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Form of workImmediate need for a talented Deviation Management Specialist . This is a 05+ Months contract opportunity with long-term potential and is located in West Point, PA(Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID: (phone number removed) Pay Range: $35- $41/hour.
Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).Key Responsibilities:Providing on-the-floor support of operational and technical issues; collaborating with the shop floor to provide immediate responses to deviations and potential deviations.Conducting real time investigations with the goal of fully understanding root cause and product impact within five days of event discovery.Performing deviation investigations and customer complaints aimed to prevent deviation/complaint re-occurrence, including determining the root cause, identifying corrective/preventative actions, identifying event scope, and conducting a product impact assessment. Where applicable, complete investigational test protocols to determine root cause, product impact, event scope, etc.Completing projects to improve the performance of our processes, including projects aimed at improving Right-First-Time performance or preventing/reducing deviations, and continuous improvement projects that seek to improve yield, reduce cost, or lower our processing cycle times.Supporting team safety, environmental and compliance objectives.Managing investigation and complaint timelines to ensure key compliance and customer due dates are met; escalating any potential misses and develop remediation plans when possible.Collaborating effectively with the area Coaches, Operators/Mechanics, support groups (Maintenance, Automation, Technology, Quality, and Planning).Actively using and championing the use of Lean Six Sigma (LSS) and Production System (MPS) tools, both in problem solving and day-to-day operational activities.Key Requirements and Technology Experience: B.S./M.S. degree in appropriate engineering/scientific field.Minimum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g.
Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry. Previous experience in writing investigations for atypical events in a manufacturing environment.Familiar with Lean Six Sigma Methodologies and proven analytical/ problem solving capabilities. Demonstrated ability to work both independently and as a part of a cross-functional team.Excellent written and verbal communication skills.Our client is a leading Pharmaceuticals organization and we are currently interviewing to fill this and other similar contract positions.
If you are interested in this position, please apply online 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.
