164 Process Equipment Jobs - Page 5

At Mott MacDonald, we are proud to be part of an ever-changing global industry, delivering transformative work thats defining our future Its our people who power that performance, Were a collection of leading experts who combine our different expertise to stay ahead of the curve and move the industry forward With so many opportunities to learn, grow and excel, the possibilities are as varied as every individual to shape the career thats right for you, Key Responsibilities/Duties Prepare Design Basis documents Develop Basic Engineering Packages (BEP) and Front-End Engineering Design (FEED) Create Process Flow Diagrams (PFD) and Piping & Instrumentation Diagrams (P&ID) Conduct Heat & Mass Balance calculations Perform Hydraulic Calculations Design process equipment such as heat exchangers, columns, and reactors Size Pressure Safety Valves (PSV) and Emergency Relief Valves (ERV) Summarize and size utilities Develop Process Control Philosophy and Control Narratives Size and specify process equipment Prepare Process Data Sheets (PDS) and Instrument Process Data Sheets (IPDS) Compile Equipment and Line Lists Essential Candidate Requirements Strong aptitude in Chemical Engineering Good understanding of process unit operations and process calculations, including principles of heat exchangers, distillation, fluid flow, and reactions Analytical thinking and problem-solving skills Can lead a team of 2 to 4 team members Excellent interpersonal skills and ability to work in a team Strong technical communication skills, with the ability to effectively communicate with other discipline engineers to understand and solve their issues Working experience with HYSYS and HTRI software Experience in designing various process equipment and engineering concepts Active participation and can conduct HAZID, HAZOP, SOP, and Process Safety development Proficiency in reviewing PFDs, P&IDs, Heat and Mass Balance calculations, and process equipment sizing Experience in risk studies and brainstorming on process units involving risk analysis and safeguards Ability to analyse, optimize, and troubleshoot chemical process plant equipment and machinery Experience in preparing and reviewing process datasheets for equipment such as distillation columns, separators, reactors, and heat exchangers Execution of debottlenecking projects and expansion studies Participation in MOC studies and recommendations, Whether you want to pursue excellence in a specialism or broaden your experience with flexible roles across our business, youre connected to a community of global experts championing you to be your best, Equality, diversity and inclusion We put equality, diversity and inclusion at the heart of our business, seeking to promote fair employment procedures and practices to ensure equal opportunities for all We encourage individual expression in our workplace and are committed to creating an inclusive environment where everyone feels they have the opportunity to contribute, Agile working At Mott MacDonald, we believe it makes business sense for you and your manager to choose how you can work most effectively to meet your client, team and personal commitments We embrace agility, flexibility and trust, Location(s): Ahmedabad, GJ, IN Mumbai, MH, IN Contract Type: Permanent Work Pattern: Full Time Market: Energy Discipline: Energy Job Ref: 9010 Recruiter Contact: Vrajesh Gajjar

Responsible for new products transferring, technical improvement such as site expansion project management, SU new products transferring in, Hazard analysis of new product, material localization, new process & equipment design, installation, validation & qualification, technical improvement to support site business growth and new products commercial launch. Be in charge of new project management to ensure project meets each milestone on time with high quality and project cost within budget. Be responsible for new product technical related such as readiness of Drawing / BOM / TP, SOP / work instruction development, manufacturing data in SAP system, new products design and validation, employee technical training & qualification, etc. Timely Technical Transfer of down filling, manufacturing technology from other global plants to support meeting production & customer demand. Initiate continuous improvement projects to drive cost saving, quality improvement such as new equipment development, current process / equipment upgrading, automation, etc. Responsible for assuring compliances to all regulatory requirements no matter for project phase new products transferring in or new process / equipment development - ISO, EHS, etc. Work with PSM & quality team for raw material localization, key supplier development & maintain relationship to improve material quality standard, reduce cost & delivery lead time. As project contact window, ensure good communication within site function team, giving site, commercial and other supporting function. Evaluate CAPEX required and interaction with E&T team and OEM. Support plant - wide strategic plan programs and activities. Other assigned tasks which are required by site leader. Organizing cross functional meeting with Global team to have smooth product transfer taking all taxation/regulatory /statutory /Change Management compliances into consideration. Who You Are: Requires a B.E/M. Tech. or equivalent, preferably in Chemical /Mechanical engineering, 10-12 years ' experience in technical or manufacturing process in pharmaceutical, biotechnology/Chemical -Fine/specialty/API or comparable environment. Technical & Professional Knowledge: Rich experience in new products transferring in, project management, process technical improvement, material localization, Process equipment Design etc. communication and interpersonal skill Lean six sigma knowledge & experience, continuous improvement mindset. GMP and product design knowledge

mechanical projects design, installation of industrial equipment, focusing on heavy machinery manufacturing & production plants engineering design and drawing skills to technical drawings, ensuring accurate fabrication and installation of machinery Required Candidate profile Applied SAP PP & SAP MM for managing production plan, materials procurement, inventory control, optimising resource allocation Developed & tracked project schedules Microsoft Project, coordination

Role & responsibilities • You will be responsible for coordinating with cross functional teams for ensuring that preventive maintenance is carried out as per schedules in SAP. • Your role involves preparing the PMP (Preventive Maintenance Plan) and maintaining the necessary records of breakdowns and maintenance activities in the PMP as per defined frequency. • Your responsibilities include handling of external contractors and agencies, reviewing and ensuring implementation of the instructions (Work Instructions and SOPs Standard Operating Procedures) related to production operation. • You will train and assist the team members during troubleshoot and breakdown of machines and commissioning of new Equipment. • You will ensure balance investigation and inventory control for all instrument spares parts. • Your role involves planning, consolidating and submitting the maintenance budget for the allotted area/unit. • You will ensure that the maintenance expense is within the budgeted amount. • You will be responsible for ensuring availability of all process equipment and regular maintenance of all process equipment spares by following up with OEMs (Original Equipment Manufacturers), external vendors and SCM (Supply Chain Management). • You will be accountable for enduring closure and completion all assigned CAPA (Corrective and Preventive Actions) on time. • You will be expected to support any technical/documentation activities at site as per instructions from Section Head. • You will be responsible for preparing, updating, and maintaining all necessary documents for audits like SOPs, formats, PM (Preventive Maintenance) books, protocols, and Machine History Books for the respective areas. • Your responsibilities include facility upkeep of respective areas as per GMP (Good Manufacturing Practices) and cGMP (Current GMP). • You will be accountable for ensuring implementation of Good Engineering Practices (GEP) at Site. Preferred candidate profile Should Have Experience in Injectables(Preferable), OSD

Job Description Ensure readiness of equipment and instrument for process. Ensure availability of the process Raw materials, accessories and consumables in process area before batch execution. Preparation, Review of process, equipment and area related SOPs and EOPs. Preparation and execution of process, area and equipment qualification / validation protocols. Preparation of various reports like process, equipment, area qualification and validation. Preparation and Review of BPR. Request and Issuance of BPR. Preparation, Review and execution of study protocols. Readiness of downstream area and other areas like corridors and washing area etc. for manufacturing operations. To ensure smooth functioning of shop floor functions during manufacturing campaigns. To raise and review change control and deviations as per the requirement. Handling of SAP related activities like process and maintenance. Operating downstream equipments for process and CIP/SIP. 11-16 Years 11 to 16 years of experience M. Sc. /B. Tech Post Graduation B. Tech in Biotechnology or Biochemistry Biosimilar manufacturing, Production planning, QMS

Required Skills Technology | Software System Development | Frontend Programming Technology | Software System Development | Backend Programming Education Qualification : Engineer - B.E / B.Tech / MCA Details: This position requires an understanding and desire to advance the programming, configuration, and lifecycle management of manufacturing process controls, automation, and field instrumentation technologies. Job Responsibilities include: 1. Develop and deploy process control applications utilizing Programmable Logic Controllers (PLC), Distributed Control Systems (DCS), Human Machine Interfaces (HMI), and Supervisory Control and Data Acquisition systems (SCADA). 2. Support of capital projects. Responsible for the application of automation engineering principles in the design, specification, construction, startup, and validation of process equipment and systems for capital projects of varying scope and complexity. 4. Development of requirements, specifications, engineering documents, SOP, and operating standards. 5. Ownership and administration of process control automation in a regulated manufacturing setting. Engage in, and execute managed process change requests per established SOP and processes. 6. Gather data and participate in technical root cause analysis, incident investigations, and troubleshooting on process control issues related to electrical, instrumentation, and control systems. 7. Design and testing of newly installed and currently installed automation-based process equipment. Support new product introductions or new technology introductions by performing engineering assessments, implementing automation system configuration changes, and supporting engineering runs. 8. Apply standard process control methods and approaches to problem solving.

Walk-in Drive @ Bangalore on 22nd June 2025 (Sunday) Strides Pharma is hosting a Walk-In Drive for multiple roles. Venue: Strides Pharma Science Ltd. (R&D office): 165/2, 3rd Main Road, Oppo. Kalyani Magnum Tech Park, JP Nagar 4th Phase, Bengaluru-560076 Open Positions Department: Production Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: Granulation, Compression, Coating, Capsule Filling, OSD Production Department: Packing Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Bangalore Key Skills: OSD Packing, Bottle Packing, Blister Packing, BQS, CVC, BPR Department: Quality Control Experience: 2-7 years Qualification: B.Pharm/M.Pharm/M.Sc. Job Location: Bangalore Key Skills: Analysis of Raw Material, Finished products, In Process, Stability Samples, for Capsules & Tablets with expertise in HPLC. Department: Formulation Development Experience: 4-7 years Qualification: M.Pharm Job Location: Bangalore Key Skills: Planning & Execution of Lab scale experiments. DOE, Quality by Design, Product Development, Stability Protocol, Regulatory Market. Department: Engineering Process Maintenance Experience: 2-7 years Qualification: Diploma/B.Tech. (Electrical, Mechanical, Instrumentation) Job Location: Bangalore Key Skills: Maintenance of RMG, FBD, Compression, Coating, Capsule filling, Blister Packing, Sachet Filling line, Bottle Packing Machines. Department: Engineering Projects & Utility Experience: 2-7 years Qualification: Diploma/B.Tech. (Electrical, Mechanical, Instrumentation) Job Location: Bangalore Key Skills: Installation, Commissioning, Equipment Qualification, DQ, IQ, OQ, PQ, Utility, Water System, HVAC, AHU, Chiller, Air Compressor, Cooling Tower, PLC, SCADA, HMI Best Regards, Talent Acquisition Team, STRIDES PHARMA SCIENCE LTD

Role & responsibilities Extensive travel for marketing to the target geography and fruit/ food/ beverage/dairy/ nutraceuticals etc. industries for business generation. Generating enquiries, making quotations as per customer requirement. Business generation by target market search, approach to propose products & solutions of the company Techno-commercial discussions, order finalization with customers to fulfil business targets. Preferred candidate profile BE/ BTech Food Engg/ Agri Engg/ Mech., MBA or higher equivalent qualification. Must have an understanding of processes like fruit pulp, food, beverage, dairy or similar sectors. Experience in marketing to the food processing industry or similar. Open to travel pan India and/or relocate as per business requirement. Perks & Benefits Best in the industry.

1.Knowledge of Oil and Gas projects, Expertise in Autodesk Inventor 3D Modeling & Drafting. Knowledge of ASME Section VIII Div. 1 & 2, , , PED. 2.Create & update 3D Model, detailed drawing, BOM, Manual as per customer specification Required Candidate profile 3) 3-D model.creation & updating. 4) 3-D model creation of tube & pipe layout. 5.General Arrangement/Assembly / foundation drawings creation / Electrical Drawings. 6. Item code creation in ERP.

1.Knowledge of Oil and Gas projects, Expertise in Autodesk Inventor 3D Modeling & Drafting. Knowledge of ASME Section VIII Div. 1 & 2, , , PED. 2.Create & update 3D Model, detailed drawing, BOM, Manual as per customer specification Required Candidate profile 3) 3-D model.creation & updating. 4) 3-D model creation of tube & pipe layout. 5.General Arrangement/Assembly / foundation drawings creation / Electrical Drawings. 6. Item code creation in ERP.

Synnat Pharma Pvt Ltd seeks a proactive Maintenance Executive to ensure equipment reliability and minimize downtime at our Visakhapatnam API manufacturing facility. You will execute preventive maintenance, troubleshoot malfunctions, manage spare parts, and collaborate on corrective actions. Responsibilities include overseeing civil/fabrication activities, adhering to SOPs, and maintaining documentation. Strong technical problem-solving skills and a commitment to quality/safety are essential. Job Details: Industry: API Manufacturing Department: Maintenance Role: Maintenance Executive Location: Visakhapatnam Compensation: 2-4 LPA Experience: 1-3 years Qualification: Bachelor's Degree in Mechanical Engineering, Electrical Engineering, or a related field Responsibilities: Develop and implement preventive maintenance schedules (PPM) for process and critical equipment, adhering to industry best practices and Synnat Pharma's SOPs. Conduct equipment inspections and performance monitoring to proactively identify and address potential issues. Analyze maintenance data to identify trends, predict equipment failures, and optimize PPM schedules. Respond to equipment breakdowns, troubleshoot issues, and perform necessary repairs on mechanical, electrical, and instrumentation systems. Manage spare parts inventory, ensuring critical items are readily available for timely repairs. Oversee basic civil and fabrication activities related to facility and equipment maintenance. Maintain accurate maintenance documentation, including manuals, SOPs, schedules, and repair records. Ensure all maintenance activities comply with regulatory requirements (FDA, cGMP). Implement corrective actions to prevent recurrence of equipment failures and improve reliability. Collaborate with production to schedule maintenance, minimizing disruption and maximizing uptime. General Expectations and Past Experiences: 1-3 years' Maintenance Executive experience in API Manufacturing (Preventive Maintenance, Troubleshooting). Hands-on experience: Civil/Fabrication, Mechanical/Electrical Systems Repair (Pharmaceutical). Solid understanding of API Manufacturing, Equipment Validation, and SOPs. Proven ability to develop Maintenance Schedules, reduce Downtime, and execute Corrective Actions. Familiarity with Procurement, Spare Parts, and Maintenance Documentation. Excellent Teamwork & Communication skills. Proficient in Maintenance Risk Assessment and Best Practices.

Role description: We are now recruiting talented individuals to fill our current vacancy for Senior Mechanical Engineer to work on our projects in Bangalore/Noida/Mumbai/ Hyderabad offices. Our Water Design and Engineering team is involved in some of the UKs most complex and stimulating projects that are diverse and technically demanding. We have an excellent reputation in the delivery of such schemes and are working closely with some of the UKs most established and recognizable companies, undertaking a vast array of projects to enhance the UKs water infrastructure and environment. As a Senior Mechanical Design Engineer, you will join our MEICA team to contribute and apply your skills on a variety of water and wastewater projects for our clients regionally and across the UK. You will be responsible for leading and supporting the mechanical design delivery of projects that promise to meet or exceed client expectations. You will represent Arcadis with direct client and stakeholder engagement, contributing towards the achievement of our business objectives and building networks within the industry. Role accountabilities: Ability to self-start and work both independently and as a team member carrying out production, checking, review or approval of mechanical design deliverables. Supporting and / or Leading design and advisory services relating to new and existing water and wastewater conveyance and treatment assets. Ensuring safety of yourself and others through design leadership and actions. Technical delivery within a multi-disciplinary team environment, in a mechanical design Lead capacity where assigned, using latest digital design processes and resources. Co-ordinate work with multi-disciplinary teams (e.g., process, civil, structural, mechanical, electrical, and ICA) Identify and develop innovative and optimised technical solutions based on client needs and drivers Establish and grow relationships with clients and capital alliance partners on project technical, commercial and progress matters Leading and supervising the design team andensure the project is delivered with high quality withinthe program and budget Liaising with the lead region to demonstrate an understanding of scope, knowledge, and experience to provide innovative design solutions as per best engineering practices. Working in collaboration with other design disciplines to ensure the integrity of the overall design Ensuring projects meet required technical, legislative, quality, safety and environmental standards and objectives. Capturing key project and technical knowledge, including innovations. Promote MEICA team capability and achievements both internally and externally. Coaching & Mentoring of junior staff Compliance to the Arcadis Health and Safety standards Internally promote and share project achievements and developments Qualifications & Experience: Degree in Mechanical Engineering or other directly related degree 10+ years experience in designing mechanical and process equipment for water supply & water treatment plants, sewerage & sewage treatment plants and drainage system. Incorporated or Chartered Engineer status (or approaching) and membership of a relevant professional institution (e.g., IMechE, IET, CIWEM) Experience of working on design and construct projects using digital design platforms Strong command of BIM / digital/data analytics software as applicable. Application of quality management systems and managing project teams Knowledge of relevant British Standards is preferable. Demonstrated delivery acumen. Experience in mechanical design, specifications, drawings and BIM models for large scale projects related to, Water and Wastewater Treatment plants, Pumping stations and other related structures, Water and wastewater conveyance systems, Drainage systems, Flood protection facilities, Hydraulic design related to above including hydraulic calculations Surge analysis and pipeline surge mitigation preferable Experience of delivering designs and reports at all stages from concept through to final project and construction delivery. Excellent oral/visual/written communication skills in English language and experience in working with remote clients and multi-disciplinary teams

1.To carry out In-process Inspection using approved QAP & Maintain records. 2.Ensure all stages of MQP have been followed in shop floor and stage wise MQP's are being signed from production and Quality team members. Required Candidate profile 3. Good drawing interpretation, Fabrication experience (2-3 yrs), Shop floor dimensional & visual inspection Basic Knowledge of Codes, MS Word, MS Excel, Report Preparation

1.Knowledge of Light and heavy fabrication. 2.Ensuring Production as per the plan with quality, cost, delivery, safety as per the company. 3.Plan & timely follow-up on put sourcing & inter department activities like lesser cutting, Messer cutting etc Required Candidate profile 4.Knowlege of Welding like TIG , MIG , Provide Process related MIN in ERP System. 5. Update Panel section weekly man- hours utilization report.Unrstanding Drawing, specification BOM, Project schedule.

Job Description 1. Qualification of process equipment, area. HVAC and Utility qualification (Compressed air, Nitrogen and PSG) and equipment qualification like Vial washing, Tunnel, Filling, Sealing and Autoclave 2. CSV validation of different category of equipment. 3. Review of CSV documents like SIA, CFRA, RAP, RAR, VA, URS, DQ, FRS, 4. CS, IQ, OQ and Qualification of water system 5. calibration / qualification / requalification / cGMP compliance of equipment / instruments / measuring devices and area on periodical basis or as and when required.

Target Industry: Pharmaceutical equipment industry (like Granulation/ Isolator) only Exp: 7-12 years in domestic pharmaceutical engineering/ pharmaceutical equipment sales Working: 6 days (1st and 3rd Sats are off)

Awareness of all fabrication standards ASME, PED, DIN AWS etc. Knowledge about the vendor development Cost and budget calculation knowledgeNDT awareness Knowledge of latest welding technology & all welding process like GTAW ,SAW ,SMAW, FCAW, GMAW Required Candidate profile Increase production, assets capacity & flexibility while minimizing unnecessary costs and maintaining current quality standard Be responsible for production output, product quality & on-time delivery

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing & Visual Inspection Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI OSD – Manufacturing / QMS (Senior Officer / Officer / Executive) Experience - 02 to 07 Years Qualification – B. Pharmacy/ M Pharmacy Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification – BE / B Tech Time and Venue : 14th June 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. *Having relevant qualification only can attend the scheduled walk-in.

Job Summary We are looking for a detail-oriented engineering team member to coordinate preventive maintenance schedules, manage breakdown records, and ensure adherence to SOPs, critical for maintaining operational efficiency and equipment reliability. This role plays a pivotal part in inventory control, and CAPA closure, contributing to seamless production operations, compliance with regulatory standards, and effective resource utilization. Roles & Responsibilities • You will be responsible for coordinating with cross functional teams for ensuring that preventive maintenance is carried out as per schedules in SAP. • Your role involves preparing the PMP (Preventive Maintenance Plan) and maintaining the necessary records of breakdowns and maintenance activities in the PMP as per defined frequency. • Your responsibilities include handling of external contractors and agencies, reviewing and ensuring implementation of the instructions (Work Instructions and SOPs – Standard Operating Procedures) related to production operation. • You will train and assist the team members during troubleshoot and breakdown of machines and commissioning of new Equipment. • You will ensure balance investigation and inventory control for all instrument spares parts. • Your role involves planning, consolidating and submitting the maintenance budget for the allotted area/unit. • You will ensure that the maintenance expense is within the budgeted amount. • You will be responsible for ensuring availability of all process equipment and regular maintenance of all process equipment spares by following up with OEMs (Original Equipment Manufacturers), external vendors and SCM (Supply Chain Management). • You will be accountable for enduring closure and completion all assigned CAPA (Corrective and Preventive Actions) on time. • You will be expected to support any technical/documentation activities at site as per instructions from Section Head. • You will be responsible for preparing, updating, and maintaining all necessary documents for audits like SOPs, formats, PM (Preventive Maintenance) books, protocols, and Machine History Books for the respective areas. • Your responsibilities include facility upkeep of respective areas as per GMP (Good Manufacturing Practices) and cGMP (Current GMP). • You will be accountable for ensuring implementation of Good Engineering Practices (GEP) at Site. Qualification Edu : Diploma in Electrical & Instrumentation Engineering or B. Tech in Electrical & Instrumentation Engineering. Responsible for coordinating and executing project development and handover activities of in-house projects in the plant In house Project Works and coordination with vendors during projects execution. Following all related SOPs, PMPs & OI's and ensuring concurrent Documentation. Maintenance & Machining of parts as per requirement. Closing of Change Controls, Job proposals, Quality, Non-Quality Impacting reports and cross checks Guiding and controlling external vendors working inside plant and arranging required material as per technical details required for work completion. Preparation of Engineering Provisions and drawings/layouts. Preparation of commissioning reports for new equipment, Instrument and submissions to Asset Team. Coordinating with CFTs for timely project execution. Training the user department and ensuring regular operation of systems implemented. Coordination with service providers during installations, commissioning and execution of qualification activities, breakdowns of systems & equipment. Technical evaluation of changes in the validated systems or processes. Responsible for addressing the deviations in external/internal audit observation in engineering processes, practices followed. Execution, Review, Installation & Commissioning of new equipment along with related documentation like DQ, IQ, OQ, PQ and related SOPs. Responsible for initiation, review of deviation management through incidents relevant to the in-house projects and incident investigation related to engineering. To Review of SOP's and OI's, coordination with QA and follow relevant SOPs. To follow the quality procedures and regulatory requirements. Monitoring of maintenance systems in SAP Responsible for planning of preventive maintenance Operation and Maintenance of pure steam generators. Responsible for taking the Periodic GXP Computerized system backup and submitting to IT department. Technical support to carry out the GxP assessment & controls for manufacturing machines. Good knowledge on PLC Programming. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

JOB PURPOSE (Briefly describe the objectives of the job) : To follow cGMP and QMS principles in calibration, maintenance and all the engineering tasks in Discovery Biology operations To prioritize and support all the calibration & maintenance related activities To co-ordinate the Qualification activities with Users, Cross functional Teams and Quality Assurance Department. To execute all the Modification projects. KEY RESPONSIBILITIES: Responsibilities: To ensure compliance to Safety at workplace and place Safety at number one priority with Engineering and Projects. Planning and executing Maintenance and calibration of instruments in Process Equipment, Lab Equipment, HVAC and Utilities. To Verify and ensure of all PM and calibration activities are completed and labels are updated on the Instruments and equipment s. To Perform and execute all the PM and breakdown calls for Discovery Biology lab equipment s. To perform PM and support the breakdown calls for all equipment s in discovery biology. To prepare and update SOPs - Maintenance, Calibration, System and Operations. To maintain spares, services, and AMC for Calibration / Maintenance. To follow and ensure Safe work environment and working methods in the workplace for all activities. To provide all requirements for OPEX related expenses for Discovery Biology. To Provide monthly data for all reports required for KPI monitoring. All SAP/Stores/Procurement related activities to be executed and processed in timely manner. To Ensure Data Integrity Compliance for Self. To Execute all the Change Control, Investigation and CAPA related Tasks.

Designation: Proposal & Costing Engineer Reporting Structure Reporting to: Sr Engineer Proposal & Costing Position reporting into this role: NA Job Description Daily working on Equipment cost /Project costing /System costing Making costing of standard equipment and approve it by management Ensuring service and application support to customers assigned Identification and encashment of project business of existing client Managing and developing relationships with customers existing client Assign by management Forecasting and reporting of sales, trends and competitor activities Receive the new enquiry from Customer on mails to verify technically & prepare costing and offer Responsible to maintain documents and records as per QMS procedure of the department Attend negotiation meeting along with management and also with Customer The offer for EPC projects tobe sent in 10-12 days The offer for Equipmentsto be sent in 4-5 days Required Skills Sales skills Leadership skills Presentation skills Negotiation skills Should be smart person Educational Qualification Graduate in Mechanical/Chemical engineering from reputed institute Work Experience Minimum 01+ yearsexperience in core costing of chemical process equipment, evaporators, pressure vessel, bio fermenter etc- Primary Internal Interactions Primary External Interactions Senior Management, employees of all levels Salary Range 25000/to 35000/- All Customers Job Location Bhosari Sector 10 Apply For This Position First Name* Middle Name Last Name* Email* Mobile Phone* Experience* Current Salary Expected Salary Available To Join (in days) Current Location Last Working Day Upload Resume* By applying, you hereby accept the data processing terms under the Privacy Policy and give consent to the processing of the data as part of this job application Contact Padmatech Industries for world-class equipment to boost your business & productivity Contact Us Contact Padmatech Industries for world-class equipment to boost your business & productivity Contact Us Show more Show less

6+ years Exp. in designing pressure vessels and heat exchangers. Software : Proficiency in PV Elite and familiarity HTRI, ANSYS is advantageous.

Walk-in Drive @ Chennai on 15th June 2025 (Sunday) Strides Pharma is hosting a Walk-In Drive for multiple roles across our Manufacturing facilities in Chennai & Pondicherry. Venue: Days Hotel by Wyndham Chennai OMR, 245/1, Rajiv Gandhi Salai, Chennai, Padur, Tamil Nadu-603103 Open Positions Department: Production Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: Granulation, Compression, Coating, Capsule Filling, OSD Production Department: Packing Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: OSD Packing, Bottle Packing, Blister Packing, BQS, CVC, BPR Department: Quality Control Experience: 2-7 years Qualification: B.Pharm/M.Pharm/M.Sc. Job Location: Chennai/Pondicherry Key Skills: HPLC, GC, UV, IR, KF, FTIR, Dissolution, LIMS, GLP Department: Quality Assurance Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: IPQA, QMS, BMR Review, BPR Review, Line Clearance, Change Control, Deviation, CAPA Department: Engineering Process Maintenance Experience: 2-7 years Qualification: Diploma/B.Tech. (Electrical, Mechanical, Instrumentation) Job Location: Chennai Key Skills: Maintenance of RMG, FBD, Compression, Coating, Capsule filling, Blister Packing, Bottle Packing Machines Department: Engineering Utility & Instrumentation Experience: 2-7 years Qualification: Diploma/B.Tech. (Electrical, Mechanical, Instrumentation) Job Location: Chennai Key Skills: Utility, Water System, HVAC, Chillers, AHU, Air Compressors, Cooling Tower, DG, LT & HT Panel, PLC, SCADA, HMI Best Regards, Talent Acquisition Team, STRIDES PHARMA SCIENCE LTD

1.Knowledge of Light and heavy fabrication. 2.Ensuring Production as per the plan with quality, cost, delivery, safety as per the company. 3.Plan & timely follow-up on put sourcing & inter department activities like lesser cutting, Messer cutting etc Required Candidate profile 4.Knowlege of Welding like TIG , MIG , Provide Process related MIN in ERP System. 5. Update Panel section weekly man- hours utilization report.Unrstanding Drawing, specification BOM, Project schedule.

Opening Sales Executive Good Communication Heat exchanger Presser Vesser working Must Reading Drawings tank Fabrication Reactors, Dryers Coordinate With Teamwork Create Quotation Lead Generation Make Offers & follow up client Contact Us :9309376374 Required Candidate profile Business Development Visit Customer Customer Handling Estimation work Quote-to-order Final work Oil Gas & Piping Structure Equipment Industry working Create Quotation & Closed Order Target Base Work