264 Job openings found

Job Summary: The SPM Operator is responsible for the operation and maintenance of Solid Preparation Machines (SPM) used in the production of pharmaceutical products. This role involves ensuring efficient and accurate processing, adhering to quality standards, and complying with regulatory requirements. Key Responsibilities: Operation of SPM Equipment: Operate Solid Preparation Machines (SPM), including ...

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 ...

Job description for the post of Production Assistant- (a) one who is able to handle all pharma reactors. (b) Able to handle glass assembly 20L, 50L, 100L, 200L, 300L.(c) Knowledge of Centrifuge 24’’ & 36’’.(d) having exposure of handling CF, multi mill, Nutseh Filter, Blender, Shifter.(e) Equipment handling(f) Knowledge of GMP ...

Responsible for supervise of production planning for in-house manufacturing.Ensuring proper Planning & execution of complete sampling activity.Optimum utilization of man & machine , material etc.Develop and maintain effective relationships with internal suppliers and customers for ensuring that required inputs are available on time.Provide forecasts and demand profiles to major suppliers Knowledge of current ...

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 ...