QC Associate II

eTeam; Fremont (CA); On-site; USD 50,000 - 80,000; Full time

Job summary

eTeam is seeking a QC Associate II in Fremont, CA for a 6-month contract. The role involves executing routine and non-routine QC testing on bulk drug substances, final products, and raw materials within a multi-product facility.

Ideal candidates have 3–5 years of industry experience and familiarity with GMP processes, UV-Vis, QPCR, and FTIR technologies. Strong attention to detail and teamwork are essential to ensure accurate, compliant results.”

Qualifications

• Bachelor's degree in Biology or Life Sciences required.
• GMP experience preferred.
• Technical laboratory skills in UV-Vis, QPCR and FTIR.

Responsibilities

• Execute routine and non-routine testing of bul k drug substance, final finish products, and raw materials.
• Maintain inventory of consumables and report anomalies promptly.
• Document work in compliance with cGMP and cGDP requirements.
• Adhere to site procedures and quality systems.

Skills

Interpersonal communication

Customer focus

Teamwork

Attention to detail

Independent work

Education

Bachelor's degree in Biology or Life Sciences

Tools

UV-Vis absorbance

QPCR

FTIR

Job description

Job Title: QC Associate II
Location: Fremont, CA 94555
Contract Duration: 6 Months
1st Shift: Mon-Fri, 8:00AM-5:00PM

Duties

As part of the QC Phys-Chem Testing team, execute and coordinate routine and non-routine testing of bulk drug substance, final finish products, and raw materials within a multi-product facility.

Perform laboratory operations independently following appropriate training, including but not limited to: UV-Vis absorbance, QPCR, FTIR and compendial testing.

Perform essential laboratory support activities such as maintaining inventory of consumables and materials, properly disposing of expired reagents, and identifying and reporting process or equipment anomalies.

Quality, Compliance, and Documentation

Deliver high-quality analytical results within established timelines, ensuring accuracy “right first time.”

Accurately document all work in compliance with cGMP and cGDP requirements.

Adhere to all site-specific procedures, regulatory standards, and quality systems.

Promptly and accurately report deviations, abnormalities, or out-of-specification results.

Maintain strict adherence to safety standards by recognizing and escalating unsafe conditions or behaviors.

Operational Excellence

Maintain laboratory workspaces in accordance with established 5S and cleanliness standards.

Ensure personal training is current and compliant with all regulatory and organizational requirements.

Skills

• 3-5 years of industry experience


• GMP experience is preferred.


• Technical skills preferred: UV-Vis absorbance, QPCR, and FTIR.

The ideal candidate can demonstrate:

• strong interpersonal and communication skills (both written and oral)


• strong customer focus, and an ability to interact with various departments and levels.


• ability to work independently and as part of a team, to meet departmental/facility goals


• able to work across functions to achieve common goals.


• strong attention to detail, and an ability to focus on details of execution.

Education

Bachelors' degree in Biology or Life Sciences required