bluedoor data·Job Postings API·bluedoor.sh ↗

HomeCompaniesCareers Alcami Icims ComSr. Compliance Specialist - Audit , GMP

Sr. Compliance Specialist - Audit , GMP

Careers Alcami Icims Com · Charleston, SC, US · Hybrid · Active · iCIMS

Job facts

FieldValue
CompanyCareers Alcami Icims Com
TitleSr. Compliance Specialist - Audit , GMP
Normalized title-
Department / teamRegulatory Compliance
LocationCharleston, SC, United States
Work modelHybrid / Hybrid
Employment typeFull Time
Salary-
Statusactive
ATS provideriCIMS
Posted / first seen2026-06-19 / 2026-06-20
Changed / last seen2026-06-20 / 2026-06-20

Related slices

PageWhat it containsOpen
Company jobsActive postings from Careers Alcami 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 Charleston.Open
Department jobsActive postings in Regulatory Compliance.Open
Work model jobsActive Hybrid 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

CompanyCareers Alcami Icims Com
Source616edbfb-b00b-461b-b6c9-d3f996abfb46
ATS provideriCIMS

Description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Are you interested in joining our team? Job Summary The Senior Compliance Specialist is accountable for driving results in a fast-paced environment by effectively performing activities directed to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting audits and supporting inspections, and maintaining quality databases. The ideal candidate will assist with the development of SOPs or other quality documents as needed. The Senior Compliance Specialist will perform the role of Lead Inspector for external audits and act as consultant with clients for all levels of regulatory issues. The Sr. Compliance Specialist will provide guidance and mentoring for other compliance employees. On-Site Expectations Hybrid position. Must be on-site for client audits. Occasional travel to other sites for audits. 1st Shift: Monday - Friday, 8:00am - 5:00pm. Responsibilities Host client audits and coordinate with clients. Coordinate with internal team members to complete responses. Write and coordinate audit responses. Perform quality review and approval of documents, data, protocols, and/or reports. May assist with supplier quality audits and/or inspections. May assist with evaluation of supplier changes and notifications and make assessment of impact accordingly. Maintain quality databases and support quality systems. Assist with development of SOPs or other quality documents as needed. Consult with clients on all levels of regulatory issues. Serve as an effective member of the Compliance team and serve as a mentor in area of expertise. Comply with company policies and SOPs. Assist with quality improvement initiatives as needed. Ensure timely completion and compliance with cGMP and all other relevant company training requirements. Other duties as assigned. Qualifications Bachelor’s degree in Chemistry, Biology, or related field with 10+ years of GMP related experience, or Master’s degree in related field with 5+ years of related experience, or equivalent educational and work experience. Client hosting experience in the pharmaceutical industry preferred. Supplier management experience in pharmaceutical industry is a plus. Client-facing experience required. Knowledge, Skills, and Abilities Strong knowledge of regulations and SOPs applicable to area of responsibility and keeps abreast of new regulations and regulatory guidance in areas of expertise. Good written and oral communication skills. Good computer skills and knowledge of Microsoft Office products. Ability to be trained and to mentor. Ability to interact well with employees at all levels. Ability to negotiate. Ability to lead audits. Ability to act as a consultant. Travel Expectations Up to 10% travel for audits. Physical Demands and Work Environment The physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee may be required to use hands to finger, handle, or feel and to reach with hands and arms. The employee is required to talk and listen. The employee is frequently required to stand, walk, and sit. The employee may be occasionally required to climb or balance.

Full job record

Job ID2e09fa5d6f90fac7cdb4a507f0cfc1ddd4a4a3aa
Org IDb460a007-52d3-42ae-8629-2d277c0dc6c6
Source ID616edbfb-b00b-461b-b6c9-d3f996abfb46
Board ID616edbfb-b00b-461b-b6c9-d3f996abfb46
Providericims
Provider Job Key2135
TitleSr. Compliance Specialist - Audit , GMP
Normalized Title
Statusactive
Activeyes
Location TextCharleston, SC, US
DepartmentRegulatory Compliance
Team
Employment Typefull_time
Workplace Typehybrid
Remote Policyhybrid
CountryUnited States
RegionSC
CityCharleston
Salary RawAt Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Are you interested in joining our team? Job Summary The Senior Compliance Specialist is accountable for driving results in a fast-paced environment by effectively performing activities directed to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting audits and supporting inspections, and maintaining quality databases. The ideal candidate will assist with the development of SOPs or other quality documents as needed. The Senior Compliance Specialist will perform the role of Lead Inspector for external audits and act as consultant with clients for all levels of regulatory issues. The Sr. Compliance Specialist will provide guidance and mentoring for other compliance employees. On-Site Expectations Hybrid position. Must be on-site for client audits. Occasional travel to other sites for audits. 1st Shift: Monday - Friday, 8:00am - 5:00pm. Responsibilities Host client audits and coordinate with clients. Coordinate with internal team members to complete responses. Write and coordinate audit responses. Perform quality review and approval of documents, data, protocols, and/or reports. May assist with supplier quality audits and/or inspections. May assist with evaluation of supplier changes and notifications and make assessment of impact accordingly. Maintain quality databases and support quality systems. Assist with development of SOPs or other quality documents as needed. Consult with clients on all levels of regulatory issues. Serve as an effective member of the Compliance team and serve as a mentor in area of expertise. Comply with company policies and SOPs. Assist with quality improvement initiatives as needed. Ensure timely completion and compliance with cGMP and all other relevant company training requirements. Other duties as assigned. Qualifications Bachelor’s degree in Chemistry, Biology, or related field with 10+ years of GMP related experience, or Master’s degree in related field with 5+ years of related experience, or equivalent educational and work experience. Client hosting experience in the pharmaceutical industry preferred. Supplier management experience in pharmaceutical industry is a plus. Client-facing experience required. Knowledge, Skills, and Abilities Strong knowledge of regulations and SOPs applicable to area of responsibility and keeps abreast of new regulations and regulatory guidance in areas of expertise. Good written and oral communication skills. Good computer skills and knowledge of Microsoft Office products. Ability to be trained and to mentor. Ability to interact well with employees at all levels. Ability to negotiate. Ability to lead audits. Ability to act as a consultant. Travel Expectations Up to 10% travel for audits. Physical Demands and Work Environment The physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee may be required to use hands to finger, handle, or feel and to reach with hands and arms. The employee is required to talk and listen. The employee is frequently required to stand, walk, and sit. The employee may be occasionally required to climb or balance.
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://careers-alcami.icims.com/jobs/2135/sr.-compliance-specialist---audit-%2c-gmp/job
Apply URLhttps://careers-alcami.icims.com/jobs/2135/sr.-compliance-specialist---audit-%2c-gmp/job
First Seen At2026-06-20 08:22:38Z
Last Seen At2026-06-20 08:22:38Z
Last Checked At2026-06-20 08:22:38Z
Last Changed At2026-06-20 08:22:38Z
Inactive At
Source Posted At2026-06-19 04:00:00Z
Source Updated At2026-06-19 19:42:58Z
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=icims/board=careers-alcami.icims.com/date=2026-06-20/2026-06-20T08-22-36-364Z-03d8872ceb6a41d94f0abe411ad5cd354d3848f10d3f4863d3aa2416ca41e56d.json
Event Fields
{
  "content_hash": "722e877639084f07a1f3b9be31ed296fcae84ef9a724e931ee70d6b8c1244e9e",
  "source_hash": "23ef1e0f22bde053e422be7b937cd7785cc5447d83da64d8ea55b427d11d1666",
  "last_changed_at": "2026-06-20T08:22:38.850Z",
  "active_status": "active"
}
Parsed Structured
{
  "dedupe": null,
  "language": "en",
  "location": {
    "raw": "Charleston, SC, US",
    "city": "Charleston",
    "region": "SC",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-20T08:22:38.800Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Charleston, SC, US",
      "city": "Charleston",
      "region": "SC",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": "hybrid",
  "salary_period": null,
  "workplace_type": "hybrid",
  "salary_currency": null
}
Extensions
{}
Native Structured
{
  "json_ld": {
    "url": "https://careers-alcami.icims.com/jobs/2135/sr.-compliance-specialist---audit-%2c-gmp/job",
    "@type": "JobPosting",
    "title": "Sr. Compliance Specialist - Audit , GMP",
    "@context": "http://schema.org",
    "datePosted": "2026-06-19T04:00:00.000Z",
    "description": "<h2> </h2>\n<p>At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.</p>\n<p> </p>\n<p>Are you interested in joining our team?</p>\n<h2>Job Summary</h2>\n<p>The Senior Compliance Specialist is accountable for driving results in a fast-paced environment by effectively performing activities directed to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting audits and  supporting inspections, and maintaining quality databases. The ideal candidate will assist with the development of SOPs or other quality documents as needed. The Senior Compliance Specialist will perform the role of Lead Inspector for external audits and act as consultant with clients for all levels of regulatory issues. The Sr. Compliance Specialist will provide guidance and mentoring for other compliance employees.</p>\n<h2>On-Site Expectations</h2>\n<ul>\n <li>Hybrid position. Must be on-site for client audits. Occasional travel to other sites for audits.</li>\n <li>1st Shift: Monday - Friday, 8:00am - 5:00pm.</li>\n</ul>\n<h2>Responsibilities</h2>\n<ul>\n <li>Host client audits and coordinate with clients.</li>\n <li>Coordinate with internal team members to complete responses.</li>\n <li>Write and coordinate audit responses.</li>\n <li>Perform quality review and approval of documents, data, protocols, and/or reports.</li>\n <li>May assist with supplier quality audits and/or inspections.</li>\n <li>May assist with evaluation of supplier changes and notifications and make assessment of impact accordingly.</li>\n <li>Maintain quality databases and support quality systems.</li>\n <li>Assist with development of SOPs or other quality documents as needed.</li>\n <li>Consult with clients on all levels of regulatory issues.</li>\n <li>Serve as an effective member of the Compliance team and serve as a mentor in area of expertise.</li>\n <li>Comply with company policies and SOPs.</li>\n <li>Assist with quality improvement initiatives as needed.</li>\n <li>Ensure timely completion and compliance with cGMP and all other relevant company training requirements.</li>\n <li>Other duties as assigned.</li>\n</ul>\n<h2>Qualifications</h2>\n<ul>\n <li>Bachelor’s degree in Chemistry, Biology, or related field with 10+ years of GMP related experience, or Master’s degree in related field with 5+ years of related experience, or equivalent educational and work experience.</li>\n <li>Client hosting experience in the pharmaceutical industry preferred.</li>\n <li>Supplier management experience in pharmaceutical industry is a plus.</li>\n <li>Client-facing experience required. </li>\n</ul>\n<h2>Knowledge, Skills, and Abilities</h2>\n<ul>\n <li>Strong knowledge of regulations and SOPs applicable to area of responsibility and keeps abreast of new regulations and regulatory guidance in areas of expertise.</li>\n <li>Good written and oral communication skills.</li>\n <li>Good computer skills and knowledge of Microsoft Office products.</li>\n <li>Ability to be trained and to mentor.</li>\n <li>Ability to interact well with employees at all levels.</li>\n <li>Ability to negotiate.</li>\n <li>Ability to lead audits.</li>\n <li>Ability to act as a consultant.</li>\n</ul>\n<h2>Travel Expectations</h2>\n<ul>\n <li>Up to 10% travel for audits.</li>\n</ul>\n<h2>Physical Demands and Work Environment</h2>\n<p>The physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee may be required to use hands to finger, handle, or feel and to reach with hands and arms. The employee is required to talk and listen. The employee is frequently required to stand, walk, and sit. The employee may be occasionally required to climb or balance.</p>",
    "directApply": true,
    "jobLocation": [
      {
        "@type": "Place",
        "address": {
          "@type": "PostalAddress",
          "postalCode": "29405",
          "addressRegion": "SC",
          "streetAddress": "4390 Belle Oaks Drive",
          "addressCountry": "US",
          "addressLocality": "Charleston",
          "postOfficeBoxNumber": "UNAVAILABLE"
        }
      }
    ],
    "validThrough": "2027-06-19T04:00:00.000Z",
    "employmentType": "FULL_TIME",
    "hiringOrganization": {
      "name": "Alcami Corporation",
      "@type": "Organization",
      "sameAs": "https://www.alcami.com"
    },
    "occupationalCategory": "Regulatory Compliance"
  },
  "detail_meta": {
    "url": "https://careers-alcami.icims.com/jobs/2135/sr.-compliance-specialist---audit-%2c-gmp/job?in_iframe=1",
    "http_status": 200,
    "content_type": "text/html;charset=UTF-8",
    "response_bytes": 35785,
    "compact_response_bytes": 5245,
    "original_response_bytes": 35785
  },
  "sitemap_job": {
    "id": "2135",
    "url": "https://careers-alcami.icims.com/jobs/2135/sr.-compliance-specialist---audit-%2c-gmp/job",
    "slug": "sr.-compliance-specialist---audit-%2c-gmp",
    "lastmod": "2026-06-19T15:42:58-04:00"
  },
  "detail_errors": []
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/2e09fa5d6f90fac7cdb4a507f0cfc1ddd4a4a3aa?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/b460a007-52d3-42ae-8629-2d277c0dc6c6JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/616edbfb-b00b-461b-b6c9-d3f996abfb46JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/2e09fa5d6f90fac7cdb4a507f0cfc1ddd4a4a3aa/eventsJSON