Pharma QC Analyst – In-Process Lab (Swing Shift)

Tucker Parker Smith Group (TPS Group); Novato (CA); On-site; USD 65,000 - 95,000; Full time

Job summary

Tucker Parker Smith Group (TPS Group) in Novato, CA, is seeking a QC Analyst to support the In-Process Analytical (QCA-IP) laboratory. You will perform analytical testing on manufacturing intermediates and drug products, ensuring cGMP compliance and accurate documentation.

The ideal candidate has a strong lab foundation, 0–3 years of experience, and familiarity with HPLC/UPLC and protein methods. The role requires swing shift participation and collaboration with QA and manufacturing teams.

Qualifications

• Bachelor's degree in Biology, Chemistry, Biochemistry, Molecular Biology, or related science.
• 0-3 years of lab experience; cGMP/regulatory exposure preferred.
• Hands-on with HPLC/UPLC and protein analyses is highly preferred.
• Strong documentation and data analysis skills.

Responsibilities

• Perform analytical testing on in-process manufacturing samples.
• Execute protein assays including A280, Bradford, UV absorbance, and activity assays.
• Analyze data vs specifications and track trends.
• Document activities per cGMP and GDP requirements.
• Prepare reagents, maintain supplies, and support lab organization.
• Assist with method validation, transfers, and equipment qualification.
• Participate in deviation investigations and process improvement.
• Maintain inspection readiness and assist with housekeeping.
• Train junior analysts on qualified methods.
• Collaborate with Manufacturing and QA to ensure timely testing.

Skills

Analytical testing

Documentation

HPLC/UPLC

Protein assays

Data analysis

SAP/BINOCS familiarity

Education

Bachelor's degree in Biology/ Chemistry/ Biochemistry/ Molecular Biology

Tools

HPLC

UPLC

A280

Bradford assay

Job description

Tucker Parker Smith Group (TPS Group) in Novato, CA, is seeking a QC Analyst to support the In-Process Analytical (QCA-IP) laboratory. You will perform analytical testing on manufacturing intermediates and drug products, ensuring cGMP compliance and accurate documentation.

The ideal candidate has a strong lab foundation, 0–3 years of experience, and familiarity with HPLC/UPLC and protein methods. The role requires swing shift participation and collaboration with QA and manufacturing teams.