KI-Beschreibung

You will participate in a pharmaceutical development project focused on optimizing dosage forms and implementing innovative strategies, while gaining mentorship and insights into biotherapeutic production processes.

• •
  Currently enrolled in a master's program
• •
  Advanced communication skills in English
• •
  Proficiency in MS Office

KI-Beschreibung

You will gain hands-on experience in drug product development, focusing on optimizing dosage forms and exploring innovative approaches to biotherapeutic production.

• •
  Currently enrolled in a master's program
• •
  Advanced communication skills in English
• •
  Proficiency in MS Office

Deine Vorteile

KI-Beschreibung

You will gain hands-on experience in drug product development, focusing on optimizing dosage forms and exploring innovative methods to enhance biotherapeutics for patients.

• •
  Currently enrolled in a master's program
• •
  Advanced communication skills in English
• •
  Proficiency in MS Office

Deine Vorteile

KI-Beschreibung

You will lead the development and execution of global CMC regulatory strategies, ensuring high-quality submissions and effective communication with stakeholders and health authorities throughout the product lifecycle.

• •
  Minimum 5 years of regulatory CMC experience
• •
  Knowledge in regulatory submission processes
• •
  Science degree or equivalent

Deine Vorteile

KI-Beschreibung

You will lead scientific strategies and oversee technical activities in drug product development, ensuring timely delivery and compliance. You will also mentor junior team members and present findings to diverse audiences.

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

Deine Vorteile

KI-Beschreibung

You will lead the development and execution of global CMC regulatory strategies, ensuring high-quality submissions and effective communication with stakeholders and health authorities throughout the product lifecycle.

• •
  Minimum 5 years of regulatory CMC experience
• •
  Knowledge in regulatory submission processes
• •
  Ability to evaluate scientific data

Deine Vorteile

KI-Beschreibung

You lead analytical development projects, coordinate cross-functional teams, and manage regulatory submissions. Your role involves supporting team growth and overseeing analytics activities for drug development to ensure high-quality outcomes.

• •
  PhD or life-science degree with experience
• •
  Leader with 5 years' team management experience
• •
  Experience in analytical areas of biologics

Deine Vorteile

KI-Beschreibung

In this role, you lead the TRD QA DDI Network and manage complex projects while ensuring compliance with GMP standards. You promote collaboration and drive improvements in processes and the use of AI tools within the organization.

• •
  10+ years in pharmaceutical industry.
• •
  Deep knowledge in GXP regulations.
• •
  Experience leading digital/
  AI initiatives.

Deine Vorteile

KI-Beschreibung

In this role, you lead the TRD QA DDI Network and support DDI projects, ensuring compliance with quality standards. You drive strategic initiatives, foster collaboration, and encourage innovative use of AI tools within the team.

• •
  10+ years in pharmaceutical industry
• •
  Deep knowledge in GXP regulations
• •
  Experience leading digital/
  AI initiatives

Deine Vorteile

KI-Beschreibung

You manage global CMC regulatory strategies and submissions, ensuring compliance and quality documentation while effectively communicating risks and leading interactions with health authorities.

• •
  At least 2 years’ regulatory CMC experience
• •
  Science degree or equivalent
• •
  Working knowledge of chemistry/
  biotechnology

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.

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

KI-Beschreibung

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

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

Deine Vorteile

KI-Beschreibung

You manage quality assurance for Data and Digital initiatives, ensuring compliance and effective project execution. Your role involves leading teams, promoting the use of AI, and maintaining regulatory standards while fostering collaboration across platforms.

• •
  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 operational activities across clinical programs and projects.

• •
  Project management
• •
  Critical negotiations
• •
  Risk management

Deine Vorteile

KI-Beschreibung

You will drive innovation and problem-solving in analytical operations, lead R&D initiatives, and provide technical guidance while engaging with external stakeholders.

• •
  Strong decision making skills
• •
  Proactive conflict resolution
• •
  Recognized expertise in specific area

Deine Vorteile

KI-Beschreibung

You lead a team of analytical experts, overseeing the release of clinical materials and stability studies while driving innovation and addressing operational challenges through strategic planning and technical guidance.

• •
  Proven track record of leading teams
• •
  Solid understanding of analytical methods
• •
  Demonstrated ability to solve analytical problems

Deine Vorteile

KI-Beschreibung

You lead the ITOT team, ensuring project delivery and collaboration with stakeholders. Your role includes managing budgets, supporting capital projects, and maintaining regulatory compliance while overseeing system reliability.

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

Deine Vorteile

KI-Beschreibung

You will design and develop system solutions for the R&D Lab, lead project delivery, troubleshoot application issues, and ensure compliance with security policies while collaborating with various teams.

• •
  Bachelor’s degree in Computer Science
• •
  Several years of experience in Pharma or IT
• •
  Expert technical understanding of Lab Applications

KI-Beschreibung

You will design and develop system solutions for the lab, lead project delivery, troubleshoot application issues, and ensure compliance with security policies while collaborating with cross-functional teams.

• •
  Bachelor’s degree in Computer Science
• •
  Several years of experience in Pharma or IT Industry
• •
  Expert technical understanding of Lab Applications

KI-Beschreibung

You manage relationships with suppliers for device components and packaging materials, ensuring effective evaluation and implementation of necessary changes.

• •
  At least 3 years experience in MS&T or QA
• •
  University degree in Engineering or equivalent
• •
  Fluent knowledge of English language

Deine Vorteile

KI-Beschreibung

You manage relationships with suppliers for device components and packaging materials, ensuring effective evaluation and implementation of necessary changes.

• •
  At least 3 years experience in MS&T or QA
• •
  University degree in Engineering or equivalent
• •
  Fluent knowledge of English language

Deine Vorteile