23 document control specialist jobs at 22 companies in Blackstone, MA
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Document Control Specialist
Andover, Massachusetts, United States
$55k-$70k/yrOnsiteFull Time
VicorNASDAQ: VICR: Designs and manufactures high-performance modular power conversion systems.
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)
LantheusNASDAQ: LNTH: Develops and commercializes radiopharmaceutical and diagnostic imaging products.
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
Document Control Specialist (Norwell, MA, US, 02061)
Norwell or Edmonton or Superior or Duluth
$30-$35/yrHybridFull Time
WECTEC Staffing Services: Provides technical staffing and contingent labor for energy industries.
2+ YOEUniversity degree or technical diploma; 2+ years in document/records management; knowledge of drawing management systems; EDMSLink, BIM-JIRA, MS Access, Excel.
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
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
Skyhawk Therapeutics: Develops small molecule drugs that modify RNA expression.
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
REXA: Designs and manufactures high-performance Electraulic actuators and valves.
3+ YOERequires 3+ years supporting a QMS in manufacturing or regulated production, ISO 9001 knowledge, audit and document control experience, strong communication, organization, and Microsoft Office skills.
Eastern BankNASDAQ: EBC: Provides personal banking, commercial lending, and wealth management services.
3+ YOEBachelor's degree and 3–5 years in loan servicing, operations, or documentation. Requires quality control, reconciliation, credit reporting, regulatory, analytical, documentation, and Microsoft Office skills.
FIS IBS Insight, eOSCAR, Microsoft Excel, Microsoft Outlook, Microsoft Word
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.
Amylyx PharmaceuticalsNASDAQ: AMLX: Develops treatments for neurodegenerative diseases and endocrine conditions.
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
ABCorp: Produces secure payment cards and provides additive manufacturing solutions.
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.
Fluor CorporationNYSE: FLR: Provides global engineering, procurement, construction, and project management services.
3+ YOEHigh school diploma/GED, 3+ years experience with PLCs, process control, and instrumentation preferred; strong troubleshooting, electrical safety (LOTO/arc flash) knowledge, ability to work off-hours and document work using CMMS (Maximo).
Tri-Mack Plastics Manufacturing: Manufactures high-temperature thermoplastic components for aerospace and defense.
2+ YOERequires 2+ years in manufacturing quality control, blueprint and GD&T proficiency, inspection and metrology experience, AS9100/ISO familiarity, technical documentation skills, and MS Office, Excel, and Outlook proficiency.
CMMs, vision inspection systems, optical comparators, Microsoft Office, Microsoft Excel, Microsoft Outlook, ISO 9001, AS9100, NADCAP, GD&T
Booz Allen HamiltonNYSE: BAH: Consulting and technology services for government and commercial clients
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.
VulcanForms: Provides industrial-scale metal additive manufacturing and precision machining services.
3+ YOE3+ years in medical device manufacturing with Final Release/Document Control; read blueprints; review DHRs/Batch Records; manage nonconformances and CAPAs.
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)