23 document control specialist jobs at 23 companies in Westminster, MA
1mo
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Document Control, Senior Specialist
Bedford, Massachusetts, United States
$111k-$185k/yr HybridFull Time
8+ YOEBS/BA and 8+ years in quality (min 5 years in document control) in pharma/medical device/biologics, experience with eDMS/eQMS (TrackWise Digital, Veeva, MasterControl), GxP documentation, technical writing, and MS Office proficiency.
TrackWise Digital, Veeva, MasterControl, eDMS, eQMS, Microsoft Office
3d
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Document Control Specialist
Andover, Massachusetts, United States
$55k-$70k/yr OnsiteFull Time
2+ YOEHigh school diploma or equivalent; Microsoft Office knowledge, technical document comprehension, SAP exposure, communication skills, and 2+ years in manufacturing with BOM and ECN experience preferred.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint, SAP S/4HANA, Master Data Governance (MDG)
2w
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Document Control Specialist I
Lowell, Massachusetts, United States
$26-$34/hr OnsiteFull Time
2+ YOEHigh school diploma or GED, 2 years of medical device document control experience, PLM and ERP experience, Microsoft Word and Excel proficiency, fluent English, and knowledge of FDA QSR and ISO 13485.
Master Control, Syteline, PLM, ERP, Microsoft Word, Microsoft Excel, CAPA, NCMR, QMS
3mo
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Document Control Specialist 1 (Sw)
Berlin or Manchester
$49k-$54k/yr OnsiteFull Time
0+ YOEDocument control for engineering projects; 0-3 years experience; HS diploma or Associate; MS Office and Adept/SharePoint familiarity; willing to travel CT/MA/NH.
Microsoft Office, Adept, SharePoint, Teams, MS Access
3w
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Document Controls Specialist
Boston, Massachusetts, United States
$108k-$120k/yr OnsiteFull Time
3+ YOEBachelor's degree or equivalent; 3+ years document control experience in transportation or construction; Microsoft Office experience; familiarity with EDMS, SharePoint, Procore, InEight, eBuilder, Bluebeam; strong organization and communication skills.
Microsoft Office, Electronic Document Management System (EDMS), Microsoft SharePoint, Procore, InEight, eBuilder, Bluebeam, Microsoft 365
2mo
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Sr. Quality Specialist, GxP Document Control
Boston, Massachusetts, United States
$105k-$128k/yr HybridFull Time
5+ YOEBachelor's in a scientific discipline (or equivalent), 5+ years QA/document control experience in regulated biotech/pharma, GxP/eQMS knowledge, audit/CAPA/training support, Smartsheet and Microsoft Excel proficiency.
electronic Quality Management Systems (eQMS), Smartsheet, Microsoft Excel
1mo
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Configuration Control Specialist
Salem, New Hampshire, United States
OnsiteFull Time
3+ YOEHigh school diploma, 3+ years related experience, familiarity with Microsoft Excel and Word, experience in document control or regulated/EMS manufacturing preferred; strong PC, organizational, and communication skills.
Microsoft Excel, Microsoft Word, Manufacturing Execution System (MES)
1w
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Documentation Control Specialist
Merrimack, New Hampshire, United States
$65k-$110k/yr OnsiteFull Time
Bachelor's degree or equivalent experience, strong Microsoft Office skills, effective stakeholder communication, task management, and eligibility for a U.S. Department of War security clearance; U.S. citizenship required.
Microsoft Office, Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Product Lifecycle Management (PLM)
2mo
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Senior Production Control Specialist
West Boylston, Massachusetts, United States
$24-$29/hr OnsiteFull Time
ERP expertise (Epicor E10 preferred), strong BOM/materials planning knowledge, MS Office proficiency, cGMP/ISO familiarity, documentation and DHR management; 3+ years planning experience in med-device manufacturing preferred.
ERP, Epicor E10, Microsoft Excel, Microsoft Word, Microsoft Outlook, Microsoft PowerPoint, Microsoft Project, Microsoft Visio
4w
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QA Specialist II - Doc Control
Bedford, New Hampshire, United States
OnsiteFull Time
10+ YOEHigh school diploma and ~10 years industry experience with at least 6 years document control in biotech/pharmaceutical/medical device; eQMS/Master Control experience; advanced cGMP and FDA 21 CFR knowledge; CSV and change control experience; strong written/verbal communication.
Microsoft Office, electronic Quality Management System (eQMS), Master Control
2w
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QA Specialist- Documentation
Waltham, Massachusetts, United States
$110k-$170k/yr OnsiteFull Time
5+ YOEBachelor's degree in a relevant field, 5+ years of GxP quality assurance experience, SOP and controlled document management, Veeva Vault QMS proficiency, FDA and ICH knowledge, and strong communication and organizational skills.
Veeva Vault QMS, Microsoft Office Suite, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
1d
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Production Specialist
Lowell, Massachusetts, United States
$17-$27/hr OnsiteFull Time
1+ YOEHigh school diploma or equivalent and 1–3 years of production or manufacturing experience. Requires manufacturing documentation, quality control, safety, basic computer, fine motor, microscope, and communication skills.
microscope
2mo
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Quality Assurance Specialist
Billerica, Massachusetts, United States
$77k-$86k/yr HybridFull Time
3+ YOEThree to five years QA/QMS experience in regulated industries, Bachelor's preferred, experience with audits, document control, change control, CAPA, and ability to access manufacturing areas and lift 25 lbs.
1w
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Quality Specialist, QMS
Cambridge, Massachusetts, United States
$82k-$92k/yr RemoteFull Time
1+ YOEBachelor's degree, 1–3 years of pharmaceutical or biotech quality experience in GMP, eQMS document control experience, GxP knowledge, audit support, and Microsoft Office proficiency.
eQMS, Veeva Vault Quality Docs, Veeva Vault Quality, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Teams
2mo
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Senior Quality Systems Specialist
Boston, Massachusetts, United States
$95k-$105k/yr OnsiteFull Time
5+ YOE5+ years in quality assurance/systems in regulated manufacturing; experience with CAPA, deviations, investigations, change and document control, audits, SOPs, root cause analysis, QMS/ERP, and strong written documentation and cross-functional collaboration.
QMS, ERP
1mo
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Quality Assurance Specialist
Charlestown, New Hampshire, United States
OnsiteFull Time
Experience in quality assurance/control, knowledge of industry quality standards and regulations, strong analytical and problem-solving skills, attention to detail, communication skills, QMS and auditing experience, and proficiency in documentation and reporting.
Quality Management Systems (QMS)
2w
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Information Security Risk Specialist
Lexington, Massachusetts, United States
$62k-$141k/yr HybridFull Time
3+ YOERequires 3+ years in cybersecurity, 2+ years with DoD RMF accreditation, Secret clearance, bachelor's degree, DoD 8140 IAM Level 1, and experience with security controls and technical documentation.
Risk Management Framework (RMF), STIGs, NIST 800-53, NIST 800-37, AWS, Xacta, eMASS, Azure, GovCloud, Kubernetes, Docker, SIEM, SOAR, Splunk, ElasticSearch, OpenSearch, Atlassian Suite, Jira, Confluence
3mo
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Final Release Specialist II - 2nd Shift
Devens, Massachusetts, United States
$23-$31/hr OnsiteFull Time
3+ YOE3+ years in medical device manufacturing with Final Release/Document Control; read blueprints; review DHRs/Batch Records; manage nonconformances and CAPAs.
ERP, QMS
2w
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Manufacturing Operation and Compliance Specialist
Billerica, Massachusetts, United States
OnsiteFull Time
5+ YOERequires a high school diploma, 5+ years supporting manufacturing or quality departments, and knowledge of GMP, quality systems, CAPAs, change controls, deviations, documentation, and compliance reporting.
Track Wise, EDMS, MasterControl
1w
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Quality Assurance Specialist II, Device Engineering
Woburn, Massachusetts, United States
$85k-$105k/yr OnsiteFull Time
4+ YOERequires 4–5 years of quality experience in a cGMP-regulated medical device, pharmaceutical, biologics, or combination product environment, plus ISO 13485, FDA QSR, design controls, risk management, validation, and GMP documentation experience.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Quality Management System (QMS), Design History File (DHF), Design Verification and Validation (DVV), Failure Mode and Effects Analysis (FMEA), Test Method Validation (TMV), Process Validation (PV), Corrective and Preventive Action (CAPA)
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