Azpipeline_org

(STEM) Science, Technology, Engineering & Mathematics

Manufacturing Production Technicians

Set up, test, and adjust manufacturing machinery or equipment, using any combination of electrical, electronic, mechanical, hydraulic, pneumatic, or computer technologies.

Salary Breakdown

Manufacturing Production Technicians

Average

$57,740

ANNUAL

$27.76

HOURLY

Entry Level

$41,450

ANNUAL

$19.93

HOURLY

Mid Level

$54,890

ANNUAL

$26.39

HOURLY

Expert Level

$68,330

ANNUAL

$32.85

HOURLY


Current Available & Projected Jobs

Manufacturing Production Technicians

14

Current Available Jobs

2,450

Projected job openings through 2024


Sample Career Roadmap

Manufacturing Production Technicians

Supporting Certifications

Core

Advanced

Specialty


Top Expected Tasks

Manufacturing Production Technicians


Knowledge, Skills & Abilities

Manufacturing Production Technicians

Common knowledge, skills & abilities needed to get a foot in the door.

KNOWLEDGE

Mechanical

KNOWLEDGE

Engineering and Technology

KNOWLEDGE

Production and Processing

KNOWLEDGE

Design

KNOWLEDGE

Mathematics

SKILL

Operation Monitoring

SKILL

Critical Thinking

SKILL

Monitoring

SKILL

Reading Comprehension

SKILL

Active Listening

ABILITY

Oral Comprehension

ABILITY

Problem Sensitivity

ABILITY

Visualization

ABILITY

Oral Expression

ABILITY

Deductive Reasoning


Job Opportunities

Manufacturing Production Technicians

  • Manufacturing Technician - Tech Grad
    Intel Corporation    Chandler, AZ 85226
     Posted about 6 hours    

    Substrate Packaging Technology Development (SPTD) is looking to hire a Manufacturing Technician to work in Assembly Test and Technology Development (ATTD) on a shift 7 (Compressed work week schedule). Manufacturing Technicians (MT) perform functions associated with all substrate production including operations, equipment, process and training.

    The Manufacturing Technician in ATTD will be expected to:

    Collect and evaluate operating data to conduct online equipment adjustment and ensure process optimization.
    Be responsible for improvement processes, troubleshooting nonstandard events in the production line, and reviewing technological health and stability.
    Be responsible for the buddy, trainer, certifies levels and is in charge of updating training manuals.
    Participate in safety forums and Emergency Response Team as required.
    Additionally, in this role:

    Work is complex and is performed within the spectrum ranging from narrowly defined parameters and limited judgment up to highly complex and nonstandard assignments in nature and broadly defined parameters.
    Normally receives general instructions on routine work, and detailed instructions on new work.
    The candidate should also exhibit the following behavioral traits and/or skills:

    Verbal and written communication skills and be comfortable presenting issues and solutions
    Willingness to work in a diverse team environment and multitask
    Work with minimal supervision and adjust to rapidly changing priorities
    Produce results in a timely manner
    Analytical problem-solving and testing skills
    Position requires frequent standing, walking, bending and reaching

    Qualifications

    This U.S. position is open to U.S. Workers Only.
    A U.S. Worker is someone who is either a U.S. Citizen, U.S. National, U.S. Lawful Permanent Resident, or a person granted Refugee or Asylum status by the U.S. Government.
    Intel will not sponsor a foreign national for this position.

    You must possess the below requirements to be initially considered for this position.
    Preferred qualifications are in addition to the requirements and are considered a plus factor in identifying top candidates.

    Requirements:

    Possess an associate's degree or bachelor's degree or Mechanical or Technical Certification or 6 months related hands-on manufacturing experience or equivalent military training.
    Work a day shift compressed work week schedule.
    Shift is twelve hours long and rotate from three to four days a week: Thursday/Friday/Saturday every other Wednesday days (Shift 7)
    Work in a clean room environment, wearing coveralls, hoods, booties, safety glasses and gloves.
    Lift up to 25 lbs., and spend the majority of time (greater than 90% less break time) on the floor working on tool sets, walking 3-5 miles a day, and/or standing/sitting for 9 hours.

    Preferred:

    6+ months of prior experience in the following areas:

    Electronics, equipment troubleshooting, installation, repair and operation in semiconductor manufacturing technology
    Read schematics and complex drawings and/or diagrams
    Inside this Business Group
    As the world's largest chip manufacturer, Intel strives to make every facet of semiconductor manufacturing state-of-the-art -- from semiconductor process development and manufacturing, through yield improvement to packaging, final test and optimization, and world class Supply Chain and facilities support. Employees in the Technology and Manufacturing Group are part of a worldwide network of design, development, manufacturing, and assembly/test facilities, all focused on utilizing the power of Moore’s Law to bring smart, connected devices to every person on Earth

    Posting Statement

    All qualified applicants will receive consideration for employment without regard to race, color, religion, religious creed, sex, national origin, ancestry, age, physical or mental disability, medical condition, genetic information, military and veteran status, marital status, pregnancy, gender, gender expression, gender identity, sexual orientation, or any other characteristic protected by local law, regulation, or ordinance....


    Seniority Level

    Some work experience (up to 5 years, non-manager)

    Industry

    Manufacturing

    Employment Type

    Full Time

  • Automation Technician
    West Pharmaceutical Services    Tempe, AZ 85280
     Posted about 13 hours    

    Automation Technician

    Tempe

    Arizona

    Working at West means having an opportunity to work by the side of our patients and customers, our global team members and the communities in which we operate - which all help contribute to a Healthier World.

    At West, we are by the side of patients. The work we do impacts patients' lives each and every day - our products are a critical part of healthcare delivery and we are proud of the role we play to improve patient health. We work by the side of our team members. We come together as one global team to deliver for our customers and help them address their challenges. We are a diverse, close-knit community of professionals, where everyone has a voice and opportunity to learn and grow through mutual trust and respect. With a 95 year plus history, we have a track record for success, which includes reported sales of $1.84B in 2019. We serve by the side of our community. Giving back is in our DNA-our team members across more than 50 sites globally are involved with hundreds of charities that have special meaning to them through our West with Without Borders team member-led giving program.

    Job Summary:

    Responsible for ensuring that existing automation equipment and systems are functioning as intended to deliver maximum output while maintaining highest product quality. Support industrialization of next generation equipment and continuous improvement initiatives in existing platform products within the proprietary product value streams in Operations, under appropriate guidance and leadership

    Essential Duties and Responsibilities:


    * Under guidance of the process and operations engineers:

    * Support production operations within the value stream to ensure operational efficiencies are met.
    * Develop, recommend and implement corrective action to improve efficiencies, as needed
    * Identify production downtime occurrences and use statistical methods to identify major downtime trends and develop robust solutions.

    * Work with project engineers/process engineers to ensure successful evaluation of all new equipment / process improvements.
    * Assist with the installation and validation of new automation equipment/process development through SAT/IQ/OQ/PQ
    * Work within timelines to ensure timely completion of assigned projects.
    * Complete project status reports and communicate to responsible engineers/project teams
    * Provide process support to the production facilities as required. Requires working knowledge of all automation equipment (i.e.: materials, molding, tooling, etc...)
    * Required to perform troubleshooting and maintenance activities as necessary
    * Implement and perform equipment preventative maintenance and calibration procedures and activities.
    * Provide direction and training to other technicians as required
    * Coordinate spares inventory management with assistance of Engineering and Maintenance to ensure minimal downtime as a result of missing spares
    * Must be able to work with minimal supervision. Must be able to work flexible hours and support business needs if required.
    * Observe all company Policies and Safety Rules and Regulations


    * Performs other duties as assigned based on business needs.

    Basic Qualifications:


    * High School or Equivalent

    * Prefer Associates degree or working toward degree in technical discipline

    * 6 - 10 Years of manufacturing experience

    Preferred Knowledge, Skills and Abilities:


    * Prefer 5 years related experience and/or training with automation systems; or a combination of equivalent education and experience.
    * Must be able to independently problem solve technical and/or mechanical issues
    * Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals
    * Ability to write reports and correspondence as needed
    * Ability to interpret a variety of instructions furnished in written, verbal, diagram or schedule form
    * Ability to work with various computer software programs
    * Must be able to manage multiple priorities
    * Willing to work overtime as needed


    * Medical device development and manufacturing background preferred
    * Knowledge of manufacturing processes, workflows, basic electrical / automation equipment and industrial techniques.
    * Must have effective problem solving and interpersonal skills.
    * Must have knowledge of sound engineering principles and practice.
    * Must possess the ability to plan work and supervise others, as needed.

    Travel Requirements:


    * 10 - 15%

    Physical & Mental Requirements:


    * Must be able to perform job duties as required with limited physical demands within clean room manufacturing requirement.

    West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a disability or special need that requires accommodation, please send an email to . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.


    Employment Type

    Full Time

  • Principal Wafer Fab Process Engineer
    Medtronic    Tempe, AZ 85282
     Posted about 14 hours    

    Principal Wafer Fab Process Engineer

    Location:

    Tempe, Arizona, United States

    Requisition #:

    20000C2G

    Post Date:

    8 hours ago

    **Principal WaferFab Process Engineer**

    **Careers thatChange Lives**

    Medtronic is the
    world’s premier medical company, providing patient benefits around the globe.
    The Tempe, Arizona location is looking for a Principal Process Engineer. The Tempe site is applying wafer fabrication
    processes to develop and produce cutting-edge medical devices. This role provides opportunities to solve novel
    material and processing technical challenges. This role will be responsible for
    the technology feasibility assessments, process and manufacturing flow development,
    and providing inputs to design and product teams.

    **Day in the Life:**

    Responsibilities
    may include the following and other duties may be assigned.

    + Lead the innovation, developmentand/or optimization of new manufacturing concepts, processes andprocedures for transfer to manufacturing operations.

    + Perform scouting and feasibilitywork, material selection, process and equipment selection, tooling /fixture and equipment installation and process development.

    + Design, execute and analyzeexperiments to establish clear understanding of fundamental processmechanisms.

    + Perform feasibility studies,process characterization and create technical reports.

    + Provide input to design andproduct teams

    + Develop project milestones andreport progress.

    + Generate and maintaindocumentation per quality system requirements.

    + Ensure processes and proceduresare compliant to regulations.

    + Champion the use of DesignReliability Manufacturing (DRM) and data-driven methods through processdevelopment

    **Must Have: Minimum Requirements**

    + B.S. in Engineering or Science with 7 years experience, or advanced degree with a minimum of 5 years of experience with wafer fab-based processes

    + Experience developing and deploying wafer fabrication process technologies, including process characterization, designed experiments, statistical process control, and data analysis.

    **Nice to Have**

    + Ph.D. or M.S. in Chemistry, Materials Science, or similar technical disciple.

    + Design for Six Sigma (DFSS) Master Black Belt, or equivalent knowledge, investment, and experience in design for reliability and manufacturing.

    + Knowledge and experience in medical device technologies

    **About Medtronic**

    Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.

    We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.

    **Physical Job Requirements**

    The physical demands described within the Responsibilities section of this job description 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. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)

    It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.


    Employment Type

    Full Time

  • Technician III - Wafer Fab Process
    Medtronic    Tempe, AZ 85282
     Posted about 14 hours    

    Technician III - Wafer Fab Process

    Location:

    Tempe, Arizona, United States

    Requisition #:

    20000BM0

    Post Date:

    9 hours ago

    **Careers that Change Lives**

    Medtronic Tempe Campus, located in Tempe,
    Arizona, is looking for a Technician III tosupport Wafer Fab Operations and the Advanced Packaging Facility
    as photolithography process technician.

    The ideal
    candidate will have a passion for the patients we serve and an unrelenting
    desire to improve our business.

    **A Day in the Life**

    In this position, your
    primary focus will be supporting wafer fab processes including patterned
    polymer/organic solution deposition on wafers. You will also conduct
    experiments, perform equipment maintenance/ troubleshooting, design and execute
    Gage RR studies and author operating specs.

    Responsibilities
    will include, but are not limited to:

    + Execute experiments,makes and records observations, collects and prepares data for evaluation.

    + Create manufacturingspecs and procedures.

    + Perform equipmentinstallation and associated documentation.

    + Provide hands-on technical support for processtroubleshooting and sustaining of manufacturing equipment.

    + Support multiple process across themanufacturing line and run product through the manufacturing line.

    + Identify, recommend and/or makeimprovements to optimize work processes.

    + Perform technical andrecord keeping duties in conformance with company and regulatory policies andstandards to meet quality and accuracy requirements

    + Adhere to safety andhousekeeping practices as required by the work area.

    + Perform technicalprocedures in one or more of the following areas: Production, Research andDevelopment, Quality Control/Assurance, and/or Compliance/Environmental.

    **Must Have – Minimum Requirements**

    + High School Diploma or GED

    + Minimum of 4 years of relevant experience and mayrequire vocational or technical education and advanced certification inaddition to prior work experience

    **Nice to Have**

    + Associate’s degree orBachelor’s degree in a related discipline

    + Demonstrated processexperience with wafer fab equipment such as spray and slot coat, screenprinting, exposure, developer, and metrology equipment.

    + Experience creatingmanufacturing specs and procedures

    + Experience working in manufacturingenvironment in a regulated industry.

    **About Medtronic**

    Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.

    We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.

    Physical Job Requirements

    The physical demands described within the Responsibilities section of this job description 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. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)

    It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.


    Employment Type

    Full Time

  • Inpatient Pharmacy Automation Technician
    Dignity Health    PHOENIX, AZ 85067
     Posted about 15 hours    

    **Overview**

    Located conveniently in the heart ofis a 571-bed, not-for-profit hospital that provides a wide range of health, social and support services. Founded in 1895 by the Sisters of Mercy, St. Joseph's was the first hospital in the Phoenix area. More than125years later, St. Joseph's remains dedicated to its mission of caring for the poor and underserved.

    We are extremely proud to be a nationally recognized center for quality quaternary care, medical education and research. St. Joseph's includes the internationally renowned,,,, and(which is verified by the American College of Surgeons). The hospital is also a respected center for high-risk obstetrics, neuro-rehabilitation, orthopedics, and other medical services.St. Joseph’s is considered a sought-after destination hospital for treating the most complex cases from throughout the world. Every day, approximately 20 percent of the hospital’s patients have traveled from outside of Arizona and the United States to seek treatment at St. Joseph’s.

    _U.S News & World Report_ routinely ranks St. Joseph's among the top hospitals in the United States for neurology and neurosurgery. In addition, St. Joseph's boasts the Creighton University School of Medicine at St. Joseph's, and a strategic alliance with Phoenix Children's Hospital.

    St. Joseph's is consistently named an outstanding place to work and one of Arizona's healthiest employers. Come grow your career with one of.

    Look for us onand follow us on.

    _For the health of our community ... we are proud_ _to be_ _a tobacco-free campus._

    **Responsibilities**

    Our Pharmacy Automation Tech provides technical support for pharmacy technology systems by performing maintenance on equipment, generating reports, setting up and configuring equipment, adjusting inventory, entering and deleting users, and completing other duties as needed.

    **Qualifications**

    **MINIMUM REQUIREMENTS:**

    A minimum of three (3) years hospital pharmacy or related experience

    High school diploma or GED

    PTCB certification

    Arizona pharmacy tech license

    Accurate typing skills (minimum 35 words per minute)

    Excellent interpersonal communication skills

    Knowledge of drug names and basic math

    Previous experience managing pharmacy automation systems

    Experience with Omnicell

    **Connect With Us!**

    Not ready to apply, or can't find a relevant opportunity?

    to learn more about a career at Dignity Health and experience #humankindness.

    Equal Opportunity

    Dignity Health is an Equal Opportunity/ Affirmative Action employer committed to a diverse and inclusive workforce. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, marital status, parental status, ancestry, veteran status, genetic information, or any other characteristic protected by law. For more information about your EEO rights as an applicant, please

    Dignity Health will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c).

    External hires must pass a post offer, pre-employment background check/drug screen. Qualified applicants with an arrest and/or conviction will be considered for employment in a manner consistent with federal and state laws, as well as applicable local ordinances, ban the box laws, including but not limited to the San Francisco and Los Angeles Fair Chance Ordinances.

    If you need a reasonable accommodation for any part of the employment process, please contact us by telephone at **(415) 438-5575** and let us know the nature of your request . We will only respond to messages left that involve a request for a reasonable accommodation in the application process. We will accommodate the needs of any qualified candidate who requests a reasonable accommodation under the Americans with Disabilities Act (ADA).

    Dignity Health participates in E-verify.

    **Job ID** _2020-122675_

    **Employment Type** _Full Time_

    **Department** _Pharmacy - Personnel_

    **Hours / Pay Period** _80_

    **Facility** _St Josephs Hospital and Medical Center_

    **Shift** _Day_

    **Standard Hours** _Mon-Fri 8am-4:30pm_

    **Work Schedule** _8 Hour_

    **Location** _AZ-PHOENIX_


    Employment Type

    Full Time

  • Manufacturing Technician
    Intiva Health    Tempe, AZ 85282
     Posted 3 days    

    Organic Biolabs is looking for a Production Technician to join our team. This position works on the warehouse and production floor, processing orders by picking and filling boxes/containers, producing gummy multivitamins, and other general responsibilities around a nutraceutical company.

    The ideal candidate has experience working in an environment that can be cold and hot during different seasons. This person will need to be able to work safely and quickly, standing for long periods while fulfilling orders.

    Responsibilities:

    + Inventory - Pick and pack products as ordered by the customer into bins, boxes, and containers. Maintain an inventory list and assist with restocking products and supplies as needed. Report defective products as discovered and maintain thorough notes and paperwork. Review and process invoices as directed by leadership and keep excellent documentation on supply and payments for recordkeeping.

    + Safety and housekeeping ? Ensure a safe warehouse environment by keeping an organized work station, alerting supervisors of any concerns, and completing continuing education for safety and hazards. Review any complaints and notify the shift leader of on-going shipping or receiving issues. Perform other related duties as assigned.

    Requirements:

    + A high school diploma or equivalent is required

    + Prior experience working with inventory control systems is preferred

    + Prior knowledge of warehouse paperwork and experience counting inventory and orders is preferred

    + Knowledge of and familiarity with any inventory system

    + Experience operating certain power equipment is a plus

    + Must be able to bend, stand reach, pull, lift and carry items in the warehouse


    Employment Type

    Full Time

  • Director of Quality Management
    Select Medical    Phoenix, AZ 85067
     Posted 3 days    

    Critical Illness Recovery Hospital

    Director of Quality Management

    Select Specialty and Regency Hospitals care for patients who are critically ill and need extended acute hospitalization for their recovery. We are currently seeking a Director of Quality Management with previous nursing experience, passion for upholding high quality standards and providing phenomenal patient care . We offer an exceptional employee experience, an environment dedicated to safety and quality, ongoing educational and skill building resources and advancement opportunities. We offer an excellent network of career opportunities across the U.S.

    As the Director of Quality Management, you will be responsible for the coordination, development and evaluation of all outcome activities including but not limited to:

    Risk Management, Quality Improvement, Survey Readiness, Running Mock Surveys, Infection Control, Coordinating and Supervising Accreditation/Certification Activities, Employee Health, Vaccination and Education.

    Why work for Select Specialty/Regency Hospital?

    + The opportunity to build a career with an established, highly successful organization in a caring and compassionate environment.

    + Focus on patient care and maintain quality standards.

    + Work collaboratively with an interdisciplinary team, consisting of hospital leaders, critical care nurses, physical, respiratory and occupational therapists, speech language pathologists and physicians.

    + Develop relationships with your employees and make a real difference.

    As the Director of Quality Management, you will be responsible for coordination, development and evaluation of all outcome activities including but not limited to: Risk Management, Quality Improvement, Survey Readiness, Infection Control, Employee Health and Education.

    Other requirements of the Director of Quality Management - DQM would include:

    + Coordinating all survey activities to assure that the facility maintains accreditation, certification, and licensure.

    + Organizing monthly interdisciplinary QAPI Team meetings with activities per QAPI Calendar

    + Receiving and reviews quarterly quality improvement reports

    + Assisting Medical Director and Quality Program Director with development and implementation of medical staff quality improvement activities

    + Leading hospital team in the performance of RCA at least annually and for every level 3-4 incident, unless otherwise indicated

    + Completing monthly quality related data entry, analysis and reporting

    + Focusing on the importance of employee training and education in the work place

    + Working with leadership team to ensure reporting requirements are met.

    As a Director of Quality Management, you must be able to deliver superior quality in all that you do. We are seeking results-driven team players who treat patients as if they were their own family members. Qualified candidates must be passionate about providing a superior quality of care. You must also be a resourceful problem solver who thrives in a fast-paced environment.

    Qualifications you must have to be successful:

    + Bachelor’s Degree, BSN or RN with relatable experience with quality improvement, infection control, employee health, accreditation and education.

    + Valid state RN license required

    + Ability to deliver superior quality of care.

    + Result-driven team player who treats patients as if they were their own family members.

    + You must also be a resourceful problem solver who thrives in a fast-paced environment.

    + Must be willing to remain hands-on and work independently.

    Benefits

    Our focus on high-quality results creates a challenging, fast-paced and rewarding environment. We offer a comprehensive benefits package with a variety of options to meet your health care needs.

    Other full-time benefits of the Director of Quality Management position include:

    + Excellent Orientation Program

    + Paid Time Off (PTO)

    + Extended Illness Days (EID)

    + Health, Dental, and Vision Insurance

    + Prescription Coverage

    + Life Insurance

    + Short- and Long-Term Disability

    + Continuing Education and Tuition Reimbursement

    + 401(k) Retirement Plan with employer matching

    + Personal and Family Medical Leave

    + Join the network of over 40,000 employees with huge growth and relocation opportunities

    Join a Select Team of Excellence Today!

    Apply now!

    EOE

    ID: 130952

    Street 2: 350 West Thomas

    External Company URL: www.selectmedical.com

    Street: SSH - Phoenix


    Employment Type

    Full Time

  • Manufacturing Technician 2
    Northrop Grumman    Chandler, AZ 85286
     Posted 3 days    

    Manufacturing and Production

    **Qualifications:**

    Manufacturing technician should be capable and experienced in working in a broad based manufacturing environment which includes:

    •Under minimal supervision, fabricate and assemble complex Space flight cable and harnesses assemblies from drawings, schematics, wire lists, or engineering sketches in conformance with government specifications and workmanship standards.

    •Support cable and harness installations to spacecraft per installation drawings and procedures.

    •A strong understanding of wiring processes, crimping, splicing, wire routing, and assembly techniques as it applies to NASA standard harness assembly operations is required.

    •Space Flight quality Hand soldering and assembly of printed circuit boards to NASA/J-Std Flight requirements.

    •Must be capable of soldering fine pitch flat pack IC's and components and have an excellent working knowledge of standard soldering practices and techniques.

    •Must be capable of performing circuit card assembly rework and repair operations as detailed by manufacturing Engineering and rework documentation.

    •Familiarization with Class Zero ESD requirements and flat pack IC lead forming capability a plus.

    1st Shift: 5am - 2:30pm or 6am - 3:30pm

    2nd Shift: 3pm - 12:30am

    **Job Category** : Manufacturing and Production

    20022685


    Employment Type

    Full Time

  • Wafer Operations Defect Metrology Engineer - Principal
    Medtronic    Tempe, AZ 85282
     Posted 3 days    

    Wafer Operations Defect Metrology Engineer - Principal

    Location:

    Tempe, Arizona, United States

    Requisition #:

    20000C7K

    Post Date:

    1 day ago

    Careers that Change Lives:

    Medtronic is the world’s premier medical company, providing patient benefits around the globe.

    The Tempe Arizona Microelectronic Solutions location is looking for a Principal Process Engineer to implement patterned wafer defect metrology. The Tempe site is applying wafer fabrication process towards medical device fabrication. This role will be responsible for the development, deployment, and sustaining of defect metrology solutions for sapphire, glass, and silicon wafers. Demonstrated knowledge and experience of both wafer fabrication and application of patterned defect metrology solutions is required.

    A Day in the Life:

    •Lead the development and implementation of technical and business systems and processes such as defect metrology inspections, libraries, process monitors, and statistical control processes.

    •Drive defect reduction across the operation/device. Work with process owners and operations to identify and eliminate sources of variation.

    •Responsible for driving material handling processes to eliminate defects and handling issues.

    •Develop, characterize, and specify processes that integrate well into a process technology for use in the medical device business. The developed processes need to provide robust and stable solutions for yield and reliability concerns.

    •Follow established procedures to perform detailed, accurate, and compliant engineering documentation for Master Validation Plans, pFMEA, Equipment Installation, Characterization, Qualification and Validation activities.

    •All activities must be performed in compliance with the Quality System.

    •Utilize Best-Known-Methods for wafer and device processes.

    •Drive definition of requirements in concert with stakeholders. Use design of experiments and applicable tools to ensure robust process capability.

    •Provide detailed engineering analysis and documentation to support process deployment and ramp into volume manufacturing.

    •Meet operational attainment of Safety, Quality, and Service goals.

    •Drive projects to successful completion using Project Management skills. Utilize technical skills associated with Six Sigma, Lean, DRM/DFSS and other appropriate improvement techniques to drive continuous improvement.

    •Performs duties in compliance with environmental, health and safety related site rules, policies, or governmental regulations.

    •Identify and work to remove barriers that slow or prevent the successful completion of projects

    BASIC QUALIFICATIONS

    •B.S. in Chemical Engineering, Materials Science, or similar technical discipline.

    •At least 7 years of relevant experience with a BS or an MS and at least 5 years of experience

    •Direct equipment/process ownership of patterned wafer defect metrology is desired.

    •Seven years of direct manufacturing experience with wafer fab based processes, microelectromechanical systems, or similar work experience.

    •Project management experience. Direct experience developing and deploying wafer fabrication process technologies, with relevant experience with process characterization, design of experiments, statistical process control, and data analysis methodologies.

    •Strong verbal and written communications skills; demonstrated ability to work in a highly cross-linked technical work environment.

    Nice to Have:

    •Ph.D. or M.S. in Chemistry, Materials Science, or similar technical disciple.

    •Design for Six Sigma (DFSS) Master Black Belt, or equivalent knowledge, investment, and experience in design for reliability and manufacturing.

    **About Medtronic**

    Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.

    We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.

    Physical Job Requirements

    The physical demands described within the Responsibilities section of this job description 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. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)

    It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.


    Employment Type

    Full Time

  • Wafer Operations Defect Metrology Engineer - Principal
    Medtronic    Tempe, AZ 85287
     Posted 4 days    

    Careers that Change Lives:
    Medtronic is the world's premier medical company, providing patient benefits around the globe.
    The Tempe Arizona Microelectronic Solutions location is looking for a Principal Process Engineer to implement patterned wafer defect metrology. The Tempe site is applying wafer fabrication process towards medical device fabrication. This role will be responsible for the development, deployment, and sustaining of defect metrology solutions for sapphire, glass, and silicon wafers. Demonstrated knowledge and experience of both wafer fabrication and application of patterned defect metrology solutions is required.
    A Day in the Life:
    * Lead the development and implementation of technical and business systems and processes such as defect metrology inspections, libraries, process monitors, and statistical control processes.
    * Drive defect reduction across the operation/device. Work with process owners and operations to identify and eliminate sources of variation.
    * Responsible for driving material handling processes to eliminate defects and handling issues.
    * Develop, characterize, and specify processes that integrate well into a process technology for use in the medical device business. The developed processes need to provide robust and stable solutions for yield and reliability concerns.
    * Follow established procedures to perform detailed, accurate, and compliant engineering documentation for Master Validation Plans, pFMEA, Equipment Installation, Characterization, Qualification and Validation activities.
    * All activities must be performed in compliance with the Quality System.
    * Utilize Best-Known-Methods for wafer and device processes.
    * Drive definition of requirements in concert with stakeholders. Use design of experiments and applicable tools to ensure robust process capability.
    * Provide detailed engineering analysis and documentation to support process deployment and ramp into volume manufacturing.
    * Meet operational attainment of Safety, Quality, and Service goals.
    * Drive projects to successful completion using Project Management skills. Utilize technical skills associated with Six Sigma, Lean, DRM/DFSS and other appropriate improvement techniques to drive continuous improvement.
    * Performs duties in compliance with environmental, health and safety related site rules, policies, or governmental regulations.
    * Identify and work to remove barriers that slow or prevent the successful completion of projects
    BASIC QUALIFICATIONS
    * B.S. in Chemical Engineering, Materials Science, or similar technical discipline.
    * At least 7 years of relevant experience with a BS or an MS and at least 5 years of experience
    * Direct equipment/process ownership of patterned wafer defect metrology is desired.
    * Seven years of direct manufacturing experience with wafer fab based processes, microelectromechanical systems, or similar work experience.
    * Project management experience. Direct experience developing and deploying wafer fabrication process technologies, with relevant experience with process characterization, design of experiments, statistical process control, and data analysis methodologies.
    * Strong verbal and written communications skills; demonstrated ability to work in a highly cross-linked technical work environment.
    Nice to Have:
    * Ph.D. or M.S. in Chemistry, Materials Science, or similar technical disciple.
    * Design for Six Sigma (DFSS) Master Black Belt, or equivalent knowledge, investment, and experience in design for reliability and manufacturing.
    About Medtronic
    Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
    We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.
    Physical Job Requirements
    The physical demands described within the Responsibilities section of this job description 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. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)
    User Supplied Image


    Employment Type

    Full Time


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