Sr Process Engineer (Hillsboro, OR) - SPC Program Focused - Ultra Clean Technology

#1
Ultra Clean Technologies (UCT), is seeking an energetic and motivated team player to fill a Sr Process Engineer role to join our fast-paced, global engineering team, based in Hillsboro, OR. This is your opportunity to develop or apply statistical theory and methods to collect, organize, interpret, and summarize numerical data. The Sr Process Engineer will report to the SPC Program Manager and is responsible to support implementation of the Corporate SPC program across all sites. This will entail problem solving and proposing systematic solutions utilizing statistical software to speed and enable decision making based on statistical analysis. You will be working directly with site engineering teams to progress the SPC program to meet our customers’ needs and provide data driven information for improved and efficient decision making. SPC Program Manager will interact directly with customers to understand customer SPC requirements and manage the implementation of those requirements at global sites.

Essential Duties and Responsibilities:

  • Demonstrate, improve and develop others to core SPC skill requirements
  • Develop SPC training program oriented specifically to operator and engineering level knowledge
  • Monitor progression of SPC program at global sites– drive CIP with site engineering
  • Participate in cross-functional site and customer SPC reviews.
  • Define, develop, and deliver standard reports for internal and external customers.
  • Work with data scientists to develop automated tracking of internal KPI’s for SPC program. Define needs specific to customer, and the overall infrastructure for SPC metric tracking.
  • Support interdepartmental needs for statistical analysis of large datasets
  • Proliferate culture of improvement - reward sites and individuals for advancing SPC program
  • Identify gaps in SPC program and propose plans for improvement
  • Evaluates work methods, procedures, and policies. Identifies, documents, and implements new business processes and efficiency improvement tools. Mentors and trains lower-level engineers; identifies training needs, updates training curriculums, and develops training programs.





Knowledge, Skills, and Abilities:

  • Application of statistical expertise within a complex manufacturing environment – requires hands-on learning for familiarity with process lines, products, metrology tools etc.
  • Project Management leadership – experience successfully leading cross-functional teams
  • Demonstrated project management skills – defining deliverables, owners, team-building
  • SQC/SPC application in Manufacturing and/or Service environment. Statistical tools proficiency – JMP, Minitab, or similar.
  • Ability to evaluate SPC charts and understand potential sources and path forward for various types of chart behavior
  • Communication skills – presenting information to internal and external customers in a concise, confident manner with data. The ability to be receptive to customer feedback and understand how to apply it. Internally, communication skills within a cross functional team with the purpose to achieve a unified goal.
  • Must possess the skills to resolve problems and ensure that critical business data integrity issues can be identified and resolved.
  • Ability and proven experience to develop effective training tools
  • Advanced statistical skill required with the ability to train others at various levels of competency

Educational/Certification Requirement:

  • Advanced statistics or engineering degree preferred. A combination of education and experience will be considered in lieu of an advanced statistical degree

Experience Requirement:
Work Experience:

  • 5+ years as a Process Engineer, or applicable statistical engineering work.
  • Advanced statistics or engineering degree. A combination of education and experience will be considered in lieu of an advanced statistical degree
  • Project Management leadership – experience successfully leading cross-functional teams
  • Statistical software proficiency – JMP, Minitab, etc
Please visit UCT's career page or respond to this post for more info!
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
Q New Job!!!-You are looking at the new Sr. Process Engineer for Overstock Covegratulations 11
R Could Factory Process Auditor and Industrial Engineer Coexist? Lean in Manufacturing and Service Industries 2
S Role of a Quality Engineer in APQP process APQP and PPAP 11
A Sample size selection for process validation - continuous data Reliability Analysis - Predictions, Testing and Standards 3
Q Failure mode, Process Excursion and Failure mode cause ISO 14971 - Medical Device Risk Management 2
Sidney Vianna IAQG News IAQG 9401-1:2022 Changes & Organization Certification Analysis Process - OCAP Demo AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
E Process capability in a single batch Capability, Accuracy and Stability - Processes, Machines, etc. 3
Ashland78 IATF Process Control Plans not including customer name Manufacturing and Related Processes 13
S Sample size considerations in medical process qualification Reliability Analysis - Predictions, Testing and Standards 11
M Process flowcharts ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
A Small Company Implementing ISO 13485 Timeline/Process/Steps Advice ISO 13485:2016 - Medical Device Quality Management Systems 5
G Help Needed: Quality Control / Assurance process Quality Manager and Management Related Issues 3
T AS9100 Process Sequence and Interaction Map Example AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
D Seeking help in validating a cleaning process. Manufacturing and Related Processes 5
R CNC process validation Manufacturing and Related Processes 1
T Process Sequence and Interaction Map AS9100 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
C Product compliance process REACH and RoHS Conversations 10
M Clinical evaluation process of FDA and MDR Medical Device and FDA Regulations and Standards News 2
V Countries without Formal Regulatory Approval Process Other Medical Device Regulations World-Wide 0
J Crimp inspection and process verification AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
Crimpshrine13 Bulk Process (Electroplating), Control Plan, and Process Change IATF 16949 - Automotive Quality Systems Standard 1
S Process Owner IATF 16949 - Automotive Quality Systems Standard 10
Bev D Development Process: FMEA, Critical Characteristics, Spec Setting and Controls Misc. Quality Assurance and Business Systems Related Topics 0
T Document Review Process Map AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
A Validation Plastic Injection Molding Process protocol ISO 13485:2016 - Medical Device Quality Management Systems 5
M Use of statistical techniques for Process Validation ISO 13485:2016 - Medical Device Quality Management Systems 9
A Question regarding new VDA_AIAG fmea approach for process FMEA FMEA and Control Plans 0
S 9001 + 14001 Internal Auditing Process checklist, flowchart or questionnaire ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
L CQI-30 Special Process: Rubber Processing System Assessment - Mixing & Molding IATF 16949 - Automotive Quality Systems Standard 4
O Process Flow Diagram, DFMEA, PFMEA, Control Plan integrated softwares FMEA and Control Plans 7
C. Tejeda Process validation of rework assembly methods (medical devices) Medical Device and FDA Regulations and Standards News 3
L Looking for feedback on Nonconformity Process Flowmap ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
M Process Flow of ECN Product User and Service Guides Process Maps, Process Mapping and Turtle Diagrams 1
R Process Maps for ISO 17025 ISO 17025 related Discussions 2
L APQP Process Flow with CFT Roles and responsibilities APQP and PPAP 4
M Having Trouble Identifying KPI for Process ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
E Please help! ! I AM FRASTRATED SO MUCH! Should inactive ingredient be included in the unit formula if it is removed during the manufacturing process? US Food and Drug Administration (FDA) 0
I Supplier Evaluation Process ISO 13485:2016 - Medical Device Quality Management Systems 4
B A template for a injection molding process sheet with upper/lower- mean value tolerances Manufacturing and Related Processes 0
P ISO 9001: Quality Management as a process ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
R How many process maps are adequate for a company for IATF 16949? Process Maps, Process Mapping and Turtle Diagrams 17
Q Process matrix 9001:2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
Q Evaluate a process audit ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 24
J Best Practices for Choosing In-process Inspection Dimensions & SPC Dimensions Inspection, Prints (Drawings), Testing, Sampling and Related Topics 2
T FDA PMA review process - advisory panel timing? Other Medical Device and Orthopedic Related Topics 0
K Process FMEA responsible For "Make to Design Parts" (Inhouse or Suppliers ?) FMEA and Control Plans 3
M Passivation Process Manufacturing and Related Processes 2
G Mfr. Process Validation BEFORE Design Transfer? Other Medical Device and Orthopedic Related Topics 1
M Clinical evaluation interface with the risk management process EU Medical Device Regulations 9
D Integrated Management System (IMS) - Process Vs Clause Based Audits ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 19

Similar threads

Top Bottom