Transfer Specialist

2 weeks ago

Ellore, Andhra Pradesh, India beBeeProject Full time ₹ 12,00,000 - ₹ 18,00,000
Job Opportunity

We are seeking a highly skilled and experienced Technical Transfer Project Manager to join our team.

This role will be responsible for managing and coordinating Technology Transfer projects, tasks, schedules, status, and project reporting to stakeholders. The successful candidate will have excellent communication skills and be able to facilitate problem-solving and decision-making with respect to project deliverables and meeting timelines.

The ideal candidate will have at least 9 years of experience in Project Management, with prior experience in Formulation Development of solid oral dosage forms, Parenteral dosage form, Liquid dosage form, Topical dosage form, Nasal spray. They should also have thorough knowledge of generic drug development cycle including 505(B2), complex generics, peptides, various regulatory guidelines, (ICH, ANVISA, USFDA, EMA) and regulations (GMP, GCP, GLP etc.).

Responsibilities
  • Manage and coordinate Technology Transfer projects, tasks, schedules, status and project reporting to stakeholders independently
  • Facilitate communication within and outside the project team.
  • Facilitate problem-solving & decision-making with respect to project deliverables and meeting timelines/tasks/'requests from project teams and other cross-functional departments.

The role requires a self-driven and dynamic individual who can work in a fast-paced environment and adapt to changing priorities. They should be capable of working independently and as part of a team, with strong analytical and problem-solving skills. Experience with EPM / MSP software and Microsoft Excel is essential.

Requirements
  • Qualification: M. Pharmacy or B. Pharmacy with MBA.
  • Experience: At least 9 years of experience in Project Management with prior experience in Formulation Development of solid oral dosage forms, Parenteral dosage form, Liquid dosage form, Topical dosage form, Nasal spray.
  • Knowledge of generic drug development cycle including 505(B2), complex generics, peptides, various regulatory guidelines, (ICH, ANVISA, USFDA, EMA) and regulations (GMP, GCP, GLP etc.)

Candidates should have excellent written and verbal communication skills, with the ability to prepare clear and concise reports and presentations. They should also be able to prioritize tasks and manage multiple projects simultaneously.

The successful candidate will be based in India and will report directly to the Director, Project Management.

Why Join Us?
  • Exciting Challenges: Every day brings new opportunities to learn and grow.
  • Supportive Environment: We foster a culture of collaboration, where your ideas are valued, and your voice is heard.
  • Career Development: We're committed to helping you reach your full potential through ongoing training and development opportunities.

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