105 Environmental Monitoring Jobs

Job Description Timely perform and plan for Calibration and maintenance of instruments. Preparation, sterilization and disposal of microbiological media and accessories. Planning and execution of Water sampling and testing (Microbial and Chemical) of OSD and Ophthalmic facility. Preparation of trend for water system and environmental monitoring. Perform the Environmental monitoring of Sterility area, Ophthalmic and OSD facility and participation in media fill activity. Planning and execution of Microbial analysis of raw material, packing material, intermediate / in-process samples, Finished Product and Stability samples for Sterility testing, Particulate matter testing, Bacterial Endotoxin testing, Antimicrobial effectiveness testing, Bio burden testing and Packing material testing. Planning and execution Growth promotion testing, Preparation of microbial culture suspensions, maintenance of microbial culture and Identification of microorganisms. Planning and execution of online documentation, Upkeep of housekeeping in laboratory. Preparation of method validation MET / Sterility / BET / other miscellaneous protocol for validation study. Proper arrangement of samples and analysis of samples performed within time line. Report any quality concerns or suggestions for improvements to Supervisors/managers. Handling of water, calibration and purchase activity through SAP. Ensure timely initiation and closure of QAMS documents such as lab incidence. Handling of all microbial testing and calibration of instrument/Equipment through LIMS. Responsible to person any other task/activity assigned by supervisor /Manager. Work Experience Experience :- 2 to 4 yrs. Education Masters in Microbiology Competencies

Roles and Responsibilities Responsible for Water sampling and analysis. Responsible for Media Preparation and consumption, sterilization. Responsible for Environmental Monitoring. Responsible for Growth Promotion test. Responsible for FG/RM/Swab/Stability/ Hold time analysis. Desired Candidate Profile Must have Experience in OSD plant (tablet & capsule)

We're Hiring: GIS Consultant Location: Vijayawada Experience: 5-10 Years | Type: Full-Time | Industry: GIS, Remote Sensing, Spatial Analytics Are you passionate about spatial data, remote sensing, and geospatial intelligence? Do you have experience integrating GIS with AI/ML and public data platforms? Join our growing team and be a part of transformative, data-driven projects. Role Overview We are looking for a GIS Consultant with strong technical skills and domain expertise to deliver impactful geospatial solutions across areas like urban planning, environmental monitoring, and AI integration. Key Responsibilities Develop GIS-based analytics and spatial data integration strategies Design interactive maps, geospatial dashboards, and predictive spatial models Integrate GIS solutions with AI and machine learning workflows Support data governance frameworks for geospatial data security and privacy Work on land use analysis, environmental monitoring, and urban planning projects Required Skills Proficiency in GIS tools: ArcGIS, QGIS, Google Earth Engine Expertise in spatial AI, remote sensing, and big data geospatial analytics Hands-on experience with geospatial databases: PostGIS, GeoServer, Spatial SQL Understanding of GIS policy frameworks, open data standards, and regulations Ability to integrate GIS with government or public data platforms Preferred Certifications Certified GIS Professional (GISP) Esri Technical Certification (ArcGIS) Certifications in Remote Sensing or Geospatial Data Science

Mandatory expectation for all roles as per Syngene safet y guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role : Microbiology analysis (Bioburden, MLT, Test for specified organisms, BET analysis) Chemical analysis for water samples Environmental Monitoring Utility Monitoring Water sampling Microbiology lab maintenance Role Accountabilities Responsible for Sample receipt of raw materials, in process, finished product and stability samples. Responsible for Microbiological analysis, Bacterial Endotoxin Test and Chemical analysis of different grades of water (PW/WFI/POW) as per the respective specification. Responsible for sample management and coordination with team for smooth operation of samples release activity. Responsible to perform the Bioburden and Microbial Limit Test. Responsible to perform the Method verification activity for BET, MLT and Bioburden test. Responsible for environmental monitoring of clean rooms in Microbiology laboratory. Responsible for all microbiological related activities like Media receipt, Media stock maintenance, Preparation of media, Sterilization, Growth Promotion for media, Culture maintenance and Media Disposal. Monitoring and review of Temperature monitoring data record of equipment and clean room. Monitoring of differential pressure in QC Microbiology Laboratory. Responsible for disinfectant preparation, cleaning, and fumigation of microbiology laboratory. Follow the required EHSS policies and Good hygiene practice. Undertake other responsibilities related to Microbiology as per requirement.

Role & responsibilities To perform the microbial limit test & validation of samples as per GLP and other different types of samples. To perform Sterility test, BET test & Preservative Efficacy testing of different samples & to perform their validation activity. To monitor the environment of the Microbiology lab. To perform the sterilization of glassware's by autoclave and dry heat sterilizer. To prepare the microbiological media and chemical reagent as and when required and perform the necessary microbial tests. Preparation of disinfectant solution Daily, quarterly and yearly calibration of the balance, pH meter and other instruments as per the master schedule. To check the performance of all instruments as per the master schedule. To review the microbiological documents. To approve the microbiological test related TRF. Documentation and writing journals related to the microbiological test and there validation. To represent the Microbiological lab during audits . Preferred candidate profile M.Sc (Micro) with 02-07 Yrs of relent experience. Interested Candidate may share their Cvs on vilshashah@torrentpharma.com

Job Description Candidate should have good knowledge about all microbiological related activity, Environmental monitoring of classified areas, Water testing Bioburden BET and Sterility. Environmental monitoring of all classified areas of DP manufacturing. Media Preparation required for Utility and area monitoring. To execute Validation / Qualification / Re-qualification as per protocol Sub culturing, serial dilution of standard cultures and GPT and Identification of isolate. Sampling, Testing of Water samples and Compressed air To perform Population Determination of Biological Indicators. Operation of Daily pH, Balance Calibration, Autoclave, DHS, Incubators, Air Samplers and particle counter. To report any Deviations/ Out of Specifications results and Safety risks to the supervisor as and when observed. The candidate should be familiar with cGMP requirements, Change Control, Deviations, OOS, Sample management, Stability Management and investigation tools. To ensure cGMP compliance and maintain the laboratory in audit ready condition. Work Experience 1 to 5 years of experience Education Post Graduation in Microbiology or Biotechnology Competencies

Walk In Drive For Microbiology Department In Formulation Division @ Corporate Office Department:- Microbiology Qualification :- B Sc | M Sc (Microbiology | Bio-Technology | Biochemistry) Division :- Formulation Fresher's :- 2023 | 2024 | 2025 Passed outs only. Interview Date:- 28-06-2025 Work Location :- MSNF Unit-II, Kothur & MSNF Unit-V, RK Puram Interview Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-30438701 | 8785 Note:- Candidate should bring Update Resume , Offer Letter, Increment Letter, CTC, Pay slips ,Bank Statement, Certificates, Aadhaar Card & Pan Card We are looking for candidates those who have experience in Production OSD Department.(Coating Operator & Compression Operator) About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Roles and Responsibilities Responsible for Water sampling and analysis. Responsible for Media Preparation and consumption, sterilization. Responsible for Environmental Monitoring. Responsible for Growth Promotion test. Responsible for FG/RM/Swab/Stability/ Hold time analysis. Desired Candidate Profile Must have Experience in OSD plant (tablet & capsule)

Role & responsibilities :- Perform routine environmental monitoring (air, surface, personnel, and water) of cleanrooms and controlled environments. Collect and analyze viable and non-viable particle data using active air samplers, settle plates, contact plates, swabs, and particle counters. Perform microbial identification and trending of isolated organisms. Ensure sampling and documentation is completed according to SOPs, cGMPs, and regulatory requirements (e.g., EU GMP Annex 1,) Support investigation of deviations, excursions, and contamination events in classified environments. Maintain accurate and timely records in logbooks, laboratory notebooks, and electronic systems. Collaborate with cross-functional teams (QA, Manufacturing, Validation) to support contamination control programs. Contribute to EM data trending, CAPA development, and continuous improvement initiatives. Preferred candidate profile :- Strong attention to detail and documentation skills. Ability to work in gown-controlled cleanroom environments for extended periods. Good communication and teamwork abilities. Understanding of risk-based environmental monitoring and alert/action level response.

JOB DESCRIPTION Job Title: QC Microbiology Analyst Job Location: Bangalore About Syngene : Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Education : M.Sc. Microbiology Equal Opportunity Employer . Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team Good speaking-listening-writing skills, attention to details, proactive self-starter Ability to work successfully in a dynamic, ambiguous environment Ability to meet tight deadlines and prioritize workloads Ability to develop new ideas and creative solutions Should be able to work in team and flexible for working in shifts Should be a focused employee Good documentation capability Experience : 1 -3 YEARS Skills and Capabilities Microbial analysis of water, OSD products, Injectable products, Environmental monitoring Education : Demonstrated Capability : Specific requirements for this role Experience : Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority. Accountabilities as a Syngene Leader (only for Leadership Hires) Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities. Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Role Accountabilities Responsible for Sample receipt of raw materials, in process, finished product and stability samples. Responsible for Microbiological analysis, Bacterial Endotoxin Test and Chemical analysis of different grades of water (PW/WFI/POW) as per the respective specification. Responsible for sample management and coordination with team for smooth operation of samples release activity. Responsible to perform the Bioburden and Microbial Limit Test. Responsible to perform the Method verification activity for BET, MLT and Bioburden test. Responsible for environmental monitoring of clean rooms in Microbiology laboratory. Responsible for all microbiological related activities like Media receipt, Media stock maintenance, Preparation of media, Sterilization, Growth Promotion for media, Culture maintenance and Media Disposal. Monitoring and review of Temperature monitoring data record of equipment and clean room. Monitoring of differential pressure in QC Microbiology Laboratory. Responsible for disinfectant preparation, cleaning, and fumigation of microbiology laboratory. Follow the required EHSS policies and Good hygiene practice. Undertake other responsibilities related to Microbiology as per requirement. Core Purpose of the Role : Microbiology analysis (Bioburden, MLT, Test for specified organisms, BET analysis) Chemical analysis for water samples Environmental Monitoring Utility Monitoring Water sampling Microbiology lab maintenance

Job Requirements: To calibrate pH meter, conductivity meter, Balance. Sampling & testing of Raw Material, Potable water, purified water by chemically as and when required. To check Temp & Humidity in microbial department. Expose plate in production area as well as microbiological section for environmental monitoring purpose. Daily documentation like log books, temp. & humidity records, cleaning records, sampling records, RDS, COA & various assigned registers entry in quantum system. To analyze RM, PM, & FG and preservative efficacy test micro biologically. To prepare media for MLT of RM, PM, & FG and preservative efficacy test as and when required. To maintain record of RM, PM, RAW WATER, POTABLE WATER & PURIFIED WATER & preservative efficacy test & finished products. To maintain instrument calibration schedule as well as calibration and its records. To checking of require media, chemicals & other relevant requirement for analysis and having requisition. In house validation of Autoclave, colony counter equipment and maintain records. Co-ordination within & other departments as and when required. As per work load ready to work overtime. Any other job as when assigned by the Senior Chemist & QC Manager. Pedigree: B.Sc/ M.Sc (Microbiology) with relevant 5-8 years of experience

-Investigate the growth, structure, development & other characteristics of microscopic organisms. -Isolate & make cultures of bacteria or other microorganisms in prescribed media. -Prepare technical reports & documents based upon research outcomes.

Job Description Candidate should have good knowledge about all microbiological related activity, Environmental monitoring of classified areas, Water testing Bioburden BET and Sterility. Environmental monitoring of all classified areas of DP manufacturing. Media Preparation required for Utility and area monitoring. To execute Validation / Qualification / Re-qualification as per protocol Sub culturing, serial dilution of standard cultures and GPT and Identification of isolate. Sampling, Testing of Water samples and Compressed air To perform Population Determination of Biological Indicators. Operation of Daily pH, Balance Calibration, Autoclave, DHS, Incubators, Air Samplers and particle counter. To report any Deviations/ Out of Specifications results and Safety risks to the supervisor as and when observed. The candidate should be familiar with cGMP requirements, Change Control, Deviations, OOS, Sample management, Stability Management and investigation tools. To ensure cGMP compliance and maintain the laboratory in audit ready condition. Work Experience 1 to 5 years experience Education Post Graduation in Microbiology or Biotechnology Competencies

Job Description Candidate should have good knowledge about all microbiological related activity, Environmental monitoring of classified areas, Water testing Bioburden BET and Sterility. Environmental monitoring of all classified areas of Drug product manufacturing. Media Preparation required for Utility and area monitoring. To execute Validation / Qualification / Re-qualification as per protocol. Sub culturing, serial dilution of standard cultures and GPT and Identification of isolate. To execute IQ/OQ/PQ of the new equipment installed in the Microbiology Section. Sampling, Testing of Water samples To perform Population Determination of Biological Indicators. Operation of Daily pH, Balance Calibration, Autoclave, DHS, Incubators, Air Samplers and particle counter. To report any Deviations/ Out of Specifications results and Safety risks to the supervisor as and when observed. Candidate should have good experience in the BET testing by using Gel clot and KTA method To perform Qualification of Equipment, Autoclave, DHS, Incubator, KTA, etc. The candidate should be familiar with cGMP requirements, Change Control, Deviations, Out of Specifications, Sample management, Stability Management and investigation tools. To perform Compressed air sampling and analysis To ensure cGMP compliance and maintain the laboratory in audit ready condition. The candidate should be familiar with SAP system. Work Experience 0 to 2 years. Education Post Graduation in Microbiology or Biotechnology Competencies

Key Responsibilities: Conduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain accurate records and documentation of environmental conditions Communicate findings and recommendations to stakeholders and management Participate in environmental remediation and restoration projects Ensure compliance with environmental regulations and standards

Job Description Daily Monitoring and Calibration: Perform daily pH, balance calibration, and temperature recording. Monitor temperature data of incubators in Lisa line. Cleaning and Disinfection: Clean and disinfect controlled areas. Sampling and Analysis: Perform compressed air sampling and analysis. Conduct water sampling, water testing, and water continuation. Perform bioburden, BET tests for water, raw materials (RM), and products. Conduct sterility testing. Environmental Monitoring: Perform environmental monitoring and prepare EM trends. Prepare a microbial library for in-house isolates identified from water and environmental monitoring samples. Microbiological Procedures: Subculture, perform serial dilution of standard cultures, and conduct CPT. Incubate exposed biological indicators (BI) in autoclave validation and report results. Perform population determination of biological indicators. Documentation and Compliance: Ensure online documentation as per GMP requirements. Prepare and review Microbiology-related SOPs, STPs, validation protocols, and reports. Perform transactions in SAP and QAMS as per authorization. Perform activities as per the authorities provided for LIMS. Change Control, Deviation, and CAPA: Initiate and manage Change Control, Deviation, and Corrective and Preventive Actions (CAPA). Work Experience 1 to 4 year Education Masters in Microbiology or Biotechnology Competencies

Job Description Candidate should have good knowledge about all microbiological related activity, Environmental monitoring of classified areas, Water testing Bioburden BET and Sterility. Environmental monitoring of all classified areas of DP manufacturing. Media Preparation required for Utility and area monitoring. To execute Validation / Qualification / Re-qualification as per protocol Sub culturing, serial dilution of standard cultures and GPT and Identification of isolate. Sampling, Testing of Water samples and Compressed air To perform Population Determination of Biological Indicators. Operation of Daily pH, Balance Calibration, Autoclave, DHS, Incubators, Air Samplers and particle counter. To report any Deviations/ Out of Specifications results and Safety risks to the supervisor as and when observed. The candidate should be familiar with cGMP requirements, Change Control, Deviations, OOS, Sample management, Stability Management and investigation tools. To ensure cGMP compliance and maintain the laboratory in audit ready condition. Work Experience 1 to 5 years experience Education Post Graduation in Microbiology or Biotechnology Competencies

About Intas Recruitment Fraud Disclaimer: Intas Pharmaceuticals does not request or accept any fees during recruitment If someone asks for payment on our behalf, it is a scam Please report the incident to the local police or cybercrime unit Your trust and safety are important to us, Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world, Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare, At Intas, our success is fundamentally built on the strength of our people Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence This approach ensures that every employee plays a meaningful role in driving both the companys growth and advancements in global healthcare, Job Title: Officer QC Micro Job Requisitions No : 13760 Job Description Purpose of Job To perform Microbiological analysis, Skill Required Microbiological skill require to perform the microbiological analysis, Roles and Responsibilites Role of microbiologist and responsibilities to perform the microbial analysis, Qualification Required Sc Relevant Skills / Industry Experience Microbiological skills required and having experience related to pharma industries, Relevant professional / Educational background Master of Science in microbiology field and having two to three years of experience, Any Other Requirements (If Any) Compensation / Reward Location: SEZ, Ahmedabad, GJ, IN, 382213 Travel: 0% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape, Date: 26 May 2025

Daily Calibration pH ad weighing balance,Water sampling&testing,Raw&finished product sampling&analysis,Pckng material analy,Subculturing,Envrnment Monitoring&fumigation in control areas,Media Preparation,Grwth Promotion Test Maintanace of log records

BUILD CAREER WITH CHIRON ! WALK IN INTERVIEW On 20 June 2025, Friday TIME: 10:00 AM to 2:00 PM Quality Assurance / Quality Control Experience 2 5 Years 1. Quality Assurance Qualification: M. Pharm / B.Pharm / B.Tech (Micro/Biotech/ Botany) IPQA/ Change Control/ DR/ CAPA /BMR/SOP Process & Cleaning Validation APQR / QMS Sterile aseptic operation Good Subject Knowledge Legible Handwriting. 2. Quality Control Qualification: M.Sc/ B.Sc Microbiology Environmental Monitoring Media Preparation Bioburden testing Positive Mindset Good Subject Knowledge Legible Handwriting Documents need to Carry Updated Resume ID Proof (Aadhaar & Pan card) Passport Size Photo Copies of Highest Educational Qualification Current company Appointment letter/ Increment letter Last 3 month Pay slips & Bank statement Previous company experience & relieving letter

The opportunity Keeping our people safe and environmentally responsible as we grow and sustain Hub APMEA s businesses through good HSE and ESG processes and practices. How you'll make an impact Manager legal requirements of HSE and comply on regular basis. Support businesses in meeting the HSE KPIs. Weekly call with all the operation leads to ensure compliance. Prepare the business in line with Hitachi Energy Management system requirements. Participate in GEMBA discussion and lead the HSE actions.Lead the mandatory training program in the business Reviewing ABRA and LSR Compliance and take actions and follow-up with team to close gaps on time. Perform safety observation tours, safety audits and inspect facilities, machinery, and safety equipment to identify and correct potential hazards, and to ensure safety regulation compliance. Manage all required documentation, operational checks and reports for the HSE Management System to be compliant with ISO standards. Compile all NCs, prepare corrective action and follow up for closure of NCRs. Coordinate and participate in the investigation of incidents and near-misses Lead in BU Carbon neutrality program.Lead and support the factories on Machine Safety Requirements and compliance. Implement the Machine Safety standards in the Factories. Manage the Legal documents and report like CTE CCA, EPR, monthly, annual environment monitoring and reporting to GPCB. Responsible to ensure compliance with applicable external and internal regulations, procedures, and guidelines. Your background Graduation in Science and engineering 10-12 years of experience in field of HSE. Recognized certificate in HSE. NEBOSH IGC Certified. Good knowledge of legal requirements Review and analyze past incidents and make action to learn from incidents Prepare and timely submit all MIS report. Proficiency in both spoken written English language is required.

The opportunity Keeping our people safe and environmentally responsible as we grow and sustain Hub APMEA s businesses through good HSE and ESG processes and practices. How you'll make an impact Manager legal requirements of HSE and comply on regular basis. Support businesses in meeting the HSE KPIs. Weekly call with all the operation leads to ensure compliance. Prepare the business in line with Hitachi Energy Management system requirements. Participate in GEMBA discussion and lead the HSE actions.Lead the mandatory training program in the business Reviewing ABRA and LSR Compliance and take actions and follow-up with team to close gaps on time. Perform safety observation tours, safety audits and inspect facilities, machinery, and safety equipment to identify and correct potential hazards, and to ensure safety regulation compliance. Manage all required documentation, operational checks and reports for the HSE Management System to be compliant with ISO standards. Compile all NCs, prepare corrective action and follow up for closure of NCRs. Coordinate and participate in the investigation of incidents and near-misses Lead in BU Carbon neutrality program.Lead and support the factories on Machine Safety Requirements and compliance. Implement the Machine Safety standards in the Factories. Manage the Legal documents and report like CTE CCA, EPR, monthly, annual environment monitoring and reporting to GPCB. Responsible to ensure compliance with applicable external and internal regulations, procedures, and guidelines. Your background Graduation in Science and engineering 10-12 years of experience in field of HSE. Recognized certificate in HSE. NEBOSH IGC Certified. Good knowledge of legal requirements Review and analyze past incidents and make action to learn from incidents Prepare and timely submit all MIS report. Proficiency in both spoken written English language is required.

The opportunity Keeping our people safe and environmentally responsible as we grow and sustain Hub APMEA s businesses through good HSE and ESG processes and practices. How you'll make an impact Manager legal requirements of HSE and comply on regular basis. Support businesses in meeting the HSE KPIs. Weekly call with all the operation leads to ensure compliance. Prepare the business in line with Hitachi Energy Management system requirements. Participate in GEMBA discussion and lead the HSE actions.Lead the mandatory training program in the business Reviewing ABRA and LSR Compliance and take actions and follow-up with team to close gaps on time. Perform safety observation tours, safety audits and inspect facilities, machinery, and safety equipment to identify and correct potential hazards, and to ensure safety regulation compliance. Manage all required documentation, operational checks and reports for the HSE Management System to be compliant with ISO standards. Compile all NCs, prepare corrective action and follow up for closure of NCRs. Coordinate and participate in the investigation of incidents and near-misses Lead in BU Carbon neutrality program.Lead and support the factories on Machine Safety Requirements and compliance. Implement the Machine Safety standards in the Factories. Manage the Legal documents and report like CTE CCA, EPR, monthly, annual environment monitoring and reporting to GPCB. Responsible to ensure compliance with applicable external and internal regulations, procedures, and guidelines. Your background Graduation in Science and engineering 10-12 years of experience in field of HSE. Recognized certificate in HSE. NEBOSH IGC Certified. Good knowledge of legal requirements Review and analyze past incidents and make action to learn from incidents Prepare and timely submit all MIS report. Proficiency in both spoken written English language is required.

Media Preparation, (GPT). Instrument like Autoclave, Hot air Oven, pH Meter, Balance, (LAF), Sampler, BOD Incubator, Deep Freezer, analysis of Water, documentation, Limit testing of Finished Product as Per Specification. Required Candidate profile Preference for Male Candidate ONLY

- Identifying and pursuing new sales opportunities - Building strong relationships with customers - Showcasing our products and services through engaging presentations and demos - Collaborating with cross-functional teams to develop marketing strategies - Staying up-to-date with industry trends and competitor activity Requirements: - B.Pharm or M.Pharm graduate - Strong understanding of pharmaceutical concepts and principles - Excellent communication, presentation, and interpersonal skills - Ability to learn quickly and adapt to new situations - Self-motivated and results-driven - Willingness to travel What We Offer: - Competitive salary and benefits package - Comprehensive training and development programs - Collaborative and dynamic work environment - Opportunities for career growth and advancement - Recognition and rewards for outstanding performance