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Quality Risk Management Jobs in Pennsylvania (NOW HIRING)

Quality & Risk Director

Mechanicsburg, PA

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

As a Quality/Risk Director, you will oversee a hospital-wide quality management program, collaborating with various stakeholders to monitor and enhance the quality of patient care services. Join a ...

Quality/Risk Director

Pittsburgh, PA

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

As a Quality/Risk Director, you will oversee a hospital-wide quality management program, collaborating with various stakeholders to monitor and enhance the quality of patient care services. Join a ...

Quality Assurance Risk Manager

Lafayette Hill, PA ยท Remote

$70K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Serve as primary contact for program management. * Aggregate and analyze data from payer Value Base ... Facilitate Quality/Risk Management meetings & discussion with members of program management ...

Drive the ongoing development of Credit Risk Management Dashboards and Reports to support Credit Risk initiatives and the ongoing analysis of Credit Risk Models, Loan Performance, Application Quality ...

Drive the ongoing development of Credit Risk Management Dashboards and Reports to support Credit Risk initiatives and the ongoing analysis of Credit Risk Models, Loan Performance, Application Quality ...

The Director of Quality, Risk & Compliance leads and coordinates quality and performance ... Partners with the Legal, Compliance, and Risk Management Department on high-risk events, complaints ...

Enterprise Risk Management, Model Risk Management Program, Third-Party Provider Program ... quality assurance for issue data and performing end user testing for system enhancements. * Assists ...

Enterprise Risk Management, Model Risk Management Program, Third-Party Provider Program ... quality assurance for issue data and performing end user testing for system enhancements. * Assists ...

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Showing results 1-20

Quality Risk Management information

See Pennsylvania salary details

$38.6K

$91.3K

$138.8K

How much do quality risk management jobs pay per year?

As of Aug 16, 2026, the average yearly pay for quality risk management in Pennsylvania is $91,266.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,700.00 and $110,300.00 per year, depending on experience, location, and employer.

What is quality risk management?

A Quality Risk Management (QRM) job involves identifying, assessing, and mitigating risks that could impact product quality, compliance, or business operations. Professionals in this role apply risk management principles to processes in industries like pharmaceuticals, manufacturing, and healthcare. They work to ensure that risk control strategies align with regulatory requirements and industry standards. Responsibilities often include conducting risk assessments, implementing mitigation plans, and maintaining compliance with frameworks such as ICH Q9. Their goal is to enhance product quality, patient safety, and business continuity.

What are typical challenges faced in quality risk management?

One common challenge in Quality Risk Management is balancing rigorous regulatory compliance requirements with operational efficiency in fast-paced environments. Professionals must often manage competing priorities, respond quickly to emerging risks, and coordinate with cross-functional teams to implement effective mitigations. You may also encounter the need to continuously stay updated on changing industry standards and regulations. Overcoming these challenges requires proactive problem-solving, strong organizational skills, and the ability to communicate complex risk scenarios clearly to both technical and non-technical stakeholders.

What are the key skills and qualifications needed to thrive in quality risk management?

To excel in Quality Risk Management, you need a strong understanding of risk assessment methodologies, quality management systems, and regulatory standards, often backed by a degree in science, engineering, or a related field. Familiarity with tools such as ISO 9001, FMEA, CAPA systems, and compliance management software is commonly required, and certifications like Six Sigma or ASQ can be advantageous. Excellent analytical thinking, attention to detail, and persuasive communication help professionals effectively identify risks and collaborate across departments. These skills are essential to design robust quality processes, mitigate operational risks, and ensure consistent compliance and product safety.

Is quality risk management a good career?

Quality risk management is a valuable career in industries such as pharmaceuticals, manufacturing, and healthcare, focusing on identifying and mitigating risks to ensure product quality and compliance. Professionals in this field often require knowledge of regulatory standards, risk assessment tools, and certifications like RAC or CQRM. It offers opportunities for advancement and specialization, with a steady demand for skilled risk managers.

What qualifications do I need to be a Quality Risk Management?

To work in Quality Risk Management, candidates typically need a bachelor's degree in a related field such as life sciences, engineering, or healthcare. Relevant certifications like Certified Quality Auditor (CQA) or Risk Management Professional (RMP) can enhance qualifications, along with strong analytical skills and experience with quality systems and risk assessment tools. Familiarity with industry standards such as ISO 14971 or ICH Q9 is also beneficial.

What are popular job titles related to Quality Risk Management jobs in Pennsylvania?

For Quality Risk Management jobs in Pennsylvania, the most frequently searched job titles are:

Infographic showing various Quality Risk Management job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, 2% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $91,266 per year, or $43.9 per hour.

Director, Enterprise Risk Management

Cabaletta Bio Inc.

Philadelphia, PA โ€ข On-site, Remote

Full-time

PTO

Posted 4 days ago


Job description

Position Director, Enterprise Risk Management
Location: Philadelphia, (hybrid)
Reports to: Chief Compliance Officer
Cabaletta Bio (Nasdaq: CABA) is a late-stage clinical biotechnology company focused on developing and launching curative targeted cell therapies designed specifically for patients with autoimmune diseases. The CABAโ„ข platform encompasses two complementary strategies which aim to advance the discovery and development of engineered T cell therapies with the potential to become deep and durable, perhaps curative, treatments for a broad range of autoimmune diseases. The lead CARTA (Chimeric Antigen Receptor T cells for Autoimmunity) strategy is prioritizing the development of rese-cel, a 4-1BB-containing fully human CD19-CAR T cell investigational therapy. Rese-cel is currently being evaluated in the RESETโ„ข (REstoring SElf-Tolerance) clinical development program spanning multiple therapeutic areas, including rheumatology, neurology and dermatology. Cabaletta Bio's headquarters and labs are located in Philadelphia, PA. For more information, please visit www.cabalettabio.com and connect with us on LinkedIn.
Uniquely Differentiated. Rapid. Elegant.
At Cabaletta, we are driven by the shared mission of developing cures, where a patients' own cells are used to fight disease. We are building a culture grounded in the knowledge that successful cures can be achieved for patients if every member of the Cabaletta is focused on the success of the team. To nurture this, we make an active commitment to the well-being and continuous growth of each employee who joins the team. In this way, we are not only working to improve the lives of patients, but of everyone involved. #CabalettaCrew.
We're proud to be a Great Place to Work-Certifiedโ„ข company! #GPTWcertified Check out what our employees say makes working here so great: Working at Cabaletta Bio Inc | Great Place to Workยฎ
About the Position:
Cabaletta Bio is seeking a Director, Enterprise Risk Management to establish and lead the company's enterprise risk management (ERM) program as we advance toward BLA submission and commercial launch. Reporting to the Chief Compliance Officer, this role will build a structured, company-wide approach to identifying, assessing, mitigating, and monitoring risk across clinical, regulatory, quality, and commercial operations. A core focus of the role is quality risk management across the product lifecycle, including risk-based oversight of the company's external manufacturing network of three CDMOs, ensuring the risk management framework scales with the organization as it prepares for its first product launch.
This is a highly visible, cross-functional role suited to someone who can stand up a program from the ground floor, engage executive leadership and functional heads, and translate risk insights into practical, prioritized action.
Responsibilities:
Enterprise Risk Management
  • Design, implement, and lead the enterprise risk management framework, including governance structure, risk taxonomy, risk appetite statements, and escalation pathways
  • Facilitate periodic enterprise risk assessments with executive leadership and functional owners; maintain the corporate risk register and heat maps
  • Partner with functional leaders (Clinical, Regulatory, Quality, CMC, Commercial, IT, Finance, Legal) to identify emerging risks, define mitigation plans, and track remediation to closure
  • Develop and deliver risk reporting to the executive team and, as appropriate, the Board or Board committees
  • Integrate risk management with related programs, including quality risk management (ICH Q9 principles), business continuity, third-party/vendor risk, and inspection readiness
  • Monitor the external environment (regulatory enforcement trends, industry events, evolving guidance) and translate implications into the risk program
Quality Risk Management & External Manufacturing Oversight
  • Lead the application of quality risk management principles (ICH Q9(R1)) across the product lifecycle, including risk assessments supporting manufacturing, supply chain, and quality operations
  • Establish and maintain a risk-based framework for oversight of the company's external manufacturing network, including three CDMOs, spanning vendor risk assessments, ongoing risk monitoring, and periodic risk reviews
  • Partner with CMC, Quality, and Supply Chain to assess and manage risks associated with CDMO performance, including deviations, change control, capacity, technology transfer, comparability, and business continuity
  • Integrate CDMO and third-party risk into the corporate risk register with clear ownership, mitigation plans, and escalation criteria; ensure risk considerations are reflected in quality agreements and governance forums (e.g., joint steering committees, quality business reviews)
  • Support risk-based prioritization of vendor audits and person-in-plant or oversight activities in partnership with GxP Quality Audit
  • Ensure risk documentation supporting external manufacturing is inspection-ready and aligned with BLA submission expectations
Program Leadership
  • Serve as a trusted advisor to the CCO and functional leadership on risk matters
  • Contribute to inspection readiness and BLA-related activities where risk management documentation and governance are in scope
  • Build scalable tools, templates, and processes appropriate for a clinical-stage company transitioning to commercial operations
  • Potential to build and manage a small team as the function grows

Required Qualifications:
  • Bachelor's degree in life sciences, business, finance, or related field
  • 10+ years of progressive experience in the biopharmaceutical industry, with significant experience in enterprise risk management and quality risk management
  • Demonstrated experience designing or leading an ERM program (framework development, risk assessments, risk registers, executive reporting)
  • Hands-on experience applying quality risk management (ICH Q9) in a GxP environment, including risk assessments supporting external/contract manufacturing
  • Experience managing or overseeing risk across multiple CDMOs or contract manufacturing partners, including vendor risk assessment and governance
  • Experience supporting or operating within a pre-launch or newly commercial organization
  • Strong facilitation, analytical, and communication skills; able to engage credibly with executives and functional experts alike
  • Comfort with ambiguity and a hands-on, roll-up-your-sleeves orientation appropriate for a clinical-stage company

Preferred Qualifications:
  • Advanced degree (MBA, MS) or relevant certification (e.g., CRMP, ARM, CQA)
  • Experience in cell and gene therapy, rare disease, or other specialty/complex products
  • Experience with cell therapy or viral vector external manufacturing networks and associated supply chain risk
  • Experience presenting to boards or board committees

Our name - Cabaletta - is derived from the operatic term that represents a rapid, repetitive, and technically challenging section of an operatic aria, designed to showcase the skills of the lead singer. Analogously, Cabaletta Bio strives to achieve rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the driver of specific autoimmune diseases without the need for long-term immunosuppression.
For more information, please visit https://www.cabalettabio.com/join-our-crew
Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans.
Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law.
Cabaletta Bio, Inc. does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Cabaletta, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Cabaletta shall not be responsible to any individual or entity for any payment relating to any form of fee or compensation.
And, if a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Cabaletta has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm.
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