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QC Compliance Associate (Temporary) - Ireland  

Company managed [?] Still accepting applications

Posted on : 26 February 2017

Project Description


QC Compliance Associate
DESCRIPTION
  • Our company is a high-performing, team based organization, where colleagues are flexible, multi-skilled and empowered to make decisions. 
  • A high level of initiative, energy and motivation are key role requirements, as well as excellent organizational skills.       
  • The initial focus of the group is to set-up an internal compliance programme encompassing self-inspection, management of executed documents (test records, logbooks and SOP’s) and defining metrics and reporting systems for highlighting issues and an escalation process for same.       
  • In addition the role will include the investigation and co-ordination of LIR’s, CAPA’s, change controls and procedural updates and the overall tracking and reporting of their status. An expertise in Trackwise is essential.        
  •  The QC Compliance Specialist will co-ordinate and organize and support the general GMP needs of the QC staff by being an available GMP resource.  
  • This position involves interaction with cross-functional departments and a close relationship with Quality Assurance.       
  • Key factors in the function of this position are flexibility, good organization, having excellent time management, solid tracking and follow up, and being self motivated to make continual progress with minimal supervision and no need for reminders.       



RESPONSIBILITIES
  • Support QC Lab Investigation Reports and Deviations.           
  • Report on the timeliness of compliance to set timelines on LIR’s, Deviations, Quality Events, Material Incidents, CAPAs, and Effectiveness Checks in Trackwise   
  • Support the internal Compliance Programme within the QC department.           
  • Self-Inspection Programme           
  • Management of GMP Records           
  • Tracking and Reporting Systems           
  • Full understanding of basic cGMP expectations; set a good example in observance of cGMP policies.            
  • Interact with the QC staff regularly to answer questions related to GMPs and help champion a compliant work environment with a Continuous Improvement Focus    
  • Lead Inspection Readiness efforts for QC           
  • Lead and Participate in Self-inspections and Compliance walk-throughs of QC.           
  • Managing Change Requests (CRs)           
  •  Work with QC staff and QA Change Control to contribute to comprehensive implementation plans for CRs           
  • Comply with cGMP Documentation & Operations           
  •  Compliance with safety guidelines           



SCOPE
The QC Compliance Specialist works within QC to ensure that the QC department has a robust compliance programme with a well-defined tracking and reporting process to ensure GMP compliance and audit readiness.       


EDUCATION
         • BA or BS in a technical discipline (physical or biological sciences preferred but not required) with 4+ years related to pharmaceutical manufacturing.        


EXPERIENCE
  •  5+ years experience in a GMP regulated environment, with exhibited knowledge or proficiency in a compliance or quality role.         
  •  Experience leading and implementing projects         
  • Demonstrated ability to influence peers and teams with no direct reporting lines.         
  •  Ability to speak, present data, and defend approaches in front of a variety of audiences.         
  • Organizational skills to contribute to department and cross-functional projects         
  • Familiarity with FDA & European GMP’s and regulatory requirements, guidelines, and recommendations.          
  • Strong proficiency with Trackwise         
  • Technical writing must be at a high level with proficient spelling, grammar, and typing skills preferred.           
  • Proficiency with standard office software applications, including MS Word, MS Excel, MS Project, MS Power Point.  
  • Experience and proficiency with other applications.       



Equal Opportunity:      
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.