ISO / Quality Associate (Onsite)

Pacheco, CA, US • Posted 9 hours ago • Updated 9 hours ago
Contract W2
12 Months
No Travel Required
On-site
Depends on Experience
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Product Development Life Cycle (PDLC)
  • IVD Development
  • In Vitro Diagnostics (IVD)
  • Biotechnology
  • Regulated Laboratory Environment
  • Research & Development (R&D)
  • GMP
  • Design Controls
  • Quality System Regulations (QSR)
  • ISO 13485
  • IVDR
  • MDSAP
  • Technical Documentation
  • Document Control
  • Design Output Documentation
  • Product Implementation
  • Product Discontinuation
  • Laboratory Operations
  • Laboratory Supplies
  • Purchase Requisitions
  • Reagent Management
  • Antibody Raw Materials
  • Inventory Management
  • Test Records
  • Data Sheets
  • Product Labeling
  • SOPs
  • Quality Assurance (QA)
  • Quality Control (QC)
  • Manufacturing
  • R&D Manufacturing
  • Marketing Collaboration
  • Cross-Functional Collaboration
  • Product Development Projects
  • Regulatory Compliance
  • Technical Writing
  • Data Organization
  • Documentation Review
  • Proofreading
  • Project Coordination
  • Communication Skills
  • Presentation Skills
  • Attention to Detail
  • Organizational Skills

Summary

Please note this is a 12-18 Month Contract Position and is ONSITE in Pacheco, CA.


Preferred Skills

  • Product development experience within an IVD, biotechnology, or regulated laboratory environment.
  • Familiarity with GMP requirements.
  • Experience with technical documentation and document control.
  • Ability to work cross-functionally with R&D, Manufacturing, QC, QA, and Marketing.
  • Strong attention to detail and organizational skills.

Required Qualifications

  • Bachelor’s degree in a scientific or technical field. (Manager will accept Associates as the least)
  • 1–3 years of related R&D experience or training.
  • Understanding of IVD development.
  • Knowledge of Design Controls and Quality System Regulations.
  • Familiarity with ISO 13485, IVDR, and MDSAP requirements.
  • Strong verbal and written communication skills.
  • Ability to effectively communicate and present complex information.

As an Associate Product Development Scientist, you will:

  • Facilitate and support product development projects.
  • Draft design outputs for review by Product Design management.
  • Assist with technical document review, including test records, data sheets, product labeling, SOPs, and design-output documentation.
  • Edit product data sheets and assist with revisions to departmental procedures.
  • Revise documentation associated with product implementations and discontinuations.
  • Participate in routine laboratory activities, including preparation of purchase requisitions and ordering laboratory supplies.
  • Monitor new reagent products through the Product Development Life Cycle (PDLC) across R&D, Manufacturing, QC, QA, and Marketing.
  • Identify potential obstacles affecting product development timelines and coordinate with cross-functional teams.
  • Support GMP-compliant product development activities.
  • Organize test results and assist with drafting, proofreading, scanning, and preparation of product-development documentation.
  • Assist with oversight of antibody raw material inventory within R&D.

This is a full-time- contract opportunity.

 

Candidates must provide their phone number. Job reference number is A5578.

 

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: NETSO
  • Position Id: A5578
  • Posted 9 hours ago
Contact the job poster
Manita Tamang

Manita Tamang

Coordinator @ NetSource, Inc.
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