AVANTOR: Quality Engineer

Elevated Resources

Radnor, Pennsylvania

JOB DETAILS
SKILLS
Active Pharmaceutical Ingredient (API), Analysis Skills, Auditing, Communication Skills, Continuous Improvement, Control Systems, Corrective Action, Cross-Functional, Data Analysis, Detail Oriented, Documentation, Experiment Design, ISO 9000, Identify Issues, Leadership, Lean Six Sigma, Manufacturing, Manufacturing/Industrial Processes, Metrology, Microsoft Excel, Microsoft Word, Minitab, Organizational Skills, Procedure Implementation, Process Analysis, Process Development, Process Improvement, Process Validation, Product Design, Product Development, Product Management, Product Reviews, Project/Program Management, Quality Assurance, Quality Assurance Methodology, Quality Engineering, Quality Management, Record Keeping, Research & Development (R&D), Risk Management, Root Cause Analysis, Statistical Process Control, Statistical Quality Control, Statistics, Statistics Software, Systems Maintenance, Team Player, Testing, United States Department of Energy (DOE)
LOCATION
Radnor, Pennsylvania
POSTED
30+ days ago

Job Description

Under general supervision, develop, modify, apply, and maintain quality evaluation and control systems/protocols. Devise and implement methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Design and analyze inspection and testing processes, mechanisms, and equipment. Conduct quality assurance tests and performing statistical analysis to assess the level of control and manage product quality risks.

Major Job Duties and Responsibilities

Knowledge, Skills and Abilities:

  • Responsible for Quality System maintenance.
  • Performs root cause analysis and implementation of corrective action for process related issues.
  • Identifies statistical methods relevant to the manufacturing process.
  • Responsible for continual improvement activities to enhance the Quality System.
  • Develops and performs training to build quality awareness throughout the company.
  • Collaborates with Manufacturing, Research and Development and Engineering to ensure transfer of newly developed products that are in accordance with approved data and analysis.
  • Conducts audits, including closing out audit findings, creating audits finding reports and works with multi-functional teams to determine proper corrective and preventive actions.
  • Assists in creation and maintaining quality documentation.
  • Implements and maintains Statistical Process Control (SPC) for products and identifies potential process improvements.
  • Conduct Active Pharmaceutical Ingredient product review.
  • Evaluate impact of process improvement effort and manufacturing deviation on process validation and product design.
  • Demonstrates good communication and project management skills.
  • Collaborate with team members to support company goals.
  • Develop experiments by applying full and fractional factorial techniques.
  • Assist in validation processes including TM validation, manufacturing process validation, cleaning validation
  • Knowledge of ISO 9000/ AS9100.
  • Knowledge and experience with LEAN, Six Sigma methodologies.
  • Familiarity in Design of Experiments (DOE), and ability to lead implementation of improvements.
  • Proficiency working with Microsoft Excel, Word.
  • Experience with Minitab or other statistical software strongly desirable.
  • Understanding of statistical process and quality control principle.
  • Skilled in metrology tools.
  • Ability to work optimally in a team environment.
  • Ability to identify problems and communicate solutions in a constructive and positive manner.
  • * Attention to detail; excellent organizational and record keeping skills.
 

About the Company

E

Elevated Resources