57 Line Clearance Jobs - Page 2

Role & responsibilities Solid Oral - Production & Packing Officer - Executive and Plant Operator - Technical Assistant : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Tablet/ Capsule - Blister Line (BQS), CVC Bottle Line Warehouse (Supervisor / Machine Operator): Officer Senior Executive and Plant Operator - Technical Assistant: RM, PM, FG, Dispensing, Dispatch , Documentation Engineering Executive/Sr. Executive: Process Equipment (Mechanical/Electrical/Instrumentation) of OSD Plant like preventive maintenance and breakdown related activities of equipment of OSD plant such as FBD, FBP, RMG, coating, compression, capsule, Packing machine ...

Role & responsibilities Solid Oral - Production & Packing Officer - Executive and Plant Operator - Technical Assistant : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Tablet/ Capsule - Blister Line (BQS), CVC Bottle Line Warehouse (Supervisor / Machine Operator): Officer Senior Executive and Plant Operator - Technical Assistant: RM, PM, FG, Dispensing, Dispatch , Documentation Engineering Executive/Sr. Executive: Process Equipment (Mechanical/Electrical/Instrumentation) of OSD Plant like preventive maintenance and breakdown related activities of equipment of OSD plant such as FBD, FBP, RMG, coating, compression, capsule, Packing machine ...

Walk-in Drive in Chandigarh for the Quality department for Baxter Ahmedabad (Injectable) plant. We are a team of motivated employees who value the importance of our mission. No matter our role, each of us understands and connects deeply to this commitment. #nowhiring experienced Quality professionals (Quality control, Microbiology, IPQA, Validation) with expertise in the injectable manufacturing facility. Department: Quality control lab Experience: 2 to 7 years Qualification: M.Sc or B.Pharm or M.Pharm Role: QC Analyst Analysis RM, PM, FP, IP, GLP and stability QMS investigation, OOS, OOT, Incident, deviation, CAPA, deviation, etc., Instruments HPLC, GC, KF, UV, IR, etc., Department: QA QMS ...

1. QA Executive Junior Level Experience Required: 24 years Salary Offered: 20,000 per month Job Summary: We are seeking motivated QA Executives with 24 years of experience to support daily quality assurance activities in a GMP-regulated pharmaceutical facility. The role will focus on documentation review, QA activities, and ensuring compliance with regulatory standards. Key Responsibilities: Review batch manufacturing and packing records Line clearance for production and packaging activities Support in handling deviations, change controls, CAPA, and incident reports Ensure compliance with cGMP and Revised Schedule M requirements Participate in in-process checks and quality monitoring Assist ...

The job involves operating machines, cleaning and sanitizing the visual inspection and packing area, handling all packing-related activities, maintaining logs as per SOP, attending training sessions as per schedule, following the preventive maintenance schedule of machines, reporting any issues to the supervisor, ensuring compliance with cGMP, Good Document Practice, and departmental discipline, and performing line clearance activities before starting operations. Candidates should have an educational background of ITI/Diploma/Graduation and possess 2 to 7 years of experience in the manufacturing/packing department of sterile manufacturing.,

You will be responsible for conducting line clearance activities before starting various operations such as dispensing, manufacturing, filling, inspection, sealing, labeling, and packing. Additionally, you will perform environment monitoring activities and ensure compliance with cGMP at the shop floor. Your role will involve process validation, cleaning validation/verification, hold time study, media fill, routine batch sampling, and in-process testing at different stages according to batch documents and SOPs. You will review executed BMRs, BPRs, environment monitoring data, water trends, printouts (CIP, SIP, autoclave, filter integrity), and different types of planner and calibration certif...

Job Title: Quality Assurance Officers (4 Positions) Company: Nourish Pharmaceutical Pvt Ltd Location: Kheda, Gujarat Job Type: Full-time Nourish Pharmaceutical Pvt Ltd is a leading pharmaceutical company committed to delivering high-quality products. We're expanding our Quality Assurance team and looking for talented professionals to join us. Positions: 1. Quality Assurance Officer - Production 2. Quality Assurance Officer - QMS 3. Quality Assurance Officer - Validation & Qualification 4. Quality Assurance Document Control Officer Job Descriptions: 1. Quality Assurance Officer - Production - Key Responsibilities: - Ensure cGMP compliance in production areas - Manage and review Batch Manufact...

We are a team of motivated employees who value the importance of our mission. No matter our role, each of us understands and connects deeply to this commitment. Hiring experienced Injectable business with expertise in Engineering and QA of the injectable manufacturing facility. Job Location: Ahmedabad Business: Quality Assurance Education: M.Pharm/M.Sc/B.Pharm/M.Pharm 1) Position: Associate, QA IPQA Experience: 3 to 8 Years Key skills: IPQA, line clearance, batch record review, in-process quality check, sampling, etc., 2) Position: Associate, QA Doc cell Experience: 3 to 8 Years Key skills: Doc control management, document and logbook issuance & retrieval, record management, CCM management, ...

To ensure cGMP compliance at facility. Responsible for online documentation, online data filling. Ensure the compliance of CAPA related to online observations Review of NQI, ensure the CAPA & closure of same Responsible for line clearance for product changeover of Powder processing area To fill the customer questionnaire & collect supportive documents Show more Show less

We are seeking skilled and dedicated individuals to join our Quality Assurance (QA) department at Fido Pharma Private Limited, an esteemed pharmaceutical company located at Plot No: 108-109, Global Industrial Park, Mauli, Barwala, Panchkula, Haryana. If you have a background in B.Pharm / M.Pharm / M.Sc. and a passion for ensuring quality in pharmaceutical products, we have the following positions available: QA Manager: As a QA Manager, you will lead our Quality Assurance department, overseeing adherence to GMP and regulatory guidelines such as EU-GMP and WHO-GMP. Your responsibilities will include managing document control, validations, change control, Vendor Qualification, CAPA, deviations,...

You will be responsible for ensuring line clearance at the start-up of the tablet section, including compression, coating, and capsule filling sections. Additionally, you will be in charge of maintaining logbooks for the Tablet section, manufacturing area, and grinding section. In-process sampling of tablets and final sampling of tablets will also fall under your responsibilities. You will be tasked with conducting online reviews of Batch Production Records (BPR) for Tablet, Capsule, and Jawkut sections. Monitoring the environmental conditions in the respective operational areas will be crucial. Issuing tablet excipients and empty capsules, as well as checking the online parameters of Tablet...

You will be responsible for ensuring optimum asset utilization and maximum production efficiency while minimizing wastage. Your duties will include maintaining the basic standard condition of machines to ensure smooth running of processes and adherence to product quality standards. Additionally, you will be required to complete line clearance after every grade/size change and operate assets at target speeds. Continuous monitoring and adjustment of processes based on observations and feedback from Quality will be crucial to your role. You will also be responsible for achieving production targets, maintaining product quality parameters, and waste reduction. Efficient utilization of raw materia...

You will be responsible for ensuring line clearance for the start-up of the tablet section including compression, coating, and capsule filling areas. Additionally, you will be in charge of accurately filling logbooks for the Tablet section, manufacturing area, and grinding section. Your duties will also include conducting in-process sampling of tablets and final sampling, as well as carrying out online reviews of Batch Production Records (BPR) for Tablet, Capsule, and Jawkut sections. Monitoring environmental conditions in the respective operational areas will be another key aspect of your role. Issuing tablet excipients and empty capsules and checking online parameters of Tablet and Capsule...

As a Validation Specialist at Piramal Pharma Solutions, your primary responsibility will involve preparing and updating various validation documents to ensure compliance with regulatory requirements. This includes developing Validation Master Plans (VMP), Process Validation protocols, Computer System Validation protocols, and reports. You will also be responsible for creating product matrices, Cleaning Validation/Verification protocols, qualification/requalification protocols for equipment/instruments, utilities, and facilities, as well as area validation protocols and reports. In addition to validation activities, you will be involved in quality risk assessments, review of calibration certi...

Role & responsibilities IPQA:- Responsible for line clearance and in process checks of Production. Responsible for Sampling of in-process, Finished Product, control samples, stability samples, and Process Validation samples as per procedure. To ensure online rejection activities and environment monitoring in manufacturing and packaging areas. To conduct periodical log review. To review of batch documents (Batch Manufacturing, Batch Packaging records, and Quality Control analysis data of the batch). To ensure online documentation during manufacturing and packaging area. To prepare and review of Quality Assurance Standard Operating Procedures. To ensure Re-processing and Re-packing activity. R...

As a Manufacturing Operator, you will be responsible for attending training sessions according to the schedule and ensuring that you apply the knowledge gained in Training Needs Identification (TNI). Your primary duties will include monitoring and performing all activities within the Manufacturing area, maintaining logs, Batch Manufacturing Records (BMRs), and other relevant documents as per Standard Operating Procedures (SOPs) and work instructions. Additionally, you will be in charge of adhering to the preventive maintenance schedule for machinery, instruments, and equipment in the manufacturing area, as well as overseeing their cleaning and sanitization. Line clearance activities before o...

You will be responsible for ensuring line clearance for the start-up of the tablet section, including compression, coating, and capsule filling sections. Additionally, you will be in charge of filling logbooks for the Tablet section, manufacturing area, and grinding section. Your duties will also include in-process sampling of tablets and final sampling of tablets. You will be required to conduct online reviews of BPR for Tablet, Capsule, and Jawkut sections. Monitoring environmental conditions in the respective operational areas is a key part of the role. Issuing tablet excipients and empty capsules and checking online parameters of Tablet and Capsule are also among your responsibilities. T...

As a Line Clearance Specialist, you will play a crucial role in ensuring the effective verification of job orders for correct resin, MB grade, packing quantity, product code, and customer details. Your responsibilities will include verifying the cleanliness and readiness of the machine and surrounding areas, ensuring compliance with FSMS requirements by removing any dust, dirt, oil, grease, loose nuts, bolts, and tools. Furthermore, you will be tasked with clearing the machine area of previous run documents, samples, raw materials, masterbatches, and regrind materials. It will be your responsibility to confirm the error-proofing mechanisms on the machine are operational, conducting visual an...

You will be responsible for performing line clearance activities before commencing operations, ensuring a clean and sanitized visual inspection and Packing area, and following the preventive maintenance schedule of machines. Operating the machines efficiently and filling the log of general areas as per SOP and work execution will also be part of your responsibilities. It is essential to adhere to cGMP, GDP, and maintain discipline in the department while ensuring that all employees comply with the same standards. Your role will involve ensuring that all equipment and production lines are in validated and calibrated status, preparing daily production reports based on achieved targets, and cre...

Role & responsibilities To take plant round and monitor production activities at shop floor. To prepare appropriate Quality related documents like SOP, BMR, BCR, BPR etc. To review BMRs, BCRs, and analysis records before release of API. To perform sampling of API's and maintain its records. To maintain control samples of API and its records. To perform and ensure the cleaning of sampling tools. To provide line clearance at the time of product changes over. To review dispatch of finished product and maintain record for the same. To Investigate the deviations identified in co-ordination with QA-Head/Designee. Product quality review of API Process and cleaning validation monitoring in plant

Carry out manufacturing activities as per Batch Manufacturing Records (BMR) and SOPs. Monitor and control production parameters to meet quality and output targets. Ensure timely completion of batches to meet production schedules. Ensure adherence to current Good Manufacturing Practices (cGMP) and company policies. Report and document any deviations, incidents, or abnormalities during production. Operate, clean, and maintain manufacturing equipment (e.g., granulators, blenders, tablet compression machines, filling machines). Perform line clearance, changeovers, and cleaning as per SOPs. Maintain accurate and timely records of all production activities. Fill out logbooks, checklists, and BMRs/...

Oversee line clearance , in-process sampling, and real-time review of batch manufacturing & packaging records (BMR/BPR) Monitor critical process parameters (e.g., weight variation, leak tests), hygiene, documentation, calibration, and equipment qualification Lead investigations for deviations, OOS/OOT results, non-conformities; drive CAPA and root cause analysis Approve/reject batches, handle change-controls and disposals, and manage legal/retention samples Support and participate in internal, external, and regulatory audits/inspections ; ensure audit readiness Prepare, review, and maintain SOPs, protocols (validation, cleaning, process), quality documentation, and MIS reporting

Role & Responsibilities: Physically verify raw materials and packaging per COA and MRN documentation Conduct routine checks on FG and SFG for pH, moisture, content, density Supervise personnel hygiene and ensure compliance with safety protocols Maintain calibration records for lab instruments Conduct pest inspections and ensure hygienic conditions Support R&D trials for quality improvements in FMCG products Perform shelf-life tracking and stock audits Ensure FoSTaC certification and food handler medical checks Follow up on market complaints and escalate quality issues Verify new packaging designs for compliance and legibility Maintain BOMs with Accounting for alignment with production and fi...

Role & responsibilities J ob Summary We are seeking an individual for the Quality Assurance team, responsible for ensuring line clearance, material verification, and conducting in-process checks according to batch manufacturing and packing records. The role includes timely sampling/testing, coordination in cleaning validation, and ensuring compliance with technology transfer and exhibit batches, including the review and certification of batch records. Roles & Responsibilities • You will be responsible for performing line clearance, material verification, start-up checks and in-process checks as per the batch manufacturing record, and batch packing record. • You will be responsible for the ti...

1.0 Key or Primary Responsibility: Role & responsibilities 1.1 Line clearance for dispensing raw materials and manufacturing activities 1.2 Document issuance, distribution, retrieval, retention, and management 1.3 In process quality check for drug substance packing process 1.4 Distribution of SOPs, controlled copies of required documents to respective departments. 1.5 Coordination and timely completion of work as per management instruction. 1.6 To make documents controlled, uncontrolled, issuance, obsolete, execution and reference copies whenever required and update the tracking sheets as well. 1.7 To retrieve the executed documents from all departments and filing properly in QA document cel...