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Gehaltsübersicht für Quality IT Specialist in Schweiz

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Gehaltsübersicht für Quality IT Specialist in Schweiz

68 400 ₣ Durchschnittliches Monatsgehalt

Durchschnittliches Gehaltsniveau in den letzten 12 Monaten: "Quality IT Specialist in Schweiz"

Währung: CHF USD Jahr: 2021 2020
Das Balkendiagramm zeigt die Änderung des Gehaltsniveaus in der Quality IT Specialist Branche in Schweiz

Verteilung des Stellenangebots "Quality IT Specialist" in Schweiz

Währung: CHF
Wie die Grafik zeigt, in Schweiz gilt Kanton Bern als die Region mit der größten Zahl der offenen Stellen in und an zweiter Stelle folgt Kanton Zürich. Den dritten Platz nimmt Kanton Waadt ein.

Ranking der Kantone in Schweiz gemäß dem Gehaltsniveau für den Beruf "Quality IT Specialist"

Währung: CHF
Wie die Grafik zeigt, in Schweiz gilt Kanton Bern als die Region mit der größten Zahl der offenen Stellen in und an zweiter Stelle folgt Kanton Zürich. Den dritten Platz nimmt Kanton Waadt ein.

Ranking der ähnlichen Stellenangebote gemäß dem Gehaltsniveau in Schweiz

Währung: CHF
Unter den ähnlichen Berufen in Schweiz gilt Directeur als der bestbezahlte Beruf. Laut unserer Webseite beträgt das Durchschnittseinkommen 131667 CHF. An zweiter Stelle folgt Director mit dem Gehalt von 120649 CHF und den dritten Platz nimmt Unix System Engineer mit dem Gehalt von 120000 CHF ein.

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Quality Supplier Specialist
Randstad (Schweiz) AG, Le Locle
We are looking for a Quality Supplier Specialist to work for a mission of 1 year at our client specialized in the medical device. It is an international company near Neuchâtel. Your mission: - You are responsible for Supplier Quality engineering functions for our swiss facility;- You participate in supplier assessments and continuous improvement activities at supplier facilities, MRB activities, and metrics activities;- You will also provide Quality Engineering support to the team;- You develop and implement Quality Systems procedures, as well as modifications to existing Inspection plans- You provide Quality Engineering Support to suppliers including audits/assessments, inspection technique support, verification /validation activities, CAPA and change management. FDA CFR part 820, EU MDR, and ISO 13485 regulations/standards will be the focus;- You ensure that activities for validation of outsourced new processes/products are performed and documented according to applicable procedures. Your profile: - You have a Bachelor’s Degree in Engineering, Life Science, or a related technical discipline.- You are experienced in performing Root Cause analysis and Special Process Validations.- You are experienced in a Medical Device manufacturing environment.- You have a solid knowledge of the QSR and ISO9001 / EN46001 / ISO13485 quality requirements- You have statistical knowledge.- You speak very good French and English.
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Michael Page, Basel
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Verfora SA, Villars-sur-Glâne
VERFORA, dont le siège est situé à Villars-sur-Glâne, est une entreprise leader dans le domaine de la santé qui fait partie du Groupe Galenica. VERFORA commercialise des médicaments et des produits de santé en vente libre ainsi que des produits de médecine complémentaire et de dermo-cosmétique. En plus d'un large portefeuille de marques propres, VERFORA distribue sur le marché suisse des produits prestigieux d'entreprises partenaires renommées. Elle propose également, sur divers marchés étrangers et par l'intermédiaire de distributeurs, une sélection de ses marques propres.Avec ses bureaux de Villars-sur-Glâne (Fribourg) et Berne, VERFORA est une entreprise suisse dynamique qui travaille activement et avec succès à bâtir le futur, dans un contexte marqué par les défis. Pour plus d'informations, consultez les sites www.verfora.ch et www.galenica.com.Pour renforcer notre équipe Quality, nous recherchons une personne engagée et fiable.Villars-sur-GlâneVos ResponsabilitésGestion des réclamations et déviations pour nos produits (depuis l'enregistrement à la clôture)Gestion des contrôles des changements, des CAPAs et des retours pour nos produits et processusGestion et rédaction des PQRAmélioration continue des processus et de la documentation en lien avec le périmètre des activitésSupport aux activités du département selon besoinVotre Profil Formation universitaire supérieure dans le domaine de la pharmacie ou de sciences naturelles ou une formation équivalenteExpérience professionnelle dans l'industrie pharmaceutique, dans les domaines de l'assurance qualité ou du contrôle qualité et de l'expertise dans la création, le maintien et l'amélioration de SOP ou de processusDe langue maternelle allemande ou française avec une très bonne maîtrise de l'autre langue ainsi que de très bonne connaissance de l'anglaisUne personne communicative, fiable et organiséeNous vous offronsUne activité intéressante et variée, dans un environnement motivant en perpétuelle évolution où votre contribution professionnelle et votre engagement personnel sont nécessaires. Vous bénéficiez de conditions d'emploi modernes et de divers avantages supplémentaires.Etes-vous motivé(e) à rejoindre un leader suisse dans le domaine de la santé ? Nous nous réjouissons d'ores et déjà de recevoir votre dossier de candidature complet. Nous vous prions de bien vouloir postuler en utilisant uniquement le lien de l'annonce, les candidatures transmises par courrier électronique ou postal ainsi que les dossiers provenant d'agences de recrutement ne seront pas traités. Verfora SAKevin ErniRoute de Moncor 10CH-1752 Villars-sur-Glânewww.verfora.chVerfora – Une entreprise du Groupe Galenica
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Quality Compliance Specialist
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Quality Supplier Specialist
Randstad AG, CH, Le Locle, Neuchâtel
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Quality Control Specialist
Approach People Recruitment, Bern, Bern-Mittelland
For one of our clients, an innovative and growing pharmaceutical company, we are currently looking for a: Quality Control Specialist Your Missions: Perform manual visual control and visual inspection tests (AQL test) Carry out visual inspections of primary packaging, analyze IPC samples. Collaborate with internal and external partners, such as laboratories and other departments Create specification requests and sampling plans, Ensure compliance with the current quality guidelines. Actively participate in process optimization and contribute to the generation of new ideas Your Ideal profile: Degree in biology, chemistry or similar First experience in a similar position Experience in a GMP environment. You are a proactive and enthusiast individual with a can-do attitude You are fluent in German and English (minimum B2) Are you looking for an exciting new challenge in a company where you can have an impact? Then we eagerly wait your application More Jobs From Approach People Recruitment
Quality Assurance Specialist
Manpower,
Votre mission The Quality Assurance Specialist provides Quality oversight of all day-to-day activities of the product lines. He or She is involved in Deviation/Change management, approval of area SOPs/Batch documentation, reviewing / approving corrective and prventive actions system.The specific duties/responsibilities include, but are not limited to: * Helps with the deployment of GMP culture. * Responsible for ensuring that manufacturing practices and operations do not affect the efficacy and safety of the products. * Handles deviation investigation process. Performs and reviews product impact assessments and investigations to ensure root cause analysis, timely resolution and, if deemed necessary, the appropriate CAPAs initiation. * Responsible for escalating significant deviations for appropriate regulatory action if necessary and for performing trending for identifying potential causes of recurring or severe non conformites. * Evaluates and performs impact assessment of changes, handles the change control. * Oversees the creation/revision and approval of QA-owned SOPs, Work Instructions, Forms or other supporting documents. Optimizes department procedures to improve efficiency. Perform Quality inspections and batch record reviews. * Responsible for QA product reviewing and approval of production SOPs/Batch documentation. * Interacts with regulatory and partner auditors/inspectors Votre profil Your ideal Background: * Experience in a biotechnology GMP environnement, ideally in diagnostic quality or technical area. * Your Mother tongue is French and/or German * Your English is fluent (oral and written) * You have a minimum of 4 years of pharmaceutical/biological manufacturing and/or QC/QA related experience. In dephth knowledge of Biologic and Device manufacturing, GMPs, associated guidelines, ISO requirements and related regulations. Ability to quickly and logically evaluate and solve problems on a daily basis, and guide others to do the same. Ability to make sound decisions and correctly evaluate decisions of others. * You have strong scientific analytical skills * You must be able to think abstactly about data and be able to work with a team toward shared goals * You must have good planning and organizing skills, manage time effectively by prioritizing tasks, taking the initiative to solve problems quickly, and knowing when to obtain assistance. Vous reconnaissez-vous ? Send us your application