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Quality Control Analyst I – DAY SHIFT
Lodi, CA, US
Scientific
Unspecified
Full Time, Temporary
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Lodi, CA, US
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Scientific
Unspecified
First Shift (Day)
Job details
PLEASE NOTE: Must be authorized to work lawfully in the United States for any employer without sponsorship. For immediate consideration, please apply.
Kelly® Science & Clinical is seeking a Quality Assurance Specialist I for temporary position (with potential to extend/convert) at a leading client in Lodi, CA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Pay Rate:
Day Shift: $26.46/Hour (non-negotiable)
Overview:
The Quality Assurance Specialist is responsible for reviewing records to comply with QSR and ISO requirements. They make recommendations for improvement and create training materials and operating manuals. This person is involved with various quality continuous improvement activities. This position is part of the Quality Assurance Specialist I and will be located in Lodi, CA.
Schedule:
Team A: Sunday/Monday/Tuesday/Every Other Wednesday, Day: 6:00 AM – 6:00 PM
- Week 1: Sunday/Monday/Tuesday
- Week 2: Sunday/Monday/Tuesday/Wednesday
Responsibilities:
In this role, you will have the opportunity to:
- Collaborating with manufacturing department for scheduling line clearance and line set up activities.
- Verify line clearance and line set-up activities by signing in relevant sections of documents.
- Reviewing the batch records online, if necessary.
- Review records and documents, for completeness and compliance with QSR and ISO requirements.
- Review batch record to support release of raw materials, work in progress and final products. This includes reagents, components and instrumentation-related products to ensure they are on the right path.
- Generate standard operating procedures to define and improve quality system functions.
Qualifications:
The essential requirements of the job include:
- High school diploma with at least 2 years of work experience in a manufacturing environment.
- Must be familiar with ISO standards and applicable regulatory requirements (CE/FDA/QSR) and GDP.
- Ability to interface well with people of varied backgrounds, and to guide groups toward effective dynamics.
It would be a plus if you also possess previous experience in:
- Experience in DNA diagnostics or other medical devices.
What Happens Next:
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.
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Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
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