ApplusVelosi

Method Validation: Support in validating analytical methods (HPLC GC UV FTIR) for raw materials and finished products. Instrument Qualification: Assist in calibration qualification (IQ/OQ/PQ) of laboratory instruments. Stability Studies: Learn and assist in stability testing as per I More...

Packaging Operations: Blister packing Primary PackingMachine Handling: Operating cleaning and maintaining packaging machines.Quality Checks: Ensure packed products meetquality standards including proper sealing labeling and batch coding.Documentation: Maintainbatch records & logbo More...

Packaging Operations: Blister packing Primary Packing Machine Handling: Operating cleaning and maintaining packaging machines. Quality Checks: Ensure packed products meet quality standards including proper sealing labeling and batch coding. Documentation: Maintain batch records & More...

Tablet Coating Operations: Operate and monitor coating equipment (Auto Coater/Conventional Coater) during trial validation and exhibit batches in technology transfer projects. Process Parameter Monitoring: Ensure adherence to defined process parameters (inlet/outlet temperature spray More...

Sterile Manufacturing Operations: Oversee aseptic filling compounding filtration and lyophilization processes to ensure product sterility and quality. Aseptic Practices & Compliance: Ensure adherence to GMP USFDA MHRA WHO and EUGMP guidelines maintaining sterility assurance in cl More...

Position: DM Level Qualification:MSc in Chemistry/BPharmacy. Relevant Experience: QC exposure of 14 to 16 Years of experience from Regulatory Approved Plant (USFDA/MHRA) of OSD facilities. Exposure Areas: Handling of QC Critical instruments Like; HPLC GC UV FTIR KF Autotitr More...

Aseptic Area Exposure: Learn and assist in sterile manufacturing processes including compounding filtration filling and sealing under aseptic conditions. Cleanroom Practices: Follow gowning procedures cleanroom discipline and contamination control measures as per SOPs. Batch Support More...

Position:DM Level Qualification: MSc in Chemistry/BPharmacy. Experience: QC/R&D exposure of 14 to 16 Years of experience from Regulatory Approved Plant (USFDA/MHRA) of OSD formulation related. Exposure Areas: Having in depth knowledge and experience of Analytical Method Va More...

Sample Handling: Assist in sampling and testing of raw materials inprocess and finished products under guidance. Analytical Support: Learn to operate basic analytical instruments like HPLC UV pH meter and balance following SOPs. Documentation: Help in preparing logbooks test records More...

Oversee and manage QMS processes including Deviation Management CAPA Change Control Risk Management and Product Quality Reviews (PQRs).Lead Quality investigations and root cause analysis for process deviations and quality events.Ensure timely closure of audit observations and effectiv More...

1. Finished product release*Release of semifinished finished product process performance qualification and hold time study related analytical data for sterile formulation facility.*Finished product batch release and approval of COA and COC for sterile products.2. Investigation*To cond More...

Microbial Testing: Perform and review microbial limit tests sterility tests endotoxin tests and preservative efficacy tests for raw materials water and finished products. Environmental Monitoring: Oversee viable and nonviable particulate monitoring surface sampling and compressed air More...

Microbial Testing: Perform and review microbial limit tests sterility tests endotoxin tests and preservative efficacy tests for raw materials water and finished products. Environmental Monitoring: Oversee viable and nonviable particulate monitoring surface sampling and compressed air More...