Home › Companies › Careers Alcami Icims Com › Sr. Compliance Specialist - Audit , GMP
Sr. Compliance Specialist - Audit , GMP
Careers Alcami Icims Com · Charleston, SC, US · Hybrid · Active · iCIMS
Job facts
| Field | Value |
|---|---|
| Company | Careers Alcami Icims Com |
| Title | Sr. Compliance Specialist - Audit , GMP |
| Normalized title | - |
| Department / team | Regulatory Compliance |
| Location | Charleston, SC, United States |
| Work model | Hybrid / Hybrid |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | iCIMS |
| Posted / first seen | 2026-06-19 / 2026-06-20 |
| Changed / last seen | 2026-06-20 / 2026-06-20 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Careers Alcami Icims Com. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through iCIMS. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Charleston. | Open |
| Department jobs | Active postings in Regulatory Compliance. | Open |
| Work model jobs | Active Hybrid 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 | Careers Alcami Icims Com |
| Source | 616edbfb-b00b-461b-b6c9-d3f996abfb46 |
| ATS provider | iCIMS |
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 ID | 2e09fa5d6f90fac7cdb4a507f0cfc1ddd4a4a3aa |
| Org ID | b460a007-52d3-42ae-8629-2d277c0dc6c6 |
| Source ID | 616edbfb-b00b-461b-b6c9-d3f996abfb46 |
| Board ID | 616edbfb-b00b-461b-b6c9-d3f996abfb46 |
| Provider | icims |
| Provider Job Key | 2135 |
| Title | Sr. Compliance Specialist - Audit , GMP |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Charleston, SC, US |
| Department | Regulatory Compliance |
| Team | — |
| Employment Type | full_time |
| Workplace Type | hybrid |
| Remote Policy | hybrid |
| Country | United States |
| Region | SC |
| City | Charleston |
| Salary Raw | 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. |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://careers-alcami.icims.com/jobs/2135/sr.-compliance-specialist---audit-%2c-gmp/job |
| Apply URL | https://careers-alcami.icims.com/jobs/2135/sr.-compliance-specialist---audit-%2c-gmp/job |
| First Seen At | 2026-06-20 08:22:38Z |
| Last Seen At | 2026-06-20 08:22:38Z |
| Last Checked At | 2026-06-20 08:22:38Z |
| Last Changed At | 2026-06-20 08:22:38Z |
| Inactive At | — |
| Source Posted At | 2026-06-19 04:00:00Z |
| Source Updated At | 2026-06-19 19:42:58Z |
| Raw Payload Uri | s3://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 |
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