

In this role, you will monitor and control the daily activities of quality inspections of incoming, in-process, final, and batch record review and release. In his position, you will manage the Quality Control team to ensure inspection process is executed in a proper and timely manner by ensuring procedures are followed and improved as part of a continuous improvement mindset.
Provides direct supervision, resolves personnel issues, conducts performance evaluations, and performs managerial discipline, as necessary.
Leads and directs the Incoming Inspection, In-Process Inspection, and Batch Release teams with a positive and patient attitude.
Maintains and instills in others a “quality at the source” mentality as it pertains to all aspects of manufacturing, including documentation, training, and other functions related to production.
Maintains and instills in others an “immediate audit readiness” mentality so that records and actions are executed in a way that ensures their accuracy, legibility, and immediate retrievability.
Ensures compliance with quality system documents, cGMPs, ISO standards and FDA regulations.
Schedule and prioritize quality inspection, testing, and batch record review and release to support Operations and release of product.
Identifies and develops opportunities to improve existing processes and procedures
Support quality assurance improvement activities by evaluating products, processes or materials in order to develop control or improvement strategies intended to improve the customer’s experience.
Work with technical staff in performing root cause failure analysis and implementing corrective and preventive actions to eliminate recurrence.
Manage the verbal communications and visual checks of work activity to ensure quality requirements are met. Ensure proper corrective actions, discrepancy reports and follow up activities are accomplished.
Reviews documentation and records for accuracy. Determines if product is impacted, can be released, or if Non-Conformance Report is required.
Manages the development of documentation and procedures during the qualification of new equipment/inspection methods.
Exhibits regular, reliable, punctual and predictable attendance.
Creates, prepares, implements and improves Quality Control KPIs metrics.
Determines/sets Goals and Objectives for the Quality control organization and training programs for team's development purposes.
Supports investigations related to Non conformances, Audit observations, CAPAs, or Issue Reviews as needed.
Ensures equipment is up to date on Preventive maintenance and calibration activities.
Maintains the QC area well organized with a 5S mindset.
Other duties as assigned
משרות נוספות שיכולות לעניין אותך

During your varied training as a Chemical Laboratory Technician (m/f/d), you will be deployed in various departments of an innovative manufacturing company. You will be surrounded by subject matter experts in your learning environment and enjoy a future-oriented work environment.משרות נוספות שיכולות לעניין אותך

In this role, you will be responsible for planning, organizing, and leading projects to support the development of new packaging systems and or components. Drive technical projects, work with cross-functional development teams, and work with strategic suppliers to develop new packaging systems. Subject matter expert for component packaging and drive technical decisions which support West's business objectives.
משרות נוספות שיכולות לעניין אותך

During your varied training as an electronics technician (m/f/d) for industrial engineering, you will be working in a modern and innovative production environment. You will be surrounded by experts in your learning environment and will have a future-oriented working environment.
משרות נוספות שיכולות לעניין אותך

Contract Details:fulltime, permanent
asap
משרות נוספות שיכולות לעניין אותך

Contract Details: fulltime, permanent
: asap
משרות נוספות שיכולות לעניין אותך

During your varied training as a Chemical Laboratory Technician (m/f/d), you will be deployed in various departments of an innovative manufacturing company. You will be surrounded by subject matter experts in your learning environment and enjoy a future-oriented work environment.משרות נוספות שיכולות לעניין אותך

In this role, you will monitor and control the daily activities of quality inspections of incoming, in-process, final, and batch record review and release. In his position, you will manage the Quality Control team to ensure inspection process is executed in a proper and timely manner by ensuring procedures are followed and improved as part of a continuous improvement mindset.
Provides direct supervision, resolves personnel issues, conducts performance evaluations, and performs managerial discipline, as necessary.
Leads and directs the Incoming Inspection, In-Process Inspection, and Batch Release teams with a positive and patient attitude.
Maintains and instills in others a “quality at the source” mentality as it pertains to all aspects of manufacturing, including documentation, training, and other functions related to production.
Maintains and instills in others an “immediate audit readiness” mentality so that records and actions are executed in a way that ensures their accuracy, legibility, and immediate retrievability.
Ensures compliance with quality system documents, cGMPs, ISO standards and FDA regulations.
Schedule and prioritize quality inspection, testing, and batch record review and release to support Operations and release of product.
Identifies and develops opportunities to improve existing processes and procedures
Support quality assurance improvement activities by evaluating products, processes or materials in order to develop control or improvement strategies intended to improve the customer’s experience.
Work with technical staff in performing root cause failure analysis and implementing corrective and preventive actions to eliminate recurrence.
Manage the verbal communications and visual checks of work activity to ensure quality requirements are met. Ensure proper corrective actions, discrepancy reports and follow up activities are accomplished.
Reviews documentation and records for accuracy. Determines if product is impacted, can be released, or if Non-Conformance Report is required.
Manages the development of documentation and procedures during the qualification of new equipment/inspection methods.
Exhibits regular, reliable, punctual and predictable attendance.
Creates, prepares, implements and improves Quality Control KPIs metrics.
Determines/sets Goals and Objectives for the Quality control organization and training programs for team's development purposes.
Supports investigations related to Non conformances, Audit observations, CAPAs, or Issue Reviews as needed.
Ensures equipment is up to date on Preventive maintenance and calibration activities.
Maintains the QC area well organized with a 5S mindset.
Other duties as assigned
משרות נוספות שיכולות לעניין אותך