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Validation Engineer I

Qualityagents · Rockville, Maryland, 20850, United States · Active · BambooHR

Job facts

FieldValue
CompanyQualityagents
TitleValidation Engineer I
Normalized title-
Department / teamValidation Services
LocationRockville, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerBambooHR
Posted / first seen2018-10-22 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-18

Related slices

PageWhat it containsOpen
Company jobsActive postings from Qualityagents.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through BambooHR.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Rockville.Open
Department jobsActive postings in Validation Services.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyQualityagents
Source7616852b-853b-48f5-83ea-0cb0b1249bb9
ATS providerBambooHR

Description

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries.  Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites.  The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach.  The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation.  The individual will coordinate validation activities with the client and meet timelines.  Documents prepared by the validation specialist must be approved by the client.  Responsibilities include: Interact with clients and works closely with site manufacturing, engineering, and QA to develop validation documents. Travel to various client sites and work independently to complete tasks. Provide qualification and validation services for cGMP manufacturing equipment, systems, and utilities at client sites. Exposure to validation aspects of facility start-up, redesign/retrofit, and expansion. Writes and executes qualification protocols for a variety of biopharmaceutical equipment and support utilities in accordance with SOPs, master plans, regulatory expectations, and industry standards. Conducts temperature mapping studies, including the operation of kaye dataloggers, or equivalent. Review and approve documented test results and maintain records for later analysis. Assist with non-conformances, investigations, and troubleshooting of equipment, utilities, and systems. Able to read P&IDs, isometric drawings, and As-built drawings. Skill Level and Requirements: Ability to problem solve and troubleshoot. Technical writing ability and use of Microsoft Word, Excel, Power point, and Project Experience with validation equipment such as the Kaye validator, wireless data loggers, or other monitoring devices is strongly desired. Experience using statistical tools is a plus to analyze data captured during validation studies. Minimum Requirements: BS in a technical discipline (Engineering, chemistry, microbiology, biology) 0-2 years of experience in at least one of the following areas:  equipment/utility qualifications, process validation, analytical method validation, or cleaning validation. Current driver’s license and auto insurance Quality Agents offers a full suite of benefits for full-time employees including: Health, dental and vision insurance Life, AD&D and disability Insurance Health savings account for participants in our health plan 401k retirement plan Paid time off Paid holidays Quality Agents accepts applications on an on-going basis in order to build a talent pool of potential candidates. These applications remain open for consideration, as positions become available, for one (1) year from the date of application. After that time, or if your application information changes, please submit your application again. Equal Opportunity & Accessibility Statement Quality Agents, LLC is an equal opportunity employer. We make employment decisions without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, veteran status, or any other protected characteristic under applicable law. We are committed to providing reasonable accommodations for individuals with disabilities throughout the application and hiring process. If you require assistance or accommodation, please contact us.

Full job record

Job ID04178b84b9ee4349d8cca744082145c081a1dec0
Org ID6c5d9442-7182-495e-9538-39cf1da6b7e2
Source ID7616852b-853b-48f5-83ea-0cb0b1249bb9
Board ID7616852b-853b-48f5-83ea-0cb0b1249bb9
Providerbamboohr
Provider Job Key1
TitleValidation Engineer I
Normalized Title
Statusactive
Activeyes
Location TextRockville, Maryland, 20850, United States
DepartmentValidation Services
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
Region
CityRockville
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://qualityagents.bamboohr.com/careers/1
Apply URLhttps://qualityagents.bamboohr.com/careers/1
First Seen At2026-05-30 05:54:30Z
Last Seen At2026-06-18 10:28:09Z
Last Checked At2026-06-18 10:28:09Z
Last Changed At2026-05-30 05:54:30Z
Inactive At
Source Posted At2018-10-22 00:00:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=bamboohr/board=qualityagents/date=2026-06-18/2026-06-18T10-28-08-336Z-2fc967c578758c79cddb1ccc87270b555f111c653d7598a728b6aef3f4592ad0.json
Event Fields
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Parsed Structured
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Extensions
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Native Structured
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    "description": "<p><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries.  Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites.  The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach.  The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation.  The individual will coordinate validation activities with the client and meet timelines.  Documents prepared by the validation specialist must be approved by the client.  Responsibilities include: </span></p>\n<p><br></p>\n<ul>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Interact with clients and works closely with site manufacturing, engineering, and QA to develop validation documents. </span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Travel to various client sites and work independently to complete tasks. </span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Provide qualification and validation services for cGMP manufacturing equipment, systems, and utilities at client sites.</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Exposure to validation aspects of facility start-up, redesign/retrofit, and expansion.</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Writes and executes qualification protocols for a variety of biopharmaceutical equipment and support utilities in accordance with SOPs, master plans, regulatory expectations, and industry standards.</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Conducts temperature mapping studies, including the operation of kaye dataloggers, or equivalent.</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Review and approve documented test results and maintain records for later analysis.</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Assist with non-conformances, investigations, and troubleshooting of equipment, utilities, and systems.</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Able to read P&amp;IDs, isometric drawings, and As-built drawings.</span></li>\n</ul>\n<p><br></p>\n<p><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Skill Level and Requirements:</span></p>\n<p><br></p>\n<ul>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Ability to problem solve and troubleshoot.</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Technical writing ability and use of Microsoft Word, Excel, Power point, and Project</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Experience with validation equipment such as the Kaye validator, wireless data loggers, or other monitoring devices is strongly desired.</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Experience using statistical tools is a plus to analyze data captured during validation studies. </span></li>\n</ul>\n<p><br></p>\n<p><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Minimum Requirements:</span></p>\n<p><br></p>\n<ul>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">BS in a technical discipline (Engineering, chemistry, microbiology, biology)</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">0-2 years of experience in at least one of the following areas:  equipment/utility qualifications, process validation, analytical method validation, or cleaning validation.</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Current driver’s license and auto insurance</span></li>\n</ul>\n<p><br></p>\n<p><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Quality Agents offers a full suite of benefits for full-time employees including:</span></p>\n<p><br></p>\n<ul>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Health, dental and vision insurance</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Life, AD&amp;D and disability Insurance</span><br></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Health savings account for participants in our health plan</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">401k retirement plan</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Paid time off</span></li>\n<li><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Paid holidays</span></li>\n</ul>\n<p><br></p>\n<p><span style=\"color: rgb(0, 0, 0); font-family: helvetica; font-size: 10pt\">Quality Agents accepts applications on an on-going basis in order to build a talent pool of potential candidates. These applications remain open for consideration, as positions become available, for one (1) year from the date of application. After that time, or if your application information changes, please submit your application again.</span></p>\n<p><br><br></p>\n<p><span style=\"font-family: helvetica; font-size: 10pt\"><span style=\"font-weight: bold\">Equal Opportunity &amp; Accessibility Statement</span></span></p>\n<p><span style=\"font-family: helvetica; font-size: 10pt\">Quality Agents, LLC is an equal opportunity employer. We make employment decisions without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, veteran status, or any other protected characteristic under applicable law. </span><span style=\"font-family: helvetica; font-size: 10pt\">We are committed to providing reasonable accommodations for individuals with disabilities throughout the application and hiring process. If you require assistance or accommodation, please contact us.</span></p>",
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    "minimumExperience": "Entry-level",
    "jobOpeningShareUrl": "https://qualityagents.bamboohr.com/careers/1",
    "employmentStatusLabel": "Full-Time"
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}
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