Formulation Development Expert

At the heart of NanoAlvand beats a relentless drive for innovation. Our Research and Development department is a thriving hub where brilliant minds converge, united by a shared passion for pushing the boundaries of modern formulations. Our scientists and researchers work in seamless harmony, fueled by a collective determination to unlock the secrets of groundbreaking formulations. With each product development, we move closer to our ultimate goal: delivering innovative solutions that shape the future of healthcare for generations to come.

Location
Simindasht Industrial Area, Karaj
Working Time
Full Time

Overview

As a Formulator in R&D team you will be responsible for new product development of products which assigned from pipeline team. You will lead the design and development of formulations and processes, scaling up for manufacturing of batches for clinical and pre-clinical trials if needed, preparation of product development reports and support for all necessary quality documentation and documentation for regulatory submissions.
In this position, you will collaborate closely with R&D manager in all internal, domestic and international inspections for constant improvement of the department.

Key Responsibilities

  • Design, conduct and interpret application experiments and studies to advance formulation development while ensuring register ability and manufacturability of the developed products

  • Writing and/or reviewing procedures, protocols and specifications needed to support product development activities

  • Developing and/or performing all testing requirements on new products and packages

  • Responsible for proposing and implementing solutions during any deviations occur during manufacturing and any changed if needed

  • Requires cross-functional interaction and relationship with Manufacturing, Sourcing, Regulatory, Supply Chain, QC

Education

  • Doctor of Pharmacy (Pharm.D)

  • Minimum - Bachelor of Science degree in Chemistry

Requirements

  • Age of 28-34

  • Extensive knowledge of current Good Manufacturing Practices (cGMP), international guidelines (e.g., FDA, EMA), and industry standards

  • Strong research skill in valid documents

  • Strong problem-solving skills, with the ability to interpret complex data and identify root causes of quality issues.

  • Excellent written and verbal communication skills for documenting results and collaborating with cross-functional teams

  • Attention to detail and a commitment to ensuring the highest quality standards are met

  • Highly proactive and results-oriented approach


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