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

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 will lead the development of global regulatory strategies and manage submission activities, ensuring compliance and quality in documentation while collaborating with cross-functional teams and health authorities.

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  Minimum 8 years regulatory experience preferred
• •
  Substantial knowledge in regulatory submission
• •
  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.

• •
  8+ years of working experience, preferably in pharma.
• •
  Expertise in analytical technologies like HPLC.
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  University degree, preferably PhD in relevant science.

Deine Vorteile

KI-Beschreibung

You manage global CMC regulatory strategies and submissions, ensuring compliance and effective communication with stakeholders while leading risk assessments and negotiations with health authorities.

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

Deine Vorteile

KI-Beschreibung

You assist in drug substance development by conducting experiments, analyzing data, documenting findings, and collaborating with the team to improve workflows.

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  Master’s program in life sciences
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  Advanced communication skills in English
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  Self-driven, team-oriented work style

Deine Vorteile

KI-Beschreibung

You contribute to the development of innovative drug candidates by conducting experiments and analyzing data, collaborating with colleagues to present findings and enhance workflows.

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  Master’s program in life sciences
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  Advanced communication skills in English
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  Self-driven, team-oriented work style

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.

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  Currently enrolled in a master's program
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  Advanced communication skills in English
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  Self-driven, team-oriented work style

Deine Vorteile

KI-Beschreibung

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

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

Deine Vorteile

KI-Beschreibung

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

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

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
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  Solid understanding of quality standards

Deine Vorteile

KI-Beschreibung

You lead the analytical sub-team, coordinating project strategies and managing analytics activities for drug development. Your role includes supporting team growth and ensuring high-quality regulatory submissions.

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

Deine Vorteile

KI-Beschreibung

You lead and support global TRD QA initiatives, ensuring compliance and quality in projects while promoting collaboration and innovation through AI technologies and strategic improvements.

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

Deine Vorteile

KI-Beschreibung

You lead and support global TRD QA initiatives, ensuring compliance and quality in projects while promoting collaboration and innovation through AI technologies and strategic engagement.

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

Deine Vorteile

KI-Beschreibung

You manage global CMC regulatory strategies and submissions, ensuring compliance and effective communication with stakeholders while leading interactions with health authorities.

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

Deine Vorteile

KI-Beschreibung

You manage global CMC regulatory strategies and submissions, ensuring compliance and effective communication with stakeholders while leading interactions with health authorities.

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  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.

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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 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 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

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 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
• •
  Critical negotiations
• •
  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
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  Bachelor's degree in Computer Science

Deine Vorteile

KI-Beschreibung

You will design and develop system solutions for the R&D Lab, ensuring timely project delivery and adherence to security policies while leading cross-functional teams and resolving application issues.

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  Expert technical understanding of Lab Applications
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  Several years of experience in Pharma or IT
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  Expert knowledge of GXP and 21CFR Part 11

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 cross-functional teams.

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  Expert technical understanding of Lab Applications
• •
  Several years of experience in Pharma or IT
• •
  Expert understanding of Lab business processes