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HomeCompaniesPolypeptideus Teamtailor ComAnalytical Validation Specialist - Torrance

Analytical Validation Specialist - Torrance

Polypeptideus Teamtailor Com · Torrance, CA, United States · Active · $80,000–$90,000 / year · Teamtailor

Job facts

FieldValue
CompanyPolypeptideus Teamtailor Com
TitleAnalytical Validation Specialist - Torrance
Normalized title-
Department / team-
LocationTorrance, CA, CA, United States
Work model-
Employment type-
Salary$80,000–$90,000 / year
Statusactive
ATS providerTeamtailor
Posted / first seen2026-03-26 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Polypeptideus Teamtailor Com.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Teamtailor.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Torrance, CA.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

CompanyPolypeptideus Teamtailor Com
Sourcebcd4ceea-e8e5-4020-8416-2e43338008a2
ATS providerTeamtailor

Description

Analytical Validation Specialist Location: Torrance, CA | Employment Type: Full-Time Why This Role Matters At PolyPeptide, analytical validation is central to how we deliver safe, reliable peptide APIs to customers worldwide. As an Analytical Validation Specialist, you will own and execute critical method validation, verification, and transfer activities that directly support development programs, GMP manufacturing, and regulatory readiness. This role offers meaningful technical ownership, regular cross-functional collaboration, and exposure to customer and regulatory interactions. If you enjoy applying analytical science in a highly regulated environment and want your work to have real-world impact, this role provides both challenge and visibility. What You’ll Do You’ll serve as a subject matter expert for analytical validation, ensuring methods are scientifically sound, compliant, and ready to support manufacturing and regulatory needs. Analytical Validation & Lifecycle Management Plan, execute, and document analytical method validation, verification, and transfer activities in alignment with ICH, FDA, EMA, and internal SOPs Draft, review, and approve validation protocols, technical reports, and supporting documentation Support analytical method lifecycle management and continuous improvement initiatives Cross-Functional Collaboration Partner closely with Analytical Development, Quality Control, Regulatory Affairs, Quality Assurance, and Project Management teams Ensure validation activities are completed on time and aligned with project timelines and customer commitments Participate in customer meetings, audits, and regulatory inspections as the analytical validation subject matter expert Data Analysis & Problem Solving Perform data analysis and interpretation using appropriate statistical tools to support validation conclusions Investigate and troubleshoot analytical methods or instrumentation issues Support deviation investigations related to validation studies, including root cause analysis and CAPA development Training & Knowledge Sharing Support training, competency assessments, and performance development of laboratory personnel as appropriate Promote best practices in Good Documentation Practices (GDP) and cGMP compliance What We’re Looking For Education Bachelor’s, Master’s, or PhD in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline Experience 3+ years of hands-on experience in analytical method validation within a pharmaceutical or CDMO environment Skills That Will Help You Succeed Technical Expertise Strong working knowledge of ICH Q2 and applicable global regulatory guidelines Hands-on experience with analytical techniques including HPLC, LC-MS, GC, UV, Karl Fischer, and related instrumentation Proficiency in statistical analysis, data interpretation, and technical report writing Experience with peptides and/or oligonucleotides is strongly preferred Professional Strengths Excellent organizational, communication, and documentation skills Ability to manage multiple priorities and adapt quickly in a fast-paced environment Strong collaboration skills across departments and functional boundaries Comfortable working independently while contributing effectively within a team How Success Is Measured On-Time Delivery: Validation projects completed within agreed timelines Compliance: High adherence to cGMP and regulatory requirements with minimal audit findings Documentation Quality: Accurate, complete, and audit-ready validation documentation Work Environment Primary work setting is a laboratory environment requiring appropriate PPE Ability to stand for extended periods and handle light-to-moderate laboratory equipment in accordance with safety guidelines About PolyPeptide PolyPeptide is a global leader in peptide-based active pharmaceutical ingredients, partnering with innovators worldwide to deliver high-quality, reliable solutions that support life-changing therapies. Our teams are driven by science, collaboration, and a shared commitment to excellence. At PolyPeptide, you’ll work alongside experts who value rigor, integrity, and continuous improvement, while building a career that makes a tangible impact on patient outcomes. If you’re ready to apply your analytical expertise in an environment where quality truly matters, we’d love to hear from you. Salary: $80k-$90k per year We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Full job record

Job IDd87c2ccfcf7fe2f485f6f5bdebb3ecdeac383362
Org IDad9e5266-447c-4ae7-816c-0b94c52377be
Source IDbcd4ceea-e8e5-4020-8416-2e43338008a2
Board IDbcd4ceea-e8e5-4020-8416-2e43338008a2
Providerteamtailor
Provider Job Key7470123
TitleAnalytical Validation Specialist - Torrance
Normalized Title
Statusactive
Activeyes
Location TextTorrance, CA, United States
Department
Team
Employment Type
Workplace Type
Remote Policy
CountryUnited States
RegionCA
CityTorrance, CA
Salary RawAnalytical Validation Specialist Location: Torrance, CA | Employment Type: Full-Time Why This Role Matters At PolyPeptide, analytical validation is central to how we deliver safe, reliable peptide APIs to customers worldwide. As an Analytical Validation Specialist, you will own and execute critical method validation, verification, and transfer activities that directly support development programs, GMP manufacturing, and regulatory readiness. This role offers meaningful technical ownership, regular cross-functional collaboration, and exposure to customer and regulatory interactions. If you enjoy applying analytical science in a highly regulated environment and want your work to have real-world impact, this role provides both challenge and visibility. What You’ll Do You’ll serve as a subject matter expert for analytical validation, ensuring methods are scientifically sound, compliant, and ready to support manufacturing and regulatory needs. Analytical Validation & Lifecycle Management Plan, execute, and document analytical method validation, verification, and transfer activities in alignment with ICH, FDA, EMA, and internal SOPs Draft, review, and approve validation protocols, technical reports, and supporting documentation Support analytical method lifecycle management and continuous improvement initiatives Cross-Functional Collaboration Partner closely with Analytical Development, Quality Control, Regulatory Affairs, Quality Assurance, and Project Management teams Ensure validation activities are completed on time and aligned with project timelines and customer commitments Participate in customer meetings, audits, and regulatory inspections as the analytical validation subject matter expert Data Analysis & Problem Solving Perform data analysis and interpretation using appropriate statistical tools to support validation conclusions Investigate and troubleshoot analytical methods or instrumentation issues Support deviation investigations related to validation studies, including root cause analysis and CAPA development Training & Knowledge Sharing Support training, competency assessments, and performance development of laboratory personnel as appropriate Promote best practices in Good Documentation Practices (GDP) and cGMP compliance What We’re Looking For Education Bachelor’s, Master’s, or PhD in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline Experience 3+ years of hands-on experience in analytical method validation within a pharmaceutical or CDMO environment Skills That Will Help You Succeed Technical Expertise Strong working knowledge of ICH Q2 and applicable global regulatory guidelines Hands-on experience with analytical techniques including HPLC, LC-MS, GC, UV, Karl Fischer, and related instrumentation Proficiency in statistical analysis, data interpretation, and technical report writing Experience with peptides and/or oligonucleotides is strongly preferred Professional Strengths Excellent organizational, communication, and documentation skills Ability to manage multiple priorities and adapt quickly in a fast-paced environment Strong collaboration skills across departments and functional boundaries Comfortable working independently while contributing effectively within a team How Success Is Measured On-Time Delivery: Validation projects completed within agreed timelines Compliance: High adherence to cGMP and regulatory requirements with minimal audit findings Documentation Quality: Accurate, complete, and audit-ready validation documentation Work Environment Primary work setting is a laboratory environment requiring appropriate PPE Ability to stand for extended periods and handle light-to-moderate laboratory equipment in accordance with safety guidelines About PolyPeptide PolyPeptide is a global leader in peptide-based active pharmaceutical ingredients, partnering with innovators worldwide to deliver high-quality, reliable solutions that support life-changing therapies. Our teams are driven by science, collaboration, and a shared commitment to excellence. At PolyPeptide, you’ll work alongside experts who value rigor, integrity, and continuous improvement, while building a career that makes a tangible impact on patient outcomes. If you’re ready to apply your analytical expertise in an environment where quality truly matters, we’d love to hear from you. Salary: $80k-$90k per year We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
Salary Min80,000
Salary Max90,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://polypeptideus.teamtailor.com/jobs/7470123-analytical-validation-specialist-torrance
Apply URLhttps://polypeptideus.teamtailor.com/jobs/7470123-analytical-validation-specialist-torrance
First Seen At2026-05-31 17:47:06Z
Last Seen At2026-06-06 10:42:11Z
Last Checked At2026-06-06 10:42:11Z
Last Changed At2026-05-31 17:47:06Z
Inactive At
Source Posted At2026-03-26 20:59:21Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=teamtailor/board=polypeptideus.teamtailor.com/date=2026-06-06/2026-06-06T10-42-11-482Z-eae5e50fce9dc111bbb8a2662791c55784e4091b8c6ba6a01a40263e7a09b4e6.json
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Parsed Structured
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Extensions
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Native Structured
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