224 Visual Inspection Jobs

As a responsible team member in the pharmaceutical manufacturing process, your role involves the following key responsibilities: - Conduct line clearance activities before starting various operations such as dispensing, manufacturing, filling, inspection, sealing, labeling, and packing. - Perform process validation, cleaning validation/verification, hold time study, media fill, and routine batch sampling according to protocol/SOP. - Review executed Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs). - Perform in-process tests at different stages as per batch documents/SOP. - Review environmental monitoring and water trends. - Review different types of calibration certificates and planners. - Receive necessary resources for environmental monitoring from the microbiology lab and ensure proper handover of monitoring items back to the lab. - Monitor cGMP compliance on the shop floor. - Review various printouts such as CIP, SIP, autoclave, and filter integrity. - Maintain issuance/reconciliation records of items/media for environmental monitoring materials. - Conduct environmental monitoring of the manufacturing clean room area based on the defined schedule. - Participate in media fill simulation studies and qualification activities of the manufacturing area. - Monitor non-viable particles in the manufacturing clean room area and compressed air/nitrogen gas, as well as personnel monitoring. - Review Media Fill Completion Document (CD) and Visual Inspector Qualification Records. Additionally, you will need to manage environmental conditions like temperature, humidity, and light during stability testing to ensure accuracy and compliance. Qualifications required for this role include a Bachelor's (B.Sc.) or Master's (M.Sc.) degree. Please note that this job description pertains to a pharmaceutical manufacturing environment where attention to detail, adherence to protocols, and compliance with regulations are crucial for ensuring product quality and patient safety.,

As a Refractory Lining Engineer, your role involves carrying out regular reliability surveys to monitor the health of Refractory Lining. You will be responsible for inspecting the Refractory lining during shutdowns, releasing observations, and providing recommendations. Monitoring day-to-day Refractory activities to ensure compliance with standards, specifications, and procedures is a key aspect of your job. Additionally, you will need to closely monitor quality checkpoints, ensure safety aspects are in place, and facilitate timely completion of tasks. Key Responsibilities: - Conduct regular reliability surveys for monitoring Refractory Lining health - Inspect Refractory lining during shutdowns and provide observations and recommendations - Monitor day-to-day Refractory activities for compliance with standards and procedures - Ensure quality checkpoints and safety aspects are monitored and adhere to timely completion - Prepare Management Information System (MIS) on summary of Refractory activities - Review contractors" efforts, check resources, and make necessary recommendations - Publish Technical Procedures related to Refractory Inspection & Maintenance - Review Technical Offers from Vendors for supply of Refractory Materials and create a historical database - Ensure compliance with MIQA requirements and adherence to heat-up & dry out schedules - Coordinate with external agencies during shutdowns and estimate resource requirements - Conduct visual inspections of Refractories upon receipt of materials at Stores - Participate in reliability studies as identified and ensure proper data entry in SAP-PM - Ensure proper execution and adherence to schedules Qualifications: - Bachelor's degree in Ceramic/Civil Engineering Experience: - 1 to 6 years of experience in a chemical/petrochemical/refinery organization - Hands-on experience in Maintenance, Reliability analysis, and Root cause analysis with standard applications. (Note: Additional details about the company were not provided in the job description),

As an experienced and detail-oriented Senior QC Engineer specializing in inspection, testing, and quality assurance for castings and metal components, you will play a crucial role in ensuring the compliance and quality of products. Your key responsibilities will include: - Conducting various types of inspections, both internal and with third-party agencies, such as visual inspection, dimensional inspection, hydrostatic pressure testing, liquid penetrant testing (LPT), ultrasonic testing (UT), and radiographic testing (RT). - Documenting and reviewing inspection reports to maintain accurate records of quality assessments. - Coordinating with third-party inspection agencies and on-site inspectors to facilitate smooth execution of inspections as per schedule and client requirements. - Implementing Quality Assurance Plans (QAPs) based on specific customer standards and project requirements to uphold quality standards. - Performing internal testing and lab analysis, including daily production testing, chemical analysis using Spectrometer (Spectro Analysis), and mechanical testing like Tensile & Hardness Testing. - Collaborating technically with NABL-accredited laboratories and ensuring compliance with national/international testing standards. - Overseeing the heat treatment process of castings to maintain quality standards. - Proficiently handling, using, and calibrating precision measuring tools and gauges for accurate measurements. You will be expected to bring your expertise in coordinating inspections, implementing quality assurance plans, conducting various tests, collaborating technically, and ensuring the accuracy of measurements and inspections.,

As a Quality Control Inspector, your role involves monitoring all shop floor activities including In process, Finish, Packaging & Labelling as per laid down procedures. Your responsibilities will include: - Inspection of all raw materials & Packaging Materials along with proper documentation - Ensuring that the product complies with product master specifications - Approval and issuance of correct labels - Analysis of defects and implementation of corrective and preventive actions - Verification of Device History Record (DHR) and other controlled/uncontrolled documents as per defined intervals and Quality Plan - Reporting any deviations or discrepancies found in In-process activities, Finished goods, Packaging & labelling to the concerned persons/seniors - Following up on feedback for in-process and finished goods and updating the hold material register - Performing Line Clearance and First Part Approval for machines and packing - Conducting patrol inspections at regular intervals and random visual inspections for finished products - Ensuring AAMI test/Pull Test is carried out for every type of product manufactured and in compliance with the Quality Plan - Conducting pouch sealing tests and monitoring data - Verifying Master Device Record (MDR) tests and 15 days tests done in the shift - Timely verification of Product release reports - Maintaining all records as per the requirements - Providing training and skill development for QC inspectors - Coordinating with the marketing team for pre-dispatch inspections - Sending samples for microbiological testing as per schedule This job requires meticulous attention to detail, strong organizational skills, and the ability to communicate effectively with different teams within the company.,

As an Assistant Manager - Solution Consulting and Delivery, your role will involve planning and executing maintenance activities such as installation of sensors, breakdown maintenance, preventive maintenance, and condition-based monitoring. You will provide Condition Monitoring Engineering support to maintain equipment integrity for ensuring safety, reliability, and efficient operations. Your responsibilities will include dashboard monitoring and reporting, providing training to customers, working with customers at on-site locations, attending disconnection issues of sensors, routers, etc., and handling replacements of sensors, routers, SMPS, and Junction Boxes as required. Additionally, you will be involved in mapping equipment for the installation of sensors, Junction Boxes, and routers, and covering nearby plants whenever necessary. Key Responsibilities: - Plan and execute maintenance activities including installation, breakdown maintenance, preventive maintenance, and condition-based monitoring. - Provide Condition Monitoring Engineering support to maintain equipment integrity. - Monitor dashboards and generate reports. - Conduct training sessions for customers. - Work with customers at on-site locations. - Attend to disconnection issues of sensors, routers, etc., as needed. - Replace sensors, routers, SMPS, and Junction Boxes at the site. - Map equipment for the installation of sensors, Junction Boxes, and routers. - Provide support to nearby plants when required. Qualifications Required: - Good communication skills. - Electrical/mechanical maintenance knowledge. - BE in Mechanical/Electrical Engineering with 5 to 8 years of experience in condition monitoring. - On-site field experience in predictive maintenance & other CBM Techniques like Thermography, Ultrasound, Visual Inspection, etc. - Proficiency in working on computers (MS Office - Excel, Word, PowerPoint, Adobe Acrobat). - Willingness to travel to different sites across West India if required.,

Knowldge about visual Inspection Fresher Candidates Can Apply Benifits - PF, ESIC , Leave, Bonus ,Uniform & Accommodation Salary - 21k-CTC ,16k Inhand Contact Person- HR Vaibhav Varpe (7722027909) Work Location : Bhiwandi

Diploma in Mechanical Engineering and B.Tech fresher candidates can apply Benifits - PF, ESIC , Leave, Bonus , Canteen Salary - 21k-CTC ,16k (Inhand ) Contact Person- HR Vaibhav 7722027909

Fresher Candidates Can Apply (Bulk Hiring) Prefect location -Wasuli Chakan Benifits - PF, ESIC , Leave, Bonus ,Uniform & Canteen Salary - 22k-CTC ,16k Inhand Contact Person- HR Pradnya 8956344606

To perform cleaning of Visual inspection equipment in fill finish facility. To Perform visual inspection of Vials, PFS and Cartridge along with documentation. Making entries in log books, batch packing record, Audit readiness and status labeling. Required Candidate profile Only BSc (Chemistry or Bio) NO MSC. Experience 1-2 years Quality Inspections Industry Pharma, Biotech or any manufacturing Perks and benefits transportation, food, Health Insurance

To perform cleaning of Visual inspection equipment in fill finish facility. To Perform visual inspection of Vials, PFS and Cartridge along with documentation. Making entries in log books, batch packing record, Audit readiness and status labeling. Required Candidate profile BSc (Chemistry or Bio) Experience 1-2 years Quality Inspections Industry Pharma, Biotech or any manufacturing Perks and benefits transportation, food, Health Insurance

Job Role: Quality Inspection Engineer (FMCG) Qualification: Mechanical Degree & ASNT Level 2 Location: Pune Experience: 5 - 8 Years+ Salary: 50,000 - 70,000 1 Year further Extendable Contract on MMK payroll. Job Description Drawing review Material verification Welding visual inspection (required ASNT level II in Visual) DP test (required ASNT level II in DP) Dimension inspection good hands-on practice of instruments handling and reading. Pressure test/water fill up witness Agitator running trial witness Documentation- report preparation Experience of customer or third-party inspection handling during FAT. Interested candidates can share their resume on: recruiter4@kushalengineers.com Connect on: 022-41556171 Only WP: 8108797259

Role & responsibilities Looking after Packing activity and Visual Inspection. Primary and Secondary Packing exposure Preferred candidate profile Worked in Injectable, Parenteral, Oncology plants Worked in USFDA approved plant. Ready to relocate to banglore

final inspection , visual inspection

Role & responsibilities Sr. Executive Visual Inspection (and Packing) : JD : Preferably with 5 to 10 Years of experience in handling visual inspection activities @ reputed Pharma / Biotech companies ( preferably in Small volume injectables ) Should be expert in KIT preparation and Qualification of Visual inspector. Should be ready to work in A/B shifts regularly. Should have GMP Audit Exposures. Handling of Packing activities and will be an advantage.

Good knowledge in Visual Inspection & Gauge Inspection Ability to identy defects in Plastic Injection & Blow Moulding Shrinkage Sinkmark ExcessMaterialDamage Scratch mark Knowledge in handling measuring Instruments Vernier Non-conformance observation

You should have 2-5 years of experience with a background in Mechanical Engineering and possess a strong knowledge of Mechanical components, along with an interest in inspection and documentation. Your responsibilities will include conducting dimensional, visual, and functional inspections of mechanical components, assemblies, and products based on drawings, specifications, and standards. You will need to utilize measuring instruments such as Vernier calipers, micrometers, height gauges, and dial indicators. Additionally, you will be responsible for performing incoming inspections, verifying welding, machining, fabrication, and surface finish requirements, preparing and maintaining inspection reports, test records, and quality documentation, reporting non-conformities (NCR), and ensuring proper documentation of deviations. It is essential to maintain calibration records of measuring instruments used in inspection. The ideal candidate must have hands-on experience in inspection, basic knowledge of ERP, knowledge of SCAR, defects identification, RCCA, knowledge of MRB process, and proficiency in handling basic instruments like Vernier, micrometer, height gauge, bevel protractor, and bore gauge. The basic requirement for this position is a Diploma in Mechanical Engineering with 2-5 years of relevant experience.,

Dalmia Cement Bharat Ltd is looking for E&I Inspector to join our dynamic team and embark on a rewarding career journey Quality Inspection: Conduct inspections and audits of products, materials, components, or systems to verify conformance with established quality standards, specifications, and requirements Regulatory Compliance: Ensure compliance with applicable laws, regulations, codes, and industry standards governing product safety, environmental protection, occupational health, and consumer protection Documentation Review: Review documentation, records, and technical specifications related to inspected items or processes to confirm accuracy, completeness, and adherence to documentation requirements Physical Examination: Perform visual inspections, measurements, tests, and examinations of physical attributes, dimensions, and properties of inspected items using specialized tools, equipment, and instruments Sampling and Testing: Collect samples, specimens, or test specimens from production batches, lots, or shipments for laboratory analysis, testing, or further evaluation as per sampling plans and testing protocols Defect Identification: Identify and document defects, non-conformities, deviations, or discrepancies observed during inspections Classify defects based on severity, impact, and risk factors to determine appropriate corrective actions Root Cause Analysis: Investigate root causes of quality issues, failures, or discrepancies detected during inspections Analyze data, trends, and patterns to identify underlying problems and recommend preventive measures Corrective Action: Recommend corrective actions, preventive measures, and quality improvement initiatives to address identified issues, prevent recurrence, and enhance overall quality performance

Dalmia Bharat Group is looking for E&I Inspector to join our dynamic team and embark on a rewarding career journey Quality Inspection: Conduct inspections and audits of products, materials, components, or systems to verify conformance with established quality standards, specifications, and requirements Regulatory Compliance: Ensure compliance with applicable laws, regulations, codes, and industry standards governing product safety, environmental protection, occupational health, and consumer protection Documentation Review: Review documentation, records, and technical specifications related to inspected items or processes to confirm accuracy, completeness, and adherence to documentation requirements Physical Examination: Perform visual inspections, measurements, tests, and examinations of physical attributes, dimensions, and properties of inspected items using specialized tools, equipment, and instruments Sampling and Testing: Collect samples, specimens, or test specimens from production batches, lots, or shipments for laboratory analysis, testing, or further evaluation as per sampling plans and testing protocols Defect Identification: Identify and document defects, non-conformities, deviations, or discrepancies observed during inspections Classify defects based on severity, impact, and risk factors to determine appropriate corrective actions Root Cause Analysis: Investigate root causes of quality issues, failures, or discrepancies detected during inspections Analyze data, trends, and patterns to identify underlying problems and recommend preventive measures Corrective Action: Recommend corrective actions, preventive measures, and quality improvement initiatives to address identified issues, prevent recurrence, and enhance overall quality performance

Fresher Candidates Can Apply Benifits - PF, ESIC , Leave, Bonus ,Uniform & Accommodation Salary - 22k-CTC ,16k Inhand Contact Person- HR Pradnya 8956344606

final inspection , visual inspection ,handling the micro meter , vernier calliper

Final inspection , visual inspection

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job-you will find purpose and pride. To perform the cleaning and lubrication of machines regularly. To ensure that machines are working smoothly and performing as per standards. To ensure that the packing activities are being performed as defined in the Standard Operating Procedure (SOP) / Batch Packing Record (BPR). To check the status label of packing material prior to take material in packing line. To ensure status labeling to avoid mix-up. To ensure that the packing activities are not started without line clearance. To check & verify the rejection generated during packing are being handled as per SOP and resolve the problem immediately. To ask questions frequently to the workers regarding productivity and quality, to make them updates with GMP. To ensure that after any break down or maintenance, no machine is taken in operation without clearance from QA. To ensure the GMP norms are followed and maintained throughout the packing. To train personnel for the critical operations like visual inspection and labeling. To perform operations like cleaning of packaging equipment, documentation of area, area clearance, line clearance, Status board update. To ensure safety features of all machine is working properly & peoples are using respective personal protective equipment during operation. To follow Standard Operating Procedure (SOP) during entry and exit to plant. To follow the SOP and guide the workers for the same. Administrative: Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our .

Responsibilities Conduct inspections and quality checks for printing and packaging materials. Monitor production processes to ensure adherence to quality standards. Identify, document, and resolve quality issues by collaborating with production and design teams. Implement corrective and preventive measures to reduce errors and improve efficiency. Maintain accurate records of inspections, audits, and test reports. Ensure compliance with internal and external quality requirements.

Role & responsibilities Department - Packing (FP) Assistant Manager Job Discription: Labelling & packing, SAP compliance, Visual inspection, QMS, SOP, MPR and BPR, cGMP Regulatory and non-regulatory audits Qualification: B.Sc/ B.Pharm/ M.Sc/ M.Pharmacy Experience: 8 - 15 years Job Description: Labeling & Packing activities, Equipment operation, SOP cGMP, Operator / Sr.Operator / Jr. Executive / Executive Qualification ITI/Diploma/B.Sc /B.Pharm /M.Sc /M.Pharmacy Experience: 2 - 8 years Preferred candidate profile

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing & Visual Inspection & Packing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspection / Packing / VI (Senior Officer / Officer / Associate) Experience - 02 to 07 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech Time and Venue : 06/09/25, Saturday 09:30 Hrs to 18:00 Hrs ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. *Having relevant qualification only can attend the scheduled walk-in.