QC Associate II

Reason: Replacement
Department: QUALITY CONTROL - USFO06
Job Category: Manufacturing/Quality
Job Title: QC Associate II
Duties:
Key Responsibilities
As part of the QC In-Process Testing (IPC) team, execute and coordinate routine and non-routine testing of bulk drug substance and intermediates within a multi-product facility. Perform laboratory operations independently following appropriate training, including but not limited to: HPLC titer, UV-Vis absorbance, endotoxin testing, pH, osmolality, total organic carbon (TOC), conductivity, and sample aliquotation.
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 expereince GMP experience is preferred.
Technical skills preferred: HPLC (titer), aseptic technique, osmolality, total organic carbon (TOC), conductivity


The ideal candidate can demonstrate:
-strong interpersonal and communication skills (both written and oral), a 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; is also able to work across functions to achieve common goals.
-strong attention to detail, and an ability to focus on details of execution.
Keywords:
Education: Bachelors' degree in Biology or Life Sciences required
Skills and Experience:
Patents: No
Publications: No
Veteran Status: No
# of Positions: 1


Location:
Fremont, CA
6397 Healthcare Drive,


Schedule:
Start Date: 06/15/2026
Estimated End Date: 12/15/2026
Hours Per Week: 38.00
Hours Per Day: 9.50
Interview Notes: 2nd Shift: Wed-12Noon-9PM, Thurs-Sun, 12Noon-11PM.
Mon-Fri, 1st shift for the first 3 months (approximately) for training. Wed-Sat, 2nd Shift after the training period.
Financials:


Currency USD


Contact Information:
MSP Contact Name: Sperry, Peggy
MSP Phone:


EEO:


"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."