243 Batch Manufacturing Jobs - Page 5

Responsibilities: * Ensure compliance with GMP, GLP & BPR review. * Conduct process validation, cleaning verification & change control. * Collaborate on batch manufacturing & release processes. * Prepare SOPs, BMRs & BPRs.

As an Enterprise Technology Architect within the Consumer Goods & Services (CG&S) Manufacturing domain, you will play a crucial role in providing specialized functional process knowledge and high-level technical expertise to analyze, define, design, and support the delivery of functional and technical capabilities for applications in the manufacturing operations space. Collaborating with various teams and partners, you will be responsible for designing and implementing efficient, scalable, and secure solutions for CG&S clients. Your key responsibilities will include: - Conceptualizing and designing manufacturing operations solutions for CG&S clients, focusing on functional processes during client pursuits and projects. - Leading and engaging in sales pursuits and presales activities to secure new projects, involving discussions and presentations to potential clients and stakeholders. - Collaborating with ecosystem partners to develop solutions for client projects and pursuits, including proof of concepts related to their latest offerings. - Driving impact assessment, due diligence, and solution blueprint activities, as well as assisting in estimating client work requests. - Leading the design and delivery of large transformation programs related to manufacturing operations, working closely with client leaders, ecosystem partners, and internal teams. - Serving as the liaison between business process and technical subject matter experts. - Taking an active role in industry-related thought leadership activities such as patents, whitepapers, proof of concepts, presentations, and capability demonstrations. Your professional and technical skills should include: - Strong knowledge of batch manufacturing, particularly in the Consumer Packaged Goods (CPG) or Food & Beverage industry, encompassing areas like manufacturing strategy, regulatory compliance, KPIs, industry standards, quality processes, track & trace, packaging, in-plant logistics, and sustainability. - Experience in driving industrial process improvement initiatives within an industrial organization or as a consultant. - Excellent thought leadership, articulation, and presentation skills, with the ability to convey complex ideas through compelling storytelling. - Knowledge of industrial automation technologies such as equipment connectivity, SCADA, HMI, Historian, MES, MOM, and QMS. - Understanding of PLM-ERP-MES connectivity and intelligent warehousing technologies like ASRS, AGVs, and AMRs. This position is based in Bengaluru and Pune and requires a minimum of 15 years of experience in the field. While a BE, BTech, or MBA is preferred, it is not mandatory for this role.,

You will be responsible for strictly following cGMP, Safety, and Environmental Practices in the manufacturing facility. This includes filling out Batch Manufacturing records and equipment cleaning records. It is crucial to adhere to Good Manufacturing practices during all operations and ensure Good Housekeeping in the plant area and its equipment. You must use the proper personnel protective equipment as required for each task. Planning and ensuring the availability of Raw Materials for daily production as per the production plan is essential. Keeping track of documents such as Issue and dispensing register is part of the responsibilities. Carrying out the manufacturing process according to the Batch Manufacturing Record without any deviation is a key aspect of the role. Ensuring adherence to data integrity in online documentation is of utmost importance. Handling hazardous operations in a safe manner is critical for the safety of yourself and others. Effective utilization of resources such as Utility, Manpower, and Machinery is required to meet production targets. It is essential to be detail-oriented, safety-conscious, and proactive in ensuring the smooth and compliant operation of the manufacturing processes.,

1. Oversee & execute production batches for OSD formulation 2.Maintaining Good housekeeping in workplace as per cGMP 3.Documentation of batch records, raw material usage & production log 4. Standard operating procedure and standard cleaning procedure Required Candidate profile 1. Minimum 5 years experience in Pharma Formulations (OSD) 2. Willing to work in Chennai/Chengalpet 3. Candidates having regulatory plant experience would be preferred

At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit. Common Responsibilities: Monitor & confirm that the established Environment, Occupational Health, Safety and Sustainability (EHSS) practices for safe work environment are followed by self & direct reports. Monitor & confirm that self & direct reports adhere to the highest standards of quality, integrity & compliance for every work activity. Complete the assigned trainings in a timely manner and comply with the training procedure & training calendar and monitor & confirm the same for the direct reports. Attend all assigned mandatory trainings related to data integrity, health, and safety measures, and monitor & confirm the same for the direct reports. Participate in & support the trainings on procedures, protocols, and On-the-Job activities. Compliance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). Report nonconformities & deviations to the respective supervisor(s) and/or line manager(s). Participate in & support for on-time initiation & closure of deviations, investigations, CAPA and change controls. Preparation, revision and review of Batch Manufacturing Records (BMR), Packing and Dispatch Record (PDR). Issue, Checking and Review of Operations documents. Preparation and review of Batch Manufacturing Records, SOPs, PDRs & Protocols. Conduct training for all DSP employees for prepared BMRs, PDRs and related documents. Review of TTD s, protocol and Quality Department Protocols related to Operations. Investigation of Batch failures in Operations. Monitor and follow good aseptic behavior inside Biologics DSP Facility. Support in hiring process and bringing quality workforce to develop a team that is highly respected and engaged towards departmental goals. Update the batch progress in PRM s and participate in client discussions. Develop and implement operating methods and procedures designed to eliminate operating problems and improve manufacturing efficiency. Safety and DI Responsibilities: Adhere to organizational policies & procedures on EHSS, POSH, Data Integrity and IT security, and monitor & confirm the same for the direct reports. Always wear the applicable PPEs and adhere to any other Environment, Health, and Safety (EHS) requirements in the workplace for individuals & lab/plant safety and monitor & confirm the same for the direct reports. Understand all necessary safety protocols and always follow the same to ensure safety for all and monitor & confirm the same for the direct reports. Proactively identify near-misses & potential incidents and communicate the same to supervisor and/or line manager or through the respective portals and disseminate learnings from those to the team members & any other concerned personnel to prevent recurrence of such events. Specific Responsibilities: Provide input to Downstream for improvement of products/process. Develop and train high potential candidates for the next generation of leaders. Serve as a mentor to develop other leaders within the department. Downstream batch plan preparation as per campaign schedule. Supervise commissioning and qualification activity of Biologics DSP Facility related equipment. Preparation of micro batch schedule and shift planning for day-to-day activities. Monitor and follow good aseptic behavior inside the Biologics DSP Facility. Support in audit and audit closure points. Involve in shipment of samples / final product as per packing and dispatch record. Prepare, revise and review of general validation protocols and reports, equipment requalification protocols, Installation, operation and performance qualification protocols and related documents. Supervise Downstream activities of buffers preparation, Harvest, purification and final filtration, Calibration of operations equipment. Monitoring and process control of specific operations of downstream. Review of Quality department protocols related to Operations. Support all site audits, inspections and client/consultant visits. Compliance to current good manufacturing practices. Facilitate & monitor the process with Engineering and Maintenance to troubleshoot process problems and identify solutions that reduce downtime in a cost-effective manner.

Key Responsibilities: Responsible to attend the training as per schedule and to ensure the training and work as per TNI. Responsible to perform and monitoring all the activities related to Manufacturing area. Responsible to fill the logs, BMRs and documents of area as per SOP and work execution. Responsible to follow the preventive maintenance schedule of machines, instruments and equipment s of manufacturing area. Responsible to ensure the cleaning and sanitization of machines, instruments and equipment s and manufacturing area. Responsible for line clearance activity before commencing the operations, CIP and SIP of Vessel Responsible to operate the machines : Manufacturing Vessel and CIP module Inform immediately to concern supervisor for any observation/disturbance found in the aseptic area. Responsible to update on self-hygiene, cleaning & sanitization of area, follow SOPs, filled the document, of area. Responsible to fill the log of area as per SOP and work execution. Responsible to ensure UAF working in area. To follow the cGMP, Good Document Practice and discipline in the department

Hi, Greetings Walk in Invitation: We are having face to face interview on 19th July 2025 Saturday in Mysore Single Round Face to face Company : A leading Pharma API Unit - in Mysore Position - Production Department Associate Work Experience Min 3 yrs in API in current Hike would be appreciable on Current CTC Note: No Charges If interested drop your CV to Priyanka Palit [ 7780363938|| jyotsna@avaniconsulting.com ] Thanks & Regards Priyanka Palit

Hi, Greetings Walk in Invitation: We are having face to face interview on 19th July 2025 Saturday in Mysore Single Round Face to face Company : A leading Pharma API Unit - in Mysore Position - Production Department Associate Work Experience Min 3 yrs in API in current Salary 20% to 25 % hike on current CTC. Note: No Charges If interested drop your CV to Priyanka Palit [ 9518220852 || priyanka@avaniconsulting.com ] Thanks & Regards Priyanka Palit

We are seeking a dedicated & skilled Production Officer to join our team. The ideal candidate should have experience in a regulatory-approved manufacturing plant with experience in handling critical production equipment & knowledge of cGMP standards.

The core job responsibilities of the position holder include: Responsible for the operation, cleaning, and primary maintenance of negative isolator, Vibro sifter, Bin blenders, and all other GEA granulation line equipment. Record activities in logbooks, Batch manufacturing record & complete documentation following cGMPs and good documentation practices. Perform all in-process checks and monitoring of intermediate processes in granulation. Select recipes, set process parameters in Blender HMI, and ensure correctness before blender revolution. Issue, utilize, clean, and retrieve sieves and handle machine change parts with inventory. Set up, changeover, and operate various manufacturing equipment in the granulation department. Report or escalate any conditions or problems affecting product quality to supervisor and HOD production. Maintain a neat, clean, and safe working environment, reporting safety concerns, accidents, or injuries to the supervisor immediately. Conduct in-process checks, monitor intermediate processes, set process parameters in PLC/SCADA per BMR before machine run in granulation area. Ensure compliance with current Good Manufacturing Practices in the Hormone Facility and follow GDP with data-integrity compliance. Complete training and training records within stipulated time. Prepare and use disinfectant and cleaning agent solutions following defined procedures. Adhere to all company policies, procedures, SOPs, and safety regulations.,

Supervising Production Teams & Production Planning Monitoring and controlling production parameters Ensuring GMP Compliance Collaborating with other departments Operating, cleaning, and maintaining manufacturing equipment & Documents BMR

You will be responsible for strictly following cGMP, Safety, and Environmental Practices in the manufacturing facility. Your duties will include filling Batch Manufacturing records and equipment cleaning records, as well as following Good Manufacturing practices during operations. It will be important to ensure Good Housekeeping in the plant area and equipment, and to use proper personal protective equipment as required. You will be in charge of planning and ensuring the availability of raw materials for daily production according to the production plan. Additionally, you will need to maintain documents such as Issue and dispensing register, and carry out processes as per Batch Manufacturing Record without any deviation. It will be crucial to adhere to data integrity in online documentation and handle hazardous operations safely. Part of your role will involve effectively utilizing resources such as utilities, personnel, and machinery to support efficient production processes.,

Job Title: Shift Incharge Production (Senior Executive Level) Location: Uppugal, Warangal, Telangana Industry: Chemical / Petrochemical / Active Pharma Department: Production / Manufacturing / Operations Experience Required: 7 to 10 years Employment Type: Full Time, Permanent Education: Diploma / B.E. in Chemical Engineering Role Category: Production / Manufacturing / Maintenance Functional Area: Production, Manufacturing & Engineering CTC: As per industry standards Job Description We are hiring a Shift Incharge Production for a reputed chemical manufacturing organization with a strong industry presence and global partnerships. Key Responsibilities: Ensure production as per SOPs and daily batch cycle Reschedule shop floor activities in line with revised production plans Plan and coordinate with Stores, Maintenance, and Dispatch departments Ensure timely manpower planning to meet shift targets Monitor inventory, equipment calibration, and safety compliance Handle non-conforming products and conduct RCA Maintain accurate production records and daily reports Train and evaluate subordinates on process and safety practices Technical Requirements: Strong knowledge of DCS systems Understanding of reactors, process parameters, and failure analysis Exposure to ISO/OSHA safety standards Skills: Planning and time management Delegation and team leadership Strong communication and coordination skills Desired Candidate Profile: Diploma / B.E. in Chemical Engineering 710 years of relevant experience in Chemical / Petrochemical / Active Pharma industries Willingness to work in shifts at the plant location Apply Now: Interested candidates can apply with their updated resume , current CTC , and notice period .

Role & responsibilities Responsible for day-to-day production activities and reports to Shift In-charge Production. Take the guidance from the supervisors and other operating personnel to carry out the production activities effectively as per the standard operating procedures. Responsible for maintaining all documents related to production. Indenting and receiving of raw materials / packing materials from stores as per requirement and same shall be checked while receiving raw materials / packing materials. Responsible for good housekeeping and keeping the production area in an orderly manner. Pack the intermediates / APIs as per customer requirements and transfer through prescribed formats. To raise the engineering requisitions related to production equipment breakdowns and preventive maintenance and co-ordinates with maintenance personnel to complete the jobs effectively. Reporting of all deviations to immediate supervisor Production. Responsible for conducting operations towards achieving 100% DDP, as per the given production plan. Responsible for conducting operations towards ensuring 100% compliance to the norms of cGMP, ISO-14001, and OHSAS-18001. Responsible for carrying out the needs of training as per him job role to ensure the adequate awareness in all of them towards the above requirements. Responsible for checking the completed BMSs for their appropriateness before submitting to QA. Review of all the filled production batch manufacturing sheets and related records ensuring that all the data is correct, complete, and signed. Should have Hands on experience with working on DCS plant operations. Suitable candidates may share your CVs to grabhilash@neulandlabs.com

Role & responsibilities Responsible for day-to-day production activities and reports to Shift In-charge Production. Take the guidance from the supervisors and other operating personnel to carry out the production activities effectively as per the standard operating procedures. Responsible for maintaining all documents related to production. Indenting and receiving of raw materials / packing materials from stores as per requirement and same shall be checked while receiving raw materials / packing materials. Responsible for good housekeeping and keeping the production area in an orderly manner. Pack the intermediates / APIs as per customer requirements and transfer through prescribed formats. To raise the engineering requisitions related to production equipment breakdowns and preventive maintenance and co-ordinates with maintenance personnel to complete the jobs effectively. Reporting of all deviations to immediate supervisor Production. Responsible for conducting operations towards achieving 100% DDP, as per the given production plan. Responsible for conducting operations towards ensuring 100% compliance to the norms of cGMP, ISO-14001, and OHSAS-18001. Responsible for carrying out the needs of training as per him job role to ensure the adequate awareness in all of them towards the above requirements. Responsible for checking the completed BMSs for their appropriateness before submitting to QA. Review of all the filled production batch manufacturing sheets and related records ensuring that all the data is correct, complete, and signed. Should have Hands on experience with working on DCS plant operations. Suitable candidates may share your CVs to grabhilash@neulandlabs.com

Long Description Role- Shift Officer - MDI Manufacturing To Supervise compliance to all CGMP or any other regulatory requirements, including EH&S requirements. Complete self-training and monitor training of team members on relevant SOP. Report any quality concerns or suggestion for improvements SOPs. Execute and supervise all tasks and activities as per the applicable SOPs. Supervision of operations, cleaning and maintenance of MDI process equipment's / area in MDI Production area of unit-3. Planning, execution, monitoring supervision of all unit operation for batch processing and Manufacturing. Co-ordination with cross-functional teams for smooth execution of production plan at shop floor. To ensure documentation of required process parameter as per SOPs. Training and development of subordinates to ensure functioning at shop floor as per cGMP requirements. To ensure status labelling of equipment, machines, area and instruments comply with the requirements. In-process checks during stage wise process as per Batch Manufacturing Record as per Standard Operating Procedure. Gap analysis of defined procedures in BMR / SOP / Protocol and initiation of corrective action. Handling of Quality Management Documents like change control, deviation, CAPA and other related documents. To ensure required inventory of approved consumables in Warehouse. To report of incident, non-conformity immediately to the manager. Competencies Developing Talent Innovation & Creativity Result Orientation Strategic Agility Process Excellence Customer Centricity Collaboration Stakeholder Management Education Work Experience

Hi, Greetings from Avani Consulting!! We have job opportunities with API Manufacturing Plant for the Production Associate/Sr Associate position, Mysore Location. Job Description: Production Department Position- Associate/Executive Work Experience - +4 in API Manufacturing Location - Mysore Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental procedures. 4. To ensure good housekeeping in the production shop floor. 5. To ensure compliance to cGMP, Safety, Health & Environment in delivering the product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date. 9. Monitoring and control of manufacturing environment and filling of daily log books. 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control. 11. To ensure the sanitization activity is performed in the department. 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required. 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality. 14. To ensure that stocks are reconciled at regular intervals. 15. Any other assignment allocated by Production head. If interested, kindly send your updated resume on whatsapp @ 7327039030 with the below details 1. Current CTC: 2. Expected CTC: 3. Notice Period: 4. Current Location: 5. Preferred Location: 6. Total Experience: 8. Relevant Experience in Production Process: 9. Experience in API Manufacturing: 10. Current company: 11. Qualification: 12. Experience in Documentation: 13. Reason for change: Thanks & Regards Monalisa Barik

1 Supervise & Monitor manufacturing and packaging activity. 2 To guide, supervise, co-ordinate, manage and lead a team of production officer and production operators in execution of manufacturing operation to achieve the stated goals. 3 Preparation, review and implementation of SOPs and Formats pertaining to manufacturing Department. 4 Preparation and review of URS for manufacturing department. 5 Imparting training of manufacturing SOPs and GDP to Production Operators and Production Officers. 6 Preparation and review of Performance Qualification batch record and protocol. 7 Executing and reviewing of manufacturing equipment qualification activity. 8 Execution and supervision of the Process Validation/Stability batches/Commercial batches. 9 Preparation and Review of Master Batch Manufacturing Records and Master Batch Packaging Record for Process Validation / Stability Batches / Commercial Batches and other relevant documents. 10 Review, execution and implementation of Batch Manufacturing Records, Process Study Protocols and Process Study Reports. 11 Management of day to day product related activities for timely execution of the assigned products through internal communications with internal departments like Purchase, Store, QA,QC,HR & Admin, Engineering, Maintenance team etc. and external communications with Tooling vendors and Equipment manufacturers. 12 Maintaining the department in accordance with the CGMP norms. 13 Responsible for initiation, assessment and closing of any deviation and change control regarding to manufacturing activity. 14 Work distribution to production officer and production operator. 15 Any work assigned by the Dept. head after proper training. 16 To raise the indent and capex as per requirement. 17 Activities other than defined in the are to be done, as per the requirement of HOD, by following HOD s instructions and guidance.

Job Responsibility: Supervision of manufacturing, processing, packaging and holding of drug product as per define and approved procedures for stability batches and commercial batches. Maintaining the area and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition. To perform online documentation with respect to departmental procedures as per good documentation. To impart training of operation and cleaning related SOP to all subordinates and operators. Co-ordination for IQ / OQ for any new equipments / system. To perform PQ for any new equipments / system. To follow all concern departmental SOPs for day to day operation and cleaning. To handle and manage material movement as per defined procedure and approved Batch Manufacturing Record / Batch Packing Record. Review, execution and implementation of Batch Manufacturing Records, Batch Packaging Records, Process Study Protocols, Process Study Reports and all relevant Documents. To follow all safety rules and departmental general instructions. To perform work other than defined in the Job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance.

To perform Machine and area clearance during dispensing, manufacturing and packaging operation. To perform sampling of blend, finished product, reserve sample, stability sample, hold time samples and other in-process samples and to manage sampling aids. To carry out in-process checks, AQL and ANSI Sampling as per respective documents viz. protocol,BMR, BPR, SOPs and other GxP documents. To ensure GMP practices at manufacturing shop floor. To verify raw material dispensing activity. To approve batch coding details during packaging operation. Review of executed batch records and release for next processing stage. Preparation and review of CPV data trend. To perform impact assessment of breakdown memo. To initiate change control, unplanned and planned deviation where ever required. To review area, equipment and cleaning log and to ensure proper labelling. To review environmental monitoring record, calibration records and executed Batch Manufacturing and packaging Records and respective electronic records. To perform calibration of IPQA instruments. To ensure appropriate labelling during manufacturing and packaging. Storage, handling and dispensing of printed packing materials. To review and approve packaging artworks, proofs and shade cards. To archive executed documents like BMR, BPR, Hold time Protocol etc. To review and approve the Quality Notification (Viz Change control and Deviation) during Batch Manufacturing/packaging. To monitor and record the environmental condition of label control room. To prepare and revise functional SOPs, wherever required. Activities other than defined in the Job Responsibility are to be done, as per the requirement of HOD, by following HODS instructions and guidance.

Role & responsibilities :- 1.Handling of oncology section , well knowledge about Batch manufacturing of oncology product and handling QMS of production 2.Planning and organising production schedules 3.Supervising and managing the work of junior staff 4.Manage production resources, including equipment and facilities, decide on and order the required resources and ensure stock levels remain adequate 5.Identify opportunities to improve processes to increase productivity, for example through lean manufacturing, and reduce costs 6.Planning and organisation skills to plan, run and monitor the production process 7.Maintaining quality standards while meeting production targets. 8.leadership skills and the ability to motivate others to meet deadlines 9.leadership and interpersonal skills ,communication skills ,team working skills.

Hi, Greetings from Avani Consulting!! We have job opportunities with API Manufacturing Plant for the Production Associate/Sr Associate position, Mysore Location. Job Description: Production Department Position- Associate/Executive Work Experience +7 in API Manufacturing Location Mysore Qualification: B.tech in Chemical// M.Sc Chemistry with 3 years in API Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental procedures. 4. To ensure good housekeeping in the production shop floor. 5. To ensure compliance to cGMP, Safety, Health & Environment in delivering the product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date. 9. Monitoring and control of manufacturing environment and filling of daily log books. 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control. 11. To ensure the sanitization activity is performed in the department. 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required. 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality. 14. To ensure that stocks are reconciled at regular intervals. 15. Any other assignment allocated by Production head. If interested, kindly send your updated resume on whatsapp @ 7015954549 with the below details 1. Current CTC: 2. Expected CTC: 3. Notice Period: 4. Current Location: 5. Preferred Location: 6. Total Experience: 8. Relevant Experience in Production Process: 9. Experience in API Manufacturing: 10. Current company: 11. Qualification: 12. Experience in Documentation: 13. Reason for change: Thanks & Regards Shweta Gupta

To Planning and implementing production operations to achieve monthly production targets as per sales plan/budget. To ensure that the Capacity Utilization, Product Quality, RM Consumption and Yield targets meet/exceed Annual Budget Required Candidate profile Batch Process knowledge People management skills Awareness of safe operating practices From Chemical Industry

Responsibilities: * Conduct BMR reviews and approvals. * Ensure compliance with GMP, API manufacturing, IPQA standards. * Collaborate with production teams on batch releases. * Monitor product quality throughout lifecycle. Food allowance Provident fund Annual bonus

Job description About Company- ACRYNOVA INDUSTRIES (P) LTD has been in operation in India for the last 40 years .The Company's product portfolio includes acrylic emulsions for textile printing, paint, adhesive, leather and paper coating applications. JD description of Deputy Production Manager We are looking for 10-15 yrs of experince in Batch processing . Most prefer the candidate who are experience in acrylic emulsion production. The incumbent will have to reside in Boisar with family The Deputy Manager is responsible for all Production activity and plant. Daily production plan as per production planning to achieve the target. Raw material planning and ensure consumption of raw material as per standard norms. Manpower planning and co-ordinate with other departments heads for smooth operation of manufacturing activities. To ensure the compliance of safety appliances by all personnel in the plant. To motivate the staff for safe working operation and take care of general safety in the manufacturing plant. The incumbent must have good knowledge and batch processing experience of emulsion polymerization. He shall be responsible for all production related activities-production planning, production supervision, meet quality targets and material handling and packaging. He will be responsible for training, mentoring and supervising the junior production staff during the emulsion polymerization reactions and the packaging process. The incumbent must be honest, sincere, hardworking and committed. Must have good communication and reporting skills. He will report to the Production Manager Required Candidate profile We are looking Qualification for this position is of BE Chemical /B.Tech chemical The ideal candidate would be one with at least 10-15 years experience in an emulsion polymerisation plant. Manufacturing emulsions for the paint, textile, adhesive and construction industries. The candidate should be first class Science graduate (BSc / BTech) with sound computer knowledge. He should be an enthusiastic and responsible person, should be honest, proactive and have good communication skills. Experience of following ISO procedures is preferred. Must be sincere and hardworking and must respect authority. He must have a good attitude and must be in a constant improvement mode. He must be proactive and aggressive. He must meet production targets and dispatch deadlines.