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Quality Control Analyst

2 months ago

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

Job Title: Quality Control Specialist I

Location: Hercules, CA

Schedule: Monday to Friday, 8:00 AM - 4:30/5:00 PM (On-site)

Duration: 6 months, potential to extend or convert to FTE

Compensation: Up to $34 per hour


Overview:

We are seeking a dedicated Quality Control (QC) Specialist I to join our team in Hercules, CA. The QC Specialist I will be responsible for ensuring that all products meet the highest quality standards through rigorous testing and documentation processes. This role requires a strong attention to detail, the ability to follow standard operating procedures (SOPs), and a commitment to maintaining a safe and compliant laboratory environment.


Key Responsibilities:

Daily Operations:

  • Review incoming batch records (Purchase Orders) each morning.
  • Utilize the QC/QA Priority list to schedule and determine the QC functional testing required.
  • Participate in daily Tier 1 meetings (9:00 AM - 9:15 AM) to discuss QC inspection/testing issues, production priorities, and additional testing needs.
  • Prepare QC standards/controls needed for functional testing to be used throughout the day.
  • Perform QC lab testing, document raw data in SOP documents, Excel sheets, and Unity Real Time application.
  • Submit completed batch records to a lead/supervisor for review before sending them to QA.
  • Utilize the Out of Specification (OOS) process if specifications are not met during QC testing, potentially initiating a Quality Notification (QN).
  • Initiate changes in SOPs and complete Document Change Orders (DCO) in the EtQc system as needed.
  • Ensure that Preventative Maintenance for lab equipment is up to date and that the lab is cleaned at the end of each business day.

Collaboration & Teamwork:

  • Collaborate closely with the CPO group and other departments to achieve business goals.
  • Support the site’s safety culture by following safety policies, reporting potential safety issues, and adhering to all safety protocols, especially those related to chemical handling, storage, and disposal.

Operational Discipline:

  • Execute assigned tasks according to SOPs with operational discipline.
  • Weigh, measure, prepare, mix, monitor, and adjust chemical materials, and operate large-scale reactors and other equipment to produce life science research products.
  • Collect and perform in-line product testing to resolve simple chemical issues before completing the production process.
  • Maintain thorough documentation in compliance with local, federal, and company regulations.

Equipment & Inventory Management:

  • Perform equipment cleaning and batch preparation, coordinating with maintenance as needed.
  • Communicate inventory, planning, and quality issues to the supervisor or appropriate department partners.


Qualifications:

Education:

  • Bachelor’s degree or equivalent in a life science (Chemistry, Biology) or related field.
  • Advanced degree preferred.
  • Experience:
  • 0-2 years in a general laboratory environment performing analyses in chemistry, biochemistry, or related life sciences.
  • Equivalent combination of education and experience will be considered.

Skills:

  • Understanding and application of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
  • Strong computer skills.
  • Experience with ERP systems, particularly SAP, is preferred.


Why Join Us?

This role offers an opportunity to work in a collaborative and dynamic environment, where you can contribute to meaningful projects in the life sciences field. If you are detail-oriented, passionate about quality control, and eager to make an impact, we encourage you to apply.