115 Job openings found

Documentation review and reconciliation. Responsible and ensuring following GMP. Granulation Process Management: Oversee all aspects of the granulation process, including equipment setup, operation, and troubleshooting. Ensure that granulation activities are carried out efficiently and in compliance with standard operating procedures (SOPs) and regulatory requirements. Team Leadership: Lead and supervise a team of granulation operators, ...

Provide analytical support for maintaining in-process control and product quality.Analysis of In-process samples and Finished Product (Syrup).Analysis of Cleaning validation and verifications samples.Documenting the activities performed online for GMP & GLP.Performed all analytical technique in Tablets, Capsules manufacturing.Responsible for Preventive maintenance of HPLC.Testing of all finish dosage form SyrupDocumentation(R.M, F.P ...

Provide analytical support for maintaining in-process control and product quality.Analysis of In-process samples and Finished Product (Syrup).Analysis of Cleaning validation and verifications samples.Documenting the activities performed online for GMP & GLP.Performed all analytical technique in Tablets, Capsules manufacturing.Responsible for Preventive maintenance of HPLC.Testing of all finish dosage form SyrupDocumentation(R.M, F.P ...

Following GMP during operation of the equipment and handling of products. Responsible for Operation of moisture analyzer and ERH apparatus. Responsible for the following SOPS and BMR’S in the area without any deviations. Responsible for integrity of punches & dies and sieves, screens, finger bags. Responsible for the Maintenance of change parts and punch ...

Receive & verify material as per SOP Good warehouse practices Dispensing & sampling as per SOP Follow FIFO & FEFO Material weighing Inventory level Adhere GMP norms Well versed with documentations related to a pharma.   Receive & verify material as per SOP Good warehouse practices Dispensing & sampling as per SOP Follow FIFO & FEFO Material weighing Inventory level Adhere GMP norms Well versed with ...

Receive & verify material as per SOP Good warehouse practices Dispensing & sampling as per SOP Follow FIFO & FEFO Material weighing Inventory level Adhere GMP norms Well versed with documentations related to a pharma.   Receive & verify material as per SOP Good warehouse practices Dispensing & sampling as per SOP Follow FIFO & FEFO Material weighing Inventory level Adhere GMP norms Well versed with ...

Provide analytical support for maintaining in-process control and product quality.Analysis of In-process samples and Finished Product (Syrup).Analysis of Cleaning validation and verifications samples.Documenting the activities performed online for GMP & GLP.Performed all analytical technique in Tablets, Capsules manufacturing.Responsible for Preventive maintenance of HPLC.Testing of all finish dosage form SyrupDocumentation(R.M, F.P ...

QMS: Maintain detailed documentation of QMS(change control, deviation, incident, market complaints, product recall) VMP: maintain and execution of Validation plan as per schedule Master index: Prepare and maintain of Master index for SOP, STP, Protocols, MFR, BMR/BPR Document control: Issue and retrieval of documents like BMR/BPR, SOP, Formats, and log books APQR: Prepare the ...

Following GMP during operation of the equipment and handling of products. Responsible for Operation of moisture analyzer and ERH apparatus. Responsible for the following SOPS and BMR’S in the area without any deviations. Responsible for integrity of punches & dies and sieves, screens, finger bags. Responsible for the Maintenance of change parts and punch ...

Should be able to work in shift Work as per IPQC SOP's Follow company's rules and regulations Follow do's and don'ts of clean room behavior's Work as er lant GMP practice     Should be able to work in shift Work as per IPQC SOP's Follow company's rules and regulations Follow do's and don'ts of clean room behavior's Work as er ...