Manufacturing Supervisor: 1st Shift
Ridgefield, NJ
9 Months contract
Pay Range: $32-42/hr on w2

JOB OVERVIEW:
Production is responsible for Aseptic manufacturing operations at Ridgefield site, manufacturing facility. Production is comprised of Upstream Operations (Formulation) and Downstream
Operations (Packaging). In either area, operational staffs are involved in cleaning and sterilization of process equipment (vessels), staging of components, aseptic processing, operating process equipment, formulation, fill operation, product sterilization and inspection. Aseptic Manufacturing consists of Senior Managers, Supervisors, Manufacturing Technicians and Associates.
Ensuring execution of production plan and manages staff performance against operational goals.

KEY ACCOUNTABILITIES:

Management
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 Genzyme s 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.

Continuous Improvements:
Working collaboratively with inter-department and cross-functional teams to lead.

If eligible share your cv on nikmit198*****mail.com
Reference : Manufacturing Supervisor: 1st Shift jobs