Research Associate - DQA

As a Pharmaceutical & Life Sciences professional, your role involves ensuring that all pharmaceutical products developed with the R&D Department meet the highest quality standards. Your key responsibilities include: - Preparing and reviewing regulatory dossier documents for DCGI, ROW, and Export market business. - Implementing and maintaining quality assurance systems and procedures for dosage preparation. - Ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratories Practices (GLP), and other relevant regulatory standards. - Collecting, organizing, and reviewing documents from F&D, ADL, and other relevant departments. - Managing quality documentation and records, including standard operating procedures (SOPs), Batch records, and Test reports. - Compiling and reviewing Product Development Reports (PDRs) to document the formulation and development process of products. - Ensuring all equipment is calibrated according to the schedule and the records are maintained. Preferred candidate profile: - Must have experience in OSD (Oral Solid Dosage) manufacturing. Please note: Any additional details of the company were not provided in the job description.,