33 Jobs in Mahad, Maharashtra

To execute analysis of finished goods / Stability samples / Raw materials / Packing materials In-process and cleaning samples along with relevant laboratory documentation. Intimation & result reporting after completion of analysis & relevant documentation. Check all the instruments on the equipment required for the analysis are in working condition and are in calibrated state. Checking and ensuring proper status labels after confirming availability of all the requirements (as applicable) for analysis such as approved control procedure, analytical protocol, reference standards, chemicals, reagents, glassware, water preparation equipment, water bath, sonication baths, mobile phase bottle etc. Ensure the online documents pertaining to day-to-day analysis are efficiently completed in timely manner. Reporting the activities daily to immediate supervisor. Destruction of QC Samples like Retention samples, analyzed samples etc. To take out the quality reports, Data / Results entry in SAP system. To prepare and maintain the working standards & documentation. Ensure timely raising and closure of deviations, quality events, change controls, OOS/OOT. Preparation and maintenance of Analytical data sheets and Excel spread sheets. Adequate knowledge of all equipment/instruments & their functioning in the laboratory & assist in equipment/instrument qualification activities. Ensuring the quality and integrity of all GxP data and documentation generated. Ensuring effective execution requirements of food regulations (US)-21 CFR Part 111. Ensure fully Engagement and Involvement regarding awareness, clarity maintained related to data integrity. Ensure the 21 CFR Part 11 compliance in the Laboratory. Ensuring good housekeeping and accident-free working in the Laboratory. To perform safe Laboratory operations (as per MSDS) ensuring proper usage of PPEs, safe, secure storage of hazardous, toxic, explosive, corrosive, irritant materials. Ensure proper maintenance of HPLC and GC column and related logbooks in QC lab. To fulfill the analytical requirements of FSSAI regulation. To undergo assigned trainings on cGMP, HSE & departmental procedures / policies. To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same.To implement QEHS policy & objectives. To ensure participation and consultation of worker. To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same. To ensure work permit system during maintenance activities. To ensure disposal of waste. In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.

To execute analysis of finished goods / Stability samples / Raw materials / Packing materials In-process and cleaning samples along with relevant laboratory documentation. Intimation & result reporting after completion of analysis & relevant documentation. Check all the instruments on the equipment required for the analysis are in working condition and are in calibrated state. Checking and ensuring proper status labels after confirming availability of all the requirements (as applicable) for analysis such as approved control procedure, analytical protocol, reference standards, chemicals, reagents, glassware, water preparation equipment, water bath, sonication baths, mobile phase bottle etc. Ensure the online documents pertaining to day-to-day analysis are efficiently completed in timely manner. Reporting the activities daily to immediate supervisor. Destruction of QC Samples like Retention samples, analyzed samples etc. To take out the quality reports, Data / Results entry in SAP system. To prepare and maintain the working standards & documentation. Ensure timely raising and closure of deviations, quality events, change controls, OOS/OOT. Preparation and maintenance of Analytical data sheets and Excel spread sheets. Adequate knowledge of all equipment/instruments & their functioning in the laboratory & assist in equipment/instrument qualification activities. Ensuring the quality and integrity of all GxP data and documentation generated. Ensuring effective execution requirements of food regulations (US)-21 CFR Part 111. Ensure fully Engagement and Involvement regarding awareness, clarity maintained related to data integrity. Ensure the 21 CFR Part 11 compliance in the Laboratory. Ensuring good housekeeping and accident-free working in the Laboratory. To perform safe Laboratory operations (as per MSDS) ensuring proper usage of PPEs, safe, secure storage of hazardous, toxic, explosive, corrosive, irritant materials. Ensure proper maintenance of HPLC and GC column and related logbooks in QC lab. To fulfill the analytical requirements of FSSAI regulation. To undergo assigned trainings on cGMP, HSE & departmental procedures / policies. To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same.To implement QEHS policy & objectives. To ensure participation and consultation of worker. To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same. To ensure work permit system during maintenance activities. To ensure disposal of waste.

Job Description Location: Additional M.I.D.C, Mahad Department: Production & Operations About Fine Finish Industries Pvt. Ltd.: Fine Finish Industries Pvt. Ltd., established in 1994, is a trusted name in the manufacturing and testing of high-quality epoxy resin systems, varnishes, marine products, and insulation materials. With ISO certifications (9001:2015, 17025, 17034, and 17043) and a strong global footprint, we are committed to delivering excellence across industries such as electrical equipment, defense & aerospace, composites, and construction. Job Summary: The Production Incharge will oversee daily production operations to ensure timely, safe, and quality manufacturing of products. This role requires coordinating resources, managing production schedules, implementing process improvements, and maintaining strict quality control. The candidate will ensure compliance with safety standards, productivity targets, and company policies. Key Responsibilities: Plan, organize, and control production activities to meet daily, weekly, and monthly output targets. Supervise production staff and allocate responsibilities to ensure efficient workflow. Coordinate with QC, R&D, and supply chain teams to ensure smooth operations. Monitor the availability and proper use of raw materials, machinery, and manpower. Implement and maintain standard operating procedures (SOPs) and safety protocols. Ensure adherence to quality standards and resolve production issues promptly. Maintain production records, including shift reports, downtime, and inventory usage. Identify and implement process improvements for productivity and cost-efficiency. Train and guide production operators and technicians on best practices. Ensure preventive maintenance schedules are followed for all equipment. Report production progress, delays, or abnormalities to management. Ensure compliance with environmental, health, and safety (EHS) guidelines. Qualifications and Skills: · Required B.Sc. in Chemistry · Minimum experience of 1-2 years in a chemical industry or manufacturing plant · Familiarity with batch processing and documentation · Knowledge of ISO, EHS, and GMP guidelines · Good communication and coordination abilities Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Cell phone reimbursement Internet reimbursement Ability to commute/relocate: Mahad, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: Production planning: 1 year (Preferred) Shift availability: Day Shift (Preferred) Overnight Shift (Preferred) Night Shift (Preferred) Work Location: In person

Job Description Location: Additional M.I.D.C, Mahad Department: Production & Operations About Fine Finish Industries Pvt. Ltd.: Fine Finish Industries Pvt. Ltd., established in 1994, is a trusted name in the manufacturing and testing of high-quality epoxy resin systems, varnishes, marine products, and insulation materials. With ISO certifications (9001:2015, 17025, 17034, and 17043) and a strong global footprint, we are committed to delivering excellence across industries such as electrical equipment, defense & aerospace, composites, and construction. Job Summary: The Production Incharge will oversee daily production operations to ensure timely, safe, and quality manufacturing of products. This role requires coordinating resources, managing production schedules, implementing process improvements, and maintaining strict quality control. The candidate will ensure compliance with safety standards, productivity targets, and company policies. Key Responsibilities: Plan, organize, and control production activities to meet daily, weekly, and monthly output targets. Supervise production staff and allocate responsibilities to ensure efficient workflow. Coordinate with QC, R&D, and supply chain teams to ensure smooth operations. Monitor the availability and proper use of raw materials, machinery, and manpower. Implement and maintain standard operating procedures (SOPs) and safety protocols. Ensure adherence to quality standards and resolve production issues promptly. Maintain production records, including shift reports, downtime, and inventory usage. Identify and implement process improvements for productivity and cost-efficiency. Train and guide production operators and technicians on best practices. Ensure preventive maintenance schedules are followed for all equipment. Report production progress, delays, or abnormalities to management. Ensure compliance with environmental, health, and safety (EHS) guidelines. Qualifications and Skills: · Required B.Sc. in Chemistry · Minimum experience of 1-2 years in a chemical industry or manufacturing plant · Familiarity with batch processing and documentation · Knowledge of ISO, EHS, and GMP guidelines · Good communication and coordination abilities Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Cell phone reimbursement Internet reimbursement Ability to commute/relocate: Mahad, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: Production planning: 1 year (Preferred) Shift availability: Day Shift (Preferred) Overnight Shift (Preferred) Night Shift (Preferred) Work Location: In person

Job Summary: The Quality Control (QC) Chemist will be responsible for conducting routine and non-routine testing of raw materials, in-process samples, and finished products in accordance with applicable specifications and standards. This role requires working in rotational shifts to support 24x7 operations and ensure timely release of batches. Key Responsibilities: Perform chemical, physical, and performance testing on raw materials, intermediates, and finished products using standard test methods (e.g., ASTM, ISO, BIS). Ensure compliance with internal specifications, customer requirements, and regulatory standards. Maintain accurate and complete documentation of test results, observations, and deviations. Calibrate and maintain laboratory equipment such as viscometers, pH meters, spectrophotometers, etc. Collect and prepare samples for analysis as per SOPs. Investigate non-conforming results and participate in root cause analysis. Assist in validation, stability studies, and method development as required. Follow all EHS and 5S practices while working in the laboratory. Coordinate with production, R&D, and QA teams for timely sample processing and batch clearance. Participate in shift handovers and communicate critical issues clearly to incoming shift personnel. Support internal and external audits by maintaining traceable records and ensuring data integrity. Qualifications: B.Sc. / M.Sc. in Chemistry or Applied Chemistry or Industrial Chemistry (preferred). 1–3 years of experience in a chemical manufacturing or resin/paint/adhesive/polymer-based QC lab. Freshers with strong fundamentals and willingness to work in shifts may be considered. Key Skills: Hands-on knowledge of wet chemistry techniques, titration, viscosity, solids content, pH, etc. Basic knowledge of spectroscopic and chromatographic techniques is an advantage. Strong documentation and data interpretation skills. Attention to detail and adherence to quality standards. Comfortable working in shifts and in a fast-paced manufacturing setup. Location: Mahad MIDC Job Type: Full-time Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Cell phone reimbursement Provident Fund Ability to commute/relocate: Mahad, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Experience: QA/QC: 1 year (Required) Quality control: 1 year (Preferred) Shift availability: Day Shift (Preferred) Night Shift (Preferred) Overnight Shift (Preferred) Work Location: In person

Job Summary: The Quality Control (QC) Chemist will be responsible for conducting routine and non-routine testing of raw materials, in-process samples, and finished products in accordance with applicable specifications and standards. This role requires working in rotational shifts to support 24x7 operations and ensure timely release of batches. Key Responsibilities: Perform chemical, physical, and performance testing on raw materials, intermediates, and finished products using standard test methods (e.g., ASTM, ISO, BIS). Ensure compliance with internal specifications, customer requirements, and regulatory standards. Maintain accurate and complete documentation of test results, observations, and deviations. Calibrate and maintain laboratory equipment such as viscometers, pH meters, spectrophotometers, etc. Collect and prepare samples for analysis as per SOPs. Investigate non-conforming results and participate in root cause analysis. Assist in validation, stability studies, and method development as required. Follow all EHS and 5S practices while working in the laboratory. Coordinate with production, R&D, and QA teams for timely sample processing and batch clearance. Participate in shift handovers and communicate critical issues clearly to incoming shift personnel. Support internal and external audits by maintaining traceable records and ensuring data integrity. Qualifications: B.Sc. / M.Sc. in Chemistry or Applied Chemistry or Industrial Chemistry (preferred). 1–3 years of experience in a chemical manufacturing or resin/paint/adhesive/polymer-based QC lab. Freshers with strong fundamentals and willingness to work in shifts may be considered. Key Skills: Hands-on knowledge of wet chemistry techniques, titration, viscosity, solids content, pH, etc. Basic knowledge of spectroscopic and chromatographic techniques is an advantage. Strong documentation and data interpretation skills. Attention to detail and adherence to quality standards. Comfortable working in shifts and in a fast-paced manufacturing setup. Location: Mahad MIDC Job Type: Full-time Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Cell phone reimbursement Provident Fund Ability to commute/relocate: Mahad, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Experience: QA/QC: 1 year (Required) Quality control: 1 year (Preferred) Shift availability: Day Shift (Preferred) Night Shift (Preferred) Overnight Shift (Preferred) Work Location: In person

Job Description: Service Engineer Position: Service Engineer – Maharashtra, We are hiring Service Engineers with 1–2 years of experience in maintaining, calibrating, and troubleshooting environmental monitoring instruments such as CEMS, AAQMS, and meteorological stations. Candidates should be proficient in installation, commissioning, and customer training. Field experience in analyzers and knowledge of safety protocols, HVAC, and data transmission to pollution control boards is preferred. Keywords: Service Engineer, CEMS, AAQMS, Instrumentation, Calibration, Environmental Monitoring Mandatory Key Skills (at least 1): Field Service of Environmental Monitoring Systems Work Experience Required: 1–2 years Industry Type: Environmental Services / Instrumentation Functional Area: Service / Maintenance / Technical Support Qualification: Bachelor's or Diploma in Instrumentation, Electronics, or related fields Industry Environmental Services Employment Type Full-time Job Types: Full-time, Permanent, Fresher Pay: ₹12,000.00 - ₹35,000.00 per month Benefits: Cell phone reimbursement Flexible schedule Health insurance Provident Fund Application Question(s): Do you hold a degree in Electrical, Electronics, Instrumentation, or Environmental Engineering? Willingness to travel: 75% (Preferred) Work Location: In person

Fine Finish Industries Pvt. Ltd. is a professionally managed, ISO: 9001-2015 certified organization engaged in manufacturing electrical insulating materials and composite matrix resins. We have an ISO/IEC: 17025-2017 NABL accredited lab for electrical, mechanical and chemical testing. This is a full-time on-site role for an Integrated Quality Manager at Fine Finish Industries Pvt. Ltd. for Mahad location responsible for entire quality system comprises regular internal auditing, analyzing and interpreting customer complaints, troubleshooting issues and ensuring compliance with safety standards. The applicant must be a graduate or postgraduate in Quality Systems Management with experience in a multi-location chemical manufacturing industry specializing in electrical insulating materials, composite matrix resins and offering laboratory services in the fields of electrical, mechanical and chemical fields. He must be proficient in procedures and equipment. Must have thorough understanding of quality management systems and safety regulations. Must be able to analyze and interpret test results leading to entire gamut of quality assurance. Strong attention to details and problem-solving skills are required. Excellent communication and team working abilities is a must. Job Type: Full-time Pay: ₹100,000.00 - ₹200,000.00 per month Benefits: Leave encashment Schedule: Day shift Rotational shift Supplemental Pay: Performance bonus Yearly bonus Ability to commute/relocate: Mahad, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: Managing Quality Systemsg: 2 years (Required) Language: Hindi, English, Marathi (Preferred) Location: Mahad, Maharashtra (Preferred) Willingness to travel: 25% (Required) Work Location: In person Application Deadline: 15/04/2025 Expected Start Date: 01/09/2025

Key Responsibilities: Experience in all aspects of Windows Server, including installation, configuration, administration, troubleshooting, and best practices. Experience with virtualization platforms (VMware, Hyper-V, Citrix XenServer). Experience with Windows Server performance tuning. Strong troubleshooting skills in resolving Windows Server issues, problem fixing, root cause analysis, and configurations. Familiarity with enterprise monitoring systems and ticketing systems. Exposure to server backups and restores. Exposure to Active Directory and Windows technologies such as DNS and DHCP. Exposure to scripting for automating daily tasks. Exposure to disaster recovery. Job Type: Full-time Pay: ₹32,000.00 - ₹35,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person

Responsible & Accountable for smooth & timely dispensing of Raw Materials for Liquid, N-Block & Vitamin-Mineral Premix products. Partially responsible & Accountable for compliance with Rules & regulations of Goods & Service Act and State Excise Act. Partially responsible & Accountable for compliance with Legal Metrology (Weights & Measures) Act Ensuring avoidance of breach of data integrity at all the levels. To follow effective sanitation activities at all the levels. Customer centricity. To follow Food safety, Quality, Environment and Occupational Health & Safety management system at RM warehouse activities of Liquid, N-Block & Vitamin-Mineral Premix products and to identify areas for improvement. To ensure compliance to the regulatory, customer, legal requirements and face audits and comply non conformities observed during the audits. To ensure compliance to the current ISO 9001:2015, ISO 14001:2015, ISO 45001:2018, D&C Act, FSS Act 2006, FSSC 22000, Kosher, Halal, RSPO, FAMI QS, WHO-GMP, UNICEF, WFP GAIN and other customer and regulatory requirements. To ensure compliance to the audit observations of RM warehousing facility of Main Plant. To follow requirements of food regulations for export market (US)-21 CFR Part 110 & 111. Imparting required training to shop floor personnel. Adherence to the requirements of EHS norms. To follow various initiatives as are suggested by corporate functions (Piramal Learning University & Quality mindset). To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same. To implement QEHS policy & objectives. To ensure participation and consultation of worker. Ensure use of PPE To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same. To ensure work permit system during maintenance activities. To implement QEHS continual improvement projects at site and monitor. To ensure disposal of waste. Authorized to prevent improper workplace conditions. Authorized for reporting of Hazards, Incident, accidents and near miss Reporting. Authorized to prepare OH&S performance document. Authorized to conduct training of workmen related to OHSMS. In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.

Responsible & Accountable for smooth & timely dispensing of Raw Materials for Liquid, N-Block & Vitamin-Mineral Premix products. Partially responsible & Accountable for compliance with Rules & regulations of Goods & Service Act and State Excise Act. Partially responsible & Accountable for compliance with Legal Metrology (Weights & Measures) Act Ensuring avoidance of breach of data integrity at all the levels. To follow effective sanitation activities at all the levels. Customer centricity. To follow Food safety, Quality, Environment and Occupational Health & Safety management system at RM warehouse activities of Liquid, N-Block & Vitamin-Mineral Premix products and to identify areas for improvement. To ensure compliance to the regulatory, customer, legal requirements and face audits and comply non conformities observed during the audits. To ensure compliance to the current ISO 9001:2015, ISO 14001:2015, ISO 45001:2018, D&C Act, FSS Act 2006, FSSC 22000, Kosher, Halal, RSPO, FAMI QS, WHO-GMP, UNICEF, WFP GAIN and other customer and regulatory requirements. To ensure compliance to the audit observations of RM warehousing facility of Main Plant. To follow requirements of food regulations for export market (US)-21 CFR Part 110 & 111. Imparting required training to shop floor personnel. Adherence to the requirements of EHS norms. To follow various initiatives as are suggested by corporate functions (Piramal Learning University & Quality mindset). To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same. To implement QEHS policy & objectives. To ensure participation and consultation of worker. Ensure use of PPE To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same. To ensure work permit system during maintenance activities. To implement QEHS continual improvement projects at site and monitor. To ensure disposal of waste. Authorized to prevent improper workplace conditions. Authorized for reporting of Hazards, Incident, accidents and near miss Reporting. Authorized to prepare OH&S performance document. Authorized to conduct training of workmen related to OHSMS.

Ensure effective functioning of Microbiology Laboratory by carrying out analysis Ensure the compliance to cGMP regulations, quality guidelines and local SOPs. Ensure online documentation. Planning and execution of Microbiological activities & online documentation. Microbiological testing of finished product, starting material, stability sample & another sample. Microbiological media preparation and its GPT. Daily monitoring of Area / room & refrigerator/ Incubators temperatures, Microbiological monitoring of classified areas. Bacterial culture maintenance and keeping records of consumption of ATCC/NCTC cultures. Sampling & Analysis of water samples for microbiological parameters. Analysis of compressed air and nitrogen gas. Report all deviations, which may have impact on safety, identity, strength, purity & quality of drug substance/ product. Issuance of QC analytical data sheets Trending & review of microbial analytical data for water samples, RM, FG samples. Monitoring & perform the calibration / validation for Instruments / Equipment in micro-Lab. Preparation and destruction of Media and culture. Preparation of Microbial inoculum. To perform safe Laboratory operations (as per MSDS) ensuring proper usage of PPEs To ensure work permit system during maintenance activities. To perform Autoclave validation. To carryout in-house Microbial flora isolation process. To perform fogging activity as per schedule. Daily review & prints out of Incubator when it required. To identify & communicate incidents, QEHS nonconformities, investigate and take corrective actions on the same. To perform Microbial assay.

To allocate manpower. Checking cleanliness of area and machines. Balance verification Verification of Raw materials in granulation. To check and monitor the dispensing, granulation and compression activities in the department as per plan. To update departmental documents and records. To do online completed batches entries and close process orders in SAP system. To impart training to the operators and workers and maintain records. To maintain inventory of machine accessories and change parts and miscellaneous items required in granulation and compression department. To give requisition of BMRs to the QA department. To check the raw material and packing material availability in SAP. Intimate material shortages to planning department. To Update KPIs. To investigate and find out root cause analysis of any identified problem. To report incident to Human resources and safety department. To make a plan of manpower requirement to meet the expected output and delivery schedules under the guidance of HOD. To utilize man, machine and material including natural resources like Electricity, Water, Steam and Compressed air to get higher productivity. To ensure proper segregation of material, quality of products, cleanliness of machines, walls, flooring, ceiling, windows and scrap area. To improve product quality and productivity. To co-ordinate with QA, QC, Stores, HR, IT, EHS and Engg. Department. To follow Good Manufacturing Practices in the department. To maintain quality products and maintain quality norms. Ensuring implementation of effective sanitation and hygiene activities at all the levels. Ensuring upkeep of area and equipment. Imparting training to colleagues / subordinates. To raise change control, deviation and CAPA. To ensure avoidance of breach of data integrity at all levels. To ensure compliance to the safety measures. To ensure the cleaning of riser filters as per SOP. To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same. To implement QEHS policy & objectives. Ensure use of PPE. To ensure compliance to Safety Measures. Implementation and Documentation of ISO 9001:2015, ISO14001:2015 and ISO 45001:2018. To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same. To ensure work permit system during maintenance activities. To implement QEHS continual improvement projects at site and monitor. To ensure participation and consultation of worker. To ensure disposal of waste. Authorised to prevent improper workplace conditions. To ensure that preventive maintenance of the machines done by maintenance department. To complete monthly production plan. To do monthly verification of weighing balances. To coordinate to external party to do calibration of instruments as per identified frequencies. Authorised for reporting of Hazards, Incident, and accidents and near miss Reporting. Authorised to prepare OH&S performance document. Authorised to conduct training of workmen related to OHSMS.

To allocate manpower. Checking cleanliness of area and machines. Balance verification Verification of Raw materials in granulation. To check and monitor the dispensing, granulation and compression activities in the department as per plan. To update departmental documents and records. To do online completed batches entries and close process orders in SAP system. To impart training to the operators and workers and maintain records. To maintain inventory of machine accessories and change parts and miscellaneous items required in granulation and compression department. To give requisition of BMRs to the QA department. To check the raw material and packing material availability in SAP. Intimate material shortages to planning department. To Update KPIs. To investigate and find out root cause analysis of any identified problem. To report incident to Human resources and safety department. To make a plan of manpower requirement to meet the expected output and delivery schedules under the guidance of HOD. To utilize man, machine and material including natural resources like Electricity, Water, Steam and Compressed air to get higher productivity. To ensure proper segregation of material, quality of products, cleanliness of machines, walls, flooring, ceiling, windows and scrap area. To improve product quality and productivity. To co-ordinate with QA, QC, Stores, HR, IT, EHS and Engg. Department. To follow Good Manufacturing Practices in the department. To maintain quality products and maintain quality norms. Ensuring implementation of effective sanitation and hygiene activities at all the levels. Ensuring upkeep of area and equipment. Imparting training to colleagues / subordinates. To raise change control, deviation and CAPA. To ensure avoidance of breach of data integrity at all levels. To ensure compliance to the safety measures. To ensure the cleaning of riser filters as per SOP. To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same. To implement QEHS policy & objectives. Ensure use of PPE. To ensure compliance to Safety Measures. Implementation and Documentation of ISO 9001:2015, ISO14001:2015 and ISO 45001:2018. To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same. To ensure work permit system during maintenance activities. To implement QEHS continual improvement projects at site and monitor. To ensure participation and consultation of worker. To ensure disposal of waste. Authorised to prevent improper workplace conditions. To ensure that preventive maintenance of the machines done by maintenance department. To complete monthly production plan. To do monthly verification of weighing balances. To coordinate to external party to do calibration of instruments as per identified frequencies. Authorised for reporting of Hazards, Incident, and accidents and near miss Reporting. Authorised to prepare OH&S performance document. Authorised to conduct training of workmen related to OHSMS. In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.

Ensure effective functioning of Microbiology Laboratory by carrying out analysis Ensure the compliance to cGMP regulations, quality guidelines and local SOPs. Ensure online documentation. Planning and execution of Microbiological activities & online documentation. Microbiological testing of finished product, starting material, stability sample & another sample. Microbiological media preparation and its GPT. Daily monitoring of Area / room & refrigerator/ Incubators temperatures, Microbiological monitoring of classified areas. Bacterial culture maintenance and keeping records of consumption of ATCC/NCTC cultures. Sampling & Analysis of water samples for microbiological parameters. Analysis of compressed air and nitrogen gas. Report all deviations, which may have impact on safety, identity, strength, purity & quality of drug substance/ product. Issuance of QC analytical data sheets Trending & review of microbial analytical data for water samples, RM, FG samples. Monitoring & perform the calibration / validation for Instruments / Equipment in micro-Lab. Preparation and destruction of Media and culture. Preparation of Microbial inoculum. To perform safe Laboratory operations (as per MSDS) ensuring proper usage of PPEs To ensure work permit system during maintenance activities. To perform Autoclave validation. To carryout in-house Microbial flora isolation process. To perform fogging activity as per schedule. Daily review & prints out of Incubator when it required. To identify & communicate incidents, QEHS nonconformities, investigate and take corrective actions on the same. To perform Microbial assay. In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.

KEY TASKS & RESPONSIBILITIES: Equipment technology, capacity upgradation for better productivity. Initiate measures for conserving natural resources like energy, water, oil etc. If required initiate suitable modifications in plant mechanism. Giving the feedback and communicating with the Engg Head about the activities and performance of the plant and processes. Monitoring and supervising the plant and machinery in good working condition. Prepare the standing operating procedures and work instructions of the department. Control on Maint. Budget - Preparation of annual budget and control. Planning for preventive maintenance, major shut down with reference to the production plan/requirements. Shut down Activity planning for duration, resources required. 3M Management (Man, Machine & Material) - Spares documentation, Critical spares identification & ensure availability. Allocation of task with ref. to individual work orientations. Adherence to Safety - Ensure all the safety rules as per OHSAS & EMS are followed for Man, Machine and Material Supplied critical organizational, analysis, and problem-solving skills to programs. Oversaw defining and resolving of critical technical and program issues and ensured engineering support to the manufacturing team.

KEY TASKS & RESPONSIBILITIES: Achieves electrical maintenance operational objectives by contributing information and recommendations to strategic plans and reviews; preparing and completing action plans; resolving problems; completing audits requirements, determining system improvements, implementing change. Provides electrical power by maintaining electrical equipment and outlets; including energy management system for lighting, security gates, security console, and mail conveyor system. Monitoring and supervising the plant and machinery in good working condition. Prepare employee shift schedule and adhere go guidelines. Maintains supplies inventory by checking electrical material stock to determine inventory levels; anticipating needed supplies. Keeps equipment operating by following operating instructions; troubleshooting breakdowns; maintaining supplies; performing preventive maintenance; calling for repairs. Inventory control - Standardization for the spares, PR control for optimum inventory. Planning for major shut down - With Ref. to the production plan/requirements. Shut down Activity planning for duration, resources required. Adherence to Safety - Ensure all the safety rules as per OHSAS & EMS are followed for Man, Machine and Material.

KEY TASKS & RESPONSIBILITIES: Achieves electrical maintenance operational objectives by contributing information and recommendations to strategic plans and reviews; preparing and completing action plans; resolving problems; completing audits requirements, determining system improvements, implementing change. Provides electrical power by maintaining electrical equipment and outlets; including energy management system for lighting, security gates, security console, and mail conveyor system. Monitoring and supervising the plant and machinery in good working condition. Prepare employee shift schedule and adhere go guidelines. Maintains supplies inventory by checking electrical material stock to determine inventory levels; anticipating needed supplies. Keeps equipment operating by following operating instructions; troubleshooting breakdowns; maintaining supplies; performing preventive maintenance; calling for repairs. Inventory control - Standardization for the spares, PR control for optimum inventory. Planning for major shut down - With Ref. to the production plan/requirements. Shut down Activity planning for duration, resources required. Adherence to Safety - Ensure all the safety rules as per OHSAS & EMS are followed for Man, Machine and Material.

KEY TASKS & RESPONSIBILITIES: To oversee, study and implement the planned activities for the entire development process of new products and programs within an organization. Analyze and collect the data regarding the process on miniature scale before submitting for commercial manufacturing. To keep track and record in form of documentations , of new development from the initial planning phase to implementation or production. Co-ordinate and sharing knowledge with technical services team on developing new process for products. Continously monitoring the ongoing processes and analyzing the data generated to the superiors. To keep updated the equipment’s and process related documentations as per ISO standards. To keep record updated regarding the old as well as new processes and produce them when required for analysing. Report the analyzed data to the superiors and implement the changes suggested in the processes. Supervise the activities carried by operators, trainees, helpers and housekeeping people. To support the department to develop a sustainable production process.

Manage daily schedules, employee shifts, and time-off requests Assign duties to employees and oversee their progress Ensure that daily sales/production goals are met Count cash at the end of the shift and manage bank deposits Train and integrate new workers Provide guidance and feedback to employees when needed Ensure industry rules and regulations are followed Handle customer and employee complaints Resolve conflicts between employees Transfer products and other objects to and from the worksite on occasion Job Types: Full-time, Permanent Pay: ₹700,000.00 - ₹800,000.00 per year Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person

Intercorp Biotech Group is a reputed manufacturer of high-quality products in Human Food Fortification, Personal & Home Care, and Animal Feed Supplements. We are committed to innovation, efficiency, and delivering impactful solutions to our customers. Job Summary: We are seeking an experienced and driven Sales Manager – Veterinary Products to lead our sales efforts in Animal Feed Supplements and Ingredients. The ideal candidate will bring a strong network within the poultry, cattle, and aquaculture feed sectors and a proven ability to build, manage, and grow key accounts across India. Key Responsibilities: Drive sales and expand the customer base for animal feed supplements across regions Build and maintain relationships with manufacturers of poultry, cattle, and aquaculture feed Develop and manage distributor/dealer networks and regional sales teams Conduct field visits with sales personnel and channel partners Formulate and execute marketing campaigns, sales schemes, trade offers, and product promotions Oversee design of packaging, labeling, marketing collaterals, and digital campaigns Conduct competitor analysis and gather market intelligence Manage product lifecycle including R&D coordination, market surveys, cost & pricing strategy, and new product introductions Stay updated on regulatory standards for veterinary products Travel 15–20 days/month as required to maintain field presence Preferred Experience: · Sales experience with feed supplements/ingredients targeted to poultry, cattle, and fish/aquaculture feed manufacturers · Familiarity with government e-procurement platforms like GEM and international procurement channels · Product management and marketing experience in animal nutrition or veterinary products Qualifications: · Bachelor’s degree in Business, Marketing, Animal Nutrition, Veterinary Science, or related field · 5+ years of relevant sales experience in animal feed or veterinary sector · Strong knowledge of animal nutrition, feed ingredients, and industry trends · Excellent communication, negotiation, and leadership skills · Ability to work independently and as part of a team · Strong problem-solving and analytical skills · Willingness to travel frequently Job Location- Maharashtra, Gujarat Job Type: Permanent Pay: ₹25,893.86 - ₹50,529.04 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Language: English (Preferred) Work Location: In person

To maintain department cleanliness. To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same. To implement QEHS policy & objectives. To ensure participation and consultation of worker. Ensure use of PPE. To identify & communicate incidents, QEHS nonconformities, investigate and take corrective actions on the same. To ensure work permit system during maintenance activities. To implement QEHS continual improvement projects at site and monitor. To ensure disposal of waste. To prepare and review departmental SOPs & load final SOPs in ENSUR. To prepare and review departmental documents. To Coordination, Monitoring and controlling of departmental activities as per cGMP norms. To get optimum productivity within specified quality by effective utilization of available resources so as to deliver the product as per market requirement. Responsible for providing quality product and maintaining quality system of company. Ensuring avoidance of breach of data integrity at all the levels. Ensuring implementation of effective sanitation activities at all the levels. To allocate manpower. Verification of raw materials and packing materials. To check and monitor the dispensing, granulation and compression and Coating activities in the department as per plan. To update departmental documents and records. To do online completed batches entries and close process orders in SAP system. To impart training to the operators and workers and maintain records. To maintain inventory of machine accessories and change parts and miscellaneous items required in granulation and compression department. To train workmen and subordinates. To give requisition of BMRs and BPRs to the QA department. To check the raw material and packing material availability in SAP. Intimate material shortages to planning department. To Update KPIs. To investigate and find out root cause analysis of any identified problem. To report near miss incident to Human resources and safety department. To make a plan of manpower requirement to meet the expected output and delivery schedules under the guidance of HOD. To utilize man, machine and material including natural resources like Electricity, Water, Steam and Compressed air to get higher productivity. To ensure proper segregation of material, quality of products, cleanliness of machines, walls, flooring, ceiling, windows, and scrap area. To improve product quality and productivity. To co-ordinate with QA, QC, Stores, HR, IT, EHS and Engg. Department. To ensure compliance to the safety measures. To ensure that preventive maintenance of the machines done by maintenance department. To complete monthly production plan. To do monthly verification of weighing balances. To coordinate to external party to do quarterly and yearly calibration of instruments. To impart training to the workmen and operators for GMP, Personal Hygiene and SOP’s, Processes and Company Policies. Preparation of Documents for ISO 9001:2015, 14001:2015 & 18001:2007 & its Compliance. Authorised to prevent improper workplace conditions. Authorized for reporting of Hazards, Incident, accidents and near Miss Reporting. Authorized to prepare OH&S performance document.

To maintain department cleanliness. To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same. To implement QEHS policy & objectives. To ensure participation and consultation of worker. Ensure use of PPE. To identify & communicate incidents, QEHS nonconformities, investigate and take corrective actions on the same. To ensure work permit system during maintenance activities. To implement QEHS continual improvement projects at site and monitor. To ensure disposal of waste. To prepare and review departmental SOPs & load final SOPs in ENSUR. To prepare and review departmental documents. To Coordination, Monitoring and controlling of departmental activities as per cGMP norms. To get optimum productivity within specified quality by effective utilization of available resources so as to deliver the product as per market requirement. Responsible for providing quality product and maintaining quality system of company. Ensuring avoidance of breach of data integrity at all the levels. Ensuring implementation of effective sanitation activities at all the levels. To allocate manpower. Verification of raw materials and packing materials. To check and monitor the dispensing, granulation and compression and Coating activities in the department as per plan. To update departmental documents and records. To do online completed batches entries and close process orders in SAP system. To impart training to the operators and workers and maintain records. To maintain inventory of machine accessories and change parts and miscellaneous items required in granulation and compression department. To train workmen and subordinates. To give requisition of BMRs and BPRs to the QA department. To check the raw material and packing material availability in SAP. Intimate material shortages to planning department. To Update KPIs. To investigate and find out root cause analysis of any identified problem. To report near miss incident to Human resources and safety department. To make a plan of manpower requirement to meet the expected output and delivery schedules under the guidance of HOD. To utilize man, machine and material including natural resources like Electricity, Water, Steam and Compressed air to get higher productivity. To ensure proper segregation of material, quality of products, cleanliness of machines, walls, flooring, ceiling, windows, and scrap area. To improve product quality and productivity. To co-ordinate with QA, QC, Stores, HR, IT, EHS and Engg. Department. To ensure compliance to the safety measures. To ensure that preventive maintenance of the machines done by maintenance department. To complete monthly production plan. To do monthly verification of weighing balances. To coordinate to external party to do quarterly and yearly calibration of instruments. To impart training to the workmen and operators for GMP, Personal Hygiene and SOP’s, Processes and Company Policies. Preparation of Documents for ISO 9001:2015, 14001:2015 & 18001:2007 & its Compliance. Authorised to prevent improper workplace conditions. Authorized for reporting of Hazards, Incident, accidents and near Miss Reporting. Authorized to prepare OH&S performance document. In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.

KEY TASKS & RESPONSIBILITIES Primary contact for Packaging QA issues Monitor Packaging’s overall safety and quality Ensure the completion of QA review of Packaging process orders and Packaging forms Lead packaging inventory counts Maintenance of master inspection characteristics for Packaging processes in ERP. Monitor Compliance with QMS, conducting regular audits of procedures and documentation Ensure timely entry QC Test results into ERP and co-ordinate with QA Manager on the release of dried harvest lots Develop and implement continuous improvement initiatives in Packaging operations, Coordinate with QA Manager and GMP Advisor to develop, implement, and maintain QMS systems and GMP for Packaging processes Perform risk assessments in Packaging and investigate non-compliances and deviations as required Provide direction supervision of Packaging QA Technician(s), provide training, feedback, and ensure completion of assigned tasks With help of the QA Manager, create and deliver performance targets and evaluations, including providing regular and consistent feedback to team Ensure adherence to GMP and SOPs during packing operations. Assist to QA manager during internal, external and customer audits by providing relevant records and data. Provide on-floor guidance to production teams on quality practices. Implement audit recommendations and support to QA team for closure of observations. Monitor personal hygiene and gowning in packing area. Identify, record and report deviations or non-conformances in packing activity. Ensure line/area clearance before packing startup.

KEY TASKS & RESPONSIBILITIES: DCS / PLC knowledge is essential. Ensure that all the processes and operations are carried out as per the standard work instructions, procedures and specifications. Organize and schedule the shop floor activities with respect to the production plan and delivery schedule. Debottleneck the problems encountered in operations. Ensure effective implementation and maintenance of QMS, EMS, OHSAS and inventory management system Manage logistics, shipping, receiving, delivery and distribution including process improvement and problem resolution. Co-ordination with the supporting documents like safety, QA/QC, ETP, Engineering, Stores etc. for smooth operations of the plant. Prepare the standing operating procedures and work instructions of the department. Initiate action to prevent the occurrence of any non-conformity related to the product, process, quality system, environment management system, OHSAS and RC. Training the subordinates as per the identified training needs. Looking after complete operation & maintenance of equipment’s in production department. Raw material consumption coefficient and yield calculation.