QC Associate II Job at 10x Genomics (Pleasanton)

Quality Control Inspector II

The Quality Control Inspector II (MRB) will be responsible for executing Quality...

Location

United States , Austin, Texas

Salary:

Not provided

Diasorin

Expiration Date

Until further notice

Requirements

H.S. Diploma or equivalent required
Associate's Degree in a technical field preferred
5+ Years relevant work experience or training required
7+ Years related experience without Associate's degree
Zeiss CMM experience preferred

Job Responsibility

Lead or assist the Material Review Board process
Process purchased materials for release
Application of GD&T practices
Take ownership and assist in core QC functions and associated activities relating to Incoming Product Control
Fulfill individual and departmental CAPP objectives
Assist and document the investigation and resolution of problems initiated through non-conformances, corrective action, customer complaints, and/or audit findings
Coordinate and/or conduct departmental maintenance and calibration of local measuring and monitoring devices
Schedule outsourced testing and services
Maintain cleanliness and integrity of facilities and working areas
Lead and assist with departmental document change control and engineering change control activities, monitor and assess impact of procedural and engineering change releases

What we offer

Receive a competitive salary and benefits package as you grow your career at Diasorin

Fulltime

New

Lab Medicine Technician II

At Boston Children’s Hospital, the quality of our care – and our inclusive hospi...

Location

United States , Boston

Salary:

19.06 - 27.64 USD / Hour

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Associates degree but Bachelors preferred with a Science background
6 months of Lab experience

Job Responsibility

Performs pre-analytical specimen preparation including stamping in, verifying ID, identification, test process and evaluating specimen quality
Performs computer functions including order entry, result entry, inquiries and worksheet and/or report maintenance
Performs waived moderately and highly complex tests under direction of supervisor, as permitted by regulatory standards
Performs daily QC and routine troubleshooting and maintenance of lab instruments and prepares reagents as necessary
Provides timely and courteous customer service for provider calling into the lab
Maintains workplace in a neat and orderly fashion and maintains supply inventory to keep work area adequately stocked
Trains new technicians and /or processing staff and interns from academic programs
Participates in departmental continuous improvement programs as necessary

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

Study Start Up Associate II

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Mexico , Mexico City

Salary:

Not provided

iconplc

Expiration Date

Until further notice

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

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

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.

Quality Control Analyst II

Quality Control Analyst II - Contract - Norton, MA. Are you passionate about qua...

Location

United States , Norton

Salary:

40.00 - 45.00 USD / Hour

Proclinical

Expiration Date

Until further notice

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

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

Medical Laboratory Scientist II - Chemistry

Join a team that’s setting the standard for safety and quality. Every day as a Q...

Location

United States , Royal Oak

Salary:

Not provided

Quest Diagnostics

Expiration Date

Until further notice

Requirements

One (1) year full-time experience or training (high complexity testing) in a clinical laboratory setting
BS/BA in Medical Technology, Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990
Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation)
United States-educated candidates must provide a detailed original transcript
Proven leadership and problem-solving skills
Must be detail-oriented, have the ability to work independently, establish work priorities and to handle several tasks simultaneously for maximum department efficiency
Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers and clients
Communication skills necessary to handle telephone inquiries from clients
Ability to deal with client information in a confidential manner
Proficiency in Microsoft Office (Word, Excel and Outlook) and Laboratory Information Systems

Job Responsibility

Perform test procedures of moderate/high complexity requiring the exercise of independent judgement and responsibility in those specialties in which they are qualified
Must demonstrate proficiency in all areas of testing and be proficient troubleshooting all applicable instruments/procedures in the department
Provides support to the department in the areas of quality control, troubleshooting complex problems, customer support, instrument and equipment maintenance, staff training, process improvement and the completion of special projects as assigned
Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met
Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient test results
Adhere to analytical schedules to maintain turnaround time of results including STATS or critical results to clients
Ensure reagents/test kits have received dates, expiration dates and if applicable opened dates
Perform and document QC analysis to ensure accuracy of clinical data and proper instrument function. Make quality control decisions regarding the disposition of an assay or test
Responsible for informing supervisory personnel of all problems associated with the proper performance of test procedures
Report any actual or potential deviation from standard or accepted testing procedures and cooperate fully with any investigation of same

What we offer

Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
Best-in-class well-being programs
Annual, no-cost health assessment program Blueprint for Wellness®
healthyMINDS mental health program
Vacation and Health/Flex Time
6 Holidays plus 1 "MyDay" off
FinFit financial coaching and services
401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
Employee stock purchase plan
Life and disability insurance, plus buy-up option

Fulltime

Specialist II, Product Quality Assurance

The Specialist, NC Product Quality Assurance (PQA) will be responsible for suppo...

Location

United States , Durham, NC

Salary:

105000.00 - 145000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Bachelors or Advanced degree in a scientific discipline
10+ years’ experience in the pharmaceutical/biotech industry in combination with drug substance/drug product manufacture, development and/or quality
Knowledge of aseptic processing, and/or cell and gene therapy is preferred
Apply Quality concepts and company policies to resolve issues of moderate complexity in an effective manner
Excellent verbal and written communication skills, detail-oriented personality, and ability to work collaboratively across functions
Knowledge of global regulations and standards
Strong team player that has a customer service approach and is solution oriented
Attention to detail and the ability to work individually as well as within a multi-disciplinary team
Excellent listening, communication and interpersonal skills with a team focus
Consistent delivery of high-quality work

Job Responsibility

Provide Quality oversight of on-the-floor activities including manufacturing shop floor presence during operations
Provide Quality oversight of QC testing
Responsible for ensuring GMP compliance with applicable procedures and production requirements in QC, manufacturing, and facilities operations
Responsible for assisting with product disposition activities of supply produced at the manufacturing facility
Real time review of batch records and labels
Review and approval of manufacturing discrepancies and associated CAPA’s
Communicating lot disposition pending issues to management
Aid in the development and ongoing improvement of applicable quality systems for the site
identifying gaps or improvements, authoring and approval of procedures, and providing training, as needed
Review and approve calibration and maintenance work orders and asset inductions

Fulltime

Operations Specialist II

The Operations Specialist II is a multi-functional role, responsible for invento...

Location

United States , San Diego

Salary:

28.00 - 30.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

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

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

New

Strategy Analyst

Strategy Analyst position at CSGM a.s. Provide analytical expertise across strat...

Location

Czech Republic , Praha - Karlín

Salary:

Not provided

Sport Vision Czechia s.r.o.

Expiration Date

Until further notice

Requirements

Master’s degree (or equivalent) in Finance, Business, Economics, Engineering, or a related field
Ideally 2–5 years’ experience in strategy consulting, corporate development, investment banking, or analytical roles
Strong proficiency in financial modeling, data analysis, and Excel/PowerPoint
Excellent research skills, with the ability to synthesize complex datasets
Comfortable working in cross-functional teams and managing projects under tight deadlines
Ability to distill technical or market data into actionable insights for executive audiences
Strong English communication skills
Detail-oriented, structured, and intellectually curious
Quick learner with strong problem-solving skills and analytical rigor
Collaborative and adaptable, thriving in small, high-performing teams

Job Responsibility

Provide analytical expertise across strategy and transformation projects
Financial modeling, market research, benchmarking
Support the CSO in answering ad-hoc CEO/Board strategic questions
Develop executive presentations
Build and maintain financial models (business cases, scenario analyses) to support strategic decision-making
Conduct in-depth market research, competitive benchmarking, and industry analysis
Translate complex data into clear insights and actionable recommendations for senior stakeholders
Prepare high-quality executive presentations and materials for the CEO, Board, and leadership team
Support the Chief Strategy Officer (CSO) in addressing ad-hoc strategic questions and priority topics
Collaborate with cross-functional teams to gather data and drive project execution

Fulltime

QC Associate II

10x Genomics

Location:
United States , Pleasanton

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 13, 2026

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Location:United States , Pleasanton

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Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:February 13, 2026

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

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Location:
United States , Pleasanton

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Not provided

Job Posted:
February 13, 2026