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<h3>Job Description</h3>
Mechanical (Sheet Metal / Hydronic) Estimator
 
Job Description:
A.O. Reed &amp; Co. is a mechanical contractor located in Los Angeles and San Diego, California. We have been in business since 1914 and are actively involved in commercial construction within Southern California. A.O. Reed is seeking a Mechanical (Sheet Metal/ Hydronic) Estimator to accurately determine the cost of mechanical projects, including HVAC, hydronic piping, and other mechanical systems.&nbsp;This person will collaborate with our sales team, engineers, vendors, and subcontractors to ensure projects are completed within budget and on schedule.&nbsp;A.O. Reed constructs various types of projects, including hospitals, laboratories, offices, hotels, and high-rise buildings. Using computer skills and onscreen Quick Pen is required. A.O. Reed not only provides health insurance for its employees, but also for their families, at no cost to the employees. Along with benefits, A.O. Reed offers a competitive salary. 
 
Qualifications:
<ul>
<li>High School Diploma</li>
<li>Must work in the construction industry for at least five years.</li>
<li>At least five years of experience estimating technical commercial construction projects, is preferred.</li>
<li>Detailed knowledge of HVAC and piping systems.</li>
<li>Proficient in Quick Pen.</li>
<li>Proficient in Microsoft Office applications.</li>
<li>A team player who has strong communication skills, produces quality work, manages multiple tasks, and meets all deadlines.</li>
<li>Team player with the ability to work with minimal supervision.</li>
<li>Works alongside and supports co-workers with enthusiasm.</li>
<li>Flexibility and willingness to learn the office operations at A.O. Reed.</li>
<li>Applicant must be detail-oriented.</li>
</ul>
 
Responsibilities:
<ul>
<li>Prepare project piping and/or mechanical estimates. Navigate in accordance with the scope of work and develop quantity take-offs. Determine manpower, equipment, materials, and subcontractor requirements.</li>
<li>Reviewing project documents: Analyzing drawings, specifications, and other documentation to understand the scope of work. </li>
<li>Preparing cost estimates: Developing detailed cost breakdowns for materials, labor, equipment, and other expenses. </li>
<li>Material take-offs: Utilizing estimating software Trimble Autobid for Sheet Metal and Hydronic piping. Plumbing is a plus.&nbsp;</li>
<li>Develop and apply labor factors based on-site conditions, work activity types, and historical performance data.</li>
<li>Sourcing materials and labor: Obtaining quotes from suppliers and subcontractors to determine the best pricing. </li>
<li>Obtain clarification of questions or conflicts that affect the estimate.</li>
<li>Could you work on constructability reviews?</li>
<li>Prepare cost studies utilizing historical data, statistical analysis, cost, and quantity comparisons.</li>
<li>Develop new techniques for piping and mechanical systems to meet the specific needs of the project.</li>
<li>Conduct bid review to finalize estimate, markup, and strategies.</li>
<li>Prepare pricing sheets, bid forms, and other proposal documents for in-house review and submittal.</li>
<li>Preparing proposals: Assembling final estimates with the Chief Estimator using Excel and Word documents. </li>
<li>Collaboration: Working with various teams, including project managers, engineers, and subcontractors, to ensure accurate cost assessments. </li>
<li>Staying current: Keeping up-to-date with industry trends, material costs, and construction techniques. </li>
<li>Maintaining records: Keeping accurate records of estimates, bids, and correspondence.</li>
<li>Assist with maintaining the estimating database.</li>
</ul>
 
 
Range: $75,000 - $125,000

Mechanical Estimator

<h3>Job Description</h3>
Client: Medical Device
 
Project Details
<ul>
<li>3-Month contract, with high possibility of permanent conversion.</li>
<li>On-site, 5 days per week.</li>
</ul>
 
Qualifications
<ul>
<li>BS in a relevant scientific or engineering discipline, with 7+ years in the medical device field.</li>
<li>The ideal candidate should have hands-on experience in risk identification, design verification, and testing.</li>
<li>Full understanding of the design control process, and ISO 13485 &amp; EU-MDR.</li>
</ul>

Sr Design Quality Engineer

<h3>Job Description</h3>
Production Lead (Production Manager)
 
Summary: 
The Production Manager for the Produce Processing Center plays a vital role in overseeing the efficient and effective production operations of perishable goods within our organization. This includes managing a team, implementing production processes, ensuring quality standards, optimizing productivity, and maintaining compliance with food safety regulations. The Production Manager is responsible for meeting production targets, maximizing efficiency, and ensuring the timely delivery of high-quality perishable products to retail stores.
 
Responsibilities:
<ul>
<li>Manage day-to-day operations of the packing center, including scheduling, production planning, and inventory management, while implementing standard operating procedures for efficiency optimization.</li>
<li>Lead, supervise, and develop a productive team by providing guidance, training, and performance management to enhance production efficiency and quality.</li>
<li>Optimize perishable processing center operations to ensure smooth workflow, efficient production, and adherence to quality standards, safety guidelines, and regulatory requirements.</li>
<li>Develop and implement production plans, schedules, and strategies to maximize operational goals, inventory management, and cost control, while meeting timely delivery requirements.</li>
<li>Collaborate with cross-functional teams, including Merchandising Managers, Store Operation, Logistics, Receiving, and Quality Control teams, to ensure quality, pricing, timely delivery, and accurate product supply.</li>
<li>Foster a culture of safety, continuous improvement, innovation, and strong relationships with suppliers and vendors to promote a safe working environment, encourage employee ideas, and support seamless production processes.</li>
<li>Analyze production data and metrics, identify trends, bottlenecks, and process optimization opportunities, and present reports and recommendations to senior management.</li>
<li>Ensure compliance with company policies, procedures, and regulatory requirements related to production operations and occupational health and safety standards.</li>
<li>Monitor production processes for inefficiencies or bottlenecks and implement corrective actions as needed to enhance productivity and quality.</li>
<li>Control production costs, including labor, materials, and operational expenses, to meet budgetary targets and maximize profitability.</li>
<li>Provide regular reports on production performance, efficiency, and quality, based on analyzed data and metrics.</li>
<li>Stay updated on industry trends, technological advancements, and best practices in perishable processing to drive operational excellence.</li>
<li>Perform other duties as assigned by management.</li>
</ul>
 
Qualification:
<ul>
<li>A Bachelor's degree in Business Administration, Operations Management, or a related field is preferred.</li>
<li>3+ years of experience in production, preferably in perishable goods or food processing, is required.</li>
<li>1+ year of experience managing a production facility is required.</li>
<li>Proficiency in Microsoft Office and other relevant software applications.</li>
<li>Familiarity with industry regulations and standards related to food safety, quality, and packaging.</li>
<li>Knowledge of perishable processing operations, quality control practices, and regulatory compliance.</li>
<li>Strong leadership skills to effectively manage and develop a team.</li>
<li>Strong communication, problem-solving, and analytical skills.</li>
<li>Strong organizational and problem-solving abilities with attention to detail and accuracy.</li>
<li>Ability to thrive in a fast-paced environment and manage multiple priorities simultaneously.</li>
<li>Bilingual proficiency in English/Mandarin or English/Spanish preferred.</li>
<li>Authorized to work in the United States without sponsorship.</li>
</ul>
 
Physical Requirements:
<ul>
<li>Prolonged periods of sitting at a desk and working on a computer.</li>
<li>This job may require standing or walking for extended periods of time, lifting up to 50 pounds, and performing repetitive motions.</li>
<li>Ability to use tools and equipment, including but not limited to knives, box cutters, electric pallet jacks, and other heavy machinery.</li>
</ul>
 
Working Conditions: 
<ul>
<li>This job is performed in a production environment that may have exposure to heat, noise, and other environmental factors associated with food production.</li>
</ul>
 
Position Details:
<ul>
<li>Employment Type: Full Time</li>
<li>Location: 6336 Regio Ave, Buena Park, CA 90620</li>
<li>Available to work 6 days a week, and may be required to work weekends, holidays, and night shifts as necessary.</li>
</ul>
 
Benefits: 
<ul>
<li>Medical, Dental, Vision, and Life Insurance.</li>
<li>401 (k) Retirement Saving Plan with 4% Company Match</li>
<li>Long-Term Services Award.</li>
<li>Employee Discount.</li>
<li>Paid Time Off</li>
</ul>
 
Compensation:
The pay range for this job starts at $70,000 per year. This is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) the responsibilities of the job, your education, skills, qualifications, experience, and location.
 
Beware of Job Scams:
We prioritize applicant safety at Tawa Group. Please exercise caution during your job search. Be wary of unsolicited offers, requests for personal information or upfront payments, poorly written job descriptions, unrealistic promises, and unprofessional communication. Research employers, verify job postings, and trust your instincts. Report any suspicious activity. For helpful guidance on identifying job scams, visit this link provided by the Indeed website: <a href="https://www.indeed.com/career-advice/finding-a-job/job-scams" target="_blank">https://www.indeed.com/career-advice/finding-a-job/job-scams</a>
 
Disclaimer:
Tawa Group dba 99 Ranch Market, is an equal opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Production Lead

<h3>Job Description</h3>
Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA editing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, we welcome you to apply.
 
Job Description: High-Throughput Screening Research Associate II, III (Biodesigner II, III)
 
Responsibilities:
<ul>
<li>Perform massively parallel reporter assays and high-throughput screens across diverse cellular contexts using cellular and molecular readouts.</li>
<li>Develop and execute molecular biology workflows such as vector design and cloning, DNA/RNA extraction, RT-PCR, qPCR, and next-generation sequencing.</li>
<li>Support cell culture activities and experiments in multiple cell lines, at small and large scales.</li>
<li>Design and execute cell-based assays (AAV/lentiviral transduction, transfection, flow cytometry, immunostaining, and other plate reader assays).</li>
<li>Engineer and characterize cell-based systems using synthetic biology tools and techniques.</li>
<li>Conduct and troubleshoot experiments, independently and in collaboration with colleagues, to optimize screening throughput, sensitivity, and specificity.</li>
<li>Proactively troubleshoot technical issues and recommend potential corrective actions based on personal observations and literature searches.</li>
<li>Prepare summaries of data and present internally to colleagues and management.</li>
<li>Draft SOPs, follow protocols, diligently document experimental data in lab notebooks, and organize and maintain electronic work records.</li>
<li>Author scientific reports and data summaries.</li>
<li>Collaborate with cross-functional teams to meet project goals, bridging early discovery with high-throughput screens to nominate and optimize candidates for further characterization.</li>
</ul>
 
Qualifications:
<ul>
<li>Bachelor’s or Master’s degree in Biology, Biochemistry, Chemical Engineering, Biological Engineering, or a related field.</li>
<li>At least 2 years of industry wet lab experience.</li>
<li>Mammalian cell culture experience (culturing, transfecting and transducing cells, and DNA/RNA purification from cells).</li>
<li>Molecular biology expertise (vector design and cloning, qPCR, primer and probe design, DNA/RNA extraction workflows)</li>
<li>Critical thinker with excellent communication skills who thrives in a multidisciplinary, fast-paced team environment.</li>
<li>Strong written and verbal communication skills.</li>
</ul>
 
Preference will be given to those who display:
<ul>
<li>High throughput screening assay development in an industry setting.</li>
<li>High motivation, with a strong work ethic and dedication to generating impact.</li>
<li>Attention to detail, with the ability to extract deep insights from data.</li>
<li>First-principles thinking, and an ability to refine one’s intuition based on additional data.</li>
<li>Ability to go from ideation to data in an independent fashion.</li>
<li>Long-term personal vision with defined career goals.</li>
<li>High EQ with team-oriented thinking.</li>
<li>Experience with pooled, high-throughput screens using next-generation sequencing-based readouts, and/or preparing screening plasmid libraries from synthesized oligo arrays.</li>
<li>Experience with CRISPR-Cas systems and/or gene editing and delivery technologies.</li>
<li>Experience preparing next-generation sequencing libraries (Illumina, PacBio, and/or Nanopore platforms).</li>
</ul>
 
If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team.
 
Please apply directly through LinkedIn.
 
Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.

High-Throughput Screening Research Associate II, III (Biodesigner II, III)

<h3>Job Description</h3>
Are you passionate about making a real impact in healthcare? Do you thrive in an environment that values integrity, curiosity and excellence? We’re looking for an Associate Principal Mechanical Engineer for a permanent position in San Diego. A unique opportunity to work with a dynamic team in the Diagnostic Group, contribute to meaningful projects, and grow both personally and professionally. If this sounds like the challenge you’ve been looking for, we’d love to meet you.
 
About Us
At Invetech, we revolutionize healthcare by developing products that make a difference. As global innovators with over 35 years of experience, we blend creativity, commercial insight, and technical expertise to drive success for our clients. Our mission is to deliver impactful solutions while continuously evolving and pushing the boundaries of what’s possible. We’re seeking talented individuals who share our values and are ready to contribute to our journey of innovation and excellence.
 
Why Join Us?
We cultivate a work environment built on trust, collaboration, humility, and continuous improvement. Here, you’ll have opportunities to learn, grow, and make a tangible difference for our clients, team and community. Whether you’re early in your career or a seasoned professional, at Invetech you’ll find a place where you can thrive.
 
What You Will Do &amp; What You Will Bring
As an Associate Principal Engineer, you will:
<ul>
<li>Lead the design of complex electro-mechanical systems, focusing on system architecture for breakthrough diagnostic products.</li>
<li>Consult with clients to capture key requirements, constraints, and engineering criteria, then architect system designs that deliver breakthrough products while meeting business, technical, and regulatory goals.</li>
<li>Direct cross-functional engineering teams, ensuring designs are robust, compliant, and delivered on time and on budget.</li>
<li>Mentor engineers, fostering technical excellence, quality, and manufacturability.</li>
<li>Provide technical leadership and mentoring to ensure quality, manufacturability, and successful transfer of products to manufacture.</li>
<li>Drive design for manufacture and assembly (DFMA), configuration management, and production-readiness across medium- and high-volume product lines.</li>
<li>Manage build activities within staged development programs and offer cross-project guidance for consumer, industrial, diagnostic, and life sciences products.</li>
<li>Champion compliance with quality, regulatory, and safety standards while promoting best practices and continuous improvement.</li>
</ul>
 
In addition, we require the following skills and experience:
<ul>
<li>Accredited Mechanical Engineering qualification or equivalent (Master’s or PhD highly regarded)</li>
<li>8+ years industrial experience in product development ideally in medical diagnostic instrument and device development or similarly complex electro-mechanical products</li>
<li>Demonstrated expertise in design transfer and manufacturing establishment</li>
<li>Familiarity with working to ISO13845 or ISO 9001</li>
<li>Exceptional problem-solving, leadership, and project management capabilities</li>
<li>Strong communication skills with a proven ability to collaborate effectively with remote teams</li>
<li>In-depth technical and engineering knowledge on designing mechanical systems in areas such as optical, thermal, fluidics, robotics devices</li>
<li>Strong knowledge in materials across metals, plastics, composites, and related manufacturing processes</li>
</ul>
 
What we offer:
Along with a great team of people to work with, at Invetech we also offer a great Benefits program, 401k matching, a comprehensive EAP, and various social clubs and events, just to name a few!
 
Ready to Make a Difference?
If you’re looking to join a company that does meaningful work and influences positive health outcomes, joining Invetech may be just the right opportunity for you. Apply today by submitting your resume and a brief cover letter outlining why you’re a great fit for this role.
 
Invetech recognizes the value of an inclusive and diverse work environment across the organization. We believe everyone deserves the same opportunities in life, regardless of gender or identity, sexual orientation, race, ethnicity, religion, disability, or age.
 
Please click here to see our Privacy Notice.
 
 
 
Pay Range
The salary range for this position is USD $130,000 - USD $150,000

Associate Principal Mechanical Engineer

<h3>Job Description</h3>
We are seeking a Product Development Tech to contribute to the completion of routine technical tasks and develops solutions to routine technical problems of specified scope. 
This is a 1st shift position. 
 
Duties and Responsibilities:
• Gathers, maintains, formats, compiles, and manipulates technical data, such as laboratory or material test results and engineering design changes. Produces engineering document, reports, and drawings (flow charts, block diagrams and schematics)
• Prepares reports and summaries, including quantitative analysis
• Provides completion of technical tasks.
• Provides technical support to engineers on a variety of technical tasks.
• Helps scope equipment for use and complete qualifications
• Works with team to on general lab functions; including calibration, implementation of safety procedures, and routine equipment maintenance
• Notifies manager or team lead upon recognition of factors that may affect project
• Helps develop prototype processes and test set-ups
• Executes designed test protocol and conducts testing
• Effectively documents and communicates test results
• Handles chemicals occasionally using provided protective equipment
• Supports hardware debugging
 
Requirements:
<ul>
<li>A minimum of training of high school or secondary school in a technical discipline with 2-4 years relevant experience in a relevant R&amp;D setting.</li>
<li>Preferred Requirement: A technical degree such as B.S. degree + 1-2 years of experience in a related field.</li>
</ul>
 
Preferred Qualifications and Experience:
<ul>
<li>Work history in physical and mechanical testing environment or education in physical/biological sciences</li>
<li>Experience in lab setting (involves handling chemicals, wearing personal protective equipment, etc.)</li>
<li>Familiarity with research/engineering documents (test protocols, coordinate drawings, equipment manuals, etc.)</li>
</ul>

Mechanical Engineering Technician

<h3>Job Description</h3>
Job Title: Manufacturing Engineer I
Location: Irvine, CA
Contract Length: 18 months

Job Summary: 
Develops and improves manufacturing processes by studying product and manufacturing methods.
Evaluates manufacturing processes by designing and conducting research programs; applying knowledge of product design, fabrication, assembly, tooling, and materials; conferring with equipment vendors; soliciting observations from operators.
Primary Responsibilities:
• Develops manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing methods and equipment; conferring with equipment vendors.
• Improves manufacturing efficiency by analyzing and planning work flow, space requirements, and equipment layout.
• Assures product and process quality by designing testing methods; testing finished- product and process capabilities; establishing standards; confirming manufacturing processes.
• Provides manufacturing decision-making information by calculating production, labor, and material costs; reviewing production schedules; estimating future requirements.
• Prepares product and process reports by collecting, analyzing, and summarizing information and trends. .
• Provides manufacturing engineering information by answering questions and requests. • Maintains product and company reputation by complying with government regulations.
• Keeps equipment operational by coordinating maintenance and repair services; following manufacturer's instructions and established procedures; requesting special service.
• Maintains product and process data base by writing computer programs; entering data.
• Completes design and development projects by training and guiding technicians.
• Maintains professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks; participating in professional societies.
• Contributes to team effort by accomplishing related results as needed.
MUST HAVE
1. Advanced Degree in Engineering or related discipline
2. Quality mindset/detailed
3. Willingness to learn and grow and take initiative to do so

Manufacturing Engineer I (Biomedical Engineering)

<h3>Job Description</h3>
Watch your work come to life in landmark projects around the world when you partner with Syska Hennessy Group! As a global leader in consulting, engineering, and commissioning services, we specialize in MEP, information and communication technology, architectural lighting, vertical transportation, and commissioning. We currently have an entry level opportunity for a Mechanical Engineering Graduate. 
Our dynamic work environment provides the optimal setting to start your career. From our supportive culture, diverse workforce, and competitive compensation to our flexible work schedules and fun social events, it is everything you will need for an exciting, challenging, and rewarding career.
Job Responsibilities:
As an entry level engineer, you will support our engineering teams working towards our designs that are inspiring, demanding and highly collaborative. You will learn from others, and they will expect to learn from you. You will share in the responsibility, rewards, and recognition of producing truly innovative solutions and complete client satisfaction.
Some responsibilities include:
<ul>
<li>Create basic designs under the direction of the senior engineer and/or senior designer</li>
<li>Learn drawing organization and company standards.</li>
<li>Perform CAD/BIM-drafting for a variety of projects and project sizes to begin to understand architectural engineering design and documentation.</li>
<li>Coordination with the designs of other trades (architectural, engineering / internal, and external) under the guidance of more senior technical staff</li>
<li>Support the design and engineering efforts of systems for new installations, system retrofits, system replacement and system upgrades for a wide variety of projects and project types.</li>
<li>Take ownership of completeness, accuracy, and timeliness of the work assignments.</li>
<li>Assists engineers with field investigations and construction site visits to observe and attend project coordination meetings.</li>
<li>Participate and regularly attend the EDT program training sessions and support activities that are part of the EDT program.</li>
<li>Attending our Engineering Development Program continuing education seminars on technical and professional enhancing topics.</li>
</ul>
Job Requirements:
The ideal candidate will enjoy a team environment and be flexible enough to work independently where needed. Candidates for this role will be eager to learn and will expand their knowledge and hands-on experience by challenging themselves and using the highly technical resources around them.
Additional job requirements:
<ul>
<li>Bachelor's Degree from an accredited university in Mechanical engineering with a graduation date of Winter 2025, Spring or Summer of 2026</li>
<li>Previous engineering internship, a plus</li>
<li>Knowledge of the latest version of MEP Auto CAD; REVIT experience is a plus.</li>
<li>Proficient in design and calculation software; MS Office Suite</li>
<li>FE and EIT preferred.</li>
</ul>
Benefits:
As an employee at Syska Hennessy, you will be part of a global firm with an amazing history! We are committed to being the best, to advancing engineering design practice, and to supporting our clients with integrity. To make all of that happen, we rely on the talent, drive, enthusiasm, and the total job satisfaction of the great people who work here.
Our Company is committed to developing engineers into respected technical experts and versatile business leaders through our Engineer Development Program (EDT).
About the EDT Program
Recent graduates interested in our Engineering Development Training (EDT) program can expect to participate in an accelerated, but thorough training curriculum. This curriculum will teach not only the technical aspects of our profession, but industry specific business aspects as well. Our senior engineers will work closely with each participant to foster a strong mentor/apprentice relationship.
This time-honored program is a trademark of Syska's commitment to the development and education of young engineers through mentoring and technical training.
As a member of our highly collaborative team, we provide our full-time employees with a flexible benefits package that reflects our respect for your workplace contributions, professional goals, and personal priorities. The personal benefits program at Syska Hennessy Group includes:
<ul>
<li>Medical, Dental, Vision insurance</li>
<li>401(k) retirement plan with employer matching</li>
<li>Individual and Dependent Life Insurance</li>
<li>Short- and Long-Term Disability</li>
<li>Health Wellness Programs including flu shots and biometric screenings</li>
<li>Training and professional development courses</li>
<li>Professional development incentive bonuses</li>
<li>Opportunities for community outreach through internal networks</li>
<li>Personal Time Off Program (PTO)</li>
<li>Transit/parking program</li>
<li>Monthly business phone stipend</li>
<li>Work from home Fridays</li>
</ul>
At Syska, we have cultivated a community that supports learning and provides guidance for professional development and furthering our culture of excellence. We promote an environment that is committed to embedding diversity and equality into the core of our business and culture. We empower our employees so they can take ownership of their work and development and strive to continually improve themselves and our firm. We rely on the talent, drive, enthusiasm and the total job satisfaction of the great people who work here for our success! Syska is a place where you can build an exceptional career and have a lasting impact on the world.
Syska Hennessy Group
Integrating the best minds and technology to help clients create exceptional environments.
The salary range listed below is for this particular job posting. Actual pay range for candidates will be commensurate with candidate's experience, skillsets and competencies and may differ based on the cost of labor in their particular location.
 
California Pay range $58,950-$88,425 USD

Mechanical Engineer I

<h3>Job Description</h3>
About ClearPath Medical
ClearPath Medical is a fast-growing, FDA-registered, ISO 13485-certified contract manufacturer specializing in the design, development, and production of custom medical cables and associated devices. We partner with leading medical device companies to deliver reliable, innovative solutions that improve patient outcomes.
 
Position Summary
We are seeking a&nbsp;hands-on Manufacturing Automation Engineer&nbsp;to join our team and drive innovation in manufacturing automation, tooling, and fixtures. This role will be responsible for assessing needs, designing solutions, and implementing automation technologies to support and scale ClearPath's production of medical devices. The ideal candidate will thrive in a collaborative environment, bringing strong technical skills and a passion for building efficient, reliable systems.
 
Key Responsibilities
<ul>
<li>Assess production processes to identify opportunities for automation and efficiency improvements.</li>
<li>Design, develop, and implement automated systems, fixtures, and tooling to support manufacturing operations.</li>
<li>Program, troubleshoot, and maintain PLC-based control systems and related automation technologies.</li>
<li>Integrate and deploy collaborative robots (cobots) for manufacturing applications.</li>
<li>Design fixturing and automation components using SolidWorks.</li>
<li>Utilize tool room equipment to fabricate, assemble, and validate automation solutions.</li>
<li>Collaborate cross-functionally with engineering, quality, and production teams to ensure solutions meet technical and regulatory requirements.</li>
<li>Provide training and support for production staff on new equipment and automation processes.</li>
</ul>
 
Qualifications
<ul>
<li>Bachelor's degree in Mechanical, Electrical, or Mechatronics Engineering (or equivalent experience).</li>
<li>Minimum&nbsp;2-3 years of focused experience in automation engineering&nbsp;within a manufacturing environment.</li>
<li>Hands-on experience with&nbsp;PLC programming and core automation principles.</li>
<li>Preferred experience with&nbsp;cobot integration&nbsp;(e.g., UR, FANUC, or similar platforms).</li>
<li>Proficiency in&nbsp;SolidWorks&nbsp;for fixturing and tooling design.</li>
<li>Practical experience building automation systems using tool room equipment.</li>
<li>Strong troubleshooting, problem-solving, and project management skills.</li>
<li>Ability to work independently and collaboratively in a fast-paced, regulated environment.</li>
</ul>
 
Why Join ClearPath Medical?
<ul>
<li>Be part of a rapidly growing company making a direct impact in the medical device industry.</li>
<li>Work on diverse projects that combine creativity, engineering, and innovation.</li>
<li>Collaborative, team-oriented culture where your contributions matter.</li>
<li>Competitive compensation and benefits package.</li>
</ul>

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