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Commercial Quality Specialist, GDP RP SK

Función del trabajo:
Fecha de publicación:
Fecha de finalización:
ID:
2607046438W

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Kenvue está reclutando actualmente para a:

Commercial Quality Specialist, GDP RP SK

Lo que hacemos

En Kenvue, nos damos cuenta del extraordinario poder del cuidado diario. Sobre la base de más de un siglo de herencia y arraigados en la ciencia, somos el hogar de marcas icónicas, incluidas NEUTROGENA®, AVEENO,® TYLENOL,® LISTERINE,® JOHNSON'S® y BAND-AID® que ya conoces y amas. La ciencia es nuestra pasión; El cuidado es nuestro talento.

Quiénes somos

Nuestro equipo global está formado por ~ 22.000 personas brillantes con una cultura laboral en la que cada voz importa y cada contribución es apreciada. Nos apasionan las ideas, innovación y comprometidos con la entrega de los mejores productos a nuestros clientes. Con experiencia y empatía, ser un Kenvuer significa tener el poder de impactar a millones de personas todos los días. Ponemos a las personas en primer lugar, nos preocupamos ferozmente, nos ganamos la confianza de la ciencia y resolvemos con coraje, ¡y tenemos oportunidades brillantes esperándote! Únase a nosotros para dar forma a nuestro futuro y al suyo. Para obtener más información, haga clic en aquí.

Role reports to:

Manager Commercial Quality BENALP (interim SVK, CZ, HU)

Ubicación:

Europe/Middle East/Africa, Slovakia, Bratislava, Bratislava

Lugar de trabajo:

Híbrido

What will you

Commercial Quality Specialist: 

  • To participate in projects and activities on cluster or regional level 

  • Support in EMEA, CE and CEE CQ projects in order to keep high level of or improve GxP compliance as well as Excellence in Execution 

  • To be the partner for the local business management of the Marketing Company (MC) in all local Quality & Compliance issues and questions 

  • To ensure that all legal requirements are respected, particularly the Cluster and country specific ones applicable for all activities/processes and products in the MC 

  • To ensure that in every business decision and process potential quality and compliance impact is assessed and respected 

  • To deploy locally all applicable Cluster, Regional and/or World-Wide Quality and Compliance Policies, processes, procedures and requirements, ensuring compliance with the JNTL Quality Policy 

  • Approval of Finished Good Specifications in Document Management System 

  • Performance of First Article Inspection (if applicable) 

  • Initiation of non-conformances (INV) and change controls (GCC) 

  • Conduct internal and external audits (supplier, distributor) following the CE audit program and ensure necessary CAPA´s are implemented 

  • Initiation of QA training for new employees 

  • To support management of local co-packing/rework operations in SK/CZ - ensure GMP & GDP compliance for products during customization and transport to / from the co-packer 

  • Communication with stakeholders  

  • To retrieve CoA´s from the system 

  • To maintain Artwork overview for release needs and share with the warehouse and ensure the data are up to date 

  • To supervise non-product related Change Control management in Slovak Republic 

 

Qualified Person SK: 

All actions are in accordance with Act No. 362/2011; Decree of MoH 128/2012 and GDP Guidelines. 

  • Communication of (potential) significant quality issues to local Health Authorities in a timely manner and in line with local requirements (for GDP responsible person). Respond to authority enquiries as required by the GDP responsible person role 

  • To record any quality issues related to product and GDP into company INV&CAPA systems and manage the ones related to GDP in Slovakia 

  • To coordinate and perform the administrative release of drug products in the local warehouse/crossdock according to local requirements and SOP 

  • To approve destructions of drug products 

  • To approve re-distribution of returned drug products 

  • To report deliveries and consumptions of drug products to HA according to local requirements 

  • To focus on accuracy and quality of records 

  • To ensure GxP relevant, MC specific suppliers and service providers are selected, qualified, audited and monitored and Quality Agreements are established according to schedule and applicable QSPs and STDs 

  • To regularly attend GDP conferences/trainings or other education programs 

  • To manage all required SOP´s in Slovakia relevant to distribution of JNTL products 

  • To ensure all involved departments and 3PL are trained on relevant SOP´s with every new revision 

  • To ensure that all implemented Quality & Compliance processes/procedures are constantly met through all local operations 

  • To ensure supplier´s and customer´s GDP & Wholesaler license validity 

  • To lead/coordinate any potential recall in Slovak Republic 

  • To handle Escalations and Field Actions 

  • To perform mock-recall 

  • To prepare and lead inspections of the Slovak MC by local HA 

  • To have a regular oversight on local requirements  

  • To have an oversight on complaints from customers 

  • To perform 3PL Inspection once per year and have an oversight on delegated actions 

  • To perform W2W in the warehouse every year 

  • To ensure self-inspection is performed every year 

Essential knowledge and skills: 

  • University degree in Pharmaceutics 

  • Knowledge and experience with quality systems 

  • Experience in production, Quality or RA or medicinal products, cosmetics, food supplements, medical devices or equivalent 

  • Knowledge and experience in working in GDP and/or GMP environment 

 

 What is in it for you:

Annual base salary for new hires in this position ranges:

21,845 - € 29,555

This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.

  • Competitive Benefit Package*

  • Paid Company Holidays, Paid Vacation, Volunteer Time & More!

  • Learning & Development Opportunities

  • Kenvuer Impact Networks

 

 

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