377 Osd Jobs - Page 2

The candidate will be responsible for the proper receipt, storage, and GMP-compliant dispensing of raw materials used in pharmaceutical production Perform raw material dispensing activity in designated dispensing booths under controlled conditions.. Required Candidate profile Receive, inspect & label incoming raw materials as per SOP Coordinate with the QA, Production & QC department during material movement Ensure adherence to GMP, GDP & safety guideline during dispensing

Roles and Responsibilities Manage warehouse operations, including inventory management, storage, and dispatch. Coordinate with production team to ensure timely delivery of raw materials (RM) and packaging materials. Ensure accurate recording of stock levels, orders, and deliveries using ERP systems. Desired Candidate Profile Experience: 2-5 years Qualification: B.A/ B.Sc./ B. Com Must have experience in OSD Formulation Warehouse operations Should be willing to work in shift operations Interested candidates can share their updated CV to jahnavi.kodali@granulesindia.com

To perform IPQA activities at shop floor in every stage of OSD manufacturing and packing. Review of BMR & BPR. Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release. Review of documents of respective areas and logbooks for adequacy and completeness. QA overview for receipt of material from warehouse to production. IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities. Review and Control of SOP’s, Specification, BPR issuance, Master Formulae and Records. Preparation & Review of process validation protocols and reports. Any job activity assigned by HOD

Walk In Drive For Engineering Services Department Formulation's Division @ Burgula Interview Date : 26-07-2025 Department : Engineering Services OSD, Formulations Qualification : Diploma | B Tech ( Mechanical | Electrical | Instrumentation ) Work Location : MSN Formulations Unit-VI, Burgula Interview Venue Details :- X59Q+P95, Mothighanapur, Burgula, Telangana 509202

Manager 1 Engineering Educational Qualification BE Mechanical / Electrical / Instrumentation Experience 15-17 years in OSD Project/Maintenance Job Summary: Handling of overall site facility maintenance, Scrap yard, online documents and QMS documentations. Responsibilities: Planning and execution: Utility section: Preparation of the material BOQ for the structural steel, pipe and pipe fittings as per company standard practices. Supervision of the fabrication work as per approved drawings for the structural and pipe and fittings for the utility services. Supervision of the insulation work, Painting works as per color coding and related activities. Measurement sheet checking and certification of work completion as per company requirement. Installation of the Utility lines and any other equipment which is part of the utility services. Unloading and shifting of the equipment as per company requirement with safety. Issuance of the work permits for above work and execution of the work with safety. Quality Improvement in mechanical works such as Machine Installation and structural fabrication work, piping and insulation works. Supporting role in installation of the process equipment used in OSD and Non OSD. Co-ordination with the external contractors and consultants for the execution of the work and modification in drawings as per site requirement if required. Reconciliation of the structural and piping material. Weekly report preparation for the status of the project work and up gradation of the same to planning department. Qualification of the equipment as per company guidelines and procedures and report closures. Plant Maintenance Brownfield projects in the OSD block and changes required in same as per company requirements. Planning, procurement and installations of the process equipment. Break down Maintenance & Preventive maintenance coordination. Material requisition slip Preparation and issuance and approval of the same. GMP Documents preparation and signing. Maintenance management (B/D and PM) of utility equipment. PR / Indenting for all Process equipment and Spares. Compliance of audit and internal observation points. Workout the energy conservation, Execution, Monitoring. Solvent storage and distribution and related activities.

Role & responsibilities Manage technology transfer activities from development to commercial manufacturing for OSD tablets. Oversee and execute process scale-up, process optimization, and validation to ensure smooth transition into commercial production. Maintain an in-depth knowledge of USFDA regulations for OSD products and ensure compliance with all regulatory requirements during tech transfer activities. Work closely with R&D, manufacturing, and quality teams to address any technical challenges during tech transfer. Preferred candidate profile Prefered candidates from OSD (manufacture Tablets , capsules,)background . USFDA experince is must Its a plant based role.

Required skill: IBM filenet P8 Added advantage AWS, FileNet BAW, Dev Ops. Responsibility. Experience in IBM FileNet BAW Administration and application maintenance. Experience in installation of FileNet P8 , ICN . Experience in installation and configuration of WebSphere 8.5/9.0. Hands on FileNet upgrades . Experience of P8 migration from on-premises to cloud environment. Experience in troubleshooting day to day user service requests /incidents on call. Experience in change request creation and implementation. Experience in working with other support/middleware teams for issues resolution. good communication & inter-personal skills. Experience in working with agile process. Deliver and Maintain high-quality application software solutions that meet Business Users . requirements. Effectively communicating through excellent written and verbal communication skills. Contributing to the development of a solution design and/or strategic deployment roadmap. Contributing to project documentation, including, but not limited to requirements documents, . technical design, test plans, and knowledge transfer documentation. Participating in multiple projects simultaneously. Demonstrating strong customer-facing skills by building and maintaining positive customer . relationships. Preparing, maintaining, and submitting weekly activity/progress reports and time recording . 100%. PART 3. Duties and Responsibilities. List in order of importance and state approximate weightage accorded to each. Deliver working software that meets the functional/non-functional requirements of business users. Deliver high quality software consistent with the principals of continuous integration. Develop and manage effective relationships peers, customers and managers. Adhere to SDLC and Allianz Technology Group Standards. 60 %. Work with the technical team in resolving complex issues and troubleshooting. Conduct code reviews of other peers and ensure code quality is not compromised. Estimate delivery costs and timeframes to meet the needs of project managers aligned with business priorities. Challenge business requirements and OSD requirements that do not deliver customer value or do not make appropriate use of technology. 30 %. Co-operate with and actively contribute to the health and safety of themselves and others within the workplace. 10 %. PART 4. Qualification, Experience, Technical and Functional Skills. Must-Have. B.E, B Tech, MCA or equivalent qualification. The candidate should have 8 to 14 years of professional experience in FileNet P8 Admin. BAW, AWS experience would be added advantage. Knowledge and understanding of on-premises and cloud enterprise software . deployments. Strong analytical, technical and problem-solving skills. Strong communication skills. Adhere to Allianz internal standards and best practices for consistent, high quality . project delivery. Good to Have. Working knowledge of any Linux, DB tools. Experience in DevOps tools like Jenkins / docker / etc. Allianz Group is one of the most trusted insurance and asset management companies in the world. Caring for our employees, their ambitions, dreams and challenges, is what makes us a unique employer. Together we can build an environment where everyone feels empowered and has the confidence to explore, to grow and to shape a better future for our customers and the world around us. We at Allianz believe in a diverse and inclusive workforce and are proud to be an equal opportunity employer. We encourage you to bring your whole self to work, no matter where you are from, what you look like, who you love or what you believe in. We therefore welcome applications regardless of ethnicity or cultural background, age, gender, nationality, religion, disability or sexual orientation. Join us. Lets care for tomorrow.

Role & responsibilities Handling of pre and post approval regulatory activities of US/EU/CA submissions. Review of developmental documents for regulatory submission. Good knowledge of handling CMC documentation for Dossier submission Compilation and Submission of Annual reports and Supplements. Having the experience of solid orals and injectables. Preparation of Sterility Assurance Package for injectable Dossiers. Preparation of Pre-IND/scientific advice meeting packages Drafting, compiling & eCTD publishing of dossiers for regulatory filings. Review of specifications and test procedure as per pharmacopoeia requirements. Providing regulatory support for customer filings and customer queries. Evaluation of regulatory authority deficiencies and preparation of action plan accordingly. Also follow up of response documents with concern stake holders. Evaluation and approval of QMS documents, wherever applicable. To update cross functional teams for different regulatory compliance & requirements. Responsible for outlining requirements for labelling, storage and packaging. Review of product development report and QBD concepts. Updating product approval package to plant team. Preferred candidate profile Should Have Formulation Regulatory Affairs Relevant Experience in US/EU/Canada Perks and benefits

Role & responsibilities Required for Quality Control(Formulations) Quality Control(QC)- Need 1 to 5 years of experience. *Analysis of Finished Product & Stability *GLP and LIMS, Documentation Preferred candidate profile Perks and benefits

We’re building an Agentic AI Platform that lets enterprises solve real business problems using Agentic AI workflows. From utility operations to legal document review; our mission is to let AI agents think, act, and deliver; fast, secure and locally. We’re looking for an Agentic AI Engineer who’s hungry to learn and ship. If you’re ready to build with cutting-edge frameworks like Lang Chain, CrewAI, Lang Graph, Google ADK and more and can translate real enterprise problems into intelligent multi-agent workflows, this role is for you. What You’ll Do Build and deploy AI agents using open-source agentic frameworks Explore and integrate models from OpenAI, Mistral, Gemini, Llama, Claude, etc. Use tools like Retrieval-Augmented Generation (RAG), knowledge graphs, and vector stores Work with product managers and domain experts to solve real problems (not just prototypes) Continuously test and refine agent behavior across different enterprise domains (utilities, legal, marketing, supply chain) Actively contribute to evolving our proprietary DataInsightAI platform Must-Have Skills At least 1+ years of hands-on experience implementing a enterprise level Gen AI project that has gone live. Strong Python skills (Async, FastAPI, LangChain/CrewAI or similar) Experience working with LLMs (OpenAI, Llama, Claude, Gemini, etc.) Familiar with agentic AI workflows, prompt chaining, and tool use Understanding of RAG, vector databases (like FAISS, Qdrant, Weaviate) Curiosity-driven mindset, fast learner, hands-on coder Ability to simplify complex problems and build MVPs fast Nice to Have Worked on multi-agent architectures or fine-tuned LLMs Used graph databases (Neo4j) or custom knowledge stores Experience deploying on Azure/AWS/GCP Familiarity with LangGraph or Google ADK Why Join Us? Work on cutting-edge agentic AI every day Be part of a lean team with real ownership Ship fast and solve real enterprise challenges Backed by InTimeTec, with a strong AI/ML engineering culture

Walk-In Interview at Vibonum Technologies Pvt Ltd, Nanjangud, Mysore We are hiring for Production, Packing and Warehouse candidates for the OSD Palnt. Date: July 26th, 2025 Venue: Vibonum Technologies Pvt Ltd, Nanjangud, Mysore Plot Numbers 6B and 7, Kallahalli KIADB Industrial Area, Nanjangud, Opposite to Govt. ITI College, Mysore District 573201, Karnataka, India. We invite B. Pharm, ITI and Diploma candidates to participate in this drive and become a part of the Vibonum family. Please carry a copy of the following documents: Updated Resume Recent Payslips, increment letter and appoinment letter Relieving Letter (if applicable) Educational Qualification Certificates We look forward to meeting passionate and skilled professionals. Take your career to the next level with Vibonum Technologies Pvt Ltd !

Key Responsibilities: Organize and supervise daily production activities to achieve defined output targets. Ensure all products comply with Pharmacopoeial standards and specified physical parameters. Supervise packing and other production-related departments as required. Ensure compliance with all regulatory and GMP documentation requirements. Manage QMS documentation related to production activities. Effectively handle manpower and ensure optimal shop floor productivity. Be audit-ready and experienced in facing regulatory, client, and internal audits. Requirements: 58 years of relevant experience in pharmaceutical production (OSD preferred). FDA approved for Tablets and Capsules . Strong knowledge of GMP, QMS, and audit preparedness. Hands-on experience in manpower management and production documentation. Qualification : M.Pharm / B.Pharm Location : Palghar Plant

We invite Engineering graduates, ITI and Diploma holders to participate in our Walk-in Drive and become a valued part of the Althera family. Please carry a copy of the following documents with you: Updated Resume Recent Payslips/Increment letter and appointment letter Relieving Letter (if applicable) Educational Qualification Certificates We look forward to meeting talented professionals like you. Join us and take the next step in your career with Althera! Vacancy for: 1. Technician/ Specialist Engineering (ITI or Diploma with 2 to 3 Years Experience) : Being a Specialist in Engineering and Maintenance, Major responsibilities include daily work, all the engineering-related routine and non-routine Activities. Execute the maintenance activities when assigned by the immediate superior. Involved in Project execution. To bring to the notice of superiors any process changes to improve productivity and quality of the product. Monitoring and daily operation of Utility equipment as per SOP. Maintaining Logs of utilities as per the SOP. Planning and doing the Preventive maintenance of all utility and Production Equipment. Execution of Calibration of all measuring equipment in the facility. To bring to the notice of the superior any accidents and injuries. To implement cGMP in the Department. Working in compliance with SOPs and Policies of the company. 2. Asst.Manager / Sr.Executive, Engineering & Projects (BE Mechanical or Electrical with 5 to 8 Years Experience in OSD) : 1. Facility Maintenance: Oversee preventive and breakdown maintenance of HVAC, utilities, & cleanroom systems. Ensure proper functioning of water systems (WFI, RO, Purified Water) and other critical equipment. 2. Utility Operations: Manage steam, compressed air, chilled water, and electrical systems. Monitor energy usage and promote energy efficiency initiatives. 3. Documentation & Compliance: Ensure GMP-compliant documentation for equipment qualification (IQ, OQ, PQ), maintenance logs, and calibration records. Handle audits (regulatory, customer, internal) and ensure compliance with cGMP, USFDA, MHRA, WHO guidelines. 4. Vendor Management: Coordinate with equipment suppliers, contractors, and service providers. Review AMCs service contracts. 5. Project Execution: Plan, schedule, and implement new projects (greenfield, brownfield, expansion, modifications). Track progress against project timelines, cost, and quality. 6. Equipment & Utility Installation: Oversee installation and commissioning of manufacturing and packaging equipment. Ensure adherence to safety and GMP requirements during execution. 7. Cross-functional Coordination: Liaise with production, quality, safety, and validation teams for seamless project integration. Coordinate with architects, consultants, & contractors during design and construction phases. 8. CAPEX Planning: Prepare capital expenditure proposals and ROI justifications. Monitor project budgets and control costs. 9. Design; Create and Review facility layouts for production, warehouse, utility, and QC areas Ensure proper flow of personnel, materials, and waste as per GMP norms.

Role & responsibilities : Only for male candidates Shri Kartikeya Pharma [Jadcherla / India] located in JADCHERLA TELANGANA, India had its last known inspection on 04 Jan 2024. There are 1 known inspections on record Preferred candidate profile Freshers,1-2 yrs

The position of Plant Head is currently available at Baddi. The ideal candidate should have a minimum of 5 years of experience as a Plant Head with a focus on OSD. The role is specifically for Plant Head and not production. The successful candidate should have a good stability record in previous roles. This is a full-time position with a day shift schedule. Interested candidates can send their resumes to admin@addiibiotech.com or contact 7719715392. Work Location: In person.,

Role & responsibilities Review of Technology data package and preparation of Gap analysis document. Preparation of technology transfer protocol and report. Co-ordination with FD for smooth Tech Transfer. Monitoring of validation batches at production site. Perform Feasibility trials, Product evaluation trials to understand critical process parameter for smooth transfer and process understanding. Review of MPCR and protocol. Planning for Execution of Process design, Process qualification batch. Coordination with Production, Quality assurance, Quality control, Engineering, Regulatory Affairs, SCM and warehouse for the TT activities. Should be part of handling deviation, change control and failure investigations. Process manufacturing parameters for Qualification batches Vs Commercial batches. Preparation and reviewing of intended batch documents for regulatory submission. Trouble shooting of existing products and process improvement to increase output or to reduce processing time or to improve the quality of products. Preferred candidate profile required from OSD pharmaceutical Executive - TT: Exp required: 04 to 06 years Dy. Manager: Exp required: 09 to 12 Years Candidate should be willing to relocate/work in Nanjangud, Mysuru Plant.

Titlle : Manager 1 Engineering Educational Qualification : B Tech/BE Electrical/ Electronics & Instrumentation Engineering Experience: 14 years & above Requirement : 1. To ensure prompt attention and resolve issues of all operational and breakdown maintenance activities related to Utilities, HVAC System, and Water System. 2. To ensure timely execution of Preventive Maintenance of Utilities, HVAC System, Water System & Process Machineries performed as per the SAP schedule and maintain accurate record of the same. 3. To provide Technical assistance & Support for efficient operation of ETP. 4. Review and approve QMS related activities in EDMS & Trackwise systems to ensure compliance and documentation Integrity. 5. Responsible for Compliance of Internal & External Audits. 6. Tracking WBS code for all, CAPEX, Projects & Aspire Projects 7. Conduct Monthly review of MTTR, MTBF & KPIs 8. Following up with OEM, third Party service s & AMC to ensure timely service delivery and issue resolution. 9. Maintaining and ensuring Safety and discipline for all engineering related work and personnel of Engineering. 10. To provide Training to Subordinates to enhance their operational efficiency. 11. To performed any other duties assigned by HOD.

Greetings from Zydus! We have an exciting opportunity for candidates who have experience in Market Complaints. Department: Packing Role: Market Complaint / Investigation Location : Ahmedabad Interested candidates are requested to send their CV on vaibhavi.harish2@zyduslife.com or whatsapp on 6358958368.

Role & responsibilities Technology transfer and scale-up activities at external/Third-party manufacturing/CMO sites. Coordinate and execute along with CMOs/internal teams for feasibility trials and commercial production. Evaluate & assure the equipment for capacity and process suitability at manufacturing site. Prepare and review documentation for feasibility/Trial batches, scale-up, exhibit /validation batches, and for commercial production. Plan, execute and monitor exhibit /validation batches for regulated markets at CMO/Third party manufacturing sites Ensure timely execution and readiness of CMOs for product transfers, validations and commercial Production. Troubleshoot technical issues at external manufacturing locations/CMOs and ensure smooth operations. Support regulatory documentation and compliance, especially for EU-regulated markets. Preferred candidate profile Experience in Tech Transfer, MS&T (Manufacturing Science and Technology transfer), and working with external manufacturing units/CMO. Process optimization and developmentfrom lab scale to commercial-scale batches. Strong knowledge in formulation and manufacturing of oral solid dosage forms (tablets/capsules). Familiarity with scale-up, validation, exhibit batches, and regulatory submissions. Experience in packaging will be added advantage Experience with European regulatory requirements will be a strong advantage. Project Management skills (planning, coordination, execution) Strong Communication, coordination, and problem-solving skills.

About the Opportunity Join a dynamic player in the IT services and enterprise technology sector, focused on delivering robust endpoint management and deployment solutions. Our organization serves a broad range of industries by enabling efficient system imaging, deployment, and configuration solutions. We pride ourselves on leveraging cutting-edge technologies to drive operational excellence and digital transformation. Role Responsibilities Manage and execute complete Windows Imaging and Operating System Deployment (OSD) processes to ensure streamlined device provisioning and lifecycle management. Configure and maintain Intune Autopilot setups, ensuring all devices are seamlessly enrolled and compliant with organizational standards. Collaborate with cross-functional IT teams to integrate imaging processes and Autopilot workflows with broader endpoint management strategies. Troubleshoot and resolve any hardware and software issues related to imaging, deployment, and configuration to maintain optimal system performance. Document procedures and maintain operational playbooks to ensure consistency, security, and compliance with IT best practices. Responsible for settig up new windows 11 systems, ensuring the approperaite hardware software requirement are met. Configuring the OS as per the company standards policies. Stay updated with emerging trends and best practices in Windows deployment strategies to advise on potential areas for improvement. Skills Qualifications Must-Have: Proven experience in Windows Imaging and OSD, including use of tools such as MDT, WDS, or SCCM. Must-Have: In-depth expertise in configuring and managing Intune Autopilot deployments. Must-Have: Strong troubleshooting skills with a focus on Windows configuration and deployment challenges. Must-Have: Ability to work on-site and collaborate closely with IT teams to ensure seamless operational transitions. Preferred: Proficiency in PowerShell scripting for automation of imaging and deployment processes. Preferred: Familiarity with ITIL frameworks and best practices in IT service management. Benefits Culture Highlights Work on cutting-edge deployment and endpoint management technologies in a collaborative, innovative environment. Engage in continuous professional development with tailored training and growth opportunities. Experience a culture that values technical expertise, teamwork, and a commitment to operational excellence. Location: India | Workplace: On-site

Technology transfer, scale-up at external/Third-party manufacturing/CMO sites. Coordinate with CMOs/internal teams for trials, validation and commercial production. Documents preparation for scale-up, validation and timely execution at CMOs. Food allowance Provident fund Health insurance

Job Location : Ahmedabad Role - Blister Machine Operators (Secondary/ Primary) Qualification ITI/Diploma Exp 2-5 Years Role - Blister Machine Officer (Secondary/ Primary) Qualification B. Pharma / Bsc Exp 3-10 Years Renu Kumari Senior Recruitment Consultant Adecco [ India] Watsapp +91, 6364920532 Email ID : renu.kumari@adecco.com

Company Name : Avantika Medex Pvt Ltd Job Title : Sr. Officer / Sr. Executive Formulation & Development (F&D) Department: Formulation & Development Formulation Location: Plant (Chachravadi Vasana) Reporting To: Manager / Senior Manager – F&D Experience Required: 3 to 8 Years Qualification: B.Pharm / M.Pharm (Pharmaceutics or relevant specialization) Job Summary: We are looking for a technically sound and motivated Formulation and Development Executive with 3 to 8 years of experience in the pharmaceutical industry. The candidate will be responsible for the development of solid oral dosage forms (tablets, capsules, etc.), execution of pre-formulation studies, lab-scale trials, and coordination for scale-up and technology transfer. Key Responsibilities: Develop formulations for oral solid dosage forms (OSDs) such as tablets, capsules, and powders. Conduct pre-formulation and excipient compatibility studies . Prepare and execute laboratory trials and pilot batches . Optimize formulations based on stability and performance results. Coordinate with Analytical, QA, RA, and Production departments for seamless project execution. Prepare product development reports (PDRs), batch manufacturing/packing records (BMR/BPR) , and technology transfer documentation. Ensure adherence to GMP, ICH, and regulatory guidelines throughout development stages. Support scale-up, exhibit batches, and validation in the manufacturing plant. Assist in investigation and troubleshooting during development and commercial stages. Keep abreast of latest developments in formulation technologies and regulatory trends. Key Skills & Competencies: Strong technical knowledge of formulation science, excipients, and process equipment. Hands-on experience in granulation, compression, coating , and packaging of OSDS. Working knowledge of QBD, DOE, AND PROCESS OPTIMIZATION . Understanding of regulatory requirements (USFDA, MHRA, EU, WHO).

Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Operations - Control, monitoring, and recording To monitor and carry out maintenance of utility equipment and review planned preventive maintenance of utility and production equipment. To provide quality service system such as, potable water, Steam, compressed air and Vacuum. To maintain and update the HVAC system. To review and update all engineering SOPs and other related documents along with quality assurance. Collaborates in the planning of new facilities and equipment or their replacement. Prepare work authorisation. Develop plant layout and prepare plans for facilities and requirements. Estimates costs of designed facilities. To ensure that the appropriate process validations, calibrations and qualification of all equipment are performed, recorded and reports are made available. To approve the instructions related to engineering operations and to ensure their strict implementation. Inspection of material received at engineering stores and approving the same and maintains the required inventory level for all equipment spares and Consumables like Lubricants, hardware etc. Follow up with the purchase department and supplier to get the required material in time. To provide quality service system such as, potable water, Steam, compressed air and Vacuum. To attend the breakdown of machineries on time so as to have less impact on quality and production. Ensure daily alarm log print taken and assessment completed within timeline. To do mechanical maintenance check as per checklist. To involve in the training conducted in the section (Scheduled Training,Training on changes, Miscellaneous). GMP To follow current Good Manufacturing Practice (cGMP). To participate in design, implementation, monitoring and continual improvement of Quality system. QMS Involvement in deviation, change control documentations, risk assessments and CAPA in consultation with quality Assurance. To operate the CipDox System, Trackwise ,Pramaan SAP System And Ariba system based on the roles and rights provided in the application. To operate the Leucine system based on roles and rights provided. Safety Strict adherence to safety, health and environment. Monitoring safely operation the machine as per SOP, with minimum rejection & maximum output. Estimating the human and material resources required for engineering services and facility management of units. Monitoring plant hygiene and adherence to Health safety and environment policy of the organisation. Training To conduct training to subordinates. Responsible for identifying staff training needs, scheduling their work, disciplinary matters. Industrial relations and manpower development. Administrative Identify areas of wastage. Identify areas of work simplification. Co-ordinates with contractors and sub-contractors for scheduling of work. Co-ordination with concerned department heads for timely execution of engineering activities. To carry out any other duties that may be allocated from time to time. Energy Management System (EnMS): Keep abreast of potential energy and water saving products. Develop a program of energy-saving projects. Measure and verify the savings achieved. Commission and supervise specialist consultants. Analyze energy consumption histories on a weekly basis (say) to detect exceptions Diagnose, investigate and rectify detected exceptions Conduct or arrange staff awareness and motivation programs. Operate an energy-saving suggestion scheme. Assist in the development of energy-conscious design, maintenance, and operation Policies. Others Discussion of the days work with Department Head. Preferred candidate profile B.E/B.Tech Mechanical with minimum 3 years in OSD Formulation Plant

Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Operation, Maintenance, Control and Monitoring: Monitoring and implementing the preventive and breakdown maintenance of all the equipments & facilities of entire unit. Ensuring the availability of power supply to the plant without any interruption. Monitoring & maintaining HVAC system as well as AHU Temperature Control system SCADA. To do mechanical and electrical maintenance check as per checklist. Ensure daily alarm log print taken and assessment completed within timeline. Monitoring and supervising the operation and maintenance of substation equipments and facilities. Ensuring the implementation of preventive maintenance for critical electrical equipments such as HT breakers, LT breakers, PCC & MCC panels, protection relays, control panel, PDB, LDB, UPSDB, capacitor bank, harmonic filter diesel generator sets, uninterrupted power supply units, material hoist, solar power panel, passenger lifts, electrical stackers, CCTV camera, etc. Maintaining the optimized inventory of spares in engineering stores. Maintaining the availability of critical spares required to avoid major production delay. Maintaining proper housekeeping and upkeep of engineering areas (substations, HT yard, MCC rooms, transformer yard, DG room, UPS room, DCS rooms, Calibration room, technical areas, hoist machine rooms, plant terrace, etc.) Executing the submission of CER / PRs as per requirement with standard specification. Coordinating with purchase and vendors for clearing technical queries and release of PO Preparing of budget for Power Consumption, OPEX and CAPEX budget. Tracking and monitoring of budget on monthly basis. Analysing the increased variance against benchmarks and implementing the actions for controlling the same. Implementing the rectification of machinery breakdowns with minimum response time to avoid the impact on quality and productivity. Encouraging team for the identification of various measures for controlling and reducing the available OPEX expenses by spare management and vendor development. Preparing the cost estimate for maintenance, major modification and project activities. Reviewing, checking, and performing contemporaneous (on time) document entries in daily logbooks of Substation, Checklists, Preventive maintenance Records, SAP, etc. Co-ordinating with concerned department in charges and heads for timely execution of engineering activities. Tracking to be done for all the activities as per plan. Preparation & sharing of reports like, monthly dashboard, daily power report, safety dashboard, CER tracking, CAPA tracking, OPEX report, FFIR report, safety compliance report, plant shutdown planner schedule, etc. Identifying new technologies and vendor development for the system improvement and ease of operation and maintenance. Ensuring on-line bill processing against the availed services for the timely payment to vendor. Designing and selecting of tools, equipments, machinery, safety and protective devices as per the norms. Planning and Co-ordinating with contractors and vendors for the scheduling of maintenance activities. Ensuring close supervision while execution of critical task for maintaining the quality and safety standards. Providing the engineering support required for the modification / upgradation / changes as per requirement. Tracking and monitoring the timelines for the completion as per target. Preparation of Annual planned preventive maintenance Schedule of process and utility equipments. Planning and reviewing of planned preventive maintenance activities for the process and utility equipments as per SOPs and approved schedule. Adhering and ensuring to meet the timelines for the completion of critical assignments related to project, modification and Safety Compliance. Reviewing and inspection of material inventory at engineering stores as per Purchase order. Initiating the request for maintaining the required inventory with coding in place for regular consumables items. To ensure that the appropriate process validations, calibrations and qualification of all equipment are performed, recorded and reports are made available. GMP: Implementing the tag numbering / coding of instruments as per the SOP. Adhering and implementing 100% compliance to the calibration of all measuring instruments of process and utility equipments as per schedule. Implementing departmental standard operating procedures (SOP) & protocols and addressing the suggestions / ideas for simplification and improvements. Preparing and updation of SOP / protocols as per the requirement and schedule. Implementing current good manufacturing practice (cGMP) for making continual improvement in quality management system. Adhering to the timely reporting and acknowledgement of non-conformances. Ensuring the timely completion of investigation with root cause analysis and appropriate CAPA in place. Following and execution of appropriate process validations, calibrations and qualification of equipments and facility under execution. Record and reports are made available. Ensuring the completion of scheduled vendor audit related to calibration laboratories. EHS: Ensuring personnel health, hygiene, plant hygiene and adherence to Health, Safety and Environment policy of the organisation. Ensuring the implementation of environment, health and safety policies and practices. Reviewing and extending the required technical support and resources for engineering services and facility management. Implementing and tracking the compliance of safety observations. Critical observations should be addressed immediately. Participating and preparing the risk assessments, hazops of non-routine maintenance activities, system, equipment and process. Preparation of Investigation report for safety incidences with root cause analysis and appropriate CAPA in place to avoid the re-occurrence. Learning and sharing to be ensured among the concerned team. Ensuring the timely investigation of safety incidences with root cause analysis and appropriate CAPA to avoid the re-occurrence. Learning and sharing should be ensured among the concerned team. Operating and reviewing the maintenance of EHS critical systems like Fire alarm system, Oxygen detection system, Hydrogen / Hydrocarbon gas detection system, NOVAC system, DSPA system, etc. Operating and executing the maintenance of CCTV system, EPABX system. Training: 3 Identifying and conducting trainings to Engineering employees & contractors for their development and improvement in skills and knowledge. QMS: Implementing 100% compliance on QMS activities like process validations, calibrations and qualification of equipments, facility & IT networks under execution. Record and reports are to be maintained Operating software systems like SAP, quality management system, EDLMS, track wise system, purified water system and Cipdox software, LMS software etc. based on roles and rights provided in the applications. To operate the Leucine system based on roles and rights provided. Maintaining the facility & equipment’s for all audit readiness. Monitoring and tracking of all the QMS tasks like, CR action, CAPA actions, deviations for timely closure. Energy Management EnMS: Identifying and implementation of energy saving measures at unit level. Adhering to energy management system (EnMS) SOPs and related documents. Ensuring the implementation of energy management guidelines & systems. Conducting internal energy audits and tracking the action plan and compliance. Developing programs for energy-saving projects & measures, verify the savings achieved. Statutory: Maintaining the statutory compliance related to substation equipment’s and facility. Co-ordinating with MSEDCL representative as per the requirement. Executing statutory legal compliances through compliance manager software. Others: Performing any other allocated assignment after ensuring appropriate training is in place. Planning and execution of plant shutdown activities. Preferred candidate profile B.E/B.Tech Electrical with minimum 3 years in OSD Formulation Plant