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Quality Assurance Specialist I
Lodi, CA, US
Scientific
High School or equivalent
Full Time, Temporary
$28.85/hr
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Lodi, CA, US
$28.85/hr
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Scientific
High School or equivalent
First Shift (Day)
Job details
Job Summary:
A leading diagnostics organization is seeking a Quality Assurance Specialist I to support quality system compliance and continuous improvement initiatives. This role is essential in reviewing documentation, supporting product release, and maintaining adherence to QSR and ISO standards. The ideal candidate will bring attention to detail, strong documentation skills, and a collaborative mindset to a fast-paced, regulated environment focused on improving healthcare outcomes.
• Location: Lodi, CA
• Pay Rate: $26.46 for Day and $28.57/hr for Night
• Shifts:
A: Sunday – Tuesday (Alternate Wed), 6am-6pm (Day)
B: Thursday- Saturday (Alternate Wed) 6am-6pm (Day)
C:Sunday – Tuesday (Alternate Sat), 6pm-6am (Night)
D: Wednesday- Friday (Alternate Sat) 6am-6pm (Night)
Duration: 12 Month assignment
Roles and Responsibilities:
• Review records and documentation for completeness and compliance with QSR and ISO standards.
• Support the release of raw materials, in-process materials, and final products, including reagents, components, and instrumentation.
• Generate and maintain standard operating procedures (SOPs) to enhance quality system functions.
• Participate in continuous improvement activities and contribute to training materials and operational manuals.
• Collaborate with cross-functional teams to ensure quality standards are met throughout the production lifecycle.
Qualifications & Skills:
• Education: High school diploma or equivalent required.
• Experience: Minimum of 2 years in a manufacturing or regulated environment.
• Must be comfortable working in an environment where you have to wear PPE at all times
Technical Skills:
• Familiarity with ISO standards and regulatory requirements (CE/FDA/QSR, GDP).
• Strong documentation and record-keeping skills.
Soft Skills:
• Effective communication and interpersonal skills.
• Ability to work collaboratively with diverse teams.
• Detail-oriented with strong organizational and time management abilities.
Opportunities:
• Contribute to the development and delivery of life-saving diagnostic tools.
• Gain experience in a global, innovation-driven company with opportunities for career advancement.
• Be part of a mission-driven team focused on improving patient outcomes worldwide.
Company Culture:
The organization fosters a collaborative, inclusive, and innovation-focused environment. Employees benefit from a strong support network, professional development opportunities, and the chance to make a meaningful impact in global healthcare.
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