Manufacturing Engineer

92589 Temecula, California Abbott

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Job Description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
+ Career development with an international company where you can grow the career you dream of.
+ Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
+ An excellent retirement savings plan with a high employer contribution
+ Tuition reimbursement, the Freedom 2 Save ( student debt program, and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.
+ A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
**The Opportunity**
This position works out of our Temecula, CA location in the Abbott Vascular division.
**WHAT YOU'LL DO:**
+ Initiates and completes technical activities leading to new or improved products or process, for current programs, next generation programs and to meet strategic goals and objectives of the company.
+ Prepares reports, publishes, and makes presentations to communicate findings.
+ Analyzes and solves problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a major breakthrough in technology.
+ Understands engineering principles theories, concepts, practices and techniques. Develops knowledge in a field to become a recognized leader or authority in an area of specialization and applies this knowledge in leadership roles in the company.
+ Incorporates business policies and procedures into task completion.
+ Understands the business needs of the company, and has knowledge of the customer needs of our business.
+ Understands the business cycle and foresight of emerging technologies trends.
+ Cultivates internal and external network of resources to complete tasks.
+ Serves has a resource in the selection orientation and training of new engineers and employees.
+ May lead a project team, determining goals and objectives for the projects.
+ Mentors employees by sharing technical expertise and providing feedback and guidance.
+ Interacts cross functionally and with internal and external customers.
+ Serves as a consultant for engineering or scientific interpretations and advice on significant matters.
+ Acts as a spokesperson to customers on business unit current and future capabilities.
+ Cultivates a wide range of internal networks and begins to develop an extensive external network of resources to facilitate completion of tasks.
+ May lead a project team of moderate scope. Provides guidance to less experienced staff. Acts as a mentor to lower level individual contributors.
+ Influence exerted at peer level and occasionally at first levels of management.
+ Plans, organizes, and prioritizes own daily work routine to meet established schedule.
+ Exercises authority and judgment within defined limits to determine appropriate action.
+ Failure to achieve results or erroneous decisions or recommendations may cause delays in program schedules and may result in the allocation of additional resources.
**EDUCATION AND EXPERIENCE YOU'LL BRING:**
**Minimum Qualifications:**
+ Bachelors Degree
+ 0-2 years related work experience
**Preferred Qualifications:**
+ Masters Degree (± 18 years)
+ 2-5 years of related work experience with a good understanding of specified functional area.
+ Working technical knowledge and application of concepts, practices and procedures.
+ General understanding of business unit/group function.
+ Will perform this job in a quality system environment.
+ Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors.
+ Exercises judgment within defined procedures and practices to determine appropriate action.
+ Has a broad knowledge of technical alternatives and an understanding of their impact on the systems environment.
Apply Now ( Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
**Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at , and on X @AbbottNews.
The base pay for this position is $50,000.00 - $100,000.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Manufacturing Engineer

92589 Temecula, California Abbott

Posted 1 day ago

Job Viewed

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Job Description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:
+ Career development with an international company where you can grow the career you dream of.
+ Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year
+ An excellent retirement savings plan with high employer contribution
+ Tuition reimbursement, the Freedom 2 Save ( student debt program and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.
+ A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
Our location in **Temecula, CA** currently has an opportunity for a **Manufacturing Engineer** **.**
**The Opportunity**
This position works out of our Temecula, CA location in the Abbott Vascular Division. Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ?ngersticks. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.
**What You'll Work On**
Provides support to the manufacturing organization by developing new processes and optimizing existing processes. Utilizes six sigma, lean, design control, and validation principles to create robust processes. This role requires completion of steps from process conception, design, validation, and implementation to manufacturing. Interfaces with Manufacturing, Quality and Research and Development organizations to integrate new processes into the existing manufacturing areas.
**WHAT YOU'LL DO**
Provides support to the Manufacturing organization to facilitate efficient operations within the production area, to optimize existing processes, and to ensure that production goals are met. Monitors performance of manufacturing lines, equipment, machines and tools and corrects equipment problems or process parameters that produce non-conforming products, low yields or product quality issues. Interfaces with Quality and other organizational functions to integrate new products or processes into the existing manufacturing area.
**Core Job Responsibilities**
Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
1. Initiates and completes technical activities leading to new or improved products or process, for current programs, next generation programs and to meet strategic goals and objectives of the company. Prepares reports, publishes, and makes presentations to communicate findings.;
2. Analyzes and solves problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a major breakthrough in technology.;
3. Understands engineering principles theories, concepts, practices and techniques. Develops knowledge in a field to become a recognized leader or authority in an area of specialization and applies this knowledge in leadership roles in the company.;
4. Incorporates business policies and procedures into task completion. Understands the business needs of the company, and has knowledge of the customer needs of our business. Understands the business cycle and foresight of emerging technologies trends.;
5. Cultivates internal and external network of resources to complete tasks. Serves has a resource in the selection orientation and training of new engineers and employees. May lead a project team, determining goals and objectives for the projects. Mentors employees by sharing technical expertise and providing feedback and guidance.;
6. Interacts cross functionally and with internal and external customers. Serves as a consultant for engineering or manufacturing interpretations and advice on significant matters. Acts as a spokesperson to customers on business unit current and future capabilities.
7. Applies manufacturing concepts like LEAN manufacturing, push versus pull, 5S, etc.
(Supervision Received) Work is monitored with autonomy. Follows specific, detailed instructions
Position Accountability / Scope
(Influence/Leadership) Begins developing a network of internal resources to facilitate completion of tasks. Individual influence is typically exerted at the peer level.;
(Planning/Organization) Completes daily work to meet established schedule with guidance from supervisor on prioritization of tasks.;
(Decision Making/Impact) May exercise authority within pre-established limits and approval. Failure to achieve results can normally be overcome without serious effect on schedules and programs.
**EDUCATION AND EXPERIENCE YOU'LL BRING**
**Minimum Education:**
Bachelor's degree plus 2-5+ years of related work experience with a basic understanding of specified functional area, or an equivalent combination of education and work experience.
**Minimum Experience / Training Required:**
(Technical/Business Knowledge (Job Skills)) Basic technical knowledge of concepts, practices and procedures. Limited understanding of business unit/group function. Will perform this job in a quality system environment adhering to medical device standards. Failure to adequately perform tasks can result in noncompliance with governmental regulations.;
(Cognitive Skills) Learns to use professional concepts and company policies and procedures to solve routine problems. Works on problems of various degrees scope/ complexity. Minimal independent decision making.
Apply Now ( more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is $60,000.00 - $120,000.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Manufacturing Lead

92589 Temecula, California Adecco US, Inc.

Posted 1 day ago

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Job Description

Adecco is hiring immediately for **Manufacturing Lead** roles in Temecula, CA. Manufacturing Leads do essential jobs with one of our premier clients. In this role, you will oversee and coordinate daily operations in our Blow Molding and Injection production area. The Manufacturing Lead will be responsible for supervising a team, ensuring production targets are met, and troubleshooting any issues related to the blow molding process and injection.
**Schedule:** 6:00am - 2:30pm / Open availability Monday - Sunday, over time is required
**Pay:** $20.00 - $3.00
**Responsibilities:**
· Led and supported production teams, ensuring training, shift communication, and adherence to safety, GMP, and SQF protocols.
· Operated and monitored blow molding machines, maintaining production flow, meeting schedule targets, and covering machines during breaks when needed.
Maintained quality standards by conducting QA checks, logging defects, verifying packouts, and ensuring compliance with SOPs and regulatory requirements.
· Collaborated across departments, including QA, Maintenance, and Planning, to resolve issues and ensure smooth operations.
· Documented production data accurately and contributed to continuous improvement efforts to enhance efficiency, reduce waste, and promote a safe work environment.
+ Support process improvements to enhance efficiency, reduce waste, and maintain high product quality
+ Keep accurate records of production data, downtime, and shift activity
**Requirements:**
· Physically capable of standing, walking, bending, reaching, and performing repetitive motions for extended periods (8+ hours), including lifting up to 25 lbs regularly and 50 lbs. with assistance.
· Able to safely navigate ladders, stairs, uneven terrain, and confined spaces, while working near loud equipment
· Strong hand-eye coordination and fine motor skills for operating tools, machinery, or performing detailed tasks with visual and auditory awareness.
· Tolerant of varying environmental conditions, including temperature changes, indoor/outdoor settings, and prolonged use of required PPE (e.g., gloves, masks, safety glasses).
**Preferred Education & Experience:**
· High school diploma required; Associate degree or technical certification in Manufacturing or Engineering preferred.
· 3-5 years of blow molding or related manufacturing experience, including at least 1 year in a leadership role.
· Skilled in operating blow molding equipment, with strong knowledge of safety standards, quality control, and production efficiency.
· Proven leadership, training, and communication abilities, with a focus on problem-solving, attention to detail, and continuous improvement (Lean knowledge a plus)
**What's in this for you?**
+ Weekly pay
+ Competitive benefits with options such as medical, dental, vision, and 401(k)
+ Temp to hire position
Click on apply now for immediate consideration for these Manufacturing Lead positions in Temecula, CA!
**Pay Details:** $20.00 to $2 .00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
+ The California Fair Chance Act
+ Los Angeles City Fair Chance Ordinance
+ Los Angeles County Fair Chance Ordinance for Employers
+ San Francisco Fair Chance Ordinance
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Quality Control Manager

92058 San Luis Rey, California TechFlow

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Quality Control Manager- Camp PendletonCompetitive Salary and EMPLOYER PAID INSURANCE!EMI Services is hiring a Quality Control Manager (QCM) to work directly with the project manager, the operations manager, the safety supervisor, as well as the United States Government. This position assures quality services to customers: reports performance levels and degrees of compliance with an established QC program. The QCM is required to test and inspect services and work performed for compliance with contract requirements and performance standards. Evaluate data and write reports to validate or indicate deviations. Recommend modifications or necessary actions to achieve optimum quality. Monitor building conditions for possible QC issues or violations, in conjunction with the Safety Supervisor. Also, monitor work assignments and projects for safety or health issues. In addition, the QCM produces and analyzes reports and makes recommendations for quality improvements, as well as, investigates complaints and report's findings to the project manager. The ideal EMI Quality Control Manager promotes quality and customer services excellence. SalaryStarting at $100,000 (DOE) plus employer paid insurance!Key Responsibilities Work closely with Project Manager, FSM, SSHO, subcontractors and QCI Staff ALL aspects Quality Control Inspection and documentation of Service and Maintenance work Develop and maintain quality surveillance and tracking system for maintenance shops and subcontractors Develop and implement QC plan, ensuring environmental plan compliance, performance monitoring, analysis and reporting Advise the Project Manager on quality control and environmental program status, strategies, issues and potential problem areas Monitor and track specialized qualifications or credentials such as licenses, certificates, degrees or training needed by personnel Enforce all regulatory, base and company specific safety rules Manage Quality Control Inspectors Lead monthly QCM with Government Execute additional duties and responsibilities as assigned and/or required to complete the project Essential Skills Effective oral and written communication skills Strong organizational, interpersonal skills Type; operate a personal computer, with emphasis on accuracy, mental alertness, and neatness Demonstrated ability to work accurately, follow procedures and schedules, and prioritize multiple tasks Ability to read and understand blueprints, specifications, and contract requirements Proficiency with all MS Office products (Word, Excel, Access, PowerPoint) Ability to work successfully in a team environment, aligning with company culture and processes Must possess a strong work ethic and values that are above-reproach Understand and adhere to policies and procedures as set by EMI Services Promote and maintain a positive image of EMI Services Maintain confidentiality of information related to EMI Services, our customers, vendors and employees Be adaptable and flexible in work situations. Establish priorities to ensure completion of tasks in a timely manner Inform the Project Manager of all pertinent problems, irregularities, and other important information within area of responsibility Adhere to safety policies and procedures to include proper use of personal protective equipment Requirements High School Diploma or equivalent 5 + years of experience as a Quality Control Manager working federal projects Experience with Government Contracts and Personnel ASQ CMQ/OE Certification Safety Certification OSHA 30 hour Construction Quality Management course within 5 years Valid driver's license Pass a pre-employment drug screening and background check Regular, dependable attendance required U.S. citizenship to obtain and maintain access to military installations *This individual is subject to Government approvalPreferred QualificationsBachelor's degree or equivalent experience (1:2 ratio) with maintenance and repair facilities Physical Requirements Carrying objects/boxes/print-outs short distances Extensive work with a personal computer Lifting and moving as much as 50 pounds with assistance Use of hands, reaching with hands and arms, talking, and walking Prolonged periods of sitting, bending, squatting, standing, twisting, or stooping Climbing ladders and entering confined spaces Work both indoors and outdoors in various temperatures (some extreme) and weather conditions *Physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Click here to follow EMI Services on Facebook Benefits Health Care Plan (Medical, Dental & Vision) Retirement Plan (401k, IRA) Life Insurance (Basic, Voluntary & AD&D) Paid Time Off (Vacation, Sick & Public Holidays) Employee Stock Ownership Plan (ESOP) Short Term and Long Term Disability Term Life Insurance What We DoEMI is an industry-leading provider of DoD base operation support services, facilities maintenance, and logistics. Our goal is to contribute to the repair and maintenance of buildings and equipment. EMI consistently delivers cost-saving through best-value innovations and quality service that exceeds our clients' expectations.What Sets Us ApartThe Right Partner: EMI has grown by gaining our customers' trust and our employees' loyalty. We've successfully performed over 60 service contracts and we understand the unique challenges facing today's military. We offer exceptional responsiveness and a strong commitment to customer satisfaction. We demonstrate this commitment by consistently earning some of the highest customer satisfaction ratings in the industry.The Right Team: The EMI team includes over 250 high-achieving professionals, administrative and trades personnel deployed in various locations throughout the United States. At times, we augment our in-house capabilities with proven and capable business partners.The Right Approach: EMI brings vast expertise and proven solutions to augment our clients' operations. We provide a platform that delivers seamless mission support and exceptional customer service in a very cost-effective and repeatable solution.#emiservices

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Quality Control Inspector

92713 Irvine, California Masimo

Posted 1 day ago

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Job Description

Job Description

Job Summary

The Quality Control Inspector is responsible for the inspection of the product at different levels of the process, in order to assure that the material meets or exceeds the requirements set forth in Company documents and procedures. The responsibilities include material handling in support of production.

Duties & Responsibilities
  • Perform Receiving, In-Process, and Final inspections of product per AP (acceptance procedure) documents;
  • Generate and complete Quality Reports in accordance with released acceptance procedures, drawings, bill of materials, assembly master records, and device master records requirements;
  • Perform functional testing per AP (acceptance procedures) and DR (drawing) requirements.
  • Release / approval of product labels
  • Review of work / job orders for compliance to internal documentation such as AMR (assembly master records), DMR (device master records), DR (drawings), DHR (Device History Record), and MB (bill of materials);
  • Identification, segregation, and NCR generation for nonconforming products and materials;
  • Keep up to date with document revision changes as they affect inspections;
  • Movement of material to designated locations in support of inspections, MRB, RMA, and Inventory processes. The material handling will include but not be limited to the physical movement of material in the warehouse and/or QC Areas, use of pallet jacks, packing and unpacking of material, palletizing material, lifting material, and verification of material quantities and documents;
  • Perform other duties or special projects as assigned.
Minimum & Preferred Qualifications and Experience

Minimum Qualifications
  • Three years of experience as a Quality Control Inspector (or similar role) within the medical device industry; or equivalent combination of education and related experience in any industry.
  • PC literate with good skills in MS Office (Word and Excel) programs;
  • Working knowledge of GDP (Good Documentation Practices)
  • Good verbal and written communication skills;
  • Must be able to work with minimum supervision.
Preferred Qualifications
  • Prior experience with quality control systems;
  • Familiar with Part 820 Quality Systems Regulation;
  • Familiar with ISO 13485 Standards;
  • Familiar with GMP (Good Manufacturing Practices);
  • Familiar with Agile, and Expandable ERP systems

Education

High School diploma or GED is required. College degree is preferred.

Compensation

The anticipated Hourly Rate range for this position is $16-21 Per Hour plus benefits. Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience.

Physical requirements/Work Environment

This position primarily works in an office, laboratory, and manufacturing environment. It requires frequent sitting, standing and walking. Daily use of a computer and other computing and digital/mechanical devices is required. Must be able to regularly lift up to 35 pounds. May sit or stand for extended periods. Some local travel is necessary, so the ability to operate a motor vehicle and maintain a valid Driver's license is required.

The physical demands and work environment 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 the essential functions.

About Us

For over thirty years, Masimo has been expanding the boundaries of noninvasive monitoring to improve patient outcomes and reduce the cost of care. Today, Masimo delivers a portfolio of hospital-trusted monitoring solutions to help increase patient safety, health, and wellness in the hospital and at home. When you join our team, you'll be part of a culture that's driven by passion, challenging the status quo, and making an impact in the lives of others.

This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: click here
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Quality Control Supervisor

92713 Irvine, California Infinite Peripherals

Posted 3 days ago

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Job Description IPCMobile (founded as Infinite Peripherals) empowers businesses to operate more efficiently through next-generation enterprise mobility solutions. With over 25 years of mobility expertise, the company provides scalable and customized solutions to a range of industries including retail, healthcare, supply chain and logistics, hospitality, and travel. From cloud-based inventory software to fully integrated payment processing solutions, IPCMobile mobilizes companies to do business anywhere, anytime. With over one million solutions deployed, IPCMobile allows companies to go paperless and is fully committed to helping reduce carbon footprints and energy consumption in businesses everywhere. With mobility, the possibilities are infinite.Quality Control SupervisorLocal candidates only. Relocation / H-1B is not offered.The Quality Control Supervisor is responsible for overseeing quality inspection and testing processes to ensure products and components meet internal and external standards. This role collaborates with engineering, compliance, QA, and production teams to interpret test results, resolve issues, and continuously improve quality practices. The ideal candidate will combine technical expertise with leadership skills to guide a team of quality control professionals in maintaining a high standard of product reliability and performance.Leadership & Supervision:Assign tasks and provide ongoing guidance, training, and performance feedback to QC personnel.Ensure team members have the tools and knowledge required to perform their duties effectively.Collaborate with management to align departmental goals with company-wide quality objectives.Support the development and implementation of performance improvement plans.Quality Control Operations:Conduct inspections of incoming goods and evaluate test results for finished products and raw materials.Review and refine test programs, methods, and procedures to maintain testing accuracy and effectiveness.Monitor product performance and suggest adjustments to improve quality outcomes.Ensure test and measurement equipment is properly maintained and calibrated.Process Oversight & Compliance:Maintain and support test and inspection procedures for both functional and performance testing of fixed and mobile devices.Ensure alignment with system-level configuration and testing management processes.Promptly document and report deviations from customer or product requirements.Utilize appropriate tools to report discrepancies, non-conformities, and compatibility issues.Cross-Functional CollaborationPartner with engineering, QA, and production teams to identify and resolve quality issues.Participate in readiness reviews and collaborate on NCMRs (Non-Conformance Material Reports) and SCARs (Supplier Corrective Action Requests).Support process improvements and corrective actions based on root cause analysis and trend reporting.This description is meant to be a guide it does not include every responsibility of roleQualifications:2-4 years of experience in quality control, engineering, or a related field.Solid understanding of quality assurance practices and standards.Familiarity with inspection and test methodologies for both hardware and software systems.Strong organizational, communication, and leadership skills.Ability to adapt and apply judgment in a fast-paced, evolving environment.Additional : Job Type: Full Time Monday - Friday (hourly)Starting wage from - $17.00 / hour- $2.00 hourHours: 8am - 5pm (TBD)Location: Irvine, CA (close to John Wayne Airport)Perks:IPCMobile offers excellent benefits including zero-deductible medical/Rx through Cigna, dental, and vision insurance coverages, Aflac, a 25,000 life insurance policy on each employee, and a 401K plan with 4% matching. Paid holidays and PTO are also offered. Employees are able to use the company gym, as well as enjoy our amazing facility which includes occasional lunches served from our gourmet kitchen, a large assortment of snacks, endless coffee, games and great people!As per company policy, official hiring will be pending background check and drug test. We use e-Verify.Equal Opportunity EmployerIPCMobile (founded as Infinite Peripherals Inc.) provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

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Quality Control Inspector

92630 Lake Forest, California AtWork - Santa Ana

Posted 4 days ago

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Job Description

AtWork has partnered with a manufacturer in Lake Forest with a commitment to excellence to uphold the highest standards in the industry. Currently seeking a skilled and motivated Quality Control Inspector to bolster our team. Schedule: First shift Benefits: PTO, Medical, 401K Role and Responsibilities: As a Quality Control Line Inspector, you will play a crucial role in ensuring the quality and accuracy of our products. Your responsibilities will include: Maintaining a keen attention to detail and focus on precision work. Utilizing equipment such as Micrometer, Comparator, and Caliper to check parts Knowledge of blueprint reading Must have previous QC experience Call or text for more info

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About the latest Manufacturing Jobs in Lake Elsinore !

Quality Control Inspector

92630 Lake Forest, California PrideStaff

Posted 4 days ago

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Job Description

Quality Control Inspector for a medical device manufacturer located in the Lake Forest area. Great opportunity and growth potential with a stable company.

This is a Temporary to Hire opportunity, hours are 1st shift, 7:00 AM - 3:30 PM, Monday-Friday. Pay rate $18-23/hr, depending on experience. Mandatory daily overtime plus 1-2 Saturdays a month. Company will complete a full background check prior to start. Excellent benefits including 100% paid medical, dental and vision for employees and 401K with 4% matching after the first year.

Responsibilities:
  • Maintain QC Policies and Procedures and ensure compliance. Adhere to QMS,ISO 13485, and FDA Rules and Regulations.
  • Inspects/Approves finished products by confirming specifications; conducting visual and measurement tests; communicating required adjustment to production supervisor.
  • Inspects/Approves in -process production by confirming specifications; conducting visual and measurement tests; communicating required adjustments to production Supervisor.
  • Inspects/Approves incoming materials by confirming specification; conducting visual and measurement tests; rejecting and returning unacceptable materials.
  • Documents inspection results by completing inspection report forms; summarizing re-work and waste.
  • Keeps measurement equipment operating by following all applicable procedures.
  • Perform other duties as assigned.
Requirements:
  • MUST have QC experience.
  • MUST be able to read blueprints.
  • MUST be able to use measuring equipment caliper, micrometer, and comparator.
  • Good verbal and written communication skills.
  • Excellent attention to detail and willing to step forward to discuss with. management any engineering change requests.


Compensation / Pay Rate (Up to): $8.00 - 23.00 Per Hour
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Quality Control Inspector

92688 Rancho Santa Margarita, California Applied Medical

Posted 4 days ago

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Job Description

Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions.

Position Description

Are you detail-oriented with a passion for maintaining the highest standards of quality in manufacturing? Join Applied Medical as a Quality Control Inspector and play a vital role in ensuring the excellence of our raw materials, components, and finished products. As part of our Quality Assurance team, you'll utilize precision measurement tools, review engineering documentation, and uphold strict compliance with industry standards.

Key Responsibilities:

  • Conduct thorough inspection activities, including receiving, in-process, and final product verification .
  • Assess raw materials, components, subassemblies, and finished products for adherence to standards, guidelines, and specifications outlined in company procedures.
  • Interpret engineering drawings, shop order operations, and process controls to ensure accuracy in production.
  • Inspect products and materials following standard operating procedures and work instructions .
  • Utilize technical measuring devices to confirm product conformance to defined specifications.
  • Document and report nonconforming materials, ensuring accurate record-keeping.
  • Maintain detailed inspection results using data management software .
Position Requirements
  • 2+ years of experience working within quality management systems (ISO 9001, ISO 13485, or 21 CFR Part 820).
  • Ability to read, write, and communicate in English effectively.
  • Understanding and adherence to Applied Medical's Quality Systems and training guidelines.
  • Compliance with safety rules and company policies .
Preferred
  • Hands-on manufacturing experience , particularly within the medical device industry .
Benefits

The base compensation range for this role is $18 - $23 per hour for positions in California . Actual compensation packages are determined based on factors such as skills, experience, certifications, and work location. The compensation range is subject to modification in the future.

Our total rewards package includes:
  • Training and mentorship programs with ongoing development opportunities.
  • On-campus wellness activities promoting health and well-being.
  • Comprehensive medical, dental, and vision coverage .
  • Education reimbursement program to support career growth.
  • 401(k) retirement program with discretionary employer match.
  • Generous vacation accrual and paid holiday schedule.

Please note that the compensation range may be based on factors such as relevant education, qualifications, experience. The compensation range may be adjusted in the future, and special discretionary bonus or incentive compensation plans may apply.

Our total reward package reflects our commitment to team member growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life.

Equal Opportunity Employer

Applied Medical is an Equal Employment Opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other basis protected by federal, state or local laws in the locations where Applied Medical operates.
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Quality Control Supervisor

92058 San Luis Rey, California MedStar Health

Posted 6 days ago

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Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES

  • Adhere to the Company's Quality Management System to ensure compliance with applicable regulatory requirements.
  • Manage daily resource utility and production workflow to ensure all daily production requirements are being met
  • Develop, coordinate, and enforce systems, policies, procedures, and productivity standards for overall quality inspections
  • Manage overall inspection methodology, including but not limited to equipment selection, inspection plans, SOP's, etc.
  • Support the transfer of new products and processes from Engineering to Production - i.e. development and implementation of inspection methodology
  • Oversee the overall calibration system for all equipment, gauging, instruments, etc.
  • Track non-conforming products and lead material review board (MRB) efforts
  • Support validation activities to meet manufacturing needs
  • Evaluate the impact of process and equipment changes on product quality conformance
  • Identify and drive continuous improvement opportunities related to product and process quality
  • Manage the review of completed device history records and the transfer of product out of Quality Control
  • Manage the training program for the inspection team - i.e. inspection methodology and standard practices
  • Provide technical guidance to the inspection team as needed
  • Provide ongoing communication and regular status updates to senior management team
  • Interface and collaborate with other departments, outside vendors, stakeholders, etc.
  • Perform other duties as required

SUPERVISORY RESPONSIBILITIES

Direct Reports: Yes N/A

  • Monitor team productivity and provide constructive feedback
  • Supervise team workflow and align performance expectations with company goals

QUALIFICATIONS

The requirements listed below are representative of the knowledge, skill, and/or ability required for this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Proficient in blueprint reading (GD&T)
  • Proficient skill with precision measuring instruments (e.g. micrometers, calipers, gauges, optical comparators, etc.)
  • Must be flexible and able to adapt to change
  • Strong written and verbal communication skills
  • Must be able to exercise independent judgment and discretion
  • Communicates and works well with employees of all positions
  • Computer literacy with standard software applications

EDUCATION AND/OR EXPERIENCE

  • High school diploma required
  • Bachelor's degree preferred
  • 5+ years of experience in a medical device manufacturing environment

CERTIFICATES, LICENSES, REGISTRATIONS

  • ASQ certification preferred (e.g. Quality Manager, Engineer, Auditor, etc.)

WORK ENVIRONMENT

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • The work environment is an industrial setting dedicated to the production and assembly of medical devices that utilizes machinery, equipment, and specialized processes to transform raw materials into finished products. The work environment also includes a typical office setting.
  • This position is based onsite and requires regular in-person attendance at the company's facility.

PHYSICAL DEMANDS

Analysis of Physical Demands

N = Never

R = Rarely Less than 1 hour per week

O = Occasional 1% to 33% of time

F = Frequent 34% to 66% of time

C = Constant over 66% of time

Activity

Frequency

Activity

Frequency

Lifting/Carrying

N

R

O

F

C

Twisting/Turning

N

R

O

F

C

Under 10 lbs

Reach over shoulder

11-20 lbs

Reach over head

21-50 lb

Reach outward

51-100 lbs

Climb

Over 100 lbs

Crawl

Pushing/Pulling

N

R

O

F

C

Kneel

Under 10 lbs

Squat

11-20 lbs

Sit

21-50 lbs

Walk-Normal Surfaces

51-100 lbs

Walk-Uneven Surfaces

Over 100 lbs

Walk-Slippery Surfaces

Other

N

R

O

F

C

Stand

Keyboard/Ten Key

Bend

Fingering (fine dexterity)

Driving

N

R

O

F

C

Handling (grasping, holding)

Automatic Trans

Repetitive Motion - Hands

Standard Trans

Repetitive Motion - Feet

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