<h3>Job Description</h3>
Job DescriptionMachine Build Supervisor – Confidential Opportunity | Metro Detroit Area
About the Opportunity A global leader in advanced manufacturing systems is seeking a Machine Build Supervisor to lead complex machinery assembly and installation projects from the shop floor to customer sites. This is a confidential opening with a long-standing, innovative company that specializes in precision production technology.
If you’re an experienced machine builder who enjoys both the technical and administrative sides of leading a build — from managing resources and schedules to overseeing installations and documentation — this role offers the perfect mix of challenge, leadership, and impact.
Key Responsibilities
<ul>
<li>
Supervise and coordinate daily machine build activities, ensuring on-time and high-quality assembly of production equipment.
</li>
<li>
Lead a small team of skilled builders and technicians, providing direction, mentorship, and problem-solving support.
</li>
<li>
Oversee mechanical and electrical installation of machinery at customer sites (domestic and international travel may be required).
</li>
<li>
Coordinate with engineering, purchasing, and project management to ensure builds align with specifications and project timelines.
</li>
<li>
Maintain build documentation, job travelers, time tracking, and reports to support project administration.
</li>
<li>
Manage inventory and tooling needs for active projects.
</li>
<li>
Participate in machine runoff, troubleshooting, and final acceptance processes.
</li>
<li>
Ensure safety, quality, and efficiency standards are met at every phase of the build.
</li>
</ul>
Qualifications
<ul>
<li>
5+ years of experience in machine building, assembly, or mechanical systems installation.
</li>
<li>
2+ years in a lead or supervisory capacity within an industrial or automation environment.
</li>
<li>
Strong mechanical aptitude with experience reading blueprints, schematics, and assembly drawings.
</li>
<li>
Proven experience in installation and commissioning of complex machinery.
</li>
<li>
Familiarity with administrative processes — scheduling, documentation, and coordination between departments.
</li>
<li>
Excellent communication and leadership skills.
</li>
<li>
Willingness to travel occasionally for installations or customer support.
</li>
</ul>
Why This Role Stands Out
<ul>
<li>
Join a respected, forward-thinking manufacturing company known for engineering excellence and precision craftsmanship.
</li>
<li>
Lead high-visibility projects that impact major global customers.
</li>
<li>
Enjoy a stable, team-oriented environment that values quality and innovation.
</li>
<li>
Competitive compensation, excellent benefits, and opportunities for long-term growth.
</li>
</ul>
Location: Farmington Hills, MI (On-site with occasional travel) Employment Type: Full-Time Compensation: Based on experience + benefits Company: Confidential (represented by Connect Force Recruiting)

Machine Builder

<h3>Job Description</h3>
Job Description
SmartTalent is looking to a hire Production Associates for a digital print company in Tukwila, WA. Ideal candidate has strong attention to detail, able to work in a fast paced environment and have flexible schedule to work 7 days during peak season (details below).
TITLE: Production Associate
LOCATION: Tukwila, WA
SCHEDULE: 1st shift, 7am-3pm +OT start or 2nd shift, 3pm-11pm 
**Must be able to work 7 days a week in December **
PAY: $21.10 - $22.10 (depending on shift)
BENEFITS OFFERED: Paid Weekly, Direct Deposit, Affordable Health Care, Full-Time, Opportunities for career growth
Summary/Objective:
The Production Associate is responsible for operating and monitoring digital printing and finishing equipment to produce high-quality printed materials. The role includes setting up print jobs, inspecting output for accuracy, performing finishing tasks such as cutting, binding, and packaging, and maintaining equipment and a clean workspace. Associates work in a fast-paced, detail-oriented environment to meet production deadlines and ensure consistent quality.
 
Key Responsibilities:
·Inspect printed materials for quality, color accuracy, and consistency.
·Sort and bin printed products according to order specifications. 
·Accurately match products with customer orders using order management software or scanners.
·Perform finishing tasks such as cutting, folding, binding, packaging, and labeling.
·Follow production schedules to ensure orders are completed on time.
·Keep work areas clean, organized, and compliant with safety standards.
·Collaborate with team members in printing, finishing, and shipping departments to ensure smooth production flow.
Requirements:
·Previous experience in print production, manufacturing, or a related environment preferred.
·Basic computer skills
·Ability to lift up to 40lbs and stand for 8+ hours per shift.
·Must be able to work 7 days a week for 4-6 weeks
·Comfortable working in a fast-paced production environment.
·Willingness to work extended hours and weekends during peak periods.
·Positive attitude, strong work ethic, and dependable attendance.
SmartTalent Staffing is an Equal Opportunity Employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, or national origin.
#STHMG

Production

<h3>Job Description</h3>
Job Description
Food manufacturer that specializes in the production of sauces/dressings is looking to hire
Production Machine operator on 2nd shift.
<ul>
<li>3pm -11:30pm</li>
<li>$19.00</li>
<li>Monday - Friday</li>
<li>Must be open to working overtime &amp; weekends as needed</li>
</ul>
Duties:
<ul>
<li>Operating machine / production of sauces</li>
<li>Mixing dry ingredients</li>
<li>Packing</li>
<li>Palletizing</li>
<li>Other duties as assigned.</li>
</ul>
Requirements:
<ul>
<li>Must count with recent warehouse experience</li>
<li>Ability to lift up to 25-50lbs</li>
<li>Must have reliable transportation</li>
<li>Fast pace environment</li>
</ul>

Food Production Machine Operator

<h3>Job Description</h3>
Job Description
Fiagon NA LLC is an established, high growth medical manufacturing company that is committed to developing and marketing innovative technologies for the rapidly changing demands of the global medical industry. We seek to help patients by creating products specifically designed to facilitate safer procedures and improved patient outcomes. We are looking for a gumptious engineer that will work with our dynamic Team where innovation isn’t just a buzzword!
The Process Engineer will play a key role in the design, development and clinical evaluation of innovative medical devices. This role combines hands-on product engineering with significant clinical and customer interaction, requiring approximately 50% travel to hospitals, clinical sites, and customer facilities.
The ideal candidate is an engineer who is ready to unleash their superpowers! One who is both technically strong and comfortable in the clinical environment capable of engaging directly with physicians and OR staff to observe product use, collect feedback, and translate insights into design improvements. This position is ideal for someone who thrives at the intersection of engineering, clinical performance, and customer experience.
RESPONSIBILITIES
Product Development &amp; Engineering
<ul>
<li>Work with team members in Product Management, R&amp;D, Quality, Regulatory, and Operations to lead the execution of new development efforts.</li>
<li>Manage execution of projects to a schedule and product development process including development phase reviews.</li>
<li>Lead or support design and development of new medical devices from concept through commercialization.</li>
<li>Understand the company Quality Management System (QMS) and follow the company procedures, policies, and methodologies for product development.</li>
<li>Develop prototypes, perform design verification/validation (V&amp;V), and support design transfer to manufacturing.</li>
<li>Conduct root-cause analysis and continuous improvement on existing products.</li>
<li>Proactively communicate project status in terms of cost, schedule, performance, issues, open risk, and action plan for meeting project goals.</li>
<li>Facilitate productivity by ensuring continued communication and alignment throughout the team.</li>
</ul>
Clinical &amp; Customer Support (≈50%)
<ul>
<li>Provide on-site technical support during clinical evaluations, product demos, and early commercial use.</li>
<li>Observe clinical procedures to understand workflow and gather actionable feedback for design improvement.</li>
<li>Develop and implement best practices to assure successful procedural outcomes with customers</li>
<li>Serve as a key liaison between engineering, clinical teams, and customers to ensure successful product adoption.</li>
<li>Support physician training, product troubleshooting, and technical presentations as needed.</li>
<li>Document field feedback and translate it into structured product requirements and design inputs.</li>
<li>Ability to travel at least 50% of the time.</li>
</ul>
Cross-Functional Collaboration
<ul>
<li>Partner closely with Clinical, Marketing, and Sales teams to align engineering activities with customer needs.</li>
<li>Communicate findings from field activities to internal design and leadership teams.</li>
<li>Participate in design reviews, project planning, and strategy sessions for next-generation products.</li>
</ul>
REQUIREMENTS:
<ul>
<li>Minimum of a Bachelor’s degree in Electrical Engineering, Mechanical, Software or Biomedical field.</li>
<li>4+ years’ of experience in medical device product development or field-based technical engineering role.</li>
<li>Background in engineering or medical devices preferred.</li>
<li>Experience in Ear, Nose, and Throat medical industry is optimal.</li>
<li>Experience and understanding of the design process for medical devices.</li>
<li>Good understanding of FDA guidelines and requirements for medical devices.</li>
<li>Self-motivated, adaptable, and able to work independently in a fast-paced environment with high attention to detail.</li>
</ul>
Company DescriptionFiagon NA, LLC, believes in the synergy of teamwork while maintaining an entrepreneurial spirit and providing an environment in which our associates develop and accomplish professional objectives. 
<h3>Company Description</h3>
Fiagon NA, LLC, believes in the synergy of teamwork while maintaining an entrepreneurial spirit and providing an environment in which our associates develop and accomplish professional objectives.

Process Engineer

<h3>Job Description</h3>
Job Description
Position : Validation Engineer
 
Location Carrollton, TX | Onsite
 
Compensation &amp; Schedule
 • Pay up to $42/hr
 • Full-time hours - Mon - Fri 
 • W2
 
ROLE IMPACT
 This role leads validation engineering efforts to ensure cGMP compliance in OTC drug manufacturing. The engineer executes qualification and validation of systems, processes, equipment, and cleaning procedures aligned with FDA regulations. Success is measured by robust, audit-ready documentation and continuous improvements in process reliability, product quality, and compliance.
 
KEY DUTIES
 • Lead execution of validation lifecycle activities: Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Cleaning Validation/Verification
 • Develop and maintain site Validation Master Plans and project schedules per 21 CFR Part 210/211
 • Conduct protocol generation, execution, data analysis, and final reporting for equipment, utilities, and process validations
 • Interface with cross-functional teams (QA, Regulatory Affairs, Engineering, Microbiology, Chemistry) to ensure alignment and documentation integrity
 • Support deviation investigations, risk assessments, and CAPA development tied to validation outcomes
 
MINIMUM QUALIFICATIONS
 • 3+ years’ validation or quality engineering experience in regulated drug, food, or cosmetic manufacturing
 • Bachelor’s degree in Engineering, Chemistry, or related scientific discipline
 • Working knowledge of cGMP, FDA validation requirements, and statistical methods (DOE, SPC)
 • Ability to author and review protocols, reports, and technical documentation with minimal oversight
 
EQUIPMENT &amp; WORK ENVIRONMENT
 • Hands-on involvement with pharmaceutical equipment and manufacturing systems
 • Exposure to hazardous waste (e.g., solvents, inks, mercury); EPA-compliant handling training required
 • Work includes interaction with cleanrooms, controlled environments, and lab-scale/production-scale machinery
 
PREFERRED SKILLS
 • ASQ certification (CQE, CRE) preferred
 • Familiarity with Six Sigma tools and process capability studies
 • Strong project management and cross-departmental collaboration skills
 
LEGAL NOTICE
 By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from CornerStone and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at: <a href="https://www.cornerstonestaffing.com/privacy" target="_blank">https://www.cornerstonestaffing.com/privacy</a>
Company DescriptionCornerStone Staffing has been servicing the Dallas-Fort Worth metroplex since 1991. We are committed to supporting our community through our core values of compassion, integrity, self discipline, and faith. CornerStone currently has 11 offices across the Metroplex to serve your needs. If you are a job seeker looking for short-term supplemental income or a full-time position that will launch a new career, we can assist you in finding the right opportunity! 
<h3>Company Description</h3>
CornerStone Staffing has been servicing the Dallas-Fort Worth metroplex since 1991. We are committed to supporting our community through our core values of compassion, integrity, self discipline, and faith.\r\n\r\nCornerStone currently has 11 offices across the Metroplex to serve your needs. If you are a job seeker looking for short-term supplemental income or a full-time position that will launch a new career, we can assist you in finding the right opportunity!

Validation Engineer

<h3>Job Description</h3>
Job Description
Overview:
Kuros Biosciences, Inc. is seeking a Production Manager to join our core Operations team to support the build-out and running of Kuros' newest manufacturing facility in Alpharetta, Georgia. The U.S. Production Manager owns the execution of manufacturing KPIs/goals as well as directing, organizing, and controlling day-to-day U.S. Operations activities and teams. The US Production Manager establishes the path and leads operations resources to manufacture Kuros' finished product in a timely manner to meet customer demand with a safety-first mentality, in the most efficient manner while ensuring sufficient capacity, and with the highest quality. Critical success factors for this role include leadership, developing people, sustaining a Lean Six Sigma culture, optimizing resource output, enforcing quality standards, and collaborating across departments to support Kuros' strategic objectives.
Key Responsibilities:
<ul>
<li>Build, lead, and develop a high-performing team of Operators, fostering a culture of accountability, continuous improvement, and operational excellence through effective coaching, performance management, and engagement.</li>
<li>Lead and manage Kuros' U.S. Operations team by leading by example and providing guidance across the operations team to embed and sustain a culture of safety-first mentality, lean manufacturing, continuous improvement, awareness, inquisitiveness, and persistence around processes and product quality improvements.</li>
<li>Develop and implement standard operating procedures (SOPs) to ensure operational efficiency, standard work and compliance.</li>
<li>Work closely with Operations in the Netherlands.</li>
<li>Implement plans and procedures that drive achievements of operations/quality goals and manufacturing improvements by managing team performance; addressing disciplinary issues, hiring, supporting people with career development, communicating information to direct reports and passing information up the management chain, administrative processing, maintaining trust and confidentiality; and ensuring the team is aligned with and accomplishing goals/objectives.</li>
<li>Support the development of Operations departmental strategy and vision to ensure adherence with customer expectations, enforce consistent and continual improvements, and monitor operation metrics.</li>
<li>With the utilization of our lean methodologies such as morning markets, manage communications between value streams to ensure Operations is meeting the build schedule and building Quality product that meets customers' expectations.</li>
<li>Provide leadership and the application of problem-solving initiatives through systemic tools such as Lean Manufacturing and Six Sigma.</li>
<li>Develop and sustain collection and analysis of Manufacturing KPIs and operational information from multiple sources to develop long-term Operations strategy and programs. Prepare monthly reports based on Manufacturing KPIs and present results to senior leadership.</li>
<li>Implement and sustain a 6S program to help foster the culture of a world-class manufacturing facility.</li>
<li>Lead production process analyses, ensuring quality standards are met and making recommendations for quality improvements.</li>
<li>Ensure compliance with regulatory requirements, ISO13485, GMP, company policies, and safety standards.</li>
<li>Work with engineering in the planning of new tools and fixture designs. Responsible for the design, development, and deployment of equipment and test systems in the manufacturing environment.</li>
<li>Ensure manufacturing systems that require calibration and maintenance are sustained through an appropriate calibration process and documented appropriately.</li>
<li>Foster a safety-first mentality while improving efficiencies through the improvement of process flow, elimination of waste, and cost reduction through leadership, example, and training.</li>
<li>Ability to influence and build strong and trusted working relationships with internal and external business stakeholders at all levels.</li>
<li>Support the development and sustainability financial budgets for U.S. Operations.</li>
</ul>
Qualifications &amp; Skills:
<ul>
<li>Education:
<ul>
<li>Bachelor's degree in Engineering, Biology, or Operational Management required. A Master's degree in related fields or an MBA preferred</li>
<li>Lean Six Sigma Green Belt or Black Belt certification preferred</li>
</ul>
</li>
</ul>
<ul>
<li>Experience:
<ul>
<li>3-5+ years in Operations management in an ISO13485 regulated industry</li>
<li>Experience with regulatory environments such as GMP, FDA, or ISO standards</li>
</ul>
</li>
<li>Skills:
<ul>
<li>Strong analytical and problem-solving skills</li>
<li>Excellent communication and interpersonal abilities</li>
<li>Proven leadership and team management expertise</li>
<li>Proficiency in lean methodologies and Six Sigma tools
<ul>
<li>Experience in the identification of the 8 wastes, line balancing and performing theory of constraints</li>
<li>Experience in developing and sustaining a 6S program</li>
<li>Experience in developing and sustaining morning markets and value stream structure organization</li>
</ul>
</li>
<li>Proficiency in data analysis tools and software such as minitab, powerBI, Tableau</li>
<li>Proficiency in ERP and Master data, preferably in Microsoft Dynamics 365</li>
<li>Experience in developing and continuously improving upon operations KPI's such as manufacturing efficiency, capacity utilizations, process cycle times, reject/scrap rates, inventory accuracy, first pass yield, and monitoring budget to fiscal year plan</li>
</ul>
</li>
</ul>
Travel Requirement:
<ul>
<li>Travel: Ability to travel domestic and international</li>
</ul>
Pay Range$120,000—$140,000 USD
Physical Requirements and Work Conditions
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.
<ul>
<li>Mobility &amp; Posture: May require occasional sitting, standing, walking, climbing, reaching, bending, or stooping.</li>
<li>Lifting/Carrying: May require lifting and carrying items 50 pounds or more, depending on the role.</li>
<li>Manual Dexterity: Frequent use of hands and fingers for typing, writing, grasping, and operating office or job-specific equipment.</li>
<li>Driving: Some roles may require the ability to operate a motor vehicle for extended periods and maintain a valid driver's license.</li>
</ul>
Specific requirements may vary by role. Contact an HR representative for details related to the position.
About Us
Kuros Biosciences is on a mission to discover, develop and deliver innovative biologic technologies.
Our Credentials
With locations in the United States, Switzerland and the Netherlands, the company is listed on the SIX Swiss Exchange. The company's first commercial product, MagnetOsTM, is a unique advanced bone graft that has already been used across four continents. For more information on the company, its products and pipeline, visit kurosbio.com.
<ul>
<li>Listing on the SIX Swiss Exchange under the symbol KURN</li>
<li>A commercial &amp; research footprint that spans &gt;20 markets</li>
<li>4 teams of internationally renowned clinical and scientific expert advisers</li>
<li>&gt;25 orthobiologics-related patents</li>
<li>&gt;400 patients evaluated in Level I, randomized controlled clinical trials</li>
<li>&gt;20 well-controlled Level I-III clinical trials initiated, including 6 that are complete</li>
<li>Level I evidence published in Spine</li>
</ul>
Kuros Biosciences is an equal opportunity employer that is 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. Kuros Biosciences complies with GDPR and the California Consumer Privacy Act (CCPA). View our CCPA Notice here.

Production Manager

<h3>Job Description</h3>
Job Description
HiFyve is hiring a Processing Technician in the manufacturing industry!
Salary: $25 – $27/hour
Shifts:
<ul>
<li>7:00 PM – 7:00 AM — Sunday, Monday, Tuesday &amp; every other Wednesday OR 7:00 PM – 7:00 AM — Thursday, Friday, Saturday &amp; every other Wednesday</li>
<li>Location: Lee’s Summit, Missouri</li>
</ul>
Job Duties and Responsibilities:
<ul>
<li>Set up and start injection molding machines, molds, and auxiliary equipment.</li>
<li>Develop, adjust, and optimize molding process parameters to achieve part quality and production efficiency.</li>
<li>Troubleshoot molding defects and make necessary process corrections.</li>
<li>Perform and assist with mold changes and machine setups.</li>
<li>Collaborate with maintenance and quality teams to identify and resolve equipment and process issues.</li>
<li>Monitor machine performance and document adjustments.</li>
<li>Ensure compliance with all safety and quality standards.</li>
</ul>
Education Requirements:
<ul>
<li>High School Diploma or GED preferred</li>
</ul>
Knowledge, Skills, and Abilities:
<ul>
<li>2+ years of plastic injection molding processing experience required (Husky equipment experience a plus).</li>
<li>Strong understanding of plastic material behavior and molding principles.</li>
<li>Ability to adjust hydraulic, pneumatic, and processing controls.</li>
<li>Familiarity with scientific molding is highly preferred.</li>
<li>Strong analytical, troubleshooting, and communication skills.</li>
<li>Flexibility to work scheduled shifts, overtime, and occasional weekends.</li>
<li>Positive safety mindset and ability to work well within a team.</li>
</ul>

Process Technician

<h3>Job Description</h3>
Job Description
About RTC Aerospace:
At RTCA, we believe in teamwork, excellence, and delivering with pride. One Team! One Mission!
RTC Aerospace is a 60-year-old aerospace manufacturer of complex, high-tolerance, difficult-to-machine parts. We have 4 facilities across the nation bringing exceptional cellular manufacturing capabilities and unique engineered solutions to our clients’ designed products. We are a company driven by ambitious individuals, working together to become an industry leader in lean-cell manufacturing. Come be a part of something exceptional at RTC Aerospace! 
How You’ll Make an Impact 
The Quality Engineering Associate I will have a detailed knowledge of outside processing purchase orders, shipping packslip, and work orders with a dedication to being part of a world class manufacturing team.
What you’ll be doing as a Quality Engineering Associate I:
<ul>
<li>Working a Full-time, onsite position at our Fife, WA location.</li>
<li>Review outside processing purchase orders, check and record spec rev levels</li>
<li>Review/ Sign shipping pack slips and ensure customer required shipping documents are included with the shipment.</li>
<li>Review and approve of raw material purchase orders.</li>
<li>Assist in Creating Certificate of Conformance Records.</li>
<li>Review and stamp newly released work orders</li>
<li>Assign and log serial numbers (for serialized parts)</li>
<li>Assist in Managing measuring tool calibration including maintenance of required records</li>
<li>Assist in Maintaining scrap log (final disposition of scrap parts)</li>
<li>Assist in Managing the final closing of completed work orders, scans the paper copy to the network</li>
<li>Assist in a variety of Document Control functions.</li>
<li>Assist in Managing the filing of records.</li>
<li>Assists in the implementation, and administration of other QA and company activities including: risk management, configuration control, training, auditing, corrective actions, continuous improvement, and preventative actions.</li>
<li>Adheres to all workplace safety guidelines, policies, and laws determined by the company, state, and federal authorities</li>
<li>Performs a variety of other duties as assigned</li>
</ul>
Required Qualifications (Education, skills, and experience):
<ul>
<li>Works independently, follows instructions, can concentrate for long periods of time and is able to tolerate multiple interruptions throughout the day</li>
<li>Able to take and successfully pass a pre-employment drug test, as well as reasonable suspicion, and post-accident drug and alcohol tests</li>
<li>Team player with a can-do attitude</li>
</ul>
Preferred Qualifications (Education, skills, and experience):
<ul>
<li>Two years experience in aerospace industry quality related roles</li>
<li>Proficiency in QMS and AS9100 requirements required</li>
<li>Experience with Microsoft Office applications and MRP systems required</li>
</ul>

Physical Demands: 
The physical demands and work environment characteristics described here are representative 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 frequently required to do the following:
<ul>
<li>Ability to lift or move up to 50lbs.</li>
<li>Reach forward, up, down and to the side in order to move equipment.</li>
<li>Continuous standing and walking throughout the workday.</li>
<li>Ability to reach with hands and arms; use hands to manipulate, handle, or feel material.</li>
<li>Access, input, and retrieve information from a computer.</li>
</ul>
Work Environment: 
A large percentage of work time is spent in a machine shop where temperatures vary from hot to cold. The environment may also include exposure to noise, dust, fumes, vapor from coolant, etc. Industry standard safety equipment is provided by the Company, and specific notice is posted in areas where safety equipment is required.
Compensation and Benefits: 
Employee Benefits: Medical, dental, vision, basic and supplemental life insurance, long-term disability and 401(k) with up to 6% QACA company match. 
The Quality Engineering Associate I Compensation range for onsite Washington applicants is $20-23/hour commensurate with experience. Some shifts may include shift differential pay rates. Other site ranges may differ.
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. 
This position must meet Export Control compliance requirements, therefore a “US Person” as defined by 22 C.F.R. § 120.15 is required. 

RTCA is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
Affirmative Action and Disability Accommodation Applicants wishing to receive information on RTCA’s Affirmative Action Plans, or applicants requiring a reasonable accommodation in order to participate in the application and/or interview process, please contact the RTCA Human Resources Department. If you are a qualified individual with a disability or a disabled veteran, you have the right to request an accommodation if you are unable or limited in your ability to use or access our career center as a result of your disability. To request an accommodation, contact the RTCA Human Resources Department. Candidates will receive consideration without discrimination in accordance with the requirements of article 9 to chapter XVIII of the City of Los Angeles Municipal Code, federal and state laws of California.

If you are a qualified individual with a disability or a disabled veteran, you have the right to request an accommodation if you are unable or limited in your ability to use or access our career center as a result of your disability. To request an accommodation, contact the Human Resources Department.

Quality Engineering Associate I

<h3>Job Description</h3>
Job DescriptionDescription:
Graceland Portable Buildings® is a national corporation manufacturing and selling high quality portable storage buildings. Our manufacturing facility in McRae, GA is seeking a top-notch builder to join our team!
<ul>
<li>Construction of portable storage sheds</li>
<li>Excellent working environment</li>
<li>All tools and equipment provided</li>
<li>Pay commensurate with experience</li>
<li>Full benefit package - Health, Dental, and Vision Insurance, Life Insurance, Paid Holidays, Paid Time Off, and more!</li>
<li>Some travel may be required - all expenses paid and travel bonuses</li>
</ul>
 
Requirements:
<ul>
<li>Quality building experience preferred</li>
<li>Highly motivated individual</li>
<li>Professional appearance</li>
<li>Strong work ethic</li>
<li>Team-oriented</li>
<li>Ability to train others</li>
<li>Positive attitude and willingness to work</li>
</ul>

Corporate Shed Builder

<h3>Job Description</h3>
Job DescriptionSalary: 
Air Controls-Billings, Montanais seeking an Electrical Designer or ElectricalEngineer to join our team!
 
Hourly wage starts at $28 - $38 per hour, DOE. Our wage packages include employer paid medical, dental, vision plans and profit share.
 
TheElectrical Designer or Electrical Engineer will work closely with our staff of mechanical and plumbing engineers to design the electrical systems in construction projects. Most projects will employ design-build strategies and will be fast paced from concepts through construction.
 
Job Duties:
<ul>
<li> Plan and design electrical systems for commercial buildings</li>
<li> Produce plans and specifications using AutoCAD or other current software</li>
<li> Address field issues involving electrical systems</li>
<li> Estimate the time, cost, labor, and materials that are needed for the projects</li>
</ul>
 
Job Requirements:
<ul>
<li>5 years experience in Commercial Construction</li>
<li>Excellent written and oral communication skills</li>
<li>Must have knowledge in AutoCAD</li>
<li>Bluebeam/Revit skills a plus</li>
<li>Passed fundamentals of engineering exam</li>
<li>Ability to travel locally to work at various types of construction sites and service locations</li>
<li>Attend training sessions as required to keep up on current trends and for continuing education</li>
<li>Bachelor's degree in Electrical Engineering or related field a plus</li>
<li>Professional Engineer (PE) License preferred but not required</li>
</ul>

6,437 Manufacturing Jobs in Maine