Title:  Regulatory Affairs Associate - Tamheer Training Program

Associate, Regulatory Affairs– Tamheer Program

• Writes submission documentations including relevant correspondences with health authorities to fulfil submission requirements in an efficient manner that complies with standards and regulations.
• Coordinates all regulatory activities for submissions throughout the regulatory life cycle from preparation, submission, deficiency letters to approvals and variations to ensure efficiency in execution for each step.
• Maintains awareness of applicable regulations and guidance to keep up to date with the relevant guidelines and information that could impact the regulatory projects.
• Coordinates and follows-up with cross functional departments to ensure that submission documents are available in time to meet submission timelines and to ensure that documents meet the authority guidelines and standards.
• Assists in data collection to contribute in the preparation of regulatory affairs department reports.
• Communicates with third parties and licensors to ensure that submission documents are available in time to meet submission timelines and to ensure that documents meet the authority guidelines and standards

Education & Qualification:

• Bachelor’s in pharmacy.
• Fresh Graduated.
• Not Registered in GOSI in last 6 months.