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Associate, QA Operation Support

4a237553 Bf3a 4a62 Ac08 Fdd8f7d3ca48 19000101 000001 · North Brunswick, NJ, US, North Brunswick, NJ · Active · $22–$25 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company4a237553 Bf3a 4a62 Ac08 Fdd8f7d3ca48 19000101 000001
TitleAssociate, QA Operation Support
Normalized title-
Department / team-
LocationNorth Brunswick, NJ, United States
Work model-
Employment typeFull Time
Salary$22–$25 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-03-27 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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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

Job Description Date 7/2025 Location 1300 Airport Road, North Brunswick NJ Title Associate, QA Operation Support Department Quality Assurance Reports to Manager, QA Operations FLSA (Exempt or Non-Exempt Exempt Role Overview This position is one of high regulatory responsibility that provides direct quality oversight for the cGMP production of Dietary Supplements and nutraceuticals. This position will help ensure compliance to SOPs, batch records, master manufacturing records, and to 21 CFR Part 111 and 117. Areas of Responsibility Level 1 - Associate, QA Operations Support Summary of the Role: Entry-level position in the QA department focused on supporting sampling and/or dispensing activities under supervision. Intended for fresh graduates or new entrants to the pharmaceutical QA function. 🔸 Key Responsibilities: Assist with material sampling and dispensing under guidance. Support line clearance and hygiene compliance checks. Label and transport sampled materials as per SOPs. Maintain basic records and area cleanliness. Learn cGMP and SOP requirements. Level 2 – Associate, QA Operations Support 🔸 Summary of the Role: Responsible for performing QA-related sampling and/or releasing , dispensing activities in compliance with SOPs and regulatory requirements. Ensures proper documentation and real-time quality assurance during material handling. 🔸 Key Responsibilities: Execute material sampling , releasing , dispensing as per approved procedures as needed. Perform line clearance and ensure area readiness. Label materials correctly and ensure segregation of sampled vs. un-sampled. Maintain logbooks, records, and data entries accurately. Report deviations or incidents to the coordinator promptly. Level 3 – Associate, QA Operations Support 🔸 Summary of the Role: Mid-level QA role with responsibility for overseeing sampling and dispensing operations. Ensures compliance, accuracy, and efficiency of all QA activities in the function. 🔸 Key Responsibilities: Supervise and coordinate QA sampling releasing , dispensing as per approved procedures as needed. Review documentation completed by associates. Ensure timely and compliant execution of sampling plans. Conduct training and mentoring for junior staff. Support audits, investigations, and CAPA implementation. Performs issuance of batch cards of Manufacturing, Coating and Packaging. Collects samples from on floor production for further testing and retention. Distributes testing samples to In-house Analytical , Elemental and Microbiology Labs Prepares In process Labels for production ,and QA samples to be provided along with the Batch Records Other Responsibilities Including Safety: Works in a safe and responsible manner in order 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: Level 1 – Associate, QA Operations Support B.Sc. / B.Pharm. or equivalent in a science-related field. Relevant QA experience working within a GMP and/or with GCP regulations. Level 2 – Associate, QA Operations Support B.Sc. / B.Pharm. (required) 1–3 years of experience in QA or related area preferred working within a GMP and/or with GCP regulations. Level 3 – Associate, QA Operations Support B.Sc. / B.Pharm. (minimum); M.Sc. / M.Pharm. preferred 3–6 years of relevant QA experience working within a GMP and/or with GCP regulations. Certifications, Licenses, Credentials: N/A Skills & Ability Level 1 – Associate, QA Operations Support Willingness to learn and follow instructions. Basic understanding of GMP (preferred). Good observational and documentation skills. Teamwork and adaptability. Level 2 – Associate, QA Operations Support Working knowledge of cGMP and SOPs. Attention to detail and strong documentation habits. Familiarity with quality systems (e.g., logbooks, traceability). Communication and coordination abilities Level 3 – Associate, QA Operations Support Strong knowledge of cGMP and quality systems. Leadership and team management skills. Effective communication and problem-solving. Ability to handle audits, deviations, and cross-functional coordination. Good documentation and review capabilities. Physical Requirements (lifting, etc.): Ability to lift up to 50 lbs.; occasionally lift and move up to 75 pounds. 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 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 environment where temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employee 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. shift schedule 1st shift: 7:00 AM - 3:30 PM, 2nd shift: 3:00 PM - 11:30 PM and 3rd shift: 11:00 PM - 7:30 AM 2nd shift - 3:00 PM to 11:15 PM

Full job record

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TitleAssociate, QA Operation Support
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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 At2026-03-27 22:16:00Z
Source Updated At—
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    "requisitionDescription": "<div><div><div><div><div><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-bottom:6.0pt;text-align:center;' id=\"isPasted\"><strong><span style=\"font-size:21px;\">Job Description</span></strong></p><div align=\"center\" style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><table border=\"1\" cellspacing=\"0\" cellpadding=\"0\" width=\"744\" style=\"width: 69%; border-collapse: collapse; border: none; margin-right: calc(19%); margin-left: calc(12%);\"><tbody><tr><td style=\"width: 10.4839%; border: 1pt solid windowtext; padding: 0in 5.4pt; height: 0.2in;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong><span style=\"font-size:13px;\">Date</span></strong></p></td><td style=\"width: 33.871%; border-top: 1pt solid windowtext; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-image: initial; border-left: none; padding: 0in 5.4pt; height: 0.2in;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><span style=\"font-size:13px;\">7/2025</span></p></td><td style=\"width: 16.129%; border-top: 1pt solid windowtext; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-image: initial; border-left: none; padding: 0in 5.4pt; height: 0.2in;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong><span style=\"font-size:13px;\">Location</span></strong></p></td><td style=\"width: 100.446%; border-top: 1pt solid windowtext; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-image: initial; border-left: none; padding: 0in 5.4pt; height: 0.2in;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><span style=\"font-size:13px;\">1300 Airport Road, North Brunswick NJ&nbsp;</span></p></td></tr><tr><td style=\"width: 10.4839%; 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: 18.4pt;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong><span style=\"font-size:13px;\">Title</span></strong></p></td><td style=\"width: 33.871%; 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:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"font-size:13px;\">Associate, QA Operation Support</span></p></td><td style=\"width: 16.129%; 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:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong><span style=\"font-size:13px;\">Department</span></strong></p></td><td style=\"width: 100.446%; 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:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><span style=\"font-size:13px;\">Quality Assurance</span></p></td></tr><tr><td style=\"width: 10.4839%; 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: 28.75pt;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong><span style=\"font-size:13px;\">Reports to</span></strong></p></td><td style=\"width: 33.871%; border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 28.75pt;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><span style=\"font-size:13px;\">Manager, QA Operations&nbsp;</span></p></td><td style=\"width: 16.129%; border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 28.75pt;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong><span style=\"font-size:13px;\">FLSA (Exempt or Non-Exempt</span></strong></p></td><td style=\"width: 100.446%; border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 28.75pt;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><span style=\"font-size:13px;\">Exempt</span></p></td></tr></tbody></table></div><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;background:white;'><span style=\"font-size:4px;\">&nbsp;</span></p><div align=\"center\" style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><table border=\"1\" cellspacing=\"0\" cellpadding=\"0\" width=\"739\" style=\"border-collapse: collapse; border: none; width: 69%; margin-right: calc(19%); margin-left: calc(12%);\"><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:\"Times New Roman\",serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><strong><span style=\"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:\"Times New Roman\",serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><span style=\"color:black;background:white;\">This position is one of high regulatory responsibility that provides direct quality oversight for the cGMP production of Dietary Supplements and nutraceuticals. This position will help ensure compliance to SOPs, batch records, master manufacturing records, and to 21 CFR Part 111 and 117.</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:\"Times New Roman\",serif;margin-top:0in;margin-right:.1in;margin-bottom:  6.0pt;margin-left:0in;text-align:justify;'><strong><span style=\"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: 3.5pt; vertical-align: top;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong>Level 1 - Associate, QA Operations Support</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;'><strong>Summary of the Role:</strong><br>&nbsp;Entry-level position in the QA department focused on supporting sampling and/or dispensing activities under supervision. Intended for fresh graduates or new entrants to the pharmaceutical QA function.</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style='font-family:\"Segoe UI Emoji\",sans-serif;'>🔸</span> Key Responsibilities:</strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Assist with material sampling and dispensing under guidance.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Support line clearance and hygiene compliance checks.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Label and transport sampled materials as per SOPs.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Maintain basic records and area cleanliness.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Learn cGMP and SOP requirements.</li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-top:0in;margin-right:.1in;margin-bottom:.0001pt;margin-left:.5in;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong>Level 2 &ndash; Associate, QA Operations Support</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;'><strong><span style='font-family:\"Segoe UI Emoji\",sans-serif;'>🔸</span> Summary of the Role:</strong><br>Responsible for performing QA-related sampling and/or releasing , dispensing activities in compliance with SOPs and regulatory requirements. Ensures proper documentation and real-time quality assurance during material handling.<strong>&nbsp;</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;'><strong><span style='font-family:\"Segoe UI Emoji\",sans-serif;'>🔸</span> Key Responsibilities:</strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Execute material sampling , releasing , dispensing as per approved procedures as needed.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Perform line clearance and ensure area readiness.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Label materials correctly and ensure segregation of sampled vs. un-sampled.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Maintain logbooks, records, and data entries accurately.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Report deviations or incidents to the coordinator promptly.</li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-top:0in;margin-right:.1in;margin-bottom:.0001pt;margin-left:.5in;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'>&nbsp;<strong>Level 3 &ndash; Associate, QA Operations Support</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;'><strong><span style='font-family:\"Segoe UI Emoji\",sans-serif;'>🔸</span> Summary of the Role:</strong><br>&nbsp;Mid-level QA role with responsibility for overseeing sampling and dispensing operations. Ensures compliance, accuracy, and efficiency of all QA activities in the function.</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style='font-family:\"Segoe UI Emoji\",sans-serif;'>🔸</span> Key Responsibilities:</strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Supervise and coordinate QA sampling releasing , dispensing as per approved procedures as needed.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Review documentation completed by associates.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Ensure timely and compliant execution of sampling plans.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Conduct training and mentoring for junior staff.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>Support audits, investigations, and CAPA implementation.</li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"font-size:15px;color:black;background:white;\">Performs issuance of</span><span style=\"font-size:15px;\">&nbsp;batch cards of Manufacturing, Coating and Packaging.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"font-size:15px;\">Collects samples from on floor production for further testing and retention.&nbsp;</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"font-size:15px;\">Distributes testing samples to In-house Analytical , Elemental and Microbiology Labs</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"font-size:15px;\">Prepares In process Labels for production ,and QA samples to be provided along with the Batch Records</span></li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-top:0in;margin-right:.1in;margin-bottom:.0001pt;margin-left:.2in;text-align:  justify;text-indent:-.2in;background:white;'><strong><span style=\"color:black;\">Other Responsibilities Including Safety:</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-top:0in;margin-right:.1in;margin-bottom:.0001pt;margin-left:.2in;text-align:  justify;text-indent:-.2in;background:white;'><strong>&nbsp;</strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Works in a safe and responsible manner in order to create an injury-free and incident-free workplace.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Complies with all job-related safety and other training requirements.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">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:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"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: 0.3in; vertical-align: top;\"><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"color:black;\">Education &amp; Qualification:</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"color:black;\">Level 1 &ndash; Associate, QA Operations Support</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">B.Sc. / B.Pharm. or equivalent in a science-related field.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Relevant QA experience<strong>&nbsp;</strong>working within a GMP and/or with GCP regulations.</span></li></ul></div><p style='margin-top:0in;margin-right:.1in;margin-bottom:0in;margin-left:.5in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"color:black;\">Level 2 &ndash; Associate, QA Operations Support</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">B.Sc. / B.Pharm. (required)</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">1&ndash;3 years of experience in QA or related area preferred working within a GMP and/or with GCP regulations.</span></li></ul></div><p style='margin-top:0in;margin-right:.1in;margin-bottom:0in;margin-left:.5in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"color:black;\">Level 3 &ndash; Associate, QA Operations Support</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">B.Sc. / B.Pharm. (minimum); M.Sc. / M.Pharm. preferred</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">3&ndash;6 years of relevant QA experience<strong>&nbsp;</strong>working within a GMP and/or with GCP regulations.</span></li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"color:black;\">Certifications, Licenses, Credentials:</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">N/A</span></li></ul></div><p style='margin-top:0in;margin-right:.1in;margin-bottom:0in;margin-left:.5in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"color:black;\">Skills &amp; Ability</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"color:black;\">Level 1 &ndash; Associate, QA Operations Support</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Willingness to learn and follow instructions.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Basic understanding of GMP (preferred).</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Good observational and documentation skills.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Teamwork and adaptability.</span></li></ul></div><p style='margin-top:0in;margin-right:.1in;margin-bottom:0in;margin-left:.5in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"color:black;\">Level 2 &ndash; Associate, QA Operations Support</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Working knowledge of cGMP and SOPs.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Attention to detail and strong documentation habits.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Familiarity with quality systems (e.g., logbooks, traceability).</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Communication and coordination abilities</span></li></ul></div><p style='margin-top:0in;margin-right:.1in;margin-bottom:0in;margin-left:.5in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"color:black;\">Level 3 &ndash; Associate, QA Operations Support</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Strong knowledge of cGMP and quality systems.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Leadership and team management skills.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Effective communication and problem-solving.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Ability to handle audits, deviations, and cross-functional coordination.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Good documentation and review capabilities.</span></li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;'><strong><span style=\"color:black;\">Physical Requirements (lifting, etc.):</span></strong><span style=\"color:black;\">&nbsp;</span></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Ability to lift up to 50 lbs.; occasionally lift and move up to 75 pounds.</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"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:\"Times New Roman\",serif;'><span style=\"color:black;\">Occasionally works from a rolling ladder or step stool.&nbsp;</span></li><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Must be able wear all PPE including lab coat, face mask, booties, gloves, safety glasses.</span></li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-top:0in;margin-right:.1in;margin-bottom:.0001pt;margin-left:.5in;text-align:justify;background:  white;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:.1in;text-align:justify;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:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0.25in;\"><li style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"color:black;\">Work is regularly performed inside a manufacturing environment where temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employee 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:\"Times New Roman\",serif;margin-right:-.1in;text-align:justify;background:white;'><em><span style=\"font-size:15px;\">&nbsp;</span></em></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:-.1in;text-align:justify;background:white;'><em><span style=\"font-size:15px;color:black;\">The above statements are intended to describe the general nature and level of work being </span></em><em><span style=\"font-size:15px;color:black;\">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&nbsp;document does not create an employment contract, implied or otherwise, other than an &quot;at will&quot; relationship.</span></em></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:-.1in;text-align:justify;background:white;'><em><span style=\"font-size:15px;\">&nbsp;</span></em></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong>USPL is proud to be an Equal Opportunity Employer.</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>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.</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong>Benefits And Compensation:&nbsp;</strong>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.</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>&nbsp;</p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong>shift schedule</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong>&nbsp;</strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>1st shift: 7:00 AM - 3:30 PM, 2nd shift: 3:00 PM - 11:30 PM and 3rd shift: 11:00 PM - 7:30 AM</p></div></div></div></div></div>\n<br/>2nd shift - 3:00 PM to 11:15 PM",
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    "url": "https://workforcenow.adp.com/mascsr/default/careercenter/public/events/staffing/v1/job-requisitions/597745?cid=4a237553-bf3a-4a62-ac08-fdd8f7d3ca48&ccId=19000101_000001&lang=en_US&locale=en_US",
    "http_status": 200,
    "content_type": "application/json;charset=UTF-8",
    "response_bytes": 40025
  },
  "detail_errors": []
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/6d824367c06cac45361de394031bc2a123ad3f19?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/f5c4df51-d5af-4907-8a20-090eca34b499JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/12aecaa3-febf-4544-8d20-69ea4b58d77dJSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/6d824367c06cac45361de394031bc2a123ad3f19/eventsJSON

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