Nordson

Quality Engineer II

Nordson$80K — $95K *
Salem, NH 03079In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 3-5 years of quality assurance experience in a manufacturing environment
  • Familiarity with FDA regulations and Good Manufacturing Practices (GMP)
  • Experience with CAPA, SCAR processes, and root cause analysis
  • Proficient in statistical process control (SPC) and quality metrics
  • Ability to read and write technical documentation including SOPs and quality plans

Responsibilities

  • Ensure manufacturing operations comply with GMP and quality standards
  • Participate in root-cause analysis and corrective actions for quality issues
  • Design and document gage R&R studies for process verification
  • Lead initiatives to reduce the cost of poor quality
  • Conduct inspections and respond to customer complaints and SCARs

Benefits

  • Participation in a multidisciplinary team to enhance quality processes
  • Opportunities for professional development and training
  • Supportive quality culture focused on continuous improvement
  • Engagement in lean initiatives to streamline quality systems
  • Collaboration with various departments to ensure quality compliance
Full Job Description
Assure that manufacturing operations follow all Good Manufacturing Practices and Procedures as defined by insuring that FDA and Quality Standards are met. • Participate in multidisciplinary teams to implement root-cause analysis, corrective and preventive action, and proof of effectiveness as quality issues are identified. • Design, execute and document gage R&R studies. • Support training on Manufacturing and Quality System documents (SOPs, PIs, MAPs, QAPs). • Actively lead process improvement events leading to reduction in cost of poor quality (COPQ). • Reduce scrap and manufacturing waste for various product lines throughout the factory. • Quality Representative for Material Review Board (NMR) for purchased and make components. • Conduct and follow up of SCAR process (SCAR issuance, Supplier notification, SCAR approval and effectiveness review) • Investigate and respond to customer complaints and customer issued SCARs. • Quality Representative for Process Validations and Transfer Validations (may require writing, reviewing, executing, analyzing and reporting on test protocols). • Prepare quality related deliverables in a timely manner. • Prepare and execute Engineering studies as needed. • Responsible for CAPA root cause investigation and actions implementation. • Implementation of SPC. • Eliminate All Escapes to the customer. Metric goal is zero. • Creates Controls plans • Meet KPI Goals,Quality deliverables. • Support Quality Culture. • . Lean QMS initiative to reduce Muda by eliminating bureaucratic processes. • Participate in Quality and Manufacturing Department meetings. • Collaborate in the clarification of specifications for quality. • Acts as a consultant for areas related to his/her expertise. • Support Supplier management process as required . Participate and assist as a part of the Internal Audit team as required. • Other duties as assigned, verbal and written. • Follow medical device manufacturing best practices (GMP, GDP, etc.), current Nordson Medical policies and procedures, ISO 13485, 21CFR Part 820 and other applicable regulations to ensure compliance to applicable customer and regulatory requirements

About Nordson

Nordson Corporation is a global manufacturer of systems that apply adhesives, sealants, and coatings to a variety of consumer and industrial products. The company's products are used in a range of industries, including packaging, nonwovens, electronics, medical, and automotive. Nordson's systems are designed to improve product quality, reduce costs, and increase efficiency for its customers. The company was founded in 1935 and is headquartered in Westlake, Ohio.
Learn more about Nordson
Size
7,200 employees
Market Cap
$13.4 billion
Industry
Net Income
$275.1 million
Founded
1935
5 Year Trend
+4.6%
Revenue
$2.1 billion
NASDAQ

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