Documentation Specialist

Your role involves establishing and maintaining a comprehensive document control system for all manufacturing processes, including batch records, standard operating procedures (SOPs), and quality control documentation. You will ensure that all documentation complies with relevant regulatory requirements, industry standards, and Good Manufacturing Practices (GMP) for Ayurvedic products. It is essential to stay informed about changes in regulations and update documentation accordingly. Your responsibilities also include compiling and reviewing batch records, as well as conducting regular audits of documentation for accuracy and completeness. You will be responsible for maintaining a systematic filing system for batch records and related documentation. Qualifications Required: - Bachelor's degree in a relevant field such as Pharmacy, Chemistry, or a related discipline - Prior experience in document control within a manufacturing environment, preferably in the pharmaceutical or Ayurvedic industry - Strong knowledge of regulatory requirements and Good Manufacturing Practices (GMP) relevant to document control - Attention to detail and excellent organizational skills - Ability to work independently and collaboratively in a team environment Additional Company Details: N/A,