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ResourceMFG | Manufacturing Workforce Specialists

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Quality Control Specialist 

1st Shift in Brea, CA

The Best Manufacturing Jobs. Start with ResourceMFG.

Expand your career with this Quality Control Specialist job opportunity! Let us get you started by offering competitive pay and benefits and FREE online skills training so you can grow in your career.

Schedule: 8AM-5PM = $20.00 hour

We Require Our Customers to Offer:

  • Safe and clean work environment
  • Employee focused workplace
  • Safety programs and training

As a ResourceMFG Quality Control Specialist We Offer You:

  • Competitive pay
  • Paid weekly (Direct Deposit or ATM Debit Card available)
  • Access to health benefits and retirement plan
  • A personal recruiter to help with job searches and assistance when at work!
  • Great for people who want to learn and start a career in manufacturing
  • FREE ONLINE skills training

Quality Control Specialist Position

  • Specialize in carrying out and implementing systems and procedures that ensure product quality within an organization
  • Managing schedules to abide by the production timeline, monitoring activities, coordinating with production and quality control personnel, assessing employee performance
  • Identify Safe Working Environment Protocols
  • Plan and coordinate all analytical R&D and QC activities and be able to schedule QC activities with team.
  • Create method development and method validation activities for QC products and equipment's.
  • Review stability study design, monitoring, reporting and data trend analysis
  • Ownership of test record review and COC creation.
  • Review product related documentation and ensure documentation is accurate and provides necessary information
  • Review internal and external complaints to determine the reason for complaint and if an investigation is necessary
  • Plans, manages, and controls programs and procedures that maintain an acceptable level of product quality.
  • Support and collaborate with all departments on issues pertaining to quality requirements and associated processes. Build and maintain positive and productive working relationships with all departments.
  • Responsible for the overall supervision, training, development, coordination and evaluation of QC department staff including Analytical Chemist.
  • Authors and/or executes protocols and reports for method validation, method transfer and USP verification
  • Provides support for complex technical investigations and projects
  • Working knowledge of analytical instrumentation
  • Complete Investigation and Deviations (Capa effectiveness) in Trackwise
  • Manage in troubleshooting of analytical test methods
  • Complies with all company policies and procedures, including safety rules and regulations
  • Carries out responsibilities in accordance with the organization’s policies, procedures, and state, Federal and local laws
  • Understanding of the principles of analytical chemistry as it applies to HPLC, GC, FTIR, UV-Vis and other general analytical techniques.
  • Ability to effectively document a process, explaining scientific and/or technical ideas in writing (technical writing skills).
  • Detail oriented with ability to identify errors and/or inconsistencies while performing tasks.
  • Knowledge of New Product Development Process, Verification and Validation

Job Requirements

  • Ability to interact positively and collaborate with co-workers and management

  • Computer proficiency with comprehensive knowledge of MS Office products, Learning Management Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as LIMS, Trackwise.

  • Ability to mentor team members

  • Attention to detail

  • Able to read ruler/tape measure or other quality tools
Apply Now