Quality Control Specialist I
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
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.