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QA Senior Shop Floor Manager

2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001 · Lee, MA, US, Lee, MA · Active · $90,000–$130,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001
TitleQA Senior Shop Floor Manager
Normalized title-
Department / team-
LocationLee, MA, United States
Work model-
Employment typeFull Time
Salary$90,000–$130,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-06-02 / 2026-06-03
Changed / last seen2026-06-06 / 2026-06-06

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Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Lee.Open
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Linked records

Company2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001
Source95b4d553-a046-4c74-bcb4-9264e4e35c82
ATS providerADP Workforce Now Recruiting

Description

Position Summary The Senior QA Shop Floor Manager serves as a senior quality leader responsible for shop floor QA oversight, batch disposition, and the site's aseptic process simulation (media fill) program. Reporting to the Director of Quality Operations, this role ensures real-time quality presence during manufacturing, drives timely and defensible batch disposition decisions, and owns the strategic and technical execution of the media fill program across all sterile product platforms. Duties and Responsibilities Duties and Responsibilities (cont’d) Shop Floor Quality Provide direct oversight of real-time QA floor coverage during aseptic manufacturing operations, ensuring cGMP compliance, aseptic technique adherence, and immediate escalation of quality events Lead and develop a team of Specialists assigned to shop floor functions, fostering a proactive quality culture and high standard of GMP behavior Review and approve in-process documentation, logbooks, and batch record entries in real time; identify trends in errors or deviations and drive targeted corrective actions Serve as the quality authority (by way of the team) for line clearance, in-process controls, and manufacturing hold/release decisions during production, as needed Batch Disposition Own the end-to-end batch disposition process, ensuring batch records are reviewed thoroughly, exceptions are appropriately investigated, and release or rejection decisions are made with scientific rigor and within defined cycle time targets Manage disposition timelines and communicate proactively with client-facing teams and Planning regarding batch status and any disposition risks Ensure batch disposition documentation meets regulatory and client quality agreement requirements across all product platforms and client accounts Track and trend disposition cycle times, batch record error rates, and right-first-time metrics; present findings and improvement plans to Quality leadership Aseptic Process Simulation (Media Fill) Program Serve as the site subject matter expert (SME) for aseptic process simulation, owning the strategy, design, execution oversight, and continuous improvement of the media fill program across all filling platforms and product types (liquid, lyophilized) Ensure media fill protocols reflect worst-case manufacturing conditions including maximum interventions, shift changes, line stoppages, and full fill durations; maintain alignment with FDA aseptic processing guidance and EU GMP Annex 1 Lead media fill failure investigations (as needed) with appropriate scientific depth, including contamination pathway assessment, barrier performance evaluation, and robust CAPA with verified effectiveness Maintain media fill trending data and present program performance, risk assessments, and improvement initiatives to site and client quality leadership Serve as the primary point of contact for media fill topics during regulatory inspections and client audits; ensure inspection-ready documentation and clear, defensible storyboards Assist scheduling team with coordination of media fills to align with semi-annual requirement Cross-Functional & Client Engagement Partner with Manufacturing, Validation, Microbiology, and Sterility Assurance teams to ensure alignment on aseptic standards, process controls, and quality expectations Support client calls and technical quality meetings related to batch disposition status, media fill performance, and manufacturing deviations Contribute to audit readiness activities and represent shop floor quality and media fill topics during regulatory inspections and client audits Regulatory Responsibilities Conduct business in a responsible manner that complies with all state, OSHA, and HIPAA regulations Maintain a detailed and comprehensive understanding of FDA, EU, and other regulatory agency requirements Supervisory Responsibilities Manage quality activities at SSM Provide leadership to the GMP team related to Quality Culture Experience Five (5) to ten (10) years’ experience working in a cGMP environment Five (5) years’ experience in a Quality role Three (3) to five (5) years’ experience supervising individuals in a cGMP environment Education Bachelor’s Degree Relevant experience may be substituted for degree Knowledge, Skills & Abilities Skilled in the use of Microsoft office applications (Word, Excel, PowerPoint) and Adobe Acrobat High attention to detail Good writing, public speaking and presentation skills Must be able to travel approximately 10% of the time Physical Requirements Ability to sit for prolonged periods of time Ability to stand for prolong periods of time as required Able to lift up to 10lbs

Full job record

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Source ID95b4d553-a046-4c74-bcb4-9264e4e35c82
Board ID95b4d553-a046-4c74-bcb4-9264e4e35c82
Provideradp_workforcenow
Provider Job Key594264
TitleQA Senior Shop Floor Manager
Normalized Title—
Statusactive
Activeyes
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Department—
Team—
Employment Typefull_time
Workplace Type—
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CountryUnited States
RegionMA
CityLee
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Salary Min90,000
Salary Max130,000
Salary CurrencyUSD
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Apply URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=2479a996-4c61-4623-bd61-684f50d6e2a0&ccId=19000101_000001&lang=en_US&type=JS&jobId=594264&jwId=9201156311178_1
First Seen At2026-06-03 09:33:06Z
Last Seen At2026-06-06 13:18:53Z
Last Checked At2026-06-06 13:18:53Z
Last Changed At2026-06-06 13:18:53Z
Inactive At—
Source Posted At2026-06-02 14:00:00Z
Source Updated At—
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Reporting to the Director of Quality Operations, this role ensures real-time quality presence during manufacturing, drives timely and defensible batch disposition decisions, and owns the strategic and technical execution of the media fill program across all sterile product platforms.</span></p></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Duties and Responsibilities</span></strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Duties and Responsibilities</span></strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>(cont&rsquo;d)</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin-left:26.3pt;text-indent:-.25in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Shop Floor Quality</span></strong></p><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;margin-left: 16.3px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Provide direct oversight of real-time QA floor coverage during aseptic manufacturing operations, ensuring cGMP compliance, aseptic technique adherence, and immediate escalation of quality events</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Lead and develop a team of Specialists assigned to shop floor functions, fostering a proactive quality culture and high standard of GMP behavior</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Review and approve in-process documentation, logbooks, and batch record entries in real time; identify trends in errors or deviations and drive targeted corrective actions</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Serve as the quality authority (by way of the team) for line clearance, in-process controls, and manufacturing hold/release decisions during production, as needed</span></li></ul></div><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin-left:26.3pt;text-indent:-.25in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Batch Disposition</span></strong></p><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;margin-left: 16.3px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Own the end-to-end batch disposition process, ensuring batch records are reviewed thoroughly, exceptions are appropriately investigated, and release or rejection decisions are made with scientific rigor and within defined cycle time targets</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Manage disposition timelines and communicate proactively with client-facing teams and Planning regarding batch status and any disposition risks</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Ensure batch disposition documentation meets regulatory and client quality agreement requirements across all product platforms and client accounts</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Track and trend disposition cycle times, batch record error rates, and right-first-time metrics; present findings and improvement plans to Quality leadership</span></li></ul></div><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin-left:26.3pt;text-indent:-.25in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Aseptic Process Simulation (Media Fill) Program</span></strong></p><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;margin-left: 16.3px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Serve as the site subject matter expert (SME) for aseptic process simulation, owning the strategy, design, execution oversight, and continuous improvement of the media fill program across all filling platforms and product types (liquid, lyophilized)</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Ensure media fill protocols reflect worst-case manufacturing conditions including maximum interventions, shift changes, line stoppages, and full fill durations; maintain alignment with FDA aseptic processing guidance and EU GMP Annex 1</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Lead media fill failure investigations (as needed) with appropriate scientific depth, including contamination pathway assessment, barrier performance evaluation, and robust CAPA with verified effectiveness</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Maintain media fill trending data and present program performance, risk assessments, and improvement initiatives to site and client quality leadership</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Serve as the primary point of contact for media fill topics during regulatory inspections and client audits; ensure inspection-ready documentation and clear, defensible storyboards</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Assist scheduling team with coordination of media fills to align with semi-annual requirement</span></li></ul></div><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin-left:26.3pt;text-indent:-22.5pt;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Cross-Functional &amp; Client Engagement</span></strong></p><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;margin-left: 16.3px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Partner with Manufacturing, Validation, Microbiology, and Sterility Assurance teams to ensure alignment on aseptic standards, process controls, and quality expectations</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Support client calls and technical quality meetings related to batch disposition status, media fill performance, and manufacturing deviations</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Contribute to audit readiness activities and represent shop floor quality and media fill topics during regulatory inspections and client audits</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Regulatory Responsibilities&nbsp;</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 16.3px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Conduct business in a responsible manner that complies with all state, OSHA, and HIPAA regulations</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Maintain a detailed and comprehensive understanding of FDA, EU, and other regulatory agency requirements</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 23.95pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Supervisory Responsibilities</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 23.95pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 16.3px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Manage quality activities at SSM&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Provide leadership to the GMP team related to Quality Culture</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 23.15pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Experience</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 23.15pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 16.3px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Five (5) to ten (10) years&rsquo; experience working in a cGMP environment</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Five (5) years&rsquo; experience in a Quality role&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Three (3) to five (5) years&rsquo; experience supervising individuals in a cGMP environment</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 19.75pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Education</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 19.75pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 16.3px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Bachelor&rsquo;s Degree</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Relevant experience may be substituted for degree</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 19.3pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Knowledge, Skills &amp; Abilities</span></strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 19.3pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 16.3px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Skilled in the use of Microsoft office applications (Word, Excel, PowerPoint) and Adobe Acrobat</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>High attention to detail</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Good writing, public speaking and presentation skills</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Must be able to travel approximately 10% of the time</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 30.1pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Physical Requirements</span></strong><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 30.1pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 16.3px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Ability to sit for prolonged periods of time</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Ability to stand for prolong periods of time as required</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Able to lift up to 10lbs</span></li></ul></div></td></tr></tbody></table></div></div>\n",
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