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<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>
Job Summary
The Staff Supplier Quality Engineer ensures that all products and services provided by suppliers meet internal and external quality standards. This role involves leading supplier audits, managing quality metrics, and driving continuous improvement initiatives across the supply base. The engineer acts as a key liaison between suppliers and internal teams, ensuring compliance with regulatory requirements and company standards.
 
Key Responsibilities:
Supplier Management &amp; Auditing
<ul>
<li>Lead and conduct supplier audits (ISO, GMP, FDA, etc.) based on annual schedules.</li>
<li>Evaluate and approve suppliers for inclusion in the Approved Supplier List (ASL).</li>
<li>Monitor supplier performance using KPIs.</li>
<li>Develop and implement supplier certification and re-certification programs.</li>
</ul>
 
Quality Systems &amp; Compliance
<ul>
<li>Ensure supplier compliance with ISO 13485, 21 CFR 820, and other applicable regulations.</li>
<li>Maintain and improve Supplier Quality Management metrics and documentation.</li>
<li>Support CAPA investigations and non-conformance resolution related to supplier issues.</li>
<li>Facilitate Manufacturing Quality Agreements (MQAs) and ensure proper documentation.</li>
</ul>
 
Product Development &amp; Validation
<ul>
<li>Collaborate with R&amp;D and manufacturing teams during design and process validation phases.</li>
<li>Provide input on statistical methods, test methodologies, and validation protocols.</li>
<li>Support process improvement initiatives and risk assessments using tools like FMEA and DOE.</li>
</ul>
 
Training &amp; Mentorship
<ul>
<li>Train internal teams and suppliers on quality tools and regulatory requirements.</li>
<li>Mentor junior engineers and support their development in supplier quality practices.</li>
</ul>
 
Post-Market Surveillance
<ul>
<li>Investigate supplier-related complaints, MDRs, and recalls.</li>
<li>Coordinate corrective actions and ensure timely closure of audit findings.</li>
</ul>
 
Qualifications:
Education
<ul>
<li>Bachelor’s or master’s degree in engineering, Life Sciences, or related technical field.</li>
</ul>
 
Experience
<ul>
<li>8+ years in Supplier Quality Engineering, preferably in medical devices or regulated industries.</li>
<li>Lead auditor experience with ISO 13485 and FDA QSRs.</li>
<li>Experience with CAPA, process validation, and statistical analysis.</li>
</ul>
 
Certifications (Preferred)
<ul>
<li>ASQ CQE/CQA</li>
<li>ISO 13485 Lead Auditor</li>
<li>Six Sigma Green/Black Belt</li>
</ul>
 
Skills
<ul>
<li>Strong analytical and problem-solving abilities.</li>
<li>Excellent communication and negotiation skills.</li>
<li>Proficiency in quality tools (FMEA, MSA, SPC) and software (MS Office, QMS platforms).</li>
<li>Ability to travel up to 30% for supplier audits and assessments.</li>
</ul>
 
Base Salary - $153,977.00 - $179,986.00

Staff Supplier Quality Engineer

<h3>Job Description</h3>
Company Description
Our mission is simple: to design a friendlier world.
 
Friendly Futures is pioneering a new placemaking typology called Neighborhood Games: bespoke, site-specific, intergenerational games that transform communities into more joyful, connected places. Our work blends architecture, landscape architecture, public art, and game design to spark play and belonging in public space.
 
Role Description
Want to help design a friendlier world? We’re hiring a part-time, remote Interdisciplinary Designer with the potential to grow into a full-time role. You’ll collaborate with our Creative Directors and design team to dream up and build playful, experimental projects, from first sketches to Rhino models to polished presentations.
 
What You’ll Do
<ul>
<li>Collaborate on the design of Neighborhood Games (spatial, experiential, and rule-based design).</li>
<li>Model concepts in Rhino and prepare drawings, diagrams, and presentation materials.</li>
<li>Contribute fresh creative input to playful, community-focused design challenges.</li>
<li>Support visual storytelling across projects (graphics, diagrams, presentations).</li>
</ul>
 
Qualifications
<ul>
<li>Proficiency in Rhino (required).</li>
<li>Background in Architecture, Landscape Architecture, Urban Design, Game Design, or related field.</li>
<li>1–2 years of experience, including internships.</li>
<li>Portfolio showing playful, experimental, or friendly design work.</li>
<li>Strong collaboration and communication skills.</li>
<li>A genuine love for play, games, and designing joyful experiences.</li>
</ul>
 
Bonus Skills
<ul>
<li>Experience teaching, facilitating workshops, or organizing clubs/community events.</li>
</ul>
 
Ideal Candidate
You might be in graduate school or recently graduated, with a strong design foundation and a playful outlook. You thrive in Rhino, enjoy bringing ideas to life visually, and want to grow as part of a small, creative team redefining placemaking. Most importantly, you’re eager to amplify our mission of designing a friendlier world — and have fun while doing it!

Interdisciplinary Designer

<h3>Job Description</h3>
Local Candidate Needed
 
The Position
We thrive to deliver more benefits to our patients as part of our 10-year Pharma vision. We serve our patients through external partnerships because access to quality products is every patient’s right. We leverage external partners in order to offer flexibility to our internal capacity at the right cost and quality. We enable our external partners to reliably deliver compliant, quality products to our supply chain customers, so that we can deliver to patients worldwide. We do this through cross-functional collaborations ensuring quality process excellence and continuous improvement.
 
The Opportunity
- Provide quality and GMP compliance oversight of CDMO/CRO operations for the delivery of products to clinical trials, including bulk drug substance (API) and bulk drug product for multiple technical platforms
- Ensure cGMP compliance and execute activities in support of disposition of clinical API and Drug Product manufactured at CDMOs, including but not limited to:
- Approval of master process and testing documentation
- Batch record review
- Leading and approving complex investigations
- Assessing and approving changes
- Ensure project milestones as well as expectations such as on time closure are met.
- Execute activities in support of global clinical trials, such as the Product Specification File
- Oversee and execute all required quality activities during the lifecycle of a CDMO/CRO, including but not limited to:
- Negotiation and maintenance of Quality Agreements
- Monitoring cGMP compliance, identifying and mitigating quality risks
- Supporting audits, ensuring audit responsiveness and CAPA implementation
 
Qualifications and Skills
B.A. or B.S. degree in life sciences
Minimum of 6 years experience in the pharmaceutical industry.
Minimum of 2 years experience in a GMP Quality Assurance role.
Must have experience making GMP release / disposition decisions and associated approval of master process and testing documentation, batch record review, resolution and quality approval of investigations, assessment of changes for clinical API and/or Drug Product, preferably synthetic molecules. Experience with SAP and Veeva is a plus. Experience with CDMO desired.
Sound knowledge of cGMP, ISO standards and international regulations for pharmaceuticals. Ability to interpret quality standards as they relate to CDMO/CRO, especially application of phase appropriate cGMP during product development for a variety of platforms, such as large molecule, synthetic molecule, conjugates, and oligonucleotides.
Demonstrated ability to apply cGMP concepts and requirements to evaluate batch disposition using sound judgment and decision making.
Strong problem solving skills using critical thinking, identifying risk based resolutions
Excellent verbal and written communication skills. Fluency in oral and written English is a must.
Strong interpersonal skills, diplomacy, and negotiation skills to influence and accomplish business objectives

Quality Specialist

<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 highly technical buildings and the systems that bring them to life. We currently have an opportunity for a Mechanical Engineering Summer Intern to join our San Diego, CA office.
Our dynamic work environment provides the optimal setting for a positive learning experience as an intern. From our supportive culture, diverse workforce, and competitive compensation, to our flexible work schedules and fun social events, it's everything you'll need for an exciting, challenging, and rewarding career. 
As an intern, 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. The pace is fast and the camaraderie is close.
Some responsibilities include: 
<ul>
<li>Assist engineers in preparing design documentation</li>
<li>Prepare AutoCAD and Revit drawings of Mechanical systems</li>
<li>Assist engineers with design calculations and sizing building Mechanical systems</li>
<li>Assist engineers with field investigations and construction site visits to observe </li>
<li>Attend intern education program lunch-and-learn sessions </li>
</ul>
Our interns will also be part of our intern education program, which consists of informational lunch-and-learn sessions that are attended by firm wide interns. These sessions consist of various topics of our business. Interns are encouraged and expected to attend these sessions as such are crucial to their development. 
Internship Requirements
The ideal candidate will enjoy a team environment and also flexible enough to work independently where needed. Candidates for this role will be eager to expand their knowledge by challenging themselves and using the highly technical resources around them.
Additional job requirements:
<ul>
<li>Pursing a bachelor's Degree from accredited university in Mechanical engineering </li>
<li>Must be at a minimum, completed your second year</li>
<li>Previous engineering internship or co-op experience a huge plus</li>
<li>Knowledge in the latest version of MEP AutoCAD and REVIT is a plus</li>
<li>Basic knowledge in design and calculation software; MS Office Suite</li>
</ul>
Benefits
As an employee with Syska Hennessy Group, 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. 
Join us this summer to prepare for your career as an Engineer through our Intern Education Program. This program consists of lunch- and- learn sessions covering various aspects of our business while gaining "hands-on" experience working with our engineers and visiting project sites. Once you graduate, jump start your career by joining Syska Hennessy Group and our EDT program.
About the EDT Program
Our Company is committed to developing engineers into respected technical experts and versatile business leaders. In keeping with that aim, interns that are hired for full time employment upon graduation can take advantage of our Engineering Development Training (EDT) program; 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. EIT/FE required.
As a member of our highly collaborative team, we also 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>Roth 401(k) Option</li>
<li>Individual and Dependent Life Insurance</li>
<li>Short- and Long-Term Disability</li>
<li>Health Wellness Program, including gym membership programs, in-house yoga, flu shots and biometric screenings</li>
<li>Training and professional development courses</li>
<li>Professional development incentive bonuses</li>
<li>A Generous Personal Time Off Program (PTO)</li>
<li>Flexible summer work schedules </li>
<li>Opportunities for community outreach through internal networks </li>
<li>Monthly transit/parking stipend </li>
<li>Monthly business phone stipend, if applicable </li>
</ul>
We are proud to be an equal opportunity workplace and an active employer to promote and foster a collaborative work space rooted in respect and powered by authenticity. We embrace an environment that is committed to embedding diversity and equality into the core of our business and culture.
Syska Hennessy Group - Creating Exceptional Environments
Let's Work Together!
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 $23-$27 USD

Mechanical Engineering Summer Intern

<h3>Job Description</h3>
Job Description
ASSEMBLER
Job Description
This position involves working on a sensor line, where sensors are assembled for single-use and then discarded. The role requires repetitive work with very small parts, using a small tool for assembly. Computer skills are essential for documentation purposes, and attention to detail is crucial.
Responsibilities
<ul>
<li>Assemble sensors using small tools.</li>
<li>Ensure accuracy and precision in assembling very small parts.</li>
<li>Document assembly processes and outcomes using computer systems.</li>
<li>Maintain attention to detail in all aspects of the work.</li>
<li>Adapt to varying tasks and responsibilities as needed throughout the day.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in assembly and production techniques.</li>
<li>Experience with hand tools, soldering, and power tools.</li>
<li>Ability to read and follow blueprints.</li>
<li>Strong computer skills for documentation.</li>
<li>Attention to detail and flexibility in task assignments.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School Diploma or GED required.</li>
<li>Experience with assembling, packaging, and using mechanical tools.</li>
<li>Ability to work on an assembly line and use a tape measure effectively.</li>
</ul>
Why Work Here?
This is a project-based position lasting until the end of the year, offering opportunities for cross-training in a supportive team environment. The company values flexibility and adaptability, providing a dynamic work setting where you can develop new skills.
Work Environment
The work environment is temperature-regulated, requiring candidates to be team players. The role involves both sitting and standing, with repetitive tasks. Candidates must ensure they have no close personal ties within the department to avoid potential conflicts of interest.
Job Type &amp; Location
This is a Contract position based out of Palm Springs, California.
Pay and Benefits
The pay range for this position is $18.00 - $20.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Palm Springs,CA.
Application Deadline
This position is anticipated to close on Oct 16, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Assembler

<h3>Job Description</h3>
HYBRID ROLES IN OAKLAND, CA OR ATLANTA, GA
 
Hello
We are looking for a Sr. QE Automation Engineer – Hybrid Roles in Oakland, CA or Atlanta, GA
Duration: 12+ months with possibility of longer term extensions
Pay Rate: $72/hr on W2
If interested, please email your resume to <a href="mailto:grace.johnson@motionrecruitment.com" target="_blank">grace.johnson@motionrecruitment.com</a>
Please Note: Client is not open to C2C, H1B, TN Visa, 1099, F1 – CPT &amp; OPT at this time
 
Role:
You will be responsible for designing, developing, and maintaining automated test frameworks and test suites to ensure the quality and reliability of our applications.
 
Key Responsibilities:
Design and implement automated test frameworks for microservices and web applications.
Develop and maintain test scripts using RestAssured for API testing and Selenium for UI testing.
Collaborate with developers, product managers, and other QA engineers to understand requirements and ensure comprehensive test coverage.
Integrate automated tests into CI/CD pipelines.
Analyze test results, identify root causes of failures, and work with development teams to resolve issues.
Maintain documentation related to test cases, test results, and automation frameworks.
Continuously improve test automation practices and tools.
 
Must-Have Qualifications and Skills:
RestAssured Framework for testing Java-based microservices.
Selenium with Java for UI automation.
Strong understanding of Java programming and object-oriented design.
Experience with test automation in CI/CD environments (e.g., GitHub Actions).
Familiarity with tools like TestNG, JUnit, Maven/Gradle.
Hands-on experience in automation testing of Java-based microservices using RestAssured and UI automation using Selenium with Java.
Experience with WebdriverIO (WDIO).
Bachelors Degree
5+ years of experience in test automation.
Knowledge of JavaScript/TypeScript.
Exposure to cloud platforms (Azure).
Experience with performance testing tools (e.g., JMeter).
Familiarity with containerization tools (Podman, Kubernetes).

Senior QE Automation Engineer

<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>

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