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Embryologist Scientist
Hcjy Fa Us2 Oraclecloud Com CX 1 · Sugar Land, TX, United States; US-Sugarland, Sugar Land, TX, US · On Site · Active · Oracle Recruiting Cloud / Fusion HCM
Job facts
| Field | Value |
|---|---|
| Company | Hcjy Fa Us2 Oraclecloud Com CX 1 |
| Title | Embryologist Scientist |
| Normalized title | - |
| Department / team | Clinical Life Science |
| Location | Sugar Land, TX, United States |
| Work model | On Site |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
| Posted / first seen | 2026-06-08 / 2026-06-09 |
| Changed / last seen | 2026-06-17 / 2026-06-18 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Hcjy Fa Us2 Oraclecloud Com CX 1. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Oracle Recruiting Cloud / Fusion HCM. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Sugar Land. | Open |
| Department jobs | Active postings in Clinical Life Science. | Open |
| Work model jobs | Active On Site postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Hcjy Fa Us2 Oraclecloud Com CX 1 |
| Source | 063b269b-849a-4216-8d0d-8fc4f7efa6f5 |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
Description
Description
About CooperSurgical
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 www.coopersurgical.com .
Work location: Sugar Land, TX (on-site)
Scope:
The Embryologist Scientist serves as a scientific subject matter expert responsible for the biological evaluation and advancement of bioassay systems used to assess the safety, efficacy, and performance of assisted reproductive technology (ART) media, consumables, and devices. The scope of this role spans research, assay development, validation, and method transfer, functioning as a critical interface between Research & Development, Quality Control, and Quality Assurance. The position has direct influence on biological risk assessment, regulatory readiness, product lifecycle decisions, and continuous improvement initiatives. Operating within a regulated laboratory environment, the role supports compliance with ISO 17025, GLP, and applicable GMP principles, and plays a key role in scientific investigations, OOS resolution, assay robustness, and next-generation bioassay development. The work performed within this scope directly impacts product quality, regulatory compliance, and patient outcomes in assisted reproduction.
Job Summary:
The Embryologist Scientist is responsible for the design, development, optimization, validation, and scientific troubleshooting of biological assays, including Mouse Embryo Assays (MEA) and sperm function assays, used to support ART product development and quality monitoring. This role conducts hands-on laboratory experimentation, performs statistical and biological data analysis, and leads scientific investigations related to assay performance, media failures, environmental influences, and OOS/OOT events. The scientist develops and validates new methods, establishes positive control systems, and transfers qualified assays into routine Quality Control use, including training and ongoing support.
The position collaborates closely with QC, QA, Manufacturing, and external partners, contributing technical expertise to CAPAs, deviations, validations, and continuous improvement initiatives, while advancing innovative bioassay strategies to support current and future ART technologies.
Responsibilities
Conduct a variety of cell-based bioassays (MEA, Sperm motility and survivability assays and Bacterial Endotoxin Test) for research and root cause analysis testing for products utilized in human assisted reproductive laboratories
Establishment and validation of medical device extraction methods following ISO 10933 methods
Improve assay sensitivity, robustness and reproducibility through endpoint selection, exposure modes, dose-response systems
Develop and validate positive control systems (e.g., embryotoxic gradients, stress models)
Evaluate emerging technologies and methodologies for embryo culture and reproductive testing
Support development of next-generation biological safety assays
Lead and execute assay validation activities, aligned with IQ/OP/PQ principes where applicable
Author validation protocols, risk assessments and final reports in alignment with ISO 17026 and GLP principles
Conduct inter-laboratory comparison and method equivalency studies
Transfer validated methods into QC laboratories and provide technical training, ongoing assay support and troubleshooting guidance
Lead scientific investigations related to OOS and OOT results (e.g., MEA failures), media performance issues and environmental or system impacts (e.g., incubator performance)
Apply structured root‑cause analysis tools, including 5 Whys and Fishbone (Ishikawa) analysis
Design hypothesis‑driven experiments to confirm root cause and corrective actions
Ensure compliance with applicable regulatory and quality standards ISO 17025 (preferred) and GLP / GMP principles where applicable
Internal quality systems (CAPA, change control, document control)
Author, review, and revise SOPs, work instructions, technical and investigation reports
Support internal, external, and regulatory audits
Ensure data integrity, traceability, and documentation accuracy
Perform statistical and trend analysis, including ANOVA, variability and reproducibility assessments and assay performance trending
Interpret biological assay data and draw scientifically defensible conclusions
Prepare technical summaries and present findings to R&D, Quality Assurance, Quality Control, Manufacturing and leadership teams
Collaborate with QC laboratories (method transfer and troubleshooting), Manufacturing (process‑related investigations), Quality Assurance (CAPA, deviations, validation support), External partners, CROs, and reagent suppliers
Support product development, lifecycle management, and continuous improvement initiatives
Travel:
This is an onsite position with minimal travel requirements (up to 10%).
Qualifications
Knowledge, Skills and Abilities:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
Significant experience in bioassay research, including experimental design and execution, with a strong focus on embryology. Excellent knowledge of bioassay methodologies, instrumentation, and data analysis techniques. Excellent organization skill and demonstrated ability to accurately complete detailed work. Strong oral and written communication skills and computer literacy. Strategic thinking and ability to translate vision into actionable plans. Knowledge of relevant regulatory requirements and compliance standards Ability to read, analyze, and interpret complex documents. Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to complete assignments accurately and with attention to detail. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Ability to analyze, organize and prioritize work under pressure while meeting deadlines. Ability to maintain detailed records and observations. Ability to process and handle confidential information with discretion. Ability to work evenings and weekends as required. Ability to work independently and/or in a collaborative environment. Ability to work under deadlines with general guidance.
Work Environment:
Weekends and holidays may be required. While performing the duties of this job, the employee is regularly required to stand and occasionally ascend/descend a ladder to perform husbandry tasks. Frequently stand, walk, twist, bend, stoop, squat, grasp lightly, use fine manipulation, grasp forcefully, perform desk-based computer task, use telephone, write by hand, lift, carry, push and pull objects over 40 pounds. Occasionally sit, kneel, crawl, reach and work above shoulders. Ability to bend, squat, kneel, stand, reach above shoulder level, and move on hard surfaces for up to eight hours. Ability to work in dusty, dirty, and odorous environment. Position may require repetitive motion. Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception, and the ability to adjust focus. Exposure to animal allergens, anesthetic gases, biohazards, radiation, sharps. Use of Personal Protective Equipment (PPE) is required (scrubs, disposable gown, exam gloves, head/beard cover, surgical mask. May require extended or unusual work hours based on research business needs. The noise level in the work environment is usually moderate.
Experience:
Min 7+ years related experience and/or training in embryology or reproductive biology laboratory, bioassay development and execution. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Significant experience in bioassay testing, particularly in routine product release and quality control within embryology and bacterial endotoxin laboratories. Sufficient computer knowledge of databases. Must possess a high level of initiative and ability to work with little supervision. Broad knowledge of biology laboratory practices. In-depth technical and scientific knowledge of embryology is desired. Previous experience in laboratory setting is highly desired.
Education:
M.S or Ph.D. or equivalent in Embryology, Reproductive Biology, Animal Science, Biochemistry, Biotechnology, or a field. The candidate should have a strong academic background in embryology, reproductive sciences or related discipline.
#LI-KA1
Our Benefits:
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 www.coopersurgical.com to learn more about CooperSurgical and the benefits of becoming a member of our team.
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.
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.
Full job record
| Job ID | 1fed0290e9b667707a6a2ac848738fd5c90d5473 |
| Org ID | fd5c005d-2102-408b-80a5-9404893f9b97 |
| Source ID | 063b269b-849a-4216-8d0d-8fc4f7efa6f5 |
| Board ID | 063b269b-849a-4216-8d0d-8fc4f7efa6f5 |
| Provider | oracle_hcm |
| Provider Job Key | 11506 |
| Title | Embryologist Scientist |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Sugar Land, TX, United States; US-Sugarland, Sugar Land, TX, US |
| Department | Clinical Life Science |
| Team | — |
| Employment Type | full_time |
| Workplace Type | on_site |
| Remote Policy | — |
| Country | United States |
| Region | TX |
| City | Sugar Land |
| Salary Raw | Description About CooperSurgical 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 www.coopersurgical.com . Work location: Sugar Land, TX (on-site) Scope: The Embryologist Scientist serves as a scientific subject matter expert responsible for the biological evaluation and advancement of bioassay systems used to assess the safety, efficacy, and performance of assisted reproductive technology (ART) media, consumables, and devices. The scope of this role spans research, assay development, validation, and method transfer, functioning as a critical interface between Research & Development, Quality Control, and Quality Assurance. The position has direct influence on biological risk assessment, regulatory readiness, product lifecycle decisions, and continuous improvement initiatives. Operating within a regulated laboratory environment, the role supports compliance with ISO 17025, GLP, and applicable GMP principles, and plays a key role in scientific investigations, OOS resolution, assay robustness, and next-generation bioassay development. The work performed within this scope directly impacts product quality, regulatory compliance, and patient outcomes in assisted reproduction. Job Summary: The Embryologist Scientist is responsible for the design, development, optimization, validation, and scientific troubleshooting of biological assays, including Mouse Embryo Assays (MEA) and sperm function assays, used to support ART product development and quality monitoring. This role conducts hands-on laboratory experimentation, performs statistical and biological data analysis, and leads scientific investigations related to assay performance, media failures, environmental influences, and OOS/OOT events. The scientist develops and validates new methods, establishes positive control systems, and transfers qualified assays into routine Quality Control use, including training and ongoing support. The position collaborates closely with QC, QA, Manufacturing, and external partners, contributing technical expertise to CAPAs, deviations, validations, and continuous improvement initiatives, while advancing innovative bioassay strategies to support current and future ART technologies. Responsibilities Conduct a variety of cell-based bioassays (MEA, Sperm motility and survivability assays and Bacterial Endotoxin Test) for research and root cause analysis testing for products utilized in human assisted reproductive laboratories Establishment and validation of medical device extraction methods following ISO 10933 methods Improve assay sensitivity, robustness and reproducibility through endpoint selection, exposure modes, dose-response systems Develop and validate positive control systems (e.g., embryotoxic gradients, stress models) Evaluate emerging technologies and methodologies for embryo culture and reproductive testing Support development of next-generation biological safety assays Lead and execute assay validation activities, aligned with IQ/OP/PQ principes where applicable Author validation protocols, risk assessments and final reports in alignment with ISO 17026 and GLP principles Conduct inter-laboratory comparison and method equivalency studies Transfer validated methods into QC laboratories and provide technical training, ongoing assay support and troubleshooting guidance Lead scientific investigations related to OOS and OOT results (e.g., MEA failures), media performance issues and environmental or system impacts (e.g., incubator performance) Apply structured root‑cause analysis tools, including 5 Whys and Fishbone (Ishikawa) analysis Design hypothesis‑driven experiments to confirm root cause and corrective actions Ensure compliance with applicable regulatory and quality standards ISO 17025 (preferred) and GLP / GMP principles where applicable Internal quality systems (CAPA, change control, document control) Author, review, and revise SOPs, work instructions, technical and investigation reports Support internal, external, and regulatory audits Ensure data integrity, traceability, and documentation accuracy Perform statistical and trend analysis, including ANOVA, variability and reproducibility assessments and assay performance trending Interpret biological assay data and draw scientifically defensible conclusions Prepare technical summaries and present findings to R&D, Quality Assurance, Quality Control, Manufacturing and leadership teams Collaborate with QC laboratories (method transfer and troubleshooting), Manufacturing (process‑related investigations), Quality Assurance (CAPA, deviations, validation support), External partners, CROs, and reagent suppliers Support product development, lifecycle management, and continuous improvement initiatives Travel: This is an onsite position with minimal travel requirements (up to 10%). Qualifications Knowledge, Skills and Abilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Significant experience in bioassay research, including experimental design and execution, with a strong focus on embryology. Excellent knowledge of bioassay methodologies, instrumentation, and data analysis techniques. Excellent organization skill and demonstrated ability to accurately complete detailed work. Strong oral and written communication skills and computer literacy. Strategic thinking and ability to translate vision into actionable plans. Knowledge of relevant regulatory requirements and compliance standards Ability to read, analyze, and interpret complex documents. Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to complete assignments accurately and with attention to detail. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Ability to analyze, organize and prioritize work under pressure while meeting deadlines. Ability to maintain detailed records and observations. Ability to process and handle confidential information with discretion. Ability to work evenings and weekends as required. Ability to work independently and/or in a collaborative environment. Ability to work under deadlines with general guidance. Work Environment: Weekends and holidays may be required. While performing the duties of this job, the employee is regularly required to stand and occasionally ascend/descend a ladder to perform husbandry tasks. Frequently stand, walk, twist, bend, stoop, squat, grasp lightly, use fine manipulation, grasp forcefully, perform desk-based computer task, use telephone, write by hand, lift, carry, push and pull objects over 40 pounds. Occasionally sit, kneel, crawl, reach and work above shoulders. Ability to bend, squat, kneel, stand, reach above shoulder level, and move on hard surfaces for up to eight hours. Ability to work in dusty, dirty, and odorous environment. Position may require repetitive motion. Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception, and the ability to adjust focus. Exposure to animal allergens, anesthetic gases, biohazards, radiation, sharps. Use of Personal Protective Equipment (PPE) is required (scrubs, disposable gown, exam gloves, head/beard cover, surgical mask. May require extended or unusual work hours based on research business needs. The noise level in the work environment is usually moderate. Experience: Min 7+ years related experience and/or training in embryology or reproductive biology laboratory, bioassay development and execution. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Significant experience in bioassay testing, particularly in routine product release and quality control within embryology and bacterial endotoxin laboratories. Sufficient computer knowledge of databases. Must possess a high level of initiative and ability to work with little supervision. Broad knowledge of biology laboratory practices. In-depth technical and scientific knowledge of embryology is desired. Previous experience in laboratory setting is highly desired. Education: M.S or Ph.D. or equivalent in Embryology, Reproductive Biology, Animal Science, Biochemistry, Biotechnology, or a field. The candidate should have a strong academic background in embryology, reproductive sciences or related discipline. #LI-KA1 Our Benefits: 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 www.coopersurgical.com to learn more about CooperSurgical and the benefits of becoming a member of our team. 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. 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. |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://hcjy.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/11506 |
| Apply URL | https://hcjy.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/11506 |
| First Seen At | 2026-06-09 11:09:24Z |
| Last Seen At | 2026-06-18 11:09:32Z |
| Last Checked At | 2026-06-18 11:09:32Z |
| Last Changed At | 2026-06-17 11:06:38Z |
| Inactive At | — |
| Source Posted At | 2026-06-08 14:57:42Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=hcjy.fa.us2.oraclecloud.com|CX_1/date=2026-06-18/2026-06-18T11-09-16-028Z-d066b4fd1cfacccc83575a8156bc6f783e280322881059767870d6c0212ced01.json |
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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 </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;\">. </span></span></p><p style=\"margin: 0in;\"> </p><p><span style=\"font-family: Arial, sans-serif;\"><strong>Work location:</strong> Sugar Land, TX (on-site)</span></p><p style=\"margin: 0in;\"> </p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Scope: </strong></span></p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">The Embryologist Scientist serves as a scientific subject matter expert responsible for the biological evaluation and advancement of bioassay systems used to assess the safety, efficacy, and performance of assisted reproductive technology (ART) media, consumables, and devices. The scope of this role spans research, assay development, validation, and method transfer, functioning as a critical interface between Research & Development, Quality Control, and Quality Assurance. The position has direct influence on biological risk assessment, regulatory readiness, product lifecycle decisions, and continuous improvement initiatives. Operating within a regulated laboratory environment, the role supports compliance with ISO 17025, GLP, and applicable GMP principles, and plays a key role in scientific investigations, OOS resolution, assay robustness, and next-generation bioassay development. The work performed within this scope directly impacts product quality, regulatory compliance, and patient outcomes in assisted reproduction.</span></p><p style=\"margin: 0in;\"> </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 Embryologist Scientist is responsible for the design, development, optimization, validation, and scientific troubleshooting of biological assays, including Mouse Embryo Assays (MEA) and sperm function assays, used to support ART product development and quality monitoring. This role conducts hands-on laboratory experimentation, performs statistical and biological data analysis, and leads scientific investigations related to assay performance, media failures, environmental influences, and OOS/OOT events. The scientist develops and validates new methods, establishes positive control systems, and transfers qualified assays into routine Quality Control use, including training and ongoing support.</span></p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">The position collaborates closely with QC, QA, Manufacturing, and external partners, contributing technical expertise to CAPAs, deviations, validations, and continuous improvement initiatives, while advancing innovative bioassay strategies to support current and future ART technologies.</span></p>",
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"ExternalQualificationsStr": "<p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Knowledge, Skills and Abilities:</strong></span></p><p style=\"margin: 0in;\"> </p><p><span style=\"font-family: Arial, sans-serif;\">To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.</span></p><ul style=\"list-style-type: disc;\"><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Significant experience in bioassay research, including experimental design and execution, with a strong focus on embryology.</span></li><li><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">Excellent knowledge of bioassay methodologies, instrumentation, and data analysis techniques.</span></span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Excellent organization skill and demonstrated ability to accurately complete detailed work.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Strong oral and written communication skills and computer literacy.</span></li><li><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">Strategic thinking and ability to translate vision into actionable plans.</span></span></li><li><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">Knowledge of relevant regulatory requirements and compliance standards</span></span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to read, analyze, and interpret complex documents. </span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to define problems, collect data, establish facts, and draw valid conclusions. </span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to complete assignments accurately and with attention to detail.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to analyze, organize and prioritize work under pressure while meeting deadlines.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to maintain detailed records and observations.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to process and handle confidential information with discretion.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to work evenings and weekends as required.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to work independently and/or in a collaborative environment. </span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to work under deadlines with general guidance.</span></li></ul><p style=\"margin: 0in 0in 0in 0.25in;\"> </p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Work Environment:</strong></span></p><ol><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Weekends and holidays may be required.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">While performing the duties of this job, the employee is regularly required to stand and occasionally ascend/descend a ladder to perform husbandry tasks.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Frequently stand, walk, twist, bend, stoop, squat, grasp lightly, use fine manipulation, grasp forcefully, perform desk-based computer task, use telephone, write by hand, lift, carry, push and pull objects over 40 pounds.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Occasionally sit, kneel, crawl, reach and work above shoulders.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to bend, squat, kneel, stand, reach above shoulder level, and move on hard surfaces for up to eight hours. </span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to work in dusty, dirty, and odorous environment.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Position may require repetitive motion.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception, and the ability to adjust focus.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Exposure to animal allergens, anesthetic gases, biohazards, radiation, sharps.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Use of Personal Protective Equipment (PPE) is required (scrubs, disposable gown, exam gloves, head/beard cover, surgical mask.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">May require extended or unusual work hours based on research business needs.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">The noise level in the work environment is usually moderate.</span></li></ol><p style=\"margin: 0in;\"> </p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Experience:</strong></span></p><ul style=\"list-style-type: disc;\"><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Min 7+ years related experience and/or training in embryology or reproductive biology laboratory, bioassay development and execution. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Significant experience in bioassay testing, particularly in routine product release and quality control within embryology and bacterial endotoxin laboratories.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Sufficient computer knowledge of databases.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Must possess a high level of initiative and ability to work with little supervision.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Broad knowledge of biology laboratory practices.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">In-depth technical and scientific knowledge of embryology is desired.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Previous experience in laboratory setting is highly desired.</span></li></ul><p style=\"margin: 0in;\"> </p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Education:</strong></span></p><ul style=\"list-style-type: disc;\"><li><p><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">M.S or Ph.D. or equivalent in Embryology, Reproductive Biology, Animal Science, Biochemistry, Biotechnology, or a field. The candidate should have a strong academic background in embryology, reproductive sciences or related discipline.</span></span></p><p> </p></li></ul><p> </p><p><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">#LI-KA1</span></span></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 </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;\"> 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>",
"InternalQualificationsStr": "<p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Knowledge, Skills and Abilities:</strong></span></p><p style=\"margin: 0in;\"> </p><p><span style=\"font-family: Arial, sans-serif;\">To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.</span></p><ul style=\"list-style-type: disc;\"><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Significant experience in bioassay research, including experimental design and execution, with a strong focus on embryology.</span></li><li><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">Excellent knowledge of bioassay methodologies, instrumentation, and data analysis techniques.</span></span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Excellent organization skill and demonstrated ability to accurately complete detailed work.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Strong oral and written communication skills and computer literacy.</span></li><li><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">Strategic thinking and ability to translate vision into actionable plans.</span></span></li><li><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">Knowledge of relevant regulatory requirements and compliance standards</span></span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to read, analyze, and interpret complex documents. </span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to define problems, collect data, establish facts, and draw valid conclusions. </span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to complete assignments accurately and with attention to detail.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to analyze, organize and prioritize work under pressure while meeting deadlines.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to maintain detailed records and observations.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to process and handle confidential information with discretion.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to work evenings and weekends as required.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to work independently and/or in a collaborative environment. </span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to work under deadlines with general guidance.</span></li></ul><p style=\"margin: 0in 0in 0in 0.25in;\"> </p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Work Environment:</strong></span></p><ol><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Weekends and holidays may be required.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">While performing the duties of this job, the employee is regularly required to stand and occasionally ascend/descend a ladder to perform husbandry tasks.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Frequently stand, walk, twist, bend, stoop, squat, grasp lightly, use fine manipulation, grasp forcefully, perform desk-based computer task, use telephone, write by hand, lift, carry, push and pull objects over 40 pounds.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Occasionally sit, kneel, crawl, reach and work above shoulders.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to bend, squat, kneel, stand, reach above shoulder level, and move on hard surfaces for up to eight hours. </span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ability to work in dusty, dirty, and odorous environment.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Position may require repetitive motion.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception, and the ability to adjust focus.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Exposure to animal allergens, anesthetic gases, biohazards, radiation, sharps.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Use of Personal Protective Equipment (PPE) is required (scrubs, disposable gown, exam gloves, head/beard cover, surgical mask.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">May require extended or unusual work hours based on research business needs.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">The noise level in the work environment is usually moderate.</span></li></ol><p style=\"margin: 0in;\"> </p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Experience:</strong></span></p><ul style=\"list-style-type: disc;\"><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Min 7+ years related experience and/or training in embryology or reproductive biology laboratory, bioassay development and execution. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Significant experience in bioassay testing, particularly in routine product release and quality control within embryology and bacterial endotoxin laboratories.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Sufficient computer knowledge of databases.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Must possess a high level of initiative and ability to work with little supervision.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Broad knowledge of biology laboratory practices.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">In-depth technical and scientific knowledge of embryology is desired.</span></li><li style=\"margin-bottom: 0in; margin-top: 0in; vertical-align: baseline;\"><span style=\"font-family: Arial, sans-serif;\">Previous experience in laboratory setting is highly desired.</span></li></ul><p style=\"margin: 0in;\"> </p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Education:</strong></span></p><ul style=\"list-style-type: disc;\"><li><p><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">M.S or Ph.D. or equivalent in Embryology, Reproductive Biology, Animal Science, Biochemistry, Biotechnology, or a field. The candidate should have a strong academic background in embryology, reproductive sciences or related discipline.</span></span></p><p> </p></li></ul><p> </p><p><span style=\"font-family: Arial, sans-serif;\"><span style=\"font-size: 10pt;\">#LI-KA1</span></span></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 </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;\"> 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>",
"OrganizationDescriptionStr": "",
"primaryLocationCoordinates": [
{
"Latitude": "29.63297",
"Longitude": "-95.60067",
"CountryCode": "US",
"GeographyId": 300000200193855,
"GeographyNodeId": 100002310795779
}
],
"ExternalResponsibilitiesStr": "<ul style=\"list-style-type: disc; padding-left: 48px;\"><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Conduct a variety of cell-based bioassays (MEA, Sperm motility and survivability assays and Bacterial Endotoxin Test) for research and root cause analysis testing for products utilized in human assisted reproductive laboratories</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Establishment and validation of medical device extraction methods following ISO 10933 methods</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Improve assay sensitivity, robustness and reproducibility through endpoint selection, exposure modes, dose-response systems</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Develop and validate positive control systems (e.g., embryotoxic gradients, stress models)</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Evaluate emerging technologies and methodologies for embryo culture and reproductive testing</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Support development of next-generation biological safety assays</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Lead and execute assay validation activities, aligned with IQ/OP/PQ principes where applicable</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Author validation protocols, risk assessments and final reports in alignment with ISO 17026 and GLP principles</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Conduct inter-laboratory comparison and method equivalency studies</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Transfer validated methods into QC laboratories and provide technical training, ongoing assay support and troubleshooting guidance</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Lead scientific investigations related to OOS and OOT results (e.g., MEA failures), media performance issues and environmental or system impacts (e.g., incubator performance)</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Apply structured root‑cause analysis tools, including 5 Whys and Fishbone (Ishikawa) analysis</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Design hypothesis‑driven experiments to confirm root cause and corrective actions</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ensure compliance with applicable regulatory and quality standards ISO 17025 (preferred) and GLP / GMP principles where applicable</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Internal quality systems (CAPA, change control, document control)</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Author, review, and revise SOPs, work instructions, technical and investigation reports</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Support internal, external, and regulatory audits </span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ensure data integrity, traceability, and documentation accuracy</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Perform statistical and trend analysis, including ANOVA, variability and reproducibility assessments and assay performance trending</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Interpret biological assay data and draw scientifically defensible conclusions </span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Prepare technical summaries and present findings to R&D, Quality Assurance, Quality Control, Manufacturing and leadership teams</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Collaborate with QC laboratories (method transfer and troubleshooting), Manufacturing (process‑related investigations), Quality Assurance (CAPA, deviations, validation support), External partners, CROs, and reagent suppliers</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Support product development, lifecycle management, and continuous improvement initiatives</span></p></li></ul><p style=\"margin: 0in;\"> </p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Travel:</strong> </span></p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">This is an onsite position with minimal travel requirements (up to 10%).</span></p>",
"InternalResponsibilitiesStr": "<ul style=\"list-style-type: disc; padding-left: 48px;\"><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Conduct a variety of cell-based bioassays (MEA, Sperm motility and survivability assays and Bacterial Endotoxin Test) for research and root cause analysis testing for products utilized in human assisted reproductive laboratories</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Establishment and validation of medical device extraction methods following ISO 10933 methods</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Improve assay sensitivity, robustness and reproducibility through endpoint selection, exposure modes, dose-response systems</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Develop and validate positive control systems (e.g., embryotoxic gradients, stress models)</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Evaluate emerging technologies and methodologies for embryo culture and reproductive testing</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Support development of next-generation biological safety assays</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Lead and execute assay validation activities, aligned with IQ/OP/PQ principes where applicable</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Author validation protocols, risk assessments and final reports in alignment with ISO 17026 and GLP principles</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Conduct inter-laboratory comparison and method equivalency studies</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Transfer validated methods into QC laboratories and provide technical training, ongoing assay support and troubleshooting guidance</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Lead scientific investigations related to OOS and OOT results (e.g., MEA failures), media performance issues and environmental or system impacts (e.g., incubator performance)</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Apply structured root‑cause analysis tools, including 5 Whys and Fishbone (Ishikawa) analysis</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Design hypothesis‑driven experiments to confirm root cause and corrective actions</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ensure compliance with applicable regulatory and quality standards ISO 17025 (preferred) and GLP / GMP principles where applicable</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Internal quality systems (CAPA, change control, document control)</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Author, review, and revise SOPs, work instructions, technical and investigation reports</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Support internal, external, and regulatory audits </span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Ensure data integrity, traceability, and documentation accuracy</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Perform statistical and trend analysis, including ANOVA, variability and reproducibility assessments and assay performance trending</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Interpret biological assay data and draw scientifically defensible conclusions </span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Prepare technical summaries and present findings to R&D, Quality Assurance, Quality Control, Manufacturing and leadership teams</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Collaborate with QC laboratories (method transfer and troubleshooting), Manufacturing (process‑related investigations), Quality Assurance (CAPA, deviations, validation support), External partners, CROs, and reagent suppliers</span></p></li><li><p style=\"margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\"><span style=\"font-family: Arial, sans-serif;\">Support product development, lifecycle management, and continuous improvement initiatives</span></p></li></ul><p style=\"margin: 0in;\"> </p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\"><strong>Travel:</strong> </span></p><p style=\"margin: 0in;\"><span style=\"font-family: Arial, sans-serif;\">This is an onsite position with minimal travel requirements (up to 10%).</span></p>",
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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: Sugar Land, TX (on-site)",
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