Quality Engineer

Posted 2 Days Ago
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Tacoma, WA, USA
In-Office
95K-125K Annually
Senior level
Pharmaceutical • Automation • Manufacturing
The Role
Maintain and improve the ISO 9001:2015 Quality Management System, manage NCR/CAPA and root cause analysis, perform audits, develop quality procedures and training, create inspection plans using manual and CMM metrology, review engineering drawings, collaborate with suppliers and cross-functional teams to ensure product and process quality.
Summary Generated by Built In

At AST, we enhance the efficiency, productivity, and safety of flexible aseptic manufacturing processes for the worldwide Life Science Industry by offering innovative products, services, and solutions. 
Do you want to contribute to a shared vision and mission? Would you like to bring your unique talents to have a significant impact on a growing company? At AST we strive to build a workplace that enables every team member to meet and exceed their capabilities. We set our expectations high and provide the environment and resources necessary to bring out the very best. AST is proud of our team. Providing challenging and rewarding work, with opportunities for personal/professional development is our key to this longevity. AST is an equal opportunity employer. 
Compensation range for onsite WA applicants is $95,000 to $125,000. All applicants are welcome to apply.  
Employee benefits include: Medical (HSA & PPO), Dental, Vision, Long/Short term disability, HSA account with employer contribution, 401(K) (Traditional & Roth options) with up to 5% company match, Education Assistance, Paid Time Off (PTO), Paid Holiday, and bonus potential. 

What can I expect in this role?

The Quality Engineer will support AST by ensuring the overall efficiency and effectiveness of the AST Quality Management System. This includes ensuring products and processes meet quality standards by working with manufacturing and assembly personnel, testing, and analyzing defects. Responsibilities include collaborating with other teams, developing quality procedures, performing audits, and developing corrective actions for implementation.

What will I be doing?
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Maintain the ISO 9001:2015 Quality Management System and ensure compliance.
  • Execute the company wide Process of Continuous Improvement (PCI).
  • Provide assistance and guidance to company in interpreting industry standards and internal policies to ensure compliance.
  • Analyze and interpret company data to provide recommendations relating to quality within the company.
  • Coordinate and maintain all aspects of the company’s Quality Management System programs.
  • Ensure documentation is completed and made available to demonstrate internal compliance, including quality manuals and plans, certifications, work instructions, and records for internal audits.
  • Interface with key suppliers to maintain internal quality standards.
  • Manage the Non-Conformance (NCR) / Corrective Action (CAPA) processes and coordinate root cause analysis.
  • Develop and conduct Quality training for all levels of employees. 
  • Review project documentation to ensure completeness with internal and customer requirements.
  • Create and implement inspection plans using manual and CMM metrology equipment.
  • Review and interpret engineering drawings to ensure internal and external quality standards are met.
  • Perform other duties as assigned.
  • Expected travel: <15%

Core Competencies, Skills and Abilities:

  • Bachelor’s degree or higher in engineering related field.
  • 5+ years of experience working within a documented ISO Quality Management System.
  • Skilled in the use of computer software for analysis of data; preferably Microsoft Excel, Access, and statistical packages.
  • Experience with GAMP or similar standards for equipment and software verification, validation testing, and documentation.
  • Training with certification in Six Sigma and LEAN.
  • Proficient with MS Office and ERP Systems.
  • Experience with identifying and implementing improvements to manufacturing processes.
  • Ability to embrace a fast-paced culture.
  • Ability to be self-driven, take initiative, and work autonomously to achieve KPI’s.
  • Lead with a results-driven mindset, reinforcing accountability to achieve and exceed metrics.
  • Excellent verbal, written, and presentation communication skills.

Eligibility Requirements:

  • Must be legally authorized to work in the United States without restriction.
  • Must be willing to take and successfully pass a drug test.

AST is proud of our team. Providing challenging and rewarding work, with opportunities for personal/professional development is our key to this longevity. AST is an equal opportunity employer.
Compensation is competitive, including salary, bonus potential, health plan options, competitive 401K match, and paid time off.

 

This is a full-time position based in Tacoma. 

*All benefits listed in this post are subject to change. 

Skills Required

  • Bachelor's degree in engineering or related field
  • 5+ years working within a documented ISO Quality Management System
  • Knowledge of ISO 9001:2015 Quality Management System
  • Skilled in use of computer software for data analysis
  • Microsoft Excel
  • Microsoft Access
  • Statistical packages
  • Experience with GAMP or similar standards for equipment and software verification and validation
  • Certification in Six Sigma
  • Training in LEAN
  • Proficient with MS Office
  • Proficient with ERP systems
  • Experience identifying and implementing manufacturing process improvements
  • Ability to work autonomously and achieve KPIs
  • Excellent verbal, written, and presentation communication skills
  • Legally authorized to work in the United States without restriction
  • Willing to take and successfully pass a drug test
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The Company
116 Employees
Year Founded: 1965

What We Do

Since 1965, AST has been a technology leader specializing in advanced aseptic filling and closing systems. The company focuses on providing innovative and flexible cGMP manufacturing systems for processing vials, syringes, and cartridges, satisfying the most challenging product and regulatory requirements for the Pharmaceutical and Biotechnology industries.

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