field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Quality Inspector 
Our client, a leading machining company, is seeking a Quality Inspector to join their team. The hours are 10:00 am to 10:00 pm, Sat, Sun, &amp; Mon
The Quality Inspector will support the Inspection Department. This role will be responsible for inspecting incoming material, work-in-process and customer shipments to achieve Client Quality and Business objectives.
Duties and Responsibilities:
<ul>
<li>Performs receiving, in-process and final inspections to verify compliance to applicable procedures including but not limited to, work instructions, product specifications, tooling and outside service certifications, external standards, and customer drawings</li>
<li>Responsible for inspecting/verifying product samples as necessary</li>
<li>Understands and uses all nonconforming materials systems (NCM Cage, DMR, DRA)&nbsp;</li>
<li>Maintains QA lab in a clean and orderly fashion in compliance with housekeeping standards</li>
<li>Responsible for completing inspection assignments within broad guidelines and general supervision</li>
<li>Performs calibrations to maintain inspection, measuring and test equipment (IM&amp;TE) systems</li>
<li>Performs all Physical Properties Testing and is capable of using all QA Lab and Customer supplied Test Equipment</li>
<li>Responsible for inventory and requisitioning of all QA lab supplies, small tools, and equipment</li>
<li>Understands and uses all nonconforming systems including tagging and scrapping of material after disposition</li>
<li>Maintains product and inspection traceability including customer supplied product</li>
<li>Understands tube manufacturing process work flow and documentation sufficiently to perform proper and effective containment activities of potentially non-conforming materials</li>
<li>Responsible for final QA signature/release to ship products</li>
</ul>
Competencies
<ul>
<li>Teamwork orientation.</li>
<li>Time Management.</li>
<li>Performance Management.</li>
<li>Results Driven.</li>
</ul>
Work Environment
<ul>
<li>This job operates in the Inspection Department which is in a shop environment. There may be exposure to any number of elements but with none present to the extent of being disagreeable.</li>
</ul>
Physical Demands
<ul>
<li>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</li>
<li>Able to stand, sit/or ambulate across the production space for long periods of time. Up to 95% of the scheduled shift.</li>
<li>Effectively handle and manipulate parts in order to identify needed specifications.</li>
</ul>
Position Type/Expected Hours of Work
<ul>
<li>Regular schedule Saturday, Sunday, and Monday 10:00 am - 10:00 pm</li>
<li>Training Schedule 10:00 am - 6:30 pm</li>
</ul>
Required Education and Experience
<ul>
<li>High School Diploma or GED.</li>
</ul>
Preferred Education/Experience
<ul>
<li>Inspection Experience</li>
<li>Ability to effectively use common measuring equipment such as micrometers, calipers, gauges (pin, thread, indicator, height), optical comparators and coordinate measuring machines</li>
<li>Demonstrated blueprint reading skills to GD&amp;T standards.</li>
<li>Blueprint reading skills</li>
<li>Ability to effectively use MS Office Products.</li>
<li>Ability to read/write in English and perform basic math functions such as addition, subtraction, multiplication and division.</li>
<li>Demonstrated verbal and written communication skills.</li>
</ul>
Other Duties
<ul>
<li>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.</li>
</ul>
If you qualify per above, apply with your resume (word format preferred) as the client is looking to interviewing ASAP.
Due to the volume of responses, only those that meet the requirements above will be contacted.
Company DescriptionPrideStaff is a national staffing organization, delivering innovative solutions to the challenges employers face every day. Over the years, PrideStaff has been a consistent industry leader, developing technology and service processes that allow our organization to deliver superior performance. With locations across the United States, we're well positioned to partner with clients and candidates to ensure a successful match of employee talent with customer needs. When it comes to your success, we leave nothing to chance! Our Mission: Consistently provide client experiences focused on what they value most. 
<h3>Company Description</h3>
PrideStaff is a national staffing organization, delivering innovative solutions to the challenges employers face every day. Over the years, PrideStaff has been a consistent industry leader, developing technology and service processes that allow our organization to deliver superior performance. With locations across the United States, we're well positioned to partner with clients and candidates to ensure a successful match of employee talent with customer needs. When it comes to your success, we leave nothing to chance! \r\n\r\nOur Mission: Consistently provide client experiences focused on what they value most.

Quality Inspector

<h3>Job Description</h3>
Job Description
ob description
Job Summary:
We are seeking a reliable and experienced&nbsp;Machine Operator / Fabricator&nbsp;to join our team. This position involves working with stone, granite, and marble to cut, shape, and finish high-quality materials for custom installations. The ideal candidate will have hands-on experience using power tools, strong attention to detail, and a solid understanding of fabrication processes.
Key Responsibilities:
<ul>
<li>Operate and maintain fabrication machinery used for cutting, grinding, and polishing stone, granite, and marble</li>
<li>Use hand and power tools to shape and finish surfaces as per specifications</li>
<li>Read blueprints, templates, and work orders to determine project requirements</li>
<li>Ensure accuracy in measurements and cuts</li>
<li>Inspect materials for defects and maintain a clean, organized work area</li>
<li>Follow all safety protocols and wear appropriate PPE</li>
<li>Assist with loading/unloading slabs and finished products</li>
<li>Work collaboratively with other team members and supervisors</li>
</ul>
Qualifications:
<ul>
<li>Proven experience working with stone, granite, and/or marble preferred</li>
<li>Proficient in using power tools and stone fabrication equipment</li>
<li>Ability to lift heavy materials and work in a physically demanding environment</li>
<li>Strong work ethic, attention to detail, and reliability</li>
<li>Willingness to work overtime as needed</li>
<li>Bilingual (English/Spanish) a plus</li>
</ul>
Benefits:
<ul>
<li>Competitive pay based on experience</li>
<li>Opportunity for overtime</li>
<li>Stable Monday–Friday schedule</li>
<li>Growth potential within the company</li>
</ul>
If you’re a skilled fabricator with a passion for quality craftsmanship, apply today to join our team!
Hours are from 6:30am-3:30pm
Job Type: Full-time
Pay: From $18.00 per hour
Expected hours: 40 per week
Benefits:
<ul>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Paid time off</li>
</ul>
Schedule:
<ul>
<li>8 hour shift</li>
<li>Overtime</li>
</ul>
Experience:
<ul>
<li>Fabrication: 3 years (Required)</li>
<li>Power tools: 2 years (Required)</li>
</ul>
Ability to Commute:
<ul>
<li>Raleigh, NC 27610 (Required)</li>
</ul>
Ability to Relocate:
<ul>
<li>Raleigh, NC 27610: Relocate before starting work (Required)</li>
</ul>

Machine Operator/Fabricator

<h3>Job Description</h3>
Job Description
EXCITING OPPORTUNITY FOR MACHINE OPERATORS – FORT WASHINGTON, PA Kelly® is in search of machine operators to work for a premier pharmaceutical company in Fort Washington, PA. Let us help you grow at work and discover the next step in your career! This is a temp role with an opportunity to be hired on permanently!
Day Shift: 6:15am-6:45pm on a rotating schedule. Night Shift: 6:15pm-6:45am on a rotating schedule. Training is Monday-Friday Pay: $23.00 per hour - $500 Retention Bonus (paid after 6 months) - $500 Retention Bonus (paid after 1 year) What’s a typical day as a Machine Operator? You’ll be: • Setting up and calibration of production equipment. • Operating machinery and ensuring proper mixing. • Utilizing attention to detail. • Working in a fast-paced environment. • Collaborating with the team to meet daily production goals. What happens next: Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more. This is a good fit if:
<ul>
<li>You have a HSD or GED equivalent</li>
<li>You have 2 years MINIMUM of machine operator or production experience</li>
</ul>
 This is a temp role with an opportunity to be hired on permanently!
Company DescriptionKelly helps companies recruit and manage skilled workers and helps job seekers find great work in industries such as accounting and finance, education, engineering, government, manufacturing and production, technology, and more. Since inventing the staffing industry in 1946, we’ve become experts in the many specialties and local and global markets we serve. With a network of suppliers and partners around the world, we connect 450,000+ people with work every year. We ensure companies have the people they need, when and where they’re needed most. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. 
<h3>Company Description</h3>
Kelly helps companies recruit and manage skilled workers and helps job seekers find great work in industries such as accounting and finance, education, engineering, government, manufacturing and production, technology, and more.\r\n\r\nSince inventing the staffing industry in 1946, we’ve become experts in the many specialties and local and global markets we serve. With a network of suppliers and partners around the world, we connect 450,000+ people with work every year. We ensure companies have the people they need, when and where they’re needed most.\r\n\r\nKelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Machine Operator

<h3>Job Description</h3>
Job DescriptionDescription:
American Plastics is a privately owned injected molded plastics company that designs and manufactures workhorse items in the United States, utilizing green processes and superior engineering. American Plastics is a growing company, with production and distribution footprints in Missouri, Ohio, Arizona, North and South Carolina.
 
The Corporate Quality Manager is responsible for the initiation, improvement and evaluation of product quality and product compliance in support of the corporate strategy of American Plastics, LLC across multiple locations in North America. This position will report to the Vice President of Quality and reside in the Innovation Center, Findlay, OH.
 
•Quality: Ensures that American Plastics products meet the customer’s expectations while complying with regulatory requirements for quality and safety.
•Quality Management System (QMS): Focused on improving the effectiveness of the critical business processes associated with the quality vision utilizing quality planning, quality assurance, quality control, and quality improvement activities.
•Product Security: Implement, improve, and evaluate existing finished good or development products according to AP and customer proprietary requirements.
•Compliance: Manage, mitigate risks, and protect the ethical integrity of American Plastics, through the implementation of policies and strict adherence to established requirements.
 
Responsibilities:
Foster an end user centric environment ensuring American Plastics meets customer and stakeholder’s expectation by taking the necessary steps to drive satisfaction. Responsible for executing the quality system across multiple locations in North America.
•Enforce a quality system that is compliant with any relevant industry standards or other specified requirements.
•Generate any deliverable or required process output through vigilant monitoring of customer feedback to introduce continuous improvement.
•Document and report any pertinent performance metrics necessary to exploit business opportunity when presented.
•Identify, manage resources for, and initiate actions needed to improve product quality or reduce product cost wherever possible.
•Lead cross-functional teams to implement FMEA, Quality control plans, 8D, Risk Assessment, and lessons learned to drive down the total cost of quality.
•Train AP personnel with regards to procedures, instructions, and quality tools to enhance corporate quality philosophy.
•Monitor enterprise-wide quality control activities to ensure company’s products comply with American Plastics and customer quality standards.
•Assemble pertinent information necessary for customer communication, supplier performance reviews, or non-conformance root cause analysis to ensure full product compliance.
 
The Corporate Quality Manager Has The Authority:
 
•To apply the required tools as needed to manage and actualize the written Quality Management System.
•To independently take the necessary actions to ensure that the management system will achieve full company-wide compliance.
•To develop Standard Operating Procedures, Work Instructions, Job Aids, or any other document or process elements needed to standardize practices throughout the organization.
Requirements:
Desired Education and Qualifications:
 
•A bachelor’s degree in technical discipline (required) with a master’s degree in business administration (preferred).
•8-10 years’ experience in a manufacturing environment, with direct quality leadership and reporting responsibilities.
•Experience with data analysis including typical Statistical Process Control (SPC) techniques.
•Plastics material and product testing to include instruments such as a Spectrophotometer (X-Rite or equivalent), Universal Test Machine (Flexural Modulus, Tensile, Product/Component performance characteristics), IZOD, FTIR, Melt Flow Index, as well as having a thorough understanding of applicable ASTM’s recognized as benchmark test methods within the plastic manufacturing industry.
•Strong leadership and communication skills including writing, presentation, influencing, and negotiation skills.
•Demonstrated ability to think critically and provide strategic insight and analysis to solve problems and make improvements.
•Ability to lead and provide guidance to multiple projects simultaneously.
•Demonstrated ability to build, develop, and lead a team of quality professionals in support of corporate goals.
•Deploy a Quality Management System to all levels of the business.
•Maintain and document product quality inspection and testing requirements.
•Any other duty as assigned by management.
 
If you are interested in joining the American Plastics team and want to work in a fast-paced, progressive environment, we want to hear from you. We offer a competitive salary &amp; benefits package including medical/dental, 401k and paid vacation.

Quality Manager

<h3>Job Description</h3>
Job DescriptionDescription:
Job Summary
 
Manages and oversees all aspects of the Quality Assurance, Quality Engineering, and Quality Control functions globally by setting, directing, and overseeing policies on quality standards and regulatory compliance; interpreting new quality and regulatory requirements/trends as they relate to all operations; and supporting and managing the firm’s relationship with external regulatory agencies. Responsible for guiding others within the organization on quality management system and regulatory compliance basics, ensuring understanding and compliance with updated requirements including US FDA, EU MDD/MDR, and other international regulatory bodies. Job holder to promote and adhere to the company values of quality and compliance with current legislation. This position is an in-office position in the Headquarters in Huntersville, NC USA. 
 
Essential Job Functions
 
The job holder will undertake some or all of the following responsibilities:
<ul>
<li>Build, lead and develop a high-performing and collaborative team of QA, QE, and QC personnel focused on local and global compliance</li>
<li>Contribute to and drive the global strategies for Quality and QMS alignment </li>
<li>Work with leaders across the business to develop strategies and plans to fulfill the mission and goals of the business while maintaining compliance with quality standards and regulatory requirements</li>
<li>Lead efforts in continuous improvement, including lean quality processes and risk-based decision-making</li>
<li>Practice and mentor others to approach situations with a risk-based approach</li>
<li>Drive a culture of compliance through influence, relationships, and partnership with cross-functional leaders</li>
<li>Collaborate with Operations, Engineering, Regulatory, and Supply Chain to ensure design transfer, manufacturing, and distribution activities meet quality standards</li>
<li>Apply various principles and techniques for developing and organizing teams and leading quality initiatives and continuous improvement within their function</li>
<li>Facilitate meetings and aspects of projects. Assist in working through resistance to change and improvement</li>
<li>Liaison with external organizations regarding Quality matters, including suppliers, Notified Bodies, external regulatory bodies, etc. </li>
<li>Support firm’s product development process and programs with resources and Quality expertise </li>
<li>Perform, and teach others to perform, root cause analysis of identified issues including identification of appropriate corrective and preventive action</li>
<li>Ensure timely and effective closeout of non-conformances, complaints, and CAPAs</li>
<li>Define and monitor quality metrics and KPIs; report quality performance to executive leadership</li>
<li>Ensure effective implementation and maintenance of Quality System appropriate to the products manufactured by and for the company and compliant with the relevant requirements of FDA Quality System Regulations (21 CFR 820), ISO 13485, EU and UK Medical Device Regulations, as well as any other applicable global regulatory body regulations at multiple locations/sites</li>
<li>Ensure the quality of the company products through the establishment, monitoring, and enforcement of a Quality Management System in compliance ISO 13485, EU and UK Medical Device Regulations and 21CFR820 requirements, as well as the requirements of any other applicable global regulatory body</li>
<li>Review documentation to ensure compliance with the relevant requirements of FDA Quality System Regulations (21 CFR 820), ISO 13485, EU, UK Medical Device Regulations, and others as applicable</li>
<li>Training of Quality personnel</li>
<li>Perform formal and informal audits as necessary</li>
<li>Oversee supplier quality management including audits of key vendors and partners, as necessary</li>
<li>Provide support or lead audits as necessary including external audits, internal audits, or supplier audits</li>
<li>Represent Quality in leadership meetings and strategic planning sessions</li>
</ul>
 
 
Requirements:
Qualifications
<ul>
<li>University degree, preferred, or relevant experience</li>
<li>Medical device industry experience of at least 10 years, with a minimum of 5 years within the Quality or Regulatory functions</li>
<li>Minimum of 4 years of management experience </li>
<li>Some experience with US FDA OTC drugs, combination devices and cGMP requirements (21 CFR 210/211) preferred </li>
<li>Thorough knowledge of US, EU, UK, and other medical device regulations, as well as ISO 13485 and ISO 14971, MDSAP requirements</li>
<li>Effective Quality leader with a demonstrated ability to build, lead, and train a team of Quality professionals</li>
<li>Proven ability to work in a fast-paced, growth-oriented environment</li>
<li>Ability to work with cross-functional partners to drive a culture of compliance</li>
<li>Computer literate and experienced in Microsoft Office applications </li>
<li>Must fit within the Safeguard Medical culture</li>
</ul>
Competencies
Demonstrates (1) ownership and accountability; Demonstrates the ability to: plan, execute, control and deliver; (2) communicate effectively both written and verbal; (3) Team-orientated personality with the ability to lead and influence others effectively without authority while creating and maintaining a positive environment; (4) Understanding of change management, conflict resolution and team dynamics; (5) respect for people with a desire to develop junior-level team members including coaching in 1:1 and team settings; (6) ability to identify project and business risks and create mitigation strategies; (7) ability to independently make sound decisions with available information, employing a risk-based approach when appropriate; (8) Effective at leading cross-functional initiatives.
 
Physical Requirements
Performing the duties of this job regularly involves: (1) sitting, (2) standing; (3) walking; (4) hearing/listening (5) repetitive hand movement; (6) vision requirements - close vision, adjust focus, color code 
 
Mental Requirements
This position requires the ability to: (1) maintain an appropriate work pace; (2) comprehend and follow instructions; (3) exercise logic and reasoning; (4) organize and prioritize; (5) read; (6) compose written communication; (7) communicate verbally; (8) problem solve (9) make decisions; (10) count and compute (11) analyze and interpret data; (12) multi-task/re-direct; (13) experience numerous interruptions, (14) This position requires the ability to maintain the highest standards of professional maturity and emotional intelligence even in difficult or stressful situations
 
Other Requirements
(1) Business travel required up to 15% of the time; (2) Must fit within the Safeguard Medical culture
 
Work Environment
The noise level in the work environment is usually (1) quiet to moderate.
Hazards in the warehouse environment are: (1) moving machinery; (2) trip hazards
 
This job description is not designed to cover an exhaustive list of duties. Other duties may be assigned, and activities may change at any time with or without notice.
Safeguard Medical is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to a work environment that supports, inspires, and respects all individuals and in which personnel processes are merit-based and applied without discrimination based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
 
Safeguard Medical believes that diversity and inclusion among our teammates is critical to our success as a global company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool.

Director, Global Quality

<h3>Job Description</h3>
Job DescriptionAbout Capricor Therapeutics
Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to developing transformative therapies for rare diseases, with a primary focus on Duchenne muscular dystrophy (DMD). We are pioneers in cell therapy and exosome-based technology, leveraging our innovative platforms, including our lead product, deramiocel (CAP-1002), and our proprietary StealthX™ platform, to engineer cutting-edge treatments. Our team is committed to harnessing advanced science and technologies to meet the unmet needs of patients living with DMD and other challenging medical conditions. Join us on our journey as we push the boundaries of medical science and pave the way for a healthier future.
About the Role
The Quality Control Associate I/II will play an essential role in supporting Capricor’s commitment to delivering high-quality therapies by ensuring the integrity of raw materials and analytical processes at our San Diego facility. This position involves hands-on quality control testing, coordination with external laboratories, and collaboration with development teams to optimize and develop assays. The associate will contribute to GMP compliance, support the release of critical materials, and drive operational excellence in a dynamic, collaborative environment. This role is ideal for a motivated individual eager to grow their expertise in quality control while making a tangible impact on the development of transformative therapies for rare diseases.
Responsibilities
<ul>
<li>
Conduct raw material inspections, including verification of Certificates of Analysis (CoAs), label checks, and documentation review per internal procedures and compendial standards.
</li>
<li>
Perform quality control testing of raw materials to support GMP release and regulatory compliance.
</li>
<li>
Coordinate with outsourced laboratories for sample receipt, testing, and timely reporting of results.
</li>
<li>
Analyze data and maintain organized records, reports, and databases.
</li>
<li>
Write technical reports, deviations, and OOS investigation documentation.
</li>
<li>
Collaborate with Process/Analytical Development to troubleshoot and optimize assays and develop new analytical methods.
</li>
<li>
Train employees on relevant techniques and procedures.
</li>
<li>
Write or revise quality control SOPs and Material Specifications.
</li>
<li>
Coordinate with third-party vendors to maintain equipment calibration.
</li>
<li>
Work with Supply Chain and Quality Assurance to resolve raw material receipt and testing issues.
</li>
<li>
Present data internally to support project goals.
</li>
</ul>
Requirements
<ul>
<li>
Bachelor’s degree in a relevant Biological Science discipline.
</li>
<li>
2+ years of experience in a GMP Quality Control laboratory or GMP/GLP setting (preferred).
</li>
<li>
Experience with laboratory methods including endotoxin detection and FTIR.
</li>
<li>
Familiarity with method qualification/validation (preferred).
</li>
<li>
Ability to independently perform laboratory analysis, troubleshoot, and improve methods.
</li>
<li>
Demonstrated history of successful, independent laboratory work.
</li>
<li>
Excellent communication, time-management, and teamwork skills.
</li>
<li>
Proficiency with Outlook, MS Office, and other electronic systems.
</li>
</ul>
Work Environment / Physical Demands
<ul>
<li>
Must be able to sit or stand for extended periods, move around the facility, communicate effectively, and lift/carry up to 40 lbs.
</li>
<li>
Ability to gown and work in a classified area as required.
</li>
</ul>
Compensation (USD)
This role offers a competitive salary based on experience and qualifications. Additional benefits include health/dental/vision insurance, paid time off, parental leave, 401k retirement plan, company stock options, and bonus eligibility.
Location Policy
This position is based at our headquarters in San Diego, California.
Come Work With Us!
Capricor Therapeutics is headquartered in San Diego, California. We offer competitive compensation and benefits, generous vacation and parental leave, flexible working hours, and a collaborative work environment. If you are excited about joining a team that’s transforming the biotech industry and making a real impact on patients’ lives, we’d love to hear from you!

Quality Control Associate I/II

<h3>Job Description</h3>
Job Description
About Us: 
At SRV Refrigeration, we provide top-notch refrigeration services to our valued customers. With a commitment to quality and customer satisfaction, we strive to maintain a positive work environment and foster professional growth. Join our team and be part of a company that values its employees!
Position Overview: 
We are seeking a skilled and motivated Refrigeration Service Technician to join our growing team. The ideal candidate will have experience in installing, repairing, and maintaining refrigeration systems in commercial settings. If you are passionate about delivering exceptional service and thrive in a team-oriented environment, we want to hear from you!
Key Responsibilities:
<ul>
<li>Install, maintain, and repair refrigeration systems, including walk-in coolers, freezers, and HVAC units. </li>
<li>Troubleshoot and diagnose issues with refrigeration systems to ensure optimal performance. </li>
<li>Perform routine preventative maintenance on refrigeration systems to ensure optimal performance. </li>
<li>Respond to service calls and provide timely and efficient solutions to customers’ problems. </li>
<li>Maintain accurate records of work performed, parts used, and time spent on each job. </li>
<li>Collaborate with team members to ensure high quality service delivery. </li>
<li>Stay up to date with industry trends, technologies, and best practices. </li>
</ul>
Qualifications
<ul>
<li>3+ years of HVAC-R service technician experience </li>
<li>3+ years of diagnosing, inspecting, repairing, and maintaining commercial grade refrigeration systems. </li>
<li>Proven experience as a refrigeration technician </li>
<li>Strong knowledge of refrigeration systems, electrical components, and HVAC principles. </li>
<li>Valid driver’s license with clean 3-year MVR. </li>
<li>Universal EPA certification required</li>
<li>Ability to work independently and as part of a team. </li>
</ul>
Benefits
<ul>
<li>Health, dental, and vision insurance</li>
<li>401(k) with 4% company match </li>
<li>Ongoing training and professional development opportunities</li>
<li>Company-provided vehicle and tools</li>
<li>PTO and 8 Holiday time off</li>
</ul>

HVAC-Refrigeration Service Technician

<h3>Job Description</h3>
Job DescriptionWe need to hire an experienced machine operator to run our bobcat skid steer. The ideal candidate would be available to work 2-3 days a week. Pay is based on experience

Part Time Landscaping Machine Operator

<h3>Job Description</h3>
Job DescriptionAbout ClassOne Experts in Advanced Electroplating and Wet Processing At ClassOne, our mission is to deliver the world’s highest performing and most elegantly designed electroplating and wet processing systems for the manufacture of advanced microelectronics. Engineered for maximum efficiency and flexibility on the manufacturing floor, our systems offer a comprehensive range of electroplating and wet systems solutions validated, tested, fab proven, and designed for top performance in both high-volume and R&amp;D fab environments. Your Job
A successful Scheduler has a strong sense of urgency and responsibility. They are about being organized while also being able to multitask daily. They are dedicated to the client experience from start to finish and maintain a strong working knowledge of client needs, our company services, and the individual skill sets of our Craftsmen. Responsibilities &nbsp;
<ul>
<li>Tracks and measures scheduling functions. Generates reports tracking performance.</li>
<li>Anticipates and prepares for short notice scheduling changes. Always has a backup plan.</li>
<li>Uses the Google forecasting document to communicate, plan, and organize schedules. Ensures it is current and accurate at all times.</li>
<li>Works to build and promote strong, loyal, and long-lasting client relationships and prevent losing clients.</li>
<li>Take responsibility for delivering work and designing the work effort</li>
<li>Proactively identify project issues and recommend viable solutions</li>
</ul>
Qualifications: &nbsp;
<ul>
<li>Three (3) years previous experience in admissions or a scheduling environment.</li>
<li>Demonstrated problem-solving skills</li>
<li>Proficient in computerized input of data</li>
<li>Good communication skills</li>
<li>Fundamental knowledge and skill in utilization of computer application.</li>
<li>Level of proficiency in the use and application of MS Office (Word, Excel, and PowerPoint) varies by department, see requisition for requirements.</li>
</ul>
 ClassOne Technology is always looking for a few more exceptional team members who share our passion for excellence. If you like the idea of working with a nimble, responsive, high-performance team – one that creates top-quality equipment that stands out and gets respect in the industry – join us at ClassOne Technology.

Real Time Scheduler ( Remote )

<h3>Job Description</h3>
Job Description
Our client, in Ames is seeking a Machine&nbsp;Operator to join their team. As a Machine&nbsp;Operator, the ideal candidate will have production experience, self-motivated and good communication skills which will align successfully in the organization. Job Title: Machine&nbsp;Operator, Ames Pay Rate: $20.00 What’s the Job? •&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Machine set-up and operation •&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Picking product, assembling, and packaging •&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ensuring quality of products •&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Inventory tasks and cycle counting Must be comfortable wearing a respirator for proper handling of powder chemical as needed. Training provided.&nbsp; What’s Needed? •&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; HS Diploma •&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Production or Assembly experience •&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ability to thrive in a high-speed, fast-paced environment •&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ability to work independently What’s in it for me? •&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Great pay - $20.00-$22 per hour &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;1st Shift: 5:00am&nbsp;- 3:30pm&nbsp;M-Th 10 hour shifts, 4 Days •&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Weekly pay Steel toe shoes/boots required and contacts are not allowed.&nbsp; Clothing must not have holes and covers legs and body, no sweat pants or spandex type pants. If this is a role that interests you and you’d like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you! ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills.

107,350 Manufacturing Jobs