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HomeCompanies9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001Senior Specialist, Sample Management QC

Senior Specialist, Sample Management QC

9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001 · Newark, DE, US, Newark, DE · Active · $49,000–$57,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001
TitleSenior Specialist, Sample Management QC
Normalized title-
Department / team-
LocationNewark, DE, United States
Work model-
Employment typeFull Time
Salary$49,000–$57,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-04-16 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from 9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Newark.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

Company9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001
Source23fd82d9-c7cc-4299-8499-ec8ee9834434
ATS providerADP Workforce Now Recruiting

Description

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS has an immediate opening for Senior Specialist, Sample Management QC supporting our Translational Medicine Department. This role is 100% desk-based. All QC activities are performed through document review, data verification, and system‑based checks. No laboratory or hands‑on QC testing is involved. The position requires extreme attention to detail, organization, multi-tasking, and comfort interacting with people who might be junior or senior to the incumbent. The ideal candidate is someone who can share responsibilities and shift priorities when necessary to do what is needed in the moment – especially in a dynamic environment. QPS's Sample Management Team ensures that client samples and other controlled materials are received, stored, distributed, tracked and returned safely, securely and without loss or damage. The process is regulated and vital to the success of clinical trials around the world. Our team is comprised of professionals from diverse backgrounds such as customer service, restaurant/retail, programming, data analysis, and various physical sciences. We work together to ensure that the biological samples received are stored, logged, tracked, distributed, and reported back to our sponsors per GLP regulations and internal & external SOP requirements. QPS’ Story: Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life. Team members enjoy challenging and rewarding work, and are encouraged to achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals. If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website ( www.qps.com ) for more information and to see all current openings. The Job Create and maintain Sample Receipt notebooks from creation to archival Use our LIMS (database) for tracking of samples through their life cycle at QPS Perform QC of Sample Receipt records against an electronic database to ensure they comply with FDA and GLP regulations, client protocol, and QPS SOPs Ensure all appropriate GLP paperwork is included with sample receipt packet Ensure shipped samples are received and reconciled per client protocol and shipping manifest Ensure any referenced client correspondence can be verified Monitor documentation of storage changes, disposal, return of samples as needed Maintain TLM Sample Receipt Table Request log and communicate any timeline issues internally to Principal Investigator Compile and/or perform QC on Sample Receipt tables prior to submission to QA QC QPS generated manifest QC various Data Management generated reports prior to submitting to Principal Investigator Assist SMT with general documentation questions Reconcile shipment packets against TLM Dashboard Communicate any new SOP revisions to the team and reconcile Employee Qualification Manuals annually Understand and abide by HIPPA & GDPR compliant privacy measures Work Location This job will be 100% QPS-office/facility based Requirements Combination of relevant education and experience that provides sufficient knowledge and skills to ensure incumbent's success in this role, such as: University/college degree in a relevant scientific discipline and/or Demonstrated experience in CRO, Clinical Research or another relevant field Experience in an FDA-related or other regulated industry laboratory is preferred Organized, with good detail-orientation Proficiency with MS Office, including Excel Good interpersonal skills Why You Should Apply Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals. Structured Career Ladders that provide excellent growth based on your personal aspirations. Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance. Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance Park-like setting in Newark, Delaware Internal committees designed with the needs and enjoyment of QPS employees in mind. QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

Full job record

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Source ID23fd82d9-c7cc-4299-8499-ec8ee9834434
Board ID23fd82d9-c7cc-4299-8499-ec8ee9834434
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Provider Job Key589813
TitleSenior Specialist, Sample Management QC
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First Seen At2026-05-31 18:25:14Z
Last Seen At2026-06-06 13:18:39Z
Last Checked At2026-06-06 13:18:39Z
Last Changed At2026-06-06 13:18:39Z
Inactive At
Source Posted At2026-04-16 17:45:00Z
Source Updated At
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    "requisitionDescription": "<div><div><div><div><div><div><div><p data-pasted=\"true\"><strong><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!&nbsp;</span></strong></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">QPS has an immediate opening for Senior Specialist, Sample Management QC supporting our Translational Medicine Department. This role is 100% desk-based. All QC activities are performed through document review, data verification, and system‑based checks. No laboratory or hands‑on QC testing is involved. The position requires extreme attention to detail, organization, multi-tasking, and comfort interacting with people who might be junior or senior to the incumbent. The ideal candidate is someone who can share responsibilities and shift priorities when necessary to do what is needed in the moment &ndash; especially in a dynamic environment.</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">QPS&#39;s Sample Management Team ensures that client samples and other controlled materials are received, stored, distributed, tracked and returned safely, securely and without loss or damage. The process is regulated and vital to the success of clinical trials around the world. Our team is comprised of professionals from diverse backgrounds such as customer service, restaurant/retail, programming, data analysis, and various physical sciences. We work together to ensure that the biological samples received are stored, logged, tracked, distributed, and reported back to our sponsors per GLP regulations and internal &amp; external SOP requirements.</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong>QPS&rsquo; Story:</strong></span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II &ndash; IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">Team members enjoy challenging and rewarding work, and are encouraged to achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.</span></p><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (<a href=\"http://www.qps.com\" target=\"_blank\" style=\"font-size: 14px;\">www.qps.com</a>) for more information and to see all current openings.</span></p><p style='margin:0in;font-size:15px;font-family:\"Arial\",sans-serif;background:#D9D9D9;' data-pasted=\"true\"><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong><span style=\"color:black;\">The Job</span></strong></span></p><ul><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Create and maintain Sample Receipt notebooks from creation to archival</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Use our LIMS (database) for tracking of samples through their life cycle at QPS</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Perform QC of Sample Receipt records against an electronic database to ensure they comply with FDA and GLP regulations, client protocol, and QPS SOPs</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Ensure all appropriate GLP paperwork is included with sample receipt packet</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Ensure shipped samples are received and reconciled per client protocol and shipping manifest</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Ensure any referenced client correspondence can be verified</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Monitor documentation of storage changes, disposal, return of samples as needed</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Maintain TLM Sample Receipt Table Request log and communicate any timeline issues internally to Principal Investigator</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Compile and/or perform QC on Sample Receipt tables prior to submission to QA</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">QC QPS generated manifest</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">QC various Data Management generated reports prior to submitting to Principal Investigator</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Assist SMT with general documentation questions</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Reconcile shipment packets against TLM Dashboard</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Communicate any new SOP revisions to the team and reconcile Employee Qualification Manuals annually</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Understand and abide by HIPPA &amp; GDPR compliant privacy measures</li></ul><p style='margin:0in;font-size:15px;font-family:\"Arial\",sans-serif;background:#D9D9D9;' data-pasted=\"true\"><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong><span style=\"color:black;\">Work Location</span></strong></span></p><ul><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">This job <strong>will be</strong> <strong>100% QPS-office/facility based</strong></li></ul><p style='margin:0in;font-size:15px;font-family:\"Arial\",sans-serif;background:#D9D9D9;' data-pasted=\"true\"><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong><span style=\"color:black;\">Requirements</span></strong></span></p><ul><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 15px; font-family: Arial, sans-serif; background: white;\" data-pasted=\"true\"><span style='font-size:14px;font-family:\"Verdana\",sans-serif;color:#262321;'>Combination of relevant education and experience that provides sufficient knowledge and skills to ensure incumbent&#39;s success in this role, such as:</span><ul><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 15px; font-family: Arial, sans-serif; background: white;\"><span style='font-size:14px;font-family:\"Verdana\",sans-serif;color:#262321;'>University/college degree in a relevant scientific discipline and/or</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 15px; font-family: Arial, sans-serif; background: white;\"><span style='font-size:14px;font-family:\"Verdana\",sans-serif;color:#262321;'>Demonstrated experience in CRO, Clinical Research or another relevant field</span></li></ul></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 15px; font-family: Arial, sans-serif; background: white;\"><span style='font-size:14px;font-family:\"Verdana\",sans-serif;color:#262321;'>Experience in an FDA-related or other regulated industry laboratory is preferred</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 15px; font-family: Arial, sans-serif; background: white;\"><span style='font-size:14px;font-family:\"Verdana\",sans-serif;color:#262321;'>Organized, with good detail-orientation</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 15px; font-family: Arial, sans-serif; background: white;\"><span style='font-size:14px;font-family:\"Verdana\",sans-serif;color:#262321;'>Proficiency with MS Office, including Excel</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 15px; font-family: Arial, sans-serif; background: white;\"><span style='font-size:14px;font-family:\"Verdana\",sans-serif;color:#262321;'>Good interpersonal skills</span></li></ul><p style='margin:0in;font-size:15px;font-family:\"Arial\",sans-serif;background:#D9D9D9;' data-pasted=\"true\"><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong><span style=\"color:black;\">Why You Should Apply</span></strong></span></p><ul><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Structured Career Ladders that provide excellent growth based on your personal aspirations.</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&amp;D and Short and Long-term Disability Insurance</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Park-like setting in Newark, Delaware</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Internal committees designed with the needs and enjoyment of QPS employees in mind.</li></ul><p><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.&nbsp;</span></p></div></div></div></div></div></div></div>\n",
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    "requisitionTitle": "Senior Specialist, Sample Management QC",
    "clientRequisitionID": "3130",
    "organizationalUnits": [],
    "postingInstructions": [],
    "additionalProperties": {},
    "requisitionLocations": [
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        "nameCode": {
          "shortName": " Newark, DE, US"
        },
        "aliasNames": []
      }
    ],
    "screeningRequirements": [],
    "sponsoredVisaTypeCodes": []
  },
  "detail_meta": {
    "url": "https://workforcenow.adp.com/mascsr/default/careercenter/public/events/staffing/v1/job-requisitions/589813?cid=9ee3716b-b93b-41d4-b702-c8728d7396d2&ccId=19000101_000001&lang=en_US&locale=en_US",
    "http_status": 200,
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    "response_bytes": 15132
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  "detail_errors": []
}
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