Quality Assurance Engineer

Thermo Fisher Scientific

  • Rochester, NY
  • Permanent
  • Full-time
  • 2 months ago
Job Description

Job Title: Quality Assurance Engineer
Requisition ID: 119844BR

When you join us at Thermo Fisher Scientific, you'll be part of a smart, driven team that shares your passion for exploration and discovery. With revenues of $22 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

Location:
This role will be based at our Penfield, NY site.

How will you make an impact?
Under the direction of the Manager, Quality Assurance Engineering and Quality Control, the Quality Engineer is responsible for assuring manufacturing processes are in compliance with Thermo Fisher Scientific ISO/cGMP Quality Management System to produce consistent quality product. The Process Quality Engineer is also responsible for identifying opportunities and supporting improvement and reduced variation in our manufacturing processes resulting in improved product quality and delivery.

What will you do?
  • Drive improved product quality through the use of Quality Assurance principles to drive towards process control.
  • Research, recommend, and implement new and improved gauging, measurement, and data acquisition systems to improve inspection efficiency and repeatability and reproducibility of measurement systems.
  • Ensure the accuracy and adequacy of quality control inspection plans (QCIP's) and standard test procedures (STP's) for purchased and manufactured components and finished goods to meet the latest quality and system specifications.
  • Communication of QCIP and STP changes to the Quality Control Department in a timely, efficient, and practical manner.
  • Serve as the Quality Assurance representative on New Product Development and Sustaining Engineering projects.
  • Use risk management tools (such as pFMEAs) to evaluate impact of change.
  • Ensure Product Development / Design Control procedures are utilized appropriately to implement new / changes to products and processes.
  • Support the Validation of molds, equipment, and processes.
  • Determine need for validation of new or changes to molds, equipment, or processes.
  • Work with Engineering to develop and document Validation Protocols and Reports (IQ, OQ, PQ) to ensure effectiveness of new or changes to molds, equipment, or processes.
  • Review and approve Validation Protocols and Reports (IQ, OQ, and PQ).
  • Support Corrective and Preventive Action (CAPA) and other Continuous Improvement Activities.
  • Review non-conformance and other manufacturing metrics to identify CAPA opportunities.
  • Facilitate CAPA investigations for customer complaints, recurring non-conformances, audit non-conformances, and other investigations using problem solving tools to identify root cause and implement effective corrective actions.
  • Analyze process capability data and other quality metrics in order to propose specification or process changes to Engineering.
  • Participate in PPI (Practical Process Improvement) projects to support achievement of business metrics (OEE, LIFR, Past Due, Scrap, and other cost savings).
  • Other duties as assigned
How will you get here?
  • This position requires a Bachelor's of Science Degree in Engineering (or equivalent experience) and 5+ years of direct Quality Engineering (or equivalent) experience.
  • Experience in a regulated medical device manufacturing environment with compliance to FDA Quality System Regulation, EU Medical Device Regulation, and ISO 13485:2016 is a plus.
  • Plastic product manufacturing experience is plus.
Knowledge, Skills, Abilities:
  • Disciplined problem solving capability: Lean / Six Sigma, Shainin, and etc.
  • Working knowledge of Excel, Word, Access, Minitab, quality software, and statistical methods (SPC, DOE, Gauge R&R, and etc.) and risk management techniques (dFMEA/pFMEA).
  • Project planning and advanced computer skills a plus.
  • Work attitude that exhibits drive, creativity, collaboration, assertiveness, good judgment, decision making, and ambition.
  • Excellent interpersonal skills that facilitate the ability to build and maintain relationships with internal and external customers in a multi-skilled, dynamic business environment.
  • Leadership Skills: Proven ability to influence others and lead significant change.
  • Strong communication skills both written and verbal.
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit .

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Job Category

Engineering, Operations, Quality

Thermo Fisher Scientific

is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Thermo Fisher Scientific