What are the responsibilities and job description for the Program Service Specialist - Deviation Management position at UL Solutions?
Job Description
The Program Service Specialist - Deviation Management is responsible for leading the investigation, assessment, resolution, and closure of product quality deviations and failing laboratory test reports across a broad portfolio of consumer packaged goods sold by a major national retailer. Product categories include cosmetics, over-the-counter (OTC) drugs, foods, dietary supplements, personal care products, household products, and general merchandise.
This role serves as the primary point of contact for managing non-conforming product issues identified through laboratory testing, retailer surveillance programs, consumer complaints, regulatory inquiries, supplier investigations, and internal quality reviews. The Deviation Manager ensures timely risk assessment, root cause analysis, corrective and preventive action (CAPA) development, and communication with suppliers, laboratories, and retailer stakeholders to support compliant and defensible disposition decisions.
The ideal candidate possesses strong technical knowledge of quality systems, regulatory requirements, laboratory testing methodologies, and consumer product safety standards, with the ability to balance compliance, business risk, and operational efficiency.
This is a full-time, hybrid (3 days in-office) position located at 200 Highland Corporate Drive, Cumberland, RI.
Responsibilities
Deviation Investigation & Resolution
About Us
A global leader in applied safety science, UL Solutions (NYSE: ULS) transforms safety, security and sustainability challenges into opportunities for customers in more than 110 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers’ product innovation and business growth. The UL Mark serves as a recognized symbol of trust in our customers’ products and reflects an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. Our science is your advantage.
About The Team
Our global network of 80 laboratories is constantly evolving, because the world around us is always changing. We embrace this — we invest in improving our equipment and our skills so we’re one step ahead of the market. One day we could be setting up a burn test and the next, simulating a tornado. And because we’re always evolving, your career will evolve alongside us, whether you’re working on brand new technology or connecting with experts around the globe. Join our team, drive the growth of our organization and deliver real change — in a changing world.
The Program Service Specialist - Deviation Management is responsible for leading the investigation, assessment, resolution, and closure of product quality deviations and failing laboratory test reports across a broad portfolio of consumer packaged goods sold by a major national retailer. Product categories include cosmetics, over-the-counter (OTC) drugs, foods, dietary supplements, personal care products, household products, and general merchandise.
This role serves as the primary point of contact for managing non-conforming product issues identified through laboratory testing, retailer surveillance programs, consumer complaints, regulatory inquiries, supplier investigations, and internal quality reviews. The Deviation Manager ensures timely risk assessment, root cause analysis, corrective and preventive action (CAPA) development, and communication with suppliers, laboratories, and retailer stakeholders to support compliant and defensible disposition decisions.
The ideal candidate possesses strong technical knowledge of quality systems, regulatory requirements, laboratory testing methodologies, and consumer product safety standards, with the ability to balance compliance, business risk, and operational efficiency.
This is a full-time, hybrid (3 days in-office) position located at 200 Highland Corporate Drive, Cumberland, RI.
Responsibilities
Deviation Investigation & Resolution
- Manage the end-to-end lifecycle of deviations, non-conformances, and failing laboratory test reports.
- Evaluate product failures involving chemical, microbiological, physical, labeling, packaging, and performance testing.
- Conduct detailed investigations to determine root cause and assess product impact.
- Review laboratory reports, Certificates of Analysis (COAs), specifications, formulations, manufacturing records, supplier documentation, and historical quality data.
- Determine appropriate product disposition, including release, rework, retesting, market withdrawal, or destruction recommendations.
- Ensure investigations are completed within established service-level expectations and retailer requirements.
- Perform risk-based evaluations to determine potential impact on consumer safety, product performance, regulatory compliance, and brand reputation.
- Assess deviations involving:
- OTC drug active ingredient levels
- Microbiological contamination
- Heavy metals and impurities
- Stability failures
- Labeling and claims compliance
- Nutritional discrepancies
- Escalate high-risk findings to senior leadership and retailer stakeholders when necessary.
- Partner with Product Development, Sourcing, Legal, Supplier Management, and Retail Quality teams.
- Communicate investigation status, risk assessments, and recommended actions to stakeholders.
- Provide technical guidance on product quality and compliance issues.
- Bachelor's degree in Food Science, Chemistry, Biology, Microbiology, Pharmaceutical Sciences, Regulatory Affairs, Quality Assurance, or related scientific discipline.
- 2 years of experience in quality assurance, quality systems, regulatory compliance, laboratory testing, or deviation management.
- Experience managing product quality investigations within consumer packaged goods, cosmetics, OTC drugs, food, dietary supplements, or related industries.
- Strong understanding of root cause analysis methodologies and CAPA systems.
- Experience reviewing laboratory testing data and technical reports.
- Excellent technical writing, documentation, and communication skills.
- Ability to manage multiple complex investigations simultaneously while meeting deadlines.
- Experience supporting major retailers testing programs
- Knowledge of OTC drug monographs, cosmetic regulations, food safety requirements, and retailer quality programs.
- Experience with supplier qualification programs and third-party manufacturing oversight
About Us
A global leader in applied safety science, UL Solutions (NYSE: ULS) transforms safety, security and sustainability challenges into opportunities for customers in more than 110 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers’ product innovation and business growth. The UL Mark serves as a recognized symbol of trust in our customers’ products and reflects an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. Our science is your advantage.
About The Team
Our global network of 80 laboratories is constantly evolving, because the world around us is always changing. We embrace this — we invest in improving our equipment and our skills so we’re one step ahead of the market. One day we could be setting up a burn test and the next, simulating a tornado. And because we’re always evolving, your career will evolve alongside us, whether you’re working on brand new technology or connecting with experts around the globe. Join our team, drive the growth of our organization and deliver real change — in a changing world.
Salary : $64,100 - $68,000