6 design manager document controller jobs at 6 companies in Massachusetts
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Document Controls Manager
Boston, Massachusetts, United States
$140k-$155k/yrOnsiteFull Time
WSPTSX: WSP: Global engineering and professional services consulting firm.
7+ YOE7+ years document control experience on design/construction projects; bachelor\u0002s degree or equivalent; EDMS implementation experience; e-Builder or InEight certification; advanced MS Office and SharePoint skills; supervisory experience.
Microsoft SharePoint, Procore, e-Builder, Bluebeam, InEight, Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Visio, MS Office
Alabama or Arizona or California or Colorado or Georgia or Illinois or Louisiana or Massachusetts or Michigan or Missouri or North Carolina or Nevada or New York or Oregon or Texas or Utah or Virginia or Washington
RemoteFull Time
Switch: Designs, builds, and operates data centers.
Coordinate design execution for hyperscale data center projects, manage RFIs/submittals/permits, oversee consultant performance, support permitting and document control, and report schedule/cost/quality metrics.
Magnendo: Medical device startup developing robotic navigation systems for neurovascular stroke and aneurysm procedures.
5+ YOE5+ years project/program management in medical-device or regulated-product development, experience with cross-functional and external partner coordination, knowledge of design controls, risk management, V&V, and regulated documentation; trained in PMP/CAPM/PMI-ACP/SAFe/Lean/Six Sigma or equivalent.
HDR: Global professional services firm specializing in architecture, engineering, and construction.
3+ YOE3+ years in A/E, design-build, P3, project management, or project controls; experience with contract management, risk, document control, claims, and project accounting; QuickBase/low-code a plus; up to 10% travel.
Lila Sciences: Builds AI and autonomous labs for scientific discovery.
4+ YOE4+ years designing complex control systems for automated labs; expertise with PLC/HMI/SCADA, industrial networking, robotics integration, engineering documentation, and vendor management.
Quality Assurance Specialist II, Device Engineering
Woburn, Massachusetts, United States
$85k-$105k/yrOnsiteFull Time
Terrestrial Bio: Private U.S. biotechnology developing needle-free microarray patches for delivering GLP-1 medicines, vaccines, and other therapies.
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)