Compliance Specialist – Technical Operations (Ref. NHRL02)

Website HeadcountGroup Headcount Solutions

Compliance Specialist – Technical Operations

The Compliance Specialist, Technical Operations is a member of the Technical Operations Team (Automation, Engineering & Facilities) and is responsible for operations support and compliance related activities for the manufacture of site products.

Responsibilities:

  • Completes investigations of technical deviations for department issues of non compliance. Ensures CAPAs are identified as appropriate and are implemented as planned; in addition, ensures CAPAs have the intended effectiveness.
  • Acts as a liaison between Technical Operations and onsite quality and regulatory groups, as well as other departments across the company, with respect to all quality instances and compliance support.
  • Provides support, information, and assistance to individuals, groups and management with the initiation, authorship, review, submission, and follow-up/completion of documents such as Change Controls, risk assessments, impact statements and corrective/prevention action plans.
  • Provide periodic review of department documentation and records such as Periodic Evaluation Reports (PER), logbooks, Life Cycle Documents and Engineering Documentation, etc. to assess for compliance with established quality standards, policies and procedures.
  • Review and approval of preventative maintenance records/work orders (corrective and scheduled) on the CMMS system to assess for compliance with established quality standards, policies and procedures.
  • Maintains knowledge of current good manufacturing practices (cGMPs) and execution of any other GMP compliance related activities as required.
  • Continuous Improvement Implementation.

Knowledge:

  • Basic knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations.
  • Proficient in Excel, PowerPoint, Visio, Word, etc. in addition to experience working within shared work environments.
  • Strong interpersonal, written, presentation, communication and investigation skills with the ability to engage with a diverse range of individuals across all levels of the organization.
  • Specialist; minimum of BA/BS in Engineering/Science discipline with 2+ years experience working in a cGMP environment.
Name
Email
Telephone
Message
Upload your CV/resume or any other relevant file. Max. file size: 256 MB.
Check the box to confirm our use of your data under GDPR regulations. To register your CV you must tick the checkbox to confirm your acceptance of our GDPR and Privacy Policy