107 Environmental Monitoring Jobs - Page 2

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

* For Quality Control (IPPT/FP, RM/PM):- To perform all test for in process product & finish product as per the specification and schedule. To investigate failure of FP / Out of specifications (OOS) and take the corrective and preventive actions (CAPA). To perform and ensure the calibration of instruments as per the schedule. To perform and ensure preparation of reagent / volumetric solution as per schedule. To perform and ensure observation of FP retained samples. To ensure that all documents related to the testing data and related papers are maintained properly. To implement Corrective and Preventive Action (CAPA). To carry out the sampling of all the materials according to Standard Operating Procedure (SOP). To carry out the testing of Raw Material and Packing Material according to approved procedure. To release Raw Material and Packing Material. To carry out the calibration of instruments as per the schedule. To prepare the working standards as per the guidelines and various pharmacopoeias. To ensure the status tag on the released material and transfer such material in the released area. To follow the Good Laboratory practices and Good Manufacturing practices (GMP). To prepare requirement list of chemical & reagent for procurement. To perform the analysis of stability sample as per current specification. To compile the data required for internal quality audit in the plant, as and when required. * For Quality Control (Stability):- To implement the change in procedure as per change control note. To check and verify the sampling of respective samples as per defined intervals for testing. To check and verify that the samples are kept at appropriate temperature and humidity as per defined procedure, which is as per the Standard Operating Procedure. To verify results of analysis conducted in respective period, and to carry out trend analysis. To coordinate with Purchase department for routine requirement and follow up for the procurement. To sign the documents related to stability studies data. To select product batches for the stability studies. In the absence of Officer, Executive will ensure his roles and responsibilities. In the absence of Executive, Sub-department Manager will ensure these roles and responsibilities. To file deviation in case of non-compliance * For Quality Control (Micro):- To ensure the clean environment for sterile preparation by implementing the Good Manufacturing Practice (GMP) norms as per the international standards and guidelines. To do sampling of Water for Injection (WFI), Double Reverse Osmosis (DRO), Single Reverse Osmosis (SRO), Raw water and pure steam. To analyze water samples for pH, conductivity, Bacterial Endotoxin Test (BET), bioburden, Total Organic Carbon (TOC), pathogens, chlorides, hardness, silt density index and other testing as per the requirements. To analyze the samples of water system after maintenance work . To observe and record the results the microbiological plates and test tubes after analysis as well as supervise discarding method of same. To perform the timely microbiological testing of finished product samples, pre-sterile samples, Raw material as well as Packing material sample as per the requirements and SOPs and record the results for the same. Candidate Profile:- Ready to work in Rotational shifts. Excellent understanding about working area. Initiator and Learner. Decision making ability. Team player and if required, can provide training to other team members. Good communication. The above mentioned requirement is for Male Candidate Only. Hence can be ready to work in rotational Shift. Candidate having Parenteral /Injectable exposure would be preferable . Candidates having Pharma exposure will only be considered for interview process. Fresher can also email their CV on Anee.Silas@otsukapharma.in

Candidate must have experience from pharma industry.

Experience Key Responsibilities: Hands-on experience in aseptic processing of biological/pharma products, including sterile filling, sealing, and packaging. Skilled in operating aseptic equipment and ensuring compliance with GMP, GDP, ISO 13485, and Health Safety standards. Maintains strict hygiene protocols and controlled sterile environments. Proficient in environmental monitoring, aseptic area upkeep, and contamination control. Accurate documentation of batch records, QC logs, and processing reports. Strong foundation in microbiology and pharmaceutical standards, backed by B.Sc./M.Sc./B.Pharm/DMLT qualifications. 1-4 years of industry experience in aseptic manufacturing and sterilization.

Role & responsibilities To follow the cGMP, Safety norms and adhere to company's policy. Performing Microbial Limit Test for Non-Sterile Products (API's), Validations, Verifications and Method developments BET analysis for water and Pharmaceutical products. Operation and handling of Instruments/Equipment's. Preparation of work sheets, SOP/GTP's and STP's for Microbiology Laboratory. Assessment of test results against specifications and Trend data. Checking of inwards registers, equipment log books and other log books for all entries. Handling of OOS and Deviations and Incidents. Attending Training classes like OJT, cGMP, SOP, External and safety programs as per schedule. Conducting Training classes like cGMP, OJT, SOP and safety programs as per schedule. Environmental Monitoring by Active and Passive air sampling methods in clean rooms and Microbiology Lab. Carryout Cleaning and Calibration of laboratory Instruments and Equipment's. Media preparation, sterilization and Growth Promotion Test of media.

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. Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a general inquiry form on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process. .

Business Division Secure Power, EcoStruxure IT Line of Business Role Description EcoStruxure IT Technical Partner Specialist Territory India Job Location India Work Type Mixed - remote, onsite, office and travel based on local regulations. Overview The EcoStruxure IT Pre-sales Technical Partner Specialist is responsible for providing Subject Matter Expertise for EcoStruxure IT technologies, supporting the sales cycle for new prospects and existing customers. EcoStruxure IT technologies include Enterprise IT Device Monitoring software, Enterprise Data Center Infrastructure Management (DCIM) Software, Netbotz Environmental Monitoring hardware, and Cooling Optimize. The role is responsible for the day-to-day Technical Pre-sales activities, presentations, and proof of concept activities for EcoStruxure IT technologies across all industries, with a primary focus on the Sales and Pre-sales activities of the Schneider Electric Secure Power business. The EcoStruxure IT Pre-Sales Technical Consultant collaborates with and takes guidance from the EcoStruxure IT Sales Manager Secure Power Commercial Account Managers when working on customer-facing opportunities and Sales pursuits. Role Responsibilities Collaborate with and take direction from EcoStruxure IT Sales Managers and Commercial Account Managers and Partners about opportunity strategy and priority. Articulate Schneider Electric EcoStruxure IT technology and product portfolio, positioning solutions to both business and technical user audience. To attend meetings with prospects and customers to determine technical and business requirements and ensure that all necessary information was collated before producing a solution proposal. Manage the technical sales bid process by responding to RFI RFP documents. Liaising with EcoStruxure IT Product Managers to provide feedback from clients about product requirements and improvements. Manage deliver compelling proof of concept technical demonstrations. Responsible for driving and managing the technical presales process with direct, enterprise, and channel customers. Confidently deliver technical presentations internally and externally to remote and in-person attendees where local guidance requires. Deliver product and technical enablement to channel partners and internal stakeholders. Create internal design configuration documentation, including network diagrams with technical explanations. Qualifications Background in Enterprise IT environments, prior experience either with IT Servers, Data Centers or related Enterprise IT software and services. Working knowledge of Operating Systems including Microsoft Windows and Linux. Basic knowledge of VMWare and virtualization technologies. Basic knowledge of Data Center protocols SNMP & Modbus. Experience with Microsoft Office suite and Salesforce.com. Business Fluent in English

Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible to perform the environment monitoring activities Responsible for Process validation, cleaning validation/verification, hold time study, media fill routine batch sampling as per protocol/SOP. Responsible for review of executed BMRs and BPRs. Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc.. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Review of Visual inspector qualification record.

Greetings from Synergy Resource Solutions, a leading Recruitment Consultancy. Our client is looking for a Technical Content Writer to join the Marketing team. In this role, you will be responsible for creating high-quality, accurate, and clear technical content that communicates complex concepts to a diverse audience. You will work closely with the marketing team and subject matter experts to ensure the content is precise and relevant. This role requires a keen eye for detail, a deep understanding of technical topics, and the ability to simplify complex information into accessible formats. Location: Ahmedabad Experience: 1 - 3 years CTC: 3.5-4 LPA Required Skills and Qualifications: Proven Writing Experience: Prior experience in technical writing related to environmental science, sustainability, or technology (preferably with a focus on air quality, environmental monitoring, or similar fields). Strong Understanding of Environmental Topics: Familiarity with environmental challenges, air quality standards, and sustainability practices. A background in environmental science is a plus. Clear Writing Skills: Ability to explain complex technical topics in simple, clear, and concise language, especially for non-technical audiences. Collaboration Skills: Ability to work with cross-functional teams, including environment, product, and marketing, to gather and communicate technical content. Attention to Detail: A keen eye for detail and the ability to spot inconsistencies, errors, or gaps in technical content. Self-Starter with Proactive Attitude: Ability to manage time effectively, prioritize tasks, and work independently, while meeting deadlines. Adaptability: Ability to manage multiple projects simultaneously and prioritize effectively in a fast-paced environment. Strong Communication Skills: Excellent written and verbal communication skills. Ability to interact with internal stakeholders to clarify complex technical concepts. Job Responsibilities: Research and Draft Technical Content: Research, write, and update high-quality technical content that is clear, accurate, and user-friendly. Collaborate with Teams: Work closely with marketing, environment, product, and sales teams to gather information for content and validate accuracy. Maintain Content Databases: Develop and organize a structured content database to ensure it remains current and easy to navigate. Optimize for SEO: Implement SEO techniques in your content creation to increase visibility and audience reach. Update Existing Documentation: Regularly update documentation based on feedback, product changes, or industry developments. Benefits: Competitive salary and benefits package Opportunities for professional growth and development A dynamic and collaborative work environment If your profile is matching with the requirement & if you are interested for this job, please share your updated resume with details of your present salary, expected salary & notice period.

Job Description 1.Microbiological analysis of raw material, in-process, cleaning validation samples, finished product samples and stability samples. 2.Environment monitoring in Microbiology Laboratory, and Manufacturing facility 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. Microbiological analysis of water samples Work Experience Education :- MSC Microbiology Experience :- 2 to 4 yrs. Education Post Graduation in Microbiology Competencies

Excellent written and verbal communication skills in Marathi and English. Excellent report writing and drafting skills in Marathi and English. Computer typing in Marathi and English. In-depth knowledge of air quality monitoring techniques, air pollution control technologies, and regulatory frameworks. Expertise in air quality data analysis, reporting, and interpretation using industry-standard software and tools. Knowledge of best practices in urban air quality management and emission reduction strategies. Strong project management skills, including the ability to streamline and execute activities within a given timeframe. Prepare EOI for Vendor identification and checking their competency and help Municipal Corporations in finalising vendor Excellent interpersonal and communication skills to engage with government bodies, industry partners, community groups, and other stakeholders. Job Responsibilities: Planning and attending meeting and preparing minutes of meeting. Development & Implementation of Air Quality Management Plans: Lead the formulation of air quality management plans aligned with the goals of the National Clean Air Programme (NCAP). Ensure the effective implementation of air quality improvement initiatives under NCAP at the local level. Monitoring & Assessment of Air Quality Data regularly and identify pollution sources within the jurisdiction of municipal corporation. Provide technical guidance on the implementation of pollution control measures to address major sources of air pollution (e.g., transportation, industrial emissions, waste management). Develop and recommend strategies for pollution reduction and improving air quality. Work closely with local, state, and central government to ensure alignment with NCAP objectives. Engage with stakeholders, including industries, NGOs, and community groups, to raise awareness and promote action on air quality improvement. Analyze air quality monitoring data, prepare detailed reports, and report findings to stakeholders. Organize workshops, seminars, and public consultations to engage local communities/groups in air Familiarity with NCAP guidelines, air quality standards, and environmental regulations. Understanding of national and local air quality management policies and practices. Minimum 2 years of experience in air quality management, environmental monitoring, or a related field, preferably with experience in the implementation of NCAP or similar air quality programs. Hands-on experience in air quality monitoring, data analysis, and preparation of technical reports. Please do not apply if you do not meet the required education, skills, knowledge, relevant experience, or eligibility criteria for this position.

" Position Executive Environment Business Unit / Function JIL-SEZ/ Environment Location Bharuch Reports to Sr. Manager Environment Summary of Job Greenbelt & Greenery Development, Environmental Facilities like ETP, STP & RO plant Operation, Monitoring & Management, Laboratory Analysis, Hazardous Wastes Management & Documentation, over all handling of on field Environment services. Key Responsibilities (Performance Indicators) Greenbelt & greenery development, monitoring & management. Environmental facilities like ETP, STP, RO etc. operation, monitoring, management, data analysis for quantitative and qualitative study on daily, weekly and monthly evaluation for performance verification. Laboratory analysis job, Laboratory & plant chemicals inventory management. Hazardous wastes management & disposal, manifest preparation, records and legal criteria fulfilment, tracking of manifested vehicle for final destruction certification. Daily check of OCEMS data associated to Effluent discharge, Source emission data along with the actual on field comparison. Online Parameters LED Board updating. Environmental compliances, monitoring & audit job planning, 3 rd party environmental monitoring & data gathering from all plants. Follow & preparation of work safety permit system. Physical inspection and monitoring for environment observations. ISO system like Responsible Care Management System RC/ISO/IMS/EnMS related documents preparation, maintain & audit job. ",

Candidates must have Injectable and Regulatory Knowledge in following areas: Aseptic Processing Handling EM excursions Viable environmental monitoring Microbial limit testing Contamination control Trend Analysis Disinfectant efficacy studies Risk Assessment for Aseptic operations Key Responsibilities: Viable Environmental monitoring Trend Analysis Handling EM excursions Computer Proficiency : LIMS, MODA Candidates should be willing to work in shifts.

Position Executive Environment Business Unit / Function JIL-SEZ/ Environment Location Bharuch Reports to Sr. Manager - Environment Summary of Job Greenbelt and Greenery Development, Environmental Facilities like ETP, STP and RO plant Operation, Monitoring and Management, Laboratory Analysis, Hazardous Wastes Management and Documentation, over all handling of on field Environment services. Key Responsibilities (Performance Indicators) Greenbelt and greenery development, monitoring and management. Environmental facilities like ETP, STP, RO etc. operation, monitoring, management, data analysis for quantitative and qualitative study on daily, weekly and monthly evaluation for performance verification. Laboratory analysis job, Laboratory and plant chemicals inventory management. Hazardous wastes management and disposal, manifest preparation, records and legal criteria fulfilment, tracking of manifested vehicle for final destruction certification. Daily check of OCEMS data associated to Effluent discharge, Source emission data along with the actual on field comparison. Online Parameters LED Board updating. Environmental compliances, monitoring and audit job planning, 3rd party environmental monitoring and data gathering from all plants. Follow and preparation of work safety permit system. Physical inspection and monitoring for environment observations. ISO system like Responsible Care Management System RC/ISO/IMS/EnMS related documents preparation, maintain and audit job.

Position: Microbiologist Experience: 2-5 Years Location: POR, Vadodara, Gujarat Job Responsibilities: Conduct microbiological sampling and analysis of: Incoming Raw Materials (RMs) Packaging Materials (PMs) Outgoing Finished Goods (FGs) Perform microbiological testing of: Water samples (process & potable) Hand and product contact surfaces Environmental air samples Handle, operate, and calibrate microbiological instruments and equipment. Maintain precise microbiological records and data logs. Prepare, handle, and document usage of microbiological media. Perform allergen swab testing for cleaning effectiveness validation. Conduct shelf-life studies of finished products (SKUs). Manage RMs, PMs, and FGs with high microbiological load effectively. Key Result Areas (KRAs): Timely and accurate reporting of microbiological test results in compliance with internal standards and regulatory guidelines. Proper handling of high microbial load materials without compromising product quality or safety. Qualifications: B.Sc. / M.Sc. in Microbiology, Biotechnology, or related field Strong knowledge of GMP, GLP, and food safety standards (e.g., FSSAI, ISO 22000, HACCP)

We are seeking a highly skilled Microbiologist to conduct microbiological tests and experiments, prepare samples and reagents for analysis, maintain laboratory equipment, and ensure compliance with safety standards.

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

May support in the development, review and approval of sterilization process and equipment validation/qualifications (IQ, OQ & PQ). Be the point of contact for suppliers/development engineers for new process development, quality issues and process improvements for assigned projects. Participate in the development and improvement of the manufacturing processes for existing and new products. Support product transfers to other plants/facilities. Review/approve nonconforming material and system documentation. Review/approve product and process change control documentation and specifications. Actively participate on teams to support new product development activities. Support design verification and validation test requirements that ensure appropriate objective evidence is available to support acceptance criteria. Specific Job Skills: Must understand the fundamentals of at least one of the following sterilization techniquesgamma irradiation, ethylene oxide (preferred), hydrogen peroxide gas plasma, moist heat, or dry heat and be an expert in one of the techniques. Demonstrated knowledge about a variety of microbiological concepts, practices, and procedures. Ability to use ISO, AAMI, USP, ANSI, EPA, EU and related guidelines toward the design, manufacturing, development, and launch of initiatives. Experience with ISO 17025, Lab Quality Management System. Desired Profile EducationM.Sc. in Microbiology ExperienceMin 5 years of experience in applied device or pharmaceutical microbiological or biological testing, research and development, or sterility assurance experience.

Backup Administration, Macro/Micro Segmentation, IOT Security Expertise in VLAN segmentation, IT/OT isolation strategies, and backup management Strong project management skills for implementing security measures across multiple sites Excellent communication skills for stakeholder engagement and leadership reporting Analytical mindset for identifying risks and designing effective mitigation strategies

Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible to perform the environment monitoring activities Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of executed BMRs and BPRs. Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring eg, plates, samplers, swabs etc. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material eg, plates, swabs, etc. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Review of Visual inspector qualification record.

Join our dynamic team to innovate and drive technology advancements, contributing to significant business growth and client success. As a Technical Program Manager in Consumer Business & Core Tech, you will drive the successful delivery of complex technology projects and programs that will help reaching business goals across the firm. Leveraging your deep knowledge of technical principles, practices, and theories is essential for developing innovative solutions, while simultaneously effectively managing resources, budgets, and high-performing teams. Your strong analytical reasoning and adaptability skills will enable you to navigate through ambiguity and change, ensuring that technology initiatives align with business goals. With advanced communication and stakeholder management abilities, you will foster productive working relationships and influence decision-making to achieve mutually beneficial outcomes. As a subject matter expert, you will contribute to the development of operational plans and risk management strategies, ensuring the highest quality and professionalism in service delivery. Job responsibilities Develop and execute comprehensive project plans, incorporating technical requirements and timelines to ensure on-time delivery. Identify and mitigate risks, proactively addressing potential roadblocks and implementing contingency plans to maintain project and program momentum. Collaborate with cross-functional teams, including engineering, product, and business stakeholders, to define program scope, objectives, and deliverables, ensuring alignment with overall business goals. Utilize advanced analytical reasoning to assess program performance, identify areas for improvement, and implement data-driven optimizations to enhance efficiency and effectiveness. Champion the adoption of agile methodologies and technical solutions, fostering a culture of continuous learning and innovation within the team. Required qualifications, capabilities, and skills 8+ years of experience or equivalent expertise in technical program management, leading complex technology projects and programs in a large organization Demonstrated proficiency in applying analytical reasoning and problem-solving techniques to break down business, technical, or operational objectives into manageable tasks and activities. Proven experience leading through the project lifecycle management, including influencing decision makers and adapting to changes as business needs evolve. Strong technical fluency, with familiarity in current and relevant platforms, software tools, and technologies Strong knowledge on agility model and working on agile dashboards Proficient in stakeholder management, with a track record of establishing productive working relationships and driving mutually beneficial outcomes Preferred qualifications, capabilities, and skills Ability to articulate project goals and updates clearly and concisely. Maintains positive attitude and adjusts plans as per project scope and timeline changes to keep project on track. Engage with stakeholders understanding their perspective and facilitates discussions. Understanding technical aspects for Test Automation and Environment monitoring projects. Proficient in creating and delivering presentations. Knowledge of Agile framework, JIRA, Scrum methodology.

Responsibility : Ensure compliance to cGMP and safety standards in the QC laboratory Conduct calibration and cleaning of laboratory equipment and instruments as per SOP. Culture Media preparation and sterilization. To perform growth promotion test of culture media. Maintenance of microbial culture. Document analytical data and calculate results. Maintain laboratory equipment, inventory and supplies. Ensure integrity, accuracy and adequacy of the analysis performed. Follow GLP activities and ensure their compliance. Conduct microbiological sampling and testing of sample. Conduct environmental monitoring. Identification of microorganism through Vitek 2 system. Daily Laboratory Monitoring including Temperature/Humidity and Testo Printout. Management of issuance and archival of log books and formats. Maintenance of various documents and records in Microbiology Lab. To assist in validation/Qualification exercise and any other assignment given by Lab. In charge / Mgr. Quality Control from time to time.

We are looking for a Sales Engineer with 2+ years of experience in Environmental Monitoring or Instrumentation. The role involves generating business leads, conducting sales presentations,meeting sales targets, and managing client relationships. Health insurance Provident fund Food allowance Annual bonus

Job Posting Form Sales Engineer Designation: Sales Engineer Job Description We are looking for a Sales Engineer with 2+ years of experience in Environmental Monitoring or Instrumentation. The role involves generating business leads, conducting sales presentations and product demos, meeting sales targets, and managing client relationships. The ideal candidate should be technically sound, have strong communication skills, and be able to contribute to business growth with strategic sales efforts.Role & responsibilities Key Responsibilities: Develop and implement effective sales strategies to achieve business growth. Identify and capitalize on new sales opportunities in the assigned region. Build and maintain strong relationships with clients, ensuring excellent customer service. Provide technical guidance and support to clients as required. Collaborate with the engineering and production teams to ensure timely project execution and product delivery. Monitor industry trends, market conditions, and competitor activities to adapt sales strategies accordingly. Prepare and present sales reports, forecasts, and updates to senior management. Requirements: Bachelor's degree in Electrical Engineering or a related field. Minimum 2+ years of sales experience in the Electrical and Instrumentation industry or a related sector. Strong technical understanding of electrical and instrumentation products and systems. Excellent communication, negotiation, and interpersonal skills. Proven ability to meet and exceed sales targets. Self-motivated, goal-oriented, and able to work independently or as part of a team. Willingness to travel as required. Preferred Qualifications: Diploma or equivalent technical qualification in Electrical, Instrumentation, or Electronics Engineering. Experience with environmental monitoring products, particularly in the water industry field Proficiency in MS Office and Excel for data analysis and reporting