CrawlJobs Logo

QC Associate II

10xgenomics.com Logo

10x Genomics

Location Icon

Location:
United States , Pleasanton

Category Icon
Category:
Manufacturing

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

31.78 - 43.03 USD / Hour
Save Job
Save Icon
Apply Position

Job Description:

As a QC Associate II, you will be responsible for inspecting raw materials, intermediates, and finished goods. The role includes biological reagent, consumable testing plus instrumental quality control tasks. In addition to ensuring a reliable supply of quality products, you will be a key contributor to the development of manufacturing infrastructure required to support commercial products in the life science field. Success in this position requires strong initiative, adaptability, and teamwork within a fast-paced life sciences environment.

Job Responsibility:

  • Conduct quality control testing on raw materials, intermediates, and finished products according to established procedures
  • Perform molecular biology techniques, including PCR, next-generation sequencing, microscopy, cell and tissue based assays, and HPLC
  • Participate in instrument QC workflows, including training to work with mechanical stages and read technical drawings and first article inspection report
  • Accurately follow work instructions and standard operating procedures, while proactively identifying and reporting discrepancies
  • Maintain comprehensive and accurate records, including QC batch files and Receiving Inspection Reports, in accordance with Good Documentation Practices
  • Efficiently communicate complications identified during QC testing and collaborate with engineers and scientists to resolve issues
  • Initiate non-conformance, deviation reports, engineering change orders (ECO) and follow up on necessary action items. Ensure that lab operations and workflow execution are compliant with ISO requirements. Drive completion of investigations and minimize disruptions to QC operations
  • Assist in root cause investigations for non-conforming lots and contribute to continual improvement efforts
  • Support process and product development activities, including process optimization, guard band and stability studies, and gauge R&R

Requirements:

  • B.S. in Biological Engineering, Molecular Biology, Analytical Chemistry, Chemical Engineering, or related discipline
  • 3 years of relevant laboratory experience in manufacturing and QC of life science products (e.g., PCR, NGS, protein analysis, HPLC)
  • Willingness to rotate through various laboratory and administrative tasks and ability to prioritize workload, and adhere to deadlines
  • Proficiency in data entry using tools such as Excel, Oracle ERP and LIMS
  • Demonstrated ability to work both independently and as part of a team
  • Strong attention to detail, organization, and commitment to quality
  • Effective communication and observational skills
  • Excellent critical and logical thinking skills to analyze and troubleshoot issues

Nice to have:

  • Proficiency with data analysis tools (e.g. Retool, Tableau, GitHub, Snowflake)
  • Extensive hands-on experience working within an ISO 13485 manufacturing environment
What we offer:
  • Equity grants
  • Comprehensive health and retirement benefit programs
  • Annual bonus program or sales incentive program
  • Health Package
  • Easy-to-use Benefits
  • Family oriented policies like parental leave
  • Generous Time Off

Additional Information:

Job Posted:
February 13, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Icon
10x Genomics - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for QC Associate II

Study Start Up Associate II

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
Mexico , Mexico City
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree completed preferably in Life Sciences
  • Minimum of 2 -4 years’ experience or understanding of clinical study start up requirements and activities. (USA sites as preference)
  • Knowledge of local and/or international regulatory processes, including submissions to regulatory authorities and ethics committees.
  • Previous experience using CTMS, goBalto, Veeva Vault, TMFs, etc.
  • Ability to read and understand clinical protocols, regulatory documents, and study-specific processes.
  • Strong attention to detail and organizational skills.
  • Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.
  • Excellent communication skills both in English
Job Responsibility
Job Responsibility
  • Proficient knowledge of ICON SOPs/WPs, ICH/GCP and applicable country regulations/guidelines and ICON systems.
  • Support Site Partners to collect, review, organize and assemble initial start-up and maintenance submission packages to Central EC/IRB, Local EC/IRB, Competent Authorities, any other local regulatory authorities as required by countries and in accordance with ICH/GCP and applicable country regulations/guidelines.
  • Support collection and assembling of all documents needed in the Critical Document Package (CDP) and/or those required for site activation, ensuring that Sponsor and Investigator obligations are being met and are in compliance with applicable requirements and ICH/GCP guidelines.
  • Support coordination of all necessary translations required for any start-up documentation.
  • Perform timely and accurate progress data entry of all documents collected from sites and of the relevant study site activation activities into the appropriate tracking systems and tools.
  • Participate to internal study review meetings with study teams to provide updates on site progress in document collection and on the executed site activation tasks.
  • Accurately forecast Site Activation plans and ensure that they are reflected accurately in ICON’s systems and proactively follow through for achievement to plan.
  • Ensure accuracy and timely completeness of Trial Master File (TMF) documents submitted during start-up and perform a Quality Control (QC) review of files before transfer to maintenance for filing in TMF.
  • Attend study team meetings as required
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Read More
Arrow Right

Quality Control Analyst II

Quality Control Analyst II - Contract - Norton, MA. Are you passionate about qua...
Location
Location
United States , Norton
Salary
Salary:
40.00 - 45.00 USD / Hour
proclinical.com Logo
Proclinical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree in biology, biochemistry, chemistry, or a related scientific field (Associate degree or Biotech Certificate considered)
  • Experience in GMP quality control within the pharmaceutical or biotechnology industry
  • Knowledge of microbiology testing and environmental monitoring/critical utility sampling
  • Familiarity with quality events such as investigations, deviations, CAPAs, and change controls
Job Responsibility
Job Responsibility
  • Conduct routine and non-routine analytical HPLC/UPLC or microbiological assays for various samples
  • Support weekend laboratory operations and maintain accurate training records
  • Adhere to testing schedules and ensure timely completion of assignments to meet project timelines and quality metrics
  • Assist in maintaining laboratory equipment and inventory for smooth operations
  • Submit data promptly and review data as needed to ensure efficiency
  • Perform operational tasks such as critical utility sampling, environmental monitoring, and product testing
  • Contribute to updating controlled documents, including SOPs, work instructions, and test methods
  • Ensure compliance with internal standards, policies, and regulatory guidelines (e.g., GMP, GLP, ICH)
  • Collaborate with QC and cross-functional teams to support quality control operations
  • Participate in inspection readiness activities and support audits and inspections
  • Fulltime
Read More
Arrow Right

Operations Specialist II

The Operations Specialist II is a multi-functional role, responsible for invento...
Location
Location
United States , San Diego
Salary
Salary:
28.00 - 30.00 USD / Hour
gomillenniumsoft.com Logo
MillenniumSoft Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor degree in Chemistry/Biology
  • Prior experience in a chemistry laboratory (2+ years)
  • Prior experience with manual and automated pipetting
  • Ability to follow standard operating procedures
  • Experience with manual (pipette) and automated filling/dispensing
  • Prior experience in a chemistry lab
  • Proficiency in MS Office Skills (Word, Excel, and PowerPoint)
  • Must possess strong organizational skills, attention to detail, and the ability to adapt to changing priorities
  • Be a self-starter, quick learner with the ability to work independently and efficiently
  • Strong interpersonal communication skills, effective written and oral communications skills
Job Responsibility
Job Responsibility
  • Ensures security and accuracy of inventory of materials and finished goods through transaction documentation and by conducting physical cycle counts and reconciliation of any discrepancies
  • Manage physical inventory within a Glovebox for raw materials, intermediate products, finished goods, analytical samples, and QA Retains
  • Perform small scale chemical reactions (dye labeling) for Quality Control testing
  • Fulfill internal requests for samples from inventory and perform sample preparation for quality testing
  • Perform Aliquoting/Vialing of air and water sensitive finished goods using manual and automated processes and equipment
  • Perform lyophilization of finished good products
  • Perform Weight Checks and Packaging of air and water sensitive finished goods within a Glovebox
  • Prepare packaged products for QA inspection and shipments, including all required documentation
  • Coordinate with QC department to ensure timely testing and release of production materials
  • Accurately complete required documentation (batch records, data entry, etc.) on time
  • Fulltime
Read More
Arrow Right
New

Specialist II, Internal Quality Assurance

The purpose of this position within the Quality Assurance department is to suppo...
Location
Location
United States , Verona
Salary
Salary:
70000.00 - 85000.00 USD / Year
arrowheadpharma.com Logo
Arrowhead Pharmaceuticals, Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BS/BA in Chemistry, Biology, Biochemistry, or related scientific field is preferred
  • 3 years of Quality Assurance experience in a GMP-regulated biotech or pharmaceutical manufacturing environment
  • Working knowledge of drug GMP regulations, as well as ICH/FDA guidance documents
Job Responsibility
Job Responsibility
  • Interact with representatives from other departments, including manufacturing, QC, and Analytical Development, to obtain the necessary information for review of documentation
  • Review and approve analytical testing data and final reports from internal and external sources with minimal supervision
  • Review and approve manufacturing batch records, forms, and associated testing with minimal supervision
  • Perform room releases as required
  • Perform QA on the floor as required
  • Assist with investigations and deviations as appropriate with minimal supervision
  • Organization and control of project related documentation
  • Issue, review, and reconcile controlled forms
  • Review, verify, and reconcile labels
  • Scan and upload executed documents to the EDMS, properly categorize within the system, and route for verification/approval
What we offer
What we offer
  • competitive salaries and an excellent benefit package
  • Fulltime
Read More
Arrow Right
New

Senior Conveyancer

We are currently recruiting a Conveyancer to join our team.
Location
Location
Australia , Melbourne
Salary
Salary:
Not provided
provey.com.au Logo
Provey Conveyancing
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Ability to handle at least 5-10 settlements per week
  • Familiarity in commercial transactions
  • Great interpersonal communication skills
  • Strong written communication and drafting skills
  • A grasp of information technology
  • Personal accountability and strong work ethic
  • Professional, able to interact with clients and other staff
  • Positive, “can do” attitude
  • A genuine interest in property law
Job Responsibility
Job Responsibility
  • Work from home available for senior conveyancer managing portfolio of conveyancing files
  • Complete responsibility and ownership over files
  • File management
  • Mentor conveyancers
Read More
Arrow Right
New

Accounts Payable Clerk

Accounts Payable Clerk - Permanent - Royal Wootton Bassett (Onsite) - Up to £35,...
Location
Location
United Kingdom , Royal Wootton Bassett
Salary
Salary:
30000.00 - 35000.00 GBP / Year
in2-consult.com Logo
IN2 Consult
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Have strong experience of working within fast paced, high volume environments
  • Strong communication skills
Job Responsibility
Job Responsibility
  • Processing high volumes of invoices
  • 3 way invoicing
  • Preparing and processing payment runs
  • Reocnciling bank accounts
  • Reconciling supplier statements
  • Fulltime
Read More
Arrow Right
New

Director senior director client team resourcing

As Head of Resourcing, you are accountable for designing and running a resourcin...
Location
Location
United States , Washington
Salary
Salary:
120000.00 - 160000.00 USD / Year
bpigroup.com Logo
Bully Pulpit International
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 8–10+ years of experience in agency operations or resource management
  • Background to negotiate win-win solutions with senior leadership
  • Expert-level understanding of project management and ERP systems (experience with NetSuite and SuiteProjectsPro is highly preferred)
  • Natural affinity for problem-solving under pressure
  • Ability to translate raw data into actionable stories and recommendations
  • Deep sense of team dynamics and personalities to build trust
  • Proven experience in educating the room and advancing a culture of operational discipline
  • Experience leading organizational transformation or change management initiatives
  • Strong grasp of agency financial drivers, including utilization rates, fee structures and freelance vs. full-time trade-offs
Job Responsibility
Job Responsibility
  • Strategic Staffing: Field and vet all inbound Client Services staffing requests
  • Lead the cultural shift from a siloed team structure to a centralized resource pool
  • Client Leader Partnership: Work with leaders across accounts to validate staff plans, identify skills gaps, and course-correct
  • Executive Partnership: Participate in high-level portfolio conversations, providing business insights to leadership
  • Operational Governance: Act as the Single Source of Truth owner, finalizing time-entry and forecasting policies
  • Develop and enforce a prioritization matrix for staffing requests
  • Workforce Planning: Design and maintain forward-looking capacity models (12-month outlook)
  • Skillset Optimization: Work with Head of Talent to map talent databases
  • Collaborate with mentors and team leads to bridge the gap between self-reported skills and actual performance
  • Use resourcing data to ensure junior talent is getting diverse experience and growth opportunities
What we offer
What we offer
  • 100% company-paid medical, dental, and vision insurance
  • 401(k) program with employer match up to 4%
  • Generous time off for vacation
  • $50 monthly phone reimbursement
  • Unlimited sick time
  • 16 weeks of paid leave for new parents
  • Fulltime
Read More
Arrow Right
New

Python Developer

Bright Vision Technologies is a forward-thinking software development company de...
Location
Location
United States
Salary
Salary:
Not provided
bvteck.com Logo
Bright Vision Technologies
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Python
  • Django
  • Flask
  • FastAPI
  • RESTful APIs
  • JSON
  • SQL (PostgreSQL, MySQL)
  • NoSQL (MongoDB)
  • Pandas
  • NumPy
What we offer
What we offer
  • H-1B sponsorship for the 2026 quota
  • Filing with level 4 prevailing wage
  • Fulltime
Read More
Arrow Right
Jobs by Category
Art and Entertainment Jobs Banking Jobs Call Center Jobs Construction Jobs Consulting Jobs Customer Service Jobs Education Jobs Energy Jobs Finance Jobs Gastronomy Jobs Health and Beauty Jobs Hospitality and Tourism Jobs Human Resources Jobs Insurance Jobs IT - Administration Jobs IT - Software Development Jobs Legal Jobs Logistics Jobs Manufacturing Jobs Marketing, Digital Marketing, SEO, SEM Jobs Media Jobs Nursing Jobs Office Administration Jobs Pharmacy Jobs Physical Work Jobs Public Relations Jobs Public Sector Jobs Purchasing Jobs Quality Control Jobs Real Estate Jobs Research and Development Jobs Sales Jobs
Job Positions Jobs by Country
United States Jobs United Kingdom Jobs India Jobs Canada Jobs Australia Jobs Germany Jobs Ireland Jobs Poland Jobs
Company
Blog About Us Contact
Follow Us
Facebook
X (Twitter)
LinkedIn
Instagram
CrawlJobs Group
ITFlashcards AllDevBlogs
© 2026 CrawlJobs Ltd. All Rights Reserved
Terms & Conditions Privacy Policy