Jobs at Spectrum Plastics Group

Operate and maintain CNC machines, perform statistical process control, replace tools, adjust offsets, deburr parts, and inspect components using precision measurement equipment. Record inspection results, communicate shift status, train others on relevant inspection equipment, and follow work instructions, safety requirements, and confidentiality policies. The role requires at least three years of related experience, basic machining skills, and the ability to use a microscope for extended periods and lift up to 50 pounds.

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

Leads quality engineering for medical device product and process development, including ISO 13485 and FDA QSR compliance, validation protocols, risk management, inspection systems, SPC, DOE, CAPA, audits, and continuous improvement. Serves as a subject matter expert for automated measurement systems and GD&T, drives eQMS and Quality 4.0 initiatives, analyzes quality data, reduces scrap and COPQ, supports customer interactions, and develops site-wide KPIs.

Supervises manufacturing operations and production staff during an assigned shift. Responsibilities include scheduling, staffing, safety, quality, equipment operation, GMP and ISO compliance, training, production records, performance metrics, housekeeping, batch record review, and complaint investigations. The role ensures efficient production, resolves operational issues, maintains organized work areas, and communicates personnel or production concerns to management.

Sales Manager responsible for profitable revenue growth of blown film products within a defined territory. Duties include developing new business, managing customer relationships, executing go-to-market strategy, presenting market intelligence, using Salesforce.com, collaborating with manufacturing and technical teams, supporting strategic planning, and representing the company at trade shows and industry events. Requires strong communication, analytical, organizational, leadership, and problem-solving skills, plus willingness to travel up to 50%.

Lead environmental health and safety programs across two manufacturing sites. Responsibilities include regulatory compliance, permits and reporting, industrial hygiene, audits, incident and injury recordkeeping, emergency and security programs, safety culture development, performance improvement, and supervision of EHS resources. The manager will partner with site leadership and corporate EHS teams, support compliance projects, and travel occasionally for training, meetings, and audits.

Leads clean room manufacturing activities by directing team assignments, reinforcing safety and environmental standards, auditing production and in-process quality, maintaining traceability records, ensuring material availability, training personnel, and supporting continuous improvement. The role uses ERP systems for production flow and recordkeeping, conducts line clearance, assists with procedures, and leads root cause analysis to resolve production issues.

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

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 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.

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.

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.

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.