PTA Manufacturing Technician III

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    "Id": "11535",
    "Title": "PTA Manufacturing Technician III",
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    "Category": "Manufacturing",
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    "JobSchedule": "Full time",
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    "workLocation": [
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        "Region1": "Essex",
        "Region2": "NJ",
        "Region3": "New Jersey",
        "Building": null,
        "Latitude": "40.78858",
        "Longitude": "-74.32236",
        "LocationId": 300000015796325,
        "PostalCode": "07039",
        "TownOrCity": "Livingston",
        "AddressLine1": "3 Regent St.",
        "AddressLine2": "suite 305",
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    "RequisitionType": "Hourly",
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    "ShortDescriptionStr": "About CooperSurgical\n\nCooperSurgical is a leading fertility and women’s healthcare company dedicated to putting time on the side of women, babies, and families at the healthcare moments that matter most in life. As a division of CooperCompanies, we're driven by a unified purpose to enable patients to experience life's beautiful moments. Guided by our shared values – dedicated, innovative, friendly, partners, and do the right thing – our offerings support patients throughout their lifetimes, from contraception to fertility and birth solutions, to women’s and family care, and beyond. We currently offer over 600 clinically relevant medical devices to healthcare providers, including testing and treatment options, as well as an innovative suite of assisted reproductive technology and genomic testing solutions. Learn more at www.coopersurgical.com. \n\nWork location: Livingston, NJ (on-site)",
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    "ExternalDescriptionStr": "<p class=\"elementtoproof\"><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\"><strong>About CooperSurgical</strong></span></span></p><p style=\"background-color: white; margin-bottom: 0in;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><span style=\"border: 1pt windowtext; padding: 0in;\">CooperSurgical is a leading fertility and women’s healthcare company dedicated to putting time on the side of women, babies, and families at the healthcare moments that matter most in life. As a division of CooperCompanies, we're driven by a unified purpose to enable patients to experience life's beautiful moments. Guided by our shared values – dedicated, innovative, friendly, partners, and do the right thing – our offerings support patients throughout their lifetimes, from contraception to fertility and birth solutions, to women’s and family care, and beyond. We currently offer over 600 clinically relevant medical devices to healthcare providers, including testing and treatment options, as well as an innovative suite of assisted reproductive technology and genomic testing solutions. Learn more at&nbsp;</span></span><a href=\"http://www.coopersurgical.com\"><span style=\"color: black; font-family: Arial, sans-serif;\"><span style=\"border: 1pt windowtext; padding: 0in;\">www.coopersurgical.com</span></span></a><span style=\"color: black; font-family: Arial, sans-serif;\"><span style=\"border: 1pt windowtext; padding: 0in;\">.&nbsp;</span></span></p><p style=\"margin: 0in;\">&nbsp;</p><p><span style=\"font-family: Arial, sans-serif;\"><strong>Work location:</strong> Livingston, NJ (on-site)</span></p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Scope:&nbsp;</strong></span></p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">This position will execute standard operating procedures (SOPs) supporting PTA manufacturing, validation, and production transfer activities at the CooperSurgical laboratory in Livingston, New Jersey.</span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Job Summary:</strong></span></p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">The PTA Manufacturing Laboratory Technician III will perform manufacturing and laboratory tasks of low to intermediate complexity while helping coordinate day-to-day production activities and supporting startup operations associated with the PTA value stream. This role will serve as a lead technician within the laboratory, supporting production execution, training, troubleshooting, and operational readiness activities during the NJ site startup and transfer phase.</span><br><br>&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">The technician will report directly to the PTA Manufacturing Manager and collaborate cross-functionally with QA, scientists, engineers, and operations teams. The primary responsibility of this role will be reagent manufacturing in a controlled laboratory environment while supporting process transfer, qualification, validation, and contamination control activities.</span><br>&nbsp;</p>",
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    "ExternalPostedStartDate": "2026-06-05T19:39:17+00:00",
    "ExternalQualificationsStr": "<p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">• Understanding of fundamental biochemical and molecular biology concepts (e.g., nucleic acid structure, PCR, pH, contamination control, etc.)</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to work effectively within a contamination-controlled processing environment</span><br><span style=\"font-family: Arial, sans-serif;\">• Strong understanding of contamination prevention practices, gowning procedures, and controlled workflow behaviors</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to follow procedures and protocols with a high degree of consistency and accuracy</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to identify operational issues and support troubleshooting activities in a manufacturing environment</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to communicate and collaborate effectively across cross-functional teams</span><br><span style=\"font-family: Arial, sans-serif;\">• Strong attention to detail, organization, and documentation accuracy</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to support training and coordination of junior laboratory personnel</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to perform repetitive pipetting and laboratory tasks for extended periods of time</span><br><span style=\"font-family: Arial, sans-serif;\">• Proficiency with Microsoft Office programs including Excel, Word, and PowerPoint</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to maintain confidentiality as required</span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Work Environment:</strong></span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">• Frequent reaching, grasping, repetitive motions, and eye/hand coordination</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to work in office and laboratory/manufacturing environments</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to don and wear contamination-controlled processing garments, gloves, eye protection, and masks for extended periods</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to sit or stand for extended periods of time</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to lift up to 50 lbs</span><br><br>&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Experience:</strong></span></p><p style=\"margin: 0in;\"><br><span style=\"font-family: Arial, sans-serif;\">• Minimum 3–5 years of relevant laboratory and/or manufacturing experience required</span><br><span style=\"font-family: Arial, sans-serif;\">• Hands-on aseptic processing experience in a laboratory, manufacturing, or contamination-controlled environment is required</span><br><span style=\"font-family: Arial, sans-serif;\">• Prior experience supporting production execution, floor coordination, or technician training activities preferred</span><br><span style=\"font-family: Arial, sans-serif;\">• Experience working in GMP or regulated manufacturing environments preferred</span><br><span style=\"font-family: Arial, sans-serif;\">• Experience supporting validation, qualification, startup, or manufacturing transfer activities preferred</span><br><span style=\"font-family: Arial, sans-serif;\">• Experience with molecular biology laboratory techniques preferred, including PCR, qPCR, DNA extraction, next-generation sequencing workflows, or related methods</span><br><span style=\"font-family: Arial, sans-serif;\">• Experience working with electronic quality systems, manufacturing systems, or laboratory information systems is preferred</span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Education:</strong></span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">• Bachelor’s degree in the sciences required</span></p><p style=\"background-color: white;\">&nbsp;</p><p style=\"background-color: white;\">#LI-KA1</p><p style=\"background-color: white;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><strong>Our Benefits:</strong></span></p><p style=\"background-color: white;\"><span style=\"color: black; font-family: Arial, sans-serif;\">As an employee of CooperSurgical, you'll receive an outstanding total compensation plan. As we believe your compensation goes beyond your paycheck, we offer a great compensation package, medical coverage, 401(k), parental leave, fertility benefits, paid time off for vacation, personal, sick and holidays, and multiple other perks and benefits. Please visit us at&nbsp;</span><a href=\"https://www.coopersurgical.com/\" target=\"_blank\" title=\"https://www.coopersurgical.com/\"><span style=\"color: rgb(0, 135, 204); font-family: Arial, sans-serif;\">www.coopersurgical.com</span></a><span style=\"color: black; font-family: Arial, sans-serif;\">&nbsp;to learn more about CooperSurgical and the benefits of becoming a member of our team.</span></p><p style=\"background-color: white;\"><span style=\"color: black; font-family: Arial, sans-serif;\">To all agencies: Please, no phone calls or emails to any employee of CooperSurgical about this opening. All resumes submitted by search firms/employment agencies to any employee at CooperSurgical via-email, the internet or in any form and/or method will be deemed the sole property of CooperSurgical, unless such search firms/employment agencies were engaged by CooperSurgical for this position and a valid agreement with CooperSurgical is in place. In the event a candidate who was submitted outside of the CooperSurgical agency engagement process is hired, no fee or payment of any kind will be paid.</span></p><p style=\"background-color: white;\"><span style=\"color: black; font-family: Arial, sans-serif;\">We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace.</span></p><p style=\"background-color: white;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">For U.S. locations that require disclosure of compensation, the starting base pay&nbsp;for this role is between&nbsp;$26.00 - $35.00 per hour. The&nbsp;actual base pay&nbsp;includes many factors and is subject to change and modification in the future. This position may also be eligible for other types of compensation and benefits.</span></span></p>",
    "InternalQualificationsStr": "<p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">• Understanding of fundamental biochemical and molecular biology concepts (e.g., nucleic acid structure, PCR, pH, contamination control, etc.)</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to work effectively within a contamination-controlled processing environment</span><br><span style=\"font-family: Arial, sans-serif;\">• Strong understanding of contamination prevention practices, gowning procedures, and controlled workflow behaviors</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to follow procedures and protocols with a high degree of consistency and accuracy</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to identify operational issues and support troubleshooting activities in a manufacturing environment</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to communicate and collaborate effectively across cross-functional teams</span><br><span style=\"font-family: Arial, sans-serif;\">• Strong attention to detail, organization, and documentation accuracy</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to support training and coordination of junior laboratory personnel</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to perform repetitive pipetting and laboratory tasks for extended periods of time</span><br><span style=\"font-family: Arial, sans-serif;\">• Proficiency with Microsoft Office programs including Excel, Word, and PowerPoint</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to maintain confidentiality as required</span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Work Environment:</strong></span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">• Frequent reaching, grasping, repetitive motions, and eye/hand coordination</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to work in office and laboratory/manufacturing environments</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to don and wear contamination-controlled processing garments, gloves, eye protection, and masks for extended periods</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to sit or stand for extended periods of time</span><br><span style=\"font-family: Arial, sans-serif;\">• Ability to lift up to 50 lbs</span><br><br>&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Experience:</strong></span></p><p style=\"margin: 0in;\"><br><span style=\"font-family: Arial, sans-serif;\">• Minimum 3–5 years of relevant laboratory and/or manufacturing experience required</span><br><span style=\"font-family: Arial, sans-serif;\">• Hands-on aseptic processing experience in a laboratory, manufacturing, or contamination-controlled environment is required</span><br><span style=\"font-family: Arial, sans-serif;\">• Prior experience supporting production execution, floor coordination, or technician training activities preferred</span><br><span style=\"font-family: Arial, sans-serif;\">• Experience working in GMP or regulated manufacturing environments preferred</span><br><span style=\"font-family: Arial, sans-serif;\">• Experience supporting validation, qualification, startup, or manufacturing transfer activities preferred</span><br><span style=\"font-family: Arial, sans-serif;\">• Experience with molecular biology laboratory techniques preferred, including PCR, qPCR, DNA extraction, next-generation sequencing workflows, or related methods</span><br><span style=\"font-family: Arial, sans-serif;\">• Experience working with electronic quality systems, manufacturing systems, or laboratory information systems is preferred</span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Education:</strong></span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">• Bachelor’s degree in the sciences required</span></p><p style=\"background-color: white;\">&nbsp;</p><p style=\"background-color: white;\">#LI-KA1</p><p style=\"background-color: white;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><strong>Our Benefits:</strong></span></p><p style=\"background-color: white;\"><span style=\"color: black; font-family: Arial, sans-serif;\">As an employee of CooperSurgical, you'll receive an outstanding total compensation plan. As we believe your compensation goes beyond your paycheck, we offer a great compensation package, medical coverage, 401(k), parental leave, fertility benefits, paid time off for vacation, personal, sick and holidays, and multiple other perks and benefits. Please visit us at&nbsp;</span><a href=\"https://www.coopersurgical.com/\" target=\"_blank\" title=\"https://www.coopersurgical.com/\"><span style=\"color: rgb(0, 135, 204); font-family: Arial, sans-serif;\">www.coopersurgical.com</span></a><span style=\"color: black; font-family: Arial, sans-serif;\">&nbsp;to learn more about CooperSurgical and the benefits of becoming a member of our team.</span></p><p style=\"background-color: white;\"><span style=\"color: black; font-family: Arial, sans-serif;\">To all agencies: Please, no phone calls or emails to any employee of CooperSurgical about this opening. All resumes submitted by search firms/employment agencies to any employee at CooperSurgical via-email, the internet or in any form and/or method will be deemed the sole property of CooperSurgical, unless such search firms/employment agencies were engaged by CooperSurgical for this position and a valid agreement with CooperSurgical is in place. In the event a candidate who was submitted outside of the CooperSurgical agency engagement process is hired, no fee or payment of any kind will be paid.</span></p><p style=\"background-color: white;\"><span style=\"color: black; font-family: Arial, sans-serif;\">We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace.</span></p><p style=\"background-color: white;\"><span style=\"color: black; font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">For U.S. locations that require disclosure of compensation, the starting base pay&nbsp;for this role is between&nbsp;$26.00 - $35.00 per hour. The&nbsp;actual base pay&nbsp;includes many factors and is subject to change and modification in the future. This position may also be eligible for other types of compensation and benefits.</span></span></p>",
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    "ExternalResponsibilitiesStr": "<p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">• Coordinate and support daily manufacturing activities according to the production schedule</span><br><span style=\"font-family: Arial, sans-serif;\">• Provide day-to-day guidance and support to laboratory technicians and operators during manufacturing activities</span><br><span style=\"font-family: Arial, sans-serif;\">• Execute a range of SOPs to perform detailed manufacturing tasks independently and in a timely manner</span><br><span style=\"font-family: Arial, sans-serif;\">• Perform reagent formulation, filling, labeling, packaging, and related manufacturing activities according to procedure</span><br><span style=\"font-family: Arial, sans-serif;\">• Execute routine quality control inspections independently according to procedure</span><br><span style=\"font-family: Arial, sans-serif;\">• Demonstrate and maintain proficiency in contamination-controlled processing techniques and contamination-controlled workflows</span><br><span style=\"font-family: Arial, sans-serif;\">• Maintain controlled laboratory practices and support contamination prevention activities during manufacturing operations</span><br><span style=\"font-family: Arial, sans-serif;\">• Support onboarding and training of new technicians during startup and transfer activities</span><br><span style=\"font-family: Arial, sans-serif;\">• Accurately complete production and test records according to good documentation practices (GDP)</span><br><span style=\"font-family: Arial, sans-serif;\">• Report process deviations, nonconformances, and operational issues in a timely manner</span><br><span style=\"font-family: Arial, sans-serif;\">• Participate in troubleshooting, root cause investigations, and continuous improvement activities</span><br><span style=\"font-family: Arial, sans-serif;\">• Support equipment qualification, process validation, and manufacturing transfer activities</span><br><span style=\"font-family: Arial, sans-serif;\">• Receive, inspect, stock, and organize production inventory and laboratory supplies</span><br><span style=\"font-family: Arial, sans-serif;\">• Routinely clean laboratory rooms, controlled areas, and manufacturing equipment</span><br><span style=\"font-family: Arial, sans-serif;\">• Perform routine laboratory and equipment maintenance activities</span><br><span style=\"font-family: Arial, sans-serif;\">• Participate in procedure reviews and updates, including SOPs, forms, and work instructions</span><br><span style=\"font-family: Arial, sans-serif;\">• Support creation and maintenance of manufacturing documentation and technical records</span><br><span style=\"font-family: Arial, sans-serif;\">• Collaborate cross-functionally with QA, R&amp;D, engineering, and operations teams to resolve process and product issues</span><br><span style=\"font-family: Arial, sans-serif;\">• Comply with all standard operating procedures, quality assurance, safety, and regulatory requirements</span><br><span style=\"font-family: Arial, sans-serif;\">• Comply with all corporate regulations, policies, and procedures</span><br><span style=\"font-family: Arial, sans-serif;\">• Perform additional duties as assigned by management</span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Travel:</strong>&nbsp;</span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">• During onboarding and initial startup activities, this role may require extended onsite training at the Houston site for approximately 1–2 months</span><br><span style=\"font-family: Arial, sans-serif;\">• Limited travel may be required afterward (&lt;10%)</span></p>",
    "InternalResponsibilitiesStr": "<p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">• Coordinate and support daily manufacturing activities according to the production schedule</span><br><span style=\"font-family: Arial, sans-serif;\">• Provide day-to-day guidance and support to laboratory technicians and operators during manufacturing activities</span><br><span style=\"font-family: Arial, sans-serif;\">• Execute a range of SOPs to perform detailed manufacturing tasks independently and in a timely manner</span><br><span style=\"font-family: Arial, sans-serif;\">• Perform reagent formulation, filling, labeling, packaging, and related manufacturing activities according to procedure</span><br><span style=\"font-family: Arial, sans-serif;\">• Execute routine quality control inspections independently according to procedure</span><br><span style=\"font-family: Arial, sans-serif;\">• Demonstrate and maintain proficiency in contamination-controlled processing techniques and contamination-controlled workflows</span><br><span style=\"font-family: Arial, sans-serif;\">• Maintain controlled laboratory practices and support contamination prevention activities during manufacturing operations</span><br><span style=\"font-family: Arial, sans-serif;\">• Support onboarding and training of new technicians during startup and transfer activities</span><br><span style=\"font-family: Arial, sans-serif;\">• Accurately complete production and test records according to good documentation practices (GDP)</span><br><span style=\"font-family: Arial, sans-serif;\">• Report process deviations, nonconformances, and operational issues in a timely manner</span><br><span style=\"font-family: Arial, sans-serif;\">• Participate in troubleshooting, root cause investigations, and continuous improvement activities</span><br><span style=\"font-family: Arial, sans-serif;\">• Support equipment qualification, process validation, and manufacturing transfer activities</span><br><span style=\"font-family: Arial, sans-serif;\">• Receive, inspect, stock, and organize production inventory and laboratory supplies</span><br><span style=\"font-family: Arial, sans-serif;\">• Routinely clean laboratory rooms, controlled areas, and manufacturing equipment</span><br><span style=\"font-family: Arial, sans-serif;\">• Perform routine laboratory and equipment maintenance activities</span><br><span style=\"font-family: Arial, sans-serif;\">• Participate in procedure reviews and updates, including SOPs, forms, and work instructions</span><br><span style=\"font-family: Arial, sans-serif;\">• Support creation and maintenance of manufacturing documentation and technical records</span><br><span style=\"font-family: Arial, sans-serif;\">• Collaborate cross-functionally with QA, R&amp;D, engineering, and operations teams to resolve process and product issues</span><br><span style=\"font-family: Arial, sans-serif;\">• Comply with all standard operating procedures, quality assurance, safety, and regulatory requirements</span><br><span style=\"font-family: Arial, sans-serif;\">• Comply with all corporate regulations, policies, and procedures</span><br><span style=\"font-family: Arial, sans-serif;\">• Perform additional duties as assigned by management</span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Travel:</strong>&nbsp;</span></p><p style=\"margin: 0in;\">&nbsp;</p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">• During onboarding and initial startup activities, this role may require extended onsite training at the Houston site for approximately 1–2 months</span><br><span style=\"font-family: Arial, sans-serif;\">• Limited travel may be required afterward (&lt;10%)</span></p>",
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