1198 Jobs in Dahej - Page 18

Hiring HR Executive for Chemical Plant for Bhavnagar 3 to 8 Years Experience Apply on sdphrsolution@gmail.com with Subject: HR Bhavnagar & Call on 9727755486 SDP HR SOLUTION have Best Walk-IN Interview Facility Training Hall Conference Room . Required Candidate profile Visit Our Bharuch Office for Your Company Recruitment SDP HR SOLUTION 610, GOLDEN SQUARE BS DMART OPP HOTEL REGENTA ABC CIRCLE GJ Best Walk-IN Facility in Bharuch City Compare to Other Hotels

Project Manager required for company into manufacturing of pressure vessels, heat exchangers & columns. Engineer should have hands on experience on MS Project & Auto Cad. Job Types: Full-time, Permanent Pay: ₹500,000.00 - ₹1,000,000.00 per year Benefits: Cell phone reimbursement Food provided Health insurance Life insurance Paid sick time Paid time off Provident Fund Work from home Work Location: In person Speak with the employer +91 9867772266

Execute and oversee all E&I installation, commissioning, and testing activities at the site. Ensure compliance with QA/QC standards and project specifications. Conduct inspections and witness tests as per ITP/QAP. Coordinate with vendors, contractors Required Candidate profile cement plant is preferable only. If you don’t get from cement plant then get field quality candidates from OGH/Thermal Power plants/Fertilizer/Steel Plants sectors.

Responsibilities: * Ensure compliance with BMR & GMP guidelines. * Collaborate with production team on quality control processes. * Conduct IPQA activities within miscellaneous industry. Food allowance Annual bonus Provident fund

Qualification: ITI Electrician / Diploma Electrical Experience : 1 to 10 Years CTC: Up to 4.5 LPA Work Location : Dahej Send CV on sdpbharuch@gmail.com with Subject: Electrician Dahej & Call on 7600033423 No Charges Share with Friends & Colleagues! Required Candidate profile Must have experience in Breakdown Maintenance, PLC, PLCC, MCC, Star Delta, SCADA, Switch Gear, Motor, and Other Maintenance Join Our WhatsApp Group: https://chat.whatsapp.com/G95zImtORl2ELbTdvS9O5s

Interview for Machine Operator for Plastic Industry in Dahej on Permanent Payroll Qualification: ITI / Diploma ANY / 10th / 12th Pass / Fail Experience: 1 to 5 Years CTC: Upto 4 LPA Budget Apply on sdpbharuch@gmail.com with Subject: Operator Dahej Required Candidate profile Twin screw extruder, Pelletizer cutter die, face cutter pelletizer, Feral extruder White & Black & Color Master Batch, PP, Filler, LL Filler, Film grade molding, Temperature setting, Kneader

Roles and Responsibilities Manage statutory compliance, including contract labour management, industrial relations, and factory acts. Ensure legal compliance by handling cases related to employment law and labor laws. Develop soft skills training programs for employees to enhance their performance and productivity. Oversee talent management initiatives to attract, retain, and develop top performers within the organization. Collaborate with senior leadership to drive business outcomes through effective people strategies.

Research In Agro Intermediate And Chemicals Doing Lab trials as per Instructions Analysis of results Follow safety rules and regulations Maintain data of all the Lab Experiments Preventive maintenance and improvement activities Statutory compliance Required Candidate profile M. Sc or Ph. D with Chemistry 2 to 9 years of Experience in Agro , Specialty Chemical , Fine chemical , Intermediate , Dyes , Pigment , Etc. Reporting to Local Unit Head - Research And Development

Responsible for all process operation / activities during the shift as per CGMP. To maintain BMR/BPR/BCR etc. for record the batches. To co-ordinate with engineering department for the shift break down jobs. To monitor the utility operation in the plant and report any abnormality to concern department. To handle manpower during the shift as per process operations. To work in safe work environment and ensure the sub ordinate are working in safe condition. To check before charging of batch, visual verification of cleanliness status of process equipment. To maintain good housekeeping in respective area. To co-ordinate for the raw material from warehouse for issuing the raw materials. To co-ordinate to QC dept. for In- process and Intermediate testing. To fill the entire document legible. To record and maintain all the documents online as per CGMP. To monitor and record temperature, Humidity and differential pressure in clean area (Level-I, Level-II & III). To check and record daily weighing balance calibration and verification. To review all filled documents after completion of activity and submitted to quality assurance department.

Essential Functions: Perform routine analysis of raw materials, intermediates, APIs, in-process samples, stability samples, and other laboratory samples as per approved specifications and methods. Carry out sampling of raw materials and packing materials in accordance with SOPs. Ensure accurate, timely, and online entry of analytical results in LIMS and relevant documentation systems. Prepare approved/rejected labels for raw materials, intermediates, and packing materials based on analysis outcomes. Conduct daily verification/calibration of analytical instruments (e.g., pH meter, balance) as per approved methods. Maintain analytical instruments in good condition and ensure logbook entries are updated regularly. Perform LIMS entries and maintain relevant analytical records for traceability and compliance. Participate in investigations related to OOS, OOT, deviations, incidents, and laboratory errors. Ensure compliance with Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and cGMP requirements in all activities. Ensure daily laboratory housekeeping and maintain laboratory safety protocols, including use of PPE. Support review and archival of analytical records and raw data as per data integrity norms. Carry out any other assignments allocated by the QC Head or Designee. Additional Responsibilities: Assist in method verification, validation, and transfer activities as required. Support review and revision of SOPs, specifications, and analytical methods. Participate in internal and external audits by providing relevant data and documents. Train junior analysts and contract staff in safe and compliant lab practices. Ensure proper retention, reconciliation, and disposal of samples as per SOPs. Support trending and analysis of analytical data (e.g., stability trends, impurity profiles). Coordinate with production and QA teams to ensure timely testing and batch release. Highlight any instrument malfunctions or quality concerns to the supervisor promptly. Qualifications :- Education: M.Sc - Chemistry / Organic Chemistry - Preferred B.Pharm / M.Pharm - Acceptable for API QC with strong analytical background Experience: 3 to 6 years of relevant experience in Quality Control - exclusively in API manufacturing environment Skills: Analysis of API, RM, Intermediate Samples - Intermediate to Advanced Instrumental Analysis (HPLC, GC, UV, KF, IR, etc.) - Intermediate LIMS Operation and Data Entry - Intermediate Handling and Review of Analytical Documentation - Intermediate OOS/OOT/Deviation Investigation Participation - Intermediate Good Laboratory Practices (GLP) - Advanced Good Documentation Practices (GDP) - Advanced Laboratory Safety and Compliance - Intermediate Data Integrity Principles - Advanced cGMP Awareness Specific to API Environment - Advanced.

Essential Functions: Participate in project planning and distribution of R&D tasks and responsibilities. Monitor and evaluate process verification schedules, plant verification batches, and prepare corresponding reports. Compare yield and quality trends of R&D verification batches and plant validation batches. Prepare, review, and interpret characterization reports for working standards, key starting materials (KSMs), and related substances. Prepare and verify documentation related to R&D process verification and validation batches. Support in plant-scale investigations and troubleshoot issues in coordination with plant and QA teams. Ensure timely submission of R&D and validation samples to Analytical Development Lab (ADL) and follow up for results. Coordinate sample dispatches (RM/intermediates/API) to the Ahmedabad API R&D division for further testing. Communicate with the Raks Ahmedabad API R&D team for technical discussions, project updates, and experimental outcomes. Assist in documentation related to Consent for Establishment (CFE), Drug Licenses, and regulatory submissions. Review of stability study data generated for development and validation batches. Perform and review routine verification and calibration of laboratory instruments used in process development. Review and approve documents related to process development (PD) and validation activities. Train junior staff or subordinates on lab safety, process understanding, and documentation practices. Additional Responsibilities: Ensure compliance with data integrity, GLP, and cGMP practices in R&D operations. Participate in technology transfer from R&D to the production plant and ensure smooth scale-up. Support generation of documents for regulatory filings, including development reports and protocols. Assist in root cause analysis and CAPA implementation related to process deviations. Maintain records of sample tracking, logbooks, and development experiments in compliance with QA requirements. Participate in internal and external audits relevant to R&D activities. Ensure upkeep and maintenance of R&D equipment and request calibration/servicing as per schedule. Drive continuous improvement and cost optimization in process development. Collaborate with QA/QC, Production, and RA teams for project coordination and compliance. Qualifications :- Education: Master Degree, M. Sc - Organic Chemistry - Preferred Ph.D - Chemistry / Pharmaceutical Sciences - Preferred Experience: 3 to 7 years of experience in API R&D/process development Skills: Process Development & Scale-Up - Advanced Plant Validation & Technology Transfer - Intermediate to Advanced Analytical Result Interpretation - Intermediate Process Troubleshooting - Intermediate Documentation Review (PD, Validation, Stability) - Advanced Communication with Cross-Functional & R&D Teams - Intermediate to Advanced Knowledge of Regulatory Documents (CFE, Drug License) - Intermediate cGMP, GLP & Data Integrity Principles - Advanced Instrument Calibration & Review - Intermediate Training & Mentorship - Intermediate

Essential Functions: Perform routine analysis of raw materials, intermediates, APIs, in-process samples, stability samples, and other laboratory samples as per approved specifications and methods. Carry out sampling of raw materials and packing materials in accordance with SOPs. Ensure accurate, timely, and online entry of analytical results in LIMS and relevant documentation systems. Prepare approved/rejected labels for raw materials, intermediates, and packing materials based on analysis outcomes. Conduct daily verification/calibration of analytical instruments (e.g., pH meter, balance) as per approved methods. Maintain analytical instruments in good condition and ensure logbook entries are updated regularly. Perform LIMS entries and maintain relevant analytical records for traceability and compliance. Participate in investigations related to OOS, OOT, deviations, incidents, and laboratory errors. Ensure compliance with Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and cGMP requirements in all activities. Ensure daily laboratory housekeeping and maintain laboratory safety protocols, including use of PPE. Support review and archival of analytical records and raw data as per data integrity norms. Carry out any other assignments allocated by the QC Head or Designee. Additional Responsibilities: Assist in method verification, validation, and transfer activities as required. Support review and revision of SOPs, specifications, and analytical methods. Participate in internal and external audits by providing relevant data and documents. Train junior analysts and contract staff in safe and compliant lab practices. Ensure proper retention, reconciliation, and disposal of samples as per SOPs. Support trending and analysis of analytical data (e.g., stability trends, impurity profiles). Coordinate with production and QA teams to ensure timely testing and batch release. Highlight any instrument malfunctions or quality concerns to the supervisor promptly. Qualifications :- Education: M.Sc - Chemistry / Organic Chemistry - Preferred B.Pharm / M.Pharm - Acceptable for API QC with strong analytical background Experience: 4 to 8 years of relevant experience in Quality Control - exclusively in API manufacturing environment Skills: Analysis of API, RM, Intermediate Samples - Intermediate to Advanced Instrumental Analysis (HPLC, GC, UV, KF, IR, etc.) - Intermediate LIMS Operation and Data Entry - Intermediate Handling and Review of Analytical Documentation - Intermediate OOS/OOT/Deviation Investigation Participation - Intermediate Good Laboratory Practices (GLP) - Advanced Good Documentation Practices (GDP) - Advanced Laboratory Safety and Compliance - Intermediate Data Integrity Principles - Advanced cGMP Awareness Specific to API Environment - Advanced.

Networking: Install, configure, and troubleshoot LAN/WAN infrastructure Manage switches, routers, access points, and structured cabling Ensure network security and uptime CCTV Systems: Install and maintain IP/analog surveillance systems Configure DVR/NVR setups and remote monitoring Perform routine health checks and incident response EPABX Systems: Set up and maintain analog/digital/IP-based EPABX systems Handle internal telephony routing and user configurations Coordinate with vendors for upgrades and repairs Public Address (PA) Systems: Install and test PA systems in commercial and industrial setups Ensure audio clarity and system integration with emergency protocols Time Attendance & Access Control: Deploy biometric/RFID-based attendance systems Configure access control panels and user permissions Monitor logs and troubleshoot authentication issues Fire Alarm Systems (FAS): Install and commission fire detection and alarm systems Conduct periodic testing and compliance checks Respond to faults and coordinate with fire safety teams Required Skills Strong technical knowledge in ELV systems Familiarity with system integration and automation Ability to read schematics and technical manuals Good communication and documentation skills Willingness to travel for on-site support

Role & responsibilities Preferred candidate profile

Supervise, plan, and implement HVAC maintenance schedules (both preventive and breakdown). Troubleshoot and resolve technical issues in HVAC systems (mechanical, electrical & controls). Monitor system performance and efficiency, suggest and execute improvements. Ensure compliance with OEM recommendations and client specifications. Coordinate with OEMs for major overhauls and retrofits. Manage HVAC technicians and site manpower, provide on-job training. Maintain records, service reports, and checklists for audits and HOTO. Ensure all safety protocols, PPE usage, and permit-to-work systems are followed. Support energy audits, AMC proposals, and client reporting. Participate in daily toolbox talks, safety briefings, and incident prevention activities. Required Qualifications: B.E. / B.Tech in Mechanical Engineering (mandatory) Minimum 10 years of experience in HVAC operation and maintenance Hands-on experience in large HVAC plants (preferably in refineries, petrochemicals, pharma, data centers, or industrial complexes) Familiar with HVAC codes, safety standards, and asset management systems (SAP/CMMS preferred) Technical Skills: In-depth knowledge of screw/centrifugal chillers, Li-Br VAMs, air-cooled chillers HVAC controls, PLC/BMS basics Thermodynamics & refrigeration cycle understanding Familiarity with refrigerant handling and leak detection norms Knowledge of HVAC balancing, ducting standards & IAQ parameters Soft Skills: Strong leadership and communication skills Client-facing and team management capability Problem-solving mindset and decision-making under pressure Certifications Preferred: HVACR Training / ASHRAE Membership Safety training (like H2S, Work at Height, Permit-to-work awareness) BMS/PLC Basic Certification (optional) Job Type: Full-time Pay: From ₹450,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Dahej, Gujarat: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Preferred) Experience: HVAC/R: 10 years (Preferred) total work: 10 years (Preferred) Work Location: In person

Essential Functions: • • Perform routine analysis of raw materials, intermediates, APIs, in-process samples, stability samples, and other laboratory samples as per approved specifications and methods. Carry out sampling of raw materials and packing materials in accordance with SOPs. Ensure accurate, timely, and online entry of analytical results in LIMS and relevant documentation systems. Prepare approved/rejected labels for raw materials, intermediates, and packing materials based on analysis outcomes. Conduct daily verification/calibration of analytical instruments (e.g., pH meter, balance) as per approved methods. Maintain analytical instruments in good condition and ensure logbook entries are updated regularly. Perform LIMS entries and maintain relevant analytical records for traceability and compliance. Participate in investigations related to OOS, OOT, deviations, incidents, and laboratory errors. Ensure compliance with Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and cGMP requirements in all activities. Ensure daily laboratory housekeeping and maintain laboratory safety protocols, including use of PPE. Support review and archival of analytical records and raw data as per data integrity norms. Carry out any other assignments allocated by the QC Head or Designee. Additional Responsibilities: Assist in method verification, validation, and transfer activities as required. Support review and revision of SOPs, specifications, and analytical methods. Participate in internal and external audits by providing relevant data and documents. Train junior analysts and contract staff in safe and compliant lab practices. Ensure proper retention, reconciliation, and disposal of samples as per SOPs. Support trending and analysis of analytical data (e.g., stability trends, impurity profiles). Coordinate with production and QA teams to ensure timely testing and batch release. Highlight any instrument malfunctions or quality concerns to the supervisor promptly. Qualifications :- Education: M.Sc – Chemistry / Organic Chemistry – Preferred B.Pharm / M.Pharm – Acceptable for API QC with strong analytical background Experience: 3 to 6 years of relevant experience in Quality Control – exclusively in API manufacturing environment Skills: Analysis of API, RM, Intermediate Samples – Intermediate to Advanced Instrumental Analysis (HPLC, GC, UV, KF, IR, etc.) – Intermediate LIMS Operation and Data Entry – Intermediate Handling and Review of Analytical Documentation – Intermediate OOS/OOT/Deviation Investigation Participation – Intermediate Good Laboratory Practices (GLP) – Advanced Good Documentation Practices (GDP) – Advanced Laboratory Safety and Compliance – Intermediate Data Integrity Principles – Advanced cGMP Awareness Specific to API Environment – Advanced. Qualifications :- Education: M.Sc – Chemistry / Organic Chemistry – Preferred B.Pharm / M.Pharm – Acceptable for API QC with strong analytical background Experience: 3 to 6 years of relevant experience in Quality Control – exclusively in API manufacturing environment

Responsible for all process operation / activities during the shift as per CGMP. To maintain BMR/BPR/BCR etc. for record the batches. To co-ordinate with engineering department for the shift break down jobs. To monitor the utility operation in the plant and report any abnormality to concern department. To handle manpower during the shift as per process operations. To work in safe work environment and ensure the sub ordinate are working in safe condition. To check before charging of batch, visual verification of cleanliness status of process equipment. To maintain good housekeeping in respective area. To co-ordinate for the raw material from warehouse for issuing the raw materials. To co-ordinate to QC dept. for In- process and Intermediate testing. To fill the entire document legible. To record and maintain all the documents online as per CGMP. To monitor and record temperature, Humidity and differential pressure in clean area (Level-I, Level-II & III). To check and record daily weighing balance calibration and verification. To review all filled documents after completion of activity and submitted to quality assurance department. Qualification : B.E. Chemical / B.Tech Chemical Engineering Experience : 3 to 6 Years

Essential Functions: Participate in project planning and distribution of R&D tasks and responsibilities. Monitor and evaluate process verification schedules, plant verification batches, and prepare corresponding reports. Compare yield and quality trends of R&D verification batches and plant validation batches. Prepare, review, and interpret characterization reports for working standards, key starting materials (KSMs), and related substances. Prepare and verify documentation related to R&D process verification and validation batches. Support in plant-scale investigations and troubleshoot issues in coordination with plant and QA teams. Ensure timely submission of R&D and validation samples to Analytical Development Lab (ADL) and follow up for results. Coordinate sample dispatches (RM/intermediates/API) to the Ahmedabad API R&D division for further testing. Communicate with the Raks Ahmedabad API R&D team for technical discussions, project updates, and experimental outcomes. Assist in documentation related to Consent for Establishment (CFE), Drug Licenses, and regulatory submissions. Review of stability study data generated for development and validation batches. Perform and review routine verification and calibration of laboratory instruments used in process development. Review and approve documents related to process development (PD) and validation activities. Train junior staff or subordinates on lab safety, process understanding, and documentation practices. Additional Responsibilities: Ensure compliance with data integrity, GLP, and cGMP practices in R&D operations. Participate in technology transfer from R&D to the production plant and ensure smooth scale-up. Support generation of documents for regulatory filings, including development reports and protocols. Assist in root cause analysis and CAPA implementation related to process deviations. Maintain records of sample tracking, logbooks, and development experiments in compliance with QA requirements. Participate in internal and external audits relevant to R&D activities. Ensure upkeep and maintenance of R&D equipment and request calibration/servicing as per schedule. Drive continuous improvement and cost optimization in process development. Collaborate with QA/QC, Production, and RA teams for project coordination and compliance. Qualifications :- Education: Master Degree, M. Sc – Organic Chemistry - Preferred Ph.D – Chemistry / Pharmaceutical Sciences – Preferred Experience: 3 to 7 years of experience in API R&D/process development Skills: Process Development & Scale-Up – Advanced Plant Validation & Technology Transfer – Intermediate to Advanced Analytical Result Interpretation – Intermediate Process Troubleshooting – Intermediate Documentation Review (PD, Validation, Stability) – Advanced Communication with Cross-Functional & R&D Teams – Intermediate to Advanced Knowledge of Regulatory Documents (CFE, Drug License) – Intermediate cGMP, GLP & Data Integrity Principles – Advanced Instrument Calibration & Review – Intermediate Training & Mentorship – Intermediate Qualifications :- Education: Master Degree, M. Sc – Organic Chemistry - Preferred Ph.D – Chemistry / Pharmaceutical Sciences – Preferred Experience: 3 to 7 years of experience in API R&D/process development

Essential Functions: Manage and oversee day-to-day administrative activities at the Dahej facility. Conduct interviews and coordinate with HR in the recruitment process. Monitor housekeeping services – from deployment of manpower to execution and cleanliness of designated areas. Ensure effective contract labor management in coordination with relevant stakeholders. Oversee site-level security operations and vendor performance. Manage canteen operations efficiently, including menu quality, hygiene, and staff coordination. Administer site transport services – ensuring timely vehicle insurance, PUC, maintenance, and coordination with accounts for payment processing. Monitor pest control services and garden/landscape maintenance. Prepare and process administrative and HR-related bills, JCRs, and coordinate with Finance for timely vendor payments. Coordinate the printing and distribution of lunch/tea/guest canteen coupons. Manage the issuance of ID cards, SEZ cards, and medical cards for employees. Prepare, renew, and maintain work orders and agreements with all admin vendors. Initiate and track Pre-Employment and Annual Medical Examinations in line with HR SOPs. Serve as POSH Coordinator for the Dahej site, ensuring compliance and training support. Prepare MIS reports and provide administrative support to Head Operations and Head HR. Oversee upkeep and smooth functioning of company guesthouse facilities. Support the HR team in induction programs, joining formalities, and interview coordination. Assist in Reward & Recognition (R&R) activities and other employee engagement initiatives. Coordinate and assist in payroll processes as needed. Schedule and coordinate meetings, travel plans, and events. Maintain inventory and order office supplies in a timely manner. Ensure proper office and facility security, including locking procedures and key control. Prepare and manage administrative files, records, and reports. Attend to employee queries and support cross-functional admin-related tasks as required. Additional Responsibilities: Organize internal audits of administrative processes and initiate corrective actions. Support regulatory audits by ensuring proper upkeep of facility-related compliance documents. Identify opportunities for continuous improvement in administrative services and cost-saving initiatives. Coordinate corporate events, celebrations, and annual functions at the Dahej site. Maintain strong vendor relationships and ensure compliance with contract terms and service level agreements (SLAs). Assist in emergency response coordination (fire drills, medical emergencies, etc.). Ensure that administrative SOPs are up to date and followed across the plant. Qualifications :- Education: MBA – HR / M.Com / MPM / IRPM / MSW – Required Experience: 5 to 8 years of relevant experience in site-level administration, preferably in manufacturing / pharma / API industry. Skills: Housekeeping & Facility Management – Advanced Canteen, Transport & Guesthouse Operations – Intermediate to Advanced Contract Labor & Vendor Management – Advanced Statutory Compliance Coordination (POSH, Medicals, etc.) – Intermediate Administrative Billing & Coordination with Finance – Intermediate Strong Communication & Interpersonal Skills – Advanced Recruitment & Induction Support – Intermediate MIS & Report Preparation – Intermediate Organizational & Event Planning – Intermediate Team Collaboration & Leadership – Intermediate. Qualifications :- Education: MBA – HR / M.Com / MPM / IRPM / MSW – Required

Essential Functions: • • Perform routine analysis of raw materials, intermediates, APIs, in-process samples, stability samples, and other laboratory samples as per approved specifications and methods. Carry out sampling of raw materials and packing materials in accordance with SOPs. Ensure accurate, timely, and online entry of analytical results in LIMS and relevant documentation systems. Prepare approved/rejected labels for raw materials, intermediates, and packing materials based on analysis outcomes. Conduct daily verification/calibration of analytical instruments (e.g., pH meter, balance) as per approved methods. Maintain analytical instruments in good condition and ensure logbook entries are updated regularly. Perform LIMS entries and maintain relevant analytical records for traceability and compliance. Participate in investigations related to OOS, OOT, deviations, incidents, and laboratory errors. Ensure compliance with Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and cGMP requirements in all activities. Ensure daily laboratory housekeeping and maintain laboratory safety protocols, including use of PPE. Support review and archival of analytical records and raw data as per data integrity norms. Carry out any other assignments allocated by the QC Head or Designee. Additional Responsibilities: Assist in method verification, validation, and transfer activities as required. Support review and revision of SOPs, specifications, and analytical methods. Participate in internal and external audits by providing relevant data and documents. Train junior analysts and contract staff in safe and compliant lab practices. Ensure proper retention, reconciliation, and disposal of samples as per SOPs. Support trending and analysis of analytical data (e.g., stability trends, impurity profiles). Coordinate with production and QA teams to ensure timely testing and batch release. Highlight any instrument malfunctions or quality concerns to the supervisor promptly. Qualifications :- Education: M.Sc – Chemistry / Organic Chemistry – Preferred B.Pharm / M.Pharm – Acceptable for API QC with strong analytical background Experience: 4 to 8 years of relevant experience in Quality Control – exclusively in API manufacturing environment Skills: Analysis of API, RM, Intermediate Samples – Intermediate to Advanced Instrumental Analysis (HPLC, GC, UV, KF, IR, etc.) – Intermediate LIMS Operation and Data Entry – Intermediate Handling and Review of Analytical Documentation – Intermediate OOS/OOT/Deviation Investigation Participation – Intermediate Good Laboratory Practices (GLP) – Advanced Good Documentation Practices (GDP) – Advanced Laboratory Safety and Compliance – Intermediate Data Integrity Principles – Advanced cGMP Awareness Specific to API Environment – Advanced. Qualifications :- Education: M.Sc – Chemistry / Organic Chemistry – Preferred B.Pharm / M.Pharm – Acceptable for API QC with strong analytical background

About BASF In India BASF has successfully partnered India’s progress for more than 130 years. As of the end of 2024, BASF had 2,411 employees in India with 8 production sites and 42 offices throughout the country. The Innovation Campus Mumbai and the Coatings Technical Center in Mangalore are both part of BASF’s global technology platform. In 2024, BASF registered sales of approximately €2.4 billion to customers in India. Further information is available on www.basf.com/in. O bjectives of the Position Functional leadership Plant Trainer (process safety) Optimise plant internal processes and procedures. Technical, Quality, and cost-effective manufacturing of Cellasto operations Value-based optimization and continuous improvement of plant equipment M ain Areas of Responsibilities and Key Activities MainTasks (Process Safety) Responsible for process optimization (procedures, automation, operator Systems etc) Responsible for process safety at plant. Responsible for the coordination and further development of the continuous improvement process Lead the implementation of process safety processes and practices according to the Responsible Care Management System Responsible for performing detailed process analysis. Responsible for implementing process changes in operations, including documentation Responsible for support by centers of competence or technology unit Responsible for operational innovations. Responsible for issues of plant safety (focus assets) Responsible for the development and documentation of plant safety, equipment investigations) Initiating and setting up of plant modifications/investments with focus on process and asset safety Collaboration in Process Manager community Act as competence center in Process Safety to provide advisory and training to the plant including support the site in preparing GU/RA audit concerning Process Safety. Coordinate all process safety programs, SHE review, MOC for the plants Plan and conduct PSM verification scheme. Manage gap analysis between existing practices and global/regional, GC requirements. Inform the plant management for upgradation as and when necessary Monitor the process safety performance and identify potential process safety issues by analyzing the incident reports and Process Safety Management verification results. Update Process Safety related guideline & regulation MainTasks (Asset Management) Define criteria for prioritization of maintenance work (in coordination with maintenance team) Support/Lead projects, Plan and execute CAPEX and OpEx plan as assigned by Plant Manager Initiate technical related improvement projects , digitalization, simplification. Development of asset condition & asset reliability. In lead to define and regularly review the maintenance- and spare parts strategy, considering the Asset Development Plan and agility plan by using integrated templates (in coordination with maintenance) Coordinate with maintenance team to develop RBM to define equipment criticality, make or buy concept, preventive maintenance strategy, equipment replacement plan & budget, FMEA, knowhow management Initiate definition of spare part strategy. Regularly review and control technical cost and relevant KPIs (monthly, quarterly) Define technical cost budget based on maintenance cost estimation and project plan (in coordination with Maintenance team) Collaboration in Asset Manager community Coordinate with maintenance team to Perform bad actor management, including data analysis, and initiate RCFA for complex issues, action plans with follow up Job Requirements Education B.E/B. in Tech (Chemical/Plastic) Working Experience 8 years & above Technical & Professional Knowledge in Chemical Process/Plastic processing machine operation

Experience in CSV, GAMP, GXP, 21CFR, Part11. Experience in Documentation Writing Good Communication skills. NP - Immediate to 15 Days

Role & responsibilities Expertise in Windows Server and VMware server administration. Strong knowledge of server virtualization technologies, such as VMware or Hyper-V. In-depth understanding of networking concepts, protocols, and services (TCP/IP, DNS, DHCP, VPN). Experience with server security practices, including access controls, patch management, and vulnerability assessments. Solid understanding of storage technologies, RAID configurations, and SAN/NAS solutions. Experience with server monitoring and management tools, such as Nagios, Zabbix, or SolarWinds. Strong problem-solving and analytical skills, with the ability to troubleshoot complex server issues. Excellent communication and teamwork skills, with the ability to collaborate effectively with cross-functional teams and stakeholders. Relevant certifications, such as Server Administrator.

Role & responsibilities Proven experience with network capacity planning, network security principles, and general network management best practices. Experience of handling customer from initial point to escalating to next level based on complexity of the issue. Good Understanding of Routing and Switching protocols like OSPF, BGP, MPLS, ISIS Understanding of TCP/IP and other networking protocols like DHCP/DNS/CDP/ARP etc. Act as a point of contact for NOC team during the shift hrs. and escalate to concerned stakeholders as defined. Good hands experience on Cisco IOS/IOS-XR and Juniper junos Responsible for providing L2 network and security operations support. Design and deploy company LANs, WANs, and wireless networks, including Routers, switches and Firewalls. Oversee installation, configuration, maintenance, and troubleshooting of end user workstation hardware, software, and peripheral devices. Working technical knowledge of current network hardware, protocols, and Internet standards, including routers, switches (layer 2/3), firewalls, remote access, DNS, BGP, OSPF, EIGRP, VLAN, QoS, DSL, Frame Relay, and Metro Ethernet. Adhere with change management process and will provide daily and weekly reports to leads/managers.

Role & responsibilities As an Electrical Maintenance supervisor you need to manage electrical maintenance activities in rotation shift basis. Should be having PLC programming experience Should be having VFD configuration experience Should be having Transformer maintenance experience Must be willing to work in rotational shift To be ready to work in any of the above locations Preferred candidate profile Qualification : : Diploma - Electrical or B.E/B.Tech - Electrical Experience : Minimum 2 Yrs of experience PLC :: Allen Bradley/ Siemens/ Mitshubishi etc. VFD :: ABB, AB, Siemens etc.