243 Batch Manufacturing Jobs

Experience in Derma Formulations, Like Cream, ointment, gel Lotion etc. (Applicable for Non- Sterile) Experience in ophthalmic Formulations, Like eye ointment, eye Gel etc. (Applicable for Sterile). Know the aseptic Process and behaviors/Practices. Required Candidate profile Knowledge of SCADA system, in various manufacturing OEM equipment, like ADAM, IWK (High speed robotic tube filling machine), trac & trace system, IMA PG, OMAG, Sachet filling machine, /auto cartonator

Responsible for sampling of In-process sample, Process validation, rinse and swab sample,FG sample, Control sample, MLT sample and Stability sample and to ensure timely submit To make necessary entries into respective register/E- log book. Responsible for activities inline in ERP, LIMS, ELOG and EDCS as per requirement. To carry out Line clearance prior to start-up of any activity and verification of dailyequipment logs. Online checking of BMR its compliance. For carrying out in-process activity at Manufacturing stage as per BMR and relevant SOPs Checking of Environment monitoring of all respective areas on shop floor. To follow EHS policies. To ensure compliance of GDP and data integrity techniques. Verification of Raw material during dispensing To participate in validation activities. To monitor the work compliance as per GMP SOPs on shop floor. Cleaning validation (cleen software) To implement GMP and cGMP activities on shop floor. Responsible for Control Sample Management. Issuance of Batch Manufacturing Record Batch Packing Record. Handling mailsFollow up of the Batches planned from PPIC. To review the BMRBPR of Primary Secondary Packing Area. Probiz ERP (Enterprise Resource Planning Software) related work (Release ofbatches BOM Approval)

The Production Chemist will be responsible for executing and monitoring API manufacturing processes, ensuring compliance with cGMP, SOPs, and regulatory guidelines . The role involves operating chemical process equipment, documentation, troubleshooting, and process optimization to achieve efficiency, safety, and quality standards. Key Responsibilities & Duties: Process Execution: Perform batch manufacturing activities in line with Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and cGMP requirements. Equipment Operation: Operate and monitor reactors, centrifuges, multi-mill, shifter, tray dryer, filtration systems, GLR, and SSR equipment . Quality Assurance & Compliance: Coordinate with QA/QC teams for batch release, deviation handling, and ensure adherence to regulatory and quality standards . Documentation: Maintain accurate production records, logbooks, and deviation reports ensuring data integrity and audit readiness. EHS & Safety Compliance: Follow Environmental, Health & Safety (EHS) protocols, participate in safety drills, and ensure a safe work environment. Process Optimization: Assist in scale-up, yield improvement, and continuous improvement initiatives for cost-effective production. Troubleshooting & Maintenance: Identify and resolve equipment or process deviations in coordination with the engineering and maintenance teams . Shift Management: Supervise shift operations, allocate tasks, and ensure smooth production workflow. Qualifications & Experience Education: B.Sc./M.Sc. in Chemistry or B.E. in Chemical Engineering. Experience: 1 - 6 years in API production / pharmaceutical manufacturing . Technical Skills: Knowledge of GMP, GLP, ICH, and regulatory compliance . Hands-on experience with clean room operations, batch documentation, and shift planning . Familiarity with process safety, scale-up, and validation activities . Preferred Attributes Strong analytical, problem-solving, and decision-making skills . Ability to work effectively in a fast-paced, regulated production environment . Good communication, teamwork, and reporting skills . Flexible to work in shifts and handle multiple tasks.

Responsibilities: Responsible for creating, maintaining, managing accurate & compliant production-related documentation. This role ensures that all documentation adheres to internal standards and external regulatory requirements.

Maintaining good housekeeping and cGMP in shop floor Preparation of New documents like BPCR and SOP Deviation , change control, OOS, activity and is compliance Plant keeps ready for audit Overall responsibility of cGMP Production should be achieved as per target. Equipment cleaning Log book and Solvent log Book to be maintained. BPCR arrangements for running batches. Review and completion of all documents like BPCR, Equipment logbook, and format as per SOP

Role Overview: As a Research Associate in the API R&D-DBH department, your primary responsibility will be to ensure the smooth and efficient operation of various research activities in the manufacturing blocks. Your role will involve following strict guidelines and procedures to maintain safety, quality, and compliance with cGMP requirements. Key Responsibilities: - Acquire training for each activity/equipment before execution - Follow entry and exit procedures of manufacturing blocks, including chemical and Pharma areas - Perform all process operations as per Batch Manufacturing Records (BMR) - Clean all equipment as per cleaning Standard Operating Procedures (SOP), Procedure, and Process Change Request (PCR) - Operate equipment such as reactors, filtration equipment, dryers, and powder processing equipment - Review and verify the status of equipment and activity logbooks - Conduct cleanliness verification of operational equipment before starting operations - Sample in-process and intermediates and send samples to Quality Control (QC) for analysis - Operate utility systems as per requirements - Calibrate/verify instruments like pH Meter and weighing balance - Ensure completion of preventive maintenance and calibration of equipment - Disposal of solid and liquid wastes along with documentation - Preparation of Batch Manufacturing Records, cleaning records, and Bill of Materials - Creation of process order in SAP for raw materials and packing materials - Recording of activities in respective logbooks as per procedure - Participation in internal, customer, and regulatory audits Qualifications Required: - M.Sc in Industrial/Organic Chemistry - 3 to 6 years of experience in a similar role Note: Person who can join within 2 months will be more preferable. Additional details about the company were not provided in the job description.,

To ensure the cleanliness of area and machines before starting the packing process. To perform challenge test of respective equipment & get it verified by packing officer To ensure availability of Batch manufacturing record before commencing the activity. To ensure the compliance of environmental conditions before commencing the activity. To ensure the line clearance from IPQA before commencing the activity. To run the machine as per approved SOP and in compliance with cGMP and record all the activities in the approved formats at the time of observation/activity is performed. To have knowledge of SOP of own working area and ensure to practice it. To escalate to supervisor for any non compliance and breakdown Ensure the housekeeping (Cleaning of the area) & safety norms are to followe'd

Job Title: Production Executive No. of Positions: 2 Company Name: The South Indian Manufacturing Company Company Website: www.saibol.com Location: Madurai (Local candidates preferred or must be willing to relocate) About the Company The South Indian Manufacturing Company is a reputed pharmaceutical manufacturer specializing in quality-driven processes and GMP-compliant production systems. Qualifications B.Pharm / M.Pharm / B.Sc Chemistry / M.Sc Chemistry Experience Freshers (0-2 years) are eligible Experienced candidates (3+ years) also welcome; higher salary will be offered based on profile Key Responsibilities Assist in ointment manufacturing (weighing, mixing, filling, packing, labeling) Ensure production follows SOPs and GMP requirements Maintain Batch Manufacturing Records (BMRs) and logbooks accurately Coordinate with QA for line clearance and documentation Support machine changeover, validation, and calibration activities Monitor cleanliness and hygiene of production areas and equipment Report any deviations, breakdowns, or non-compliance issues promptly Desired Candidate Profile Fresh graduates or experienced pharma professionals welcome Knowledge of pharma production processes and GMP documentation preferred Ability to work in a regulated pharma environment Disciplined, detail-oriented, and a strong team player Key Skills Pharma Production | Ointment Manufacturing | GMP Compliance | Batch Records | Line Clearance | SOP Adherence | Pharma Documentation Compensation Gross Salary: 14,000 - 25,000 per month (depending on experience and qualifications)

To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities: Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeovers and line clearance activities. Identify and report deviations or equipment malfunctions to the supervisor. Ensure compliance with cGMP, safety, and environmental regulations. Participate in continuous improvement and troubleshooting initiatives. Qualifications: ITI / Diploma / B.Sc or equivalent; technical diploma preferred. 4-6 years of experience in pharmaceutical manufacturing, preferably in granulation. Familiarity with cGMP, USFDA guidelines, and pharmaceutical documentation practices. Ability to read and interpret batch records and SOPs. Basic computer skills and understanding of production documentation. Preferred Skills: Attention to detail and strong documentation habits. Mechanical aptitude for operating and troubleshooting equipment. Team player with good communication skills. Forklift certification (if required for material handling).

With HOD and reliever discuss: - Special requirement/ instruction/target, last 2 shift issues, another 3 shifts schedule and additional task if any. Take quick round with the reliever in the entire area: - During round try to touch each and every people and have some specific question may be which are most critical to last 2 shifts issues/area etc. Charge will be taken during round physically area: - Any abnormality observed need to be objected; also, information should go to HOD. Abnormality should be cleared by the doer before leaving the workplace. Come to planning board well advanced (before shift start) and see the schedule status on the board updated and people reporting in the shift on time. Stand at the entry point and ensure: - Everybody reports on time at workplace and charge handover happening at workplace only. Operator handover running machine to the reliever. Proper allocation of part time and full-time employee considering absenteeism if any. Ensure each and every individual should know the shift plan and what to deliver in the shift before going to workplace. It should be predefined, and changes can be only re-communicated. Again, discuss in depth with all concerns (reliever, HOD, department planner, miscellaneous responsible persons) for schedule, investigation and CAPA to incident if any, productivity, quality issues, documents and department works to perform in the shift, this is the understanding for pre and post 3 shifts. Report to the concern workplace: - Instruct offline/ concern people to make arrangement of blend /SFG and any other materials for coming two shift operations. Make responsible offline/concern people to close quality issues, perform quality activity and other miscellaneous activities (like BMR, Training & other arrangements). Batch Manufacturing: - During area round ensure: - People, quality systems, machine, accessories, documents, materials and all other things are in place. Ensure things are in their designed place and vice versa. Interact with Supervisor and understand that they know shift target for output and quality. Ask few casuals that they should know what they are doing and our requirement. Ensure training record of casual if any. Perform critical challenge test and in process checks. Ensure no machine functioning parameters/facility by passed. Talk the same with line people simultaneously. Check the line documents entries (BMR, Logbooks and any formats). Cross verifies with vigilance that correct document, product and manpower used. Ensure and discuss with people that if any special precaution (like staggering during breaks, sensitive product, new product, new market, offline activity, special/critical product, new manpower, machine issues etc. Get pending work from previous shift; get it done from them only. Go through the BMR, blend and machine and ensure correct dose and material used. Evaluate and challenge the working of manpower for correctness and if required retrain them. Ensure no human intervention at any places and correct procedure being followed. Check people should know the batch completion time, SFG quantity, batch yield will give etc. Must be consider for the following: - After completion of round in department report finding to the HOD. No documentation noncompliance and manipulation on dose and process. Keep required manpower on the line. Focus the improvements project like Yield, Quality, Safety, Cost saving and Man hour reduction. All report must be completed like Shift report, DPR etc. Safety, hygiene, discipline and ISO requirements shall be followed in the department. Ensure everybody in shift follow their responsibility. Spend some time for innovation and initiatives in the department. Spend time to train the people. Spend time on other department activities like procurement, change parts, other department issues, meeting and discussion. Ensure people should report and taking permission for each non routine jobs. Spend some time to interact with people. Ensure activities are on- line. Face abnormality and talk to supervisor immediately. Ensure and pass communication in such way that nobody should get of any partial communications; also, it shall not be transferred to other shift people. Ensure special precaution in night shift so that people should not be sleepy. Ensure manpower allocation for each and every activity (like operational lines, wash area, change parts, HK etc.). Be ready to give time to next shift reliever and to take round with him.

Efficiencies to work long working hours (like as 10 to 11 Hrs.)Excellent knowledge of computer reservation process and MS Office.Shall be responsible for booking of Hotels/Flights/ Transportation as per the schedule sharedTo maintain the CRS on daily

Division Department Sub Department 1 Job Purpose Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift. Key Accountabilities (1/6) Operate the equipment efficiently without error and deviation as per SOP to meet shift targets Perform unit operations as per SOP and unit processes as per batch manufacturing record Optimize the utilization of available resources for achieving production in shift Maintain equipment, facility and block premises as per SOP for audit readiness Key Accountabilities (2/6) Provide suggestions for optimization of processes to manufacture quality product Identify the deficiency in area and errors in documents and rectify them as per requirement Propose and implement new idea to enhance production, optimise the use of consumable goods and maximum utilization of resources Key Accountabilities (3/6) Execute and update online documentation to meet cGMP requirements Maintain online documentation and timely entries in BMR and supporting documents Check documentation before submission to ensure data integrity Key Accountabilities (4/6) Deliver training to workmen and adhere cGMP and safety guidelines in production process to ensure smooth operations Conduct training related to cGMP, equipment operation, safety and housekeeping for workmen Optimize the use of resources in housekeeping Ensure good housekeeping and sanitisation as per the guidelines Ensure usage and maintenance of PPEs by workmen during shifts Report any near-miss to officer in-charge in time Key Accountabilities (5/6) Key Accountabilities (6/6) Major Challenges Meeting shift targets due to unavailability of adequate resources. Overcome by efficient work load distribution and resource optimisation Meeting production targets due to lapses in knowledge transfer between shifts. Overcome by bridging gaps between inter-shift communication Key Interactions (1/2) Engineering & Utility for system and equipment related queries (Daily) Safety for safety rounds and PPE (Weekly) Formulation Technical Support for troubleshooting in products (Case Basis) Formulation Tech Transfer for support in new products (Project Basis) Key Interactions (2/2) Equipment manufacturer for troubleshooting in machine (Case Basis) Dimensions (1/2) Number of dosage forms : 2 Number of tech transfer supported per month : 2 Number of batches executed per month : 35-40 Achieve internal OTIF more than 90% Meet percentage utilisation of plant as per the plan 0% errors in documentation Zero reportable accidents / incidences during manufacturing Achieve 0% failures / deviations target 100% compliance to SOP Dimensions (2/2) Key Decisions (1/2) Scheduling house-keeping activities Key Decisions (2/2) Equipment Selection to Section Head Modification in plant and equipment to Production Officer Education Qualification Diploma in Pharmacy / Mechanical Relevant Work Experience 0-2 years of experience in a manufacturing organisation preferably in pharmaceutical industry

Role Overview: As a Production Chemist specializing in UV Gel Nail Paint, your main responsibility will be to oversee the scale-up and production of formulations from lab-scale to production-scale batches. You will create and adhere to batch manufacturing records (BMRs), monitor production floor procedures including mixing, heating, and filling processes. Key Responsibilities: - Convert lab-scale formulations to production-scale batches. - Create and follow batch manufacturing records (BMRs). - Monitor mixing, heating, and filling procedures on the production floor. Quality Control (QC): - Test raw materials, in-process batches, and final products for: - Viscosity - Cure speed (UV/LED) - Color consistency - Shelf life stability - Ensure compliance with cosmetic regulations such as FDA, EU, and REACH. Safety & Compliance: - Handle hazardous chemicals (e.g., acrylates) safely. - Maintain MSDS/SDS. - Adhere to GMP and workplace safety standards. Qualification Required: - Previous experience in production chemistry, preferably in cosmetics or related industry. - Knowledge of cosmetic regulations and quality control procedures. - Strong attention to detail and adherence to safety protocols. Please note the job type for this position is full-time with the work location being in person.,

As a Production Planning & Execution specialist, you will be responsible for executing daily production activities on the shop floor according to the approved production schedule. Your role will involve planning and allocating manpower shifts, distributing work effectively with proper supervision, and monitoring utilities to meet production schedules and ensure continuous functionality. Your coordination with various departments will be crucial for the smooth operation of production activities. You will liaise with Warehouse/Stores/Procurement to ensure timely availability of raw materials, coordinate with the QC Department for timely analysis and approval of samples, and work closely with the QA Department to ensure compliance with GMP and ISO requirements. Line clearance before manufacturing and packaging activities, monitoring critical steps, and ensuring timely completion of batch manufacturing records will be part of your responsibilities. You will also be required to maintain accurate documentation in compliance with GMP and ISO standards and ensure good housekeeping practices in production areas. Overseeing calibration and maintenance of machines, addressing troubleshooting issues, and managing installation of new equipment will be essential for efficient production operations. You will also report and assist in the investigation of deviations, incidents, and out-of-specification results. Your role will involve performing sampling activities, adhering to SOPs, and ensuring compliance with GMP, SOPs, and regulatory guidelines. Additionally, you will review batch manufacturing records, support audits, and focus on continuous improvement in quality management. Training and development of production staff on shop floor activities, GMP, and SOPs will be part of your responsibilities. You will also support manpower development in areas of quality, productivity, and cost efficiency. This is a full-time, permanent position with benefits including cell phone reimbursement. The work location is in person.,

Job Description for Executive API Technology Transfer Responsibilities: To evaluate process and scale up studies/exhibit batch of commercial site. To understand chemistry reaction mechanism and process of APIs and Intermediate from Lab scientists. To observe lab batches and provide inputs for the process development that are safe, robust, scalable, reproducible, and commercially viable. To develop, optimize and integrate scalable chemical process technologies to pilot plant / commercial plant using Multimax, RC1e, Syrris and Lasentec (PAT Tool) To accomplish and review literature search for advanced tools used in scale up. To execute the pilot plant batches To conduct demonstration and validation of the process at the Manufacturing sites. To involve into various technical issues, trouble shooting, OOS / OOT / Deviation To evaluate equipment fitment for pilot plant batch/exhibit batch To evaluate stability data To carry out complete documentation of projects To evaluate pilot plant batches To execute GMP batch at LLM site To evaluate process safety data during scale up and EB. To perform evaluation and impact assessment for the change control proposals To contribute towards minimising the environment & safety hazards and make operations safe and Eco-friendly . To prepare Tech transfer documents like MFC, PDR etc. J ob Description for Executive Pilot plant operations Responsibilities : Operating equipment as per standard operating procedures (SOPs). Batch manufacturing exposure in Intermediate & API process at Pilot or plant scale. Hands-on experience of Different unit operation (e.g : Reaction, Filtration (Nutch filter, Centrifuge), Drying (ATD, VTD, RCVD, FBD),Extraction, Different type of vacuum unit (Ejector, Oil ring Vacuum pump), Different type of Utilities etc. Implementation of instructions relating to pilot plant operations, including the in-process control & Log book entries. Coordination with engineering for breakdowns / routine maintenance of equipments. Ensuring compliance of cGMP and safety during operations. Coordinating with tech transfer engineers/ R & D chemist for execution of batch and sharing critical observations / feedback. Housekeeping of premises and equipment. Hands-on experience of SCADA system is preferable.

As a QA Manager at Systacare, a trusted name in the pharmaceutical industry, your primary responsibility will be to ensure adherence to regulatory requirements and maintain the highest standards of compliance in injectable manufacturing. With a strong focus on innovation, compliance, and patient safety, Systacare is expanding its team and is seeking passionate professionals to join the organization. You will lead and manage the QA team to ensure compliance with cGMP, regulatory standards, and company SOPs. Your role will involve overseeing quality systems, including deviation management, change control, CAPA, OOS, and OOT investigations. It will be crucial for you to ensure quality assurance in sterile injectable manufacturing processes, emphasizing aseptic practices and cleanroom compliance. In addition, you will be responsible for preparing, reviewing, and approving batch manufacturing/packaging records, protocols, and reports. You will also play a key role in conducting internal audits and supporting external audits such as regulatory inspections and customer audits. Monitoring vendor quality and ensuring raw materials/packaging compliance will be part of your routine tasks. To excel in this role, you should have a Bachelor's or Master's degree in Pharmacy or a related field, along with 5-10 years of experience in the pharmaceutical industry, specifically with a minimum of 5 years in injectable manufacturing (sterile/aseptic). A strong understanding of cGMP and regulatory guidelines from bodies like USFDA, MHRA, EU, and WHO is essential. Hands-on experience in handling audits, documentation, and compliance processes will be beneficial, along with excellent leadership, problem-solving, and communication skills. This is a full-time position that requires in-person work at the Amritsar location of Systacare. If you are passionate about ensuring quality in pharmaceutical manufacturing processes and are committed to upholding the highest standards of compliance, we encourage you to apply for this role and be a part of our dynamic team at Systacare.,

Greetings from FocusR...!!! Exciting Opportunity to Shift Your Career to an IT Sector. If you are currently working in Manufacturing, Production, Procurement, Logistics, Quality, Inventory or Supply Chain industries, this is your chance to shift your career into the IT sector!!! Great opportunity of becoming an "Oracle SCM Consultant" Complete On-Job Training will be given by FocusR (with salary) on ORACLE SCM MODULE as per of the permanent employment. Manufacturing sector experience: 2-5 years required Qualification: Any UG/PG Degree Notice Period: Immediate - 30 Days preferred Job Location: Salem and Chennai (Training will be mandatory in Salem) Willing to take Oracle Supply Chain Management as career. Good Exposure in Production process, Supply chain, Inventory, Procurement, Quality, Logistics or Manufacturing process. Must be a team player. Willing to learn new concepts. Good in communication. We prefer candidates without any constraints in travelling as we have projects across India and abroad. We prefer candidates who can work with us for minimum duration of 30 months.

Role & responsibilities Responsible for all in process Quality Assurance Activities Document issuance and control Preparation and review of SOPs, Protocols, Reports, BMR, BPR and QC Specifications Issuance and review of BMR and BPR and other quality system documents Internal audit and its compliance related activity Ensuring compliance to cGMP Prepare Annual Training Plan in co-ordination with Head of QA Schedule and coordinate the cGMP training session Assist in the delivery of new employee orientation training Assure training records are maintained for regular, temporary and contractors/consultants Check monthly log book and calibration of IPQA instrument and balance Stability and control sample management Preferred candidate profile Should be worked in QA Department Well versed with computers, MS officer knowledge is must. documentation skills required

*Operate and monitor injectable (DPI)production equipment in compliance with cGMP standards. *Execute manufacturing processes compounding, aseptic filling, vial washing, autoclaving, and lyophilization. *Maintain (BMR) and related documentation. Required Candidate profile *Ensure adherence to safety, hygiene, & quality standards during production activities. *Familiarity with regulatory guidelines (USFDA, MHRA, WHO, etc.). *Good documentation and communication skills.

Junior Executive/ Executive - Production (API) Job Criteria: B.E-B.Tech (Chemical Engg.) / M.Sc./B.Sc. 1 to 5 years of experience Job Role: Ensure that the products are manufactured as per the cGMP and handle critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc. Maintain documentation as per regulatory requirement like change control, deviations. Highlight technical problems and take corrective actions, and maintain safety practices. Technical Officer/ Junior Executive/ Executive-Production+Packing (OSD) Production Job Criteria: M. Pharm/B. Pharm/DME/ITI 2 to 7 years of experience Job Role: Manage granulation, compression, coating, pelletization and capsule filling area. Packing Job Criteria: M. Pharm/B. Pharm/DME/ITI 2 to 7 years of experience Job Role: Manage blister packing, bulk/bottle packing, documentation, Track and Trace and serialization. Technical Officer/ Junior Executive/ Executive- Production (Injectable) Job Criteria: M.Pharm/ B.Pharm/ Diploma/ITI 2 to 7 years of experience Exposure to aseptic practices and good documentation practices are must. Job Role: Handle manufacturing skids, Fedegari autoclaves ,Isolator, lyophilizers, vial washing and tunnel, vial/ ophthalmic /PFS filling and aseptic filtration, FFS, CIP/SIP, filters, microsphere refiner, active freeze drying System. Execute manufacturing activities as per SOP. Operation, cleaning, sterilization, qualification and maintenance of solution preparation systems.

As an Enterprise Domain Architect for CG&S Manufacturing, you will provide deep functional process and high-level technical expertise to analyze, define, design, and support the delivery of functional and technical capabilities for an application/group of applications in the manufacturing operations space for Consumer Goods and Services (CG&S) clients. This role involves collaborating with various teams and ecosystem partners to design and implement efficient, scalable, and secure solutions for CG&S clients. Conceptualization and design of manufacturing operations solutions for CG&S clients, from a functional process perspective as part of client pursuits and projects. Actively leading and participating in sales pursuits and presales engagements, with responsibility for new project wins. This will involve multiple discussions and presentation of our capability and solution to potential clients and other stakeholders/leaders. Work with top ecosystem partners towards building solutions for client pursuits and projects and proof of concepts especially around their niche and latest offerings. Facilitate and drive impact assessment, due diligence, and solution blueprint activities and assist in developing and reviewing estimates for client work requests. Lead solution design and delivery of large and complex transformation programs around manufacturing operations, working with the rest of the organization, client leaders, and ecosystem partners to bring the best tools and delivery methods. Acting as the go-to-person between business process and technical SMEs. Active participation and leadership in driving industry-related thought leadership activities like patents, authoring whitepapers/POVs, proof of concepts, conference/academia presentations, capability presentations, etc. Professional & Technical Skills: Strong knowledge of batch manufacturing (preferably in CPG/Food & Bev. industry) and supply chain domain, including manufacturing strategy, regulatory compliance norms, KPIs, industry trends and standards, quality processes (in-line and process completion), Track & Trace, Packaging, in-plant logistics, sustainability, etc. Driving industrial process improvement engagements in own industrial organization or as a consultant. Strong thought leadership, articulation, and presentation skills with the ability to articulate through compelling storytelling. Knowledge of industrial automation involving equipment connectivity, SCADA, HMI, Historian, MES-MOM-QMS knowledge for any package. Knowledge of PLM-ERP-MES connectivity. Intelligent Warehousing & Plant Logistics, ASRS, AGVs, AMRs, etc. Additional Information: This position is based at Bengaluru, Pune location. A BE/BTech, MBA (not mandatory) is required.,

About The Role Project Role : Enterprise Technology Architect Project Role Description : Support sales teams in solution development, managing an internal matrix team to scope and price solutions. Lead customers through the design process. Work directly with Internal Accenture Domain Architects, Partner Architects, Client Architects, and Accenture project teams to design solutions. Must have skills : Manufacturing Operations Good to have skills : NA Minimum 15 year(s) of experience is required Educational Qualification : BE or BTech or MBA not mandatory Summary :As an Enterprise Domain Architect for CG&S Manufacturing, you will provide deep functional process and high-level technical expertise to analyze, define, design and support the delivery of functional and technical capabilities for an application/ group of applications, in the manufacturing operations space for Consumer Goods and Services (CG&S) clients. This role involves collaborating with various teams and ecosystem partners to design and implement efficient, scalable, and secure solutions for CG&S clients. Roles & Responsibilities:-Conceptualization and design of manufacturing operations solutions for CG&S clients, from a functional process perspective as part of client pursuits and projects.-Actively leading and participating in sales pursuits and presales engagements, with responsibility for new project wins. This will involve multiple discussions and presentation of our capability and solution to potential clients and other stakeholders/ leaders.-Work with top ecosystem partners towards building solutions for client pursuits and projects and proof of concepts esp. around their niche and latest offerings. -Facilitate and drive impact assessment, due diligence and solution blueprint activities and assist in developing and reviewing estimates for client work requests.-Lead solution design and delivery of large and complex transformation programs around manufacturing operations, working with rest of organization, client leaders and ecosystem partners to bring the best tools and delivery methods.-Acting as the go-to-person between business process and technical SMEs.-Active participation and leadership in driving industry related thought leadership activities like patents, authoring whitepapers/ POVs, proof of concepts, conference/ academia presentations, capability presentations etc.Professional & Technical Skills: - Must have Skills: Strong knowledge of batch manufacturing (preferably in CPG/ Food & Bev. industry) and supply chain domain, including manufacturing strategy, regulatory compliance norms, KPIs, industry trends and standards, quality processes (in-line and process completion), Track & Trace, Packaging, in-plant logistics, sustainability etc. -Driving industrial process improvement engagements in own industrial organization or as a consultant.-Strong thought leadership, articulation and presentation skills with the ability to articulate through compelling story telling.-Good to Have Skills: Knowledge of industrial automation involving equipment connectivity, SCADA, HMI, Historian, MES-MOM-QMS knowledge for any package -Knowledge of PLM-ERP-MES connectivity.-Intelligent Warehousing & Plant Logistics, ASRS, AGVs, AMRs etc. Additional Information:-This position is based at Bengaluru, Pune location.-A BE/ BTech, MBA (not mandatory) is required. Qualification BE or BTech or MBA not mandatory

1. Monitor raw material dispensing activity. 2. Perform daily IPQA activities as per SOP-defined frequency and ensure timely closure of IPQA observations. 3. Conduct validation sampling as per approved validation protocols. 4. Review BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for accuracy and compliance. 5. Perform ERP-related transactions of IPQA. 6. Check BSR (Batch Summary Record) and Shipper inspection as per SOP. 7. Manage issuance, review, and reconciliation of formats across all departments. 8. Conduct IPQA rounds and share observations with concerned HODs for corrective action and compliance. 9. Ensure cleaning, sanitation, and hygiene in all departments to maintain GMP compliance at all times. 10. Perform sampling of In-process, Semi-Finished Goods (SFG), and Finished Goods (FG) as per procedure. B.Pharm / M.Pharm / M.Sc. in relevant discipline. 2-5 years of experience in IPQA or Quality Assurance within the pharmaceutical industry.

Ensure the compliance of cGMP & EHS. Follow the cGMP requirement with appropriate housekeeping and documentation in manufacturing area. Co-ordination with other department for safe, successful and timely batch execution. Achieving plant production target w.r.t quality and yield. Active involvement in facing quality audits by vendor audit & regulatory audits. Lead from front to ensure safe behaviour / GMP culture on the shop floor. Comply with online documentation with complete data integrity. Undergo safety, quality and operational training & comply with requirement. Maintain housekeeping standard to ensure a clean and safe workplace. Follow the SOP practices. Preparation to comply statutory audit, customer audit and regulatory audit. Batch charging and process work out as per written instruction. Shift handover / instruction/ information communication. Operation & cleaning of Equipments. Suggests changes in working conditions and use of equipment to increase efficiency of equipment. Initiates or suggests plans to motivate workers to achieve work goals. Maintaining cleanliness and hygienic practices in the plant premises.

Responsible for Operation, cleaning and primary maintenance of negative isolator, Vibro sifter, Bin blenders and all other GEA granulation line equipment. Responsible for recording of activity in logbooks, Batch manufacturing record complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP s and good documentation practices. To perform all in-process checks and monitoring of all intermediate processes in granulation. To select recipes and set process parameters in Blender HMI ensure its correctness before blender revolution. Responsible for Issuance, utilization, cleaning, and retrieval of sieves and proper handling of machine change parts with its inventory. Responsible for set up, changeover, and operation of various manufacturing equipment s but not limited to granulation department. Responsible for reporting and/or escalating any conditions or problems that may affect the quality or integrity of product to supervisor and HOD production. Responsible for maintaining a neat, clean and safe working environment always and notifies supervisor immediately of any safety concerns, accidents or injuries observed. To ensure all in-process checks and monitoring of all intermediate processes, to check set process parameters in PLC/SCADA as per BMR before machine run in granulation area. Compliance of current Good Manufacturing Practices in the Hormone Facility to follow GDP with data-integrity compliance. To Complete the training and training record as per stipulated time. Responsible for preparation and usage of Disinfectant and cleaning agent solution as per defined procedures. To adhere to all Company policies, procedures, SOPs and Safety regulations. In absence of the position holder, the sub-ordinate Executive / Manager working in the section or the authorized designee (as applicable) shall be responsible for day to day working Role: Assembly Line Operator Industry Type: Medical Devices & Equipment Department: Production , Manufacturing & Engineering Employment Type: Full Time, Permanent Role Category: Operations, Maintenance & Support Education UG: Any Graduate PG: Any Postgraduate