OQ SPECIALIST

We are looking for an OPERATIONAL QUALITY SPECIALIST for a manufacturing company.
As Operational Quality Specialist staff you will be responsible for supporting in implementing and maintaining an effective and robust quality management system.
You will also perform day to day quality operations to ensure lean and efficient ways of working to meet compliance standards.
This role will provide YOU the opportunity to lead key activities to progress YOUR career.
These responsibilities include some of the following.
Perform quality oversight directly on the shop floor, guaranteeing that all the GMP standards are met during operations Execute and deliver quality objectives, quality improvement plan, and trends against the quality key performance indicators to drive continuous improvement Monitor quality performance and key performance indicators assigned to third parties to ensure quality and compliance issues are identified, communicated, and resolved Support the Quality Manager to ensure that an effective local product incident process is in place and manage any product quality related issues and train staff as appropriate Develop local processes to conduct root cause analysis; identify where corrective/preventative actions plans are required and ensure they are effectively implemented, monitored, and closed out Perform activities to support the risk management process to ensure effective management, timely reporting, review and escalation of quality risks Ensure all product specifications and related documents are maintained and compliant to current registered details Support the local change control process to ensure all planned major changes are effectively and compliantly managed Support the complaints management process to ensure potential issues are determine quickly, linked to the adverse events, reported, and follow up on product complaints Support Quality Manager in ensuring product storage and distribution performed by third party warehousing and distribution service providers Ensure as appropriate documentation of batch records and retention of samples Basic Qualifications and Skills.
Bachelor’s degree in a science-related field Previous experience in the role Experience in quality assurance systems particularly in the areas of batch manufacturing and release, product incidents and performing self-inspection Experience with regulatory requirements pertaining to good manufacturing practices and good documentation practices Experience working with effective quality documentation systems   Preferred Qualifications & Skills.
Previous role as a quality associate or specialist for sterile manufacturing Excellent written and verbal communication skills Analytical thinker with good attention to detail and problem-solving skills in a structured process Team player with the ability to work in cross-functional teams Ability to work under pressure Identify areas of continuous improvement and innovative ways of working Ability to demonstrate flexible thinking Strong general computer literacy with Intermediate skills in Microsoft Word, Excel, Power Point and Outlook   Facciamo parte di Gi Group Holding (www.
igroupholding.
t) la prima multinazionale italiana del lavoro, nonché una delle principali realtà a livello mondiale nei servizi dedicati allo sviluppo del mercato del lavoro.
Il nostro Gruppo è attivo nei seguenti campi.
lavoro temporaneo, Permanent e Professional Staffing, Ricerca e Selezione, Consulenza HR, Formazione, Outsourcing, supporto alla ricollocazione e attività complementari.
Siamo presenti in più di 30 Paesi in Europa, Asia e America con un team di oltre persone.
I valori che ci contraddistinguono.
attenzione, passione, apprendimento continuo e innovazione, collaborazione, sostenibilità, responsabilità.
Consulta tutti i nostri annunci su www.
igroup.
t Gi Group S.
.
.
è autorizzata ad operare dal Ministero del Lavoro (Aut.
Min.
PROT.
- SG).
L’offerta si intende rivolta a candidati am