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Accountabilities:

  • Provide technical support for new product development, technology transfers, and routine manufacturing.
  • Drive Product Lifecycle Management activities and technical risk assessments.
  • Collaborate with cross-functional teams to ensure product quality and regulatory compliance.

Requirements:

  • Master's or PhD in Pharmacy or Pharmaceutical Sciences with relevant experience.
  • Strong knowledge of cGMP, regulatory requirements, and quality management systems.
  • Excellent communication, stakeholder management, and problem-solving skills.

Benefits:

  • Remote working arrangement and full-time employment.
  • Exposure to diverse pharmaceutical dosage forms and technical projects.
  • Inclusive and collaborative environment promoting professional growth.

Confidential

This partner company in the pharmaceutical industry focuses on drug product development and manufacturing across various dosage forms. It offers an inclusive and collaborative working environment that encourages professional growth.

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