Our success as the global leader in UV curing systems starts with our people. For more than three decades, our engineers, chemists, business managers, and other staff members have been committed to developing innovative, eco-friendly technologies that push the industry forward. We work hard, and we care deeply—for our technology, our customers, and for one another. Joining the Miltec family means the potential to change both your career trajectory and the world as we know it. Shape the Future Become a part of the sustainable solution that is UV curing and positively impact the environment for generations to come. Join our Family Team dinners. Service projects. Gratitude luncheons. Our family-owned business is a tight-knit group and we look forward to welcoming new faces. Grow with Us Our small team dynamic gives you the flexibility to cross-collaborate, explore different specialty areas, and learn new skills. Our Core Values Teamwork Contributions Respect Success Trust Integrity Our Hiring Process Our hiring process is simple and direct, and we are with you every step of the way, keeping you informed and introducing you to our culture. If you application meets all requirements, we’ll reach out to schedule a brief phone call. Interviews We’ll meet with you online or in person to talk about your qualifications. Qualified candidates will complete two interviews. Profile Assessment Next, we’ll give you a task or scenarios to see how you respond in certain situations. Offer Finally, we’ll make you an offer that includes compensation and benefits. Current Openings Position: Document Control Administrator Location: Stevensville , MD Job Id: 154 # of Openings: 0 Document Control Administrator Location:Stevensville, Maryland Employment Type:Full-Time ABOUT USFor over 36 years, Miltec has been a global leader in the UV curing industry, proudly serving more than 30 diverse manufacturing market segments. We specialize in delivering high-quality, custom-designed UV curing systems and replacement parts, all made in the USA. POSITION OVERVIEWThe Document Control Administrator is a key member of the Quality Department, providing support across all departments and ensuring the effective administration of the Document Control and Quality Management Systems. This role requires a high level of proficiency in document control and quality system processes, with a strong focus on accuracy, compliance, and consistency. The ideal candidate demonstrates exceptional attention to detail, strong communication skills, and the ability to train and support employees in the proper use of Document Control and Quality Management System processes as outlined in the duties and responsibilities. Document & Records ManagementCreate, revise, format, release, distribute, and archive controlled documents including Standard Operating Procedures (SOPs), Work Instructions, Forms, Engineering Drawings, Specifications, and Engineering Change Orders (ECOs).Maintain document control system to ensure proper version control, revision history, and document traceability.Manage electronic and physical document storage, retrieval, retention, and disposition activities.Verify documentation for completeness, accuracy, proper approvals, and compliance with established procedures before release.Ensure obsolete documents are removed from points of use and appropriately archived.Coordinate controlled distribution of documents to authorized employees and departments.Support departmental staff with document creation, updates, formatting, and revision activities.Maintain document indexes, logs, and tracking systems to ensure accessibility and traceability. Engineering Change & Configuration ManagementAdminister the Engineering Change Order (ECO) process from initiation through implementation and closure.Prepare, route, track, and maintain ECO documentation and approval records.Update Bills of Material (BOMs), Bills of Manufacturing (BOMfg), part numbers, and associated records within Miltec's MRP system.Coordinate with Engineering, Manufacturing, Quality, and Materials teams to ensure timely implementation of approved engineering changes.Maintain configuration control of engineering drawings, product specifications, and revision-controlled records.Schedule and facilitate change review meetings to support timely processing of engineering changes. Quality Management System AdministrationSupport the maintenance and effectiveness of Miltec's Quality Management System.Administer Corrective Action Reports (CARs), Supplier Corrective Action Reports (SCARs), and associated quality system workflows.Coordinate corrective action activities, assign tasks, monitor progress, and maintain quality records.Track quality system metrics and maintain associated databases and reports.Assist with quality system reviews, process improvements, and continuous improvement initiatives.Ensure quality records are maintained in accordance with retention and internal process requirements. Training Management & ComplianceEvaluate document revisions to determine training requirements and employee impact.Coordinate training activities associated with new or revised procedures, work instructions, forms, and quality system requirements.Notify trainers, supervisors, and affected employees of required training activities.Maintain accurate employee training records, including:Training datesRevision levelsTraining materialsTrainer approvalsCompetency verificationEnsure training records are linked to document revisions for complete traceability.Conduct and support training related to document control processes, QMS requirements, ECO processes, CAR processes, and related systems. Audit & Compliance SupportPrepare and organize documentation for internal, customer, and other audits.Provide timely retrieval of records and objective evidence during audit activities.Support audit findings, corrective actions, and follow-up activities.Assist in auditing internal processes and supplier quality systems as assigned.Verify documentation practices comply with company procedures, customer requirements, and applicable quality standards. Data Management & ReportingDevelop and maintain tracking databases, dashboards, and reporting tools supporting quality and document control activities.Generate status reports for document revisions, ECOs, CARs, SCARs, training compliance, and audit activities.Analyze trends and performance metrics to identify opportunities for process improvement.Support management reviews with data collection and reporting activities.Ensure the integrity, security, and accessibility of quality-related data and records.Cross-Functional Support & Continuous ImprovementServe as a subject matter resource for document control and quality system processes.Collaborate with Engineering, Manufacturing, Materials, Operations, and Quality teams to improve workflow efficiency.Recommend improvements to document management systems, workflows, and business processes.Participate in continuous improvement initiatives that enhance compliance, efficiency, and effectiveness.Support special projects and additional Quality Department initiatives as assigned. Minimum QualificationsEducationAssociate degree preferred; Engineering, Technical, Business, or Quality-related discipline.Equivalent combination of education and relevant experience may be considered. Experience3-5 years of experience in Document Control, Quality Systems, Engineering Administration, or a related function within a manufacturing environment.Experience managing document lifecycles, revisions, approvals, retention schedules, and controlled records.Experience supporting corrective action systems and engineering change management processes preferred.Experience using Affinity Designer, Adobe InDesign, and Canva is a plus. Technical SkillsProficiency with SharePoint, Microsoft Office Suite, and document management systems.Experience with SolidWorks PDM or comparable Product Data Management (PDM) systems preferred.Experience with ERP/MRP systems and Bill of Material maintenance.Working knowledge of Quality Management Systems and compliance requirements.Database development, reporting, and data analysis experience preferred. Core CompetenciesAttention to DetailOrganization and PlanningProcess DisciplineQuality OrientationAccountabilityCommunication SkillsCollaboration and TeamworkProblem SolvingInitiative and Self-DirectionTime ManagementContinuous Improvement MindsetDependability and Integrity Physical RequirementsWork is sedentary in nature – regularly required to sit, walk and stand. Must be able to talk and hear in-person and by telephone. Must be able to use hands repetitively to operate standard office equipment. WHY JOIN US?BENEFITSMiltec offers a comprehensive benefits package including:Flexible work schedule optionsHealth InsuranceDental InsuranceVision InsurancePaid Time Off (PTO)401k matchingOpportunities for professional development and growth. WORK HOURSMiltec business hours are Monday through Friday, 8 am to 5 pm. We offer three optional flexible work schedules:Plan A – Monday through Friday, 8:00 a.m. to 5:00 p.m., 1 hour lunch (40 hours)Plan B – Monday through Thursday 7:00 a.m. to 6:00 p.m., 1 hour lunch OR 7:00 a.m. to 5:30 p.m., 30-minute lunch (40 hours) – Friday offPlan C – Tuesday through Friday 7:00 a.m. to 6:00 p.m., 1 hour lunch OR 7:00 a.m. to 5:30 p.m., 30-minute lunch (40 hours) – Monday off Pay Range:$27 - $31 per hour Working at Miltec means stability and security. We offer employees a competitive package of benefits, including:
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