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/hrOnsiteFull Time
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
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
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
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)
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)
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
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.
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.
Quality Assurance Specialist II, Device Engineering
Woburn, Massachusetts, United States
$85k-$105k/yrOnsiteFull Time
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)