9 document control specialist jobs at 9 companies in Eliot, ME

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Document Control Specialist I
Lowell, Massachusetts, United States
$26-$34/hr OnsiteFull Time
Cirtec Medical
Cirtec Medical: Outsourced design and manufacturing for complex medical devices.
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
2mo
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Document Control Specialist 1 (Sw)
Berlin or Manchester
$49k-$54k/yr OnsiteFull Time
Eversource Energy
Eversource EnergyNYSE: ES: Delivers electricity, natural gas, and water to New England customers.
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
1w
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Document Control - Qlty
Arundel, Maine, United States
$20-$35/hr OnsiteFull Time
Align Precision
Align Precision: Manufactures high-precision metal components for aerospace and defense sectors.
1+ YOEEntry-level role requiring high school education or equivalent, 1–3 years relevant experience or steady employment, computer skills, attention to detail, arithmetic, and ability to use inspection tools.
Microsoft Excel, Microsoft Word, Microsoft Outlook, micrometers, calipers
3w
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Configuration Control Specialist
Salem, New Hampshire, United States
OnsiteFull Time
Electronic Instrumentation & Technology
Electronic Instrumentation & Technology: Provides comprehensive electronic manufacturing and engineering services.
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)
4d
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Documentation Control Specialist
Merrimack, New Hampshire, United States
$65k-$110k/yr OnsiteFull Time
BAE Systems
BAE SystemsLondon Stock Exchange: BA: Provides advanced defense, aerospace, and security technology solutions.
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)
3w
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QA Specialist II - Doc Control
Bedford, New Hampshire, United States
OnsiteFull Time
PCI Pharma Services
PCI Pharma Services: Integrated pharmaceutical development, manufacturing, and global packaging services.
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
2mo
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Quality Assurance Specialist
Billerica, Massachusetts, United States
$77k-$86k/yr HybridFull Time
Nova Biomedical
Nova Biomedical: Develops and manufactures blood testing analyzers and diagnostic equipment.
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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Manufacturing Operation and Compliance Specialist
Billerica, Massachusetts, United States
OnsiteFull Time
Sun Pharma
Sun PharmaNSE: SUNPHARMA: Develops and manufactures generic and specialty pharmaceutical products worldwide.
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
6d
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Quality Assurance Specialist II, Device Engineering
Woburn, Massachusetts, United States
$85k-$105k/yr OnsiteFull Time
Terrestrial
Terrestrial: Develops micro-array patch technology for patient-friendly drug delivery.
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)