Aktuell 99 Jobs mit Home-Office in Schaftenau 6336 & Umgebung

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, refining 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 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 be at the forefront of developing analytical data packages for drug-device combination products, coordinating tasks across teams, and ensuring compliance with regulatory standards. Your expertise will shape the analytical strategies that drive successful product registrations.

• •Master or PhD in engineering, chemical/bio analytics, or equivalent
• •Proven knowledge in late phase parenteral analytical development
• •Leadership experience in managing development projects

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing analytical data packages for drug-device combination products, coordinating tasks across teams, and ensuring compliance with regulatory standards. Your expertise will shape the analytical strategies that drive product success.

• •Master or PhD in engineering, chemical/bio analytics, or equivalent
• •Proven knowledge in late phase parenteral analytical development
• •Leadership experience in managing development projects

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 Medical Device Technical Transfer Lead, you will oversee the transition of assembly and packaging processes from development to commercial operations, ensuring compliance and efficiency throughout the production cycle.

• •At least 3 years of related experience with medical devices or 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 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.

• •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, all while supporting the release of safe medicines.

• •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 meet high-quality standards for clinical trials and commercial use while collaborating with cross-functional teams.

• •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 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

As a Senior QA Compliance Specialist, you will dive into complaint investigations, ensuring quality and compliance while collaborating 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 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

In this role, you will dive into the world of primary packaging, assess solutions, and ensure compliance while collaborating with stakeholders. Your day-to-day responsibilities will involve problem-solving, preparing documentation, and supporting audits to enhance medical device development.

• •Bachelor or master’s in engineering, materials science, pharmaceutical technology, or related discipline
• •Experience in primary packaging, medical device, combination product, or pharmaceutical
• •Strong communication skills and cross-functional understanding

Deine Vorteile

KI-Beschreibung

In this role, you will become a key player in primary packaging development, focusing on selecting and assessing packaging solutions while ensuring compliance and collaborating with stakeholders to meet high customer expectations.

• •Bachelor or master’s in engineering, materials science, pharmaceutical technology, or related discipline
• •Experience in primary packaging, medical device, combination product, or pharmaceutical
• •Strong communication skills and ability to connect across functions

Deine Vorteile

KI-Beschreibung

In this role, you will blend laboratory work with documentation, developing and optimizing analytical methods for drug development. You will collaborate with teams, interpret results, and contribute to innovative solutions that enhance efficiency and quality.

• •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 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 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 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 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 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
• •2+ years work experience within the pharmaceutical industry

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 and project management

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, leading and influencing in global matrix organization

Deine Vorteile

KI-Beschreibung

In der Rolle des Technical Stewards bist du verantwortlich für Technologie-Transfers und die kontinuierliche Verbesserung der pharmazeutischen Herstellungsprozesse. Dein Alltag umfasst die Zusammenarbeit mit verschiedenen Schnittstellen und die Sicherstellung, dass die Produkte 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 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 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