201 quality documentation jobs at 126 companies in Attleboro, MA
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Quality Documentation Supervisor
Mansfield, Massachusetts, United States
$90k-$125k/yrOnsiteFull Time
EmersonNYSE: EMR: Engineering industrial automation and software solutions for global industries.
1+ YOE2+ MgmtHigh school diploma or GED, 2+ years supervisory experience, 1–2 years manufacturing QA experience, proofreading, process improvement, multitasking, independent work, and deadline management.
Microsoft Office, Microsoft Excel, Microsoft Access
Gainesville or Caguas or Boston or United States or Dominican Republic or Mexico or Germany or Canada or South America
OnsiteFull Time
Mentor Technical Group: Provides engineering and compliance services for life sciences industry.
Bachelor's degree in Engineering, Science or related; knowledge of cGMP and FDA regulations; strong documentation and communication skills; experience in regulated industries preferred; Microsoft Office proficiency; bilingual (English/Spanish) preferred.
Tri-Mack Plastics Manufacturing: Manufactures high-temperature thermoplastic components for aerospace and defense.
2+ YOE2+ years manufacturing quality control experience (preferably AS9100 aerospace); proficiency in blueprint reading, GD&T, metrology/CMM/vision inspection, MS Office; ability to prepare FAI packages and ensure traceability; must pass background check and be authorized to work in the U.S.
AS9100, ISO, NADCAP, Geometric Dimensioning and Tolerancing (GD&T), CMMs, vision inspection systems, optical comparators, ballooning and inspection software, manual and digital handheld inspection instruments, metrology tools, gauges, Microsoft Office, Microsoft Excel, Microsoft Outlook
TransMedicsNASDAQ: TMDX: Preserving and transporting donor organs for medical transplantation.
3+ YOE3-5 years in documentation control; HS diploma; familiar with eQMS; knowledge of FDA 21 CFR Part 820/Part 11, ISO 13485, EU MDR; strong attention to detail and communication; MS Office proficiency.
Plansee Group: Global manufacturer of high-performance molybdenum and tungsten components.
Associate's degree preferred, experience with document control, AS9100 familiarity, SAP and Microsoft Office proficiency, attention to detail, and basic quality administration skills.
SAP, Microsoft Excel, Microsoft Word, Microsoft Outlook
CAS Holdings: Provides industrial automation products and integrated engineering services.
2+ YOE2+ years quality/document control or related experience preferred; practical ISO 9001 understanding; strong written communication; Excel, Outlook, Teams, and SharePoint skills; high school diploma or equivalent required.
NetSuite, MaintainX, SharePoint, Microsoft Excel, Microsoft Outlook, Microsoft Teams
Waltham or United States or Puerto Rico or North America
$78k-$113k/yrHybridFull Time
SanofiEuronext Paris: SAN: Researches, develops, and manufactures medicines and vaccines globally.
5+ YOEBachelor's degree or equivalent; minimum 5 years experience in training, learning management, quality, compliance, documentation, or QA; LMS and iLearn experience preferred; familiarity with GxP training requirements.
VulcanForms: Provides industrial-scale metal additive manufacturing and precision machining services.
3+ YOE3+ years in medical device or aerospace quality with knowledge of FDA requirements, ISO 13485/AS9100/ISO9001, QMS, CAPA, NCR, document control, procedure writing, audits, and quality metrics/KPIs.
The Middlesex Corporation: Constructs heavy civil infrastructure including highways, bridges, and rail.
2+ YOEBachelor's in engineering or construction management; 2+ years in construction quality control management; strong QA/QC, planning, and documentation skills; PM software experience.
Project management software, Construction QA/QC tools
PAVmed Inc.NASDAQ: PAVM: Diversified medical technology developing diagnostic and health solutions.
3+ YOEBachelor's in engineering or life sciences, 3+ years in FDA/ISO 13485 medical device quality environments, QMS knowledge (document control, CAPA, audits), eQMS and Microsoft Office proficiency.
Microsoft Office, eQMS, quality documentation systems
Quantic Evans: Manufactures high-energy density capacitors for aerospace and defense.
Experience in quality or manufacturing roles, familiarity with ISO 9001/AS9100, NC/CAPA processes, document control, audit support, Excel/ERP proficiency, strong written/verbal communication and attention to detail.
Microsoft Excel, Microsoft Office, ERP, FMEA, CAPA, IPC standards
Optos: Develops and manufactures ultra-widefield retinal imaging devices.
Experience with calibration, first/second party audits, device history records, inspections, document control, and ISO 13485 internal auditing training preferred.
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.
Plansee Group: Manufactures high-performance materials and tools from molybdenum and tungsten.
Support QMS and document control per AS9100, assist audits, track nonconformances and deviation waivers, perform data entry and reporting; associate's degree preferred and SAP/MS Office experience helpful.
SAP, Microsoft Excel, Microsoft Word, Microsoft Outlook
Tango TherapeuticsNasdaq Capital Market: TNGX: Develops precision cancer medicines using synthetic lethality principles.
8+ YOEManage and continuously improve QMS for GxP compliance, document control, training, records, CAPA, metrics, and audit readiness; 8+ years QA/Compliance and bachelor\u0002s in life sciences/quality required.
Charles River Center: Provides residential and vocational support for people with disabilities.
3+ YOE3+ years human services experience preferred; experience with DDS regulations, audits, data analysis, documentation review, training, and quality improvement.
ZOLL Medical: Manufactures medical devices and software for emergency care.
2+ YOEBachelor's in engineering or related,2+ years quality/product engineering experience in regulated industry,experience with complaint investigations,risk management,CAPA,and documentation;strong communication and data analysis skills.
Access Vascular: Develops biomaterial catheters that reduce clinical complications during intravenous therapy.
5+ YOEBachelor's in Engineering or Life Sciences; 5+ years quality systems in medical devices; QMS experience (FDA 21 CFR Part 820, ISO 13485); CAPA, document control, audits; CQE/CMDA or ISO Lead Auditor a plus.
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