75+ Jobs mit Home Office in Söll

KI-Beschreibung

In dieser Rolle bist du maßgeblich an der Planung und Abwicklung kleiner Projekte im Bereich Flüssiggasanlagen beteiligt. Dein Alltag umfasst die Erstellung von Angeboten, die Koordination der Ausführung und die enge Zusammenarbeit mit Behörden sowie dem Team.

• •Technische Ausbildung (z.B. HTL, technische:r Zeichner:in, Installations-/Gastechnik etc.)
• •Grundlegende CAD-Kenntnisse (idealerweise AutoCAD)
• •Selbstständige, strukturierte Arbeitsweise

Deine Vorteile

KI-Beschreibung

As a Senior Expert - Device Project Leader, you will guide cross-functional teams in managing the drug-device combination product portfolio, ensuring compliance and supporting regulatory processes while driving project success.

• •Master or PhD in natural science, engineering, pharmaceutical field, or equivalent
• •Minimum 2-4 years of experience in the pharmaceutical industry, preferably in drug-device combination product technical development
• •Understanding and awareness of regulatory guidelines for drug-device combination products, including relevant ISOs and cGMP

Deine Vorteile

KI-Beschreibung

In this role, you will guide cross-functional project teams, ensuring compliance with regulations while managing resources and budgets. Your expertise will be crucial in leading discussions, evaluating device technologies, and supporting regulatory preparations.

• •Master or PhD in natural science, engineering, pharmaceutical field, or equivalent
• •Minimum 2-4 years of experience in the pharmaceutical industry
• •Understanding of regulatory guidelines for drug-device combination products

Deine Vorteile

KI-Beschreibung

In this role, you will drive collaboration with third parties to develop medical devices and combination products, ensuring quality and compliance while fostering strategic partnerships. Your day-to-day responsibilities will involve leading teams, implementing sourcing strategies, and managing vendor relationships.

• •Over 10 years’ experience in pharma/biotech with deep knowledge of drug, device, packaging, and combination product development, including quality and regulatory requirements
• •Advanced degree in life science or related field
• •Proven leadership in matrix or line functions

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing analytical data packages for drug-device combination products, coordinating project tasks, and collaborating with cross-functional teams to ensure compliance and successful product registrations.

• •Master or PhD in engineering, chemical/bio analytics, or equivalent
• •Some working experience in pharmaceutical industry in combination product development
• •Proven knowledge in late phase parenteral analytical development

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing analytical data packages for drug-device combination products. Your day-to-day responsibilities will involve coordinating analytical tasks, managing resources, and collaborating with cross-functional teams to ensure compliance and successful product registrations.

• •Master or PhD in engineering, chemical/bio analytics, or equivalent
• •Some working experience in pharmaceutical industry in combination product development
• •Proven knowledge in late phase parenteral analytical development

Deine Vorteile

KI-Beschreibung

In this role, you will lead a dynamic team to drive effective partnerships for drug-device combination products. Your day-to-day responsibilities will involve strategizing sourcing models, ensuring quality governance, and fostering collaboration across various stakeholders.

• •Over 10 years’ experience in pharma/biotech with deep knowledge of drug, device, packaging, and combination product development
• •Advanced degree in life science or related field
• •Proven leadership in matrix or line functions

Deine Vorteile

KI-Beschreibung

In this role, you will oversee the transfer of medical device assembly and packaging processes from development to commercial operations, ensuring compliance and efficiency throughout the process.

• •At least 3 years of related experience with medical devices/combination products
• •University degree in engineering, pharmaceutical technology, or similar discipline
• •Thorough understanding of development processes and state-of-the-art technology/equipment

Deine Vorteile

KI-Beschreibung

In this role, you will lead innovative packaging design projects while collaborating with various teams. Your day-to-day responsibilities will involve defining packaging strategies, ensuring technical excellence, and sharing your expertise across the organization.

• •At least 5 years of experience in the Pharmaceutical Environment or Medical Devices
• •Technical degree in Engineering, material science, or equivalent
• •Experience in packaging design development

Deine Vorteile

KI-Beschreibung

In this role, you will lead innovative packaging design projects while collaborating with various teams. Your day-to-day responsibilities will involve defining packaging strategies, ensuring technical excellence, and sharing expertise across the organization.

• •At least 5 years of experience in the Pharmaceutical Environment or Medical Devices
• •Technical degree in Engineering, material science, or equivalent
• •Experience in packaging design development

Deine Vorteile

KI-Beschreibung

As a Supply Chain Manager, you will play a crucial role in shaping clinical supply plans, ensuring timely trials by harmonizing strategies, optimizing inventories, and collaborating with various stakeholders to deliver breakthroughs to patients faster.

• •5+ years of experience in chemical or pharmaceutical industry or 3+ years specialized expertise
• •Solid expertise in supply chain or closely related field
• •Strong understanding of drug development process

Deine Vorteile

KI-Beschreibung

As a Supply Chain Manager, you will play a crucial role in shaping clinical supply plans, ensuring timely trials by harmonizing strategies, optimizing inventories, and collaborating with various stakeholders to deliver breakthroughs to patients.

• •5+ years of experience in chemical or pharmaceutical industry, or 3+ years specialized expertise
• •Solid expertise in supply chain or closely related field
• •Strong understanding of drug development process

Deine Vorteile

KI-Beschreibung

As a QA Operations Expert, you will play a vital role in ensuring product quality and compliance with global standards. Your daily tasks will involve overseeing GxP functions, managing regulatory requirements, and collaborating on audits to uphold the highest quality assurance practices.

• •University Degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology or equivalent
• •Professional experience in pharmaceutical industry with direct experience with Pharmaceuticals, Biopharmaceutical or API products and at least 2 years within QA
• •Thorough knowledge of cGMP requirements and proven track record with FDA / EMA and other Health Authorities

Deine Vorteile

KI-Beschreibung

As a QA Operations Expert, you will play a vital role in ensuring product quality and compliance with global standards. Your daily tasks will involve overseeing GxP functions, managing regulatory requirements, and collaborating on audits to uphold the highest quality assurance practices.

• •University Degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology or equivalent
• •Professional experience in pharmaceutical industry with direct experience with Pharmaceuticals, Biopharmaceutical or API products and at least 2 years within QA
• •Thorough knowledge of cGMP requirements and proven track record with FDA / EMA and other Health Authorities

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing innovative combination products, ensuring that device components are integrated seamlessly and meet the highest quality standards for both clinical trials and commercial use.

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

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 while collaborating with cross-functional teams to deliver safe and effective solutions.

• •5+ years of experience in development of medical devices or combination products
• •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

In this role, you will dive into complaint investigations, ensuring quality and compliance while coordinating with various departments. Your day-to-day responsibilities will involve managing samples, identifying improvements, and preparing for audits to uphold high standards.

• •Degree in natural sciences (pharmacy, chemistry, medicine, biology, microbiology)
• •Experience in manufacturing medicinal products for human use
• •Working experience in GMP production, Quality Assurance, or Quality Control

Deine Vorteile

KI-Beschreibung

As a Senior QA Compliance Specialist, you will dive into complaint investigations, ensuring quality and compliance while coordinating with various departments. This role also involves managing samples, identifying improvements, and preparing for audits, all while upholding high health and safety standards.

• •Degree in natural sciences (pharmacy, chemistry, medicine, biology, microbiology)
• •Experience in manufacturing medicinal products for human use
• •Working experience in GMP production, Quality Assurance, or Quality Control

Deine Vorteile

KI-Beschreibung

In this role, you will engage in method development and optimization for pharmaceutical processes, collaborating with teams to ensure compliance and efficiency. Your work will blend laboratory experiments with documentation, making a significant impact on healthcare advancements.

• •University degree in pharmaceutical technology, biotechnology, biochemistry, chemistry, chemical engineering, or relevant natural science discipline
• •At least 3 years (PhD) or 6 years (MSc) of working experience in the (bio)pharmaceutical industry
• •Expertise in Biologics DS and DP process development applying QbD principles

Deine Vorteile

KI-Beschreibung

In this role, you will engage in method development and optimization for pharmaceutical processes, collaborating with teams to ensure quality and efficiency. Your work will blend laboratory experiments with documentation, making a significant impact on healthcare advancements.

• •University degree in pharmaceutical technology, biotechnology, biochemistry, chemistry, chemical engineering, or relevant natural science discipline
• •At least 3 years (PhD) or 6 years (MSc) of working experience in the (bio)pharmaceutical industry
• •Expertise in Biologics DS and DP process development applying QbD principles

Deine Vorteile

KI-Beschreibung

In this role, you will oversee critical project tasks while authoring essential documentation. Your work will involve managing stability studies and validations, ensuring compliance, and supporting the lab team in resolving complex issues.

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

Deine Vorteile

KI-Beschreibung

In this role, you will oversee critical project tasks while authoring essential documentation. Your work will involve managing stability studies and validations, ensuring compliance, and collaborating with the lab team to resolve complex issues.

• •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

In this role, you will lead the development of innovative testing methods for container closure integrity, ensuring the quality of pharmaceutical products. Your work will involve collaboration with experts, troubleshooting challenges, and mentoring students in a dynamic environment.

• •Bachelor’s, Master or PhD degree in engineering or natural sciences
• •Strong knowledge of container closure integrity testing and sterile drug products filling
• •Strong skills in cross-functional coordination, project management, leading and influencing in global matrix organization

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing and validating cutting-edge testing methods for container closure integrity, ensuring the quality of pharmaceutical products. Your work will involve collaboration with experts, troubleshooting challenges, and mentoring students, all while contributing to innovative solutions in a dynamic environment.

• •Bachelor’s, Master or PhD degree in engineering or natural sciences
• •Strong knowledge of container closure integrity testing and sterile drug products filling
• •Strong skills in cross-functional coordination, project management, and influencing in global matrix organization

Deine Vorteile

KI-Beschreibung

In dieser Rolle als Technical Steward bist du verantwortlich für Technologie-Transfers und Prozessvalidierungen. Du arbeitest eng mit verschiedenen Abteilungen zusammen, um sicherzustellen, dass die Produktionsprozesse kontinuierlich verbessert werden und den höchsten Standards entsprechen.

• •Abgeschlossenes Studium in Pharmazie, Chemie, Biotechnologie oder vergleichbar
• •Mehrjährige Erfahrung in der pharmazeutischen Produktion, Technologie-Transfer oder MS&T
• •Fundierte Kenntnisse in cGMP, Validierung und regulatorischen Anforderungen

Deine Vorteile

KI-Beschreibung

In dieser Rolle als Technical Steward bist du verantwortlich für Technologie-Transfers und Prozessvalidierungen. Du arbeitest eng mit verschiedenen Abteilungen zusammen, um sicherzustellen, dass die Produktionsprozesse kontinuierlich verbessert werden und den höchsten Standards entsprechen.

• •Bachelor- oder Masterabschluss in Pharmazie, Chemie, Biotechnologie oder vergleichbar
• •Mehrjährige Erfahrung in pharmazeutischer Produktion, Technologie-Transfer oder MS&T
• •Fundierte Kenntnisse in cGMP, Validierung und regulatorischen Anforderungen

Deine Vorteile

KI-Beschreibung

In this role, you will leverage MES expertise to enhance pharmaceutical manufacturing processes, ensuring quality and efficiency. Daily activities will involve implementing software solutions, training staff, and collaborating with engineers to drive continuous improvement.

• •Experience in food, drug, or medical device regulated industry for at least 3 years
• •Experience in an MES system
• •Background in IT, Engineering, Computer Science, or related field

Deine Vorteile

KI-Beschreibung

In dieser Rolle bist du für die Vorbereitung von Werkzeugen und Materialien sowie die Durchführung von Wartungsaufträgen verantwortlich. Du überwachst die Qualität der Arbeiten und dokumentierst alle Vorgänge sorgfältig, während du technische Beschwerden zeitnah meldest.

• •Abgeschlossene Lehre in einem einschlägigen Fachbereich
• •Technisches Verständnis von korrektiver und präventiver Wartung
• •Problemlösung über Funktionsbereiche hinweg

Deine Vorteile

KI-Beschreibung

In dieser Rolle bist du Teil eines dynamischen Teams, das für die Wartung und Optimierung von 80 Anlagen zuständig ist. Du bereitest Materialien vor, führst Wartungsaufträge aus und sorgst dafür, dass alles reibungslos läuft, um die Versorgung mit hochwertigen Arzneimitteln sicherzustellen.

• •Abgeschlossene Lehre in einem einschlägigen Fachbereich
• •Technisches Verständnis von Wartung
• •Problemlösungsfähigkeit über Funktionsbereiche hinweg

Deine Vorteile

KI-Beschreibung

In dieser Rolle als Automation Technician bist du an der Schnittstelle von Wissenschaft und Automatisierung tätig. Du entwickelst und wartest moderne Automatisierungslösungen, programmierst SPS-Systeme und treibst die Automatisierung wissenschaftlicher Workflows voran.

• •Erfahrung mit SPS-Programmierung, Robotik und Systems Engineering
• •Technisches Verständnis von Wartung in Automatisierungssystemen
• •Verständnis von Automatisierungs- und Integrationstests

Deine Vorteile