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Lead, Quality Control Chemist

4a237553 Bf3a 4a62 Ac08 Fdd8f7d3ca48 19000101 000001 · North Brunswick, NJ, US, North Brunswick, NJ · Active · $85,000–$90,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company4a237553 Bf3a 4a62 Ac08 Fdd8f7d3ca48 19000101 000001
TitleLead, Quality Control Chemist
Normalized title-
Department / team-
LocationNorth Brunswick, NJ, United States
Work model-
Employment typeFull Time
Salary$85,000–$90,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-04-03 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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Linked records

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

Description

Job Description Date 02/2024 Location 1300 Airport Road, North Brunswick NJ Title Lead, Quality Control Chemist Department Quality Control Reports to Manager, Quality Control Laboratory FLSA (Exempt or Non-Exempt Exempt Role Overview The Lead, QC Chemist performs specific routine analysis of samples of raw materials, in process, and finished products according to established (official and/or in-house) test procedures. Testing assesses the strength, identify, purity of the test samples and/or raw materials. The Chemist prepares reagents, standards, and solutions and may monitor and verify quality in accordance with statistical process and other control procedures. The Chemist maintains & organizes testing’s and compliance while working in a fast-paced environment with changing priorities. The duties and responsibilities described for each level are not limited to those outlined and are not intended to be a comprehensive list of all activities, functions, or responsibilities required of the position. Management reserves the right to modify, assign, or reassign duties and responsibilities at any time based on business needs. Areas of Responsibility Performs assigned sampling, physical, chemical tests and assay on raw materials, active dietary ingredients, in-process, finished, and stability products in an FDA regulated lab environment. Uses a variety of wet chemicals, physical and instrumental techniques as well as routine QC instruments HPLC, GC, IR, Auto Titrator, Bulk Density, UV Spectrophotometer, Dissolution, Karl Fisher (KF), Potentiometer. Troubleshoots HPLC, GC, QC instruments for specific tests in order to assist in determining the root cause of aberrant results and help in performing Lab investigations / OOS. Evaluates daily raw data sheets for product samples and release, if needed. Coordinates annual review of STPS / SOPS as per USPL procedures. Prepare new methods and test procedures for new or existing raw materials and finished products. Ensures compliance with company and customer specifications as well as federal, state and local regulatory requirements. Perform floor supervision of QC Chemists for routine testing, if required. Prepares and reviews QC related documents during and finishing of testing of sample. Submit all testing related documents like data sheets, chromatograms, spectras, instruments print outs in timely manner to Qc Documentation department to release the batch of raw material / finished product. Prepares and/or Reviews Test Procedures, SOP's and Protocols as assigned. Performs maintenance and calibrations of laboratory instruments /equipment, if required to help in-house calibrations. Assures GMP compliance according to FDA CFR Part 111 and USPL SOPs / guidelines. Complies with all regulatory/ in-house requirements (may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, GLP, documentation) when performing the assigned activity. Trains new QC Chemists to perform instrumental testing. Must be able to work extended hours as needed and occasional weekends. Other duties and responsibilities as assigned by QC in-charge / management. 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: BS/MS in Chemistry or related scientific disciplines. Five (5) years of basic chemistry techniques (can be academic) is a plus. Minimum of 5 years QC lab work experience in handling HPLC, GC, KF, Dissolution, DT and other sophisticated lab instruments in dietary supplements, food or OTC / Pharmaceutical manufacturing industry. Certifications, Licenses, Credentials: N/A Skills & Ability Ability to maintain integrity and honesty at all times and to communicate with transparency. Ability to work independently or as part of a team. Solid understanding of cGMP’s and GLP and is familiar with 21 CFR Part 11. Strong working knowledge of Microsoft Word, Excel. Good documentation practices and able to write simple, clear reports. Meets commitments on time and practices time-management skills. Seeks to identify continuous improvement needs. Experience with Shimadzu LC2010, Nexera, GC2010, Thermo ICP-MS, Labsolution and Waters Empower Lab Software a plus. Physical Requirements (lifting, etc.): Ability to navigate office, lab, and/or plant floor working environments. Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances and leaning over equipment as well as kneeling on the floor to clean under the equipment. Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators. On occasion may need to lift up to 20lbs Work Environment (Office, Warehouse, temperature extremes, etc.): Work is regularly performed inside a laboratory 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. May execute up to 20% of their work at the bench level either standing or sitting on a stool. Work performed in a standard office environment is without unpleasant or hazardous conditions. 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 accommodation.

Full job record

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Source ID12aecaa3-febf-4544-8d20-69ea4b58d77d
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Provideradp_workforcenow
Provider Job Key598730
TitleLead, Quality Control Chemist
Normalized Title—
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CountryUnited States
RegionNJ
CityNorth Brunswick
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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 At2026-04-03 22:45:00Z
Source Updated At—
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    "requisitionDescription": "<p>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;</p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:6.0pt;text-align:center;background:white;' data-pasted=\"true\"><strong><span style=\"font-size:21px;color:#414141;\">Job Description</span></strong></p><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" width=\"630\" style=\"width: 92%; border-collapse: collapse;\" data-pasted=\"true\"><colgroup><col style=\"width: 10.1623%;\"><col style=\"width: 27.3271%;\"><col style=\"width: 21.3493%;\"><col style=\"width: 41.1614%;\"></colgroup><tbody><tr><td style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; height: 0.2in;\"><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;text-align:justify;'><strong><span style=\"font-size:15px;\">Date</span></strong></p></td><td style=\"border-top: 1pt solid windowtext; 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border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; padding: 0in 5.4pt; height: 18.4pt;\"><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;text-align:justify;'><strong><span style=\"font-size:15px;\">Title</span></strong></p></td><td style=\"border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 18.4pt;\"><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;'><span style=\"font-size:15px;\">Lead, Quality Control Chemist</span></p></td><td style=\"border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 18.4pt;\"><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;text-align:justify;'><strong><span style=\"font-size:15px;\">Department</span></strong></p></td><td style=\"border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 18.4pt;\"><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;'><span style=\"font-size:15px;\">Quality Control</span></p></td></tr><tr><td style=\"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: 0.2in;\"><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;text-align:justify;'><strong><span style=\"font-size:15px;\">Reports to</span></strong></p></td><td style=\"border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 0.2in;\"><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;'><span style=\"font-size:15px;\">Manager, Quality Control Laboratory</span></p></td><td style=\"border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 0.2in;\"><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;text-align:justify;'><strong><span style=\"font-size:15px;\">FLSA (Exempt or Non-Exempt</span></strong></p></td><td style=\"border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 0.2in;\"><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;'><span style=\"font-size:15px;\">Exempt</span></p></td></tr></tbody></table><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;text-align:justify;background:white;'>&nbsp;</p><table border=\"1\" cellspacing=\"0\" cellpadding=\"0\" width=\"666\" style=\"width: 94%; margin-left: -13.75pt; border-collapse: collapse; border: none;\" data-pasted=\"true\"><colgroup><col style=\"width: 100%;\"></colgroup><tbody><tr><td valign=\"top\" style=\"border: 1pt solid windowtext; background: rgb(208, 206, 206); padding: 0in 5.4pt; height: 12.35pt; vertical-align: top;\"><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:0in;text-align:justify;line-height:115%;'><strong><span style=\"color:black;\">Role Overview</span></strong></p></td></tr><tr><td valign=\"top\" style=\"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: 12.35pt; vertical-align: top;\"><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:12.0pt;text-align:justify;line-height:115%;background:white;'><span style=\"color:black;\">The Lead, QC Chemist performs specific routine analysis of samples of raw materials, in process, and finished products according to established (official and/or in-house) test procedures. Testing assesses the strength, identify, purity of the test samples and/or raw materials. The Chemist prepares reagents, standards, and solutions and may monitor and verify quality in accordance with statistical process and other control procedures. The Chemist maintains &amp; organizes testing&rsquo;s and compliance while working in a fast-paced environment with changing priorities.&nbsp;</span></p><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:12.0pt;text-align:justify;line-height:115%;background:white;'><span style=\"color:black;\">The duties and responsibilities described for each level are not limited to those outlined and are not intended to be a comprehensive list of all activities, functions, or responsibilities required of the position. Management reserves the right to modify, assign, or reassign duties and responsibilities at any time based on business needs.</span></p></td></tr><tr><td valign=\"top\" style=\"border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; background: rgb(208, 206, 206); padding: 0in 5.4pt; height: 12.35pt; vertical-align: top;\"><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:0in;text-align:justify;line-height:115%;'><strong><span style=\"color:black;\">Areas of Responsibility</span></strong></p></td></tr><tr><td valign=\"top\" style=\"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: 130pt; vertical-align: top;\"><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Performs assigned sampling, physical, chemical tests and assay on raw materials, active dietary ingredients, in-process, finished, and stability products in an FDA regulated lab environment. Uses a variety of wet chemicals, physical and instrumental techniques as well as routine QC instruments HPLC, GC, IR, Auto Titrator, Bulk Density, UV Spectrophotometer, Dissolution, Karl Fisher (KF), Potentiometer.&nbsp;</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Troubleshoots HPLC, GC, QC instruments for specific tests in order to assist in determining the root cause of aberrant results and help in performing Lab investigations / OOS.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Evaluates daily raw data sheets for product samples and release, if needed.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Coordinates annual review of STPS / SOPS as per USPL procedures.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Prepare new methods and test procedures for new or existing raw materials and finished products.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Ensures compliance with company and customer specifications as well as federal, state and local regulatory requirements.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Perform floor supervision of QC Chemists for routine testing, if required.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Prepares and reviews QC related documents during and finishing of testing of sample. Submit all testing related documents like data sheets, chromatograms, spectras, instruments print outs in timely manner to Qc Documentation department to release the batch of raw material / finished product.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Prepares and/or Reviews Test Procedures, SOP&#39;s and Protocols as assigned.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Performs maintenance and calibrations of laboratory instruments /equipment, if required to help in-house calibrations.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Assures GMP compliance according to FDA CFR Part 111 and USPL SOPs / guidelines.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Complies with all regulatory/ in-house requirements (may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, GLP, documentation) when performing the assigned activity.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Trains new QC Chemists to perform instrumental testing.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Must be able to work extended hours as needed and occasional weekends.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Other duties and responsibilities as assigned by QC in-charge / management.</span></li></ul><p style='margin-right:.1in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:12.0pt;margin-bottom:.0001pt;text-align:justify;line-height:  115%;'><strong><span style='font-family:  \"Times New Roman\",serif;'>Other Responsibilities Including Safety:</span></strong></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>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: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Complies with all job-related safety and other training requirements.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;margin-right:.1in;text-align:justify;line-height:       115%;\"><span style='font-family:\"Times New Roman\",serif;'>Keeps management informed of area activities and of any significant problems.</span></li></ul></td></tr><tr><td valign=\"top\" style=\"border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; background: rgb(208, 206, 206); padding: 0in 5.4pt; height: 11.3pt; vertical-align: top;\"><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:0in;text-align:justify;line-height:115%;'><strong><span style=\"color:black;\">Requirements</span></strong></p></td></tr><tr><td valign=\"top\" style=\"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: 0.3in; vertical-align: top;\"><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:6.0pt;margin-bottom:0in;text-align:justify;line-height:115%;'><strong>Education &amp; Qualification:</strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: -0.25in;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\">BS/MS in Chemistry or related scientific disciplines.</li><li style=\"margin:0in;font-size:16px;font-family: initial;\">Five (5) years of<span style=\"color:black;background:white;\">&nbsp;basic chemistry techniques (can be academic) is a plus.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\">Minimum of 5 years QC lab work experience in handling HPLC, GC, KF, Dissolution, DT and other sophisticated lab instruments in <span style=\"color:black;background:  white;\">dietary supplements, food or OTC / Pharmaceutical manufacturing industry.</span></li></ul></div><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:0in;text-align:justify;line-height:115%;'><strong>Certifications, Licenses, Credentials:</strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: -0.25in;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>N/A</span></li></ul></div><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:0in;text-align:justify;line-height:115%;'><strong>Skills &amp; Ability</strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: -0.25in;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\">Ability to maintain integrity and honesty at all times and to communicate with transparency.&nbsp;</li><li style=\"margin:0in;font-size:16px;font-family: initial;\">Ability to work independently or as part of a team.&nbsp;</li><li style=\"margin:0in;font-size:16px;font-family: initial;\">Solid understanding of cGMP&rsquo;s and GLP and is familiar with 21 CFR Part 11.</li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>Strong working knowledge of Microsoft Word, Excel.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>Good documentation practices and able to write simple, clear reports.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>Meets commitments on time and practices time-management skills.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>Seeks to identify continuous improvement needs.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\">Experience with Shimadzu LC2010, Nexera, GC2010, Thermo ICP-MS, Labsolution and Waters&nbsp;</li><li style=\"margin:0in;font-size:16px;font-family: initial;\">Empower Lab Software a plus.</li></ul></div><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:0in;text-align:justify;'><strong>&nbsp;</strong></p><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:0in;text-align:justify;'><strong>Physical Requirements (lifting, etc.):</strong>&nbsp;</p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: -0.25in;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>Ability to navigate office, lab, and/or plant floor working environments.&nbsp;</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances and leaning over equipment as well as kneeling on the floor to clean under the equipment.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>On occasion may need to lift up to 20lbs</span></li></ul></div><p style='margin-right:.1in;margin-left:  0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:0in;text-align:justify;line-height:115%;background:white;'><strong><span style=\"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;margin-left: -0.25in;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>Work is regularly performed inside a laboratory 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.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>May execute up to 20% of their work at the bench level either standing or sitting on a stool.&nbsp;</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Times New Roman\",serif;'>Work performed in a standard office environment is without unpleasant or hazardous conditions.&nbsp;</span></li></ul></div></td></tr></tbody></table><p style='margin-right:-.1in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:0in;text-align:justify;background:white;'><em><span style=\"color:black;\">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 &quot;at will&quot; relationship.</span></em></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-bottom:6.0pt;text-align:justify;'><br></p><p style='margin-right:0in;margin-left:.2in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:6.0pt;text-align:center;'><strong><span style='font-family:\"Times New Roman\",serif;'>USPL is proud to be an Equal Opportunity Employer.</span></strong></p><p style='margin-right:0in;margin-left:.2in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:6.0pt;text-align:center;'><br></p><p style='margin-right:0in;margin-left:.2in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:6.0pt;text-align:justify;'><span style='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-right:0in;margin-left:.2in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:6.0pt;text-align:justify;'><span style='font-family:\"Times New Roman\",serif;'>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&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-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-bottom:6.0pt;text-align:center;'><strong><u><span style='font-family:\"Times New Roman\",serif;'>Job Description Acknowledgement</span></u></strong></p><p style='margin-right:0in;margin-left:-.1in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:6.0pt;text-align:justify;'>&nbsp;</p><p style='margin-right:0in;margin-left:-.1in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:6.0pt;text-align:justify;'><span style='font-family:\"Times New Roman\",serif;'>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 accommodation.</span></p><p style='margin-right:0in;margin-left:-.1in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:6.0pt;text-align:justify;'><br></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-bottom:6.0pt;text-align:justify;'><br></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;'><br></p><p style='margin-right:0in;margin-left:.2in;font-size:16px;font-family:\"Calibri\",sans-serif;margin:0in;margin-top:0in;margin-bottom:6.0pt;text-align:center;'><strong>&nbsp;</strong></p>\n",
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