19 Line Clearance Jobs

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 materials, preventive and breakdown maintenance, as well as working on CAPA to reduce quality defects will be part of your responsibilities. Ensuring shift production targets, ISO compliance, production reconciliation, and adherence to safety practices to achieve zero accidents/incidents are essential aspects of the role. Maintaining 5S and housekeeping standards in accordance with company GMP guidelines will also be a key responsibility. This is a full-time, permanent position with benefits including food provision, health insurance, leave encashment, life insurance, paid sick time, and Provident Fund. The work schedule involves rotational shifts and includes a yearly bonus. The work location is in Pithampur, Madhya Pradesh, and reliable commuting or relocation is preferred. The ideal candidate should have at least a Higher Secondary (12th Pass) education and a minimum of 5 years of experience in baby diaper machine operation. If you are detail-oriented, proactive, and have a strong background in machine operation, this role offers an opportunity to contribute to the efficient production processes and quality standards of the company.,

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 will also be part of your responsibilities. This is a full-time, permanent position with benefits such as internet reimbursement, leave encashment, and paid sick time. The work schedule will be during the morning shift. A background in pharmaceuticals or herbal medicine is preferred, and a Bachelor's degree is preferred for this role. The work location will be in person.,

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 certificates, issuance and archival of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR), preparation of Annual Product Quality Review (APQR), line clearance for manufacturing, packing, and dispensing activities, sampling of bulk and finished goods, and review of production records. Furthermore, you will play a key role in managing change controls, deviations, and CAPA (Corrective and Preventive Actions), conducting complaint handling, updating departmental SOPs, providing training as per schedule, coordinating training programs with HR, and ensuring documentation management as per SOP. You will also be responsible for providing necessary documents/data to meet internal and external quality, environmental, health, and safety requirements. Moreover, you will be involved in compliance monitoring through self-inspection programs, audit compliance coordination, preparation of responses to audit reports, and execution of food/dietary supplements regulations for export markets. You will also oversee the implementation of sanitation programs, adherence to EHS norms, and various corporate initiatives. Piramal Group values equal employment opportunity, ensuring that all applicants and employees are treated fairly based on merit, qualifications, skills, and performance. As part of a globally integrated network of facilities, Piramal Pharma Solutions offers a wide range of services across the drug life cycle, making it a trusted partner for innovators and generic companies worldwide.,

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. Responsible to perform Acceptance Quality Limit and Pre Dispatch Inspection of finished product. Responsible for preparation of Annual Product Quality Review. Responsible to maintain the document as per current Good Manufacturing Practices. Responsible to initiate Change control\Deviation\Incident\Market complaint\non-conformance investigation. To assist the Head of Department for preparation of regulatory inspection. Any other responsibility assigned by Head of Department. Quality Management System:- 1. To coordinate with cross functional department for execution of training planners and maintain training record for same. 2. To master, issue and retrieve of SOPs/BMR/BPR/QC dockets and other documents in-line with the laid down procedure. 3. To maintain vendor related documents and conduct vendor audits. 4. To investigate and prepare Market Complaint investigation report. 5. To take follow up and communicate with customer/vendor regarding Complaint. 6. To handle Change control/Deviations/Incidents/NCR/CAPA. 7. Review of quality technical agreements.

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 operations, Clean-in-Place (CIP), and Steam-in-Place (SIP) of Vessel operations will be under your responsibility. You will operate specific machinery such as the Manufacturing Vessel and CIP module. It is crucial that you promptly report any observations or disturbances in the aseptic area to the relevant supervisor. Maintaining personal hygiene, cleanliness, and following SOPs while documenting all activities within the area will be essential tasks. Furthermore, you must ensure that the Unit Area File (UAF) is up to date and operational within the designated area. Compliance with current Good Manufacturing Practices (cGMP), Good Documentation Practices, and maintaining discipline within the department are also key aspects of this role. Qualifications: - Qualification Requirement: ITI/ Diploma in Mechanical Engineering - Experience: 3-6 years - Skilled Operator needed for CIP & SIP of Vessel, Filter integrity checks, and Batch manufacturing activities - Prior experience in the aseptic area for Manufacturing Injectable Products is preferred If you meet the qualifications and possess the necessary skills, we encourage you to apply for this position and contribute to our manufacturing operations effectively.,

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. This is a full-time, permanent position with benefits such as internet reimbursement, leave encashment, and paid sick time. The work schedule is during the morning shift. A background in pharmaceuticals or herbal medicine is preferred for this role. A Bachelor's degree is preferred for this position. The work location is in person.,

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 and functional tests on line clearance samples, and promptly documenting test results for timely decision-making and communication. In addition, you will be required to provide line clearance reference samples and first shot approvals to the machine operator, conduct visual inspections and testing of finished goods according to approved sampling plans, and make decisions in alignment with applicable Acceptable Quality Levels (AQLs), with all results accurately recorded in the relevant forms. Identifying non-conforming products, blocking them in the Alpla production system, updating the Non-Conformance Report (NCP) tracker, monitoring rework activities, sampling, inspection, and documenting results will also be part of your duties. You will perform functional testing as per the specified frequency, make decisions based on the outcomes, and document the results accordingly. Moreover, as a detail-oriented professional, you will conduct dimension inspections of products as per the approved sampling plan, make decisions in line with the applicable AQLs, and document the results accurately. You will also be responsible for managing and maintaining monitoring and measuring equipment by performing internal calibrations of laboratory equipment as per the required schedule. Working with us, you can expect a range of benefits including free transportation, a positive working culture, a clear growth path, subsidized canteen meals, free uniforms, provided personal protective equipment (PPE), on-time salary disbursement, national and festival holidays, various celebrations, and opportunities for continuous training and development.,

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 creating production plans on a monthly and daily basis according to material availability. Handling tasks such as change control, deviations, CAPA, investigations, and document management including BMRs, BPRs, and master SOPs will be part of your duties. You will also be involved in the preparation, review, revision, control, and implementation of standard operating procedures within the sterile manufacturing department. Conducting line clearance activities before commencing various operations such as manufacturing, sterilization, and filling, as well as checking and maintaining records and logbooks related to manufacturing processes, garment washing, drying, and equipment sterilization are key aspects of your role. Additionally, you will be required to perform any activities as instructed by the HOD, provide training to subordinates, technicians, and operators, and stay updated on self-hygiene practices. Attending training sessions as per the schedule and ensuring compliance with the Training Need Identification (TNI) will also be part of your responsibilities. Qualifications required for this role include M.Sc., B.Pharm, or M.Pharm degree.,

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/BPRs (Batch Production Records) as per regulatory standards. Coordinate with QA, QC, maintenance, and warehouse departments to ensure smooth workflow. Support validation activities, including equipment qualification and process validation.

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 finance Lead GMP, HACCP, and FSSAI audit readiness efforts Coordinate fire safety drills, hygiene inspections, and corrective action Preferred Candidate Profile: 5 -10 years in FMCG, food production, or confectionery Proficient in HACCP, FSSAI guidelines, and FoSTaC Strong recordkeeping and documentation mindset Proficient in Telugu, Hindi. Experience in managing audits and lab instruments

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 timely sampling/testing of In-process, reserve, and finished samples and stability samples/environmental monitoring. • You will be responsible for coordination in cleaning validation, performing sampling and compliance. • You will implement and comply with Technology Transfer and initiation of exhibit batches. • You will review batch manufacturing and batch packing records and certification of the same after execution. educational qualification: A Bachelors degree in Pharmacy, Chemistry, Chemical Engineering, or a related field Minimum work experience : 4 to 7 years of experience in pharmaceutical manufacturing or a similar role Technical Skills • Knowledge of microbiology and aseptic practices, cleaning validation activities, sampling and relevant standards. • Proficiency in performing line clearance, material verification, start-up checks, and in-process checks following batch manufacturing and packing records. • Experience in timely sampling and testing of in-process, reserve, and finished samples, as well as stability samples and environmental monitoring. • Skilled in reviewing batch manufacturing and batch packing records, ensuring accuracy and certification after execution. Behavioral Skills • Attention to detail in performing line clearance, verification, and record reviews. • Skilled in time management and coordination for sampling, testing, and execution of batch manufacturing and packing activities. • Communicates effectively with team members and stakeholders regarding batch-related activities and compliance. • Applies problem-solving skills in addressing issues related to line clearance, sampling, and record certification. • Demonstrates a focus on maintaining high-quality standards and adhering to regulatory compliances in manufacturing processes.

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 cell. 1.8 To prepare lists of documents retrieved from all departments and documents available in QA document. 1.9 Stamp management and maintaining properly under lock and key. 1.10 To arrange and label the files in QA document cell. 1.11 Preparation, coordination, and execution of vendor audit. 2.0 Secondary Responsibility: 2.1 Supporting the regulatory department for licensing activities 2.2 Issuance and retrieval of daily and monthly documents. 2.3 Controlling & distribution of the new SOPs to the respective departments, retrieving and destruction of the old-controlled copies of documents/ SOP's 2.4 Responsible for undergoing training in BGL policies and following BGL policies. Preferred candidate profile 3.0 Knowledge and skill set: 3.1 Effective communication skills and Good at Microsoft document editing 3.2 Ability to manage cross functional departments 3.3 Good in handling documentation

Outlines quality assurance procedures and policies Oversees implementation of quality assurance procedures Ensures the efficiency of inspections through hands-on guidance Ensures data integrity and accuracy Prepares reports on the results of quality inspections Evaluates outcomes of quality inspections and proposes corrective measures. Preferred skills : IPQA, Line clearance, BMR/BPR preparation and & Exposure in review Qualification of equipment and HVAC (DQ, IQ, OQ, PQ) Process validation, Protocol preparation and review Documentation, Change Control, deviation, Market Complaint, CAPA, etc.

Online documentation checking in plants to check the compliance of SOP's and to conduct random audits in different manufacturing blocks. To check the adherence to the Quality Management System (QMS) elements, such as change control, incident management, and CAPA (Corrective and Preventive Actions) management on the shop floor. Verification of online filling of BPR/BMR Responsible for conducting line clearance in manufacturing facilities. To verify whether the manufacturing facility always meets basic Good Manufacturing Practice (GMP) requirements, including facility upkeep, environmental conditions, segregation of materials, and status labeling. To verify that manufacturing activities i.e.sampling activities, charging/discharging of material to/from the equipment, weighing balance calibration/verification, cleaning of equipment (PCO and periodic cleaning), powder processing activities and other GMP related activities are being performed as per established procedures. Verification during process validation and Equipment Qualification activities.

A. Job Objective Monitor and review In Process quality control checks to meet the required quality compliance as per specifications. Strategic and planning Functional Core:- Review and provide decision based on the IQC sheet Online feedback to production for correction Daily plant round for ensuring compliance of SOPs, GDP, GMP guidelines etc. on the shop floor Refer ZMIC for special instruction during color change/ product change and guide the IQC operator for the same. Review the implementation of the same. Monitoring CAPA during shifts. Investigation of internal stranger/failure to identify the Root cause analysis and take corrective/preventive action for the same. Track instance of repeat failure from operators and take measures/set processes to avoid re-occurrence of the same and to ensure FTR. Line clearance of camera inspections, HCM, ATS, printing machines and Final Inspection System Ensuring document verification generated during shift on daily basis against defined standards Internal process Preparation of various reports Maintenance and verification of gauges to ensure proper calibration of these equipments on a regular basis in each shift Ensure verification of shade against master and Macbeth report Verification of daily profiles and online graphs Periodically conduct process, product and systems Audit. To provide data for annual product quality review & Participate in APQR and finalise the recommender's People development Ensure proper manning and shift handling, shift activities. Effective training to the operators with evaluation for compliance. Effective manning to utilization of available sources.

Exciting opportunity for IPQA Executive at our EU approved OSD Manufacturing faculity (UNIT 1) @ Moraiya, Ahmedabad!! Company : Unison Pharmaceuticals Pvt Ltd Website : www.unisonpharmaceuticals.com Location : UNIT 1 , Moraiya, Ahmedabad Experience : 4 - 9 Years Dept. & Sub Dept. : QA - IPQA - OSD MFG Designation : Executive Job description (Not limited to): Collect in-process and Finished sample as per Specifications and Protocol. Check documents like equipment log books, temperature & humidity records. Line clearance of machine & manufacturing area . Checking of batch manufacturing record. Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position. Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career.

Role & responsibilities We are looking for candidate on below criteria at our Nalagarh Plant Himachal Pradesh location. Candidate must have completed Pharma, M.Sc. or B.Sc. in Chemistry. Experience of regulatory industry would be preferred. Candidate should have 1-3 years of working experience Preferred candidate profile Responsible for Line clearance in Warehouse and Production area during dispensing, MFG, Filling and Packing & review of log books and status label of each equipments before start of activity. Responsible to carry out in-process checks as per respective Batch Production Record in Manufacturing, packing and warehouse. To ensure that the manufacturing and packing operations are carried out as per the instructions given in the Batch Production Record. Responsible for collection of in-process samples, FP sample, control samples, validation & stability samples. Responsible to make SAP entries, Release of inspection lot of SFG & FG, Physical sampling confirmation, Approval of Batch Production Records for printing and additional page issuance. Responsible for online review of Batch Production record and make entry of data required for trending in maintained excel sheet for preparation of APQR. Responsible for Line clearance in Warehouse and Production area during dispensing, MFG, Filling and Packing & review of log books and status label of each equipment’s before start of activity. Responsible to carry out in-process checks as per respective Batch Production Record in Manufacturing, packing and warehouse. To ensure that the manufacturing and packing operations are carried out as per the instructions given in the Batch Production Record. Responsible for collection of in-process samples, FP sample, control samples, validation & stability samples. Responsible to make SAP entries, Release of inspection lot of SFG & FG, Physical sampling confirmation, Approval of Batch Production Records for printing and additional page issuance. Responsible for online review of Batch Production record and make entry of data required for trending in maintained excel sheet for preparation of APQR. Perks and benefits