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HomeCompaniesElement Ext Hub Icims ComQuality Specialist I

Quality Specialist I

Element Ext Hub Icims Com · Concord, CA, US · On Site · Active · $30–$34 / hour · iCIMS

Job facts

FieldValue
CompanyElement Ext Hub Icims Com
TitleQuality Specialist I
Normalized title-
Department / team-
LocationConcord, CA, United States
Work modelOn Site
Employment typeOTHER
Salary$30–$34 / hour
Statusactive
ATS provideriCIMS
Posted / first seen2024-06-06 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Element Ext Hub Icims Com.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through iCIMS.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Concord.Open
Work model jobsActive On Site postings.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

CompanyElement Ext Hub Icims Com
Sourcee32bc6d9-b280-4d89-a0c1-37d1da1c798f
ATS provideriCIMS

Description

Overview Element Materials Technology currently has an opening for a Quality Specialist I to join our growing team in Concord, CA . The Concord laboratory specializes in pharmaceutical and life sciences testing services, supporting developers and manufacturers with microbiology, virology, environmental monitoring, analytical chemistry, sterility, and rapid sterility testing solutions. The site is FDA and DEA registered, cGMP certified, and ISO/IEC 17025:2017 accredited. The Quality Specialist I is responsible for ensuring laboratory services remain compliant with the Quality Manual, client requirements, and applicable regulatory standards. This role plays a key part in supporting the laboratory’s pharmaceutical quality and compliance operations while helping maintain the integrity, accuracy, and reliability of testing services provided to clients. Primary responsibilities include monitoring the effectiveness of the Quality Management System (QMS), supporting internal compliance initiatives, assisting with audits and quality investigations, and helping implement continuous improvement activities. The Quality Specialist I also provides guidance, training, and quality support to laboratory personnel to ensure adherence to regulatory and client requirements in a highly regulated GMP environment. This position is ideal for candidates interested in supporting pharmaceutical quality systems within a fast-paced laboratory environment focused on patient safety, regulatory compliance, and operational excellence. Pay Range: $30–$34/hour DOE Site Status: 100% On-Site (no exceptions) Site Page: EMT Concord Responsibilities Comply to and enforce data integrity requirements(21 CFR Part 11, 210, and 211) Maintain QA files and training matrixes Review Certificates of Analysis, raw data files, in-house documentation, and logbooks Scan data and files records Submit data and Certificates to clients Document management and archival Release Media and Reagents Initiate and participate in quality event investigations using eQMS MasterControl Support client Audits Other duties as assigned Skills / Qualifications A B.S. in science is desired with typically 0-2 years of pharmaceutical/biotechnology/GMP industry experience. Follows company and regulatory quality standards. Basic knowledge of industry and governmental quality regulations. Audits and reviews quality data according to existing procedures. Involved in root cause investigations. Excellent time management and prioritization, strong interpersonal skills, attention to detail, plans tasks to meet deadlines, good critical thinking skills, and demonstrates Element Values. #LI-TK1 Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world’s most trusted testing partner”. All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c) “If you need an accommodation filling out an application, or applying to a job, please email [email protected]

Full job record

Job ID153af2428e7e46e557e3830a2f2494189c4747a4
Org ID6ee70033-59d3-4e39-8afd-8fd159acc71d
Source IDe32bc6d9-b280-4d89-a0c1-37d1da1c798f
Board IDe32bc6d9-b280-4d89-a0c1-37d1da1c798f
Providericims
Provider Job Key19241
TitleQuality Specialist I
Normalized Title
Statusactive
Activeyes
Location TextConcord, CA, US
Department
Team
Employment TypeOTHER
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionCA
CityConcord
Salary RawOverview Element Materials Technology currently has an opening for a Quality Specialist I to join our growing team in Concord, CA . The Concord laboratory specializes in pharmaceutical and life sciences testing services, supporting developers and manufacturers with microbiology, virology, environmental monitoring, analytical chemistry, sterility, and rapid sterility testing solutions. The site is FDA and DEA registered, cGMP certified, and ISO/IEC 17025:2017 accredited. The Quality Specialist I is responsible for ensuring laboratory services remain compliant with the Quality Manual, client requirements, and applicable regulatory standards. This role plays a key part in supporting the laboratory’s pharmaceutical quality and compliance operations while helping maintain the integrity, accuracy, and reliability of testing services provided to clients. Primary responsibilities include monitoring the effectiveness of the Quality Management System (QMS), supporting internal compliance initiatives, assisting with audits and quality investigations, and helping implement continuous improvement activities. The Quality Specialist I also provides guidance, training, and quality support to laboratory personnel to ensure adherence to regulatory and client requirements in a highly regulated GMP environment. This position is ideal for candidates interested in supporting pharmaceutical quality systems within a fast-paced laboratory environment focused on patient safety, regulatory compliance, and operational excellence. Pay Range: $30–$34/hour DOE Site Status: 100% On-Site (no exceptions) Site Page: EMT Concord Responsibilities Comply to and enforce data integrity requirements(21 CFR Part 11, 210, and 211) Maintain QA files and training matrixes Review Certificates of Analysis, raw data files, in-house documentation, and logbooks Scan data and files records Submit data and Certificates to clients Document management and archival Release Media and Reagents Initiate and participate in quality event investigations using eQMS MasterControl Support client Audits Other duties as assigned Skills / Qualifications A B.S. in science is desired with typically 0-2 years of pharmaceutical/biotechnology/GMP industry experience. Follows company and regulatory quality standards. Basic knowledge of industry and governmental quality regulations. Audits and reviews quality data according to existing procedures. Involved in root cause investigations. Excellent time management and prioritization, strong interpersonal skills, attention to detail, plans tasks to meet deadlines, good critical thinking skills, and demonstrates Element Values. #LI-TK1 Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world’s most trusted testing partner”. All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c) “If you need an accommodation filling out an application, or applying to a job, please email [email protected]
Salary Min30
Salary Max34
Salary CurrencyUSD
Salary Periodhour
Source URLhttps://element-ext-hub.icims.com/jobs/19241/quality-specialist-i/job
Apply URLhttps://element-ext-hub.icims.com/jobs/19241/quality-specialist-i/job
First Seen At2026-05-31 18:48:46Z
Last Seen At2026-06-06 08:39:56Z
Last Checked At2026-06-06 08:39:56Z
Last Changed At2026-06-06 08:39:56Z
Inactive At
Source Posted At2024-06-06 08:39:47Z
Source Updated At2026-05-18 13:20:58Z
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=icims/board=element-ext-hub.icims.com/date=2026-06-06/2026-06-06T08-39-34-478Z-ff01b292593b9a6dd0bec1452684fe1b306fc2a684efaad282390257877fe956.json
Event Fields
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Parsed Structured
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Extensions
{}
Native Structured
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