247 Sop Preparation Jobs - Page 2

Role & responsibilities Preparation of SOP, STP and Protocols as per requirement. Perform the Instrument calibration/ verification as per SOP. Involving in analytical method validation /verification and technology transfer activity. Handling of equipment the UV Spectrophotometer, SDS PAGE, RT-PCR, ELISA. Implementing all documentation as per GMP, cGLP & WHO GMP guidelines. Follow the established procedures and policies of the company Pertaining to EHS management system. Preferred candidate profile Execution of biochemical analysis like total protein Content, mycoplasma testing and DNA content etc., Perform cell culture analysis and virus titration performing micro biological tests such as micro bio identification, micro biological testing of material/intermediate products, Sterility testing, BET, mycoplasma and mycobacterial testing Performing Environmental monitoring Perfuming water testing (bio Chemical & Microbiology) Job Location: Kadi, Gujarat ( Bus facilities are available)

Role & responsibilities Handled Microbiology QMS Activities. Should have experience in OOS,OOT protocol review Preferred candidate profile Male Candidate Preferred

Record day-to-day accounting transactions in Tally/Zoho/Excel Assist in GST, TDS, and income tax filings Support internal audits and financial reviews Help draft SOPs and client working papers Coordinate with senior team for client reporting Perks and benefits Reimbursement based on client visits

Content writer, SOP Writer, crafting narratives for abroad university admissions, writing personal statements, essays, and scholarship applications, authentic stories, narrative angles representing students while meeting university requirements

Job Title: Quality Engineer. Experience: 4 to 10 years Location: Mysuru Notice Period: immediate to 15 days Mandatory Skill: QMS, Capa, GMP/Gdp/ GLP, Change Control, Deviation, Sop Preparation JD : Good understanding of Pharmaceutical GMP/GLP/GDP practices. *Experience in Pharma QMS activities like, handling Change Controls, Deviations, vendor qualifications and SOP updates. *Understanding of Internal Audits and CAPA closures. *Supporting for Quality metrics program. *Proficient experience with MS-office is required. *Strong written and verbal communication skills are essential *Experience working with virtual teams • Understanding of ISO 9001:2015 is required. *Strong communication, teamwork, data analysis, inductive reasoning and root cause analysis skills are required.

Immediate requirement for Executive - Regulatory function for one of the leading pharma company Position : Executive ( Regulatory function ) Educational qualification: MSc/MPharm Experience : 3 to 6 years of relevant experience. CTC : up to 6 LPA Contract Period: 1 Year (It can be extended based on performance ) Work Location : Thane office (Maharashtra) Transport provided : Yes (from Thane station) Working Mode ( Remote / Hybrid ) : Work from office. Shift timings : 9 am to 5.30pm Main Responsibilities: KEY RESPONSIBILITIES 1) To maintain high degree of quality of documents required for submissions to get the approval without deficiency / non-critical deficiency. 2) Timely readiness and submission of documents / dossier for variation / new submissions and renewals in different countries. 3) To follow Global Working Instructions and local SOPs for new submissions, variations and renewals and also support DRA initiatives. 4) Proven expertise in scientific writing and regulatory documentation Strong project management capabilities and ability to work independently Familiarity with global regulatory requirements and submission processes Key Competencies: Ability to diligently communicate with both internal and external stakeholders. Strong ability to collaborate within the team and also with all other functions. Excellent written/spoken communication skills. Computer Literacy. Interested candidates share cv : busiraju.sindhu@manpower.co.in Whats App : 7013970562

Role & responsibilities Biological (Therapeutical Protein) sample analysis by HPLC, UV, pH meter, Osmometer, ELISA and SDS-PAGE methods. Calibration of instruments and equipment as per the SOP. Responsible for analysis of in-process, finished products and stability samples. Raw material sampling and outsourcing activity. Preparation of certificate of analysis. Preparation of standard operating procedures, specifications, Protocols and standard testing procedures Operation of High Performance Liquid chromatography, UV spectrophotometer, Osmometer, pH Meter, gel power pack, Plate reader and stability chambers. Initiation of QMS events like lab event, Deviation, OOS, CAPA and Change controls Daily Maintenance of QC laboratory as per GMP requirement. Supervision of AMC and CMC activities for all instruments in the QC. Work in Shifts Preferred candidate profile

Oversees QC activities, staff training, SOPs, calibrations, GLP compliance, audits, records, and lab investigations (OOS/OOT) and aligns QC goals with production and ensures lab standards (candidates having approval from Raj. FDA will be preferred).

Job Role: ERPNext Functional Consultant (Manufacturing) Key Responsibilities Manufacturing Module Implementation Set up production plans, bill of materials (BOMs), workstations, and routing. Lead implementation and configuration of the ERPNext Manufacturing module. Configure production orders, job cards, and material consumption tracking. Align shop floor operations with inventory, procurement, and sales modules. Requirement Gathering & Analysis Collaborate with clients and internal teams to assess production workflows and supply chain processes. Translate manufacturing and operations needs into ERP configurations Conduct GAP analysis and prepare functional requirement documents. ERP Configuration & Customization Implement workflows, scripts, and automations using ERPNext/Frappe. Customize dashboards and production reports as per business requirements. Ensure system alignment with industry practices such as lean manufacturing and MRP. Training & Support Deliver hands-on training to production planners, supervisors, and floor staff. Provide post-go-live support, including issue resolution and system optimization. Act as a bridge between production teams and development/technical teams. Documentation Maintain detailed documentation of configurations, workflows, and system changes. Create user manuals and SOPs for manufacturing operations within ERPNext. Qualifications & Requirements Bachelors degree in Engineering, Industrial Management, or a related field. Minimum 35 years of experience with ERPNext or similar ERP systems. Proven expertise in ERPNext Manufacturing module implementation. Strong understanding of production planning, inventory, and shop floor processes. Skills in requirement analysis, process mapping, and functional documentation. Excellent interpersonal and communication skills. Ability to conduct user workshops and training independently. Preferred Qualifications (Good to Have) ERPNext Certification (Functional or Manufacturing specialization). Experience with ERPNext integrations (e.g., barcode/RFID, IoT devices). Familiarity with SQL and basic scripting using the Frappe framework. Experience in discrete or process manufacturing environmentsRole & responsibilities

Role & responsibilities Handle E&S insurance submissions , including reviewing, compiling, and forwarding complete and compliant submission packets. Ensure timely completion of all reports, trackers, and assigned operational deliverables. Conduct thorough quality checks on documentation and data before submission. Regularly update SOPs to reflect changes in process, compliance, or carrier requirements. Communicate professionally and clearly via email with underwriters, brokers, and internal stakeholders. Demonstrate proactive communication and ownership of assigned tasks. Maintain flexibility to support business requirements across different time zones, if needed. Utilize MS Office tools effectively (Excel, Word, Outlook, etc.) for reporting, documentation, and communication. Preferred candidate profile Knowledge of insurance Proactive communication Flexibility Ready for nigh shift MS Office Knowledge If Interested Kindly shared your updated resume on sakshi@beanhr.com Thanks & Regards, Sakshi Kala Bean HR Consulting-"Ahead Your Search" https://beanhr.com Locations:- Ghaziabad (Delhi-NCR) / Dehradun

Job Summary: We are looking for a highly experienced and dedicated Dairy Technologist based in Hyderabad , who will be responsible for improving the quality and yield of milk and milk products through rigorous testing, real-time MIS tracking, and field audits. The role demands regular travel to chilling centers and the main plant for quality monitoring, surprise audits, and operational oversight. Key Responsibilities: Quality Control & Field Audits: Conduct weekly and surprise audits at chilling centers and dairy plant to enforce quality and hygiene standards. Oversee milk testing protocols (fat/SNF/microbiological) and guide QA teams. Drive continuous improvements in product quality , process hygiene, and compliance with regulatory standards (FSSAI/ISO/HACCP). MIS & Reporting: Prepare daily, weekly, and monthly Plant MIS and Procurement MIS reports, with insights into procurement quality, production efficiency, and deviations. Generate quality dashboards and KPI reports for internal review. Maintain real-time data accuracy through coordination with procurement, production, and quality teams. Product Testing & Yield Management: Lead testing and analysis of milk and milk products to ensure optimal yield and quality recovery . Identify and troubleshoot yield losses in fat, SNF, and final products. Provide actionable recommendations for improving milk utilization efficiency. Reconciliation & Inventory Oversight: Manage reconciliation of milk procurement, SNP materials, stores, and finished goods . Coordinate with accounts and inventory teams for accurate tracking and reporting . Minimize stock losses and ensure correct reporting across the supply chain. Qualifications & Skills: Degree in Dairy Technology / Dairy Science / Food Technology . 810 years of experience in dairy production, quality control, and MIS reporting. Strong analytical background with practical experience in milk yield, quality monitoring , and product testing . Proficient in Excel , MIS systems , and ERP tools. Familiarity with FSSAI , ISO , and HACCP compliance standards. Must be willing to travel weekly/monthly to field and plant locations. Performance Metrics: Yield optimization improvements Quality non-conformance reduction Accuracy & timeliness of MIS reports Reconciliation closure percentage Audit compliance scores

Role & responsibilities Experience with QMS handling (Incident, OOS, OOT, OOC, Deviation, Change Control, and CAPA). Prepare of SOP and Specification and standard testing procedure Preparation of trends (QMS, Other lab trends). Ensure compliance with GLP standards in QC activities. Familiar with instrument knowledge (Like, Conduct advanced testing techniques such as RT-PCR, ELISA, Virus Titer, and TOC.) Operate laboratory instruments like Autoclave, Vitek 2, Colony Counter, Heating Block, pH Meter, and Conductivity Meter. Perform microbial analysis including sterility testing, BET, water analysis, and microbial culture activities. Strong understanding of QMS and GLP practices

KEY REQUIREMENTS: Experience of handling Internal Audit of listed and large Private Limited companies with a team of qualified Chartered Accountants. Preferably should have also worked on internal audit Documentation Software and analytical tools during audit. Execution and ownership of Internal audit engagements of various clients. Strong analytical, problem-solving, and critical-thinking skills are crucial for evaluating internal controls and identifying potential risks. Proficiency in audit techniques and procedures, risk analysis, and internal control evaluation is essential. Strong interpersonal skills are needed to effectively collaborate with stakeholders at all levels. KEY RESPONSIBILITIES Worked in Risk Advisory Services (Internal Audits, IFC Designs Testing, SOP Design, Process Reviews). The candidate should have good communication, analytical and report writing skills, command over excel, have worked on clients in Manufacturing/ Healthcare/ Service Industry. Handling Internal Audits. Preferred candidate profile Candidate should have good working experience in Internal Audits, handling good clients and available to join the firm with notice 30 Days or less. Immediate Joiners are preferred.

We are seeking a skilled QA Executive / Officer to join our Quality Assurance team. The ideal candidate will have hands-on experience in SOP preparation, internal audits, validation, cleaning validation, and quality systems (QMS). Key Responsibilities: - SOP Preparation, Revision & Training: Conduct gap analysis against QA SOPs, prepare and revise SOPs using Control Document Management System (CDMS), and conduct classroom training sessions for approved SOPs. - Audit & Inspection Readiness: Prepare annual internal audit schedules, conduct internal audits, and prepare audit reports. Raise CAPAs in TrackWise and verify effectiveness post-implementation. - Periodic Product Review (PPR): Prepare PPR for assigned products as per regulatory expectations. - Product Transfer & Validation Support: Support contract manufacturing sites during product transfers and validations. - Qualification Activities: Perform change control assessments from a validation perspective, prepare and maintain Site Validation Master Plan (SVMP), present monthly validation reports to the steering committee, and track and manage re-qualification schedules. - Cleaning Validation: Prepare protocols and reports for cleaning validation, conduct Clean Equipment Hold Time (CEHT) & Dirty Equipment Hold Time (DEHT) studies. - Quality Management Systems (QMS): Conduct gap analysis against QMS standards, handle and document change controls, deviations, and CAPAs, and perform risk assessments for process changes or new product introductions. Interview Details: Walk-in Interviews: Monday to Friday, 2:00 PM 4:00 PM. Please carry your updated resume and passport-size photograph. Interview Address: Unit G-14, 15, 16, 17, PRABHADEVI INDUSTRIAL ESTATE, 408, Swatantryaveer Savarkar Rd, Prabhadevi, Mumbai, Maharashtra 400025. Job Type: Full-time Experience: Relevant - 5 years (Required) Expected Start Date: 01/08/2025,

As a Senior Associate in Receivable & Inventory Controls based in Bangalore, your main responsibility will be focused on managing receivable and inventory controls, ensuring accurate reconciliation between our company's accounts and customer records. Your key responsibilities will include: - Conducting regular receivable and inventory reconciliations at the order level, with a focus on continuous improvement and process automation. - Collaborating with warehouse and supply chain management teams to address operational challenges in inventory financial reporting. - Ensuring the correct weighted average cost at the style code level is accurately reflected in the financial accounting system, coordinating with the technology team as needed. - Tracking the absorption of direct and indirect overheads and maintaining an audit trail of adjustments to product costs and closing stock. - Periodically reviewing internal processes and inventory health, identifying risks, and reporting to regional and corporate management. - Coordinating internal and external audits, including bank and stock audits, and ensuring necessary corrections are incorporated into the warehouse management system. - Managing statutory compliances and maintaining related trackers. - Preparing standard operating procedures (SOPs), conducting periodic reviews, and ensuring effective operation related to warehousing and manufacturing. The ideal candidate for this role would be: - A self-starter who can work with minimal supervision. - Strong in establishing and adhering to systems and processes. - Highly focused on cost accounting and controls. - Demonstrates high integrity, energy, and collaborative skills. - Chartered Accountant with 8-10 years of relevant experience. - Experience working in the E-Commerce ecosystem is mandatory. - Proficient in managing and processing large volumes of data. - Ability to work in an unstructured environment and set up systems and processes from scratch. - Good communication skills and the ability to represent the organization externally. - Capable of efficiently managing internal and external stakeholders. If you possess the above attributes and experience, and you are looking for a challenging role in receivable and inventory controls, we encourage you to apply for this position.,

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.

Job Responsibilities Operations Build successful relationships with Life Sciences (LS) client stakeholders to promote confidence in quality and compliance, as well as forward planning. Provide management and leadership direction for the development and implementation of quality and compliance programs. Collaborate with other Life Sciences accounts to proactively accumulate, share and reapply all learnings, successes as well as best practices. Collaborate with Global Life Sciences Quality Vertical for development, revision and implementation of QMS and quality documents. Responsible for ensuring Lide Sciences facilities teams adhere to the required training and ensuring in compliance to clients QMS and quality training requirements. Responsible for ensuring that the work conducted by the Facilities team, and its subcontractors is in full compliance with contractual requirements, clients SOPs, GxP, FDA and other regulations. Able to perform/support internal JLL compliance audits and prepare SOPs, and training materials for use by the Life Sciences facilities team in the performance of their work. Guide Life Sciences facilities team in closing recommendations from clients audit. Expected to interface with the clients quality personnel to ensure that all of the clients SOPs are followed, work performed by the LS facilities team is properly documented for traceability in the framework of GDP. Sustain quality assurance support and develop a Quality Engineering Maintenance program for a controlled-environment manufacturing and laboratory facility as it relates to the facilities maintenance of this plant. Conduct investigations and drive accountability for all quality events. Lead programs to create value for client to ensure program deliveries meet or exceed expectations. Facilitate quality-relevance investigation via structured Root Cause Analysis. As part of career development, lead Life Sciences accounts as an IFM leader.Reporting Manage and report on critical & key performance measurements. Develop and submit periodic site status reports related to the Quality Program. People Management Effectively lead and guide a Life Sciences Quality team by clearly communicating expectations, accountabilities and providing performance feedback for continuous improvement. Ensure Life Sciences Operations team members complete relevant quality and compliance training. Coach new Life Sciences team members on quality and compliance for their adaptation into specific Life Sciences accounts. Mentor, develop and train peer and direct report team members. Provides direction/information to vendors, facilities staff and service providers as required to ensure that quality assurance expectations are communicated and followed.Others Any other quality-relevant duties and tasks assigned. Knowledge, Skills & Abilities. MINIMUM REQUIRED / PREFERRED - Education/training Bachelor degree preferred Degree in science, technical or relevant discipline Sound fundamental knowledge in process utilities. 6+ Years of relevant experience preferred with minimum 4+ years in Quality and Compliance discipline in GxP manufacturing or laboratory environment. Six-Sigma and Root Cause Analysis training is essential. Skills and knowledge Background in technical documentation Work independently and within a team. Strong mindset of compliance and client-focus. Communicate effectively with technical, quality assurance and other personnel. Proficient in Word, Excel and other Microsoft Office Suite programs Ability to investigate, recognize and diagnose trends and patterns. Solid understanding of cGMPs as they relate to the performance of maintenance and repairs to facilities, utilities and equipment utilized for the manufacturing plants and laboratories for drug products. Experience working at an FDA regulated manufacturing facility in a quality assurance or quality control capacity. Support investigations and corrective action plans for appropriate discrepancies. Investigation of compliance issues as required, collaborating with relevant Compliance Partner(s) Understanding of FDA regulations including 210 CFR part 210 and 211. Strong commitment to quality assurance, and a willingness to help develop a quality first culture on the site. Knowledge of Quality Engineering techniques, CMMS systems, and Quality Management Systems English communication is essential Other abilities Good oral and written communication skills including the ability to communicate to all levels of management and willing to interface with a diverse customer base including technical and non-technical personnel.Physical work requirements and work conditions Familiar with process utilities and GxP environment.

Preferred candidate profile More than 4 Years of Experience of the proposed resource in undertaking Report preparation/ Capacity Building/processes preparation/ SOP development/ business process re-engineering/ inter-departmental coordination/ bid process management for State Government/Centre Government/Board and Corporation Coordination with Application team for development

Job Summary: The Documentation Engineer will be a key member of the execution team, responsible for managing and maintaining documentation related to installation, commissioning, and qualification of process and utility equipment. This role is ideal for mid-level professionals (3-5 years of experience) looking to advance their expertise in installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) for equipment used in pharmaceutical, chemical, and food processing industries. Key Responsibilities: Prepare and maintain IQ, OQ, PQ documentation for micronizing mills, containment isolators, bulk handling systems, and fluid bed dryers. Ensure documentation aligns with industry GMP, FDA, and other regulatory standards for equipment validation. Support audits by maintaining structured records for qualification processes on day to day basis. Assist in the installation, commissioning, and qualification of high-containment and powder-handling equipment. Coordinate with internal teams and vendors for proper setup and troubleshooting of process equipment, Provide technical support for operation and maintenance of containment solutions. Work with senior engineers to troubleshoot automation systems, PLCs, and electrical components. Analyze equipment efficiency and contribute to continuous improvement initiatives. Maintain electrical consumption reports to optimize operational performance.

Job Role Title Production Manager Business Segment Bentonite plant Educational Qualification: BE /BTech/ Diploma / M.Sc. (Mechanical/Electrical/Production/Chemicals/Chemistry) Technical Qualification: 8 to 15-year experience in production management Relevant field, Chemical / Agrochemical / Starch/ Engineering / Soda Ash / Silica / Any powder handling facility Key Accountabilities 1.Production planning and Plant operations 2.MIS reporting / API Audit / Quality management system 3.Cost control and Manpower optimization 4.Internal or external team co-ordination 5.Quality control and Process optimization 6.Hose keeping and 5-S managements 7.Team building and contract labour managements 8.New product developments 9.Plant safety / KAIZEN 10.Inventory managements for Raw material, Packing material and Finished Goods 11.Plant Equipment's and Material handling equipment's handling 12.SOP, CCP creation and implementation Type of Equipments :-Dryer, Belt conveyer, grinding system, Pulverizer, packing machine, Forklift, Loader, Weighing system, Screw conveyer, Elevators, Silos, Mixer, Dosing system, Reactors, Kiln, Roller grinder, Pneumatic system, laboratory Equipments, Filter press, ETP, HAG

Role & responsibilities To review that all relevant quality management systems of Hosur manufacturing site are implemented and well maintained. To review, monitor and improve Quality performance of Hosur manufacturing site. To promote quality attitude, awareness, and mindset of the site by all proper means including training to the cross functional team members. Implement, audit, and develop quality management system, in line with Global quality policy/ manual and procedures relevant to area. Ensure the required process controls are in place wherever they are necessary. To review that testing and inspection of all raw materials, packaging materials and finished goods are carried out as per documented testing procedures and specifications. To review that the release of all raw materials, packaging materials, bulk as per approved SOP before they are used for further production activities. To review the release process of all finished goods as per approved SOP and global requirements including GFS before they are released for distribution. To review all RM and PM used in manufacturing process are from approved suppliers and with the required quality before it reaches Hosur manufacturing site including COA verifications against the documented specifications. To review all the internal lab/ External labs are conducting the testing processes as per the documented procedures and specifications. Ensure appropriate investigation are carried out throughout the manufacturing site in case of any quality related issue and ensure the corrective and preventive actions are implemented to mitigate the identified root causes for the quality issue. Ensure the preparation of training calendar and adherence to the same. To support and conduct self-inspection quality audits across all the QMS areas and continuously improve the QMS implemented at site. To ensure that all audit points/recommendations highlighted in the audit reports are followed up and closed effectively as per the agreed timelines. Review the performance of suppliers on a regular basis. To support all key initiative at the site as key member of the site. To support the site in conducting management review meetings as per the schedule. To accept and execute other responsibilities assigned by the management time to time.

Purpose of the Job This is a Subject Matter expertise profile which requires a detail-oriented and experienced Regulatory Reporting professional to join our team. The ideal candidate will have a strong background in banking, possess relevant regulatory knowledge Candidate will be responsible for preparing, reviewing, and submitting timely and accurate regulatory reports regulators. 1. Prepare and submit regulatory reports as per jurisdictional guidelines 2. Review, validate, and reconcile data sources used for regulatory reporting, ensuring accuracy and completeness 3. Collaborate with internal teams including Finance, Risk, and Compliance to gather data and ensure accuracy in reports 4. Maintain strong documentation and audit trails for all submissions 5. Assist in the implementation of new regulatory reporting requirements and upgrades to reporting systems The incumbent is expected to act as a catalyst for management of the Entire Control management across the entity Life-cycle (Onboarding, post-Modifications, and Closure) of entities identified by the bank SoP for performance of any onboarding related consequence management or control actions The Incumbent is expected to be well versed with the extant norms, guidelines of various regulatory bodies such as RBI , UIDAI, CERSAI, NeSL , CRILIC, Ministry of Corporate Affairs, and all relevant URLs, Sites in the Corporate/ mSME/ Non Individual domain. The Incumbent has to provide thought leadership and process improvement initiatives by demonstrating Control across Audit observations, good performance across RISK scorecards and ensure Compliance for reporting to relevant external and Internal authorities and control functions. Deliverables 1. Updation of SoPs basis guidelines and compliances laid by Regulator(s) ( like RBI , UIDAI, CERSAI etc.) with respect to Manual Onboarding Operations. 2. Periodic Onboarding Due Diligence Such as Creation / Management / Closure, of Accounts , Name Screening for Individual and Non- Individual entities (including BCs and BC Agents), and Individuals as Authorized Signatories of these entities 3. Ensure Clean Compliance and reporting , nil Audit observations , Process adherence from the team as per SoP and Way-of-Working 4. Interacting with team(s) like Product, IT, CBS, CX, Risk , Audit, Compliance, Internal Control (Control Functions) Demonstrate Customer centric, Innovation, dynamism, Industry benchmarking, Collaborative, Analytical, & Alive to customer needs.

The Production Engineer is responsible for ensuring that production targets are met with quality while maintaining employee morale and safety.

JOB TITLE : Production Engineer COMPANY : Torrecid India Pvt Ltd COMPANY PROFILE Torrecid is a Multinational Business Group founded in 1963, dedicated to provide products, services, solutions and future trends to the Ceramic and Glass Sector. Torrecid Group is present in 29 countries around the world with customers in more than 130 countries. Its headquarters are located in Alcora - Castelln, in Spain. LOCATION : Vadodara QUALIFICATIONS: Bachelor's or Masters degree in chemical, mechanical, ceramic or related field. Fresher’s can apply but prior experience in a production role will also be welcomed WHAT WE ARE LOOKING FOR: Fast learning ability Resolute people focused on goals achievements WINNING MENTALITY Creative problem-solving Excellent communication and interpersonal skills, with the ability to communicate complex technical information to non-technical stakeholders. Bold people with adventure spirit WARRIORS Long term commitment Strong leadership skills and the ability to manage and motivate a team. Strong project management skills and the ability to manage multiple projects simultaneously. Experience with production budgeting and financial management. Knowledge of the latest trends and advancements in technology and their potential impact on the organization. Experience working in a fast-paced, dynamic environment. JOB RESPONSIBILITIES: Track all materials, equipment, and operator, and report daily production figures. Monitor the productivity of staff, materials, and equipment to ensure maximum efficiency. Ensure the work areas are clean and organized. Participate in troubleshooting along with identifying the root cause of production issues Uphold all health and safety procedure Identifying, documenting, and reporting unsafe practices. Regular reporting work to management based on company culture. Design and construct new effective SOP’s for making current production process more effective. Ensure proper inventory rotation. Research and propose new innovative products to produce in our existing facility. Draft, manage, and revise technical documents, reports, and presentations Keeping abreast of advancements in engineering and production, and sharing knowledge with co-workers. Scheduling and participate in the meetings with relevant departments and stakeholders. SALARY PACKAGE & OTHER BENEFITS As per Industry Standards Health Insurance Life Insurance Performance-Linked Increment CTC 3.5 to 4 Per Annum THINGS WE BELIEVE IN We believe in Ethics, sustainability, passion, commitment, the initiative to learn, critical thinking, self-confidence, creativity, a sense of humour, effective communication, and care for our stakeholders are just some of the key aspects that guide our actions. We believe in differentiation through our innovations, actions and our company culture. HOW YOU WILL GROW AT TORRECID Additionally, our commitment to internal promotion, based on meritocracy, ensures that individual growth is determined by each person’s dedication and potential. We offer transparent communication with experience colleagues and learning opportunities. At Torrecid, we believe that our company culture not only reflects our identity but also provides a strong foundation for both personal and professional development. Our culture drives the opportunities for growth and empowers every team member to reach their full potential. Why Us, we are one of the fastest-growing large technical companies in the world, with offices in 29+ countries across the globe and 3500 + employees our company is extremely diverse with vivid nationalities represented. We offer the opportunity to work with colleagues across the globe. we offer most ethical work environment, invested in your growth, offering learning and build your career at every level to help you find your own unique spark. CONTACT INFORMATION hr.india@torrecid.com

Roles and Responsibilities Responsible for GPCB work, SOP Preparation, Periodic Revision of EHS SOP, Work Permit System, Documentation work etc. ETP and STP Knowledge. Plastic Waste (ERP) related Knowledge. Knowledge of CGWA. should knowledge of EC compliance uploading process on Parivesh Portal. Knowledge of MEE. Responsible for Regulatory Compliance Responsible for Statutory Audit, Safety Audit. Responsible for Risk Assessment, Incident Investigation, Hazard dentification. Responsible for Safety Training to new joiners. Responsible for Legal Compliance. Responsible for Environment Audit.