Build scientific relationships with healthcare professionals and key thought leaders in endocrinology to support patient access to innovative therapies.
Responsibilities
Engage internal and external stakeholders in balanced, high-quality exchange of scientific information
Identify and validate unmet medical needs and help define appropriate standards of care
Generate actionable medical insights and share them cross-functionally to support patient access to new therapeutic options
Identify emerging issues within the endocrinology therapeutic area and contribute to well-founded activities and solutions
Support local data generation initiatives, including investigator-initiated studies, real-world evidence and observational research, and publications
Requirements
Bachelor’s degree in Pharmacy
Master’s degree in a related field (life sciences, biotechnology, biology, nursing)
As a QA Operations Intern, you drive GMP compliance across our pharmaceutical site within the Quality Operations team.
Compensation
€ 400 - € 800/mese
Responsibilities
Review analytical batch records and manufacturing documentation to ensure compliant release of commercial product batches and analytical laboratory data
Perform rigorous quality assurance data integrity audits across analytical testing activities, identifying anomalies and preventing procedural deviations
Drive continuous process improvements by assessing and integrating practical artificial intelligence tools into team workflows
Review qualification and validation protocols for site equipment and manufacturing processes, collaborating with cross-functional departments to uphold all regulatory standards and maintain inspection readiness
Requirements
Degree in Pharmaceutical Sciences or related scientific discipline
Responsible for preparation of Distribution Key Design Decisions & deployment activities, ensuring adherence to harmonization targets
Drive business process change on an operational level as a change agent while ensuring process simplification & process/system standardization
Identifies areas for process improvement & works with relevant stakeholders (e.g., ITSEs, Data Experts) to implement change
Develops detailed process documentation & maintains up-to-date records of all design and deployment activities
Synthesizes information & provides strong recommendations incorporating business context & dependencies while establishing clear prioritization criteria to determine tradeoffs
Betreuung und Förderung von Kindern im Alter von 1-3 Jahren gemäß hessischem Bildungs- und Erziehungsplan in einer Kindertagesstätte
Compensation
Eine attraktive Vergütung nach dem Chemietarif in Vollzeit mit 37,5 Std./Woche und 30 Urlaubstagen im Jahr, selbständige ganzjährige Urlaubsplanung, zahlreiche Sozial- und Zusatzleistungen (z.B. Urlaubsgeld, betriebliche Altersvorsorge, Nutzung des betrieblichen Gesundheitsmanagement)
Responsibilities
Betreuung und Förderung der Kinder im Alter von 1-3 Jahren
Planung und Durchführung des Tagesablaufs
Organisation von Tagesplänen und administrativen Tätigkeiten
Dokumentationsarbeiten
Konzeptionelle Arbeit des Hauses umsetzen und weiterentwickeln
Requirements
staatliche Anerkennung als Erzieher/in, Heilpädagoge/in, Kindheitspädagoge/in, Elementarpädagoge/in oder Sozialpädagoge/in
Medical Science LiaisonNewThe businesses of Merck KGaA, Darmstadt, Germany · Seoul, South Korea