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Open nowPosted yesterday

Quality Specialist 3

Hologic106 open roles

Where
Marlborough, MA, United States
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Your applicationOpen nowQuality Specialist 3Hologic · Marlborough, MA, United States

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The clock on this job

Early applications get read.

12.4% of postings close within 7 days. Measured by our own scanner across the market. Hologic postings stay open a median of 14 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.4%7 days
  4. 20.0%14 days
  5. 35.5%30 days
  6. 58.6%60 days
This job: posted yesterday

Hologic median: 14 days open

The posting

Job Description

We are looking for senior-level QMS Specialist responsible for serving as a CAPA, Nonconformance, and Quality Compliance SME to drive compliant, sustainable QMS improvements, support remediation and inspection readiness, and partner cross-functionally across regulated medical device quality system workstreams.

Knowledge

  • Quality Management System (QMS) requirements in a regulated medical device environment
  • CAPA, Nonconformance (NC), and quality compliance processes, methodologies, and best practices
  • FDA 21 CFR 820 / QMSR, ISO 13485, ISO 14971, EU MDR, MDSAP, and other applicable global regulatory standards
  • Root cause analysis, risk assessment, corrective actions, containment, disposition, and effectiveness checks
  • Internal audits, external audits, change control, management review, and quality data trending
  • Audit and inspection readiness, including FDA inspections, Notified Body audits, MDSAP audits, and internal audits
  • Quality metrics, dashboards, reporting tools, and data-driven continuous improvement
  • Statistics and statistical analysis, preferred
  • Product Lifecycle Management systems such as Agile, preferred
  • Reporting systems such as Qlik, PowerBI, or equivalent tools

Skills

  • Ability to serve as a Subject Matter Expert for CAPA, NC, and quality compliance processes
  • Strong root cause analysis, risk assessment, problem-solving, and analytical skills
  • Ability to lead or support remediation of QMS processes, procedures, and records
  • Strong technical writing skills for regulatory documentation, investigations, CAPAs, NCs, and quality records
  • Ability to develop sustainable corrective actions and effectiveness checks
  • Ability to manage dashboards, metrics, reports, and quality performance tracking
  • Strong written and verbal communication skills, including executive-level updates
  • Ability to present information to director-level leadership
  • Ability to lead cross-functional teams and manage multiple workstreams
  • Ability to train, coach, and mentor junior staff and cross-functional teams
  • Strong organization and program management skills

Behavior

  • Hands-on, accountable individual contributor with SME-level ownership
  • Detail-oriented with a strong focus on compliance, effectiveness, sustainability, and quality
  • Proactive in identifying gaps, trends, systemic risks, and process improvement opportunities
  • Collaborative and able to partner effectively across functions, sites, and divisions
  • Comfortable advising teams on complex or systemic quality issues
  • Adaptable and able to operate in high-visibility, fast-paced environments
  • Strong escalation judgment for CAPA, NC, and compliance issues
  • Continuous improvement mindset
  • Able to coach others and promote process adherence and regulatory expectations

Experience

  • 2–5 years of Quality Systems experience with a technical bachelor’s degree, or 1–3 years with a master’s degree
  • Experience in a regulated industry, preferably medical devices
  • Experience managing or working with CAPA, NC, and other QMS processes across multiple sites
  • Experience supporting QMS compliance workstreams, including CAPA, NC, audits, change control, and quality data trending
  • Experience supporting remediation activities in response to audit findings, inspection observations, enforcement actions, or continuous improvement initiatives
  • Experience preparing for or supporting FDA inspections, Notified Body/MDSAP audits, and internal audits
  • Experience working cross-functionally with process owners, CAPA/NC owners, remediation leads, and quality teams
  • Experience using Agile or equivalent PLM systems
  • Experience using Qlik, PowerBI, or other metric reporting systems
  • Ability to travel up to 15%, including potential international travel

Why join Hologic?

We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.

The annualized base salary range for this role is $85,200 - $133,300 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.

Agency and Third-Party Recruiter Notice

Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

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