CrawlJobs Logo

Quality Control Associate I, Instruments

United States, Austin, Texas · Job Posted February 03, 2026
Apply Position
Job Link Share

Job Description

The Quality Control Associate I, Instruments is responsible for performing the prescribed intermediate and final QC test procedures, and generate test reports according to the department policies and procedures and assuring the instrument products meet Luminex Quality Standards, performing equipment maintenance, calibration, test area cleanliness, and to assist in continuous process improvement and assisting with continuous process improvement. This position will have frequent intra-department interaction as well as frequent inter-department interfaces with Quality Assurance, Instrument Manufacturing, Manufacturing Engineering, Materials and Production Planning, Purchasing, Shipping, and Document Control.

Job Responsibility

  • Assist in core QC functions and associated activities relating to Intermediate and Finished Product Control
  • Fulfill individual and sectional CAPP objectives
  • Coordinate and/or conduct sectional maintenance and calibration of local measuring and monitoring devices
  • Assist in the maintenance, cleanliness and integrity of Test area(s)
  • Schedule outsourced testing and services
  • Monitor section supplies, maintain focused supplies and generate Purchase Orders as needed
  • Assist in compilation of section metrics
  • Assist in the development of departmental test methods
  • Assist in specification development for raw materials, products, acceptance, etc.
  • Assist in validations of section test methods, equipment, and processes
  • Assist in section document change control and engineering change control activities
  • Assist in continuous improvement projects
  • Assist in the resolution of section audit findings, observations, and recommendations
  • Assist in investigations initiated through non-conformances, corrective action, or customer complaints
  • Participate in design and implementation of new quality initiatives and programs
  • Document non-conformances
  • Conduct quality record Completeness Reviews
  • Participate in applicable departmental and interdepartmental training
  • Interface with other departments and participate in meetings as required
  • Assist in training of section personnel
  • Ensure personal compliance and facilitate sectional compliance with the Quality System and Health and Safety policies
  • Other duties as assigned

Requirements

  • Associate's Degree Associate degree in technical field or more than 3 years related experience and/or training.
  • 2+ Years of relevant work experience or training

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Quality Control Associate I, Instruments

8 matching positions

Sr. Associate I, Quality Control

This is where you make a difference in our patients’ safety. As a member of the ...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • To investigate failure of finished product (FP) / In-process (IP) product, in case of any out of specification (OOS) / Laboratory error / deviation and take corrective and preventive actions
  • To ensure that preparation of reagents and volumetric solution and standardization on time
  • To perform periodic observation of retained sample
  • To initiate Change control (CcM), Non conformation report (NCR), Out of Specification (OOS), Document change record (DCR) etc.. QMS related documents
  • To do the work allocation in shift and ensure it complete within timeline
  • To assess the results of testing of In-process sample and finish products to ensure alignment with standard operating procedure (SOP) and regulatory guidelines
  • To review results of the tests against the specification & standard test procedure performed by team members
  • To investigate out of specification (OOS), Non-conformity and Laboratory Error Report (LER) related to In-Process Product Testing (IPPT) & Finished Product Testing (FP) and take corrective and preventive actions
  • To follow and ensure Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) inside QC
  • To ensure availability the working & impurities standards as per various pharmacopoeias
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right

Sr. Associate I, Quality Control

This is where you make a difference in our patients’ safety. As a member of the ...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • To investigate failure of finished product (FP) / In-process (IP) product, in case of any out of specification (OOS) / Laboratory error / deviation and take corrective and preventive actions
  • To ensure that preparation of reagents and volumetric solution and standardization on time
  • To perform periodic observation of retained sample
  • To initiate Change control (CcM), Non conformation report (NCR), Out of Specification (OOS), Document change record (DCR) etc.. QMS related documents
  • To do the work allocation in shift and ensure it complete within timeline
  • To assess the results of testing of In-process sample and finish products to ensure alignment with standard operating procedure (SOP) and regulatory guidelines
  • To review results of the tests against the specification & standard test procedure performed by team members
  • To investigate out of specification (OOS), Non-conformity and Laboratory Error Report (LER) related to In-Process Product Testing (IPPT) & Finished Product Testing (FP) and take corrective and preventive actions
  • To follow and ensure Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) inside QC
  • To ensure availability the working & impurities standards as per various pharmacopoeias
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
Read More
Arrow Right

Sr. Associate I, Quality Control

This is where you make a difference in our patients’ safety. As a member of the ...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Detail Oriented
  • Continuous Learner
  • Courageous
  • Collaborative
  • Critical Thinker
  • Influential
Job Responsibility
Job Responsibility
  • To investigate failure of finished product (FP) / In-process (IP) product, in case of any out of specification (OOS) / Laboratory error / deviation and take corrective and preventive actions
  • To ensure that preparation of reagents and volumetric solution and standardization on time
  • To perform periodic observation of retained sample
  • To initiate Change control (CcM), Non conformation report (NCR), Out of Specification (OOS), Document change record (DCR) etc.. QMS related documents
  • To do the work allocation in shift and ensure it complete within timeline
  • To assess the results of testing of In-process sample and finish products to ensure alignment with standard operating procedure (SOP) and regulatory guidelines
  • To review results of the tests against the specification & standard test procedure performed by team members
  • To investigate out of specification (OOS), Non-conformity and Laboratory Error Report (LER) related to In-Process Product Testing (IPPT) & Finished Product Testing (FP) and take corrective and preventive actions
  • To follow and ensure Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) inside QC
  • To ensure availability the working & impurities standards as per various pharmacopoeias
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
Read More
Arrow Right

Associate Quality Control

At Amgen, if you feel like you’re part of something bigger, it’s because you are...
Location
Location
United States , Thousand Oaks
Salary
Salary:
62571.90 - 84656.10 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High school/GED + 2 years of Quality experience OR Associate’s + 6 months of Quality experience OR Bachelor’s
Job Responsibility
Job Responsibility
  • Responsible for one or more of the following activities in QC: analytical testing, sample and data management and equipment maintenance
  • Perform routine laboratory procedures such as sample analysis, standard and solution preparation
  • Responsible for documenting, compiling, interpreting, reviewing and entering laboratory data
  • Providing and communicating results, maintaining/operating specialized equipment and drafting and revising documents such as Analytical Methods, SOPs and technical reports
  • Support introduction of new methods/techniques into the lab
  • Perform basic assay and instrument troubleshooting
What we offer
What we offer
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models, including remote and hybrid work arrangements, where possible
  • Fulltime
Read More
Arrow Right

Senior Scientist I, Quality Control

This position is within the Quality Control structure, under the Quality Organiz...
Location
Location
United States , Verona
Salary
Salary:
90000.00 - 108000.00 USD / Year
arrowheadpharma.com Logo
Arrowhead Pharmaceuticals, Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • M.S. in Chemistry (or related field) with 7+ years relevant laboratory experience
  • B.S. in Chemistry (or related field) with 9+ years of relevant laboratory experience
  • Fully knowledgeable of cGMP and ICH laboratory requirements and operations
  • Proficient and demonstrated experience with analytical instrumentation, test methodology/validations/transfers, data acquisition systems, and typical cGMP policies/practices
Job Responsibility
Job Responsibility
  • Fully knowledgeable of cGMP requirements and ICH guidelines
  • Works independently to meet project timelines and deliverables with minimal supervision to no supervision
  • Collaborates routinely with Analytical Development on procedural method transfers and may participate in the execution of method validation protocols
  • Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and stability samples using established test methods and procedures
  • Proficient with various analytical instrumentation theory and practice
  • Executes training requirements for assigned SOPs and participates in department specific training modules
  • Independently completes complex instrumentation for testing according to written test methods and procedural documents to analyze samples
  • Demonstrates proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, Endotoxin plate readers, and/or Raman spectroscopy) and will assist in training on instrumentation
  • Is a subject matter expert in technical aspects of both instrumentation and workflow management and prioritization
  • Performs analyses in a timely and efficient manner to support ongoing prioritized studies
What we offer
What we offer
  • competitive salaries and an excellent benefit package
  • Fulltime
Read More
Arrow Right

Associate I, Quality Laboratory

The Quality Lab Associate I encompasses the biological, chemical and physical an...
Location
Location
United States , Round Lake
Salary
Salary:
64000.00 - 88000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in chemistry or science related degree with 6 months or more of experience
  • Knowledge of Empower CDS and LIMS is preferred but not required
  • Knowledge of GLP, cGMP requirements and familiar with USP/ICH guidelines is preferred but not required
  • Excellent communication (oral and written) and interpersonal skills
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude in a highly dynamic environment
  • Ability to lift up to 50 pounds when required
  • Must not be color blind
  • 20/20 vision with or without correction
  • A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials
Job Responsibility
Job Responsibility
  • Conduct critical chemical and physical analyses on Raw Materials, Initial, In-process and Final products, and samples collected from environmental monitoring programs
  • Use sophisticated laboratory instrumentation (HPLC, FTIR, UV, GC etc) and computer systems to collect and record data
  • Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles
  • Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations
  • Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality
  • Perform laboratory and manufacturing audits as required
  • Audit and update, as required, plant SOPs
  • Perform equipment maintenance and calibrations as required
  • Document the completion of testing in Notebooks, Controlled documents, Forms and LIMS and maintain accurate and complete quality records
  • Follow, understand and comply with Baxter SOP’s and policies on cGMP’s and safety
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Medical and dental coverage that start on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan (RSP)
  • Flexible Spending Accounts
  • Fulltime
Read More
Arrow Right

Associate I, Quality Laboratory

The Quality Lab Associate I encompasses the biological, chemical and physical an...
Location
Location
United States , Round Lake
Salary
Salary:
64000.00 - 88000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in chemistry or science related degree with 6 months or more of experience
  • Knowledge of Empower CDS and LIMS is preferred but not required
  • Knowledge of GLP, cGMP requirements and familiar with USP/ICH guidelines is preferred but not required
  • Excellent communication (oral and written) and interpersonal skills
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude in a highly dynamic environment
  • Ability to lift up to 50 pounds when required
  • Must not be color blind
  • 20/20 vision with or without correction
  • A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials
Job Responsibility
Job Responsibility
  • Conduct critical chemical and physical analyses on Raw Materials, Initial, In-process and Final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities
  • Use sophisticated laboratory instrumentation (HPLC, FTIR, UV, GC etc) and computer systems to collect and record data
  • Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles
  • Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations
  • Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality
  • Perform laboratory and manufacturing audits as required
  • Perform equipment maintenance and calibrations as required
  • Document the completion of testing in Notebooks, Controlled documents, Forms and LIMS and maintain accurate and complete quality records
  • Follow, understand and comply with Baxter SOP’s and policies on cGMP’s and safety
  • Investigate deviations and write exception/OOL/OOS/OOT documents
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Medical and dental coverage that start on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan (RSP)
  • Flexible Spending Accounts
  • Fulltime
Read More
Arrow Right

Associate I, Quality Laboratory

The Quality Lab Associate I encompasses the biological, chemical and physical an...
Location
Location
United States , Round Lake
Salary
Salary:
64000.00 - 88000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in chemistry or science related degree with 6 months or more of experience
  • Knowledge of Empower CDS and LIMS is preferred but not required
  • Knowledge of GLP, cGMP requirements and familiar with USP/ICH guidelines is preferred but not required
  • Excellent communication (oral and written) and interpersonal skills
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude in a highly dynamic environment
  • Ability to lift up to 50 pounds when required
  • Must not be color blind
  • 20/20 vision with or without correction
  • A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials
Job Responsibility
Job Responsibility
  • Conduct critical chemical and physical analyses on Raw Materials, Initial, In-process and Final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities
  • Use sophisticated laboratory instrumentation (HPLC, FTIR, UV, GC etc) and computer systems to collect and record data
  • Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles
  • Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations
  • Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality
  • Perform laboratory and manufacturing audits as required
  • Audit and update, as required, plant SOPs
  • Perform equipment maintenance and calibrations as required
  • Document the completion of testing in Notebooks, Controlled documents, Forms and LIMS and maintain accurate and complete quality records
  • Follow, understand and comply with Baxter SOP’s and policies on cGMP’s and safety
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Medical and dental coverage that start on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan (RSP)
  • Flexible Spending Accounts
  • Fulltime
Read More
Arrow Right