USA-Manufacturing Technician III (Manufacturing/Quality) 1st Shi
Immediate need for a talented Senior Manufacturing Technician. This is a 12+ Months contract opportunity with long-term potential and is located in Pleasantview Terrace; Ridgefield NJ(Onsitenbsp;nbsp;Please review the job description below and contact me ASAP if you are interested.Job ID: 23-30224 Pay Range: $3035/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work locationKey Responsibilities: Manage the Component Preparation area which includes two steam sterilizers, parts washers, intermediate solution preparations and the area personnel to work effectively as a team to support manufacturing operations to deliver high quality products within the budget.
Providing leadership and direction to Manufacturing Leads while embodying the principles of the Global Leadership Model. Managing and developing the performance of direct reports by setting clear SMART goals, providing timely performance feedback, recognizing and rewarding.
High achievers, and holding reports accountable for underperformance. Ensuring timely issue escalation to manufacturing senior management and crossfunctional support teams. Ensures adherence to production schedules, while holding Leads and teams responsible for compliance to all safety and quality regulations.
Ensuring that appropriate levels of trained resources are available to meet production schedules. Ensuring adherence to PM and validation schedules. Working with recruiters to maintain staffing levels and meet approved hiring plans, conducting performance appraisals and career development assessments for all direct reports.
Training /Deviations /Compliance-Utilizing quality systems to measure, analyze, and improve team performance. Participating in/leading scheduling, project, and staff meetings, providing updates of department activities and project statuses. Designing Department Training Plan, managing execution and monitoring training of direct reports.
Ensuring Inspection Readiness of assigned manufacturing areas. Participating in inspections conducted by external regulators and ensuring success of audits for department. Responsible for on-time completion of investigations, CAPAs for major and critical deviations and QEs.
Participating in formal FMEAs and RAs. Review and approval of Quality Reports, validation protocols and validation reports. Manage Change Controls Overseeing implementation of CAPAs. Complying with requirements from Genzymes Safety Program including Health and Safety regulations and OSHA requirements.
Production-Oversee day to day activities of second shift of the Autoclave and Parts preparation areas. Provide technical support and guidance as it impacts production processes and resolution of exceptions and investigations. Perform daily walk through of production areas.
Overseeing departmental projects and ensuring that the appropriate controls, approvals, and validation requirements are implemented. Monitoring projects through major milestones and completion. Obtaining additional resources from supporting departments as needed to be successful in the implementation of projects.Our client is a leadingPharmaceutical organization and we are currently interviewing to fill this and other similar contract positions.
If you are interested in this position, please apply today for immediate consideration.Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
#Mor
Providing leadership and direction to Manufacturing Leads while embodying the principles of the Global Leadership Model. Managing and developing the performance of direct reports by setting clear SMART goals, providing timely performance feedback, recognizing and rewarding.
High achievers, and holding reports accountable for underperformance. Ensuring timely issue escalation to manufacturing senior management and crossfunctional support teams. Ensures adherence to production schedules, while holding Leads and teams responsible for compliance to all safety and quality regulations.
Ensuring that appropriate levels of trained resources are available to meet production schedules. Ensuring adherence to PM and validation schedules. Working with recruiters to maintain staffing levels and meet approved hiring plans, conducting performance appraisals and career development assessments for all direct reports.
Training /Deviations /Compliance-Utilizing quality systems to measure, analyze, and improve team performance. Participating in/leading scheduling, project, and staff meetings, providing updates of department activities and project statuses. Designing Department Training Plan, managing execution and monitoring training of direct reports.
Ensuring Inspection Readiness of assigned manufacturing areas. Participating in inspections conducted by external regulators and ensuring success of audits for department. Responsible for on-time completion of investigations, CAPAs for major and critical deviations and QEs.
Participating in formal FMEAs and RAs. Review and approval of Quality Reports, validation protocols and validation reports. Manage Change Controls Overseeing implementation of CAPAs. Complying with requirements from Genzymes Safety Program including Health and Safety regulations and OSHA requirements.
Production-Oversee day to day activities of second shift of the Autoclave and Parts preparation areas. Provide technical support and guidance as it impacts production processes and resolution of exceptions and investigations. Perform daily walk through of production areas.
Overseeing departmental projects and ensuring that the appropriate controls, approvals, and validation requirements are implemented. Monitoring projects through major milestones and completion. Obtaining additional resources from supporting departments as needed to be successful in the implementation of projects.Our client is a leadingPharmaceutical organization and we are currently interviewing to fill this and other similar contract positions.
If you are interested in this position, please apply today for immediate consideration.Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
#Mor
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