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<h3>Job Description</h3>
Job DescriptionDescription:
RxSight® is an ophthalmic medical technology corporation headquartered in Aliso Viejo, California that has commercialized the world’s first and only adjustable intraocular lens (IOL) that is customized after cataract surgery. The company’s mission is to revolutionize the premium cataract surgery experience by allowing surgeons to partner with their patients to achieve optimized results for every unique eye.
 
OVERVIEW:
The Senior Manufacturing Engineer will play a vital role in supporting and leading the sustaining efforts aimed at continuous improvement and maintaining robust manufacturing processes related to the Light Adjustable Lens and Insertion device manufacturing. As a vital member of the Manufacturing Engineering team, this individual will closely collaborate with Manufacturing, Design Engineering and Quality Control/Assurance departments to ensure production line sustainability, compliance with regulations, and quality systems requirements. The Senior Manufacturing Engineer will be responsible for deploying lean manufacturing methodology and implementing the culture of continuous improvement to improve overall safety, quality, on-time delivery, and productivity of our LAL and Insertion device manufacturing and processes. This individual will also guide and mentor the engineering team and other departments in resolving manufacturing and production issues, improving engineering and project systems, and identifying and resolving product or process issues.
 
Requirements:
ESSENTIAL DUTIES AND RESPONSIBILITIES:
<ul>
<li>Lead effort in support of continuous improvement initiatives aimed at enhancing production efficiency, ensuring business continuity, and maintaining regulatory compliance.</li>
<li>Implement corrective and preventive actions for production non-conformances.</li>
<li>Establish and execute validation strategies (IQ/OQ/PQ) for new processes, and equipment in compliance with ISO 13485 and FDA regulations.</li>
<li>Implement corrective and preventive actions for production non-conformances.</li>
<li>Provide troubleshooting expertise for equipment-related issues and offer technical support to operators and technicians as required.</li>
<li>Initiate documents such as drawings, work instructions, and reports ensuring proper routing through the quality management system.</li>
<li>Perform training necessary for the implementation of processes/tooling changes as necessary.</li>
<li>Set up, operate, and maintain various manufacturing equipment and tools.</li>
<li>Perform diagnostics, troubleshoot, and repair complex electrical, mechanical, network and software issues.</li>
<li>Participate in root cause analysis and implement corrective actions for manufacturing issues.</li>
<li>Perform analysis and provide input to mitigate risk due to obsolete or high-risk equipment and parts.</li>
<li>Ability to stay on tasks with minimal supervision and minimal direction.</li>
</ul>
REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES:
<ul>
<li>Demonstrates a hands-on approach to problem solving, ensuring prompt task closure.</li>
<li>Familiarity with SolidWorks PDM software (desired).</li>
<li>Proficient in conducting training sessions and initiating engineering change requests.</li>
<li>Prior experience working in a cleanroom environment/ or medical device manufacturing is highly preferred.</li>
<li>Experience with optical measurement systems (Keyence, NEMO, or similiar)</li>
<li>Demonstrate strong problem-solving skills and can ask critical questions without being the subject matter expert.</li>
<li>Professional, responsible, energetic, and accountable.</li>
<li>Strong interpersonal skills – the ability to communicate effectively at multiple organizational levels including technicians, Engineering, Chemistry, and Production operators.</li>
<li>Clear communicator – understands how to distill information to have substantive discussions with the right audience.</li>
<li>Strong Organizational skills – the ability to balance and prioritize multiple studies, and manufacturing builds.</li>
<li>Continued appetite to learn about our technology, its performance characteristics, and its manufacturing process – our process and our technology are unique!</li>
<li>Self-motivated, proactive, and able to work effectively under minimal supervision.</li>
</ul>
EDUCATION, EXPERIENCE, and TRAINING:
<ul>
<li>Bachelor’s degree in Biomedical, Electrical, or Mechanical Engineering with a minimum of 7 years of technical experience.</li>
<li>Master’s degree in Biomedical, Electrical, or Mechanical Engineering with a minimum of 5 years of technical experience.</li>
<li>Continuous improvement experience.</li>
<li>Familiarity with regulatory standards (ISO 13485).</li>
<li>Familiarity with good manufacturing practices (GMP) and good documentation practices (GDP). Experience with good laboratory practices (GLP) is a plus. </li>
<li>Training to be completed per the training plan for this position as maintained in the document control system</li>
<li>The training requirements on TRN-10007 Insider Trading Policy, TRN-10008 Global Anti-Bribery and Anti-Corruption Policy and TRN-10009 Code of Business Conducts and Ethics must be diligently completed within 30 days from the hiring date and on an annual basis</li>
</ul>
COMPUTER SKILLS:
<ul>
<li>Microsoft Word; Microsoft Excel; Teams</li>
<li>MiniTab</li>
<li>Project Management System (SmartSheet preferred)</li>
<li>CAD (SolidWorks or PRO/E proficiency preferred)</li>
</ul>
Notice to Staffing Agencies and Search Firms:
RxSight does not accept unsolicited resumes or candidate submissions from staffing agencies or search firms for any employment opportunities. All agency engagements must be authorized in writing for a specific position by RxSight’s Talent Acquisition department. Any resumes or candidate information submitted without such specific engagement will be considered unsolicited and the property of RxSight. No fees will be paid in the event a candidate is hired under these circumstances.

Senior Manufacturing Engineer

<h3>Job Description</h3>
Job DescriptionThis role is in Coldwater, MI. 
POSITION SUMMARY: Investigation, Development, Presenting Themes, Project Management, Budgeting, Scheduling, Installation, Start-up functions, Training, Document Development (Ops Stds, PM’s, PQCT Etc…) of newly installed, line movement, re-build of equipment pertaining to the machining of Cast Iron Castings. Review new Technologies in Machining Functions for overall improvements in Safety, Quality, Manpower Efficiencies and Cost.
ESSENTIAL FUNCTIONS
· Read and interpret blueprints, technical drawings, schematics, and computer-generated reports.
· Confer with engineers and other personnel to implement operating procedures, resolve system malfunctions, and provide technical information.
· Research and analyze customer design proposals, specifications, manuals, and other data to evaluate the feasibility, cost, and maintenance requirements of designs or applications.
· Specify system components or direct modification of products to ensure conformance with engineering design and performance specifications.
· Research, design, evaluate, install, operate, and maintain mechanical products, equipment, systems and processes to meet requirements, applying knowledge of engineering principles.
· Investigate equipment failures and difficulties to diagnose faulty operation, and to make recommendations to maintenance crew.
· Assist drafters in developing the structural design of products using drafting tools or computer-assisted design (CAD) or drafting equipment and software.
· Provide feedback to design engineers on customer problems and needs.
· Oversee installation, operation, maintenance, and repair to ensure that machines and equipment are installed and functioning according to specifications.
· Conduct research that tests and analyzes the feasibility, design, operation and performance of equipment, components and systems.
· Recommend design modifications to eliminate machine or system malfunctions.
· Develop and test models of alternate designs and processing methods to assess feasibility, operating condition effects, possible new applications and necessity of modification.
· Develop, coordinate, and monitor all aspects of production, including selection of manufacturing methods, fabrication, and operation of product designs.
· Estimate costs and budget control for submitted bids for engineering, construction, or extraction projects, and prepare contract documents.
· Perform personnel functions such as supervision of production workers, technicians, technologists and other engineers, or design of evaluation programs.
· Research new business and provide technical customer service.
· Establish and coordinate the maintenance and safety procedures, service schedule, and supply of materials required to maintain machines and equipment in the prescribed condition.
· Study industrial processes to determine where and how application of equipment can be made.
· Write performance requirements for product development or engineering projects.
· Apply engineering principles and practices to emerging fields such as robotics, waste management, and biomedical engineering.
· Design test control apparatus and equipment and develop procedures for testing products.
· Achieve company and department business plans for Health and Safety Goals
 
<ul>
<li>Education: Bachelor's Degree in Mechanical Engineering, Manufacturing Engineering, or a related field.</li>
<li>Experience: Minimum of 5 years of experience in machining or manufacturing engineering roles.</li>
<li>Skills: 
<ul>
<li>Proficiency in CAD software and familiarity with engineering principles.</li>
<li>Proficiency in CNC programming and G-Code to write CNC programs.</li>
</ul>
</li>
<li>Excellent leadership and project management skills, with the ability to motivate a team.</li>
<li>Strong analytical and problem-solving skills for cost estimation and project planning.</li>
<li>Effective communication skills for collaboration across departments.</li>
</ul>

Machining Staff Engineer

<h3>Job Description</h3>
Job DescriptionDescription:
Welcome to the future of wound care. AVITA Medical is a therapeutic, acute wound care company leading the development and commercialization of novel wound therapy technologies and skin reconstruction solutions designed to Heal at the Speed of Life™. Our portfolio includes the RECELL® System, which uses a patient’s own cells to stimulate healing and repigmentation in the wound bed, Cohealyx®, a collagen dermal matrix to support cellular migration and revascularization, and PermeaDerm®, a biosynthetic wound matrix that serves as a wound temporizer or primary dressing.
 
As an organization, we believe:
<ul>
<li>Patients are at the heart of everything we do</li>
<li>Our employees are the lifeblood of AVITA Medical</li>
<li>Passion is key to making a difference</li>
<li>Quality impacts everything we do</li>
<li>Integrity is essential to our success</li>
</ul>
The Senior Manufacturing Engineer is a technical resource for manufacturing of AVITA Medical products and as an interface with AVITA Medical contract manufacturers and suppliers. This role will support Engineering development, validation activities, and lead coaches and other engineers on technical requirements to help optimize quality and efficiency. Additionally, assure product control documents are current and properly implemented at suppliers. In charge of designing and recommending processes and equipment for efficient and appropriate manufacturing, and lead the validation and implementation of those processes or equipment. 
Requirements:
<ul>
<li>Competence in engineering skills set (CAD, drawings, manufacturing systems).</li>
<li>Ability to analyze data, identify additional needed information, determine root cause, and offer solutions to problems.</li>
<li>Attention to details and all aspects of medical device quality.</li>
<li>Proficient in communication and working with teams that consist of diverse personnel and scattered locations.</li>
<li>Bachelor’s or Master’s Degree in mechanical, Biomedical, or Industrial Engineering.</li>
<li>5+ years of equivalent industry experience</li>
<li>Medical Device Sterile Packaging and Sterilization experience. </li>
<li>Proven success in working with and improving medical device operations. Knowledge of both FDA QSR and ISO standards. Demonstrated knowledge in product validation and introduction.</li>
<li>This is a full-time position 40 hours per week.</li>
<li>Travel: Approximately 10% </li>
</ul>
Responsibilities
<ul>
<li>Working understanding of statistics for process development including sample size selection, data distribution analysis, process capability, Design of Experiments (DOE), and Analysis of Variance (ANOVA).</li>
<li>Working understanding of inspection methods and procedures (Test Method Validation).</li>
<li>Demonstrate strong problem-solving skills and have the ability to ask critical questions without being the subject matter expert.</li>
<li>Work with product development to design and prototype novel manufacturing processes and equipment.</li>
<li>Establish and execute validation strategies (IQ/OQ/PQ) for new products, processes, and equipment in compliance with ISO 13485 and FDA regulations.</li>
<li>Skilled in fixture design and development, including mechanical design, tolerance analysis, material selection, and CAD-based engineering drawings.</li>
<li>Create and maintain necessary Manufacturing Process Instructions (MP’s), test methods, product drawings, and component specifications.</li>
<li>Ensure product is manufactured in accordance with engineering best practices, AVITA's quality system, international standards and regulations, and specific AVITA requirements.</li>
<li>Provides technical support and performing failure analysis for non-conforming components, assemblies, and process defects.</li>
<li>Implement corrective and preventive actions for production non-conformances.</li>
<li>Continuous process monitoring, evaluation, and improvement for quality, efficiency, and costs to prevent issues before they occur.</li>
<li>Support concurrent engineering efforts within development projects. </li>
<li>Design, document, and implement methods for process control, process improvement, testing, and inspection. </li>
<li>Participate in change control, material review boards, quality system reviews as the engineering representative.</li>
<li>Provide leadership and coaching to other engineers and within operations to optimize quality and efficiency.</li>
<li>Other duties as assigned.</li>
</ul>
AVITA Medical is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on qualifications, merit, and business need. 
Your Physical Work Environment Will Require: The physical demands described here are representative of those that must be met by an individual to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
While performing the duties of this job, the employee is regularly required to sit, talk, and hear, stand, walk and/or balance, use hands and fingers to type, handle, feel, grasp, push, and pull. Hand-eye coordination necessary to operate computers and various pieces of office equipment. Specific vision abilities required by this job include close vision and the ability to adjust focus. The individual is frequently required to reach with hands and arms, and repetitive motion. The individual is occasionally required to stoop, kneel, or crouch. The individual may occasionally lift and/or move up to 25 pounds. 
AVITA Medical is an E-Verify participant. 
 
AVITA Medical recognizes the role of information security in ensuring that users have access to the information they require to carry out their work in a secure manner. AVITA Medical is committed to protecting the security of its information and information systems. As such, each role within AVITA Medical must demonstrate the same commitment to information security.

<h3>Job Description</h3>
Job DescriptionDescription:
Job purpose
 
The Process Engineer I is responsible for evaluating and improving manufacturing processes to reduce cost, improve yields, and reduce variation. This position performs new process design and implementation, process validations and process qualifications. Process Engineers also participate in technology transfer to ensure the processes necessary for new products are effectively translated to manufacturing from R&amp;D. Process Engineer I makes use of statistical analysis methods, critical thinking, process development, and scaling principles to achieve the objectives mentioned above.
 
Duties and responsibilities
 
<ul>
<li>Plan and execute process optimization, equipment qualification, and process validation or process qualification projects.</li>
<li>Use LEAN Manufacturing principles to analyze processes and make recommendations for improvements.</li>
<li>Lead and perform equipment qualifications, process validations or process qualifications, including writing of protocols and reports.</li>
<li>Lead efforts to solve problems using formal problem resolution techniques and root cause analysis.</li>
<li>Create, communicate, and follow project plans with detailed tasks and timelines necessary for project completion. Communicate to management of performance against plan.</li>
<li>Identify and resolve insufficiencies in routine manufacturing and provide constant support to manufacturing team.</li>
<li>Develop standard operating procedures (SOPs) for newly designed or optimized processes, while ensuring compliance with safety and quality standards. </li>
<li>Assess processes, take measurements, and interpret data.</li>
<li>Develop and monitor process and equipment metrics to use for optimization analysis.</li>
<li>Comply with FDA and AATB tissue banking standards.</li>
<li>Other duties as assigned.</li>
</ul>
 
Requirements:
Qualifications
 
Qualifications include:
<ul>
<li>BS in Biomedical, Mechanical or Industrial Engineering or other applicable engineering discipline. Advanced degree (Master’s) a plus.</li>
<li>1-3 years of experience in Tissue Banking, Device, Biologics, or Pharmaceutical industry in a relevant engineering role preferred.</li>
<li>Strong analytical, planning, project management, critical thinking, troubleshooting, clear communication, and problem-solving skills.</li>
<li>Ability to effectively communicate with multidisciplinary teams. </li>
<li>Excellent technical skills and writing.</li>
<li>Strong knowledge of LEAN manufacturing principles preferred.</li>
<li>Working knowledge of 21 CFR 1271 regulations and AATB guidelines preferred.</li>
<li>Proficient in project planning software. Microsoft Project preferred.</li>
<li>CTBS certified (or certified within two years of employment).</li>
<li>Strong work ethics.</li>
</ul>
 
Working conditions
 
Job requires working in office. Must be willing to work weekends and evening hours as necessary. Must be willing to accommodate travel if necessary. The job may require work to be performed inside the controlled clean room processing area where the engineer would be exposed to tissue processing. 
 
Physical requirements
 
The job may entail the occasional requirement to stand for extended periods of time and lifting heavy objects of up to 30 lbs. and do repetitive tasks with few breaks while executing engineering plans.
 
Direct reports
No direct reports

Process Engineer I

<h3>Job Description</h3>
Location: Woburn, MA
 
Vaxess is a NIH and venture-funded company developing a pipeline of next-generation vaccines and therapeutics on the MIMIX platform. With only five minutes of wear-time on the skin, the self-applied MIMIX patch enables up to two weeks of sustained delivery. The platform combines high temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world.
 
Research &amp; development at Vaxess is cross-disciplinary, integrating mechanical, industrial, biomedical, and chemical engineering with chemistry, biology, and human factors to address important unmet medical needs. We are seeking a talented, collaborative, and highly motivated engineer to join our growing team. This role offers a unique opportunity to build manufacturing capacity from the ground up to bring innovative technology to the global vaccine and therapeutic market. 
 
Responsibilities
<ul>
<li>Characterize and improve manufacturing process unit operations by designing, executing, and analyzing process development experiments; communicate results via written reports and oral presentations to internal and project teams</li>
<li>Support manufacturing scale-up by assessing novel equipment, work flows, analytical techniques/PAT, and process configurations</li>
<li>Support manufacturing operations by incorporating equipment and process improvements within established processes and equipment trains, and by revising manufacturing batch records, SOPs, and other controlled documents to reflect changes; contribute to implementing and maintaining Vaxess’ Quality System.</li>
<li>Supervise and mentor junior engineer(s) and technicians, including a direct report</li>
<li>Collaborate closely with cross-functional teams to support product development and manufacturing activities.</li>
</ul>
 
Qualifications
<ul>
<li>BS in Mechanical Engineering, Biomedical Engineering, or a related discipline</li>
<li>5 – 7 years of relevant direct R&amp;D experience within the medical device or biopharmaceutical industries; experience working on combination products is highly desirable</li>
<li>Demonstrated success using empirical and first-principles models to inform and analyze experiments; experience with statistical methodologies and working with large data sets (e.g. Six Sigma, DoEs, multivariate techniques) is a plus</li>
<li>Excellent time and project management skills and proven ability to meet goals and deadlines</li>
<li>Demonstrated abilities to learn new skills and fields, creatively solve challenging technical problems, think independently, and work collaboratively in diverse multidisciplinary teams</li>
<li>Entrepreneurial spirit and drive to positively impact global human health</li>
</ul>
 
Vaxess is building a team of exceptional people to rapidly advance product development. We work closely as a team and thrive in a dynamic, exciting, and engaging work environment. If you’re interested in joining the Vaxess team, please submit your CV/resume to <a href="mailto:careers@vaxess.com" target="_blank">careers@vaxess.com</a>.

Process Engineer III

<h3>Job Description</h3>
Job Title: Manufacturing Engineer III
 Locations:
Newark, CA – 2 Openings (DFM-Focused Roles)
 
About the Role
<ul>
<li>We are seeking experienced Manufacturing Engineers to join our Advanced Manufacturing Engineering – Powertrain Battery Production team. The primary objective is to support the ramp-up of a greenfield mass production facility for powertrain batteries by improving throughput through process optimization, equipment enhancements, headcount planning, and quality improvements.</li>
</ul>
 
Key Responsibilities
<ul>
<li>Work hands-on with production equipment, manufacturing teams, and quality departments to enhance operational efficiency.</li>
<li>Identify production bottlenecks, conduct root cause analysis, and implement effective solutions.</li>
<li>Design, modify, and optimize manufacturing equipment and processes.</li>
<li>Collaborate cross-functionally with controls, equipment, and quality teams.</li>
<li>Support multiple product/line launches from commissioning through ramp-up.</li>
</ul>
 
Required Qualifications
<ul>
<li>Experience: Minimum 5+ years in manufacturing engineering, process engineering, or industrial engineering.</li>
</ul>
 
Backgrounds of Interest:
<ul>
<li>Manufacturing equipment or process engineering in high-volume automation environments.</li>
<li>Systems integrator or equipment builder experience (design/building of automation equipment, robotics, feeder systems, end-of-arm tooling).</li>
<li>Powertrain or battery manufacturing (cylindrical, NMC, or LFP preferred).</li>
</ul>
 
Technical Skills
<ul>
<li>CAD proficiency (CATIA preferred; SolidWorks, Fusion, AutoCAD acceptable).</li>
<li>GD&amp;T and tolerance stack-up analysis.</li>
<li>Root cause analysis, Six Sigma methodologies, and process flow optimization.</li>
<li>Experience with robotic programming, vision systems, and DC tool optimization (preferred).</li>
</ul>
 
Industry Flexibility
<ul>
<li>Equipment design experience from related industries (biomedical, material handling, etc.) is acceptable if automation is heavy.</li>
<li>Pure process experience without battery exposure is less likely to be a fit.</li>
</ul>
 
Day-One Expectations
<ul>
<li>Identify and troubleshoot equipment/process issues immediately.</li>
<li>Design equipment using 2D/3D CAD tools.</li>
<li>Apply GD&amp;T principles and tolerance analysis without supervision.</li>
</ul>
 
Performance Metrics (KPIs)
<ul>
<li>Overall Equipment Effectiveness (OEE) improvement.</li>
<li>First-Time-Through (FTT) quality rates.</li>
<li>Downtime reduction and throughput increase.</li>
</ul>
 
Interview Process
<ul>
<li>Conversational review of work history and experience.</li>
<li>Technical deep dive into problem-solving methods and past improvement projects.</li>
<li>Possible senior engineer panel for specialized areas.</li>
<li>Presentation or portfolio of past work (equipment design examples).</li>
</ul>
 
Disqualification Criteria
<ul>
<li>Lack of automation or equipment background.</li>
<li>Primarily manual process experience without high-volume automation exposure.</li>
<li>No proven hands-on design or troubleshooting experience.</li>
</ul>

Manufacturing Engineer

<h3>Job Description</h3>
Job Description
AUTOMATION ENGINEER
 
POSITION SUMMARY: 
The Automation Engineer within the Production Engineering Group contributes to the implementation of automation systems and workflows to support the processing of samples in a clinical diagnostics laboratory environment. This individual collaborates with teams to implement and support solutions designed to optimize the performance and increase the efficiencies of the laboratory processes.
PRIMARY RESPONSIBILITIES:
<ul>
<li>Program and deploy liquid handling robots and work cells</li>
<li>Support production through troubleshooting down liquid handling robots and work cells</li>
<li>Build rapport with end-users, and engineering colleagues</li>
<li>Deploy, optimize, support and test the automation systems and related software tools.</li>
<li>Promptly complete documentation utilizing good documentation practices.</li>
<li>Prepare User Requirement and Testing Procedure, Standard Operating Procedures, and related documentations</li>
<li>Perform the functional testing and qualification</li>
<li>Additional responsibilities as needed</li>
</ul>
QUALIFICATIONS:
<ul>
<li>BS degree in Biomedical engineering, closely related scientific field, or equivalent</li>
<li>2+ years of laboratory automation engineering experience required</li>
<li>Technical proficiency and experience in automation and systems development and integration for the life science industry; especially with robotics and liquid handling systems. </li>
<li>Experience in computer programing is required.</li>
</ul>
KNOWLEDGE, SKILLS, AND ABILITIES:
<ul>
<li>Strong project management skills, organizational skills, and written and verbal communication skills are required. </li>
<li>Flexibility and self-initiative required to support several simultaneous automation projects. </li>
<li>Biotech, pharmaceutical, Lab automation providers, or clinical-laboratory experience is highly desirable</li>
</ul>
The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.San Carlos, CA $112,000—$140,000 USD
OUR OPPORTUNITY
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
For more information, visit <a href="http://www.natera.com" target="_blank">www.natera.com</a>.
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
If you are based in California, we encourage you to read this important information for California residents. 
Link: <a href="https://www.natera.com/notice-of-data-collection-california-residents/" target="_blank">https://www.natera.com/notice-of-data-collection-california-residents/</a>
Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
For more information: - BBB announcement on job scams - FBI Cyber Crime resource page

Automation Engineer

<h3>Job Description</h3>
Job Description
Lexington Medical is a medical device company, developing and manufacturing minimally invasive surgical stapling solutions in the Boston area. With the highest standards in design engineering and smart manufacturing, our team delivers disruptive technology to health care providers which improves surgical outcomes for their patients in a thriving $6B+ Surgical Stapler market. 
Rooted in a talent dense culture, we are committed to innovation, foster continuous growth and achieve great heights, together. At Lexington Medical, you will have the opportunity to impact the lives of millions of patients worldwide and thrive in a growing company. 
As a Manufacturing Engineer at Lexington Medical, you'll design and commission both simple and complex equipment to serve the needs of our in-house production environment. Our ideal candidate will have demonstrated hardware experience and is looking to apply it to manufacturing and scaling production lines. A successful applicant will embrace working on a different challenge every day and thrive in an environment with many competing and shifting priorities. At Lexington Medical, we are proud to have our manufacturing facility in Massachusetts, which offers our manufacturing engineers the ability to be hands-on and interact directly with the products that we build. 
Responsibilities:
<ul>
<li>Design, manufacture, and implement production fixturing and equipment as well as the processes that surround them.</li>
<li>Work with external vendors to commission custom equipment for Lexington Medical's production environments.</li>
<li>Serve as the primary engineer supporting certain production processes and equipment.</li>
<li>Document and maintain manufacturing process written instructions.</li>
<li>Provide training to production personnel on manufacturing processes.</li>
<li>Assist in Equipment Qualification and Validation testing. </li>
</ul>
Qualifications: 
<ul>
<li>BS or MS in Mechanical, Biomedical, Manufacturing, or Industrial Engineering.</li>
<li>Experience in manufacturing environments and working with mechanical and/or electromechanical products.</li>
<li>Working knowledge of various production methods and 3D CAD tools (SolidWorks preferred).</li>
<li>Experience designing, fabricating, and debugging mechanical systems.</li>
<li>Continuous improvement mindset, driven to find opportunities for positive change.</li>
<li>(Preferred, but not required) Experience working with industrial automation, wiring, and programming. </li>
</ul>

<h3>Job Description</h3>
Job Description
Lexington Medical is a medical device company, developing and manufacturing minimally invasive surgical stapling solutions in the Boston area. With the highest standards in design engineering and smart manufacturing, our team delivers disruptive technology to health care providers which improves surgical outcomes for their patients in a thriving $6B+ Surgical Stapler market. 
Rooted in a talent dense culture, we are committed to innovation, foster continuous growth and achieve great heights, together. At Lexington Medical, you will have the opportunity to impact the lives of millions of patients worldwide and thrive in a growing company.
We have an exciting opportunity for a Product Engineer. In this role, you will play a pivotal role in defining, designing, and developing best-in-class surgical devices. Our ideal candidate will embrace working in a fast-paced, entrepreneurial and collaborative environment; be a self-starter, independent, results-oriented team player with a demonstrated ability to manage multiple projects and deadlines including shifting priorities. If you enjoy wearing many hats and are looking to have an immediate impact, this job might be exactly the opportunity you've been looking for!Responsibilities:
<ul>
<li>Provide engineering input during all stages of product development.</li>
<li>Convert validated product prototype (Prototype Model) to manufacturing ready model (Production Model).</li>
<li>Create Production Model Design Documentation.</li>
<li>Assist Product Manager with New Model Development Process.</li>
<li>Create and execute design of experiments for testing new materials and/or manufacturing processes to enhance product quality, functionality and potential reduction in manufacturing time.</li>
<li>Develop incremental design improvements based on customer feedback.</li>
<li>Develop Lexington Medical product knowledge as well as hands-on ability to operate.</li>
<li>Work independently across functions including with Research &amp; Development and Manufacturing Engineering.</li>
</ul>
Qualifications:
<ul>
<li>BS in Mechanical or Biomedical Engineering.</li>
<li>Medical device design experience preferred.</li>
<li>Working knowledge of 3D CAD tools (SolidWorks preferred).</li>
<li>Experience in product development and product lifecycle management.</li>
<li>Demonstrated theoretical and practical engineering fundamentals.</li>
<li>Exceptional technical zeal, problem-solving skills and reasoning ability.</li>
<li>Mechanical aptitude to use experimental engineering techniques in the lab.</li>
<li>Demonstrated motivation, curiosity and creativity.</li>
</ul>

Product Engineer

<h3>Job Description</h3>
Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
The position reports to the Head of Product Development and Manufacturing, and is responsible for meeting site production, safety, and quality requirements by developing and establishing automated systems for mRNA synthesis, quality control experiments, high throughput gene synthesis platform and other emerging molecular biology service lines at the Redmond site of the GenScript Innovation Center.
Responsibilities:
<ol>
<li>Independently manage or contribute to all laboratory automation projects including conception, design, development, acquisition, process implementation and execution of automation solutions for manufacturing</li>
<li>Define scope of project in consultation with supervisor and stakeholders. Individually or collaboratively through leadership of project team, define alternative solutions, and decision criteria used to evaluate alternatives.</li>
<li>Develop and optimize automation solutions for RNA synthesis by in vitro transcription and purification, and high throughput nucleic acid synthesis platforms. Script for automated platforms based on project needs.</li>
<li>Provide support for the DNA and RNA production line by leveraging automation tools to achieve revenue goals. Troubleshoot issues, if occur, with automation systems, propose effective solutions and coordinate system updates and enhancements to optimize performance.</li>
<li>Oversee preventative maintenance and calibration of automated system instruments, ensuring optimal performance and reliability. Collaborate with the equipment engineering team, internal stakeholders including QA team, production team and external vendors to provide technical input, review and approve testing documents and protocols of automation systems as needed.</li>
<li>Acquire new technologies to develop, optimize and improve existing high throughput laboratory automation systems.</li>
<li>Provide day-to-day maintenance and production support for the manufacturing equipment and staff.</li>
</ol>
Qualifications
<ol>
<li>BS in Engineering Discipline or Biology/ Biochemistry/ Molecular Biology/ Biomedical Instrumentation/ related subjects with 2+ years of automation experience in manufacturing</li>
<li>Proven track of workflow design and process optimization with automation</li>
<li>Experience in transforming bench work process to automation solutions</li>
<li>Knowledge of commercial automated liquid handlers, experience in handling/maintaining automated liquid handlers, e.g., Tecan, Beckman, PerkinElmer, etc.</li>
<li>Basic understanding of hands-on molecular biology experiments is required</li>
<li>Knowledge of automated production line is a plus</li>
<li>Ability to effectively interact with individuals at all levels and good organizational and project management skills.</li>
<li>Patient, attend to details and is able to follow SOPs</li>
<li>Flexible to work in non-standard work hours in the case of emergency situations</li>
</ol>
Benefit:
<ul>
<li>Medical Insurance/ Vision Insurance/ Dental Insurance</li>
<li>401(k) &amp; Retirement Savings Plan (RSP)</li>
<li>Short Term Disability Insurance</li>
<li>New Child Leave</li>
<li>Paid Time Off</li>
<li>Paid Company Holidays per year</li>
<li>Paid Sick Days (earned based on hours worked)</li>
<li>Compassionate Leave</li>
<li>Jury Duty Leave</li>
<li>Float day</li>
<li>Personal days</li>
</ul>
Perks: 
<ul>
<li>Free colleague meals during shift</li>
<li>Onsite massage Charis</li>
<li>Onsite gyms</li>
</ul>
Compensation: Salary range: $85,000 – $130,000, depending on experience and qualifications.
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

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