Between $18.00 and
$20.00
Per Hour
DOE (Depends on Experience)
Position range in Dallas $14.01 - $23.02 Per hour
Lab Technician Analyst
BEPC INCORPORATED
Occupation: Medical and Clinical Laboratory Technicians
Location: Irving, TX - 75038
Positions available: 1
Job #: 16909436
Source: WorkInTexas
Posted: 8/21/2025
Updated: 8/24/2025
Expires: 9/20/2025
Web Site: WorkInTexas
Onsite / Remote: Work onsite all of the time
Job Type: Regular, Full Time (30 Hours or More), Permanent Employment, Rotating Shift
Job Requirements and Properties Help for Job Requirements and Properties. Opens a new window.
Job Requirements and Properties
Help for Job Requirements and Properties. Opens a new window.
Work Onsite
Full Time
Education
Bachelor's Degree
Experience
06 Month(s)
Schedule
Full Time
Job Type
Regular
Duration
Permanent Employment
Shift
Rotating Shift
Benefits
Help for . Opens a new window.
Help for . Opens a new window.
: Lab Technician Analyst
Our company is looking for a detail-oriented and highly skilled Lab Technician Analyst, performing laboratory tests and analyses to ensure the quality and accuracy of materials and products. Proficient in operating and maintaining a wide range of laboratory equipment, analyzing data, and preparing detailed reports. Committed to ensuring high standards of precision and reliability in all laboratory procedures.
Position Duties & Responsibilities
Performs raw material, in-process and/or finished goods tests and reviews.
Able to work in an environment with chemicals safely.
Inspects, tests and/or evaluates the precision and accuracy of products, and/or testing equipment.
Monitors and reviews environmental charts and/or numeric data.
Performs chemical and sterility release of product.
Performs sterility, environmental, moisture, residual ethylene oxide, and triclosan testing.
Carries out difficult calculations and prepares documentation that shows the results for the test performed.
Prepares media and performs quality assurance control checks per USP.
Investigate and write out of specification reports.
Read and interpret results, performs trend analysis as required.
Recommends, amends, and analyzes sampling procedures, test methods, standard operating procedures, and/or inspection measures to lean processes or simplify current practices.
Performs other duties assigned as by any member of Laboratory Management.
Execute simple microbiology analyses in-process sample and finish products (Microbial count, Environmental Monitoring, and sterility test) to comply with current procedures and Pharmacopoeias.
Basic knowledge on microbiology principles, theories, practices and methodology.
Basic Technical writing techniques knowledge to perform preliminary laboratory investigation.
Completes record of inspection results, acceptance, rejection and disposition for entry into logbooks or computer systems (i.e. LIMS).
Support process improvement teams for departmental and company continuous improvement activities (Lean, compliance laboratory processes, etc.)
Responsible to ensure adequate systematic control of nonconforming product.
Recommends and implements revisions, corrections and changes to test equipment, procedures and methods.
Experience on proper use and basic troubleshooting on the following laboratory instrumentations: UPLC, HPLC, GC, FTIR, pH, KF, Particle counter, RCS.
Participates on special requests for product testing, such as qualification protocols
Initiates and coordinates discussions with quality, engineering, and other relevant departments to develop corrective actions for reoccurring problems
Conducts training for lower-level technicians and operations.
Cross-trains to support other functional areas.
Ensures proper safety and environmental procedures and practices are utilized
Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001).
Education & Experience Requirements
University / Bachelor's Degree or Equivalent is required with major on science preferred.
Good interpersonal relations and communication skills required.
Knowledge of Microsoft Office, LIMS, Empower and other computer software recommended.
Demonstrated knowledge and expertise in quality processes and regulatory requirements.
Experience working in an FDA regulated environment (21 CFR Part 211 and 211, 21 Part 820, ICH Q7 and/or 21 CFR Part 4).
Basic Spectroscopy knowledge (theorical and practical) to evaluate and troubleshoot chromatography analysis, document, and review chromatography and/or spectroscopy (GC, UPLC, HPLC, FTIR, etc.) results that could impact the results for the test performed.
Basic wet chemistry techniques related to qualitative and quantitative
Help for Employer Information. Opens a new window.
$20.00
Per Hour
DOE (Depends on Experience)
Position range in Dallas $14.01 - $23.02 Per hour
Lab Technician Analyst
BEPC INCORPORATED
Occupation: Medical and Clinical Laboratory Technicians
Location: Irving, TX - 75038
Positions available: 1
Job #: 16909436
Source: WorkInTexas
Posted: 8/21/2025
Updated: 8/24/2025
Expires: 9/20/2025
Web Site: WorkInTexas
Onsite / Remote: Work onsite all of the time
Job Type: Regular, Full Time (30 Hours or More), Permanent Employment, Rotating Shift
Job Requirements and Properties Help for Job Requirements and Properties. Opens a new window.
Job Requirements and Properties
Help for Job Requirements and Properties. Opens a new window.
Work Onsite
Full Time
Education
Bachelor's Degree
Experience
06 Month(s)
Schedule
Full Time
Job Type
Regular
Duration
Permanent Employment
Shift
Rotating Shift
Benefits
Help for . Opens a new window.
Help for . Opens a new window.
: Lab Technician Analyst
Our company is looking for a detail-oriented and highly skilled Lab Technician Analyst, performing laboratory tests and analyses to ensure the quality and accuracy of materials and products. Proficient in operating and maintaining a wide range of laboratory equipment, analyzing data, and preparing detailed reports. Committed to ensuring high standards of precision and reliability in all laboratory procedures.
Position Duties & Responsibilities
Performs raw material, in-process and/or finished goods tests and reviews.
Able to work in an environment with chemicals safely.
Inspects, tests and/or evaluates the precision and accuracy of products, and/or testing equipment.
Monitors and reviews environmental charts and/or numeric data.
Performs chemical and sterility release of product.
Performs sterility, environmental, moisture, residual ethylene oxide, and triclosan testing.
Carries out difficult calculations and prepares documentation that shows the results for the test performed.
Prepares media and performs quality assurance control checks per USP.
Investigate and write out of specification reports.
Read and interpret results, performs trend analysis as required.
Recommends, amends, and analyzes sampling procedures, test methods, standard operating procedures, and/or inspection measures to lean processes or simplify current practices.
Performs other duties assigned as by any member of Laboratory Management.
Execute simple microbiology analyses in-process sample and finish products (Microbial count, Environmental Monitoring, and sterility test) to comply with current procedures and Pharmacopoeias.
Basic knowledge on microbiology principles, theories, practices and methodology.
Basic Technical writing techniques knowledge to perform preliminary laboratory investigation.
Completes record of inspection results, acceptance, rejection and disposition for entry into logbooks or computer systems (i.e. LIMS).
Support process improvement teams for departmental and company continuous improvement activities (Lean, compliance laboratory processes, etc.)
Responsible to ensure adequate systematic control of nonconforming product.
Recommends and implements revisions, corrections and changes to test equipment, procedures and methods.
Experience on proper use and basic troubleshooting on the following laboratory instrumentations: UPLC, HPLC, GC, FTIR, pH, KF, Particle counter, RCS.
Participates on special requests for product testing, such as qualification protocols
Initiates and coordinates discussions with quality, engineering, and other relevant departments to develop corrective actions for reoccurring problems
Conducts training for lower-level technicians and operations.
Cross-trains to support other functional areas.
Ensures proper safety and environmental procedures and practices are utilized
Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001).
Education & Experience Requirements
University / Bachelor's Degree or Equivalent is required with major on science preferred.
Good interpersonal relations and communication skills required.
Knowledge of Microsoft Office, LIMS, Empower and other computer software recommended.
Demonstrated knowledge and expertise in quality processes and regulatory requirements.
Experience working in an FDA regulated environment (21 CFR Part 211 and 211, 21 Part 820, ICH Q7 and/or 21 CFR Part 4).
Basic Spectroscopy knowledge (theorical and practical) to evaluate and troubleshoot chromatography analysis, document, and review chromatography and/or spectroscopy (GC, UPLC, HPLC, FTIR, etc.) results that could impact the results for the test performed.
Basic wet chemistry techniques related to qualitative and quantitative
Help for Employer Information. Opens a new window.
Job ID: 490791506
Originally Posted on: 8/26/2025
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