KI-Beschreibung

As a Drug Product Project Leader, you will drive the late-stage development of biologics, ensuring strategic alignment and timely delivery of high-quality documentation. You will foster collaboration across global teams and engage with regulatory authorities.

• •
  Ph.D. in pharmaceutical technology, biotechnology, chemical engineering, or equivalent
• •
  Minimum of 8 years of relevant industry experience
• •
  Proficiency in quality principles, Quality by Design (QbD), Good Manufacturing Practice (GMP), and regulatory requirements

Deine Vorteile

KI-Beschreibung

As a Drug Product Project Leader, you will drive the late-stage development of biologics, ensuring strategic alignment and timely delivery of high-quality documents while leading a global team of experts and engaging with key stakeholders.

• •
  Ph.D. in pharmaceutical technology, biotechnology, chemical engineering, or equivalent
• •
  Minimum of 8 years of relevant industry experience
• •
  Proficiency in quality principles, Quality by Design (QbD), Good Manufacturing Practice (GMP), and regulatory requirements

Deine Vorteile

KI-Beschreibung

As the Associate Director of Analytical Operations, you will lead a dedicated team in Austria, guiding them through technical and project management challenges while ensuring compliance and fostering professional growth. This role involves strategic oversight of Late-Phase projects, collaboration with stakeholders, and driving operational excellence.

• •
  Strong experience in biotechnological Chemistry Manufacturing Control (CMC) development
• •
  Minimum of 10 years of experience in the pharmaceutical industry
• •
  Minimum of 5 years in a leadership position

Deine Vorteile

KI-Beschreibung

As the Associate Director of Analytical Operations, you will lead a dedicated team in Austria, guiding them through technical and project management challenges while ensuring compliance and fostering professional growth. This role involves strategic oversight of Late-Phase projects and collaboration with various stakeholders to drive operational excellence.

• •
  Strong experience in biotechnological Chemistry Manufacturing Control (CMC) development
• •
  Minimum of 10 years of experience in the pharmaceutical industry
• •
  Minimum of 5 years in a leadership position

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of generating and analyzing critical data for medical devices, ensuring compliance with regulations, and leading innovative lab projects. Your day-to-day responsibilities will involve testing, documentation, and collaboration with project teams to enhance product quality.

• •
  Apprenticeship or secondary school, or bachelor's or master's degree in Technical/
  Engineering/
  Life-Sciences area with substantial relevant work experience
• •
  Knowledge in Environment, Experiments Design, Health And Safety (EHS), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, SOP (Standard Operating Procedure), Technical Writing, Waterfall Model

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of generating and analyzing critical data for medical devices, ensuring compliance with regulations, and leading innovative projects. Your day-to-day responsibilities will involve testing, documentation, and collaboration with project teams to enhance product quality.

• •
  Apprenticeship or secondary school, or bachelor's or master's degree in Technical/
  Engineering/
  Life-Sciences
• •
  Experience in Environment, Experiments Design, Health And Safety (EHS), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, SOP (Standard Operating Procedure), Technical Writing, Waterfall Model

Deine Vorteile

KI-Beschreibung

As a Senior Manager in RA CMC, you will shape global regulatory strategies for drug development, ensuring compliance while driving innovation. Your role involves leading submission activities, managing documentation, and engaging with Health Authorities to navigate the regulatory landscape.

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

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.

• •
  Minimum 5 years of regulatory CMC experience or pharmaceutical industry experience
• •
  Knowledge in regulatory submission and approval processes
• •
  Ability to critically evaluate data from scientific disciplines

Deine Vorteile

KI-Beschreibung

In this role, you will actively support the development of innovative drug candidates by conducting experiments and analyzing data. You will also document your findings and collaborate with the team to enhance processes, gaining valuable insights into drug substance development.

• •
  Enrollment in a Master’s program in life science
• •
  Interest or knowledge in data science, statistical data analysis, process modeling, simulation, automation, and basic programming
• •
  Advanced communication skills in English

KI-Beschreibung

In this role, you will actively support the development of innovative drug candidates by conducting experiments and analyzing data. You will also collaborate with a dedicated team, documenting findings and presenting them to enhance drug substance processes.

• •
  Enrollment in a Master’s program in life science
• •
  Interest or knowledge in data science, statistical analysis, and basic programming
• •
  Advanced communication skills in English

KI-Beschreibung

In this role, you will actively support the development of innovative drug candidates by conducting experiments and analyzing data. You will also collaborate with a dedicated team, document findings, and present them to enhance drug substance processes.

• •
  Enrollment in a Master’s program in life science
• •
  Interest or knowledge in data science, statistical data analysis, process modeling, simulation, automation, and basic programming
• •
  Advanced communication skills in English

KI-Beschreibung

In this role, you will lead the scientific strategy for developing Biologic Drug Products, overseeing everything from technical activities to regulatory submissions. Your day-to-day responsibilities will involve collaborating with teams, interpreting results, and mentoring junior scientists, all while driving innovative solutions in a dynamic environment.

• •
  PhD or Master in pharmaceutical technology, biotechnology, chemical engineering, or relevant discipline
• •
  Experience of 2-5 years in biotech/
  pharmaceutical industry with focus on formulation or manufacturing processes development, technical transfer, validation, and submission for biological drug products
• •
  Solid understanding of quality standards and regulations in pharmaceutical industry

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 bodies and supporting team growth, as well as overseeing critical analytics activities in drug development.

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

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 the growth of the team, overseeing all analytics activities in drug development.

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

Deine Vorteile

KI-Beschreibung

In this role, you will drive global CMC regulatory strategies and oversee submission activities, ensuring compliance and quality throughout the product lifecycle. Your expertise will guide interactions with health authorities and support project teams in navigating regulatory challenges.

• •
  Science degree or equivalent
• •
  At least 2 years’ experience in regulatory CMC or pharmaceutical industry
• •
  Demonstrated working knowledge of chemistry/
  biotechnology, analytics or pharmaceutical technology

Deine Vorteile

KI-Beschreibung

In this role, you will drive global CMC regulatory strategies and oversee submission activities, ensuring compliance and quality throughout the product lifecycle. Your expertise will guide interactions with health authorities and support project teams in navigating regulatory challenges.

• •
  Science degree or equivalent
• •
  At least 2 years’ experience in regulatory CMC or pharmaceutical industry
• •
  Working knowledge of chemistry, biotechnology, analytics, or pharmaceutical technology

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing user-friendly drug delivery devices. Daily responsibilities include conducting human factors studies, collaborating with diverse teams, and ensuring that products meet regulatory standards while prioritizing the end-user experience.

• •
  3+ years of experience in human factors engineering, preferably in medical devices or combination products
• •
  Strong understanding of usability engineering standards (e.g., IEC 62366, ISO 14971)
• •
  Experience with qualitative and quantitative research methods

KI-Beschreibung

In this role, you will be at the forefront of developing user-friendly drug delivery devices. Your work will involve conducting human factors studies, collaborating with diverse teams, and ensuring that products meet regulatory standards while prioritizing the end-user experience.

• •
  MSc in Human Factors Engineering, Cognitive Sciences, Behavioral Sciences, Biomedical Engineering, Psychology, Product Design, or Mechanical Engineering
• •
  3+ years of experience in human factors engineering, preferably in medical devices or combination products
• •
  Strong understanding of usability engineering standards (e.g., IEC 62366, ISO 14971)

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.

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

Deine Vorteile

KI-Beschreibung

In this role, you will oversee the integration of new technologies in TRD and drive digitalization strategies. Your day-to-day responsibilities will include managing QA oversight for projects, promoting AI usage, and ensuring compliance with GMP standards while collaborating with various teams.

• •
  5+ years of relevant experience in development quality environment
• •
  Experience in project management or operations 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.

• •
  Functional breadth
• •
  Critical negotiations
• •
  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.

• •
  Functional breadth
• •
  Critical negotiations
• •
  Project management

Deine Vorteile

KI-Beschreibung

In this role, you will lead the Site ITOT organization, focusing on enhancing automation and IT processes. Your daily responsibilities will include managing a dedicated team, collaborating with global counterparts, and ensuring operational excellence and compliance.

• •
  Minimum of 7 years of experience in Automation or IT in a GMP Pharma environment
• •
  In-depth knowledge of automation systems and IT infrastructure
• •
  Bachelor's degree in Computer Science, Information Technology, automation, engineering, or related field

Deine Vorteile

KI-Beschreibung

In this apprenticeship, you will immerse yourself in automation technology, working closely with experts to install systems, maintain machinery, and engage in programming PLC controls and robots, all while building valuable teamwork skills.

• •
  Technical interest in mechanics and electronics
• •
  Careful and precise working style
• •
  Enthusiasm and commitment

KI-Beschreibung

In this apprenticeship, you will dive into the world of metalworking, mastering the creation of precision molds and the operation of advanced machinery while ensuring that tools are well-maintained and functional.

• •
  Excellent compulsory school diploma or higher-level school diploma
• •
  Passion for craftsmanship and strong interest in technology
• •
  Eagerness to learn and enjoyment of new challenges

KI-Beschreibung

In this role, you will be actively involved in the manufacturing process, executing tasks to ensure products are produced on time and meet quality standards. You will also manage important documentation and support operational activities while adhering to safety and GMP guidelines.

• •
  Operations management and execution
• •
  Transportation classification expertise (i.e. IATA or DOT)
• •
  Manufacturing process execution