Manoucher Jandaghi

• Quality Control Manager/ Quality assurance member (May 2016 ‐ Jul 2022)/ Responsible pharmacist (Apr 2015 ‐ Apr 2016)/ R&D department (Mar 2014 ‐ Mar 2015).

-Product Development Strategy (bring new products to market for product portfolio management / modify existing products to create new business).

- Monitor environmental conditions to comply with current Good Manufacturing Practices (cGMP) requirements.

-Prepare and implement procedures for periodic inspection and calibration of laboratory equipment, and plant level process control instruments and equipment.

- Performing stability testing to assess product suitability.

- Preparation of GMP, DMF, and CTD compliance documents for newly introduced products.

- Supervision of all regulations of the Food and Drug Administration regarding the production of pharmaceutical products (including formulation, manufacturing, control, packaging and storage).

- Performing relevant duties in different departments in a Pharmaceutical Manufacturing Company such as production, quality control, warehouses, health and safety, training and research, etc.

• Provided counseling to clients on their use of medications, natural remedies, over-the-counter products and other services as necessary.
• Contacted doctors and other health practitioners to discuss prescription changes or renewals.
• Accurately processed new prescriptions and re-fill requests Professional filling of prescriptions (right medication, right dosage, right amount).
• Manufacturing, compounding, and preparation of drugs in accordance with the scientific principles of pharmacy and the notified rules and standards.
• Participating in screening programs and referring patients to doctors in order to enable early disease diagnosis.
• Helping to improve patient safety and drug safety by following clinical and pharmaceutical protocols and guidelines.
• Sending quick and timely reports of unwanted side effects of drugs and other health products, and providing adequate training to patients.
  
  

• Conducted research on breast cancer treatments, drugs and developed new radiopharmaceuticals.
• Collaborated with interdisciplinary teams of scientists and physicians to design and implement preclinical and clinical studies.
• Conducted research on the use of radiopharmaceuticals in the diagnosis and treatment of breast cancer.
• Designed and implemented experiments to evaluate the efficacy and safety of radiopharmaceuticals.
• Analyzed radiopharmaceuticals for radiochemical purity, biological activity, and stability.
• Developed strong communication and organizational skills through working on group projects.
• Organized and detail-oriented with a strong work ethic.
• Self-motivated, with a strong sense of personal responsibility.
• Proven ability to learn quickly and adapt to new situations.