Jobs at Spectrum Plastics Group

Maintains the quality management system and ensures compliance with applicable regulations, ISO standards, customer requirements, and business objectives. Leads CAPA completion, supports complaints and MRB processes, coordinates internal, customer, and supplier audits, prepares management review reports, and manages employee training records. Reviews material purity information and provides guidance on quality procedures, standardization, and requirements.

Lead quality for medical-device product/process development ensuring ISO 13485 and FDA QSR compliance. Develop/execute validation protocols (TMV, IQ/OQ/PQ), maintain risk files and FMEAs, program and validate CMM/vision systems, drive inspection method qualification and SPC/DOE analysis, implement eQMS and Quality 4.0, lead CAPA investigations, train staff, and support Lean Six Sigma continuous improvement and KPI reporting with PowerBI.

Lead plant operations to achieve productivity, quality, safety, and on-time delivery. Develop manufacturing processes, manage tooling and capacity, recruit and mentor operations teams, drive continuous improvement and budgeting, support new business quoting and resource planning, and collaborate with executive leadership to meet growth and profitability objectives.

Supervise shift operations in a medical sterile packaging converting environment, ensuring safety, GMP/ISO compliance, product quality, staffing, training, documentation, inventory control, and continuous improvement while resolving production issues and communicating metrics to leadership.

Develops CMM and Vision System programs and fixtures for product development, supports quality activities, mentors technicians, and manages measurement projects.

The Toolmaker III assembles molds, manages workflows, diagnoses tool issues, performs maintenance, and ensures quality and safety standards in production.

The Planner-Scheduler role involves creating and maintaining production schedules, managing raw material planning, coordinating supply chain activities, and ensuring inventory and production efficiency. The role requires collaboration with manufacturing and supply chain teams to address production issues and maintain material availability.

Lead daily thermoplastics manufacturing operations to meet quality, delivery, cost, and performance targets. Drive process development, continuous improvement, cross-functional collaboration, and program execution. Manage budgets, metrics, documentation (BOMs, ECOs), and escalated production issues while building and mentoring high-performing teams to ensure customer satisfaction and on-time delivery.

Lead the site Quality organization for blown-film extrusion and converting, maintain and improve the Quality Management System (ISO 9001, FSSC 22000), ensure food-safety and medical-packaging compliance, drive audits and CAPA, deploy SPC/PFMEA/control plans and structured problem-solving (5 Why, A3, 8D), reduce variation and defects, and develop the quality team while partnering with Operations, Engineering, Supply Chain, and Commercial.

Lead site EHS for a 24/7 blown-film extrusion and converting facility: own EHS management system, regulatory compliance, incident investigation, risk management, contractor safety, environmental stewardship, training, audits, and continuous improvement while developing the EHS team and partnering across operations and support functions.

The role involves driving accurate pricing outcomes through technical estimations and customer engagement, ensuring efficient cost processes and collaboration with multiple teams.

Lead end-to-end development and scale-up of medical films and flexible packaging—from translating customer requirements to prototype, pilot-scale process development, IQ/OQ/PQ validation, and tech transfer to commercial manufacturing—ensuring regulatory compliance, quality, and cross-functional project leadership.

Lead and deliver QMS and cross-functional projects to ensure compliance with ISO 9001, FSSC 22000, and ISO 13485. Establish project governance, schedules, risk management, and stakeholder communication. Coordinate CAPA execution, internal audit readiness, supplier and production readiness, and change implementation. Drive continuous improvement, documentation, reporting, and measurable results while partnering with Quality, Operations, Engineering, and Supply Chain.

The Regional Business Manager drives growth by managing customer accounts, developing business opportunities, and executing sales strategies in the medtech sector.

Provides administrative support to HR including managing agency staff interviews/onboarding, visitor management, badge administration (Lenel), recordkeeping, time reporting, orientations, clerical tasks, event support, and coordination with IT for accounts.

Lead site quality assurance activities to maintain ISO and FDA regulatory compliance, manage audits, develop and train on QMS, perform root-cause analysis, maintain quality documentation (PFMEA, control plans), manage metrics, and support an ISO Class 8 cleanroom environment.

Lead process and technology improvements for flexible packaging manufacturing: implement new products/processes, manage capital equipment projects, reduce costs and scrap, ensure quality, validate processes, and support cross-functional commercial and risk management activities.

Design, develop, procure, qualify, and support silicone processing tooling and equipment (molding, extrusion). Troubleshoot and maintain production tooling, lead mold design reviews, manage tooling projects, support DFM/FMEA and continuous improvement, and coordinate with cross-functional teams and suppliers.

Lead extrusion process development as the enterprise SME, establish standardized methodologies (DOE, IQ/OQ/PQ), drive technology adoption (micro/multi-material extrusion, IIoT), support regulatory compliance (FDA, ISO 13485) and cross-site technology transfer, mentor engineers, and solve complex materials and tooling challenges for medical device manufacturing.

Design, develop, and maintain tooling and extrusion processes for medical device production. Coordinate with customers and vendors, perform statistical analysis and validation (IQ/OQ), select/procure equipment, and support new product introductions and production troubleshooting.