Executive - Compression

Job Description Role Overview: As an Officer, your main responsibility will be the supervision of manufacturing, processing, packaging, and holding of drug products as per defined and approved procedures for stability batches and commercial batches. You will also be in charge of maintaining the area and equipment in an orderly manner as per cGMP requirements in a good state of repair and sanitized condition. Additionally, you will need to perform online documentation with respect to departmental procedures and impart training on operation and cleaning related SOPs to all subordinates and operators. Key Responsibilities: - Co-ordinate for IQ / OQ for any new equipment / system - Perform PQ for any new equipment / system - Follow all concern departmental SOPs for day-to-day operation and cleaning - Handle and manage material movement as per defined procedure and approved Batch Manufacturing Record / Batch Packing Record - Review, execute, and implement Batch Manufacturing Records, Batch Packaging Records, Process Study Protocols, Process Study Reports, and all relevant Documents - Follow all safety rules and departmental general instructions - Perform work other than defined in the Job responsibility as per the requirement of HOD, by following HODs instruction and guidance Qualifications Required: - Bachelor of Pharmacy - Minimum 3 years of experience Additional Details: The company emphasizes a strong adherence to cGMP requirements and safety rules, ensuring that all operations are conducted in a compliant and efficient manner. Your role will involve not only overseeing the production processes but also contributing to the training and development of subordinates and operators. Role Overview: As an Officer, your main responsibility will be the supervision of manufacturing, processing, packaging, and holding of drug products as per defined and approved procedures for stability batches and commercial batches. You will also be in charge of maintaining the area and equipment in an orderly manner as per cGMP requirements in a good state of repair and sanitized condition. Additionally, you will need to perform online documentation with respect to departmental procedures and impart training on operation and cleaning related SOPs to all subordinates and operators. Key Responsibilities: - Co-ordinate for IQ / OQ for any new equipment / system - Perform PQ for any new equipment / system - Follow all concern departmental SOPs for day-to-day operation and cleaning - Handle and manage material movement as per defined procedure and approved Batch Manufacturing Record / Batch Packing Record - Review, execute, and implement Batch Manufacturing Records, Batch Packaging Records, Process Study Protocols, Process Study Reports, and all relevant Documents - Follow all safety rules and departmental general instructions - Perform work other than defined in the Job responsibility as per the requirement of HOD, by following HODs instruction and guidance Qualifications Required: - Bachelor of Pharmacy - Minimum 3 years of experience Additional Details: The company emphasizes a strong adherence to cGMP requirements and safety rules, ensuring that all operations are conducted in a compliant and efficient manner. Your role will involve not only overseeing the production processes but also contributing to the training and development of subordinates and operators.