Dear All, We are conducting Walk-in Interview at Ahmedabad for our OSD manufacturing Facility based out of our Ahmedabad (SEZ-II), please find the below details. Date : 22nd June 2025 (Sunday) Interview Location: Ahmedabad Timings: 9:00 am 5:00 pm Interview Venue: PTC-Sigma Block No. 2, 3, 4, 5, Sigma Commerce Zone,Nr Iskon Mandir BRTS Bus Stand, Ambli Bopal Road, Ahmedabad - 380015 . Job Location: Ahmedabad Education Qualification: ITI/Diploma/BSC/ B.E/B.Tech Departments are as follows : Production- OSD : Plant Operator/ Technical Assistant : ITI / Diploma having 3 - 8 years of experience in operating machines like Granulation (ACG, Glatt, Tapasya, GEA), Fitzpatrick Roll Compactor, Compression machines (Fette), Wurster Coater (ACG, Glatt, Anish), imprinting, Visual Inspection. Perform line clearance, operation and cleaning of equipment / instrument / auxiliary items Executive/ Sr Executive: B. Pharma with 3 - 8 years of experience in Tablet/ Capsule department with experience in Granulation, Compression, Coating, Inspection . Responsible to plan for the manufacturing of batches in coordination with PPMC. To monitor line clearance, cleaning of equipment, instrument, auxiliary items. To carry out qualification activities. To initiate QMS activities (Change control, deviation, CAPA, investigation) and E-BMR. To handle manpower and allocate daily activities.. Engineering: Technician : Diploma / ITI with 3- 8 years of experience in plant maintenance & Process Equipment (Electrical/ Instrumentation) and Instrumentation . Candidates should have experience in Plant maintenance, preventive maintenance and breakdown maintenance of OSD plant equipment. Troubleshooting of mechanical and electrical equipment . Instrument and calibration of OSD plant equipment. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration activities. Sr. Executive/ Assistant Manager: B.E/ B.Tech with 5-10 Years Process Equipment( Electrical / Instrumentation), . Candidates should have experience in Plant maintenance, preventive maintenance and breakdown maintenance of OSD plant equipment. Troubleshooting of mechanical and electrical equipment . Instrument and calibration of OSD plant equipment and Utility. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration . QMS documentation exposure is required. Warehouse: Officer to Senior Executive B.Sc./M.Sc. / B. Pharma graduate with 5 to 10 years of experience in handling of warehousing activities. Exposure of handling Raw Material, Packing Material receipt Dispatch and issuance activities. Having good knowledge of QMS area and equipment qualification related activities. Well versed with SAP MM module with WMS. Handling of expired, rejected, non-moving and obsolete inventory. Having exposure of USFDA/MHRA and other regulatory audits. For all the positions, candidate should have exposure in pharmaceutical company and exposure to regulatory requirements of documentation and cGMP will be added advantage. Interested candidates Please Walk-in for an interview along-with their Aadhar Card, Passport size Photograph, updated CVs, Salary Structure, Salary Slip and relevant documents(original as well as Photocopies) as per the schedule.

Walk-in Interview for Zydus Lifesciences Ltd. Moraiya - Ahmedabad at Moraiya| 22nd June 2025 | We are recruiting for our Ahmedabad Units at Moraiya, Ahmedabad. Walk-in Interview Details Date : 22nd June 2025 Interview Location: Moraiya, Ahmedabad Timings: 9:00 am 3:00 pm Interview Venue: Zydus Lifesciences Limited, Moraiya Opp. Akshar industrial Park, Survey No.417,419&420, Sarkhej- Bavla N.H. No.8A, Village: Moraiya, Tal: Sanand, Dist: Ahmedabad- 382210, Gujarat, India Job Location: Ahmedabad Education Qualification: M.Sc. / M. Pharm / B. Pharm / B.sc /Diploma/ ITI Experience: 3 13 Years Production- OSD: Officer / Assistant manager : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Plant Operator/ Technical Assistant : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Packing: Plant operator/Technical Assistant: Blister Line(BQS), CVC Bottle Line, Sachet Packing (Wraptech) Warehouse: Officer / Sr. Executive: RM, PM, FG, Dispensing, Dispatch , Documentation Plant operator/Technical Assistant: RM, PM, Dispensing and dispatch Engineering Technician: Instrument Technician - Fitter/Electrical/Process equipments/ HVAC Operation/HVAC Validation/ Instrumentation/ Water system Quality Assurance (IPQA) Officer / Assistant Manager: IPQA in process (Mfg. and Pkg.) / QMS

Receive and Log Complaints : Record and evaluate complaint submissions from customers regarding manufacturing defects or issues. Ensure all complaints are logged accurately in the complaint management system. Investigate Complaints : Conduct thorough investigations to determine the root cause of the complaint. Coordinate with internal departments (Quality Assurance, Regulatory Affairs, Production) to gather necessary information. Communicate with Stakeholders : Communicate with customers to understand their concerns and provide updates on the investigation. Liaise with healthcare providers, if applicable, to acquire relevant complaint information. Regulatory Compliance : Ensure timely processing of complaints in accordance with regulatory requirements. Generate and submit reports to appropriate authorities and government agencies as required. Corrective Actions : Recommend and implement corrective and preventive actions (CAPA) to address and prevent recurrence of issues. Monitor the effectiveness of implemented actions. Documentation and Reporting : Maintain detailed records of all complaint investigations and resolutions. Prepare trend reports and metrics to capture and analyze complaint data. Audit Preparation : Participate in activities to prepare for audits and inspections. Ensure all documentation is compliant with GMP (Good Manufacturing Practices) standards.

Walk-In Interview Exciting IT Career Opportunities in SAP S/4 & Microsoft Technologies & Infrastructure & Compliance Opportunities @ ZYDUS Location : Zydus Corporate Park, Scheme No. 63, Survey No. 536, Khoraj (Gandhinagar), Nr. Vaishnodevi Circle, S.G. Highway, Ahmedabad 382481 Date : Saturday, 28th June 2025 Time : 10:00 AM to 03:30 PM Job Location : Ahmedabad About the Company: Zydus is an innovation-led global healthcare provider dedicated to discovering, manufacturing, and marketing a wide range of healthcare therapies. With over 23,000 employees worldwide, including more than 1,400 scientists engaged in research, we are committed to creating healthier communities globally. Website: https://www.zyduslife.com/zyduslife/ SAP S/4 HANA Opportunities: 1.SAP FICO Consultant Experience: 5+Years in SAP FI, FM, PS, CO, and S/4HANA. Education: BE/BTech/MCA in IT/Computer/Graduate & SAP Certification is added advantage Location: Ahmedabad Profile: Design and implement SAP FI/FM solutions, integrate with MM, SD, and PPQM modules, and drive process improvements. 2. SAP ABAP Developer Experience: 5+ Years in OOABAP, SmartForms, IDocs, and SAP HANA Education: BE/BTech/MCA in IT/Computer/Graduate & SAP Certification is added advantage Location: Ahmedabad Profile: Design, develop, and optimize ABAP programs supporting SAP applications. 3. SAP MM/WM Consultant Experience: 5 - 8 Years with S/4HANA and knowledge of warehouse management is a plus. Education: BE/BTech/MCA in IT/Computer/Graduate & SAP Certification is added advantage Location: Ahmedabad Profile: Drive SAP MM implementations and integrations with SD, PP, QM, WM, and FI modules 4. SAP BW Consultant Experience: 5 Years Education: BE/BTech/MCA in IT/Computer/Graduate & SAP Certification is added advantage Location: Ahmedabad Profile: Expertise in SAP BW and BO. Analytical skill must be required. Strong development and maintenance skills. Good knowledge about SAP Process, which helps to develop dashboard and excellent communication skill Microsoft Technology Opportunities: 1. Full Stack Developer (Dotnet + Angular) Experience: 57 Years with Azure DevOps, AKS, and Microsoft SQL Server Education: BE/BTech/MCA in IT/Computer Location: Ahmedabad Profile: Design and develop scalable solutions using .NET Core, Angular, and MS SQL. 2. Dotnet Developer / ASP.NET Developer Experience: 5-8 Years with .NET Framework, IIS, WCF, and MS SQL Server Education: BE/BTech/MCA in IT/Computer Location: Ahmedabad Profile: Design and develop robust solutions using ASP.NET WebForms, MVC, and Core technologies.Support existing systems, handle SLA-driven tasks, and contribute to feasibility discussions. 3. Sharepoint Developer Experience: 6-12 Years with Office 365, remote event receivers, and SharePoint migrations (20102016). Education: BE/BTech/MCA in IT/Computer Location: Ahmedabad Profile: Design and develop solutions using SharePoint Online, SPFx, React, PowerApps, and Power Automate. Support existing systems, manage SLA-driven tasks, and lead feasibility discussions. Infrastructure & Compliance 1.IT CSV (Computer System Validation) Experience: 03-5 Years Education: BE/BTech/MCA in IT/Computer Location: Ahmedabad Profile: Role involves 24x7 user access management (activation, reset, changes, deactivation), maintaining the Privilege and User Access Matrices, and handling IT QMS activities including Change Control, Deviation, CAPA, and Incident Management. Responsibilities also include supporting software assessments, network maintenance, conducting risk-based failure tests, and representing IT processes during audits and regulatory inspections. Note: This walk-in interview is for experienced professionals. Freshers are encouraged to apply online for future opportunities.Priority will be given to candidates who can join immediately and are willing to relocate to the job location.

Role & responsibilities Vaccine Manufacturing (Cell Culture) Responsible for cell revival, subculture, cell counting of MRC-5 cells. Preparation of MCB/WCB. Experience in handling Roller bottles, Cell stacks, TCFs. Quality Control (Bacterial/Viral) Candidate should have good knowledge of Product testing techniques like : Biochemical, Chromatography, Electrophoresis, Immuno assay, Cell culture & Molecular techniques. Experience in handling HPLC, Dionex, UV-Spectrophotometer, Multimode plate reader and ELISA. Shall be well versed with Biochemical assays (Protein, O-acetyl) immuno-chemical assays and electrophoresis, Education: - Post-Graduate M.Sc. in Biochemistry, Biotechnology, Microbiology, Lifesciences. Experience: - 1-6 years of hands-on experience in relevant field, preferred Vaccine/Biotech background.

Manufacturing (OSD) Officer/Executive: B. Pharma/M. Pharma with 2 - 7 years of experience in Tablet/ Capsule department with experience in Granulation, Compression, Coating, Inspection. Responsible to plan for the manufacturing of batches in coordination with PPMC. To monitor line clearance, cleaning of equipment, instrument, auxiliary items. To carry out qualification activities. To initiate QMS activities (Change control, deviation, CAPA, investigation). To handle manpower and allocate daily activities. Plant Operator / Technical Assistant: ITI / Diploma having 3 - 8 years of experience in operating machines like, Granulation (Glatt, GEA), Cadmach Roll Compactor, Compression machines (Cadmach-26STN). Perform line clearance, operation and cleaning of equipment / instrument / auxiliary items. Semi-Solid : Tube Filling Operator: ITI / Diploma having 3 - 8 years of experience in operating machines like; Wimco. Taking care of Machine operations, Machine Set-up and Trouble shooting. Ensuring accurate measurements, proper mixing and precise reaction conditions. Packing Department Transdermal (Semi Solid) Plant Operator / Technical Assistant – Packing: ITI / Diploma with 3 - 8 years of experience in packing department. Candidates should have exposure to Cartonator machine operation / Track & Trace, Check Weigher, Vision inspection System. Quality Control Department: Officer / Executive/Sr. Executive (Analyst/Reviewer): B. Pharm / M.Sc. with 3 to 8 years’ experience in handling analytical instruments like HPLC, GC, dissolution apparatus and UV visible spectrometer and able to work in different sections like RM, FP, Stability and GLP. Candidates should also have experience in GMP compliance and self-inspection of analytical labs, document review and finished product release in LIMS. Candidates must have exposure of QMS trending for Lab review of various types of reports and protocols. Interview Date : 29th June 2025 Interview Venue: Zydus Healthcare Ltd, Block 2,3,4,5, Sigma Commerce Zone, Nr, Isckon Mandir, BRTS Bus Stand, Ambli Bopal Road, Ahmedabad - 380015. Interview Location: Ahmedabad Interview Timings: 9:00 AM – 04:00 PM Job Location: Pharmez – Matoda -Ahmedabad

Greetings from Zydus Lifesciences Ltd.! We have an exciting opportunity at our Zydus SEZ-1, Matoda. Department : Engineering Skills : Water System, Electrical Interested candidates can mail their Resumes at vaibhavi.harish2@zyduslife.com

# Work from Office only. Role & responsibilities: Role Digital Team Member Person will be part of digital team and helping the digital team members for digital initiatives and implementing various digital tool at the manufacturing site. Individual Contributor Location – Ahmedabad, Manufacturing Site / Corporate Department – Digitization (Central Team driving Digital and Industrial Automation across Mfg and Quality verticals) Reporting – Team Lead – Digitalization Roles & Responsibilities: Working with leaders across the organization for identifying and conceptualizing potential digital transformation solutions on the manufacturing shop floor. Drive digital Business Process Transformation solutions for Manufacturing operations in collaboration with respective digital & process excellence teams. Conceptualize potential new digital platform business models and solution opportunities with an aim of creating competitive advantage and new business models. Drive multiple digital projects from concept till launch and ensure delivery of digital solutions as per budgeted cost, timelines and quality. Contribute in building Digital Quotient across the organizations through Trainings & Workshops on new & emerging digital technologies and their potential use cases. Ensure successful adoption and scale-up of digital programs. Working effectively with cross functional team members Adherence to Digital Product/Solution Development best practices and processes such as Design Thinking & Agile Scrum for ensuring optimum program outcomes. Managing and grooming the users on the manufacturing site and external partner management. Defining and leading execution of technology proof of concepts to evaluate disruptive technologies. Driving solution adoption and scale up as per defined product roadmap for ensuring planned value realization. Required Technical and Professional Expertise Minimum 5+ years of experience in leading Digital Transformation Initiatives with excellent understanding of digital technologies such as Mobility, AI, IoT & Computer Vision. Proven success in driving Digital Solution / Platforms / Digital Product development and management in Pharmaceutical company. Ability to think strategically & creatively. Good understanding of Digital Platform Thinking and ability to create Digital Business Models. B. Tech / B.E. / B.S. /M.sc / M.Pharma Ability to prioritize and manage multiple initiatives simultaneously. Ability to lead and manage a Team of Business Analysts, Project Managers, Partners and Technology Specialists. Proven success in driving programs as per agile methodologies and apply design thinking process for developing innovative and cutting edge technologies digital solutions.

1. Technology transfer activity End to End, lead role for ANK location. 2. Site transfer and Block transfer activities for ANK location. 3. Managing Tech. Transfer and Process Engg (TT and PE) team. 4. Ensure for smooth technology transfer from Research and development to plant with minimum concerns w.r.t. scale-up. 5. Coordination with desired stake holders for getting timely execution of plant validation campaign. 6. Smooth planning of lab demo and detailed studies on negative experiments, holding studies, identifying process criticalities, etc. w.r.t. Scale-up. 7. Freezing lab process w.r.t. Scale-up to avoid deviations at plant. 8. To manage for making EHS friendly process. 9. Detailed discussion and finalizing the process for all site transfer molecules. 10. Coordinate with team for equipment mapping at plant for new and site transfer molecules. 11. Planning, coordination, and effective communication for Execution of trial and validation batches at plant. 12. Exploring of new technologies and its implementation at plant. 13. Managing of smoothly performing related EHS studies including HAZOP and HAZAN studies for new / site transfer projects.

Role & responsibilities To perform and be responsible for all the activities and documentation of formulation and filling process development and should have strong knowledge of optimization of different vaccine formulations, stabilizer selection, excipient selection, selection and preparation of adjuvants such as aluminium salts, Oil-In-Water emulsions, Liposome-based adjuvants with TLR agonists and saponin, LNP formulation and preparation, aseptic filling and Lyophilization cycle designing for new vaccine products and troubleshooting for existing vaccines. To perform all the activities and documentation of the formulation and filling process, development and execution of clinical drug product manufacturing for the clinical batches, planning and execution of media fill activities Prepare and Maintain R/D lab documents, equipment and area qualifications as per GMP requirements and Responsible for preparation of process validation and technology transfer protocols as per GMP requirements and co-ordinates with QA, QC, Engineering department for viral vaccine development activities. Responsible to ensuring proper hygiene and entry exit procedures in the respective formulation and filling section and preparation of adjuvant, buffer solutions and other materials & ensuring proper arrangements for their preparation and supply. To coordinate with the central warehouse department for receipt and entry of RM and PM materials. Preparation / supervision of disinfectant solution, cleaning solution, integrity testing of hydrophobic and hydrophilic filters, sanitization and disinfection activities of R/D formulation department. Responsible for QMS such as deviations, MDD, investigation, observation and ensuring its timely closure. Preparation of standard operating procedure and Batch manufacturing records, QRM and protocol related to R/D formulation and filling section. To supervise washing, drying, packing and sterilizations of materials required for R/D development and GMP clinical batch preparation. Preferred candidate profile PhD/MSc in science (Biotechnology, Biochemistry and Microbiology), masters degree in pharmacy or engineering with biotechnology. Candidate should have experience in vaccine industry Candidate should be able to work on bench and this position has one reporting.

Role & responsibilities Analyze and manage cost accounting processes and reports. Lead or support SAP HANA implementation and integration with finance modules. Collaborate with cross-functional teams to ensure accurate cost allocation and reporting. Monitor and improve cost control systems and procedures. Provide insights and recommendations for cost optimization. Preferred candidate profile Someone with Professional Experience of not less than 8 years.

Role & responsibilities 1. Engineering Maintenance & Reliability Ensure efficient preventive, predictive, and breakdown maintenance of all plant equipment and utilities. Lead cross-functional engineering teams to achieve zero unplanned downtime and maximum equipment uptime. Implement root cause analysis and continuous improvement in maintenance practices. 2. Utilities Management Manage all utility systems (boilers, chillers, HVAC, air compressors, cooling towers, etc.) to ensure uninterrupted supply to manufacturing. Drive energy e iciency and utility optimization initiatives across the plant. 3. Instrumentation & Automation Ensure calibration, maintenance, and performance of critical instrumentation and process control systems. Work with cross-functional teams to support automation and control upgrades. 4. Engineering Stores Oversee stores management for engineering spares and consumables with optimal inventory levels. Ensure availability of critical spares and compliance with GMP documentation requirements. 5. Budgeting & Capex Management Prepare and manage annual engineering budget (Opex & Capex) for maintenance, projects, and utilities. Plan and execute Capex projects related to facility upgrades, new installations, expansions, and regulatory requirements. Ensure cost control, vendor coordination, procurement support, and timely project execution. 6. Compliance & Safety Ensure compliance with cGMP, GEP, statutory norms (Factory Act, Electrical safety, Boiler Act, etc.), and EHS requirements. Lead readiness for internal and external audits including USFDA, EDQM, WHO, and other regulatory agencies. Implement engineering controls to enhance safety and environment performance. 7. People Management Lead and develop a high-performing engineering team. Identify training needs, performance development, and succession planning. Preferred candidate profile Educational Qualification: Full-time B.E / B.Tech in Mechanical / Electrical / Instrumentation Engineering (Mandatory) Industry Preference: Candidates must be from API / Bulk Drug Manufacturing environment Experience: 18+ years in Engineering, with at least 5 years in a leadership role

Preparation of Qualification documents: URS, DQ, FDS, Risk Assessment, IQ, OQ, PQ and Operation SOP of different equipment / instrument / utility. Initiation of change controls and CAPA related to Equipment / instrument / utility. Person should have hands on experience in qualification of autoclave, vial washer, depyrogenation tunnel, Filling Machine, capping machine, lyophilizer etc. Person should have exposure / understanding of qualification of packing equipment

Role & responsibilities Responsible for RM/PM Dispensing SAP Basic documentation Preferred candidate profile Pharmaceutical experience is a must. Interested candidates can share their CV/Resumes to noor.m.judge@zyduslife.com

Role & responsibilities Responsible for cell revival, subculture, cell counting of MRC-5 cells. Preparation of MCB/WCB. Experience in Preparation of media and in process buffers in media mixing vessels. Experience in handling Roller bottles, Cell stacks, TCFs. Experience in working in GMP conditions / production department of viral vaccines. Preparation of SOP, BMR’s, Protocols related to cell culture / virus culture. Experience in virus infection, virus harvesting procedures. Experience in working with Chicken embryo fibroblast cells, pooling of embryos, seeding of RB’s . Preparation of Media, in process solutions using preparation vessels. Preferred candidate profile Candidate should have experience in Cell Culture vaccine 6 days work from office based at Ahmedabad

Dear All, We are conducting Walk-in Interview at Indore for our OSD manufacturing Facility based out of our Ahmedabad (SEZ-II), please find the below details. Date : 13th May 2025 (Sunday) Interview Location: Indore Timings: 9:00 am 5:00 pm Interview Venue: Enrise By Sayaji Rau, Survey No. 27/1 27/2, Village Pigdambar Rau Tehsil Mhow Ab Road Job Location: Ahmedabad Education Qualification: ITI/Diploma/BSC/ B.E/B.Tech/B.Pharma Departments are as follows : Production- OSD : Plant Operator/ Technical Assistant : ITI / Diploma having 3 - 8 years of experience in operating machines like Granulation (ACG, Glatt, Tapasya, GEA), Fitzpatrick Roll Compactor, Compression machines (Fette), Wurster Coater (ACG, Glatt, Anish), imprinting, Visual Inspection. Perform line clearance, operation and cleaning of equipment / instrument / auxiliary items Executive/ Sr Executive: B. Pharma with 3 - 8 years of experience in Tablet/ Capsule department with experience in Granulation, Compression, Coating, Inspection . Responsible to plan for the manufacturing of batches in coordination with PPMC. To monitor line clearance, cleaning of equipment, instrument, auxiliary items. To carry out qualification activities. To initiate QMS activities (Change control, deviation, CAPA, investigation) and E-BMR. To handle manpower and allocate daily activities.. Engineering: Technician : Diploma / ITI with 3- 8 years of experience in plant maintenance & Process Equipment (Electrical/ Instrumentation) and Instrumentation . Candidates should have experience in Plant maintenance, preventive maintenance and breakdown maintenance of OSD plant equipment. Troubleshooting of mechanical and electrical equipment . Instrument and calibration of OSD plant equipment. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration activities. Sr. Executive/ Assistant Manager: B.E/ B.Tech with 5-10 Years Process Equipment( Electrical / Instrumentation), Instrumentation, Water System and Utility . Candidates should have experience in Plant maintenance, preventive maintenance and breakdown maintenance of OSD plant equipment. Troubleshooting of mechanical and electrical equipment . Instrument and calibration of OSD plant equipment and Utility. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration . QMS documentation exposure is required. Quality Assurance (Qualification) Assistant Manager / Deputy Manager / Associate Manager: B.Pharm with 10-20 years QA & MFG Qualification. Candidates should have experience in Qualification, Validation. They would have to prepare, execute and review of equipment/ instrument/ system /utility /area qualification program. Review of data backup activity, data restoration and its compliance. QMS documentation exposure is required. completion of CAPAs and to perform change control/CAPA effectiveness. Associate Manager: CSV B.Pharm with 15-20 years with experience in Issuance and retrieval of documents. Candidate should have experience in Review of various Qualification and CSV Documents. Review of system audit trail, system security user privileges and ensure the compliance. Review of data backup activity, data restoration and its compliance. To ensure timely completion of CAPAs and to perform change control/CAPA effectiveness. Quality Control: Assistant Manager & Deputy Manager: Planning & review of reports in Raw Material & Packing material section Executive / Sr. Executive : Analyst - Expertise in analysis of In-process, process validation, FP and method transfer of solid dosage forms (Tablets / capsules) and Raw material with hands on experience in HPLC, UV, Dissolution, GC, IR, Polarimeter, Malvern 3000 etc For all the positions, candidate should have exposure in pharmaceutical company and exposure to regulatory requirements of documentation and cGMP will be added advantage. Interested candidates Please Walk-in for an interview along-with their Aadhar Card, Passport size Photograph, updated CVs, Salary Structure, Salary Slip and relevant documents(original as well as Photocopies) as per the schedule.

Great Opportunity to work withs us in QA - Investigation team . Role & responsibilities Handling of the deviation, OOS, OOT, Market complaint, Lab incident, CAPA. Handling of audits and compliance. Shop floor investigation to identify the root cause. To form CFT for investigation and lead the investigation. To review an investigation plan. To provide necessary information and data for the investigation. To ensure investigation is completed within time line. If investigation is not completed in time, to ensure Interim Report is prepared, reviewed and request for extension is approved by QA head. To prepare and review investigation report and cause or probable cause for finding cause of failure. Discuss the findings and improvement areas based on trend analysis in Quality Review Meetings. Preparation, review and approval of trend analysis reports. Identification of improvement areas based on trend analysis report and providing feedback to the site management. To propose an investigation plan and evaluation of the impact of failure on already distributed batches, batches under manufacturing or in staging/ Process area. To find out root cause or contributory factor for most probable root cause. To carry out impact assessment and risk assessment. To notify the other functional head to carry out investigation Preferred candidate profile Qualification should be M.Sc. Organic chemistry/ PhD with organic chemistry. Person shall be 3-5 year experience in PD Lab/ R&D/QA

Role & responsibilities Familiar with Process safety management , Risk assessment techniques, conducting safety trainings, Safety meetings, BBS , Workplace safety, Record keeping , Incident investigation techniques, SAP activities. ISO -14K ISO45K documentation and compliances, Strengthen Fire hydrant system., Mock drill preparedness Preferred candidate profile Post graduation with 7- 8 years of experience OR graduation with 10-12 years of experience in Safety department.

Qualifications and Education Requirements ICWA or CA Experience 9 to 15 years Location - Ambarnath, Thane, Mumbai ROLE AND RESPONSIBILITIES: CONTROLLING: Product costing run in SAP on monthly / quarterly basis Controlling and review of product cost and analysis of budget v/s. actual cost variance Product wise budgeted OH allocation. Analysis of under/over absorption of overhead Perform cost-benefit analysis and ad-hoc/Standard reporting as per business requirement BOM / Recipe verification in SAP based on BMR and regular updation in SAP to reflect current level of operation Monthly RMC and manufacturing saving calculation Scrap and solvent sales review and release of sales order. Activity rate updation in SAP including Update equipment wise activity rates Driving cost reduction related projects, Product Profitability Analysis (PPA) for new development product. Handling Cost audit & helping in internal & statutory audit. Support to site in costing and system related issues. Monthly TECO of Process orders in SAP. Review of code to code transactions in SAP. Material code extension in consultation with MDM cell PR release activity & coordination with concerned function for errors, if any. Carry forward of FRN/PR/PO at year end FINANCE: Facilitate clearing of GR/IR and Accounts payable Monitor budget and actual utilization of fund and issue of FRN based on request from concerned functions Valuation of inventory and analysis of variances Expense provision scrutiny for month end closing Physically verification of inventory once in a year and entire fixed assets once in 3 years as per planned schedule Inventory controlling- Monthly review and discuss B & R stock with site head. Coordinate Fixed assets Transfer/sales etc. as per SOP. MIS: Month end MIS preparation and review of budget v/s. actual (Monthly and YTD) Daily product wise batch wise yield report Daily report for usage of fresh and recovered solvent Automation of daily reports Preparation of budget with close coordination of all functions Other activity which may be required from time to time BUSINESS PROCESS REENGINEERING: Driving process related changes to make system more automated. Exception reporting PREFERRED SKILLS 1) Excellent communication skill 2) Self-starter and go getter 3) Inter and intra departmental coordination 4) Challenge the status quo 5) Exploratory skills 6) Knowledge of SAP and Excel