7 supervisor jobs found

The Quality Supervisor is responsible for maintaining, implementing, and continuously improving the Quality Management System. This role emphasizes hands-on application of quality tools, development and delivery of training, and facilitation of systems that build organizational knowledge while driving measurable improvements in processes, products, and performance. The Quality Supervisor facilitates SPC and Gage R&R programs, serves as the Corrective Action Request (CAR) system coordinator, and supports managers with root cause analysis and corrective/preventive action development. Essential Responsibilities Drive continuous improvement through execution of improvement activities such as PIT teams, capability studies, SPC, and Gage R&R. Serve as backup ISO/QS Management Representative for the QA Manager. Develop and conduct training programs to establish a common understanding of quality tools,...

EHS Leader – Nashoba Valley Area Comp Target; $120-130K + bonus Role Overview We are seeking a seasoned EHS and Facilities Supervisor with a strong background in manufacturing or industrial environments. This role is responsible for the dual oversight of our Environmental, Health, and Safety (EHS) management systems and the operational integrity of our facility. You will be the primary lead for regulatory compliance, risk mitigation, and the continuous improvement of our physical infrastructure. Key Responsibilities Environmental, Health & Safety (EHS) Leadership System Administration: Own and administer the site EHS management system in full compliance with OSHA , EPA, and all applicable state and local regulations. Policy Development: Create, implement, and maintain comprehensive EHS policies, procedures, and detailed work instructions. Risk Management: Lead hazard identification, formal risk assessments , and robust...

Quality Manager Littleton, MA – $140-150K + bonus Position Summary We are seeking a senior, hands-on Quality Manager to lead all aspects of manufacturing quality for our high-complexity medical imaging and therapeutic systems. Reporting directly to the Director of QA/RA, you will serve as the primary owner of manufacturing quality affairs, responsible for day-to-day execution on the production floor, driving robust quality systems, and leading continuous improvement initiatives. The successful candidate will work cross-functionally with Manufacturing, Engineering, and Supply Chain leadership. You must be comfortable making independent quality decisions while aligning with the broader corporate Quality and Regulatory strategy. This role manages the QC Supervisor and Quality Engineers and is expected to be a visible leader capable of identifying risk, driving root cause analysis, and implementing sustainable corrective actions. Essential Functions Quality...

? Now Hiring: Senior Facilities Specialist (High-Tech Manufacturing) Are you a veteran Facilities Technician who thrives in complex, mission-critical environments? We are looking for a technical lead to oversee a state-of-the-art facility in Littleton, MA . This isn’t your typical “handyman” role. We need a specialist who understands the heartbeat of a regulated industrial environment—from UPS systems and industrial chillers to complex HVAC and emergency generators. Why this role stands out: Technical Ownership: You’ll be the senior resource for a high-tech facility, managing advanced troubleshooting and preventive maintenance. Project Impact: Lead infrastructure upgrades, equipment installations, and site renovations. Competitive Compensation: $38.00 – $43.00 / hour (First Shift). Autonomy: Report directly to the EHS & Facilities Supervisor in a role that values leadership and minimal supervision. What we’re looking for: ? 7–10+...

The Senior Manufacturing Engineer is a key contributor to the design and development of manufacturing processes, tools, and procedures. Provides direct engineering support for New Product Introduction (NPI), development of  assembly & test processes, tools, and inspection methods. Identifies and leads and continuous improvement activities  and projects. Responsible for manufacturing process verification & validation and employee training effectiveness. Ensures the smooth running of manufacturing processes with the highest possible quality and efficiency. Principal Responsibilities  ? Designs, develops and documents manufacturing systems, processes and tools for new products, product & process changes, to meet targets for quality, efficiency, and reliability. ? Creates and maintains manufacturing plans, procedures, process FMEAs, flowcharts, workflows, layouts, routings, time standards, and...

Planner II – Littleton, MA – $85K Description Position Summary The Planner II is responsible for end-to-end planning and execution of material and production plans for complex, long-lead, engineered-to-order medical systems and service assemblies. This role operates at the system and project level, translating MRP outputs, engineering releases, and SIOP commitments into executable production plans that support on-time system delivery, service fulfillment, and regulatory compliance. The Planner II acts as a cross-functional integrator, working closely with Manufacturing, Purchasing, Engineering, Quality, and Program Management to manage schedules, material readiness, and execution risk across assigned systems or service programs. Key Responsibilities Develop and maintain system-level production plans aligned to approved SIOP and master schedules Create, release, and manage work orders, jobs, and build packages in ERP/MRP systems Plan and sequence production...

Overview The Senior Quality Management Systems Engineer is responsible for maintaining, improving, and ensuring compliance of the company’s Quality Management System in accordance with ISO 9001, ISO 13485, FDA 21 CFR Part 820, and other applicable regulatory requirements.  This role supports continuous improvement initiatives, internal and customer audits, CAPA processes, and documentation control to ensure product quality and regulatory compliance. This position is responsible for developing and maintaining the company’s QMS documentation including SOPs, work instructions, and related forms and specifications The position is also responsible for ensuring individuals within the company are effectively trained to the QMS documentation applicable to their roles and responsibilities. Principal Responsibilities Quality System Maintenance & Compliance Maintain and improve the company’s Quality Management System (QMS) to ensure...