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Compliance Specialist

  • ... Posted on: Feb 21, 2026
  • ... Blackfield Associates
  • ... Hampshire, Tennessee
  • ... Salary: Not Available
  • ... Full-time

Compliance Specialist   

Job Title :

Compliance Specialist

Job Type :

Full-time

Job Location :

Hampshire Tennessee United States

Remote :

No

Jobcon Logo Job Description :

Blackfield Associates are supporting a globally renowned beauty organisation to recruit for an experienced Compliance Specialist, to lead site-level compliance initiatives within a fast-paced GMP manufacturing environment. This role is responsible for ensuring adherence to regulatory requirements and corporate quality standards through robust documentation systems, audit readiness, and effective training programmes.Key ResponsibilitiesMaintain and enhance GMP-compliant policies, procedures, and quality systemsLead internal audits and drive audit readiness activitiesManage deviations, change controls, CAPAs, complaints, and product recallsOversee controlled documentation lifecycle (SOPs, batch records, protocols)Coordinate Annual Product Reviews and product stability programmesDevelop and deliver GMP training aligned with regulatory expectationsRequirementsMinimum 5 years’ experience in a GMP-regulated manufacturing environmentStrong knowledge of quality systems, document control, and audit preparationExperience with product quality reviews and compliance investigationsExcellent communication skills and ability to work cross-functionallyProficient in Microsoft Office and electronic quality management systems (SAP preferred)This is an excellent opportunity for a proactive, detail-oriented quality professional looking to make a meaningful impact within a regulated manufacturing setting.

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Jobcon Logo Position Details

Posted:

Feb 21, 2026

Employment:

Full-time

Salary:

Not Available

City:

Hampshire

Job Origin:

APPCAST_CPC

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Blackfield Associates are supporting a globally renowned beauty organisation to recruit for an experienced Compliance Specialist, to lead site-level compliance initiatives within a fast-paced GMP manufacturing environment. This role is responsible for ensuring adherence to regulatory requirements and corporate quality standards through robust documentation systems, audit readiness, and effective training programmes.Key ResponsibilitiesMaintain and enhance GMP-compliant policies, procedures, and quality systemsLead internal audits and drive audit readiness activitiesManage deviations, change controls, CAPAs, complaints, and product recallsOversee controlled documentation lifecycle (SOPs, batch records, protocols)Coordinate Annual Product Reviews and product stability programmesDevelop and deliver GMP training aligned with regulatory expectationsRequirementsMinimum 5 years’ experience in a GMP-regulated manufacturing environmentStrong knowledge of quality systems, document control, and audit preparationExperience with product quality reviews and compliance investigationsExcellent communication skills and ability to work cross-functionallyProficient in Microsoft Office and electronic quality management systems (SAP preferred)This is an excellent opportunity for a proactive, detail-oriented quality professional looking to make a meaningful impact within a regulated manufacturing setting.

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