Job Details

ID #45977945
State Pennsylvania
City Westpoint
Job type Contract
Salary USD BASED ON EXPERIENCE BASED ON EXPERIENCE
Source Alpha Consulting Corp.
Showed 2022-09-25
Date 2022-09-24
Deadline 2022-11-22
Category Manufacturing
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Deviation Specialist

Pennsylvania, Westpoint, 19486 Westpoint USA

Vacancy expired!

DEVIATION SPECIALIST WEST POINT, PA Onsite. Project Description:

  • 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 Client's Production System tools, both in problem solving and day-to-day operational activities .
Required Skills:
  • B.S./M.S. degree in appropriate engineering/scientific field.
  • Minimum of 0-3 years post-bachelor's 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.
This 12+ month position starts ASAP. Please E-MAIL your resume (attachment to email) with rate and availability to Angie: ALPHA'S REQUIREMENT #22-02638 MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE

Vacancy expired!

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