QA Documentation Specialist - San Francisco, United States - Rose International

    Rose International
    Rose International San Francisco, United States

    1 week ago

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    Permanent Engineering / Architecture
    Description

    Date Posted: 05/17/2024

    Hiring Organization: Rose International

    Position Number: 464270

    Job Title: QA Documentation Specialist

    Job Location: Newton, MA, USA, 02466

    Work Model: Onsite

    Shift: Shift 1; M-F (9:00 AM - 5:00 PM)

    Employment Type: Temporary

    Estimated Duration (In months): 3

    Min Hourly Rate ($): 28.00

    Max Hourly Rate ($): 28.00

    Must Have Skills/Attributes: Documentation, Engineering, Quality Assurance, SAP

    Nice To Have Skills/Attributes: Agile, CAPA, Medical device, Quality Engineer


    Job Description


    Only those lawfully authorized to work in the designated country associated with the position will be considered.


    Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.


    Job Title: QA Documentation Specialist

    Schedule: Shift 1; M-F (9:00 AM - 5:00 PM)


    Responsibilities:


    • Disposition non-conforming material (NCMR).


    • Lead and/or participate in product complaint investigations leading to root cause.


    • Propose, lead, initiate and follow-up on Corrective Action and Preventive Actions (CAPA).


    • Ensuring that all changes and associated documents are managed in accordance with internal and external standards, policies, and procedures.


    • Ensuring the accuracy (Quality) of documents with regards to numbering formatting, revisions, and content per approved changes.


    • Incoming part inspection; 70% Mechanical, 30% Electrical.


    • In-process Inspection.


    Required Knowledge/Skills, Education, and Experience


    • College degree in engineering and 2+ years related experience; or HS Diploma or GED with 5+ years related experience.


    • 2-5 yrs. combined experience of Document Control, Inspection, and/or Quality Assurance experience


    • Working knowledge of SAP PLM (1-2 yrs.)


    • Proficient with MS WORD and EXCEL


    • Strong organizational skills, detail oriented, and the ability to meet changing deadlines on a fast-moving environment


    • Ability to communicate effectively within a technical environment


    • Team player who is customer driven


    • No travel required.


    Preferred Knowledge/Skills, Education, and Experience


    • Prior Medical Device/Biotech experience


    • Prior experience with a Document Control Platform such as Arena or Agile


    • Ability to work semi-independently within a regulated environment


    Benefits:

    For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.


    California Pay Equity:

    For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.