Quality Assurance Manufacturing

A WHO GMP CERTIFIED MANUFACTURER OF DRUG FORMULATIONS IN EXTERNAL PREPARATION AND ORAL LIQUID FINISHED DOSAGES LOOKING FOR PHARMA QUALITY ASSURANCE MANAGER (PHARMACEUTICAL MANUFACTURING) HAVING THE BELOW SKILLS AND QUALIFICATIONS.A. MINIMUM WORK EXPERIENCE OF 7 YEARS IN PHARMACEUTICAL MANUFACTURING QUALITY ASSURANCE REQUIRED.B. MINIMUM BACHELOR OF SCIENCE OR...

**Position**: Executive **Educational Qualification**: B. Pharm / M. Pharm / M.sc. **Experience**: 3 to 5 years of experience in Pharmaceutical Quality Assurance. To review batch manufacturing and packaging documentation for solid oral dosage forms. To review Annual Product Quality Review (APQR) reports. To monitor and close change controls in 21 CFR...

Job Description- To ensure all the products manufactured and distributed by the bottling operation conform to the specifications through assurance of processes from supply to consumer. The QAE supports the identification, planning, documentation, and management of the practices, activities and resources needed to meet quality goals and objectives in a manner...

This position is responsible for managing all cGMP aspects of Quality Assurance Operations of a WHO-GMP approved Tablets and Capsule manufacturing facility.Specific Responsibilities:In-Process Quality Assurance (IPQA) performing checks during manufacturing, such as sampling, manufacturing, packing, and line clearance,Review and approve SOPs, Batch Records,...

**Quality Assurance Executive** **No. of Vacancy - 01** **Job Summary** The Quality Assurance Executive will be responsible for monitoring, inspecting, and proposing measures to correct or improve the company’s final products and processes in order to meet established quality standards in notebook manufacturing. **Key Responsibilities** - **Quality...

Review and update standard operating procedures (SOPs) to align with changing regulations and best practices. Documentation And Records Management - Maintain and manage documentation related to quality assurance activities, including batch records, investigation reports, change controls, and validation documentation. - Ensure accurate and timely completion...

Job Responsibility Knowledge Required OOS, OOT Deviation Incident Change Control Process Validation Cleaning Validation Site master file Drug Master File - Responsible for the quality assurance of the batches manufactured - Responsible for identifying the training requirements of the manufacturing and maintenance personnel and - imparting the...

**Shift Job (8 Hours)** Surat Gujarat India **Quality assurance (QA)**: **Manufacturing**: - Skill & Responsibility: - Documentation Quality assurance is related to the document related activities which includes Training, Quality Management System, Document Issuance, Market Compliant, Audit Compliance etc. **Required Skills and Abilities**: - M.pharm -...

Key Responsibilities:· Establish inspection criteria, testing methods, and quality assurance plans for various stages of product development and manufacturing· Conduct inspections and testing: Perform routine inspections of raw materials, in-process components, and finished products to verify conformance to specifications· Responsible for all quality...

Quality Assurance SpecialistWe are seeking a highly skilled Quality Assurance Specialist to assume key responsibilities in our quality management system. This role involves ensuring compliance with Good Manufacturing Practice (GMP) and Good Hygiene Practice (GHP) standards.Process control and clearance of raw materials, packing materials, semi-finished...