KI-Beschreibung

In dieser Teilzeitposition übernimmst du die stellvertretende Leitung des TANN-Markts in Wörgl. Du führst das Team, unterstützt bei der Warenpräsentation und sorgst für eine persönliche Beratung der Kund:innen.

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  Abgeschlossene kaufmännische Ausbildung
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  Berufserfahrung im Einzelhandel
• •
  Erste Führungserfahrung

Deine Vorteile

KI-Beschreibung

In dieser Rolle bist du maßgeblich an der Führung des TANN-Marktes beteiligt, indem du betriebswirtschaftliche Kennzahlen im Blick behältst und das Team aktiv unterstützt. Dein Alltag dreht sich um die Koordination von Warenannahme und -präsentation sowie die persönliche Beratung der Kund:innen.

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  Abgeschlossene kaufmännische Ausbildung (HAK, HAS, HLW, Einzelhandelslehre)
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  Berufserfahrung im Einzelhandel
• •
  Idealerweise erste Führungserfahrung

Deine Vorteile

KI-Beschreibung

Du leitest ein kleines Team und sorgst für ein herausragendes Kundenerlebnis. Dabei schaffst du ein motivierendes Arbeitsumfeld, entwickelst Nachfolgestrategien und maximierst die Leistung deines Geschäfts.

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  Kürzliche Erfahrung als Supervisor
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  Selbstbewusste Führungspersönlichkeit
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  Leidenschaft für den Einzelhandel und Menschen

Deine Vorteile

KI-Beschreibung

In dieser Rolle als Senior Marketing Manager treibst du eigenständig spannende Großprojekte voran und kümmerst dich um die Umsetzung neuer Funnels und Anzeigen. Dein Alltag umfasst die Koordination von AD-Shootings und die Entwicklung von Automatisierungen, während du das E-Mail-Marketing aktiv gestaltest.

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  Mehr als 4 Jahre Berufserfahrung im Marketing
• •
  Grundlegende Copywriting-Skills und Verständnis von technischen Marketingprogrammen
• •
  Perfekte Deutschkenntnisse in Wort und Schrift

Deine Vorteile

KI-Beschreibung

In dieser Rolle gestaltest du innovative Reiseprodukte und führst ein engagiertes Team. Du analysierst Markttrends, optimierst das Produktportfolio und pflegst wichtige Partnerschaften, während du aktiv im Tagesgeschäft mitwirkst.

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  Mehrjährige Erfahrung im Produktmanagement oder Hoteleinkauf – inklusive Verhandlungserfahrung
• •
  Fundierte Kenntnisse in ATCOM sowie sicherer Umgang mit Microsoft 365
• •
  Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift

Deine Vorteile

KI-Beschreibung

Du leitest ein interdisziplinäres Team im Therapiebereich und bist verantwortlich für die Weiterentwicklung der Qualitätsstandards. Dabei planst und überwachst du die Therapieprozesse und arbeitest eng mit der ärztlichen Leitung zusammen.

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  Abschluss in Physiotherapie oder Ergotherapie
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  Mehrjährige Berufserfahrung in der Rehabilitation
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  Sehr gute Deutschkenntnisse

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of shaping global CMC regulatory strategies for innovative projects. Your day-to-day responsibilities will involve leading submission activities, ensuring compliance, and collaborating with cross-functional teams to drive successful interactions with Health Authorities.

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  Minimum 8 years regulatory experience or pharmaceutical industry experience
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  Substantial knowledge in regulatory submission and approval processes
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  Science degree or equivalent

Deine Vorteile

KI-Beschreibung

You manage and coordinate extractables and leachables projects, conducting studies and analyses while ensuring compliance with regulatory standards and promoting collaboration across teams.

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  8+ years of working experience
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  Expertise in analytical technologies
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  University degree in relevant science discipline

Deine Vorteile

KI-Beschreibung

You manage global CMC regulatory strategies and submissions, ensuring compliance and quality documentation while effectively communicating risks and coordinating with stakeholders throughout project lifecycles.

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  Minimum 5 years of regulatory CMC experience
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  Knowledge in regulatory submission processes
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  Proven ability to evaluate scientific data

Deine Vorteile

KI-Beschreibung

You will develop and implement global regulatory strategies for CMC, manage submission activities, and ensure compliance while collaborating with cross-functional teams and engaging with health authorities.

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  Minimum 8 years regulatory experience preferred
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  Substantial knowledge in regulatory submission
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  Proven ability to evaluate scientific data

Deine Vorteile

KI-Beschreibung

As a Senior Manager in RA CMC, you will shape global regulatory strategies and oversee submission activities, ensuring compliance while driving innovation. This role involves collaborating with teams, managing risks, and engaging with Health Authorities to support product development.

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  Minimum 5 years of regulatory CMC experience or pharmaceutical industry experience
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  Knowledge in regulatory submission and approval processes
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  Science degree or equivalent

Deine Vorteile

KI-Beschreibung

In this role, you will lead E&L project activities, applying scientific expertise to manage studies and collaborate with internal labs and external partners. Your work will involve designing protocols, interpreting results, and ensuring compliance with evolving regulations.

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  University degree (preferably PhD) in Pharmacy, Polymer or Food Chemistry, Life Sciences or relevant science discipline
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  8+ years of working experience in pharma/
  biopharmaceutical industry or relevant industry
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  Expertise in analytical technologies: Headspace-GC/
  MS, LI-GC/
  (HR)MS, HPLC/
  (HR)MS, and related sample preparation techniques

Deine Vorteile

KI-Beschreibung

You manage the technical development and integration of medical devices, ensuring compliance with regulations and quality standards while supporting audits and addressing inquiries from health authorities.

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  5+ years experience in medical device development
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  Bachelor, Master or PhD degree in engineering
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  Experience in developing plastic and metal components

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing innovative combination products, ensuring that device components meet high-quality standards for clinical trials and commercial use while collaborating with cross-functional teams.

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  5+ years of experience in development of medical devices or combination products
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  Bachelor, Master, or PhD degree in engineering or equivalent
• •
  Experience in developing plastic and metal components, tolerance analysis, modelling, and testing

Deine Vorteile

KI-Beschreibung

You lead and develop a team of Qualified Persons, ensuring compliance in product releases and quality management while collaborating with various departments to tackle quality challenges.

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  Minimum 7 years in Quality Assurance
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  Minimum 4 years as a certified Qualified Person
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  Experience in leading teams in regulated environments

Deine Vorteile

KI-Beschreibung

As a QA Operations Team Leader, you will guide a team of Qualified Persons to ensure the compliant release of pharmaceutical products. This role involves managing resources, resolving quality issues, and fostering a culture of continuous improvement.

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  Minimum 7 years of experience in Quality Assurance within the pharmaceutical industry
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  Minimum 4 years of experience as a certified Qualified Person (QP)
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  Qualified Person (QP) as per EU Directive 2001/
  83/
  EC

Deine Vorteile

KI-Beschreibung

You manage critical project tasks and create essential documentation while ensuring compliance with quality standards. Additionally, you assist the lab team in resolving complex issues and maintaining operational efficiency.

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  Master’s degree in relevant field
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  At least 4 years strong industry experience
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  Proven experience within GMP environment

Deine Vorteile

KI-Beschreibung

In this role, you will play a crucial part in developing new biologic drugs, overseeing project tasks, and ensuring compliance through documentation and quality investigations, all while collaborating with the lab team in a hybrid environment.

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  Master’s degree in biotechnology, biochemical engineering, biology, chemistry, biochemistry, or similar
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  At least 4 years relevant industry experience or PhD in relevant field or equivalent
• •
  2+ years work experience within the pharmaceutical industry

Deine Vorteile

KI-Beschreibung

In this role, you will oversee critical project tasks and author essential documentation. Your work will involve managing the release and stability studies of new biologic drugs, ensuring compliance and quality throughout the process.

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  Master’s degree in biotechnology, biochemical engineering, biology, chemistry, biochemistry, or similar
• •
  At least 4 years relevant industry experience or PhD in relevant field or equivalent
• •
  2+ years of work experience within the pharmaceutical industry

Deine Vorteile

KI-Beschreibung

You lead scientific strategies and oversee technical activities in drug product development, ensuring timely delivery and compliance with quality standards while mentoring junior team members.

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  2-5 years in biotech/
  pharmaceutical industry
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  PhD or Master in relevant discipline
• •
  Solid understanding of quality standards

Deine Vorteile

KI-Beschreibung

As an Analytical Project Leader, you will drive the analytical development strategy, ensuring timely delivery of high-quality documents while managing a cross-functional team. This role involves engaging with regulatory authorities and supporting team growth, overseeing all analytics activities related to drug development.

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  PhD or university life-science degree with industry experience
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  Minimum of 5 years' experience in managing teams/
  projects
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  Excellent understanding of regulatory expectations and IND/
  BLA submission

Deine Vorteile

KI-Beschreibung

You ensure compliance with quality standards and regulatory requirements while managing GxP functions. Your role includes overseeing audits, addressing complaints, and supporting process changes and documentation.

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  At least 2 years in QA within Pharmaceuticals
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  University Degree in Pharmacy or related field
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  Fluent German and intermediate English

Deine Vorteile

KI-Beschreibung

As a Senior QA Operations Specialist, you will ensure compliance with cGMP regulations and Novartis Quality Standards while overseeing product quality and regulatory adherence. This role involves managing investigations, supporting audits, and collaborating on process improvements to maintain high-quality operations.

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  Professional experience in Pharmaceutical industry with direct experience in Pharmaceuticals, Biopharmaceutical or API products and at least 2 years in QA
• •
  University degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology, or finalized apprenticeship in Pharmaceutical industry
• •
  Fluent German and intermediate English

Deine Vorteile

KI-Beschreibung

You conduct human factors studies and user research, collaborating with various teams to translate user needs into design requirements while providing actionable insights to support regulatory submissions.

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  3+ years of experience in human factors engineering
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  MSc in relevant engineering or sciences
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  Strong understanding of usability engineering standards

KI-Beschreibung

You oversee quality assurance for Data and Digital projects, ensuring compliance and effective execution. Your role involves leading initiatives, promoting the use of AI, and maintaining communication across teams to enhance quality processes.

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  5+ years of relevant experience
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  Demonstrated experience in project management
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  Strong quality background

Deine Vorteile

KI-Beschreibung

You oversee quality assurance for Data and Digital projects, ensuring compliance and effective execution. Your role involves leading initiatives, promoting the use of AI, and maintaining regulatory standards while collaborating with various teams.

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  5+ years of relevant experience
• •
  Demonstrated experience in project management
• •
  Strong quality background

Deine Vorteile

KI-Beschreibung

You manage quality assurance and compliance initiatives, ensuring adherence to regulations and fostering continuous improvement in clinical programs while addressing quality issues and supporting corrective actions.

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  Functional breadth
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  Critical negotiations
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  Project management

Deine Vorteile

KI-Beschreibung

You manage quality assurance tasks, ensuring compliance with regulations and supporting initiatives to improve quality performance across clinical programs and operational activities.

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  Functional breadth
• •
  Critical negotiations
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  Project management

Deine Vorteile

KI-Beschreibung

You lead the ITOT team, ensuring project delivery and operational support while collaborating with various stakeholders. Your role includes managing the budget, overseeing compliance, and maintaining high system reliability.

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  Minimum of 7 years in Automation or IT
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  In-depth knowledge of automation systems
• •
  Bachelor's degree in Computer Science

Deine Vorteile

KI-Beschreibung

Du akquirierst Neukunden und entwickelst Key Accounts, während du innovative Technologien präsentierst. Dein Alltag umfasst den Vertrieb von Softwarelösungen, die Steuerung von Ausschreibungen und die Pflege von Partnernetzwerken.

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  Mindestens 5 Jahre B2B-Vertriebserfahrung
• •
  Nachweisbare Erfahrung im Aufbau von Neukunden
• •
  Verhandlungssicherheit auf C-Level

Deine Vorteile