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Senior Coordinator, Quality Assurance

4a237553 Bf3a 4a62 Ac08 Fdd8f7d3ca48 19000101 000001 · North Brunswick, NJ, US, North Brunswick, NJ · Active · $60,000–$75,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company4a237553 Bf3a 4a62 Ac08 Fdd8f7d3ca48 19000101 000001
TitleSenior Coordinator, Quality Assurance
Normalized title-
Department / team-
LocationNorth Brunswick, NJ, United States
Work model-
Employment typeFull Time
Salary$60,000–$75,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-01-27 / 2026-05-31
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 North Brunswick.Open
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Linked records

Company4a237553 Bf3a 4a62 Ac08 Fdd8f7d3ca48 19000101 000001
Source12aecaa3-febf-4544-8d20-69ea4b58d77d
ATS providerADP Workforce Now Recruiting

Description

Role Overview The Senior QA Coordinator plays a key role in supporting the Quality Assurance department by ensuring compliance to SOPs, batch records, master manufacturing records, GMP documentation and to 21 CFR Part 111 and 117 and other relevant quality standards in the nutraceutical manufacturing environment. This position will be responsible for coordinating quality assurance programs designed to ensure continuous production of products and includes tracking products, materials, status, and location. Involved in the issuance /review of batch records, on floor collection of samples , preparation of Master compliance documents and participating in audit preparations . Areas of Responsibility Oversee and maintain GMP documentation systems, including SOPs, batch records, deviations, CAPAs, change controls, and training records. Issuance of Manufacturing / Coating / Packaging Batch Cards Collects samples from on floor production for further testing and retention Distributes testing samples to Inhouse testing Analytical , Elemental and Microbiology Lab Preparation of different types of In process Labels for production , QA samples to be provided along with the Batch Records Scanning , photocopy, filing of GMP documents per Batch Product requirements Coordinate Finished Product release in Syspro Performs Sampling of materials / products per procedures as needed Reads and understands approved specifications/standards assigned to the project Keeps up to date with the regulatory requirements around documentation and implements changes if necessary. Work with internal teams to obtain an in-depth understanding of the processes and documentation requirements. Collaborate with Manufacturing, R&D, QC, and Regulatory teams to ensure seamless execution of quality processes. Play an active role on quality management team within the organization Any other duties which may be assigned from time to time Other Responsibilities Including Safety: Works in a safe and responsible manner to create an injury-free and incident-free workplace. Complies with all job-related safety and other training requirements. Keeps management informed of area activities and of any significant problems. Requirements Education & Qualification: Bachelor’s degree in Life Sciences, Chemistry, Biology, or a related field. Minimum 3–5 years of QA experience in a nutraceutical, dietary supplement, or pharmaceutical manufacturing environment. Strong knowledge of GMP, 21 CFR Part 111,117 and other relevant quality standards. Detail-oriented with strong organizational and documentation skills. Proficient in Microsoft Office; experience with electronic Quality Management Systems (eQMS) preferred. Excellent communication and problem-solving skills. Certifications, Licenses, Credentials: N/A Skills & Ability In-depth understanding of nutraceutical manufacturing processes and regulatory compliance. Proficient in QA documentation, process audits, and deviation handling. Strong analytical and decision-making skills. Familiar with QMS tools, GMP documentation, and data integrity principles. Working knowledge of SOP writing, change control, and risk assessment. Physical Requirements (lifting, etc.): Ability to lift up to 35 lbs.; occasionally lift and move up to 50 pounds. Must stand and walk on production floor a minimum of 6 hours per shift Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from waist, or squatting, walking short distances. Occasionally works from a rolling ladder or step stool. Must be able to wear all PPE including lab coat, face mask, booties, gloves, safety glasses. Work Environment (Office, Warehouse, temperature extremes, etc.): Work is regularly performed inside a manufacturing and packaging environment where temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employees can be exposed daily to chemicals and cleaning agents. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all the job responsibilities, duties, skill, or working conditions. In addition, this document does not create an employment contract, implied or otherwise, other than an "at will" relationship. USPL is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law. Benefits And Compensation: Our benefits are designed to help you move forward in your career, and in areas of your life outside of USPL. From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&D insurance. We also offer a matched 401(k) savings plan. Employees have the opportunity to receive compensation in the form of premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment. Job Description Acknowledgement I have read and understand the job requirements, responsibilities, and expectations set forth in the job description provided for my position. I attest that I can perform the essential job functions as outlined with or without any reasonable accommodations. shift schedule :- General Shift 8.30am – 5.00 pm or extended

Full job record

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Source ID12aecaa3-febf-4544-8d20-69ea4b58d77d
Board ID12aecaa3-febf-4544-8d20-69ea4b58d77d
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Provider Job Key590250
TitleSenior Coordinator, Quality Assurance
Normalized Title—
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Activeyes
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CountryUnited States
RegionNJ
CityNorth Brunswick
Salary Raw60000.00 To 75000.00 (USD) Annually
Salary Min60,000
Salary Max75,000
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First Seen At2026-05-31 18:18:23Z
Last Seen At2026-06-06 11:26:48Z
Last Checked At2026-06-06 11:26:48Z
Last Changed At2026-06-06 11:26:48Z
Inactive At—
Source Posted At2026-01-27 16:49:00Z
Source Updated At—
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    "requisitionDescription": "<div><p><br></p><div align=\"center\" style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;' id=\"isPasted\"><table border=\"1\" cellspacing=\"0\" cellpadding=\"0\" width=\"739\" style=\"border-collapse: collapse;border: none;width: 739px;\"><tbody><tr><td valign=\"top\" style=\"width: 739px; border: 1pt solid windowtext; background: rgb(191, 191, 191); padding: 0in 5.4pt; height: 12.35pt; vertical-align: top;\"><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>Role Overview</span></strong></p></td></tr><tr><td valign=\"top\" style=\"width: 739px; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; background: white; padding: 0in 5.4pt; height: 12.35pt; vertical-align: top;\"><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;background:white;'>The <strong>Senior QA Coordinator</strong> plays a key role in supporting the Quality Assurance department by ensuring compliance to SOPs, batch records, master manufacturing records, GMP documentation and to 21 CFR Part 111 and 117 and other relevant quality standards in the nutraceutical manufacturing environment.&nbsp;</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;background:white;'>&nbsp;</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;background:white;'>This position will be responsible for coordinating quality assurance programs designed to ensure continuous production of products and includes tracking products, materials, status, and location. Involved in the issuance /review of batch records, on floor collection of samples , preparation of Master compliance documents and participating in audit preparations .</span></p></td></tr><tr><td valign=\"top\" style=\"width: 739px; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; background: rgb(191, 191, 191); padding: 0in 5.4pt; height: 12.35pt; vertical-align: top;\"><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>Areas of Responsibility</span></strong></p></td></tr><tr><td valign=\"top\" style=\"width: 739px; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; padding: 0in 5.4pt; height: 22pt; vertical-align: top;\"><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>Oversee and maintain GMP documentation systems, including SOPs, batch records, deviations, CAPAs, change controls, and training records.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>Issuance of Manufacturing / Coating / Packaging Batch Cards&nbsp;</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>Collects samples from on floor production for further testing and retention&nbsp;</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>Distributes testing samples to Inhouse testing Analytical , Elemental and Microbiology Lab</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>Preparation of different types of In process Labels for production , QA samples to be provided along with the Batch Records</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>Scanning , photocopy, filing of GMP documents per Batch Product requirements</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>Coordinate &nbsp;Finished Product release in Syspro</span></li></ul><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;\"><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;\">Performs Sampling of materials / products per procedures as needed</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;\">Reads and understands approved specifications/standards assigned to the project</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;\">Keeps up to date with the regulatory requirements around documentation and implements changes if necessary.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;\">Work with internal teams to obtain an in-depth understanding of the processes and documentation requirements.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;\">Collaborate with Manufacturing, R&amp;D, QC, and Regulatory teams to ensure seamless execution of quality processes.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;\">Play an active role on quality management team within the organization</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;\">Any other duties which may be assigned from time to time</span></li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:.0001pt;margin-left:.2in;text-align:  justify;text-indent:-.2in;background:white;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>Other Responsibilities Including Safety:&nbsp;</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:.0001pt;margin-left:.2in;text-align:  justify;text-indent:-.2in;background:white;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;\"><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Works in a safe and responsible manner to create an injury-free and incident-free workplace.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;\">Complies with all job-related safety and other training requirements.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;\">Keeps management informed of area activities and of any significant problems.</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 739px; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; background: rgb(191, 191, 191); padding: 0in 5.4pt; height: 11.3pt; vertical-align: top;\"><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>Requirements</span></strong></p></td></tr><tr><td valign=\"top\" style=\"width: 720px; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; background: white; padding: 0in 5.4pt; height: 76pt; vertical-align: top;\"><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>Education &amp; Qualification:</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;\"><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Bachelor&rsquo;s degree in Life Sciences, Chemistry, Biology, or a related field.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Minimum 3&ndash;5 years of QA experience in a nutraceutical, dietary supplement, or pharmaceutical manufacturing environment.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Strong knowledge of GMP, 21 CFR Part 111,117 &nbsp;and other relevant quality standards.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Detail-oriented with strong organizational and documentation skills.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Proficient in Microsoft Office; experience with electronic Quality Management Systems (eQMS) preferred.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Excellent communication and problem-solving skills.</span></li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>Certifications, Licenses, Credentials:</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;\"><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">N/A</span></li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>Skills &amp; Ability</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;\"><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">In-depth understanding of nutraceutical manufacturing processes and regulatory compliance.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Proficient in QA documentation, process audits, and deviation handling.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Strong analytical and decision-making skills.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Familiar with QMS tools, GMP documentation, and data integrity principles.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Working knowledge of SOP writing, change control, and risk assessment.</span></li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>Physical Requirements (lifting, etc.):</span></strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>&nbsp; &nbsp; &nbsp;&nbsp;</span></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;\"><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Ability to lift up to 35 lbs.; occasionally lift and move up to 50 pounds.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Must stand and walk on production floor a minimum of 6 hours per shift</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from waist, or squatting, walking short distances.</span></li><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Occasionally works from a rolling ladder or step stool.&nbsp;</span></li></ul></div><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-right:.1in;margin-bottom:6.0pt;text-align:       justify;background:white;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>Must be able to wear all PPE including lab coat, face mask, booties, gloves, safety glasses.</span></li></ul><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;background:white;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;color:black;'>Work Environment (Office, Warehouse, temperature extremes, etc.):</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;\"><li style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><span style=\"font-size:15px;color:black;\">Work is regularly performed inside a manufacturing and packaging environment where temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. &nbsp;</span><span style=\"font-size:15px;color:#00000A;\">Employees can be exposed daily to chemicals and cleaning agents.</span></li></ul></div></td></tr></tbody></table></div><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><em><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></em></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>The above statements are intended to describe the general nature and level of work being&nbsp;performed by people assigned to this job. They are not intended to be an exhaustive list of all the job responsibilities, duties, skill, or working conditions. In addition, this document does not create an employment contract, implied or otherwise, other than an &quot;at will&quot; relationship.</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>USPL is proud to be an Equal Opportunity Employer.</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law.</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>Benefits And Compensation: </span></strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>Our benefits are designed to help you move forward in your career, and in areas of your life outside of USPL. From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&amp;D insurance. We also offer a matched 401(k) savings plan. Employees have the opportunity to receive compensation in the form of premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment.</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><br></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:0in;margin-bottom:3.0pt;margin-left:-.1in;text-align:center;' data-pasted=\"true\"><strong><u>Job Description Acknowledgement</u></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:0in;margin-bottom:3.0pt;margin-left:-.1in;text-align:center;'><br></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:-.1in;text-align:justify;'><span style=\"font-size:15px;\">I have read and understand the job requirements, responsibilities, and expectations set forth in the job description provided for my position. I attest that I can perform the essential job functions as outlined with or without any reasonable accommodations.</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>shift schedule :- &nbsp;General Shift &nbsp;8.30am &ndash; 5.00 pm or extended&nbsp;</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><strong><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;text-align:justify;'><span style='font-size:15px;font-family:\"Times New Roman\",serif;'>&nbsp;</span></p><p><br></p></div>\n",
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