Top 6 Quality control lab technician Jobs in Milpitas, Ca

QC Specialist - Full time & Temporary
Bionova Scientific LLC —Fremont, CA
- $48 - $60 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor of Science
10d
Quality Control Laboratory Technician
viva —Fremont, CA
- $17 - $22 an hour
- Weekends as needed
- High school diploma or GED
- Ability to lift 50 pounds
- Associate's degree
1d
Manufacturing Lab Technician (Pharma/Biotech)
Vanator —Fremont, CA
- $20 - $27 an hour
- Contract
- High school diploma or GED
- Computer skills
- In-person
Quick Apply
QC Analyst II *PC 610
Miltenyi Biotec, Inc. —San Jose, CA
- $38.75 - $45.63 an hour
- Microsoft Word
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
QC Specialist - Full time & Temporary
Asahi Kasei —Fremont, CA
- $48 - $60 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor of Science
10d

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QC Specialist - Full time & Temporary
Bionova Scientific LLC —Fremont, CA
As part of the rapidly growing QC team, you will be able to influence decisions and develop your own talent with the team to meet project goals that ultimately…
$48 - $60 an hour
10d
Quality Technician, Bulk Release
BeneFit Cosmetics —San Francisco, CA
Bachelor's degree in Chemistry, Biology, Pharmacy, Cosmetics Science, or a related scientific field preferred. Retest expired bulk as needed.
$34.62 - $43.27 an hour
8d

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Raw Materials Sampler (10am-6:30pm)
kdc/one —Groveport, OH
Inspect and sample all incoming raw materials following SOPs and Work Instructions. Strong problem-solving, analytical, and technical skills.
Quick Apply
18h
Manager QA/QC Lab - Ethanol Plant
Valero —Bloomingburg, OH
Bachelor's degree (or higher degree) in a related scientific or technical field required. Ensure city, county, state, and federal regulations relating to the QA…

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QC Specialist - Full time & Temporary

Bionova Scientific LLC -
Fremont, CA

Apply Now

Job Details

Full-time
$48 - $60 an hour
10 days ago

Qualifications

Optimizing workflow processes
Safe work practices
Data integrity assurance
Biology
Bachelor's degree in biological science
Stability testing
Instrumentation troubleshooting
Immunological assays
Laboratory inventory control
Laboratory safety
Microsoft Excel
Content creation for technical audiences
Quality records maintenance
Microsoft Outlook
Stability studies in drug product development
Sample preparation
Immunological laboratory techniques
Bachelor of Science
Continuous improvement (laboratory quality control method)
Production deviation management
Good documentation practices (GDP)
Corrective and preventive actions (CAPA)
GMP
Assay development
Bachelor's degree in biology
Data summary reports
Analysis skills
Laboratory reports
Laboratory equipment repair
Laboratory quality control records management

Full Job Description

Bionova is seeking a motivated and innovative QC Specialist to contribute to our expanding business. As part of the rapidly growing QC team, you will be able to influence decisions and develop your own talent with the team to meet project goals that ultimately will improve patient outcomes.

Location: Fremont, California

Bionova B1 building 3100 W. Warren ave, Fremont, CA 94538

Temporary role - Full Time

Company Summary:

Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems.

Because our success depends on our ability to exceed our clients' expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team.

Essential Duties and Responsibilities:

Perform cell‑based assays, ELISA, and qPCR testing to support method qualification, in‑process testing, release, and stability studies while maintaining accurate GMP documentation.
Participate in the development, transfer, and validation of analytical and instrument‑based test methods (Bioassay, ELISA, qPCR).
Author and review technical documents, including method validation/qualification protocols and reports, as well as regulatory filing documents as required by project needs.
Complete, review, and maintain QC documentation, logbooks, and data records with accuracy and compliance.
Perform routine equipment maintenance in accordance with established procedures.
Prepare buffer solutions required for analytical procedures.
Manage inventory by monitoring stock levels and critical reagents, placing timely orders, and ensuring essential supplies remain available.
Support the development, revision, and adherence to SOPs, protocols, and quality documentation.
Independently troubleshoot and resolve issues related to analytical techniques and instrumentation.
Maintain adherence to GMP and quality standards. Support regulatory inspections and contribute to observation responses.
Identify and implement process improvements to enhance efficiency and robustness of bioassay testing.

Working Conditions:

This position required to work in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 20 pounds independently.

Qualifications:

BS in Biological Sciences or a related discipline. Preferred candidates have 5-7 years of experience with Bioassays and/or ELISA, and at least 3-5 years in a regulated QC GMP laboratory environment.
Strong hands‑on experience with Bioassay, ELISA, qPCR, proper laboratory documentation, and safe laboratory practices; with proven experience in method validation, transfer, and regulatory compliance in a GMP environment.
Proficiency with SpectraMax and QuantStudio instruments.
Ability to follow and execute SOPs, protocols, and regulatory requirements.
Ability to interpret data and communicate results clearly.
Strong quality mindset, including knowledge of GDP, Data Integrity principles, and ALCOA+.
Knowledge of quality standards and global regulatory guidelines.
Experience with deviations, CAPA, change control, and related quality systems.
Demonstrated ability to work independently and collaboratively on cross‑functional teams, with strong analytical and logical problem‑solving skills.
Effective verbal and written communication skills.
Self‑motivated, organized, and able to manage multiple tasks in a fast‑paced environment.
Proficiency in Microsoft Office Suite (Word, Excel, Outlook).

The base compensation range for this role is $48 to $60 an hour. Base Compensation is influenced by many factors including, but not limited to: time in the role, previous experience, skills, knowledge, performance, work requirements, internal equity, and business / economic conditions.

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quality control lab technician jobs in milpitas, ca

QC Specialist - Full time & Temporary

Quality Control Laboratory Technician

Manufacturing Lab Technician (Pharma/Biotech)

QC Analyst II *PC 610

QC Specialist - Full time & Temporary

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