PpLincotek, headquartered in Rubbiano, Parma, Italy, is a global contract manufacturer for services in markets including Industrial Gas Turbines, Aerospace and Medical Device applications, as well as a leading manufacturer of industrial coating equipment and one of the most respected producers in the Additive Manufacturing field. The Group has more than 1,800 employees located in 18 production facilities across Europe, North America and Asia. /p h3About The Role /h3 pThe Quality Control Senior Supervisor is responsible for managing and overseeing all activities related to the inspection of raw materials, semi‑finished, and finished products during manufacturing and final release phases, ensuring compliance with required quality standards in accordance with technical specifications, regulatory requirements, and internal procedures. This role leads a team and ensures the effectiveness of incoming, in‑process, dimensional, functional, and quality controls, guaranteeing compliance of manufactured medical devices with applicable standards, including both implantable devices and surgical instruments. The position is also responsible for managing inspection and measurement equipment, ensuring proper selection, qualification, calibration, maintenance, and suitability for intended use, in compliance with Quality System requirements and applicable regulations. It ensures measurement traceability and proper calibration record management, guaranteeing that all equipment is used under controlled and appropriate conditions. /p h3Main Responsibilities /h3 ul liTeam Management Lead, manage, and supervise the Quality Control team (7 direct reports) /li liPlan activities, shifts, and operational priorities /li liPromote a Quality culture focused on continuous improvement Quality Control /li liDefine and optimize incoming and in‑process quality control plans /li liEstablish sampling plans and statistical rationale in line with customer specifications and applicable standards /li liCoordinate and supervise: Incoming inspections (raw materials, components, semi‑finished goods) /li liDimensional and functional checks (using metrology tools such as calipers, micrometers, CMM) /li liQuality inspections on semi‑finished and finished products /li liEnsure compliance with technical specifications and regulatory requirements /li liAdvanced Metrology CMM Program and optimize Coordinate Measuring Machines (CMM) /li liDefine measurement strategies and automated inspection cycles Validate measurement methods ensuring repeatability and accuracy /li liSupport the team in advanced CMM usage Statistical Analysis Data Management /li liApply and monitor process statistical indicators (Cp, Cpk) /li liAnalyze data and produce process performance reports Support capability studies and process validation activities /li liTechnical Interpretation Interpret technical drawings and product specifications at an advanced level /li liCollaborate with Engineering, Quality Assurance, and Production in case of deviations, concessions, and technical clarifications Deviation, Non‑Conformity CAPA Management /li liCollaborate with Engineering and Quality Assurance in managing internal deviations and non‑conformities identified during inspections Issue non‑conformity reports to suppliers and maintain related databases /li liOversee supplier claims through resolution /li liSupport root cause analysis and CAPA implementation with QA, Engineering, and Plant Manager /li liMonitor effectiveness of corrective and preventive actions Regulatory Compliance (Medical Sector) /li liEnsure compliance with applicable quality and regulatory requirements (ISO 13485) /li liSupport the creation and update of operating procedures /li liSupport internal and external audits (certification bodies, customers) /li liEnsure proper traceability and documentation of inspection activities /li liContinuous Improvement Identify and promote opportunities to optimize quality controls and manufacturing processes /li liImplement and promote Lean methodologies /li liSupport industrialization and production transfer activities, ensuring compliance with quality requirements /li /ul h3Requirements /h3 ul liEducation: Degree in Engineering (Mechanical, Materials, Biomedical) or equivalent technical disciplines /li liExperience: At least 5 years of experience in Quality Control within manufacturing environments /li liExperience in the Medical Device Industry is strongly preferred /li liTechnical Skills: Strong knowledge of Applied statistics (Cp, Cpk, SPC), Sampling plans (ISO 2859‑1, ISO 3951), excellent ability to read and interpret technical drawings, ability to understand technical standards and international regulations, experience in drafting and reviewing technical documentation /li liAdvanced Metrology Expertise: CMM Programming Skills (ZEISS Contura Preferred) /li liSoft Skills: Leadership and team management, structured problem‑solving approach, high attention to detail and accuracy, excellent command of English (both written and spoken) /li /ul h3Altre informazioni /h3 h3WORK ENVIRONMENT /h3 pThis job operates in both an office environment and a manufacturing environment. The role routinely uses standard office equipment, such as computers, phones, photocopiers, filing cabinets and fax machines. The individual will be required to adhere to safety policies and procedures on the manufacturing floor. /p h3PHYSICAL DEMAND /h3 pLimited physical demand may be needed. Physical demands will involve standing, walking, and occasionally moving or lifting material. /p h3POSITION TYPE/EXPECTED HOURS OF WORK /h3 pThis is a full‑time position, with business core hours of Monday through Friday 8am to 5.30pm, with additional hours as business needs necessitate. /p h3TRAVEL /h3 pOccasional overseas and domestic travel may be required to support the rapid growth of the company. /p pLincotek provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law. /p /p #J-18808-Ljbffr