Home › Companies › Americanregent › Validation Engineer II
Validation Engineer II
Americanregent · New Albany, OH · Deleted · Workday Recruiting
Job facts
| Field | Value |
|---|---|
| Company | Americanregent |
| Title | Validation Engineer II |
| Normalized title | - |
| Department / team | - |
| Location | New Albany, OH, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | - |
| Status | deleted |
| ATS provider | Workday Recruiting |
| Posted / first seen | 2026-04-10 / 2026-05-30 |
| Changed / last seen | 2026-06-06 / 2026-06-03 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Americanregent. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Workday Recruiting. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in New Albany. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Americanregent |
| Source | 3e6241e5-b100-4b1d-bb11-8ff49b40d4fe |
| ATS provider | Workday Recruiting |
Description
The Validation Engineer II will develop and execute validation plans, protocols and reports that support the business needs of the company. The position will oversee and support the qualification and validation of the pharmaceutical manufacturing processes and ensure that the facility, systems and processes perform according to internal specifications, comply with current GMPs and are maintained in a validated state. This position will report into the Manager, Validation.
Essential Duties and Responsibilities
Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.
The incumbent will act as a Subject Matter Expert (SME) for a designated discipline/s. Focusing on Packaging, Equipment and Facilities and/or Cleaning Validation, the incumbent will develop and execute validation protocols associated with the installation, operation and performance qualification and requalification of equipment, utilities and processes used in the manufacture of aseptically produced parenteral pharmaceuticals, including lyophilized solutions. The SME will provide technical expertise during design, evaluation and procurement of new equipment, utilities or processes. Maintain life cycle documentation for equipment and systems, including User Requirements Specifications, Functional Specifications, Hardware Design Specifications, Software Design Specifications, and Configuration Specifications. Support all aspects of the Validation Life Cycle, from design through operation and improvement. Plan, coordinate and manage site-specific validation project activities including protocol development/approval, work schedules and lifecycle documentation. Review qualification/requalification packages for completeness and accuracy, sound rationale, compliance with validation policies and procedures and accurate data analysis. Provide and document training to personnel performing validation activities. Provide the technical input to address validation deviations and provide assessments for change requests and identify qualification requirements to ensure compliance to GMP’s and that the validated state is maintained. Coordinate protocol approvals and produce accurate summary reports. Develop or contribute to the development of SOPs related to equipment or processes for which the incumbent serves as SME. Remain current with FDA guidance’s and requirements regarding the validation of aseptic manufacturing processes; ensures all work is performed and documented in accordance with existing Company policies and procedures, as well as cGMP and health and safety requirements. Provide technical and troubleshooting assistance for identifying and addressing manufacturing anomalies or deviations. Interface with Quality, Manufacturing, Packaging and Engineering groups to facilitate and drive validation execution and completion. Perform any other tasks/duties as assigned by management. Education Requirements and Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.
Bachelor’s Degree in Life Sciences, Engineering or equivalent and 3 years of validation experience in a Pharmaceutical or related industry OR Associate’s Degree and 5 years of validation experience in a Pharmaceutical or related industry OR High School Diploma / GED and 8 years experience in a Pharmaceutical or related industry Strong knowledge and understanding of cGMP regulations and practices pertaining to validation principals, manufacturing processes, quality systems, engineering design fundamentals, regulatory agency expectations and industry trends. Ability to read/interpret engineering drawings and design documents. Strong knowledge of MS-Office software and PC Skills required. Good technical writing skills. Excellent communication, problem-solving, planning and organization skills. Ability to work independently with minimum supervision, including making sound decisions and managing priorities that are in alignment with departmental and site directives. Ability to mentor and direct junior team members. Ability to work within a team-oriented environment. Ability to work overtime as needed. Travel for off site training and projects may be required on occasion ( Physical Environment and Requirements
Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees. Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. PPE is essential for the health and safety of employees. Employee must be able to occasionally lift and/or move up to 15 pounds. American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.
Applicants have rights under Federal Employment Laws.
FMLA poster: https://www.dol.gov/whd/regs/compliance/posters/fmlaen.pdf
Know Your Rights: Know Your Rights: Workplace discrimination is illegal ( eeoc.gov )
Employee Polygraph Protection Act: https://www.dol.gov/whd/regs/compliance/posters/eppac.pdf
Alert: We’re aware of individuals impersonating our staff to target job seekers. Please note:
· All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address.
· Our recruiting process includes multiple in person and/or video interviews and assessments.
· If you are unsure about the legitimacy of a message, contact John Rossini at [email protected] before responding.
· We never request payment, bank information, or personal financial details during our offer process.
Your security is important to us, and we encourage you to stay vigilant when job searching.
American Regent Inc. endeavors to make https://careers.americanregent.com/ accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email [email protected] .
Full job record
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| Board ID | 3e6241e5-b100-4b1d-bb11-8ff49b40d4fe |
| Provider | workday |
| Provider Job Key | /job/New-Albany-OH/Validation-Engineer-II_R-103187 |
| Title | Validation Engineer II |
| Normalized Title | — |
| Status | deleted |
| Active | no |
| Location Text | New Albany, OH |
| Department | — |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | OH |
| City | New Albany |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://americanregent.wd1.myworkdayjobs.com/American_Regent_Careers/job/New-Albany-OH/Validation-Engineer-II_R-103187 |
| Apply URL | https://americanregent.wd1.myworkdayjobs.com/American_Regent_Careers/job/New-Albany-OH/Validation-Engineer-II_R-103187 |
| First Seen At | 2026-05-30 05:46:47Z |
| Last Seen At | 2026-06-03 10:25:04Z |
| Last Checked At | 2026-06-06 09:42:25Z |
| Last Changed At | 2026-06-06 09:42:25Z |
| Inactive At | 2026-06-06 09:42:25Z |
| Source Posted At | 2026-04-10 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://bluework-jobs-prod-raw-590183727216/raw/provider=workday/board=americanregent.wd1.myworkdayjobs.com|americanregent|American_Regent_Careers/date=2026-06-03/2026-06-03T10-25-00-442Z-8ea483345c48195f6321b0a5e55d26361b64dac7057242e2f0c249aa550e896a.json |
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"jobDescription": "<p>The Validation Engineer II will develop and execute validation plans, protocols and reports that support the business needs of the company. The position will oversee and support the qualification and validation of the pharmaceutical manufacturing processes and ensure that the facility, systems and processes perform according to internal specifications, comply with current GMPs and are maintained in a validated state. This position will report into the Manager, Validation.</p><p><b>Essential Duties and Responsibilities</b></p><p>Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.</p><ul><li>The incumbent will act as a Subject Matter Expert (SME) for a designated discipline/s. Focusing on Packaging, Equipment and Facilities and/or Cleaning Validation, the incumbent will develop and execute validation protocols associated with the installation, operation and performance qualification and requalification of equipment, utilities and processes used in the manufacture of aseptically produced parenteral pharmaceuticals, including lyophilized solutions.</li><li>The SME will provide technical expertise during design, evaluation and procurement of new equipment, utilities or processes. </li><li>Maintain life cycle documentation for equipment and systems, including User Requirements Specifications, Functional Specifications, Hardware Design Specifications, Software Design Specifications, and Configuration Specifications.</li><li>Support all aspects of the Validation Life Cycle, from design through operation and improvement.</li><li>Plan, coordinate and manage site-specific validation project activities including protocol development/approval, work schedules and lifecycle documentation.</li><li>Review qualification/requalification packages for completeness and accuracy, sound rationale, compliance with validation policies and procedures and accurate data analysis.</li><li>Provide and document training to personnel performing validation activities.</li><li>Provide the technical input to address validation deviations and provide assessments for change requests and identify qualification requirements to ensure compliance to GMP’s and that the validated state is maintained.</li><li>Coordinate protocol approvals and produce accurate summary reports.</li><li>Develop or contribute to the development of SOPs related to equipment or processes for which the incumbent serves as SME.</li><li>Remain current with FDA guidance’s and requirements regarding the validation of aseptic manufacturing processes; ensures all work is performed and documented in accordance with existing Company policies and procedures, as well as cGMP and health and safety requirements.</li><li>Provide technical and troubleshooting assistance for identifying and addressing manufacturing anomalies or deviations. </li><li>Interface with Quality, Manufacturing, Packaging and Engineering groups to facilitate and drive validation execution and completion.</li><li>Perform any other tasks/duties as assigned by management.</li></ul><p><b>Education Requirements and Qualifications</b></p><p>To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.</p><ul><li>Bachelor’s Degree in Life Sciences, Engineering or equivalent and 3 years of validation experience in a Pharmaceutical or related industry OR</li><li>Associate’s Degree and 5 years of validation experience in a Pharmaceutical or related industry OR</li><li>High School Diploma / GED and 8 years experience in a Pharmaceutical or related industry</li><li>Strong knowledge and understanding of cGMP regulations and practices pertaining to validation principals, manufacturing processes, quality systems, engineering design fundamentals, regulatory agency expectations and industry trends.</li><li>Ability to read/interpret engineering drawings and design documents.</li><li>Strong knowledge of MS-Office software and PC Skills required.</li><li>Good technical writing skills.</li><li>Excellent communication, problem-solving, planning and organization skills.</li><li>Ability to work independently with minimum supervision, including making sound decisions and managing priorities that are in alignment with departmental and site directives.</li><li>Ability to mentor and direct junior team members.</li><li>Ability to work within a team-oriented environment.</li><li>Ability to work overtime as needed.</li><li>Travel for off site training and projects may be required on occasion (<10%)</li></ul><p><b> Physical Environment and Requirements</b></p><ul><li>Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees.</li></ul><ul><li>Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. PPE is essential for the health and safety of employees. </li></ul><ul><li>Employee must be able to occasionally lift and/or move up to 15 pounds.</li></ul><p><span style=\"color:#000000\">American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.</span></p><p><span style=\"color:#000000\">Applicants have rights under Federal Employment Laws. </span></p><ul><li><p><span style=\"color:#000000\">FMLA poster: </span><a target=\"_blank\" href=\"https://linkprotect.cudasvc.com/url?a=https%3a%2f%2fwww.dol.gov%2fwhd%2fregs%2fcompliance%2fposters%2ffmlaen.pdf&c=E,1,e7MTuJKPMcGBUQSBja_9gRcH_uIiF8PloXVJrgsr-QJMtlBkKsdA4_QnK012agsZDURLxw6DAkszmgxMKrBDUo5eHojPl2QB1yH63TNQD1mlBe9d1OI,&typo=1&ancr_add=1\"><span style=\"color:#000000\">https://www.dol.gov/whd/regs/compliance/posters/fmlaen.pdf</span></a></p></li><li><p><span style=\"color:#000000\">Know Your Rights: </span><a target=\"_blank\" href=\"https://linkprotect.cudasvc.com/url?a=https%3a%2f%2fprotect.checkpoint.com%2fv2%2fr01%2f___https%3a%2fwww.eeoc.gov%2fsites%2fdefault%2ffiles%2f2023-06%2f22-088_EEOC_KnowYourRights6.12ScreenRdr.pdf___.YzJ1Ompqa2VsbGVyOmM6bzpjNjhjZmFmZDNmMjIwNGI4Nzc2YzJiZDM4OTU1YmVjMTo3OjI0ZGI6OGRmZDZjYzU0MjI0ZmQ5NzcwY2UxNWI5Y2Q1NDMyMDQyNzhjYzVlNThkN2ZlMWUyZGQzZTQxMmU0NzVjOWNkMTpoOlQ6Tg&c=E,1,vPNBSsNCZkiDYKdJbiUoASO06l2hz5TjOrkElSpCGo6rKM9_UnDDdiUiisVe_u_hDnErnMyZrrYFajU_1WYes4xp8wKLMNsIfkk5lC-byLk,&typo=1\"><span style=\"color:#000000\">Know Your Rights: Workplace discrimination is illegal (</span></a><a target=\"_blank\" href=\"https://linkprotect.cudasvc.com/url?a=https%3a%2f%2feeoc.gov&c=E,1,cjVpBwdOiOtIADcWufJyfSjNG1dODoJmyp3miK_HRnBe1o97PTgDuyjnNDBLz4pwjrhg65ahvhoVDUbCpxbsGZWpK7Z3h9FuUpX-E9DwaP40lueDsMZ4&typo=1&ancr_add=1\"><span style=\"color:#000000\">eeoc.gov</span></a><span style=\"color:#000000\">)</span></p></li><li><p><span style=\"color:#000000\">Employee Polygraph Protection Act: </span><a target=\"_blank\" href=\"https://linkprotect.cudasvc.com/url?a=https%3a%2f%2fwww.dol.gov%2fwhd%2fregs%2fcompliance%2fposters%2feppac.pdf&c=E,1,oHcPK-z_gYZlaKfXH04MY5FHYlmjPRxZ6mzOox7dO-jRqcAnoi0bEVENBbNnFTGRT69Q-Fe5g-fsUeT3CooY-hk7oQXIuTljgKFHvzEiYZsJgaT3Fw,,&typo=1&ancr_add=1\"><span style=\"color:#000000\">https://www.dol.gov/whd/regs/compliance/posters/eppac.pdf</span></a></p></li></ul><p></p><p><span style=\"color:#a33600\"><b>Alert: We’re aware of individuals impersonating our staff to target job seekers. Please note:</b></span></p><p><span style=\"color:#000000\"><span style=\"font-size:10pt\">·</span><span style=\"font-size:7pt\"> </span>All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address.</span></p><p><span style=\"color:#000000\"><span style=\"font-size:10pt\">·</span><span style=\"font-size:7pt\"> </span>Our recruiting process includes multiple in person and/or video interviews and assessments.</span></p><p><span style=\"color:#000000\"><span style=\"font-size:10pt\">·</span><span style=\"font-size:7pt\"> </span>If you are unsure about the legitimacy of a message, contact John Rossini at </span><a target=\"_blank\" href=\"mailto:jrossini@americanregent.com\"><span style=\"color:#000000\"><u>jrossini@americanregent.com</u></span></a><span style=\"color:#000000\"> before responding.</span></p><p><span style=\"color:#000000\"><span style=\"font-size:10pt\">·</span><span style=\"font-size:7pt\"> </span>We never request payment, bank information, or personal financial details during our offer process.</span></p><p><span style=\"color:#000000\">Your security is important to us, and we encourage you to stay vigilant when job searching.</span></p><p></p><p><span style=\"color:#000000\">American Regent Inc. endeavors to make </span><a target=\"_blank\" href=\"https://americanregent.com/Careers\"><span style=\"color:#000000\">https://careers.americanregent.com/</span></a><span style=\"color:#000000\"> accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email </span><a target=\"_blank\" href=\"mailto:hrtalentacquisition@americanregent.com\"><span style=\"color:#000000\">hrtalentacquisition@americanregent.com</span></a><span style=\"color:#000000\">. </span></p>",
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