Job Description
PE Global is currently recruiting for a Warehouse Compliance Specialist for a leading multi-national Pharma client based in Carlow. This is an 11 month contract position. Role: Work as directed by the Warehouse & Weigh and Dispense Area Manager(s) according to Company safety policies and cGMP. Required to drive compliance with Merck Global policies, procedures and guidelines and regulatory requirements and execute Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions. Required to comply with Merck Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job Provide support for the SCM/Warehouse/Weigh and Dispense with respect to the following: Support the updating of Standard Operating Procedures, Shipping & Receipt Documents, protocols and associated reports and any other documentation/ administration of these documents in direct support to the SCM/Warehouse/Weigh and Dispense. Archiving/retrieval of the SCM/Warehouse/Weigh and Dispense documentation. Maintaining and controlling the SCM/Warehouse/Weigh and Dispense documentation areas. Acts as compliance point of contact for all SCM/Warehouse/Weigh and Dispense documentation Assist in the review of SCM/Warehouse/Weigh and Dispense operational procedures, training materials and procedures for various systems. Support documentation in support of investigations, non-conformances, protocols, reports and change controls. Assist in the review of data for periodic reviews as Drive continuous improvement for all aspects of documentation control/ Provide support with audit/inspection requirements to ensure department compliance/readiness. Liaise with site QA Document Control Provide support with audit/inspection requirements to ensure department compliance/readiness. Participate in internal and external audits and inspections. Participate in SCM/Warehouse/Weigh and Dispense Tier daily meetings and ensure effective communication of relevant information. Requirements: 3-5 years experience in a quality role (QC/ QA), ideally in a pharmaceutical manufacturing environment. Knowledge of cGMP and GDP preferred Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices. Extensive knowledge of the following systems: Change Control Deviation Management Self-Inspections Report, standards, policy writing skills required Interested candidates should submit an updated CV. Please click the link below to apply, or alternatively send an up to date CV to . ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland*** Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert. Skills: Change Control Deviation Management Self-Inspections