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Job Requirements of QC Analyst I:
-
Employment Type:
Full-Time
-
Location:
South San Francisco, CA (Onsite)
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QC Analyst I
Tailored Management Services Inc
South San Francisco, CA (Onsite)
Full-Time
Job Title: Quality Analyst (QC Analyst I)
Shift: 1st Shift (8:00 AM – 5:00 PM)
Location: 1 DNA Way, South San Francisco, CA 94080 (On-site)
Duration: 6-month contract (with potential for extension or permanent conversion)
Pay Rate: $28 – $37.78/hour (W2)
Benefits: Weekly pay, Medical, Dental, and Vision coverage
Work Model: Fully On-site (Lab-Based)
Interview Process:
Position Overview
The Quality Analyst (QC Analyst I) will join the PTCC Analytical Development & Quality Control – US Testing group. This role is responsible for performing biochemical, immunological, and cell-based assays to support clinical and commercial products within a cGMP laboratory environment. The position contributes to process development, product characterization, stability testing, and lot release activities using established procedures.
Key Responsibilities
Qualifications
Shift: 1st Shift (8:00 AM – 5:00 PM)
Location: 1 DNA Way, South San Francisco, CA 94080 (On-site)
Duration: 6-month contract (with potential for extension or permanent conversion)
Pay Rate: $28 – $37.78/hour (W2)
Benefits: Weekly pay, Medical, Dental, and Vision coverage
Work Model: Fully On-site (Lab-Based)
Interview Process:
- Round 1: Virtual
- Round 2: On-site
Position Overview
The Quality Analyst (QC Analyst I) will join the PTCC Analytical Development & Quality Control – US Testing group. This role is responsible for performing biochemical, immunological, and cell-based assays to support clinical and commercial products within a cGMP laboratory environment. The position contributes to process development, product characterization, stability testing, and lot release activities using established procedures.
Key Responsibilities
- Perform routine sample preparation and laboratory testing using established cGMP procedures
- Execute biochemical, immunological, and cell-based assays to support development and release testing
- Review, document, and release assay data (electronic and paper-based) in compliance with GMP standards
- Prepare reagents and materials required for laboratory testing
- Present and summarize experimental results as required
- Monitor assay performance and quality metrics
- Adhere to Good Documentation Practices (GDP) and ALCOA+ principles
- Maintain data integrity and ensure compliance with cGMP requirements
- Perform routine laboratory maintenance and housekeeping activities
- Follow all EHS and laboratory safety guidelines
Qualifications
- Bachelor’s degree (B.S.) in Biological Sciences with 1–5 years of relevant laboratory experience
- Hands-on experience with immunological or cell-based assays, including ELISA, PCR, flow cytometry, and cell-killing assays
- Aseptic cell culture experience is required
- Ability to work independently and collaboratively in a team environment
- Strong organizational skills with the ability to manage multiple priorities
- High attention to detail with a proactive, results-driven mindset
- Effective verbal and written communication skills
- Ability to thrive in a fast-paced laboratory environment
- Proficiency with computer applications, data management tools, and electronic documentation systems
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Preferred experience with:
- Benchling
- BD FACSDiva / FACSLyric
- FlowJo
- GxP-compliant systems such as SoftMax Pro, Single LIMS, and Veeva QMS
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