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Key Responsibilities - Provide details about our Pharma QMS solutions to prospective clients - Implement and maintain Quality Assurance systems and procedures. - Study & Prepare, review Project scope documentation, SOPs, protocols, and reports for customers - Conduct and participate in internal, customer, vendor, and regulatory audits. - Study and assess manufacturing and quality processes to ensure GMP compliance at customer site. - Participate in customer meeting & presentations. Required Education Qualifications UG: - B.Pharma - B.Sc (Chemistry) - Diploma in Chemical Engineering - B.E./B.Tech (Chemical Engineering) PG (Preferred): - M.Pharma - M.Sc (Chemistry/Biochemistry) - M.E./M.Tech in Chemical Engineering Required Skills - Quality Assurance (QA) - GMP, GLP, and QMS Implementation - SOP Preparation and Documentation - Process Validation - Regulatory Compliance - Internal and External Audits - CAPA, Deviations, and Change Control - ISO Documentation - Vendor and Customer Audits - Strong English Communication Skills - Strong Presentation skills - Good Computer Proficiency Preferred Experience - Experience in API, Bulk Drug, or Formulation manufacturing companies. - Exposure to US FDA, MHRA, EU GMP, and other regulatory inspections. - Experience in handling customer queries and audit observations. Candidate Profile - Robust understanding of pharmaceutical quality systems and regulatory requirements. - Detail-oriented with excellent documentation skills. - Good analytical and problem-solving abilities. - Ability to work effectively with cross-functional teams. - Confident in interacting with customers and regulatory authorities. .