Jobs
>
Scarborough

    Supplier Quality Engineer - Scarborough, United States - Abbott

    Abbott
    Abbott Scarborough, United States

    2 weeks ago

    Default job background
    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.


    JOB DESCRIPTION:
    About Abbott


    Abbott Rapid Diagnostics is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.

    The Opportunity


    The position of Supplier Quality Engineer is within our Infectious Disease Developed Markets business unit located at all sites under Abbott Diagnostics Scarborough QMS.

    This role will perform daily activities required to ensure that all purchased or otherwise received materials, products and services that can impact the quality of product or service provided conform to predefined requirements and quality attributes.

    What You'll Do
    Maintain the Supplier Quality Function, working closely with and supporting Purchasing and the New Product Development and Engineering team(s).
    Respond in a timely and professional manner to internal and external suppler requests that pertain to quality.
    Manage supplier changes through the change management system.
    Review Supplier Validation Protocols to ensure they meet regulatory and customer requirements.

    Work closely with the engineering team to schedule and drive and review purchased product first article inspections, capability studies, gage R&Rs, etc.

    Investigate and drive to completion root cause analysis of product quality issues and defects for new and sustaining purchased products and implement solutions to resolve issues; assist other personnel, as required, with the Corrective Action process specific to purchased components and/or services.

    Manage the Supplier corrective action process, drive improvement to the ASL.

    Utilize supplier Scorecards/metrics and analytical tools to quantify performance levels of individual suppliers and work with those suppliers to develop improvement plans to achieve quality performance goals.

    Establish and execute priorities to achieve expectations.
    Identify and implement continual improvement opportunities to streamline quality systems and processes.

    Perform external audits, as required, based on the published audit schedule and/or as needed if suppliers are struggling to achieve established quality metrics.

    Required Qualifications
    BS in Engineering, Manufacturing, Biology or related discipline or equivalent combination of education and experience.
    2+ years' experience in medical device industry, preferably in Quality or Supplier Engineering.
    Demonstrated proficiency using Microsoft Word, PowerPoint, and Excel

    Preferred Qualifications

    Familiarity with federal and other regulations, e.g. QSR's, ISO 13485, CMDR,
    IVDD/IVDR. Working knowledge of the General Provisions of 21 CFR Part 11 for
    Electronic Records and Electronic Signatures preferred.
    High level of proficiency in Microsoft Office Suite of software applications
    High level of attention to detail and accuracy
    Strong organizational skills and ability to prioritize tasks
    Exceptional documentation and technical writing skills
    Excellent verbal and written English language skills
    Ability to establish and maintain strong, effective working relationships with internal employees and external customers
    Ability to react quickly and adapt to changes in priorities, circumstances and direction.
    Must be able to reason independently and work with minimum supervision
    Ability to interpret data and make sound judgments based on those interpretations.
    Must be able to adapt to quickly changing priorities and schedules.
    Ability to maintain good working relationships with all co-workers and outside contracts.

    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 .
    Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
    Health care and well-being programs

    including medical, dental, vision, wellness and occupational health programs,

    Medical Benefits start day 1
    Vacation - 3 weeks of accrued vacation (1st yr is prorated) + vacation buy program + 3 personal days + 10 paid holidays
    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.

    The base pay for this position is
    $57, $114,700.00
    In specific locations, the pay range may vary from the range posted.


    JOB FAMILY:
    Operations Quality


    DIVISION:
    IDDM ARDx Infectious Disease Developed Markets


    LOCATION:
    United States > Scarborough : 6 Lincoln Avenue


    ADDITIONAL LOCATIONS:

    WORK SHIFT:
    Standard


    TRAVEL:
    Yes, 5 % of the Time


    MEDICAL SURVEILLANCE:
    Not Applicable


    SIGNIFICANT WORK ACTIVITIES:
    Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)

    Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

    EEO is the Law link - English:

    EEO is the Law link - Espanol:
    #J-18808-Ljbffr

  • GForce Life Sciences

    Quality Engineer

    1 week ago


    GForce Life Sciences Scarborough, United States

    Quality Engineer – Scarborough, ME · Must be able to work on a W2 · Job Summary · Manufacturing Line Quality Engineers operate as independent Quality resources, partnering with Production to ensure compliance with GMP, GDP, and quality standards. They are responsible for assist ...

  • GTT, LLC

    Quality Engineer

    1 week ago


    GTT, LLC Scarborough, United States

    Quality Engineer · Contract Duration 3 Months · Main Purpose of Role · Manufacturing Line Quality Engineers operate as an independent Quality resource partnered with Production to facilitate GMP, GDP, and Client quality standard compliance. · Responsible for assisting in the impl ...

  • Intellectt Inc

    Quality Engineer

    1 week ago


    Intellectt Inc Scarborough, United States

    Role: Quality Engineer I · Location: Scarborough, ME · Duration: 4 Months · MAIN RESPONSIBILITIES · • Responsible for performing line clearance, shift change activities, set up verification and label verification. · • Independently contribute to Quality System processes which m ...

  • ATR International

    Quality Engineer

    1 week ago


    ATR International Scarborough, United States

    MAIN PURPOSE OF ROLE · Manufacturing Line Quality Engineers operate as an independent Quality resource partnered with Production to facilitate GMP, GDP and Abbott quality standard compliance. Responsible for assisting in the implementation and maintenance of an effective Quality ...

  • Global Technical Talent

    Quality Engineer

    1 week ago


    Global Technical Talent Scarborough, United States

    Quality Engineer Contract Duration 3 MonthsMain Purpose of Role Manufacturing Line Quality Engineers operate as an independent Quality resource partnered with Production to facilitate GMP, GDP, and Client quality standard compliance. Responsible for assisting in the implementatio ...

  • Planet Pharma

    Quality Engineer

    5 days ago


    Planet Pharma Scarborough, United States

    The position of Manufacturing Line Quality Engineer is within our Infectious Disease Developed Markets business unit. In this role you will provide support for product quality assurance, process improvements and all quality system program at the Westbrook Site. · This job descri ...

  • GTT

    Quality Engineer

    1 week ago


    GTT Scarborough, United States

    Quality Engineer · Contract Duration 3 Months · Main Purpose of Role · Manufacturing Line Quality Engineers operate as an independent Quality resource partnered with Production to facilitate GMP, GDP, and Client quality standard compliance. · Responsible for assisting in the i ...

  • GTT

    Quality Engineer

    1 week ago


    GTT Scarborough, United States

    Quality Engineer · Contract Duration 3 Months · Main Purpose of Role · Manufacturing Line Quality Engineers operate as an independent Quality resource partnered with Production to facilitate GMP, GDP, and Client quality standard compliance. · Responsible for assisting in the i ...

  • INTELLECTT INC

    Quality Engineer

    5 days ago


    INTELLECTT INC Scarborough, United States

    Role: · Quality Engineer I · Location: · Scarborough, ME · Duration: · 4 Months · MAIN RESPONSIBILITIES · • Responsible for performing line clearance, shift change activities, set up verification and label verification. · • Independently contribute to Quality System processe ...

  • Planet Pharma

    Quality Engineer

    1 week ago


    Planet Pharma Scarborough, United States

    The position of Manufacturing Line Quality Engineer is within our Infectious Disease Developed Markets business unit. In this role you will provide support for product quality assurance, process improvements and all quality system program at the Westbrook Site. · This job descri ...

  • The Fountain Group

    Quality Engineer

    2 weeks ago


    The Fountain Group Scarborough, United States

    The Fountain Group is currently seeking a · Line Quality Engineer · for a prominent client of ours. This position is located in · Scarborough, ME · Details for the position are as follows: · Payrate: $44/hr W2 · Job Title: Line Quality Engineer · Location: Scarborough, ME · ...

  • GForce Life Sciences

    Quality Engineer

    2 weeks ago


    GForce Life Sciences Scarborough, United States

    Internal Title: Engineer, Quality · Duration: 6-month · Location: Onsite in Scarborough, ME · Responsibilities · production with resolution of quality issues in accordance with established procedures. · production on the manufacturing floor, ensuring adherence to procedures and ...

  • TechLink Systems

    Quality Engineer

    1 week ago


    TechLink Systems Scarborough, United States

    Job Description · Job Description · Job Title: Quality Engineer I · Location : Scarborough, ME (onsite) · Contract Duration: Contract until 09/30/2024 · Work Hours: 9am-6:00pm · MAIN PURPOSE OF ROLE · Manufacturing Line Quality Engineers operate as an independent Quality resour ...

  • NESC Staffing Corp.

    Quality Engineer

    5 days ago


    NESC Staffing Corp. Scarborough, United States

    Quality Engineer Job Description: · The purpose of this position is to initiate medical device quality assurance activities. These activities must be by FDA Quality System Regulation, ISO13485, and other international standards. This position will also support device complaint in ...

  • ATR International

    Quality Engineer

    1 week ago


    ATR International Scarborough, United States

    MAIN PURPOSE OF ROLE · Manufacturing Line Quality Engineers operate as an independent Quality resource partnered with Production to facilitate GMP, GDP and Abbott quality standard compliance. Responsible for assisting in the implementation and maintenance of an effective Quality ...

  • The Fountain Group

    Quality Engineer

    2 weeks ago


    The Fountain Group Scarborough, United States

    The Fountain Group is currently seeking a Line Quality Engineerfor a prominent client of ours. This position is located in Scarborough, MEDetails for the position are as follows: · Payrate: $44/hr W2 · Job Title: Line Quality Engineer · Location: Scarborough, ME · Duration: 7 ...

  • Techlink Systems

    Quality Engineer

    1 week ago


    Techlink Systems Scarborough, United States

    Job Description · Job DescriptionJob Title: Quality Engineer I · Location : Scarborough, ME (onsite) · Contract Duration: Contract until 09/30/2024 · Work Hours: 9am-6:00pm · MAIN PURPOSE OF ROLE · Manufacturing Line Quality Engineers operate as an independent Quality resource pa ...

  • The Fountain Group

    Quality Engineer

    1 week ago


    The Fountain Group Scarborough, United States

    Job Description · Job DescriptionManufacturing Line Quality Engineers operate as an independent Quality resource partnered with Production to facilitate GMP, GDP and quality standard compliance. Responsible for assisting in the implementation and maintenance of an effective Quali ...

  • Cynet Systems

    Quality Engineer

    1 week ago


    Cynet Systems Scarborough, United States

    Mandatory: · HS Diploma (but must have experience). · Prefer bachelors or associates. · Some experience in quality environment. · Experience with batch records, SOPs, structured documentation. · Excellent communication an · ...


  • Abbott Laboratories Scarborough, United States

    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 bra ...