{"schemaVersion":"jobsearcher.job.v1","id":"aef2347adc0c35e3e8c4c2dc","url":"https://jobsearcher.com/jobs/aef2347adc0c35e3e8c4c2dc","canonicalUrl":"https://jobsearcher.com/jobs/aef2347adc0c35e3e8c4c2dc","title":"Document Control Specialist","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\n\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\n\nDocument Control Specialist\n\nDescription:\n\nManage controlled documents (SOPs, batch records, protocols, forms) and maintain version control.\nWork with multiple departments to ensure accuracy and quality of document change processes.\nWork with SME's to prepare, update, and review for submission of controlled documents.\n\nQualifications:\n\nBachelor's degree in Science, Pharmacy, Biology, Chemistry, or Business/Administration.\nMinimum 3 years' experience in document control within the pharmaceutical, biotech, or regulated manufacturing environment.\nStrong written and verbal communication skills in both Spanish and English (bilingual).\nProven experience managing controlled documents (SOPs, batch records, protocols, forms) and maintaining version control.\nFamiliar with regulatory requirements (cGMP, FDA, EMA) and compliant document lifecycle practices.\nSkilled in document management systems (DMS) and Microsoft Office (Word, Excel, PowerPoint); experience with enterprise QMS tools preferred.\nAbility to review and improve document formats and structure for clarity, compliance, and usability.\nCoordinate and track training on SOPs and document-related procedures; ensure field resources are trained and records are maintained.\nDetail-oriented, excellent proofreading/editing skills, and capable of producing clear, professional documentation.\nFlexible schedule; willing to work occasional additional hours and rarely on Saturdays when required to meet project deadlines or support critical activities.\n\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\n\nExcited to build something meaningful together? We look forward to hearing from you.\n\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","company":"Validation","rawCompany":"validation","city":"Washington","state":"DC","isRemote":false,"isActive":false,"createdAt":"2026-09-06T14:00:32.405Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"15-1299.03","title":"Document Management Specialists","slug":"document-management-specialists"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"}],"industries":[{"code":"561410","title":"Document Preparation Services","slug":"document-preparation-services"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Document Control Specialist","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\n\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\n\nDocument Control Specialist\n\nDescription:\n\nManage controlled documents (SOPs, batch records, protocols, forms) and maintain version control.\nWork with multiple departments to ensure accuracy and quality of document change processes.\nWork with SME's to prepare, update, and review for submission of controlled documents.\n\nQualifications:\n\nBachelor's degree in Science, Pharmacy, Biology, Chemistry, or Business/Administration.\nMinimum 3 years' experience in document control within the pharmaceutical, biotech, or regulated manufacturing environment.\nStrong written and verbal communication skills in both Spanish and English (bilingual).\nProven experience managing controlled documents (SOPs, batch records, protocols, forms) and maintaining version control.\nFamiliar with regulatory requirements (cGMP, FDA, EMA) and compliant document lifecycle practices.\nSkilled in document management systems (DMS) and Microsoft Office (Word, Excel, PowerPoint); experience with enterprise QMS tools preferred.\nAbility to review and improve document formats and structure for clarity, compliance, and usability.\nCoordinate and track training on SOPs and document-related procedures; ensure field resources are trained and records are maintained.\nDetail-oriented, excellent proofreading/editing skills, and capable of producing clear, professional documentation.\nFlexible schedule; willing to work occasional additional hours and rarely on Saturdays when required to meet project deadlines or support critical activities.\n\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\n\nExcited to build something meaningful together? We look forward to hearing from you.\n\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","datePosted":"2026-09-06T14:00:32.405Z","dateModified":"2026-09-06T14:00:32.405Z","hiringOrganization":{"@type":"Organization","name":"Validation","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Washington","addressRegion":"DC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"aef2347adc0c35e3e8c4c2dc"},"url":"https://jobsearcher.com/jobs/aef2347adc0c35e3e8c4c2dc"}}