At Hikma we put better health within reach, every day in more than 50 countries around the world. For more than 40 years, we've been creating high-quality medicines and making them accessible to the people who need them. Headquartered in the UK, we are a global company with a local presence across the United States (US), the Middle East and North Africa (MENA) and Europe, and we use our unique insight and expertise to transform cutting-edge science into innovative solutions that transform people's lives. We're committed to our customers, and the people they care for, and by thinking creatively and acting practically, we provide them with a broad range of branded and non-branded generic medicines. Together, our 8,600 colleagues are helping to shape a healthier world that enriches all our communities. We are a leading licensing partner, and through our venture capital arm, are helping bring innovative health technologies to people around the world. For more info Disclaimer: EMPLOYMENT RECRUITMENT FRAUD ALERT Please be advised that the Hikma Pharmaceuticals Group does not ask its employees or prospective employees to wire any money either to its bank accounts or to any third party, and does not conduct employment interviews via any social media platform, Google Hangouts, Yahoo! Messenger, text message, or e-mail. Unfortunately, employment scams are increasingly common and it is important to remain vigilant when conducting a job search. For more information about these scams, see the UK National Fraud Intelligence Bureaus website and the US Better Business Bureaus article on the subject. If you receive a request to send money through any means or a request for personal information from anyone claiming to be a Hikma recruiter, DO NOT REPLY. Instead, please forward the communication(s) to us at [email protected] so that we may provide it to relevant law enforcement agencies, as appropriate.

Website

http://www.hikma.comJob description:Descriptif du poste :

Rattach la direction Qualit, le superviseur Validation et calibration participe activement, en collaboration avec les autres dpartements et services, la mise en place et le suivi de la politique Qualit de Promopharm S.A.

Le titulaire du poste aura les responsabilits suivantes :

• Mettre en uvre les moyens (locaux, matriel, personnel, documents etc.) ncessaires lapplication des B.P.F. et des exigences rglementaires par ses collaborateurs et ce dans le cadre de leurs activits. Cela englobe les aspects suivants :
• Le contrle de lenvironnement dans les ateliers de fabrication et de contrle des mdicaments et de stockage des matires premires et des produits finis ;
• La mtrologie des instruments et appareils de mesure ;
• La qualification des quipements et installations ;
• La validation des procds de fabrication ;
• La validation de nettoyage des quipements de production.
• La validation des systmes dinformation
• Mettre en place et veiller loptimisation et la ralisation des plannings des activits cits ci-dessus.
• Dfinir et proposer les investissements ncessaires au bon fonctionnement du dpartement ;
• Grer le budget de la qualit technique CAPEX et OPEX relatives aux activits du dpartement
• Sassurer de la bonne utilisation, le suivi et de lentretien du matriel utilis dans le cadre des activits du dpartement
• Participer la ralisation de Plan dAction dAmlioration de la Qualit
• Participer la formation du personnel et lorganisation du dpartement en accord avec sa hirarchie
  

Diplme & Formation

Bac+5 ans ou plus Formation Scientifique et Technique, (exemple :ingenieur en chimie, Technique danalyse et contrle qualit, Master en Instrumentation Scientifique et Qualit dans les Bio-industries).

Exprience dans un poste similaire exigeSeeked profile:Diplme & Formation :

Bac+5 ans ou plus Formation Scientifique et Technique, (exemple :ingenieur en chimie, Technique danalyse et contrle qualit, Master en Instrumentation Scientifique et Qualit dans les Bio-industries).