123 Gmp Compliance Jobs - Page 4

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Job Title: Officer/Senior Officer Location: Ankleshwar Experience: 2-5 Year Department: Production Role and Responsibilities: Production Operations Check labels and verify identity of raw materials, packing materials, and solvents before use. Maintain appropriate storage conditions for raw materials and intermediates in the plant. Execute batch processes as per approved Batch Production Records (BPRs). Follow instructions from Shift In-charge or Production Manager for batch charging and monitoring. Monitor and maintain process parameters during manufacturing. Complete allocated tasks within the stipulated timeline with accuracy. Ensure contamination-free production and proper packing/repacking of materials. Adhere to proper gowning, hygiene, and entry protocols for classified production areas. Operate plant equipment and utilities safely and efficiently. Maintain cleanliness and proper segregation in the production area as per SOP. Documentation & SAP & GDP Perform online documentation of BPRs, cleaning logs, and equipment usage records during the shift. Maintain differential pressure, centrifuge bag records, and other PP/Intermediate area logs. Update SAP transactions for material consumption, yield recording, and inventory movements. Ensure timely entries in equipment logbooks and SAP-based process entries . Label all process equipment, HDPE/fiber drums, and accessories correctly per batch and SOP requirements. Ensure Good Documentation Practices (GDP) by making real-time, legible, complete, and traceable entries in all logs and records. GMP & Compliance Guide and train workmen on cGMP practices and technical SOPs. Ensure finished product yield and quality meet predefined specifications. Participate in internal audits, regulatory inspections, and SOP reviews. Perform calibration of instruments such as weighing balances and pH meters. Keep equipment status boards updated and follow QMS standards. Safety & Environmental Compliance Understand MSDS of all materials handled and ensure safe handling practices. Supervise plant operators to ensure chemical and equipment handling safety. Use scrubbers and proper exhaust systems to control emissions and avoid air pollution. Coordinate with the EHS department for required safety permits and compliance. Wastage Reduction Prevent solvent/material spillage and reduce wastage through proper process control. Ensure utilities (valves, pumps) are turned off when not in use to conserve resources. Cross-Functional Coordination Coordinate with QC for sample analysis and batch release. Liaise with engineering for breakdown and preventive maintenance activities during shift. Work closely with Warehouse, QA, and EHS departments for smooth operations. Interested candidate can share there cv at meet.chauhan@cadilapharma.com .

Roles & Responsibilities: Daily R.M. /P.M. planning and issuing as per production schedule. Manpower allotment in shifts and to give and take proper shift charge from reliever. To review BMR, BCR, documents and to submit to QA. To check the processing is being done as per instructions written in BMR. To report any kind of deviation/abnormal incident to HOD immediately. To ensure safety, GMP, discipline & housekeeping in plant. To ensure that all production related documents are filled on line & accurately. To give training to subordinates, prepare and maintain training related all activity and documents. To prepare, issue and submit all documents like BMR, BCR, SOP etc. as draft for production processes and to get approval from QA. To ensure that all persons working in plant are fit as per predetermined fitness criteria. To report any kind of maintenance job immediately & ensure completion of it. To ensure that equipment cleaning is done as per schedule and ensures approval of QA to cleaning after completion of campaign before starting the next campaign. To ensure process related deviation, CAPA, change control to QA and get it documented To ensure that sampling of finished product is done and the same is transferred to ware house after approval. To ensure the quality & yield of batches within acceptable limits. To ensure tracking of department objectives & take actions accordingly. To ensure PSD and complete analysis results and pack final material as per customer requirements. To ensure the process and cleaning validation is done as per schedule. Ensure that all work relevant to his area is carried out under his supervision in Accordance with company procedures as regards Safety, Health and Environmental protection. To perform the internal audit and prepared the audit report. Desired Candidate Profile: Experience: 8-10 years of experience in pharmaceutical industry with expertise in Batch Manufacturing Records, Continuous Improvement, Documentation & Reporting, Gmp Compliance, Regulatory Compliance. Qualification: Bachelor's degree in Chemistry (B.Sc)& Master's degree in Science (MS/M.Sc) Job Location: Boisar (Tarapur).

QA Head Seeking a QA Head to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 4+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to train & improve Jr.

Ensure machine availability to production to achieve monthly production targets. Ensure effective preventive maintenance programme to minimize machine breakdowns and to increase machine operational time. Ensure that highest standards of safety are being followed for all engineering related activities Support the cross functional teams for specific projects and activities like Lean Management, validation activities etc. at site. To raise Change Requests, Planned Deviations and Exceptions in system. To track and complete all QMS (Quality Management System) related activities. To verify all records related to QMS activities. To ensure that best Engineering & GMP practices are being followed while executing all engineering related work. Documentation preparation and maintenance as per QA / cGMP guidelines and Engineering Standards To ensure that facility is maintained as per cGMP requirements. To execute work assigned by the superiors on timely basis Government related formalities compliance for Metrology Department (Weight & Measures and Stamping). Raising RCEs (Request For Capital Expenditures) for various projects and equipment s and to monitor cost tracking for same. To follow all Engineering related SOP s and ensure that all records are updated accordingly. To update CO2 and Envision data required for Senior Management team. To maintain spares of machines pertaining to liquid section. To handle all responsibilities in Manufacturing and Utility blocks, while working in shifts. To provide support during c HVAC validation activity. To handle all job responsibilities in absence of Mr. Suraj Naik. To provide technical support for instrumentation related activities of entire plant Leading DMS (Daily Management System) meeting for daily work planning Tracking of Opex (Operational Expenses) for Engineering Department. To deliver the training at site on GMP topics, SOPs and other technical topics.

Role & responsibilities : ISO 9001/ISO 13485. Manage the Quality Management System. To provide QA support in all quality related matters and to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements. Risk Management & CAPA. Establishing procedures and records as per requirement of standards and regulatory authorities. Responsible for establishing, managing, and implementing Records Management policy, Records. Retention and retrieval procedures are in place. To manage and execute internal and external audit schedules and follow up on action plan, Quality Auditing of External suppliers - maintain an annual auditing program. Regular Internal Quality Audit and maintain the company anytime audit ready. Participate in and/or lead audits, manage action plans and follow up on agreed upon CAPAs & NCs. To monitor & handle market complaints. Conduct Management review at site. Conduct Calibration of instrument & Maintain Calibration Matrix . Ensure that a respective Change Control procedure is in place and adhered to . Process validation protocol preparation & implementation. Provide leadership and expertise on all aspects of product regulatory compliance to ensure that products are successfully introduced and maintained domestically and globally pursuant to regulatory compliance. Must be capable to handle all types of Audit. To Lead and face the regulatory audits and close all queries and NC in stipulated time. To maintain all documents related to compliances. Create Maintain & update Device Master/ Product Technical File. Preferred candidate profile: Graduate in Science or Engineering . Post Graduation preferred. Thorough Experience in quality and regulatory areas. Thorough experience in ISO 13485, GMP, US FDA, EU MDR, CDSCO, ISO 9001. Regulatory functions throughout the organization including monitoring , improvement , audits, and team building. Thoroughly conversant with technical documentation requirement and preparation. Excellent MS office skills. Should have faced multiple audits from multiple agencies Should have thorough knowledge of the applicable standards Perks and benefits: Medical Insurance for Spouse , 2 Kids Below 18 years upto Rs. 3lac.

Roles & Responsibilities: Associate Manager Responsible for shift activities Responsible for extension of method Validation/ transfer Responsible for review of the analytical report Responsible on need basis in line with the requirements day to day basis Senior Executive Responsible for analysis of Raw Material In process, Intermediate finished Products using GCP, HPLC, IR, Potentiometric Responsible for calibrations, WS Generation and lab readiness for audits Responsible for GMP/GLP procedure in QC Lab Executive Hands on Experience on Trouble Shooting Knowledge in PH Meter/KF/ Potentiometric Exposure in Regulatory audits Good Documentation practice Preferred candidate profile Male Candidate with M.Sc Chemistry background and having strong Understanding of GMP /GLP procedure in QC Lab Hands on experience in HPLC/GC/IR Regulatory Exposure Immediate joiners are preferred Perks and benefits As per Industry Standnard

Roles :- * Knowledge of cosmetic and personal care product manufacturing processes (e.g., mixing, filling, emulsifying, packaging) * Understanding of GMP and regulatory compliance * Familiarity with batch processing, SOPs, and quality documentation

The job involves preventive maintenance of production equipments and utilities (chiller, blowers, HVAC etc), coordination for validation of equipments, maintain GMP compliances, participate in new equipment installations, general maintenance of buil

Role & responsibilities Key Responsibilities: Strategic & Policy Development: Define, implement, and continuously improve QA/QC policies, procedures, and standards aligned with global best practices (e.g., ISO, GMP, Six Sigma). Develop strategic quality plans in alignment with organizational objectives. Team Leadership: Lead and manage the QA/QC team, including hiring, training, mentoring, and performance evaluation. Foster a high-performing team culture with a strong focus on accountability, results, and continuous improvement. Quality Management System (QMS): Monitor and improve the organizations QMS to ensure effectiveness and compliance with applicable standards. Lead quality system implementations, upgrades, and documentation control. Audits & Compliance: Plan, coordinate, and execute internal and external audits. Ensure ongoing compliance with regulatory and customer requirements. Develop and track corrective and preventive actions (CAPAs) from audit findings. Customer Feedback & CAPA: Review and analyze customer complaints and feedback. Lead root cause investigations and implement robust CAPA processes to prevent recurrence. Cross-Functional Collaboration: Partner with Production, Engineering, R&D, and Supply Chain teams to integrate quality into all operations. Promote quality best practices across the value chain. Data Analysis & KPI Monitoring: Analyze quality metrics and KPIs to identify trends and areas for improvement. Report on performance against targets, and develop action plans for gaps. Supplier Quality Management: Oversee supplier quality performance and conduct supplier audits. Develop and maintain strong relationships with suppliers to ensure quality standards are met. Training & Culture Building: Lead organization-wide quality training initiatives. Promote a proactive culture of quality, compliance, and continuous improvement. Reporting & Communication: Present quality performance metrics, risk assessments, and improvement strategies to senior leadership. Provide recommendations for strategic quality initiatives. Preferred candidate profile Bachelors or Masters degree in Engineering, Quality Management, or a related field. 8+ years of experience in Quality Assurance/Quality Control, with at least 3 years in a leadership role. Strong knowledge of QMS standards (e.g., ISO 9001, ISO 13485, GMP, Six Sigma). Proven experience with internal/external audits, CAPA, and risk management. Excellent analytical, problem-solving, and decision-making skills. Strong interpersonal and leadership capabilities. Certifications such as Six Sigma (Black Belt), Lead Auditor, or ASQ Certified Quality Manager are a plus.

Job Title: FDA & International Pharma Compliance Consultant (Excipients, API & Ingredients & Formulations) Location: Kutch, Gujarat (Remote advisory with periodic on-site presence) Experience: 2025 years in pharmaceutical manufacturing and regulatory compliance Salary: Competitive Education: Bachelors or Master’s in Pharmacy, Pharmaceutical Sciences, Chemistry or related discipline Kindly get in touch for career advancement opportunities with us at rupsha.saha@antal.com Roles & Responsibilities Guide the upgrade and development of plant infrastructure and systems to achieve compliance with: WHO-GMP Regulatory requirements of Russia, Australia/New Zealand, African authorities Ultimate readiness for UK MHRA and US FDA audits Provide expert support on: WHO-GMP and GLP compliance for excipients, APIs, and formulation ingredients Equipment qualification (DQ/IQ/OQ/PQ) and cleanroom classification Process and cleaning validation Quality Management Systems (QMS), documentation (SOPs, BMRs, BPRs) and change control protocols Advise on regulatory documentation strategy for DMF and CTD/ACTD filings, including supplier qualification Assist in product selection and formulation pipeline development, identifying high-potential excipients and formulations for domestic and export markets Train and mentor QA, QC, production, and R&D teams on global pharmaceutical standards and best practices Desired Profile 20–25 years’ experience in excipients, API or formulations manufacturing, with a top-tier pharmaceutical company Proven track record of preparing and leading facilities through US FDA, MHRA or TGA audits Deep working knowledge of: ICH Q7/Q8/Q9/Q10 WHO GMP and EU GMP Annexes Indian D&C Act & Schedule M Hands-on experience supporting DMF submissions and familiarity with USP, EP, BP and IP Prior consulting or leadership roles serving regulated export markets Strong grasp of product lifecycle management, export documentation and quality risk management for emerging markets Tech-savvy, with exposure to digital QMS or e-BMR systems (desirable) Awareness of sustainability and EHS standards for global audit readiness Excellent cross-functional collaboration skills spanning production, QA/QC, R&D and supply-chain teams About Antal Antal International is a 30-year-old global executive search and placement firm with a network of over 800 people across 35+ countries, originally based out of the UK.

Roles and Responsibilities Ensure compliance with GMP guidelines during API manufacturing processes. Monitor equipment performance and troubleshoot issues related to piping systems. Maintain accurate records of production data, quality control tests, and inventory management. Experience needed: Production - 0 -4 years Engineering production-6-8 yrs

Reporting to Sr. Director - Regulatory Affairs Experience required: 5-8 Years Education: B. Pharm / M. Pharm Department: Regulatory Affairs Key Responsibilities: Prepare the status of all documents related to submission. Compile and review Regulatory submission documents required in line with the relevant guidelines. Coordinate with all stakeholders of the manufacturing plant for the collection of documents. Evaluation of change control: evaluate all post-approval changes. Review of specifications (API, Intermediate, FP, and Shelf life) executed BMRs, BPRs, COA, Method transfer report, Method verification, Analytical chromatograms intended for regulated or non-regulated market submission. General Review of plant Site Master File, layouts, and valid GMP Compliance Certificate for its adequacy to support regulatory submission. Effectively implement post-approval commitment. Preferred candidate profile Review of CMC (Chemistry, Manufacturing, and Controls) Documents Self-motivated, detail-oriented, and highly organized professional Proven ability to collaborate and communicate effectively with diverse teams Proficient in Microsoft Word, Excel, and PowerPoint Fluent in English, with strong skills in speaking, comprehension, reading, and writing. Strong technical expertise in reviewing manufacturing site documentation.

Role & responsibilities Ensuring compliance to GMP during day-to-day activities on shop floor. Review of day-to-day and online compliance. Performing SAP transaction as required. Timely performing sampling at different stages as per the requirement. Ensuring and giving clearance for various stages during day-to-day activities like, Line clearance in Dispensing, Mixing, Autoclave, Washing, Depyrogenation Tunnel, Filtration, Filling, Terminal sterilization, visual Inspection, labelling, packing. Collection of various samples as per the requirement. To review of GMP document. Identification of deviation through review and observation. Handling over the shift base change for continued operation. To review Manufacturing, Packing document, etc. To raise deviation in case of any abnormality found and inform to Section Manager for the same. To prepare BMR/ BPR by verification against DMBD, respective process Standard Operating Procedure and Validation recommendation and get it reviewed. To issue standard formats. To execute routine IPQA monitoring like volume check, critical control step verification during manufacturing of the product, sampling and periodic verification activities and to report to Section Manager in case of any abnormality is observed and will file deviation for the same. To review the GDP issues in production / QC / QA and logbooks. To review Preventive Maintenance, Breakdown maintenance and perform risk assessment and suggest immediate corrective actions. Report conclusion of preventive maintenance and breakdown maintenance to Section Manager. To verify raw material, primary packing material at the time of material issuance and material dispensing against Standard Material Requirement Form and approve the process step. To perform routine IPQA monitoring like volume check, critical control step verification during manufacturing of the product, sampling and periodic verification activities and if any deviation / abnormal observation in terms of noncompliance to Good Manufacturing Practice (GMP) observed, bring to the notice of Process Manager. To verify headspace oxygen and dissolve oxygen during in process monitoring. To verify secondary packing material at the time of issuance against Standard Material Requirement Form and approve the process step. Preferred candidate profile Result orientated Communication skills Presentation skills Analytical skills Lateral coordination

We are looking for Quality Head, who has worked at least 10years in SGI Casting speciality in Manhole cover division. Maintain QMS, with computer knowledge. Job location-Howrah(WB),Salary-35k-45k Monthly. Walk in Interview. Contact : +91 7687919790

Role & responsibilities Handling and management of the Engineering department. Overall responsible for the maintenance of the plant, Machinery, Utilities, Building, and premises Coordination with concerned department heads for the timely execution of engineering activities. Planning and scheduling preventive maintenance of Production, QC, Warehouse equipment, and utility as per the preventive maintenance planner. Review of SOPs, protocol & reports, and preventive maintenance planner and checklist. To provide technical guidance to the engineering team and top management. Responsible for the selection and design of equipment, plant layout, materials handling, and ordering of material. Up-dation of facilities as per regulatory guidelines such as man material handling, HVAC system and utility etc. The monitoring of compliance with the requirements of Good Manufacturing Practice. Handling of QMS activities related with engineering department. Ensure that environmental, Health and Safety, Engineering, Quality standards and procedures are adhered to review the technological system that supports a more environmentally friendly approach. Requirement and skills: Proven working experience as a Manager-Engineering. People-oriented and results-driven. Candidates having pharmaceutical experience of working in liquid and tablet products, Equipment, utility, and maintenance will be the preference. Preferred candidate profile Applicants must be stay in Modinagar (Ghaziabad).

Open Positions: Officer / Executive / Sr Executive Quality Assurance & Quality Control : Analytical Skill on HPLC, Electrophoresis, Microbiology, Document Review, IPQA, Quality Systems, GMP Compliance, QA-QMS Biosimilars Manufacturing: Downstream (Operation of Chromatography systems) & Upstream (Handling of Single use and Stainless-steel bioreactors) Experience: 2 to 10 years of relevant experience in Biopharmaceutical Qualification: B Sc / B. Pharm/B Tech / M Sc in Microbiology / Biotechnology / Chemistry/M. Pharm Date : 01st June 2025, Sunday Time : 08:30 AM to 06:00 PM (Registration will be closed by 12:00 PM) Venue : Hotel Pride , 5, University Rd, Narveer Tanaji Wadi, Shivajinagar, Pune, Maharashtra 411005, India Note: All positions are based out at Pune, Gotawade.

Responsible for aligning production schedules with demand forecasts, optimal raw material availability & minimizing downtime & inventory costs Coordinate with production, R&D, QA/QC & procurement teams to ensure timely & efficient batch planning Required Candidate profile 6–8 years in production planning and control (PPC) in specialty chemical or polymer manufacturing Strong understanding of Batch Manufacturing, EHS, GMP & compliance protocols ERP Software is must

Roles and Responsibilities Ensure compliance with EHS regulations, policies, and procedures at API manufacturing facilities. Provide training on EHS best practices to employees at all levels within the organization. Develop, maintain, and update safety documents such as SOPs, risk assessments, and incident reports. To ensure safety in process plants / sections in shift, by on the job monitoring /CAPA. Issuing of the work permit's with verification of job, Supervision & monitoring. To operate ETP in shift & ensure discharge of treated effluents as per MPCB norms. To maintain in order all PPE's, FFE's, SCBA's, OHC, MCP's, Fire water pumps, safety shower, smoke detector etc. Desired Candidate Profile 2-5 years of experience in Environment Health & Safety (EHS) role in pharmaceutical industry. B.Sc / MS/M.Sc(Science) degree in Chemistry or related field; Adavance Diploma in Industrial Safety. Strong knowledge of GMP compliance.

The Junior Executive – Warehouse will support day-to-day operations within the warehouse to ensure the proper handling, storage, and dispatch of pharmaceutical products in compliance with regulatory and company standards. The role involves inventory

Job Objective - Maintain machine continuity, quality of production, reduce wastages and adherence to cGMP in-shift for the allocated machines. Roles and Responsibilities - Check the allocated machine in each shift as per the CTQ (critical to Quality) checklist (Machine checking report), pin lubrication monitoring. Blade change, jaw/cheek change, collet change) under the supervision of Shift supervisor Dip Bath, greaser, blade, Replacement of dome wiping felt and oiling, collet oiling and cleaning as per SOP. Colour change (removal and insertion of dip bath, machine cleaning) as per SOP Attending tripping on HCM and bring the machine back to running condition. In certain cases, seek help from Maintenance Operator to bring the m/c to normal condition. Cut length graph plotting and take corrections on the machine as per SOP. Hourly Weight monitoring and take corrective steps in case of deviations. Process parameter recording and inform to the supervisor for any corrective actions to be taken. Implement CAPA for any customer complaint related to HCM as per the instructions from Supervisor/Hall In charge. Machine cleaning (1s, 2s) Shift handover and takeover. Helping other operator in case of colour change or break down on HCM. Numbering of capsules in case of defect identification as per SOP Making downtime entries on daily machine performance report Safety

NOTE : IMMEDIATE JOINERS ARE PREFERRED 1) Receive different kind of PR and requirement from different department (Production Consumables, Microbiology, BT, R&D, QC, Russia Project, Maintenance (Asset, Domestic, Import, Service), Pharmacopeias of RA from our End User. 2) Source Vendors according to material and float enquires for the quotation. Minimum 2-3 quotes require for comparison. 3) After getting the quote, take technical confirm with our end user and check all the technical points of quotation like delivery time, payment terms, warranty, inclusion, exclusions etc. 4) Discuss and negotiate with vendor for the best price and delivery time of material. 5) Accordingly prepare comparison sheet and budget sheet and handover that sheets to reporting HOD for approval. 6) After finalization of all the things, check that vendor is our existing vendor or not in SAP. If existing vendor is not there we have to create that vendor in SAP by taking required documents from Vendor. 7) After checking all the things in PR (proper material description, quantity, uom, cost centre etc.) will proceed to raise PO in SAP. 8) After completion of creating purchase order in SAP will give it to reporting HOD for authorization of PO. Then the signed po will send to vendor after that get the acknowledgement from the vendor for PO receipt. 9) After PO, will take follow-ups with suppliers for the material, Service, All the required data, FAT, Service reports and other documents which is required by our user, store person, Finance and QA department for the utilization of material/Service. 10) Coordinating with stores department for material receipt confirmation (GRN) and also discuss with finance for timely payments for suppliers. 11) Will do GRN and SRN of material and Services related to Russia Project and Head Office. 12) If any break down happens, we have to arrange service Engineer or material as soon as possible by coordinating with suppliers and Engineers. 13) We have to Prepare PR Tracker sheet, Material Tracker sheet, logistic follow up, Pending payment sheet to keep track of all the materials and services to avoid any kind of confusion and not to miss any important PR or PO.

Job Summary: We are seeking a motivated and skilled QC Microbiologist to join our Quality Control team. The successful candidate will be responsible for performing microbiological testing on raw materials, in-process samples, finished products, water systems, and environmental monitoring to ensure compliance with GMP and regulatory standards. Key Responsibilities: Conduct microbiological testing of raw materials, in-process samples, finished products, and stability samples. Perform environmental monitoring of manufacturing areas including viable and non-viable particle counts, surface monitoring, and air sampling. Carry out water analysis (e.g., Total Microbial Count, Endotoxin, TOC). Execute Sterility testing, Microbial Limit Tests (MLT), Endotoxin testing (LAL method), and Growth Promotion Tests (GPT). Maintain proper documentation of all microbiological activities in compliance with cGMP and GLP. Participate in method validation, media preparation, and equipment qualification. Investigate microbiological deviations, OOS/OOT results, and support implementation of CAPA. Ensure calibration and maintenance of all microbiological instruments (e.g., incubators, autoclaves, particle counters). Support internal and external audits by regulatory authorities. Comply with all lab safety protocols and procedures. Exp.- Fresher or 1 year of experience in a pharmaceutical microbiology lab. Location-Por GIDC, Gujarat

Job Title: Shift Executive Packaging Department: Production / Packing Reporting To: Deputy Manager Location: Moga, Punjab Shift: Rotational (Morning, Evening, Night) Key Responsibilities: . Shift Management: Manage the entire food packing operations during the assigned shift. Ensure smooth start-up, operation, and handover of the shift with proper documentation. Allocate manpower as per line requirements and optimize workforce utilization. Packing Operations: Monitor packing lines for sachet, pouch, or bulk packing formats. Ensure product packaging is as per specifications (weight, sealing, labeling, coding). Coordinate with Quality Assurance for in-process checks and compliance. Documentation & Reporting Team Supervisio n:-Supervise packers, helpers, and machine operators. GMP & Hygiene: Ensure adherence to Good Manufacturing Practices (GMP), hygiene, and safety protocols. Desired Candidate Profile: Education: Diploma / B.Sc / B.Tech in Food Technology or related discipline Experience: 4-5 years in a food processin g or FMCG plant in packing operations Skills: Team handling, shift management, documentation, quality awareness, basic troubleshooting. Salary - Hike on last Hand on experience on SAP is Mandatory More Details connect me at mansi.sharma@manpower.co.in

Strategic: Representative for QMS activities in Drug product/ Drug substance area. Timely initiation and closure of QMS elements. Documentation related to Drug product/ Drug substance area. Training need identification for all the employees Assist the validations and routine validations of equipment and facility. Identify and implement the manufacturing and warehouse procedures with compliance to current GMP requirements. Coordination during customer and vendor audits. Coordinating with engineering and validation department for calibration and preventive maintenance. Coordination and implementation of software based QMS solutions like Track-wise, LMS, SAP etc. Operational: Initiation of change controls, deviations, Investigation and CAPAs and closure of the same. Tracking of QMS activities and coordinating with cross functional departments to complete the QMS activities like investigation for OOS, complaints, deviations. Identification, preparation and implementation of SOP’s. This position will prepare SOPs related to the machines which are undergoing commissioning and procedures which are proposed to implement in Drug product area. Preparation and review of URS, CLIA, SLIA, QRM, IQ and OQ documents. Involvement in the qualification activities of equipment and area in drug product area People: Champion the OneSource Core Values and lead by example by acting a member of a team to achieve organizational and common objectives. Identify business successors and coach, mentor, nurture and develop people towards leading the business as non-fungible assets in the organization with a succession and continuity plan. Preparation and execution of training modules on SOP’s in the department. Preparation and execution of QMS documents in the department. Preparation and execution of training modules on QMS and safety SOP’s in the department. Preparation and execution of training on soft skills to develop the team. Finance: Ensure activities, services and tasks engaged / managed meets or improves on budget, cost, volume and efficiency targets (KPIs) in line with business objectives. Ensure the availability / adequacy of resources to implement and maintain the pharmaceutical quality system and continually improve its effectiveness by applying resources to specific product, process or site.