Performs and leads computer system validation projects related to authoring and executing validation documentation for laboratory instruments/equipment and systems according to the ISPE GAMP 5 ...
Quick apply
Performs and leads computer system validation projects related to authoring and executing validation documentation for laboratory instruments/equipment and systems according to the ISPE GAMP 5 ...
Quick apply
Performs and leads computer system validation projects related to authoring and executing validation documentation for laboratory instruments/equipment and systems according to the ISPE GAMP 5 ...
Basic computer skills including experience in the use of Microsoft word, Excel, etc preferred ... Ellab Validator), desired preferred * Experience working with cross functional teams preferred
New
Basic computer skills including experience in the use of Microsoft word, Excel, etc preferred ... Ellab Validator), desired preferred * Experience working with cross functional teams preferred
New
Basic computer skills including experience in the use of Microsoft word, Excel, etc preferred ... Ellab Validator), desired preferred * Experience working with cross functional teams preferred
New
Basic computer skills including experience in the use of Microsoft word, Excel, etc preferred ... Ellab Validator), desired preferred * Experience working with cross functional teams preferred
New
Join our validation engineering team as a Validation Engineer III (Computer Systems Validation - CSV) , where you will ensure product quality and regulatory compliance across pharmaceutical ...
Join our validation engineering team as a Validation Engineer III (Computer Systems Validation - CSV) , where you will ensure product quality and regulatory compliance across pharmaceutical ...
Durham, NC ยท On-site
$133K - $183K/yr
Experience in Data Integrity, computer system validation/IT quality in an FDA regulated manufacturing environment. Demonstrated expert knowledge of 21CFR, Part 11, and/or EU Annex 11 as well as ...
Durham, NC ยท On-site
$133K - $183K/yr
Experience in Data Integrity, computer system validation/IT quality in an FDA regulated manufacturing environment. Demonstrated expert knowledge of 21CFR, Part 11, and/or EU Annex 11 as well as ...
Join our validation engineering team as a Validation Engineer III (Computer Systems Validation - CSV) , where you will ensure product quality and regulatory compliance across pharmaceutical ...
Join our validation engineering team as a Validation Engineer III (Computer Systems Validation - CSV) , where you will ensure product quality and regulatory compliance across pharmaceutical ...
$133K - $183K/yr
Experience in Data Integrity, computer system validation/IT quality in an FDA regulated manufacturing environment. Demonstrated expert knowledge of 21CFR, Part 11, and/or EU Annex 11 as well as ...
$133K - $183K/yr
Experience in Data Integrity, computer system validation/IT quality in an FDA regulated manufacturing environment. Demonstrated expert knowledge of 21CFR, Part 11, and/or EU Annex 11 as well as ...
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards ...
Quick apply
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards ...
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards ...
Quick apply
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards ...
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards ...
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards ...
Specialist IS Business Systems Analyst - Technology Computer Validation SME What you will do Let's do this. Let's change the world. In this vital role, you will join the Amgen North Carolina (ANC ...
Specialist IS Business Systems Analyst - Technology Computer Validation SME What you will do Let's do this. Let's change the world. In this vital role, you will join the Amgen North Carolina (ANC ...
Clayton, NC ยท On-site
Serve as a member of the QC computer validation team, ensuring compliance with regulatory and internal validation standards. * Support additional computerized systems within the QC environment ...
Clayton, NC ยท On-site
Serve as a member of the QC computer validation team, ensuring compliance with regulatory and internal validation standards. * Support additional computerized systems within the QC environment ...
Durham, NC ยท On-site
$140 - $200/hr
Contribute to SDLC and computer validation practices where applicable. What We're Looking For 8-12+ years of experience in manufacturing; pharmaceutical manufacturing experience strongly preferred. A ...
New
Durham, NC ยท On-site
$140 - $200/hr
Contribute to SDLC and computer validation practices where applicable. What We're Looking For 8-12+ years of experience in manufacturing; pharmaceutical manufacturing experience strongly preferred. A ...
New
Specialist IS Business Systems Analyst - Technology Computer Validation SME What you will do Let's do this. Let's change the world. In this vital role, you will join the Amgen North Carolina (ANC ...
Specialist IS Business Systems Analyst - Technology Computer Validation SME What you will do Let's do this. Let's change the world. In this vital role, you will join the Amgen North Carolina (ANC ...
The Position Provide subject matter expertise in Computer Systems Validation, process improvement, and IT compliance service delivery management across the site. Ensure that IT solutions are ...
The Position Provide subject matter expertise in Computer Systems Validation, process improvement, and IT compliance service delivery management across the site. Ensure that IT solutions are ...
The Position Provide subject matter expertise in Computer Systems Validation, process improvement, and IT compliance service delivery management across the site. Ensure that IT solutions are ...
The Position Provide subject matter expertise in Computer Systems Validation, process improvement, and IT compliance service delivery management across the site. Ensure that IT solutions are ...
The Position Provide subject matter expertise in Computer Systems Validation, process improvement, and IT compliance service delivery management across the site. Ensure that IT solutions are ...
The Position Provide subject matter expertise in Computer Systems Validation, process improvement, and IT compliance service delivery management across the site. Ensure that IT solutions are ...
Write and execute process, packaging, computer,facility, and cleaning validation protocols and summary reports. * Interface with Manufacturing, Packaging, Logistics, Engineering, and external vendors ...
Write and execute process, packaging, computer,facility, and cleaning validation protocols and summary reports. * Interface with Manufacturing, Packaging, Logistics, Engineering, and external vendors ...
Atlanta, GA ยท On-site
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards ...
Atlanta, GA ยท On-site
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards ...
At least 4 years' experience validating equipment At least 2 years' experience validating laboratory instruments with computer systems Initiates and leads change control for implementation of new ...
At least 4 years' experience validating equipment At least 2 years' experience validating laboratory instruments with computer systems Initiates and leads change control for implementation of new ...
$9.61 - $15.85
2% of jobs
$15.85 - $22.08
9% of jobs
$22.08 - $28.32
1% of jobs
$28.32 - $34.56
4% of jobs
$38.34 is the 25th percentile. Wages below this are outliers.
$34.56 - $40.79
15% of jobs
$40.79 - $47.03
9% of jobs
The median wage is $52.23 / hr.
$47.03 - $53.27
13% of jobs
$58.23 is the 75th percentile. Wages above this are outliers.
$53.27 - $59.50
29% of jobs
$59.50 - $65.74
12% of jobs
$65.74 - $71.97
2% of jobs
$71.97 - $78.21
5% of jobs
$9
$49
$78
| Aspect | Computer Validation | Quality Assurance Specialist |
|---|---|---|
| Required Credentials | GxP, 21 CFR Part 11, validation certifications | ISO standards, QA certifications, GxP knowledge |
| Work Environment | Pharmaceutical, biotech, regulated industries | Manufacturing, healthcare, regulated industries |
| Employer & Industry Usage | Regulated industries requiring validated systems | Ensuring quality compliance across processes |
Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

Full-time
This job post hasย expired today.ย Applications are no longer accepted.
Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Computer System Validation Specialist.
Responsibilities:
Qualifications:
Quality Chemical Laboratories (QCL) is a rapidly growing pharmaceutical testing and manufacturing lab in Wilmington, NC. We are seeking highly motivated candidates for multiple positions throughout the company in the areas of analytical data review, LabWare LIMS development/configuration/validation, Document Control, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in Mass Spec, LC, GC, QC compendial testing, Wet Chemistry, Microbiology, Sterility, Synthetic Chemistry, Biotech, Pharmaceutical Formulation and Manufacturing (requires knowledge of manufacturing equipment), Validation Engineers, Metrology, Report Generation, Sample Log-In Associates, and HVAC Technicians. Special attention given to candidates with an advanced degree in Chemistry or related science and experience in method development/validation. Special consideration also given to experienced GMP data reviewers.
QCL offers competitive salaries commensurate with experience and an excellent benefits package, as well as great potential for career advancement and leadership in a rapidly growing company. We now also offer subsidized childcare at our newly acquired childcare facility.
QCL is an equal opportunity employer.
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Pharmaceutical and medicine manufacturing
51 - 200 Employees
Wilmington, NC, US
1998