Burke Porter, an Ascential Technologies Brand

Quality Engineering Manager

SAN DIEGO, CAPosted 30+ days ago

Job summary

  • Job post source

    This job is directly from Burke Porter, an Ascential Technologies Brand

  • Job overview

    The Quality Engineering Manager at Burke Porter leads the Quality Engineering team to ensure product quality and regulatory compliance in medical and life sciences projects, driving innovation in healthcare and diagnostics.

  • Responsibilities and impact

    The manager leads and develops the Quality Engineering team, oversees design controls, risk management, process validation, supplier quality, CAPA, compliance with FDA and ISO standards, and supports manufacturing process transfers.

  • Compensation and benefits

    The position offers an annual salary range of $132,000 to $165,000 based on experience, along with a comprehensive benefits package including health insurance and other standard employee benefits.

  • Experience and skills

    Candidates must have a Bachelor's degree in Engineering or related field with 7-10 years in Quality Engineering in life sciences, 3-5 years of management experience, relevant certifications like ASQ CQE, Six Sigma Green Belt or Black Belt, and expertise in FDA and ISO standards.

  • Career development

    The role offers opportunities to lead a multidisciplinary team and contribute to high-impact projects in a leading medical and life sciences company, fostering professional growth through leadership and technical challenges.

  • Work environment and culture

    The company promotes a culture of quality, continuous improvement, and collaboration across departments, emphasizing leadership, innovation, and compliance in a professional on-site environment.

  • Company information

    Burke Porter, part of Ascential Technologies, specializes in precision engineering and automation solutions for medical devices, diagnostics, and life sciences, focusing on innovation and regulatory compliance.

  • Team overview

    The candidate will join and lead a multidisciplinary Quality Engineering team, managing engineers and collaborating closely with R&D, manufacturing, and supply chain teams.

  • Job location and travel

    This is an on-site position located in San Diego, with limited travel required.

  • Unique job features

    The role involves managing complex quality engineering functions including regulatory inspections, process transfers, and continuous improvement initiatives using Lean and Six Sigma methodologies.

Company overview

Burke Porter, now part of Ascential Technologies, is a global leader in advanced automation, testing, and inspection solutions for industries such as automotive, life sciences, and specialty manufacturing. The company generates revenue by designing, engineering, and delivering custom machinery and integrated systems that help clients improve quality, efficiency, and compliance in their production processes. Founded in 1953 and headquartered in Grand Rapids, Michigan, Burke Porter has a long history of innovation, including pioneering end-of-line testing equipment for automotive manufacturers. Its integration into Ascential Technologies has expanded its global reach and technological capabilities, positioning it as a key player in the industrial automation sector. Candidates should be aware of Burke Porter’s reputation for engineering excellence, customer collaboration, and continuous technological advancement.

How to land this job

  • Position your resume to emphasize your leadership and management experience in Quality Engineering, particularly in life sciences, highlighting your ability to lead teams and manage cross-functional projects.

  • Focus on showcasing your expertise with FDA QSR (21 CFR 820), ISO 13485, ISO 9001, and ISO 14971 standards, along with your skills in design controls, risk management, process validation, and supplier quality management.

  • Apply to this role through Burke Porter's corporate careers page and also on LinkedIn, ensuring your application is visible across multiple platforms to increase your chances.

  • Connect with current Quality Engineering managers or team members at Burke Porter on LinkedIn; start conversations by complimenting recent company innovations in medical device quality or asking about their experience managing quality processes under FDA regulations.

  • Optimize your resume for ATS by integrating keywords from the job description such as 'Quality Engineering Manager,' 'FDA QSR,' 'ISO 13485,' 'risk management,' 'process validation,' and 'supplier quality,' ensuring your resume passes automated screenings.

  • Leverage Jennie Johnson's Power Apply feature to automate applying through multiple sites, tailor your resume with the right keywords, and identify LinkedIn contacts to network with, saving you valuable time and improving your job search effectiveness.

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