Quality Assurance Specialist

2 weeks ago


Irvine, United States Tucker Parker Smith Group (TPS Group) Full time

Quality Assurance Specialist

Location: Irvine, CA

Hours: 7:00 AM - 3:30 PM, Onsite

Pay Rate: $27/hr.

9 month contract (Great potential to extend or convert)


On behalf of our client a pharmaceutical company focused on the development of medical devices for the life science industry. We are seeking an Entry-Level Documentation Specialist to join their team in Irvine, CA. As a Documentation Specialist, you will play a vital role in ensuring the smooth operation of our manufacturing processes by meticulously creating, processing, and reviewing production batch records in accordance with established GDP/GMP procedures.


Duties:

  • Review documents for format, accuracy, and compliance with established procedures, collaborating with subject matter experts to provide feedback on content.
  • Efficiently process Change requests in alignment with ISO/quality/change management standards by coordinating with team members.
  • Execute production tasks following prescribed procedures and work instructions.
  • Perform inventory and quality transactions in the SAP Inventory System.
  • Complete required documentation accurately and promptly, adhering to Good Documentation Practices (GDP).


Education and Experience

  • Bachelor’s degree in science, or an Associate’s degree or equivalent (preferably in a science field).
  • 1-2 years of experience in a regulated industry (experience in medical device, pharmaceutical, or biotechnology sectors preferred).
  • Familiarity with ERP systems such as SAP and Product Lifecycle Management is advantageous.
  • Must have experience with batch records, CAPA's, and SOP's
  • Basic understanding of Good Documentation Practices (GDP) is a plus.


Please submit your resume in a Word or PDF format to be considered.



  • Irvine, United States Tucker Parker Smith Group (TPS Group) Full time

    Quality Assurance SpecialistLocation: Irvine, CAHours: 7:00 AM - 3:30 PM, OnsitePay Rate: $27/hr.9 month contract (Great potential to extend or convert)On behalf of our client a pharmaceutical company focused on the development of medical devices for the life science industry. We are seeking an Entry-Level Documentation Specialist to join their team in...


  • Irvine, United States Tucker Parker Smith Group (TPS Group) Full time

    Quality Assurance SpecialistLocation: Irvine, CAHours: 7:00 AM - 3:30 PM, OnsitePay Rate: $27/hr.9 month contract (Great potential to extend or convert)On behalf of our client a pharmaceutical company focused on the development of medical devices for the life science industry. We are seeking an Entry-Level Documentation Specialist to join their team in...


  • Irvine, United States Laird Connectivity Full time

    The Senior Quality Assurance Specialist is responsible for, but not limited to, development, maintenance, coordination and implementation of the Quality Business System in assigned facility. The incumbent will apply knowledge of quality systems and interact with/and provide guidance to functional managers, engineers, and operators in order to meet quality...


  • Irvine, United States Actalent Full time

    Description: • Manage and process RMA. Process and monitor corrective actions, Internal Audits (customer and internal) for resolution and effectiveness. Maintain documentation of corrective and preventive action activities. • Plan, manage and conduct internal audits and serve as a Lead or Internal Auditor. • Creates, maintains, and distributes...


  • Irvine, United States Conduent Full time

    About Conduent: Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments creating exceptional outcomes for our clients and the millions of people who count on them. You have an opportunity to personally thrive, make a difference and be part of a culture where...


  • Irvine, United States Inari Medical Full time

    **Description**: The Quality Assurance Associate, under direct supervision, supports efficient operation of the Quality Assurance department and compliance to FDA GMP, ISO 13485, MDSAP and other applicable regulatory requirements. **Responsibilities** - Organize and digitize Quality files. - Review training records for manufacturing personnel. - Compile...


  • Irvine, United States Brothers Desserts Full time

    Job DescriptionJob DescriptionJOB SUMMARY: The Quality Assurance Technician will play a critical role in ensuring the quality and safety of our products. Your primary responsibility will be to monitor and test our ice cream products at various stages of production to ensure compliance with quality standards, food safety regulations, and customer...


  • Irvine, United States Kelly Services, Inc. Full time

    #x. A 0; Review all QC HPLC, GC, CE , AAS. TOC, UV, KF, FTIR and NIR assay and impurity results for Raw Materials, Finished Goods, Stability Products. Monitor all Controlled Products, Raw materials, Standards receiving, usage and inventory. Deacom Ti Quality Assurance, Assurance, QA Manager, Quality, Senior, Technology, Staffing


  • Irvine, United States Pharmaron Full time

    Job DescriptionJob DescriptionAre you ready to embark on an exciting journey with a company that's passionate about making a difference? Look no further - As Pharmaron continue to grow, we are seeking to add a highly skilled and experienced Quality Assurance Associate Director to join our team to play a key role in the implementation of our quality...


  • Irvine, United States TekWissen LLC Full time

    Job DescriptionJob DescriptionOverview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. Our client is a company operating a marketplace for consumers, sellers, and content creators. It offers merchandise and content purchased for resale from vendors and those offered by thirdparty sellers. Job...


  • Irvine, United States Voluspa Full time

    Company Profile: An introduction to Voluspa unveils stunning packaging design coupled with rare exotic fragrances, as the brand invites fans to seek everyday chic illumination. Founded in 1999, Voluspa is an industry leading luxury home fragrance brand. Voluspa designs, markets, manufactures, and distributes its products worldwide. About our Culture:...


  • Irvine, United States Voluspa Full time

    Company Profile:An introduction to Voluspa unveils stunning packaging design coupled with rare exotic fragrances, as the brand invites fans to seek everyday chic illumination. Founded in 1999, Voluspa is an industry leading luxury home fragrance brand. Voluspa designs, markets, manufactures, and distributes its products worldwide. About our Culture:Voluspa...


  • Irvine, United States Voluspa Full time

    Company Profile:An introduction to Voluspa unveils stunning packaging design coupled with rare exotic fragrances, as the brand invites fans to seek everyday chic illumination. Founded in 1999, Voluspa is an industry leading luxury home fragrance brand. Voluspa designs, markets, manufactures, and distributes its products worldwide. About our Culture:Voluspa...


  • Irvine, United States Voluspa Full time

    Company Profile:An introduction to Voluspa unveils stunning packaging design coupled with rare exotic fragrances, as the brand invites fans to seek everyday chic illumination. Founded in 1999, Voluspa is an industry leading luxury home fragrance brand. Voluspa designs, markets, manufactures, and distributes its products worldwide. About our Culture:Voluspa...


  • Irvine, United States ACE Partners Full time

    A leading medical device organization are seeking a skilled Quality Assurance Software Engineer to join their team on a W2 contract basis.Duration: 6-9 Months (opportunity to convert FT after this period)Rate: $43-48.64ph DOE (W2). No C2C or 1099Location: Irvine, CA (Onsite)Duties:Participates in Quality Management System (QMS) activities in compliance with...


  • Irvine, United States ACE Partners Full time

    A leading medical device organization are seeking a skilled Quality Assurance Software Engineer to join their team on a W2 contract basis. Duration: 6-9 Months (opportunity to convert FT after this period) Rate: $43-48.64ph DOE (W2). No C2C or 1099 Location: Irvine, CA (Onsite) Duties: Participates in Quality Management System (QMS) activities in...


  • Irvine, United States ACE Partners Full time

    A leading medical device organization are seeking a skilled Quality Assurance Software Engineer to join their team on a W2 contract basis.Duration: 6-9 Months (opportunity to convert FT after this period)Rate: $43-48.64ph DOE (W2). No C2C or 1099Location: Irvine, CA (Onsite)Duties:Participates in Quality Management System (QMS) activities in compliance with...


  • Irvine, United States ACE Partners Full time

    A leading medical device organization are seeking a skilled Quality Assurance Software Engineer to join their team on a W2 contract basis.Duration: 6-9 Months (opportunity to convert FT after this period)Rate: $43-48.64ph DOE (W2). No C2C or 1099Location: Irvine, CA (Onsite)Duties:Participates in Quality Management System (QMS) activities in compliance with...


  • Irvine, United States PRISMATIK DENTALCRAFT, INC. Full time

    Position at Prismatik Dentalcraft, a subsidiary of GlidewellEssential Functions:Leads the ongoing implementation of Quality Management System (QMS) in conformance with US FDA Quality System Regulations and ISO 13485 Design Controls, through the integration of internal and external/medical device industry best practices.Responsible for the administration of...


  • Irvine, United States PRISMATIK DENTALCRAFT, INC. Full time

    Position at Prismatik Dentalcraft, a subsidiary of GlidewellEssential Functions:Leads the ongoing implementation of Quality Management System (QMS) in conformance with US FDA Quality System Regulations and ISO 13485 Design Controls, through the integration of internal and external/medical device industry best practices.Responsible for the administration of...