QC Associate II

The Fountain Group; Fremont (CA); On-site; USD 38,572 - 52,348; Full time

Job summary

The Fountain Group is seeking a QC Associate II in Fremont, CA to perform routine and non-routine physical and chemical testing of bulk drug substances, finished products, and raw materials. The position emphasizes rigorous adherence to cGMP/cGDP requirements and meticulous documentation in a multi-product laboratory.

Ideal candidates will have 3–5 years of QC laboratory experience and proficiency with UV-Vis, qPCR, FTIR, and compendial testing, along with strong inventory management and reagent

Qualifications

• 3–5 years of industry experience in QC laboratory testing.
• Proficiency in UV-Vis, qPCR, FTIR and compendial testing.
• Experience handling bulk drug substances, finished products, and raw materials.
• Document results in a cGMP/cGDP environment and maintain inventory records.
• Knowledge of reagent handling and disposal procedures.

Responsibilities

• Perform routine and non-routine physical and chemical testing of bulk drug substances, finished products, and raw materials.
• Execute analytical tests and support laboratory operations in a multi-product lab.
• Maintain accurate laboratory documentation and ensure compliance with cGMP/cGDP requirements.
• Support inventory management and reagent handling/disposal.
• Contribute to laboratory readiness and quality compliance.

Skills

QC testing

UV-Vis spectroscopy

qPCR

FTIR spectroscopy

Compendial testing

Bulk drug testing

cGMP/cGDP documentation

Inventory management

Reagent handling

Job description

The Fountain Group is currently seeking a QC Associate II for a prominent client of ours. This position is located in Fremont, CA.

Details for the position are as follows:

Job Title: QC Associate II– Physical & Chemical Testing

Location: Fremont, CA

Pay Rate: $33.26/hour W2

Duration: 6-Month Contract

Job Description

Seeking a QC Analyst to perform routine and non-routine physical and chemical testing of bulk drug substances, finished products, and raw materials in a multi-product laboratory. Responsibilities include executing analytical testing, supporting laboratory operations, maintaining laboratory inventory, documenting results in compliance with cGMP/cGDP requirements, and ensuring laboratory readiness and quality compliance.

Required Skills

• 3–5 years of industry experience
• Quality Control (QC) laboratory testing
• UV-Vis absorbance
• qPCR
• FTIR spectroscopy
• Compendial testing
• Analysis of bulk drug substances, finished products, and raw materials
• Laboratory documentation in a cGMP/cGDP environment
• Laboratory inventory management
• Reagent handling and disposal

Preferred Skills

• GMP-regulated laboratory experience
• Experience testing biologics or pharmaceutical products
• Experience supporting multi-product QC laboratories
• Knowledge of 5S laboratory organization and compliance