Engineer - QC Lab Job at Alleima Precision Tube (Mehsana, Gujarāt)

QC Associate II

As a QC Associate II, you will be responsible for inspecting raw materials, inte...

Location

United States , Pleasanton

Salary:

31.78 - 43.03 USD / Hour

10x Genomics

Expiration Date

Until further notice

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

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

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

Fulltime

Qc chemist

As a QC Chemist, you need quality control. You will report to QC Manager. And yo...

Location

China , Wuhu

Salary:

Not provided

PPG Industries

Expiration Date

Until further notice

Requirements

Bachelor or above degree in Chemistry or equivalent
Over 2 years chemical engineering or chemistry disciplines background
Master in the knowledge and skill about the chemical and instrument analysis, understand the chemical properties, safety and production process
Adapted to shift work

Job Responsibility

Conduct the routine QC tests and color match according to the relative SOP on in-process and finished products to ensure the quality within the specifications, record and feedback all the test results timely and correctly. Approve the qualified products to pass, control the unqualified products, take the appropriate action according to SOP, avoid shipping to customer
Investigate on quality anomalies and customer’s complaint, analyze on the root cause of the quality issues, offer the solution and improvement plan, participate the activity for the quality improvement and continuous improvement
Understand and meet all related requirements regarding Quality Management Systems and EHS Management Systems, QC lab’s cleaning and maintenance, 5S promotion

Fulltime

QC Lab Technician

Cariboo Pulp is currently recruiting for a Quality Control Lab Technician. Locat...

Location

Canada , Quesnel

Salary:

70000.00 - 83000.00 / Year

West Fraser

Expiration Date

Until further notice

Requirements

Technical certificate, diploma, or post-secondary science degree
Excellent interpersonal and presentation skills
Strong organizational and analytical skills
Strong computer skills, including familiarity with Microsoft Word and Excel
High commitment to safety
Strong communication skills including technical or procedural writing
A valid driver’s license
Available to occasionally work evenings and weekends when required

Job Responsibility

Perform pulp physical testing
Perform asbestos testing
Prepare chemicals for mill control tests
Calibrate and maintain testing equipment
Collect/analyze chemicals and samples from various stages of production
Troubleshoot upset conditions and develop corrective actions for the impact on quality
Analyze historical data for diagnoses of quality excursions
Support the QA department in maintaining QMS certifications
Tabulate and report analytical data in a clear and concise manner
Train and evaluate operators on test methods as required

What we offer

Annual bonus opportunity
Outstanding benefits package including medical, dental, pension, life insurance, disability, accident insurance, vacation, and holidays

Fulltime

Production Associate

10x Genomics is looking for a Production Associate to join its consumable manufa...

Location

United States , Pleasanton

Salary:

30.00 - 36.00 USD / Hour

10x Genomics

Expiration Date

Until further notice

Requirements

B.S./M.S. in one of the following disciplines – Molecular Biology, Analytical Chemistry, Chemical Engineering, or equivalent
3 years of relevant laboratory experience in manufacturing or QC of Life Science products
Ability to multi-task and prioritize work load to meet strict deadlines under supervision
Effective communicator skilled in collaborating with cross-functional teams to clearly relay production issues and updates
Motivated to contribute to a fast-paced, evolving organization by driving continuous improvement in products and processes

Job Responsibility

Execute production operations according to defined Standard Operating Procedures (SOPs) and ensure the integrity and quality of products
Perform reagent formulation while safely handling corrosive/flammable chemicals and fragile glassware
Operate liquid handling robotic system and complex manufacturing equipment for production biochemistry under supervision
Operate and maintain laboratory to clean room standards required in the production of Life Science products
Process work orders accurately using an ERP system in a timely manner
Draft Non-Conformance Reports (NCRs) and troubleshoot moderate manufacturing issues to support continuous improvement and compliance efforts
Ensure accurate tracking and documentation of production, testing, and inventory data
Disposition material based on QC and production data
Provide guidance and support to peers to ensure successful execution
Identifies issues in production labs and escalate issues appropriately

What we offer

comprehensive health benefit program
competitive and comprehensive health benefits package
competitive easy-to-use benefits that promote wellbeing
family friendly policies like parental leave
generous time off

Fulltime

Sr. QC Associate I

10x Genomics is looking for a Sr. QC Associate I to join our Quality Control tea...

Location

United States , Pleasanton

Salary:

37.64 - 50.91 USD / Hour

10x Genomics

Expiration Date

Until further notice

Requirements

B.S. in Analytical Chemistry, Biochemistry, or a related field
5+ years of laboratory experience specifically in a QC environment
Strong hands-on experience with NGS and tissue-based assays (including immunofluorescence and flow cytometry)
Proficiency in PCR, qPCR, spectrophotometry, spectrofluorometry, and HPLC
Experience collaborating with R&D and QA on risk-based QC strategy assessment including assay robustness, assay cost, and alignment of QC checkpoints to the manufacturing process
A solid understanding of New Product Introduction (NPI) and manufacturing processes
Ability to manage and track diversified QC assays and projects in a rapidly evolving environment
Strong critical thinking, logical problem-solving skills, and the ability to communicate effectively with stakeholders

Job Responsibility

Execute QC Testing: Perform quality control operations according to defined procedures to ensure the integrity and quality of raw materials, intermediates, and finished goods
Data Analysis & Disposition: Complete QC testing in a timely manner and disposition materials based on established acceptance criteria
Product Development and Sustaining Support: Serve as the primary QC point of contact to oversee project completion, providing expert guidance on assay setup and assisting in the introduction and optimization of new products and processes
Assay Cross-Training: Cross-train on various inspections, including first article inspection, metrology, microscopy, analytical assays, and NGS
Documentation: Maintain quality control batch records and ensure Good Documentation Practices (GDP) under ISO requirements. Accurately track QC test data, calibration records, and inventory. Draft Work Instructions in collaboration with the Manufacturing Systems & Engineering team
Quality Compliance: 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
Problem Solving: Effectively identify and communicate complications arising from QC testing with minimal supervision. Work closely with scientists to establish and maintain technical solutions. Drive completion of investigations and minimize disruptions to QC operations

What we offer

Equity grants
Comprehensive health and retirement benefit programs
Annual bonus program or sales incentive program
Generous time off
Competitive and comprehensive health benefits package
Family friendly policies like parental leave

Fulltime

Production Associate-Reagent

10x Genomics is looking for an outstanding individual to join its consumable man...

Location

United States , Pleasanton

Salary:

30.00 - 36.00 USD / Hour

10x Genomics

Expiration Date

Until further notice

Requirements

B.S./M.S. in one of the following disciplines – Molecular Biology, Analytical Chemistry, Chemical Engineering, or equivalent
3+ years of relevant laboratory experience in manufacturing or QC of Life Science products
Basic understanding of DNA sequencing, PCR or other nucleic acid based technologies required
Ability to multi-task and prioritize work load to meet strict deadlines under supervision
Good documentation skills and ability to write procedures and reports
Desire to be part of a rapidly evolving organization and taking products and processes to the next level

Job Responsibility

Execute production operations according to defined procedures and ensure the integrity and quality of products
Perform formulation and dispensing of reagent consumables and assemble into final kit configurations
Operate liquid handling robotic system and complex manufacturing equipment for production biochemistry under supervision
Operate and maintain laboratory to clean room standards required in the production of Life Science products
Process work orders accurately using an ERP system in a timely manner
Maintenance of production batch records and good documentation under ISO requirement
Initiate Non-Conformance Material or Deviation report and follow up on progress and action items
Accurate tracking of production data, test data and inventory
Disposition material based on QC and production data
Assist in writing and revising work instructions and production batch records

What we offer

Equity grants
Comprehensive health and retirement benefit programs
Annual bonus program or sales incentive program
Generous time off
Competitive and comprehensive health benefits package
Family friendly policies like parental leave

Fulltime

Sr Program Manager Tech - Gen AI

Lead program delivery and client engagement in the domain of AI training and eva...

Location

United States , Sunnyvale; San Francisco; New York

Salary:

167000.00 - 185500.00 USD / Year

Uber

Expiration Date

Until further notice

Requirements

7+ years of overall experience, with specific familiarity in software engineering, ML engineering, ML ops domains
Familiarity and experience in leading or managing client interactions (i.e., AI labs, foundation LLM companies, agentic AI companies) for data annotation, training, evaluation, performance benchmarking in the area of coding and development for foundational AI/LLM/ML is required
Experience in client facing service delivery management, solutioning, governance - with external client stakeholders at senior levels and/or their AI teams
Familiarity with strategies for delivery and QC processes in this domain is required
Track record of driving innovation and thought leadership in AI/ML/LLM training and evaluation services
Strong ability to communicate, bring clarity of thought in messaging for senior management as well as broader teams
Strong collaboration skills and abilities - working across silos and team structures to drive impact effectively
Ability to work in a global organization across locations and time zones

Job Responsibility

Client engagement for presales support - partner with Sales to interact with prospective clients to shape the project scope, evangelise our capabilities, design the delivery solution, and governance approach
Client engagement for program delivery - represent the service delivery organization and collaborate with them in order to drive ongoing governance, enable troubleshooting, find up/cross sell opportunities, bring thought leadership with client teams
Program delivery - help to manage US/onshore based delivery of annotation / training/ evaluation of AI/LLM/ML for coding and data areas, where required
Innovation and thought leadership - demonstrate deep understanding and expertise of coding and data analytics related AI training/evals including agentic AI with prospective clients
Sourcing strategy and implementation inputs - collaborate with our Supply team to help source and develop worker pools in the US/onshore with technical expertise for coding and data related training/evals
Tech platform capability and roadmap inputs - collaborate with our Product and Engineering teams to help develop a roadmap for tech and tooling required specific to coding and data analytics related tasking
Stakeholder management - represent the coding and data AI capabilities at senior leadership level interactions and forums, evangelise our capabilities, drive sponsorship and backing for initiatives
Best practices - continually improve ways of work, enhance delivery maturity, elevate governance and impact

What we offer

Eligible to participate in Uber's bonus program
May be offered an equity award & other types of comp
Eligible for various benefits

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

Engineer - QC Lab

Alleima Precision Tube

Location:
India , Mehsana, Gujarāt

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
April 10, 2026

Expiration:
April 29, 2026

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Expiration:April 29, 2026

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