Current jobs related to QA/ Document Control Coordinator - New Hope - Ultimate Staffing


  • New Hope, Pennsylvania, United States ORCHESTRA BIOMED, INC. Full time

    About Orchestra BioMedOrchestra BioMed is a pioneering biomedical innovation company that accelerates high-impact technologies to patients through strategic partnerships with leading medical device companies. Our vision is to revolutionize medical innovation by forging collaborative relationships with industry leaders to drive successful global...


  • New York, New York, United States QA Mentor, Inc. Full time

    Job Title: Project Test CoordinatorQA Mentor, Inc. is seeking a highly skilled Project Test Coordinator to manage the System Acceptance testing phase for a 3-month consulting opportunity. The ideal candidate will have experience in implementing strategy, best practices, and offshore resource management.Key Responsibilities:Create a comprehensive Test Plan...


  • New Hope, United States Orchestra BioMed Full time

    About Orchestra BioMedOrchestra BioMed is a biomedical innovation company accelerating high-impact technologies to patients through risk-reward-sharing partnerships with leading medical device companies. Orchestra BioMed’s vision is to accelerate medical innovation to patients through risk-reward-sharing partnerships with leading medical device companies....


  • hope, United States Orchestra BioMed Full time

    About Orchestra BioMedOrchestra BioMed is a biomedical innovation company accelerating high-impact technologies to patients through risk-reward-sharing partnerships with leading medical device companies. Orchestra BioMed’s vision is to accelerate medical innovation to patients through risk-reward-sharing partnerships with leading medical device companies....


  • New Brunswick, United States Intellectt Inc Full time

    Role: Documentation Control LeadLocation: New Brunswick, NJDuration: 24+ MonthsJob Description:The Document Control/QA Specialist will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols, ensuring compliance with internal and regulatory...


  • New Brunswick, United States Intellectt Inc Full time

    Role: Documentation Control LeadLocation: New Brunswick, NJDuration: 24+ MonthsJob Description:The Document Control/QA Specialist will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols, ensuring compliance with internal and regulatory...


  • New Brunswick, United States Intellectt Inc Full time

    Hello,One of my clients is looking Role: Documentation Control Lead, if you’re interested or your skills matches, please share with me your updated resume to sushma@intellectt.comRole - Documentation Control LeadLocation: New Brunswick, New Jersey, United StatesDuration: Long-TermNote: NO C2CThe Document Control/QA Specialist will be responsible for...


  • New Brunswick, United States Intellectt Inc Full time

    Hello,One of my clients is looking Role: Documentation Control Lead, if you’re interested or your skills matches, please share with me your updated resume to sushma@intellectt.comRole - Documentation Control LeadLocation: New Brunswick, New Jersey, United StatesDuration: Long-TermNote: NO C2CThe Document Control/QA Specialist will be responsible for...


  • New Brunswick, United States Pharmatek Consulting Inc Full time

    Job DescriptionThe Document Control/QA Specialist will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols, ensuring compliance with internal and regulatory standards.Key Responsibilities:• Manage validation documentation in automated systems,...

  • QA Coordinator

    2 months ago


    New Albany, United States Pharmavite Full time

    HELP US BRING THE GIFT OF HEALTH TO LIFE.Working at Pharmavite is an experience like no other. With a focus on complete nutrition for all, each endeavor is urgent and every day counts. You'll have the opportunity to work on the #1 selling national vitamin and supplement brand, Nature Made, as well as an exciting portfolio of other products that are shaping...


  • New York, New York, United States Pride Now Full time

    Job OverviewWe are seeking a highly organized and detail-oriented Document Control Specialist to join our team at PrideNow. The successful candidate will have a minimum of three years of experience in administrative assistance or document control, with a strong background in computer software systems.As a Document Control Specialist, you will be responsible...


  • New York, New York, United States EXP Full time

    Job OverviewAs a Document Controls Specialist at EXP, you will play a vital role in ensuring the smooth operation of our engineering projects. Your primary responsibility will be to coordinate the electronic, printing, and distribution process for engineering drawings and documents. This includes performing basic system maintenance, managing access requests,...

  • Document Controller

    2 weeks ago


    New Orleans, United States Robert Half Full time

    Job DescriptionJob DescriptionWe are seeking a Document Controller for our client in New Orleans, Louisiana. This role is integral to the Project Services Department and offers a short-term contract to full time employment opportunity. As a Document Controller, you will be tasked with numerous responsibilities including document control, overseeing project...

  • QA Tester

    1 week ago


    New York, New York, United States Deca Games Full time

    About DECA GamesWe believe that games should be played for decades, but many are abandoned even when a loyal community is screaming to keep them alive.DECA specializes in acquiring games from other developers and reinvigorating them to continue to entertain for decades.We see a fantastic set of problems to solve and a huge opportunity in every old game.Our...


  • New York, New York, United States Parsons Corporation Full time

    About the Role:We are seeking a highly skilled Senior Document Control Specialist to join our team at Parsons Corporation. As a key member of our Critical Infrastructure team, you will play a critical role in supporting our portfolio of projects.Key Responsibilities:Support capital and non-capital rail-transit projects by applying appropriate and proper...

  • QA Tester

    1 month ago


    New York, New York, United States Deca Games Full time

    About DECA GamesWe believe that games should be played for decades, but many are abandoned even when a loyal community is screaming to keep them alive.DECA specializes in acquiring games from other developers and reinvigorating them to continue to entertain for decades.We see a fantastic set of problems to solve and a huge opportunity in every old game.Our...


  • New York City, United States Michael Page Full time

    The Sanctions QA Consultant will focus on delivering sanctions quality assurance by collaborating with stakeholders, testing, and reviewing sanctions-related operations, advisory functions, and investigations. The role requires expertise in sanctions compliance, audit practices, and maintaining documentation standards to ensure a strong sanctions compliance...


  • New Brunswick, New Jersey, United States Aviva Natural Supplements Full time

    Job Title: Document Control SpecialistCompany: Aviva Natural SupplementsLocation: New Brunswick, NJJob Type: Full-timeAbout Us: Aviva Natural Supplements is a GMP & USDA Organic turnkey contract manufacturer specializing in custom formulation, blending, encapsulations, compression, and high-speed packaging lines.Job Description:We are seeking a highly...

  • Document Control Lead

    4 weeks ago


    New Brunswick, New Jersey, United States Pharmatek Consulting Inc Full time

    Job DescriptionThe Document Control Lead will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols, ensuring compliance with internal and regulatory standards.Key Responsibilities:Manage validation documentation in automated systems, including...


  • New Brunswick, United States Aviva Natural Supplements Full time

    Company DescriptionAviva Natural Supplements is a GMP & USDA Organic turnkey contract manufacturer located in New Brunswick, NJ. Specializing in custom formulation, blending, encapsulations, compression and high-speed packaging lines, Role DescriptionThis is a full-time on-site role for a SOP Document Control Specialist at Aviva Natural Supplements in New...

QA/ Document Control Coordinator

4 months ago


New Hope, United States Ultimate Staffing Full time

Job Summary:


Responsible for developing and maintaining processes, forms, and databases for Manufacturing and Quality Assurance. This role ensures the accuracy and accessibility of records essential for operations.


Primary Responsibilities:


  • Develop process documents based on input from various sources, ensuring approval and distribution for use in QA and manufacturing.
  • Provide clerical support to Engineering, Quality, and Manufacturing departments.
  • Maintain a master document list with current revisions and locations
  • Update Technical Change Management (TCM) and Item Data.
  • Manage a computerized master file for quality system forms.
  • Organize and maintain long-term document storage.
  • Maintain training files and ensure training documentation is in order for all employees.
  • Create and update Quality Plans and First Cure Records.
  • Generate and manage Certificates of Compliance for product shipments.
  • Conduct audits as assigned.
  • Manage various QA files (Shelf-life report, Audits, Procedures, Work Instructions, CARs, MRBs, MRRs, RMAs, FAIs, etc.).
  • Perform Quality inspections as required.


Skills and Knowledge:

  • 1 to 2 years of work experience in a document control / quality assurance position in a manufacturing environment. Will consider recent grads with manufacturing, engineering, or a plastics education who want to get into quality engineering
  • Proficiency in Microsoft Word, Excel, and Access.
  • Familiarity with ISO 9001 quality systems.


Additional Info:

  • Pay range: $25-35/hr
  • Schedule: M-F 7:30 am - 4:00 pm or 8:00 am - 4:30 pm (there may be some flexibility if needed)
  • Location: 100% In-Office
  • Type: Direct hire or contract to hire after 6 months; they are open to both hiring options


All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.