mechanical, electrical, and software components.</li>
<li>Assist in root cause analysis and contribute to Corrective and Preventive Action (CAPA) activities.</li>
<li>Manage the Nonconforming Material (NC) process end-to-end—from identification and evaluation to coordination of the Material Review Board (MRB) for timely and effective disposition of nonconforming product.</li>
<li>Assist in supplier quality management activities, including performance monitoring, documentation maintenance, and follow-up on Supplier Corrective Actions (SCARs) to ensure root cause resolution and sustainable improvements.</li>
<li>Collaborate with Manufacturing and Engineering teams to evaluate process improvements and product quality concerns.</li>
<li>Support incoming inspection process, verification of components, and evaluation of test data.</li>
<li>Review Engineering Change Orders (ECOs) for quality impact under supervision.</li>
<li>Contribute to risk management documentation (e.g., FMEA) as part of design and process evaluations.</li>
<li>Assist in managing the calibration program for measurement equipment and support investigations of out-of-tolerance (OOT) tools.</li>
<li>Assist in the documentation of complaint investigations and return analysis reports.</li>
<li>Participate in internal audits, supplier evaluations, and quality improvement projects.</li>
<li>Maintain detailed records, forms, and reports in accordance with QMS and regulatory requirements.</li>
</ul>
JOB SKILLS:
<ul>
<li>Solid understanding of quality engineering principles (e.g., CAPA, NCRs, risk analysis).</li>
<li>Familiarity with FDA 21 CFR 820, ISO 13485, and ISO 14971 requirements.</li>
<li>Familiarity with medical device standards such as IEC 60601 is advantageous.</li>
<li>Ability to read and interpret engineering drawings and specifications.</li>
<li>Working knowledge of basic inspection tools and techniques.</li>
<li>Strong analytical and problem-solving skills, including root cause analysis techniques.</li>
<li>Effective communication skills and ability to work in cross-functional teams.</li>
<li>Attention to detail, organizational skills, and the ability to manage multiple priorities.</li>
<li>Detail-oriented with a commitment to quality and continuous learning.</li>
<li>Basic understanding of statistical analysis and sampling methods is a plus.</li>
</ul>
QUALIFICATIONS:
<ul>
<li>Bachelor’s degree in Biomedical, Mechanical, Industrial, or related engineering field.</li>
<li>2 to 5 years of experience in a Quality or Manufacturing Engineering role, preferably in a medical device or regulated industry.</li>
<li>Experience with CAPA, and nonconformance systems preferred.</li>
<li>Working knowledge of risk management tools (FMEA) and quality planning.</li>
<li>Certification such as ASQ Certified Quality Engineer (CQE) is a plus.</li>
<li>Advanced problem-solving skills including troubleshooting and root cause analysis</li>
<li>Familiarity with sterilization validation, environmental monitoring, and cleanroom protocols is desirable.</li>
<li>Effective written and verbal communication skills in English.</li>
<li>Basic knowledge and understanding of Quality Management System regulations including but not limited to ISO 13485 and 21CFR820. </li>
</ul>
ADDITIONAL INFORMATION:
<ul>
<li>Department: QA</li>
<li>Reports To: Sr. Manager, Quality Assurance</li>
<li>FLSA Status: Exempt</li>
<li>Base Salary: $80,000 - $118,000 DoE</li>
<li>Travel: 10% </li>
<li>Work Location: This job will be primarily onsite; the percentage of supplier-visit work will be defined by the management</li>
</ul>

Quality Engineer

<h3>Job Description</h3>
Job Description
 
Quality Engineer
Reporting directly to the Quality Assurance and Lab Manager, this position uses critical thinking and technical writing skills to research, develop and document key quality processes such as process and software validations, procedures, risk assessments, PFMEAs, as assigned in a timely manner. This role supports all levels of operations, quality, laboratory, and engineering departments in the development, management and execution of testing and validation protocols. This position will service all aspects of the businesses at PCNA. This role supports the Engineering team with maintaining the facilities’ master validation plan. Facilitates the company’s Management of Change (MOC) process. Maintain outgoing process data for statistical analyses, trending purposes to ensure the process is maintained as validated. Continuous Improvement Coach and Coordinator. Perform data analyses using ERP, PowerBI, Excel, etc.
 
POSITION REQUIREMENTS
Education, Credentials, Licenses:
<ul>
<li>Bachelor’s degree in Engineering (Biomedical, Mechanical, etc), Science (Chemistry, Biology, Physics, etc.), or Math (Statistics) required</li>
</ul>
Kind &amp; Length of Experience:
<ul>
<li>Minimum of 5 years of experience in an industrial manufacturing environment with a quality system designed to meet the requirements of the FDA Quality System required</li>
<li>Proficient in Microsoft Office is required </li>
<li>GMP in Cosmetics or Pharmaceuticals experience is preferred</li>
<li>Certifications in quality, engineering, Six Sigma, or Lean Manufacturing are preferred</li>
<li>Experience with Microsoft Business Dynamics preferred </li>
<li>Experience with Power BI preferred</li>
</ul>
IV. PERFORMANCE MEASURES AND STANDARDS
Quality Improvement
<ul>
<li>Perform root cause investigation and CAPA (corrective action preventative action) to deliver non-repeatable issues, measure effective performance of CAPA solutions.</li>
<li>Develop, lead and drive optimization Kaizens related to top quality losses.</li>
<li>Lead data collection, analysis and assignment of standard Quality loss trees in support of operational KPI reporting.</li>
<li>Support the development of PFMEA documents, perform risk assessment and updated PFMEA documents for equipment and processes as needed.</li>
<li>Partner with department leaders to execute validations and provide support for validation including report writing, and participation.</li>
</ul>
ISO Documentation
<ul>
<li>Create new SOPs and modify current SOPs using the established structured format; which will allow for production operator to perform and produce the same outcome every time the process is executed.</li>
</ul>
ISO Management System
<ul>
<li>Leads, develops and manages the layered process audit program.</li>
<li>Manage and ensure compliance with the quality management system through communication, training and internal/external audits.</li>
<li>Assess training and development needs related to the quality program.</li>
<li>Ensure that all training activities associated with validation activities are performed in a timely manner.</li>
<li>Implement and verify site calibration and maintenance program for inspection, measuring and testing equipment. Coordinate performance of quality measurement equipment capabilities studies.</li>
<li>Initiate and support Management of Change (MOC) per requirements.</li>
<li>Support the documentation of maintenance procedures to ensure the production of quality products. Provide insights to trends and performance of processes through data analysis.</li>
<li>Support efforts to implement and maintain the all company certification and regulations including, SQF, ISO 9001, ISO/IEC 17025, and RC14001/EHS&amp;S management system; </li>
</ul>
Innovation
<ul>
<li>Support innovation funnel activities with key customers by partnering with process engineering and operations departments to support IQ/OQ/PQ processes.</li>
<li>Develop timely validation and test protocols for new processes, computer software, or equipment in conjunction with the engineering group.</li>
<li>Establish and maintain systems to maintain raw materials, finished goods within specification.</li>
<li>Supports and participates in structured quality improvement activities related to customers, consumer issues/complaints and PQ gaps.</li>
</ul>
Peter Cremer Training Required
<ul>
<li>We will follow the company written training program for this position.</li>
</ul>
Customer Service, Teamwork &amp; Code of Conduct 
<ul>
<li>Maintain a safe, legal and environmentally protective operation </li>
<li>Listen to our customers, suppliers and employees </li>
<li>Respond quickly to customer concerns </li>
<li>Follow set guidelines for GMP, quality and food safety requirements </li>
<li>Maintain training on applicable procedures in quality, GMP, and food safety </li>
<li>Report any food safety, security, and / or quality issues to management or the HACCP team to initiate action</li>
<li>Provide flexible and innovative strategies to support new business opportunities </li>
<li>Be cost effective in the utilization of our resources, thereby contributing to the profitability of Peter Cremer North America, LP and our customers </li>
<li>Strive for continued improvement </li>
<li>Willing and eagerness to learn</li>
<li>Maintain positive attitude.</li>
</ul>
We are an equal opportunity employer. Applicants are considered for positions without regard to sex, race, color, ancestry, religion, national origin, disability, age, marital status, disabled veteran or Vietnam era veteran status, genetic information, sexual orientation, pregnancy, including childbirth or any related condition, gender identity or expression, citizenship, or any other characteristic protected by applicable state, federal or local laws.

<h3>Job Description</h3>
Job Description
Sightpath Medical Laser Engineer
In addition to learning the latest innovations in the ophthalmic industry, Sightpath Medical offers a challenging and rewarding environment where you’ll work with smart, fun and energetic people. We are interested in candidates with all areas of experience (entry level to experienced)
<ul>
<li>Sightpath Medical is the premier cataract and LASIK mobile services provider in the U.S.</li>
<li>We provide an independent working atmosphere</li>
<li>We provide on the job training to help you become an expert in our area of expertise</li>
<li>Salary position with quarterly bonus eligibility</li>
<li>401(k) plan</li>
<li>Medical Benefits including medical, dental, vision, health savings account, short term disability, long term disability</li>
<li>Health and Wellness Program</li>
</ul>
Responsibilities:
<ul>
<li>Requires the ability to install/de-install and operate transportable lasers and related equipment on one business unit at customer sites.</li>
<li>Responsible for calibration and programming of equipment for surgeon’s approval prior to surgery being performed.</li>
<li>Responsible for the operation of both lasers when they are both required.</li>
<li>Provide routine preventative maintenance and repairs on the laser systems to maximize usage and minimize downtime.</li>
<li>Ability to troubleshoot, remove and replace components of the laser and calibrate to vendor specifications.</li>
<li>Responsible for maintaining all company assets in good working order.</li>
<li>Adherence to company standard operating procedures that meet/exceed standard of care.</li>
<li>Ability to complete Annual and Semi-Annual Preventative Maintenance checks and services on all assigned equipment. Successfully completes all PM paperwork during and at the end of PM.</li>
<li>Understands and adheres to proper sterile technique.</li>
<li>Willing and able to do manual labor</li>
<li>Other duties as required</li>
</ul>
Qualifications:
<ul>
<li>Degree in Laser Electro-optics, Biomedical Equipment Technology, Biomedical Electronics, Electronics or military training equivalent.</li>
<li>Proficiency with basic electronics and associated test equipment.</li>
<li>Able to work a varied work schedule and travel.</li>
<li>Able to work in a team environment.</li>
<li>Valid Driver’s License</li>
<li>Ability to pass company administered road test.</li>
<li>Ability to occasionally lift 50 lbs.</li>
<li>Ability to stand for extended periods of time.</li>
<li>Able to work a varied work schedule and travel.</li>
<li>Great customer service skills.</li>
</ul>
SIGHTPATH is an equal opportunity employer. In accordance with applicable law, we prohibit discrimination based on race, color, religion, creed, gender, pregnancy or related medical conditions, age (40 and over), national origin or ancestry, physical or mental disability, genetic information or any other consideration protected by federal, state or local laws. Our commitment to equal opportunity employment applies to all persons involved in our operations and prohibits unlawful discrimination by any employee, including supervisors and coworkers.
 
PM25

Laser Engineer

<h3>Job Description</h3>
Job Description
Description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines &amp; Values:
<ul>
<li>We empower and support our colleagues</li>
<li>We commit to client success at every turn</li>
<li>We have the courage to do the right thing</li>
<li>We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.</li>
<li>We constantly acquire new skills and learn from our experiences to enhance our collective expertise</li>
</ul>
Responsibilities:
Entry level Deviation Investigator / CQV Engineer position in the Pharma industry. Employer will train hired resource on Deviation Investigation.
Requirements
<ul>
<li>Deviation investigation remediation experience is a plus but is not necessary</li>
<li>Undergraduate Engineering/STEM degree preferred (mechanical, chemical, biomedical, etc.)</li>
<li>1-3 years' experience</li>
<li>Salary dependent on experience</li>
<li>Some Pharma experience preferred but not absolutely required</li>
<li>New college grads with internship experience encouraged to apply</li>
<li>Proficiency using PC and Microsoft Office tools</li>
<li>Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms</li>
<li>Ability to work as part of a team</li>
<li>Strong problem-solving and critical thinking skills</li>
<li>Excellent organizational and time management skills</li>
<li>Strong attention to detail</li>
<li>Strong interpersonal skills and clear communication capabilities</li>
<li>Experience with and tolerance for high levels of challenge and change</li>
<li>Onsite requirement in Indianapolis, IN</li>
</ul>
For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
*Verista is an equal opportunity employer.
National (US) Range$59,951—$93,541 USD
Benefits
Why Choose Verista?
<ul>
<li>High growth potential and fast-paced organization with a people-focused culture</li>
<li>Competitive pay plus performance-based incentive programs</li>
<li>Company-paid Life, Short-Term, and Long-Term Disability Insurance.</li>
<li>Medical, Dental &amp; Vision insurances</li>
<li>FSA, DCARE, Commuter Benefits</li>
<li>Supplemental Life, Hospital, Critical Illness and Legal Insurance</li>
<li>Health Savings Account</li>
<li>401(k) Retirement Plan (Employer Matching benefit)</li>
<li>Paid Time Off (Rollover Option) and Holidays</li>
<li>As Needed Sick Time</li>
<li>Tuition Reimbursement</li>
<li>Team Social Activities (We have fun!)</li>
<li>Employee Recognition</li>
<li>Employee Referral Program</li>
<li>Paid Parental Leave and Bereavement</li>
</ul>
Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details. 
For more information about our company, please visit us at Verista.com

5935- Deviation Investigator / Validation Engineer

<h3>Job Description</h3>
Job Description
SLD Laser, a world leader in commercialization of gallium nitride (GaN) based laser light sources, was acquired by KYOCERA Corporation and has commenced operations as a wholly owned subsidiary and group company of KYOCERA Corporation under the name KYOCERA SLD Laser, Inc. (KSLD). KSLD is commercializing a new generation of gallium nitride-based laser light sources. KSLD's high luminance LaserLightTM sources are utilized in a myriad of applications including automotive &amp; mobility, specialty &amp; portable lighting, entertainment &amp; outdoor, projection &amp; AR/VR displays, biomedical instrumentation &amp; therapeutics, and industrial imaging &amp; material processing.
 The company is ISO 9001 certified and automotive compliant to IATF 16949, and operates facilities in Santa Barbara, CA and in Fremont, CA. KSLD's high luminance LaserLightTM sources are UL and IEC safety certified. 
The company has also been named Fortune's "Best Workplaces in Manufacturing &amp; Production," having promoted an employee-centric corporate culture since its founding
KSLD will continue to pioneer the future of light by developing, manufacturing and marketing innovative laser-based products with high efficiency and luminance for mobility, specialty lighting, consumer, and industrial applications. To learn more about KSLD, visit <a href="http://www.kyocera-sldlaser.com" target="_blank">www.kyocera-sldlaser.com</a> or contact the company at <a href="mailto:info@kyocera-sldlaser.com" target="_blank">info@kyocera-sldlaser.com</a> or 1-866-753-5273.
SLD Laser, a world leader in commercialization of gallium nitride (GaN) based laser light sources, was acquired by KYOCERA Corporation and has commenced operations as a wholly owned subsidiary and group company of KYOCERA Corporation under the name KYOCERA SLD Laser, Inc. (KSLD). KSLD is commercializing a new generation of gallium nitride-based laser light sources. KSLD's high luminance LaserLightTM sources are utilized in a myriad of applications including automotive &amp; mobility, specialty &amp; portable lighting, entertainment &amp; outdoor, projection &amp; AR/VR displays, biomedical instrumentation &amp; therapeutics, and industrial imaging &amp; material processing.
The company is ISO 9001 certified and automotive compliant to IATF 16949, and operates facilities in Santa Barbara, CA and in Fremont, CA. KSLD's high luminance LaserLightTM sources are UL and IEC safety certified. The company was recently ranked 7th in Fortune magazine's "2021 Best Workplaces in Manufacturing &amp; ProductionTM," having promoted an employee-centric corporate culture since its founding.
KSLD will continue to pioneer the future of light by developing, manufacturing and marketing innovative laser-based products with high efficiency and luminance for mobility, specialty lighting, consumer, and industrial applications.
To learn more about KSLD, visit <a href="http://www.kyocera-sldlaser.com" target="_blank">www.kyocera-sldlaser.com</a> or contact the company at <a href="mailto:info@kyocera-sldlaser.com" target="_blank">info@kyocera-sldlaser.com</a> or 1-866-753-5273.
 
Job Description:
As an MTS Epi Process Development Engineer, you will be responsible for product-driven development of gallium nitride based epitaxial deposition processes using Metal Organic Chemical Vapor Deposition (MOCVD). This position will be responsible for planning and execution of MOCVD experiments, analysis and review of metrology data, and working closely with process engineering to ensure necessary process controls for uniform and high yielding MOCVD processes. This position is additionally responsible for close cross-functional work with chip fabrication teams to identify and contribute to co-optimization of epitaxy and chip designs toward product requirements.
Job Responsibilities:
<ul>
<li>Development and execution of product-driven epitaxial processes via MOCVD</li>
<li>Analyze and review metrology data associated with epitaxial processes and equipment</li>
<li>Contribute to development and optimization of yield and process control metrics for epi</li>
<li>Coordinate with chip fabrication team to plan and execute necessary epi experiments for co-optimization of epi and chip; may serve as member on cross-functional project team(s)</li>
<li>Support quality systems requirements and new product introduction (NPI) requirements</li>
<li>Additional duties as assigned</li>
</ul>
Required Qualifications:
<ul>
<li>B.S. and MS or PhD in engineering (materials, electrical engineering, physics or related discipline)</li>
<li>5+ years industry experience in epitaxial process development, semiconductor or manufacturing process engineering for product</li>
<li>Experience with a variety of thin film metrology and characterization techniques</li>
<li>Fabrication and/or test experience with LED, laser diode or similar optoelectronic devices</li>
</ul>
Preferred Qualifications:
<ul>
<li>Epitaxial growth experience in gallium nitride MOCVD, preferably in production environment</li>
<li>Laser device design and chip fabrication knowledge; technical background to effectively support epi/chip design co-optimization for various applications</li>
<li>Strong analytical programming and/or data analysis skills (JMP, Python, MATLAB, Mathematica, etc)</li>
<li>Strong critical thinking, creative, innovative and analytical problem-solving skills</li>
<li>Self-motivated and resourceful</li>
<li>Excellent verbal and written communication skills</li>
<li>Flexible and team player mentality</li>
</ul>
The full-time base salary range for the MTS Epi Process Development Engineer position is $157,000 to $185,000 per annum. The range reflects the minimum and maximum possible base salary for new hires for the role, based on the advertised location. Individual pay is determined by several factors including work location, job-related skills, experience, and relevant education and training. For more information about the base salary range applicable to the work location, talk to the recruiter. 
Kyocera SLD Laser, Inc. is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), gender identity, gender expression, national origin, ancestry, citizenship, age, physical or mental disability, legally protected medical condition, military or veteran status, marital status, domestic partner status, sexual orientation, genetic information, or any other basis protected by local, state, or federal laws.
The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties, and requirements of personnel as classified. 
 Benefits:
Medical, Dental, Vision, 401K

Member of Technical Staff Epi Process Development Engineer

<h3>Job Description</h3>
Job Description
Description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines &amp; Values:
<ul>
<li>We empower and support our colleagues</li>
<li>We commit to client success at every turn</li>
<li>We have the courage to do the right thing</li>
<li>We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.</li>
<li>We constantly acquire new skills and learn from our experiences to enhance our collective expertise</li>
</ul>
We are seeking a highly motivated Project Engineer with proven experience in risk management within the pharmaceutical or medical device industry. This role will be responsible for leading and supporting cross-functional projects that ensure product and process compliance while minimizing risks throughout the product lifecycle. Candidates with experience or familiarity in Turbo AC (Air Conditioning or Turbo Compressor) systems are highly desired.
Project Engineer – Risk Management (Pharma/Med Device) Responsibilities:
<ul>
<li>Lead and support risk management activities (e.g., FMEA, Fault Tree Analysis, Risk Registers) throughout the product lifecycle</li>
<li>
Coordinate with cross-functional teams (QA, Regulatory, Manufacturing, R&amp;D) to ensure risk mitigation strategies are effectively implemented
</li>
<li>
Drive the development, execution, and documentation of engineering project plans, timelines, and deliverables
</li>
<li>
Analyze and interpret engineering specifications, user needs, and technical drawings to support risk assessments and product safety evaluations
</li>
<li>
Manage technical issues and provide solutions that align with project objectives and compliance standards
</li>
<li>
Prepare and deliver clear project updates, risk reports, and design documentation to stakeholders
</li>
<li>
Support product verification and validation (V&amp;V) efforts, ensuring alignment with regulatory and industry standards
</li>
<li>
Contribute technical expertise, especially where Turbo AC systems are applicable in the design or manufacturing environment
</li>
</ul>
Requirements:
<ul>
<li>
Bachelor's degree in Engineering (Mechanical, Biomedical, Electrical, or related field)
</li>
<li>
Minimum 3–5 years of experience in risk management within the pharmaceutical or medical device industry
</li>
<li>
Deep understanding of relevant FDA/EMA regulations
</li>
<li>
Strong project engineering and cross-functional collaboration skills
</li>
<li>
Excellent problem-solving and analytical skills
</li>
<li>
Experience or working knowledge of Turbo AC systems / or QMSpace
</li>
<li>Local resource (Indianapolis) is desired but remote is possibility for a candidate that is a solid fit</li>
</ul>
For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
*Verista is an equal opportunity employer.
National (US) Range$80,465—$132,593 USD
Benefits
Why Choose Verista?
<ul>
<li>High growth potential and fast-paced organization with a people-focused culture</li>
<li>Competitive pay plus performance-based incentive programs</li>
<li>Company-paid Life, Short-Term, and Long-Term Disability Insurance.</li>
<li>Medical, Dental &amp; Vision insurances</li>
<li>FSA, DCARE, Commuter Benefits</li>
<li>Supplemental Life, Hospital, Critical Illness and Legal Insurance</li>
<li>Health Savings Account</li>
<li>401(k) Retirement Plan (Employer Matching benefit)</li>
<li>Paid Time Off (Rollover Option) and Holidays</li>
<li>As Needed Sick Time</li>
<li>Tuition Reimbursement</li>
<li>Team Social Activities (We have fun!)</li>
<li>Employee Recognition</li>
<li>Employee Referral Program</li>
<li>Paid Parental Leave and Bereavement</li>
</ul>
Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details. 
For more information about our company, please visit us at Verista.com

5868 - Project Engineer / Risk Management (Pharma/Med Device)

<h3>Job Description</h3>
General Summary
John Moriarty &amp; Associates of Virginia (JMAV) is seeking a Summer 2026 Intern in the Raleigh, NC area.
 
Interns with Moriarty are responsible for assisting the project team with direction to ensure that the project is built according to plan, specification, schedule, and quality.
 
The intern should be located within daily driving distance of the Raleigh, NC area.
 
Roles &amp; Responsibilities:
The intern must have the basic ability to read and interpret plans &amp; drawings, understand the importance of jobsite safety, and be able to effectively present information. Some responsibilities include:
<ul>
<li>Assist field personnel in their site-specific responsibilities.</li>
<li>Assist field personnel in quality control inspections and documentation.</li>
<li>Ability to perform construction material takeoffs and make estimates for future needs.</li>
<li>Understand company / project safety plan.</li>
<li>Assist with administration of subcontractor safety training and compliance.</li>
<li>Asist with coordinating subcontractor deliverables for project execution.</li>
<li>Assist in processing submittals.</li>
</ul>
Education:
<ul>
<li>Working towards a 4-year degree preferred, in Building Construction or relevant subject.</li>
</ul>
 
Work Experience: 
<ul>
<li>0-2 years of project management experience, in Construction is preferred.</li>
</ul>
 
Knowledge, Skills, and Abilities:
<ul>
<li>Excellent communication skills, both verbal and written</li>
<li>Adaptable team players, with strong client service skills</li>
<li>Basic understanding of construction drawings and specifications</li>
<li>Basic understanding area schedules</li>
<li>Basic knowledge of Microsoft Excel and Smartsheet scheduling</li>
</ul>
 
Physical Requirements:
<ul>
<li>This position will require moderate physical activity</li>
<li>Driving between sites, climbing stairs and ladders, walking on rough terrain, standing for extended periods of time</li>
</ul>
 
Work Environment:
<ul>
<li>Work onsite, outdoors, in all weather conditions. The noise in these work environments is usually moderate to very loud. The employee will be regularly exposed to outside weather conditions.</li>
</ul>
 
The Company:
John Moriarty &amp; Associates of Virginia (JMAV) is a privately held general contractor that specializes in large scale, urban, ground-up projects such as mixed-use, multi-family, hotels, senior living, student housing and bio-medical and is one of the faster growing contactors in the DC-Metro area. Exceptional for the industry, 100% of our projects are negotiated with over 85% being with repeat clients.
 
Our approach is characterized by transparency, collaboration, attention to detail and hands-on leadership. Our projects are set up for success by our strong emphasis on pre-construction services and planning, proper staffing and hiring best-in-class subcontractors. Our growth has been a result of outstanding execution in every phase of project delivery and an unparalleled employee retention of the best people in the industry.
 
Our parent company, John Moriarty &amp; Associates (JMA), was founded in 1985 in Winchester, MA and is one of the most respected general contracting firms in the industry. Learn more about us at <a href="http://www.jma-va.com" target="_blank">www.jma-va.com</a> and <a href="http://www.jm-a.com" target="_blank">www.jm-a.com</a>.
 
John Moriarty &amp; Associates of Virginia participates in E-Verify for all hired employees. E-Verify is a web-based system that allows enrolled employers to confirm the eligibility of their employees to work in the United States by electronically matching information provided by employees on the Form I-9 against records available to the Social Security Administration and the Department of Homeland Security. More information can be found at <a href="http://www.e-verify.gov" target="_blank">www.e-verify.gov</a>.

Field/Office Engineer Intern (Summer 2026)

<h3>Job Description</h3>
General Summary
John Moriarty &amp; Associates of Virginia (JMAV) is seeking a Summer 2026 Intern in the Charlottesville, VA area.
 
Interns with Moriarty are responsible for assisting the project team with direction to ensure that the project is built according to plan, specification, schedule, and quality.
 
The intern should be located within daily driving distance of the Charlottesville, VA area.
 
Roles &amp; Responsibilities:
The intern must have the basic ability to read and interpret plans &amp; drawings, understand the importance of jobsite safety, and be able to effectively present information. Some responsibilities include:
<ul>
<li>Assist field personnel in their site-specific responsibilities.</li>
<li>Assist field personnel in quality control inspections and documentation.</li>
<li>Ability to perform construction material takeoffs and make estimates for future needs.</li>
<li>Understand company / project safety plan.</li>
<li>Assist with administration of subcontractor safety training and compliance.</li>
<li>Asist with coordinating subcontractor deliverables for project execution.</li>
<li>Assist in processing submittals.</li>
</ul>
Education:
<ul>
<li>Working towards a 4-year degree preferred, in Building Construction or relevant subject.</li>
</ul>
 
Work Experience: 
<ul>
<li>0-2 years of project management experience, in Construction is preferred.</li>
</ul>
 
Knowledge, Skills, and Abilities:
<ul>
<li>Excellent communication skills, both verbal and written</li>
<li>Adaptable team players, with strong client service skills</li>
<li>Basic understanding of construction drawings and specifications</li>
<li>Basic understanding area schedules</li>
<li>Basic knowledge of Microsoft Excel and Smartsheet scheduling</li>
</ul>
 
Physical Requirements:
<ul>
<li>This position will require moderate physical activity</li>
<li>Driving between sites, climbing stairs and ladders, walking on rough terrain, standing for extended periods of time</li>
</ul>
 
Work Environment:
<ul>
<li>Work onsite, outdoors, in all weather conditions. The noise in these work environments is usually moderate to very loud. The employee will be regularly exposed to outside weather conditions.</li>
</ul>
 
The Company:
John Moriarty &amp; Associates of Virginia (JMAV) is a privately held general contractor that specializes in large scale, urban, ground-up projects such as mixed-use, multi-family, hotels, senior living, student housing and bio-medical and is one of the faster growing contactors in the DC-Metro area. Exceptional for the industry, 100% of our projects are negotiated with over 85% being with repeat clients.
 
Our approach is characterized by transparency, collaboration, attention to detail and hands-on leadership. Our projects are set up for success by our strong emphasis on pre-construction services and planning, proper staffing and hiring best-in-class subcontractors. Our growth has been a result of outstanding execution in every phase of project delivery and an unparalleled employee retention of the best people in the industry.
 
Our parent company, John Moriarty &amp; Associates (JMA), was founded in 1985 in Winchester, MA and is one of the most respected general contracting firms in the industry. Learn more about us at <a href="http://www.jma-va.com" target="_blank">www.jma-va.com</a> and <a href="http://www.jm-a.com" target="_blank">www.jm-a.com</a>.
 
John Moriarty &amp; Associates of Virginia participates in E-Verify for all hired employees. E-Verify is a web-based system that allows enrolled employers to confirm the eligibility of their employees to work in the United States by electronically matching information provided by employees on the Form I-9 against records available to the Social Security Administration and the Department of Homeland Security. More information can be found at <a href="http://www.e-verify.gov" target="_blank">www.e-verify.gov</a>.

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