Quality Control Supervisor

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 Control Supervisor at Burke Porter leads the QC team to ensure product quality and regulatory compliance in medical and life sciences manufacturing, impacting overall quality management and innovation.

• Responsibilities and impact

  The supervisor manages daily QC operations, oversees inspections, maintains compliance with FDA and ISO standards, leads the QC team, coordinates with other departments, supports audits, and drives continuous improvement.

• Compensation and benefits

  The position offers an annual salary range of $70,000-$91,000 based on experience, with a comprehensive benefits package including health insurance and retirement plans.

• Experience and skills

  Candidates should have 3-5 years in QC within life sciences, 1-2 years supervisory experience, knowledge of FDA QSR, ISO standards, Lean/Six Sigma, and strong leadership and communication skills.

• Career development

  The role supports professional growth through team leadership, performance evaluations, and involvement in audits and continuous improvement initiatives.

• Work environment and culture

  The company promotes a positive, collaborative environment focused on quality, compliance, and safety, reflecting core values and professionalism.

• Company information

  Ascential Medical and Life Sciences specializes in precision engineering and automation for medical devices and diagnostics, emphasizing innovation and regulatory compliance.

• Team overview

  The candidate will supervise a team of QC inspectors and technicians, fostering a collaborative and compliant work environment.

• Job location and travel

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

• Unique job features

  The role involves leading quality control in a regulated medical device environment with opportunities to influence process improvements and participate in high-level audits.

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

• Tailor your resume to emphasize leadership experience in supervising Quality Control teams, highlighting your ability to manage workflow, train staff, and enforce compliance with FDA QSR, ISO 13485, and ISO 9001 standards, as these are critical for the Quality Control Supervisor role at Burke Porter, an Ascential Technologies Brand.

• Focus on showcasing your expertise in quality control operations including inspection, testing, documentation, and handling non-conforming materials, as well as your familiarity with regulatory audits and continuous improvement initiatives like Lean or Six Sigma methodologies.

• Apply through multiple channels such as Burke Porter's corporate careers page, LinkedIn job postings, and relevant job boards to maximize your chances of being noticed by recruiters for this position.

• Connect with current employees or managers in the Quality Control or Quality Assurance divisions at Burke Porter on LinkedIn, using ice breakers like commenting on their recent projects related to medical device quality or asking about how their team integrates quality standards in daily operations to build rapport and gain insights.

• Optimize your resume for ATS by incorporating keywords from the job description such as 'Quality Management System,' 'FDA 21 CFR Part 820,' 'ISO 13485,' 'team leadership,' 'inspection,' 'non-conforming materials,' and 'continuous improvement' to ensure your resume passes automated screenings effectively.

• Leverage Jennie Johnson's Power Apply feature to automate applying through multiple platforms, tailor your resume with relevant keywords, and identify LinkedIn contacts for networking, allowing you to focus your time on preparing for interviews and strategic networking.