12 Inprocess Checks Jobs

As a Quality Assurance Officer, you will be responsible for the following key responsibilities: - Issuing documents related to the shop floor. - Conducting line clearance activities. - Performing in-process checks for Tablets, Capsules, Pellets, DC granules, Dry syrups, and Packing. - Calibration of IPQA instruments. - Online documentation and review. - Monthly log book review. - Sampling and cross-checking of semi-finished, finished, reference, and stability samples. - Reviewing master documents like BMR, BPR of Tablets, Capsules, Pellets, DC granules, and Dry syrups, as well as Validation Protocols. - Batch closing and entering QQF in the ERP system. - Verifying rubber stereo indent, impre...

Role Overview: As a Quality Assurance professional at our company, your primary responsibility will be to ensure the online documentation of batch manufacturing and batch packing records. You will also be in charge of carrying out in-process checks of pre-determined process parameters as per BMR/BPR and withdrawing in-process/FP/Reference & stability samples following SOP. Additionally, monitoring the environmental condition of critical areas and reviewing & approving QA SOPs will fall under your purview. Key Responsibilities: - Ensure online documentation of batch manufacturing and batch packing record - Carry out in-process checks of pre-determined process parameters as per BMR/BPR - Withd...

Role Overview: As a Production Operator in the granulation department, your main responsibilities will include: Key Responsibilities: - Operate, clean, and perform primary maintenance on negative isolator, Vibro sifter, Bin blenders, and all other GEA granulation line equipment. - Record activities in logbooks, Batch manufacturing record, and complete documentation following cGMPs and good documentation practices. - Perform all in-process checks and monitoring of intermediate processes in granulation. - Select recipes, set process parameters in Blender HMI, and ensure correctness before blender revolution. - Issue, utilize, clean, and retrieve sieves and handle machine change parts with inve...

Role Overview: As a Team Member in IPQA for Injectables/OSD, you will be a skilled professional with over 5 years of experience in real-time monitoring of manufacturing and packaging processes. Your responsibilities will include line clearance, in-process checks, and reviewing Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) to ensure compliance with GMP and regulatory standards. You will also be involved in deviation handling, documentation, and providing audit support for injectable and oral solid dosage forms. Key Responsibilities: - Real-time monitoring of manufacturing and packaging processes - Conducting line clearance and in-process checks - Reviewing Batch Manufactur...

You will be responsible for machine setting, operation, and cleaning of machines according to the operating instructions and standard operating procedures. Your role will involve meeting the pilot production schedule and ensuring adherence to the delivery timeline. You will execute pilot-bio/clinical trial/trial batches as per manufacturing instructions and record process parameters during batch manufacturing, online documentation, log books, and status labeling. Adherence to quality and safety procedures & policies at manufacturing sites will be a key aspect of your responsibilities. As part of your duties, you will be responsible for the calibration of instruments as per the schedule and a...

As an operator in our team, your primary responsibility will be to operate herbal extraction equipment such as Extractor reactors, filtration units, evaporators, and other associated machinery. You will diligently follow batch processing instructions and Standard Operating Procedures (SOPs) to ensure efficient and accurate production processes. In addition to operating the equipment, you will be responsible for maintaining detailed batch records, Batch Manufacturing Records (BMR), logbooks, and ensuring compliance with Good Manufacturing Practices (GMP). Your role will also involve conducting in-process checks on parameters such as temperature, pH levels, moisture content, and other relevant...

You will be responsible for conducting In-Process Quality Assurance (IPQA) activities on the shop floor throughout the various stages of sterile manufacturing and packing process. This includes performing sampling at each stage or when necessary during product manufacturing, filling, and packaging activities. Your duties will also involve conducting in-process checks of manufacturing, filling, and packaging processes. You will be required to perform Acceptable Quality Level (AQL) checks after completing visual inspection of products. Additionally, you will need to carry out audit trail and electronic data reviews batch-wise and as per the designated schedule. Furthermore, you will be tasked ...

You will be responsible for documenting inspection results by preparing detailed reports, summarizing rework and waste, and entering data into the quality database. Ensuring the accuracy of measurement equipment is crucial, which involves following calibration protocols and coordinating with line managers. Regular quality inspections at specified intervals throughout the day will be part of your routine. You will conduct thorough inspections at various stages, including raw material receipt, in-process checks, final product review, and dispatch. Utilizing appropriate methods such as standard comparisons, dimensional measurements, and functionality testing, you will inspect samples to maintai...

The Quality Assurance (QA) Executive API (Bulk Drugs) role based in Savli, Gujarat requires a candidate with 2-5 years of experience and a qualification of B.Sc / M.Sc. As a QA Executive, your responsibilities will involve ensuring compliance with cGMP, ICH, and regulatory guidelines in API (bulk drug) manufacturing. You will be responsible for preparing, reviewing, and controlling SOPs, BMRs, BPRs, change controls, deviations, and CAPAs. In addition, conducting in-process checks for manufacturing and packaging activities, handling investigations for deviations, OOS/OOT results, and supporting root cause analysis are key components of this role. You will also be involved in participating in ...

As a Shift Executive at our Krishnagiri location, you will be responsible for efficiently managing the shift manpower to enhance productivity. Your primary duties will include ensuring the timely completion of the day's production schedule, monitoring processes, conducting in-process checks, and coordinating with other departments to achieve the desired output. Additionally, you will be tasked with maintaining production records, optimizing yield, streamlining workflow to minimize downtime, and planning preventive maintenance activities. Training and developing both migrant and new manpower will be crucial aspects of your role, along with overseeing housekeeping practices, ensuring complianc...

The core job responsibilities for the position holder include: Responsible for operating, cleaning, and performing primary maintenance on negative isolator, Vibro sifter, Bin blenders, and all other GEA granulation line equipment. This includes recording activities in logbooks, Batch manufacturing records, and completing documentation required for product manufacturing and equipment cleaning, while following cGMPs and good documentation practices. Performing all in-process checks and monitoring of intermediate processes in granulation. Selecting recipes and setting process parameters in Blender HMI, ensuring correctness before blender operation. Issuing, utilizing, cleaning, and retrieving s...

The core job responsibilities of the position holder include: Responsible for the operation, cleaning, and primary maintenance of negative isolator, Vibro sifter, Bin blenders, and all other GEA granulation line equipment. Record activities in logbooks, Batch manufacturing record & complete documentation following cGMPs and good documentation practices. Perform all in-process checks and monitoring of intermediate processes in granulation. Select recipes, set process parameters in Blender HMI, and ensure correctness before blender revolution. Issue, utilize, clean, and retrieve sieves and handle machine change parts with inventory. Set up, changeover, and operate various manufacturing equipme...