Management and Administration of Quality Control Dept, ensuring Timely testing & quality check of Raw, Packing and Finished Products. Complying all the regulatory requirements of FDA, MOH Guideli ... view more

• quality assurance manager
• fda
• quality control manager
• moh
• CGMP
• glp

Roles and Responsibilities 1. Responsible for all sections of production area and plan and execute production to meet business requirements within timelines. 2. Ensure data integrity and compliance ... view more

• Vial Filling
• Manufacturing
• Vial Washing
• Formulations
• Injectable
• Production
• Regulatory Requirements
• Sterile Formulations
• Lyophilization
• PFS
• Sealing

Roles and Responsibilities Protein analysis by HPLC, ELISA, OD280 methods and electrophoresis methods. Operation of HPLC, UV spectrophotometer, TOC analyzer, gel doc and stability chambers. Samp ... view more

• HPLC
• UV Spectrophotometer
• Quality Control
• ELISA

1.  Supervision of Packing section & job assigned as an when required. 2.  Timely check up & fill up of related GMP document. 3.  On line documentation. 4.  On line job ... view more

• Production
• packing

Purpose: To lead & manage the Integrated Engineering and Infrastructure Projects function With the objective of Ensuring maximum availability of equipment and facilities, both Plants and Labs for ... view more

• Civil Engineering
• Instrumentation Engineering
• Mechanical Engineering
• Automation Engineering
• Engineering Projects
• Electrical Engineering

Roles and Responsibilities Responsible for receipt, storage, control, and the issue of Raw materials, Packing Materials. PDS Chemicals inventory control and maintain the statutory compliance records ... view more

• Inventory Control
• Chemical Handling
• Team Handling
• Issuance of Raw Materials
• Raw Material
• Issue
• Material Requirement Planning
• Inventory Management
• Safety Compliance
• Statutory Compliance

candidate must have well-versed experience in the field of Quality Assurance. Having sound knowledge of QMS. candidate must have exposure in API process validation, Cleaning validation equipment q ... view more

• Cleaning Validation
• Process Validation
• GMP
• MHRA
• Corporate Quality Assurance
• USFDA
• QC
• Cqa
• QMS
• Equipment Qualification
• Pharma
• CGMP
• Bulk Drugs
• Quality Assurance
• API Manufacturing

1.Planning and monitoring of daily work of stability section. 2.Receiving of stability samples and maintaining their records. 3.Responsible for Charging / loading and withdrawal of stability samples. ... view more

• Stability Chamber Management
• Stability Samples
• Quality Control Management
• Cgmp

Roles and Responsibilities 1. Reports to Designee/HOD. 2. Guides the operating personnel to carry out the production activities effectively as per the standard operating procedures. 3. Responsible ... view more

• online Documentation
• Production
• Production Planning
• CGMP
• Packaging
• SLR
• Bulk Drugs
• GLR
• Standard Operating Procedures
• API Manufacturing
• Batch Manufacturing

Promoted by the late Mr. Amrut Mody, a pioneer of the Indian pharmaceuticals business, Unichem Laboratories has grown to become one of India's most respected pharmaceutical companies. It is commi ... view more

• Data Integrity
• QMS
• Quality Assurance
• Capa
• Validation
• OOS
• SOP
• Documentation
• Production
• CGMP