Medical Device Test Engineer
Newton, MA · On-site
Develop and implement test methods for verification of complex medical robotic systems . * Execute system and subsystem verification testing during verification and validation (V&V) phases.
Newton, MA · On-site
Develop and implement test methods for verification of complex medical robotic systems . * Execute system and subsystem verification testing during verification and validation (V&V) phases.
Newton, MA · On-site
Develop and implement test methods for verification of complex medical robotic systems . * Execute system and subsystem verification testing during verification and validation (V&V) phases.
Canton, MA · On-site
This includes conducting equipment and method Validation/Verification as appropriate * Ensure the Raw Materials laboratories remains current with all changes to applicable compendia and ability to ...
Canton, MA · On-site
This includes conducting equipment and method Validation/Verification as appropriate * Ensure the Raw Materials laboratories remains current with all changes to applicable compendia and ability to ...
Canton, MA · On-site
This includes conducting equipment and method Validation/Verification as appropriate * Ensure the Raw Materials laboratories remains current with all changes to applicable compendia and ability to ...
Canton, MA · On-site
This includes conducting equipment and method Validation/Verification as appropriate * Ensure the Raw Materials laboratories remains current with all changes to applicable compendia and ability to ...
This includes conducting equipment and method Validation/Verification as appropriate * Ensure the Raw Materials laboratories remains current with all changes to applicable compendia and ability to ...
This includes conducting equipment and method Validation/Verification as appropriate * Ensure the Raw Materials laboratories remains current with all changes to applicable compendia and ability to ...
A key focus will be the internalization of validated mRNA methods into the North Carolina Quality Control laboratory, strengthening inhouse testing capabilities and longterm operational resilience.
A key focus will be the internalization of validated mRNA methods into the North Carolina Quality Control laboratory, strengthening inhouse testing capabilities and longterm operational resilience.
A key focus will be the internalization of validated mRNA methods into the North Carolina Quality Control laboratory, strengthening in-house testing capabilities and long-term operational resilience.
A key focus will be the internalization of validated mRNA methods into the North Carolina Quality Control laboratory, strengthening in-house testing capabilities and long-term operational resilience.
Billerica, MA · On-site
$74K - $82K/yr
Execute method validation protocols related to product testing * Author summary reports for executed method validations * Author deviation reports and microbiological assessment reports related to ...
Billerica, MA · On-site
$74K - $82K/yr
Execute method validation protocols related to product testing * Author summary reports for executed method validations * Author deviation reports and microbiological assessment reports related to ...
Danvers, MA · On-site
$100K - $120K/yr
... methods, specifications, and engineering drawings • Apply Gage R&R (repeatability ... validated inspection methods and best practice Salary Range $100,000-$120,000 years TCS Employee ...
Danvers, MA · On-site
$100K - $120K/yr
... methods, specifications, and engineering drawings • Apply Gage R&R (repeatability ... validated inspection methods and best practice Salary Range $100,000-$120,000 years TCS Employee ...
Fall River, MA · On-site
$78K - $99K/wk
Oversee and verify method validation reports, comparisons, and study documentation. * Monitor laboratory operations for cGLP compliance and ensure SOPs are followed. * Review and assess standard ...
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Fall River, MA · On-site
$78K - $99K/wk
Oversee and verify method validation reports, comparisons, and study documentation. * Monitor laboratory operations for cGLP compliance and ensure SOPs are followed. * Review and assess standard ...
Support analytical method validation, transfer, and troubleshooting to ensure compliance with cGMP standards. * Collaborate with the Process/Formulation Development teams to ensure seamless ...
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Support analytical method validation, transfer, and troubleshooting to ensure compliance with cGMP standards. * Collaborate with the Process/Formulation Development teams to ensure seamless ...
$160K - $190K/yr
Support analytical method validation, transfer, and troubleshooting to ensure compliance with cGMP standards. * Collaborate with the Process/Formulation Development teams to ensure seamless ...
$160K - $190K/yr
Support analytical method validation, transfer, and troubleshooting to ensure compliance with cGMP standards. * Collaborate with the Process/Formulation Development teams to ensure seamless ...
Devens, MA · On-site
Author and execute computer system validation scripts using ALM or paper-based methods. * Own change controls related to qualification of QC instruments and associated software. * Update the asset ...
Devens, MA · On-site
Author and execute computer system validation scripts using ALM or paper-based methods. * Own change controls related to qualification of QC instruments and associated software. * Update the asset ...
Beverly, MA · On-site
$108K - $163K/yr
Test Method Validation; polymer rheological characterization; Mechanical & Chemical property testing of polymer; and DMAIC process, root cause analysis, and implementation of corrective action.
Beverly, MA · On-site
$108K - $163K/yr
Test Method Validation; polymer rheological characterization; Mechanical & Chemical property testing of polymer; and DMAIC process, root cause analysis, and implementation of corrective action.
Cambridge, MA · On-site
$160K - $190K/yr
Support analytical method validation, transfer, and troubleshooting to ensure compliance with cGMP standards. * Collaborate with the Process/Formulation Development teams to ensure seamless ...
Cambridge, MA · On-site
$160K - $190K/yr
Support analytical method validation, transfer, and troubleshooting to ensure compliance with cGMP standards. * Collaborate with the Process/Formulation Development teams to ensure seamless ...
Devens, MA · On-site
Author and execute computer system validation scripts using ALM or paper-based methods. * Own change controls related to qualification of QC instruments and associated software. * Update the asset ...
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Devens, MA · On-site
Author and execute computer system validation scripts using ALM or paper-based methods. * Own change controls related to qualification of QC instruments and associated software. * Update the asset ...
Candidate should be an analytical expert who can lead method transfer/validation independently. Description: The Analytical Chemist will join Client's growing Technical Operations Analytical team and ...
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Candidate should be an analytical expert who can lead method transfer/validation independently. Description: The Analytical Chemist will join Client's growing Technical Operations Analytical team and ...
Beverly, MA · On-site
$108K - $163K/yr
Test Method Validation; polymer rheological characterization; Mechanical & Chemical property testing of polymer; and DMAIC process, root cause analysis, and implementation of corrective action.
Beverly, MA · On-site
$108K - $163K/yr
Test Method Validation; polymer rheological characterization; Mechanical & Chemical property testing of polymer; and DMAIC process, root cause analysis, and implementation of corrective action.
Lee, MA · On-site
$95K - $110K/yr
Represent the validation department in multi-disciplinary teams focused on production and ... Demonstrated ability with engineering methods, process controls and manufacturing systems;
Lee, MA · On-site
$95K - $110K/yr
Represent the validation department in multi-disciplinary teams focused on production and ... Demonstrated ability with engineering methods, process controls and manufacturing systems;
Beverly, MA · On-site
$108K - $163K/yr
Test Method Validation; polymer rheological characterization; Mechanical & Chemical property testing of polymer; and DMAIC process, root cause analysis, and implementation of corrective action.
Beverly, MA · On-site
$108K - $163K/yr
Test Method Validation; polymer rheological characterization; Mechanical & Chemical property testing of polymer; and DMAIC process, root cause analysis, and implementation of corrective action.
Devens, MA · On-site
Author and execute computer system validation scripts using ALM or paper-based methods. * Own change controls related to qualification of QC instruments and associated software. * Update the asset ...
Devens, MA · On-site
Author and execute computer system validation scripts using ALM or paper-based methods. * Own change controls related to qualification of QC instruments and associated software. * Update the asset ...
$24.68 - $30.19
2% of jobs
$30.19 - $35.70
6% of jobs
$35.70 - $41.22
13% of jobs
$42.94 is the 25th percentile. Wages below this are outliers.
$41.22 - $46.73
13% of jobs
$46.73 - $52.24
11% of jobs
The median wage is $55 / hr.
$52.24 - $57.76
12% of jobs
$57.76 - $63.27
9% of jobs
$67.52 is the 75th percentile. Wages above this are outliers.
$63.27 - $68.78
13% of jobs
$68.78 - $74.30
13% of jobs
$74.30 - $79.81
6% of jobs
$79.81 - $85.32
3% of jobs
$24
$56
$85
To excel in Method Validation, a strong background in analytical chemistry, laboratory techniques, and scientific data analysis is typically required, often supported by a degree in chemistry, biochemistry, or a related field. Familiarity with validation protocols, industry regulations (such as GLP, GMP, or ISO standards), and analytical instrumentation (e.g., HPLC, GC, MS) is essential. Strong attention to detail, problem-solving skills, and effective collaboration and documentation abilities help professionals thrive in this position. These skills are vital to ensure that laboratory methods are reliable, regulatory-compliant, and suitable for their intended purposes.
A Method Validation job involves assessing and verifying analytical methods to ensure they produce reliable, accurate, and reproducible results. Professionals in this role typically work in pharmaceutical, biotechnology, or chemical industries, following regulatory guidelines such as ICH, USP, or FDA requirements. Their responsibilities include designing validation protocols, performing experiments, analyzing data, and documenting results. Method validation ensures compliance with industry standards and guarantees product quality and safety.
As a Method Validation professional, you will design, conduct, and document experiments to confirm that laboratory methods produce accurate and reproducible results under specified conditions. Typical daily tasks include preparing protocols, running validation samples, analyzing data, and preparing comprehensive validation reports for internal or regulatory review. You’ll work closely with scientists, quality assurance teams, and regulatory specialists to ensure compliance with industry standards. This collaborative environment provides opportunities to contribute to critical product development stages and to build expertise that supports career progression into quality management, regulatory affairs, or advanced analytical roles.

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11 - 50 Employees
Alpharetta, GA, US
2007