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Qms Manager Jobs in Delaware (NOW HIRING)

Hologic

Sr Quality Systems Specialist

Newark, DE · On-site

$85.20K - $133.30K/yr

Working understanding of Quality Management Systems (QMS), especially Management Review, Quality System audits, CAPA, nonconformances, and quality planning. * Knowledge and experience with ISO 13485 ...

Hologic Inc.

Sr Quality Systems Specialist

Newark, DE · On-site

$85.20K - $133.30K/yr

Working understanding of Quality Management Systems (QMS), especially Management Review, Quality System audits, CAPA, nonconformances, and quality planning. * Knowledge and experience with ISO 13485 ...

Hologic

Sr Quality Systems Specialist

Newark, DE · On-site

$85.20K - $133.30K/yr

Working understanding of Quality Management Systems (QMS), especially Management Review, Quality System audits, CAPA, nonconformances, and quality planning. * Knowledge and experience with ISO 13485 ...

Hologic

Project Manager, NPI

Newark, DE · On-site

$78K - $122.10K/yr

Manages projects from initiation through launch, including planning, resourcing, scheduling ... Use internal phase/gate and QMS processes; ensure required Operations documentation is created and ...

Hologic Inc.

Project Manager, NPI

Newark, DE

$78K - $122.10K/yr

Manages projects from initiation through launch, including planning, resourcing, scheduling ... Use internal phase/gate and QMS processes; ensure required Operations documentation is created and ...

Datwyler

Quality Assurance Manager

Middletown, DE · On-site

Leads the Regulatory and External Customer Audits including preparation, execution and follow-up. * Maintains and continuously improves the site's Quality Management System (QMS) in alignment with ...

Datwyler

Quality Assurance Manager

Middletown, DE

Leads the Regulatory and External Customer Audits including preparation, execution and follow-up. * Maintains and continuously improves the site's Quality Management System (QMS) in alignment with ...

Hologic Inc.

Quality Assurance Engineer 2

Newark, DE

$97.60K - $152.70K/yr

Knowledge * Quality Management Systems (QMS) for medical devices * GMP, GDP principles and basic regulatory frameworks * Medical device Quality System Regulations (21 CFR 820), ISO 13485, MDD ...

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Qms Manager information

See Delaware salary details

$24K

$86.2K

$158.1K

How much do qms manager jobs pay per year?

As of May 28, 2026, the average yearly pay for qms manager in Delaware is $86,234.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a QMS Manager, and why are they important?

To thrive as a QMS Manager, you need expertise in quality management systems, regulatory compliance, and process improvement, typically supported by a relevant degree and experience in quality assurance. Familiarity with ISO standards (such as ISO 9001), audit management tools, and quality software platforms is essential. Strong leadership, problem-solving skills, and effective communication help drive a culture of continuous improvement and team alignment. These competencies ensure that organizational processes meet regulatory requirements and consistently deliver high-quality outcomes.

How does a QMS Manager typically collaborate with other departments to ensure compliance and continuous improvement?

A QMS Manager regularly works cross-functionally with departments such as production, engineering, and procurement to implement and maintain quality standards. This involves coordinating audits, facilitating training sessions, and gathering feedback to identify areas for process improvement. Effective communication and negotiation skills are essential, as the QMS Manager must align diverse teams toward compliance goals and foster a culture of continuous improvement. Regular meetings and collaborative problem-solving are part of ensuring that quality objectives are met across the organization.

What are QMS Managers?

QMS Managers, or Quality Management System Managers, are professionals responsible for developing, implementing, and overseeing an organization's quality management system. They ensure that processes and products meet established quality standards and comply with relevant regulations. Their duties often include conducting audits, managing documentation, training staff on quality procedures, and driving continuous improvement initiatives. QMS Managers play a crucial role in maintaining customer satisfaction and supporting organizational efficiency.

What is the difference between Qms Manager vs Quality Assurance Supervisor?

AspectQms ManagerQuality Assurance Supervisor
CertificationsISO 9001 Lead Auditor, CQEISO 9001 Lead Auditor, CQE
Work EnvironmentOversees quality management systems across departmentsSupervises quality assurance team and daily testing activities
Industry UsageUsed in manufacturing, aerospace, automotiveCommon in manufacturing, pharmaceuticals, food industry
Primary FocusDeveloping, maintaining, and improving QMSMonitoring product quality and compliance

The Qms Manager and Quality Assurance Supervisor roles share similar certifications and industry usage, but the Qms Manager focuses on managing the entire quality management system, while the Supervisor concentrates on daily quality assurance activities. Both positions are vital for ensuring product quality and compliance within manufacturing and related industries.

What are popular job titles related to Qms Manager jobs in Delaware? For Qms Manager jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Qms Manager jobs in Delaware look for? The top searched job categories for Qms Manager jobs in Delaware are:
Qms Manager jobs near you
Sr Quality Systems Specialist

Sr Quality Systems Specialist

Hologic

Newark, DE • On-site

$85.20K - $133.30K/yr

Full-time

Posted 12 days ago

Hologic rating

7.9

Company rating: 7.9 out of 10

Based on 24 frontline employees who took The Breakroom Quiz

154th of 415 rated machine equipment manufacturers

Job description

Job Description
Hologic is seeking a Senior Quality Systems Specialist to strengthen and sustain our Quality Management System (QMS) and quality operations. In this role, you'll work across engineering, supply chain, regulatory, marketing, and other functions to investigate process, product, and system issues, support audits and inspections, and help develop and refine quality procedures. You'll use data-driven tools to analyze trends, support continuous improvement, and ensure our systems are audit-ready. If you enjoy solving diverse quality challenges, partnering cross-functionally, and owning impactful quality system initiatives in a regulated environment, this role is a strong fit.
Knowledge
  • Working understanding of Quality Management Systems (QMS), especially Management Review, Quality System audits, CAPA, nonconformances, and quality planning.
  • Knowledge and experience with ISO 13485, MDSAP, EU MDR, and 21 CFR 820/QMSR in a medical device or IVD environment.
  • Familiarity with internal and external audit expectations and documentation needs (front-room/back-room).
  • Understanding of GMP concepts and quality system processes such as Quality Agreements, Quality Plans (QPLs), and Periodic Review.
  • Beneficial: Basic understanding of statistics and statistical analysis for quality metrics and KPIs.
  • Beneficial: Experience with Agile or equivalent PLM systems.

Skills
  • Excellent computer skills, including use of word processing, spreadsheet, and database applications (data entry, querying, and report generation).
  • Strong technical writing skills for drafting procedures, quality system documentation, audit responses, and investigation reports.
  • Ability to apply auditing knowledge to help build robust, audit-ready systems and documentation.
  • Experience with Quality Management Systems, particularly Management Review, CAPA, and quality system audits.
  • Capable of documenting technical work and leading/assisting investigations and improvements in a GMP-regulated environment.
  • Able to modify, maintain, and create procedures and processes related to QMS elements.
  • Comfortable presenting materials and quality system status to director-level leadership.
  • Strong interpersonal skills to collaborate with junior staff, peers, and senior stakeholders across the organization.

Behaviors
  • Models Hologic's quality values, promoting defect prevention, reduction of variation and waste, and continuous improvement.
  • Detail-oriented and thorough, ensuring quality records, procedures, and outputs are accurate and compliant.
  • Collaborative and communication-focused, working effectively with cross-functional teams at all levels.
  • Uses sound judgment in selecting methods and techniques to solve diverse quality system problems.
  • Proactive and self-directed, requiring little day-to-day instruction while responding effectively to new assignments.
  • Comfortable networking with senior internal and external personnel within area of expertise.

Experience
  • College Degree required; Technical Bachelor's Degree preferred (e.g., Engineering, Life Sciences, or related field). With a non-technical college degree: 3-5 years in the medical device or IVD industry. Or with a technical Bachelor's degree: 2-4 years of experience; 1-3 years with a Master's degree.
  • Experience in a certified medical device or pharmaceutical manufacturing environment.
  • Hands-on experience with QMS elements such as Management Review, audits, CAPA, and quality planning.
  • Experience supporting internal and external audits and/or FDA inspections is beneficial.

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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