Quality Project Manager

Altus Spine

• $88K — $105K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's in Engineering or related field plus 5+ years of relevant experience; or Associate's degree plus 7+ years; or High School diploma plus 10+ years in a quality or engineering role.
  • Proven ownership of CAPA investigations from initiation through to closure and effectiveness verification.
  • Experience managing cross-functional quality projects with defined parameters.
  • Competence in root cause analysis, risk assessments, and quality systems within regulated sectors.
  • Familiarity with medical device regulations and ISO standards; knowledge of ISO 13485:2016 and 21 CFR Part 820 required.
  • Skilled in mechanical inspection using calipers and micrometers; RAM experience is a plus.
  • Proficient in Microsoft Office and CAD software, especially Creo.

Responsibilities

  • Own and manage the CAPA process from initiation to closure.
  • Lead structured investigations while coordinating input from various functional teams.
  • Establish methods for verifying the effectiveness of CAPA activities.
  • Maintain CAPA records and present status updates to management.
  • Analyze data to identify trends and opportunities for continuous improvement.
  • Lead quality projects involving remediation plans and regulatory transitions.
  • Coordinate the internal audit program, including scheduling and closure management.

Benefits

  • Multiple health insurance plans, including a no-cost HSA option for eligible employees.
  • Affordable dental and vision benefits.
  • 100% covered uniforms for all employees.
  • 401(k) with employer matching contributions.
  • Generous PTO: 100 hours during the first year.
  • Access to wellness coaching and support programs for employees and families.
  • Paid training opportunities for certifications and licenses.
Full Job Description
Now Hiring: Quality Project Manager

Full-Time| On-Site| West Chester, PA

We are seeking a Quality Project Manager to lead CAPA investigations, root cause analysis, and cross-functional quality projects while supporting inspection, compliance, and continuous improvement across the product lifecycle.

What We Offer

  • Competitive salary
  • Multiple health insurance plans, including a no-cost HSA health plan for eligible employees
  • Affordable dental and vision benefits
  • 100% paid uniforms
  • 401(k) with employer match
  • 100 hours of PTO during your first year
  • Work-Life Services Benefit Program (Employee + Family)
  • Group Life Insurance
  • Seven paid holidays every year
  • Investing in you: paid training for certifications and licenses
  • Wellness Coach Program access


Your Impact

  • Own and manage the Corrective and Preventive Action (CAPA) process from initiation through effectiveness verification and closure.
  • Lead structured root cause investigations, coordinating cross-functional input from Engineering, Operations, Suppliers, and Customers.
  • Establish effectiveness verification methods and evidence requirements for CAPA activities and ensure effectiveness is demonstrated prior to closure.
  • Maintain CAPA records, aging metrics, and escalation activities while presenting CAPA status, trends, and systemic themes to Quality Management.
  • Analyze data from complaints, nonconformities, returns, supplier performance, and inspection results to identify trends and continuous improvement opportunities.
  • Lead cross-functional quality projects involving remediation plans, validation activities, regulatory and standards transitions, and electronic quality management system changes.
  • Maintain project trackers identifying project owners, deliverables, and due dates, and provide project summaries for Management Review.
  • Coordinate the internal audit program, including audit scheduling, scope, auditor assignments, finding classification, and closure of findings.
  • Coordinate validation of quality management system software applications and maintain revalidation records following configuration changes.
  • Perform first production lot inspections for new and changed part numbers using calibrated inspection equipment and document results according to established procedures.
  • Perform targeted inspections on parts with elevated nonconformance, complaint, or return rates to support data analysis and improvement initiatives.
  • Provide backup inspection support during employee absences or production surges, including magnification inspection of small-font laser etching.
  • Support quality and regulatory activities associated with product commercialization, including 510(k) submission packaging and Management Review.
  • Apply working knowledge of applicable medical device regulations and standards, including ISO 13485:2016, 21 CFR Part 820, and ISO 14971:2019.


What You Bring

  • Bachelor's degree in Engineering or a technical field plus 5+ years of experience; Associate's degree plus 7+ years; or High School diploma plus 10+ years of experience in a quality or engineering role within a regulated environment. Medical device experience is preferred.
  • Experience owning CAPA investigations from initiation through effectiveness verification and closure.
  • Experience managing cross-functional projects with defined scope, schedules, and deliverables.
  • Experience with root cause analysis, risk-based analysis, and quality systems within a regulated environment.
  • Working knowledge of medical device regulations, ISO standards, and quality management systems.
  • Ability to use calipers, micrometers, and mechanical inspection instrumentation. RAM and Overlay experience is a plus.
  • Proficiency with Microsoft Office and experience with CAD software; Creo preferred.
  • Experience with or willingness to train and/or obtain certifications related to ISO 13485, ISO 14971, cGMP, and other quality and regulatory systems supporting medical device compliance and safety.
  • Valid driver's license.
  • Strong organizational skills with a detail-oriented and quality-focused approach.
  • Excellent communication and customer service skills, with the ability to conduct investigations with tact and professionalism.

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