7 Inprocess Checks Jobs

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 factors to maintain product quality. Ensuring cleanliness and sanitation of the equipment and work area will be crucial to maintain a hygienic production environment. You will be expected to promptly report any deviations from standard procedures or equipment issues to the relevant teams to address them efficiently. Collaborating with Quality Control (QC) and maintenance teams will be essential for seamless operations and continuous improvement. This is a full-time, permanent position with benefits including leave encashment and Provident Fund. The work schedule may involve day shifts, night shifts, or rotational shifts based on operational requirements. The work location is on-site, requiring your presence in person. We are looking for a detail-oriented and proactive operator to join our team, with an expected start date of 06/06/2025. If you are passionate about herbal extraction processes and maintaining high standards of production quality, we welcome your application for this role.,

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 with managing control samples and stability samples. Your role will also include participating in the qualification of master kit approval for visual inspection activities. You will be expected to review and approve all relevant documents related to the qualification of visual inspectors. Overall, your attention to detail and adherence to quality standards will be crucial in ensuring the production of high-quality sterile products.,

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 maintain quality standards. The company you will be working for, Shri Bhagavati Bright Bars Limited (SBBBL), was founded in the 1980s with a focus on manufacturing cold-drawn bright bars. Established officially in 1991, SBBBL aimed to diversify its product range to meet the evolving demands of the Indian iron and steel market. Adapting to the changing landscape, SBBBL transitioned towards steel products in response to market trends. With a commitment to meeting customized requirements and minimizing downtime, machining, and labor costs for customers, SBBBL expanded its offerings to include custom-shaped bars, profile bars, and bars and wires in custom sizes. The company maintains an average inventory of 1,000 metric tonnes to facilitate just-in-time delivery, reducing idle time and optimizing inventory turnover for its clientele.,

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 internal audits, regulatory audits (USFDA, EU, WHO, etc.), and vendor audits. Maintaining documentation for batch release, validation protocols, and quality systems, ensuring adherence to data integrity and good documentation practices (GDP), and supporting qualification and validation activities are crucial aspects of this position. Collaboration with cross-functional teams such as Production, QC, and R&D is essential for ensuring smooth operations. This is a full-time, permanent position with benefits including health insurance and Provident Fund. The work schedule is day shift with additional perks such as performance bonus and yearly bonus. The work location is in person.,

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 compliance with Good Manufacturing Practices (GMP), and implementing the 5S methodology to uphold a safe working environment. Ideally, you should possess 2-5 years of experience, with a background in Bakery and Confectionery being an added advantage. A Bachelor's degree in Food Technology, Mechanical, or Electrical Engineering (B.E/B.Tech) is required to qualify for this position. If you are a proactive individual with excellent organizational and leadership skills, we encourage you to apply and contribute to our team's success.,

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 sieves, as well as handling machine change parts inventory appropriately. Setting up, changing over, and operating various manufacturing equipment within the granulation department. Reporting or escalating any conditions or problems that may impact product quality or integrity to the supervisor and HOD production. Maintaining a neat, clean, and safe working environment at all times, and promptly notifying the supervisor of any safety concerns, accidents, or injuries observed. Conducting in-process checks and monitoring of intermediate processes, verifying process parameters in PLC/SCADA according to BMR before machine operation in the granulation area. Ensuring compliance with current Good Manufacturing Practices in the Hormone Facility and following GDP with data-integrity compliance. Completing training and training records within the stipulated time frame. Preparing and utilizing disinfectant and cleaning agent solutions following defined procedures. Adhering to all company policies, procedures, SOPs, and safety regulations.,

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 equipment in the granulation department. Report or escalate any conditions or problems affecting product quality to supervisor and HOD production. Maintain a neat, clean, and safe working environment, reporting safety concerns, accidents, or injuries to the supervisor immediately. Conduct in-process checks, monitor intermediate processes, set process parameters in PLC/SCADA per BMR before machine run in granulation area. Ensure compliance with current Good Manufacturing Practices in the Hormone Facility and follow GDP with data-integrity compliance. Complete training and training records within stipulated time. Prepare and use disinfectant and cleaning agent solutions following defined procedures. Adhere to all company policies, procedures, SOPs, and safety regulations.,