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Manager, QA Operations

6fdcb75d 12f7 487c B0b2 Fa6ea2c6c2ea 19000101 000001 · Idaho Falls, ID - 4IDF, Idaho Falls, ID, US, Idaho Falls, ID · On Site · Active · $100,000–$125,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company6fdcb75d 12f7 487c B0b2 Fa6ea2c6c2ea 19000101 000001
TitleManager, QA Operations
Normalized title-
Department / team-
LocationIdaho Falls, ID, United States
Work modelOn Site
Employment typeFull Time
Salary$100,000–$125,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-04-10 / 2026-05-31
Changed / last seen2026-06-18 / 2026-06-18

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City jobsActive postings in Idaho Falls.Open
Work model jobsActive On Site postings.Open
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Linked records

Company6fdcb75d 12f7 487c B0b2 Fa6ea2c6c2ea 19000101 000001
Source114dadd0-e35f-43b8-8dad-cb3efaa506b5
ATS providerADP Workforce Now Recruiting

Description

PharmaLogic is the fastest-growing SPECT & PET radiopharmaceutical solutions provider and contract development and manufacturing organization (CDMO) with radiopharmacies across North America. We are passionate about expanding the power of radiopharmaceutical technology to provide transformative diagnostic and therapeutic agents to patients from bench to bedside. PharmaLogic offers you an exceptional opportunity to join our dynamic team as a QA Operations Manager! If you have a passion for nuclear medicine and want to make a significant contribution to patient care while working in a stimulating and dynamic environment, then this opportunity is for you. Purpose and Scope The QA Operations Manager is responsible for managing Quality Assurance support for manufacturing operations, focusing on aseptic processing, terminal sterilized products, sterility assurance, and contamination control. This role ensures compliance with current Good Manufacturing Practices (cGMP) following 21 CFR 210/211, internal procedures, and regulatory requirements while driving continuous product quality and operational excellence improvement. The QA Operations Manager also serves as the quality representative on cross-functional project teams and collaborates with internal and external alliance partners to support the consistent delivery of safe, high-quality pharmaceutical products. Essential Duties & Responsibilities Provide quality oversight for all sterile manufacturing operations, including aseptic processing, terminally sterilized processes, and related support areas. Manage the QA team to provide coverage and decision-making support across a variable radiopharmaceutical manufacturing schedule, including off-shift and potential weekend operations as needed. Ensure the integrity of sterile product manufacturing through robust sterility assurance practices. Build and oversee the facility electronic Quality Management System (eQMS) for the site. Manage QA review and approval of cGMP documentation, including procedures, protocols, deviations, out of specifications, CAPAs and change controls. Act as a subject matter expert (SME) during regulatory inspections and internal/external audits for quality assurance operations. Lead, coach, and develop quality team members to maintain a high-performing, quality-focused, and engaged workforce, to maintain compliance and foster continuous improvement. Monitor and report on key quality performance metrics to monitor performance and drive continuous improvement initiatives including management of an internal audit program. Collaborate with cross-functional departments (Manufacturing, QC, Engineering, Safety, Regulatory, etc.) to resolve quality-related issues and support new products and product lifecycle management. Serve as a QA representative on cross-functional project teams to ensure quality requirements are built into new processes, equipment, and products from the outset. Promote a proactive quality culture focused on patient safety, product quality, and regulatory compliance. Knowledge, Skills & Abilities Strong knowledge of cGMP regulations (21 CFR Parts 210/211), FDA Guidance for Aseptic Processing. Strong technical understanding of aseptic processing, sterilization methods, cleanroom classifications, and contamination control practices Understanding of contamination control practices and sterility assurance principles preferred. Experience with quality systems, deviation/investigation management, change control, and CAPA. Excellent written and verbal communication skills; capable of presenting quality topics to regulators and senior leadership. Ability to analyze complex problems, identify root causes, and drive corrective actions. Strong leadership, interpersonal, organizational skills and the ability to influence cross-functional teams. Education & Experience Bachelor’s degree in scientific discipline preferred. Five or more years’ experience in the pharmaceutical industry (210/211) in a quality role required. 5 years in sterile injectables preferred. Four or more years’ previous experience in a supervisory role required. PharmaLogic offers a competitive compensation package and superior benefits. Come join our winning team and begin a fulfilling career with us by applying today. PharmaLogic is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other protected class. Benefits Include: 401(k) retirement benefit program Medical Dental care Disability insurance Employee assistance program Extended health care Life insurance On-site parking Paid time off Vision care 9 am to 5 pm 40 hours per week

Full job record

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Source ID114dadd0-e35f-43b8-8dad-cb3efaa506b5
Board ID114dadd0-e35f-43b8-8dad-cb3efaa506b5
Provideradp_workforcenow
Provider Job Key558313
TitleManager, QA Operations
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Activeyes
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Department—
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CountryUnited States
RegionID
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First Seen At2026-05-31 18:17:55Z
Last Seen At2026-06-18 13:45:36Z
Last Checked At2026-06-18 13:45:36Z
Last Changed At2026-06-18 13:45:36Z
Inactive At—
Source Posted At2026-04-10 14:09:00Z
Source Updated At—
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    "requisitionDescription": "<div><div><div><p id=\"isPasted\"><span style=\"font-family: georgia, serif; font-size: 16px;\">PharmaLogic is the fastest-growing SPECT &amp; PET radiopharmaceutical solutions provider and contract development and manufacturing organization (CDMO) with radiopharmacies across North America. We are passionate about expanding the power of radiopharmaceutical technology to provide transformative diagnostic and therapeutic agents to patients from bench to bedside. &nbsp;<br></span></p><p><span style=\"font-family: georgia, serif; font-size: 16px;\">PharmaLogic offers you an exceptional opportunity to join our dynamic team as a QA Operations Manager!&nbsp;</span></p><p><span style=\"font-family: georgia, serif; font-size: 16px;\">If you have a passion for nuclear medicine and want to make a significant contribution to patient care while working in a stimulating and dynamic environment, then this opportunity is for you.&nbsp;</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\"><br></span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;' id=\"isPasted\"><span style=\"font-family: georgia, serif; font-size: 16px;\"><strong><u>Purpose and Scope</u></strong></span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">The QA Operations Manager is responsible for managing Quality Assurance support for manufacturing operations, focusing on aseptic processing, terminal sterilized products, sterility assurance, and contamination control. This role ensures compliance with current Good Manufacturing Practices (cGMP) following 21 CFR 210/211, internal procedures, and regulatory requirements while driving continuous product quality and operational excellence improvement. The QA Operations Manager also serves as the quality representative on cross-functional project teams and collaborates with internal and external alliance partners to support the consistent delivery of safe, high-quality pharmaceutical products.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\"><strong><u>Essential Duties &amp; Responsibilities</u></strong></span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Provide quality oversight for all sterile manufacturing operations, including aseptic processing, terminally sterilized processes, and related support areas.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Manage the QA team to provide coverage and decision-making support across a variable radiopharmaceutical manufacturing schedule, including off-shift and potential weekend operations as needed.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Ensure the integrity of sterile product manufacturing through robust sterility assurance practices.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Build and oversee the facility electronic Quality Management System (eQMS) for the site.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Manage QA review and approval of cGMP documentation, including procedures, protocols, deviations, out of specifications, CAPAs and change controls.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Act as a subject matter expert (SME) during regulatory inspections and internal/external audits for quality assurance operations.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Lead, coach, and develop quality team members to maintain a high-performing, quality-focused, and engaged workforce, to maintain compliance and foster continuous improvement.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Monitor and report on key quality performance metrics to monitor performance and drive continuous improvement initiatives including management of an internal audit program.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Collaborate with cross-functional departments (Manufacturing, QC, Engineering, Safety, Regulatory, etc.) to resolve quality-related issues and support new products and product lifecycle management.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Serve as a QA representative on cross-functional project teams to ensure quality requirements are built into new processes, equipment, and products from the outset.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Promote a proactive quality culture focused on patient safety, product quality, and regulatory compliance.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\"><strong><u>Knowledge, Skills &amp; Abilities</u></strong></span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Strong knowledge of cGMP regulations (21 CFR Parts 210/211), FDA Guidance for Aseptic Processing.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Strong technical understanding of aseptic processing, sterilization methods, cleanroom classifications, and contamination control practices</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Understanding of contamination control practices and sterility assurance principles preferred. Experience with quality systems, deviation/investigation management, change control, and CAPA.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Excellent written and verbal communication skills; capable of presenting quality topics to regulators and senior leadership.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Ability to analyze complex problems, identify root causes, and drive corrective actions.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Strong leadership, interpersonal, organizational skills and the ability to influence cross-functional teams.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\"><strong><u>Education &amp; Experience</u></strong></span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Bachelor&rsquo;s degree in scientific discipline preferred.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Five or more years&rsquo; experience in the pharmaceutical industry (210/211) in a quality role required.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">5 years in sterile injectables preferred.</span></p><p style='color: rgb(0, 0, 0); font-family: \"Times New Roman\"; font-size: medium; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'><span style=\"font-family: georgia, serif; font-size: 16px;\">Four or more years&rsquo; previous experience in a supervisory role required.</span></p><p id=\"isPasted\"><span style=\"font-family: georgia, serif; font-size: 16px;\">PharmaLogic offers a competitive compensation package and superior benefits. &nbsp;&nbsp;</span></p><p><span style=\"font-family: georgia, serif; font-size: 16px;\">Come join our winning team and begin a fulfilling career with us by applying today.<br><br>PharmaLogic is an Equal Opportunity Employer. &nbsp;&nbsp;</span></p><p><span style=\"font-family: georgia, serif; font-size: 16px;\">All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other protected class.&nbsp;<br></span></p><p><span style=\"font-family: georgia, serif; font-size: 16px;\"><strong><u>Benefits Include:</u></strong>&nbsp;</span></p><ul><li style=\"font-family: georgia, serif; font-size: 16px;\"><p>401(k) retirement benefit program&nbsp;</p></li><li style=\"font-family: georgia, serif; font-size: 16px;\"><p>Medical &nbsp;</p></li><li style=\"font-family: georgia, serif; font-size: 16px;\"><p>Dental care&nbsp;</p></li><li style=\"font-family: georgia, serif; font-size: 16px;\"><p>Disability insurance&nbsp;</p></li><li style=\"font-family: georgia, serif; 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