105 Environmental Monitoring Jobs - Page 4

Job Role: QC Executive - Microbiologist Job Location: Jaipur Education: BSC Microbiology / MSC Microbiology Experience: 3-5 Years About Brand: Minimalist (https://www.beminimalist.co) is a science-backed Indian skincare brand built on the core values of efficacy, transparency, and comprehensiveness. Known for its ingredient-first approach, the brand formulates high-performance skincare products using proven activities and clean formulations. The company believes in creating high-quality products using best-in-class ingredients at its own manufacturing facility. Minimalist empowers consumers with knowledgeclearly stating what goes into each product and whyso they can make informed choices. With a commitment to 'Hide Nothing,' the brand champions authenticity and honesty in skincare, creating solutions that work, without the fluff. With a robust portfolio of 60+ SKUs spanning Skincare, Haircare, and Bodycare, the brand is rapidly expanding its footprint. Focused on enhancing product availability, it is strategically deepening its penetration while strengthening both Modern Trade (MT) and General Trade (GT) channels in India. The brands global presence now extends across 15+ countries, including key markets such as the UK, USA, UAE, Malaysia, Indonesia, Germany, France & Italy. Roles and Responsibilities: Maintain and update the Quality Control (QC) tracker to accurately reflect product quality data and metrics. Ensure timely and precise recording of quality issues, test results, and corrective actions. Coordinate with production teams to implement corrective and preventive actions to improve product quality. Assist in creating, revising, and maintaining quality process documents, including standard operating procedures (SOPs) and work instructions. Ensure compliance with industry standards and regulatory requirements relevant to personal care products Prepare and present detailed reports on quality performance, including trends, issues, and improvement actions to management. Qualifications : 3-5 years of experience. Btech, Bsc, Msc in any specialisation is preferred Strong understanding of quality control principles, methodologies, and best practices. Proficiency in using quality control tools, software, and tracking systems. Ability to work collaboratively with cross-functional teams and handle multiple priorities. Knowledge of manufacturing processes and quality control techniques specific to personal care products. Apply Here : https://forms.gle/VxmsWbrqwkoToKxe9

Role & responsibilities Environmental clearance & Expansion ,Statutory Clearance from State Pollution Control Board & legal required documentation ( consent to established /Operate /Hazardous / Water etc. ) To ensure Environment and Healthy safety across the entire site and coordinate EHS activates . Responsible of matters relating to site safety inspection , behavior safety observations , safety audits , corporate audits and other external EHS audits . To ensure all necessary EHS related legal compliances are done within the time frame and submitted to statutory bodies like Fire & Safety . Environmental monitoring and analysis of various Environment ( like emission , ambient air quality, noise monitoring , drinking water &waste water etc.). Ensuring that to complying all the statutory compliances , submission of various monthly ,quarterly ,half yearly and yearly returns and plantation reports to statutory authorities. Liasioning with government authorities ,regulatory bodies and other external agencies . Data collection for ESG( Environment ,Sustainability & Governance ). Comprehensive understanding of Environment Rules & Regulations and adopt the changing requirements . Hazardous waste management and solid wasted Management: Environmental Statutory Compliance , monitor & control of EHS parameters . Environmental , Social and Governance ( ESG ) compliances . Preferred candidate profile B.SC /M.SC / B.Tech /MTech Environment Science qualified candidate with 6-8 yrs experience in Environment Science .

JOB RESPONSIBILITIES QC Executive ( Microbiology )Quality Control Head Quarter : Faridabad Purpose of the position : - To ensure that water sampling, media preparation and used media destruction is done as per approved procedure. Job Responsibilities :- 1. Responsible for all type of water sampling & analysis. 2. Responsible for operation and calibration of pH meter and weighing balance. 3. Responsible for destruction of used media/used plates and used cultures. 4. Responsible to verify logbook of autoclave, water sample inward, media management, pH meter, Laminar Air Flow and weighing balance etc. 5. Responsible for media preparation in absence of other team member. 6. Responsible for Analysis of Bioburden Sample testing of in-process, finished product & raw materials samples as per approved standard operating procedure. 7. Responsible for timely submission, review, approved and release of reports related to microbiology section. 8. Responsible for culture management as per approved protocol. 9. Responsible for Preparation of culture Suspension. 10. Responsible for Growth Promotion Test for all the dehydrated media as per standard operating procedure. 11. Responsible for Revival and Sub culturing of Microorganisms. 12. Responsible for Environmental Monitoring by Settle Plate Method & Surface swab method. 13. Responsible for performing Preservative Efficacy Test. 14. Responsible for all admin related work. 15. Responsible for reporting any Non conformity/OOS/Deviation related to water and bio burden samples. 16. Responsible for reporting of DCR for any changes related to microbiology section. . 17. To provide practical training to newcomer of QC-Microbiology Section. 18. Responsible for maintaining stock of media & materials needed for analysis. 19. Functional reporting shall be as per departmental organogram. 20. Responsible to ensure the compliance of the SOP’s applicable to QC-Microbiology. 21. Any other task assigned by your Reporting Manager. The Job Responsibilities may be reviewed / added as per company requirements from time to time.

Role & responsibilities Performing routine microbiological testing on raw materials, in-process samples, and finished products to ensure they meet quality and safety standards. Conducting environmental monitoring of clean rooms and other controlled environments Documenting and interpreting test results accurately and timely Ensuring adherence to Good Manufacturing Practices (GMP) and Hazard Analysis and Critical Control Points (HACCP) Monitoring and maintaining water systems for safety Assisting in achieving standards accreditation Validating and verifying cleaning and sanitation practices through microbiological testing Preferred candidate profile Qualification :- B.SC or M.SC (Microbiology) Work Experience :- 2-4 Years

Lead and manage the entire Environmental Impact Assessment (EIA) process. Ensure compliance with environmental laws and regulations Prepare and submit reports, such as Environmental Impact Statements (EIS) To attend SEAC/MoEF meeting for presentation Required Candidate profile 1. B.E./M.E./Masters’ in Science or above 2. Accredited by NABET for EIA Coordinator 3. Approved for minimum 4 sectors, (either sectors 16, 17, 22, 29 or other approved sectors) 4. Willing to travel

-Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems. About the Role Major accountabilities: Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance -Support exception investigations -Review and approval of production, QC, and AS and T records -MBR review -Support OpEx improvement projects Qualified Person - Executes batch release in compliance with registration -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Key performance indicators: On-time and GMP-compliant release of dosage forms -No complaints about inspections by authorities in your own area of responsibility without these being noticed and communicated beforehand -Successfully support continuous improvement projects -Executes batch release in compliance with registration Minimum Requirements: Work Experience: Functional Breadth. QC/ QA in pharmaceutical ind./ biotech with environmental monitoring . Collaborating across boundaries. cleanliness zones. Skills: QMS BMR/ BPR review Batch Release process Quality Management Regulatory compliance checks Languages : English.

-Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems. Major accountabilities: Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance -Support exception investigations -Review and approval of production, QC, and AS and T records -MBR review -Support OpEx improvement projects Qualified Person - Executes batch release in compliance with registration -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Key performance indicators: On-time and GMP-compliant release of dosage forms -No complaints about inspections by authorities in your own area of responsibility without these being noticed and communicated beforehand -Successfully support continuous improvement projects -Executes batch release in compliance with registration Minimum Requirements: Work Experience: Functional Breadth. QC/ QA in pharmaceutical ind./ biotech with environmental monitoring . Collaborating across boundaries. cleanliness zones. Skills: Continuous Learning. Dealing With Ambiguity. Gmp Procedures. Qa (Quality Assurance). Quality Control (Qc) Testing. Quality Standards. Self Awareness. Technological Expertise. Technological Intelligence. Languages : English.

-Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems. Key Responsibilities: Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance -Support exception investigations -Review and approval of production, QC, and AS and T records -MBR review -Support OpEx improvement projects Qualified Person - Executes batch release in compliance with registration -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Essential Requirements: On-time and GMP-compliant release of dosage forms -No complaints about inspections by authorities in your own area of responsibility without these being noticed and communicated beforehand -Successfully support continuous improvement projects -Executes batch release in compliance with registration Desirable Requirements: Work Experience: Functional Breadth. QC/ QA in pharmaceutical ind./ biotech with environmental monitoring . Collaborating across boundaries. cleanliness zones. Skills: Continuous Learning. Dealing With Ambiguity. Gmp Procedures. Qa (Quality Assurance). Quality Control (Qc) Testing. Quality Standards. Self Awareness. Technological Expertise. Technological Intelligence. Languages : English.

-Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems. Key Responsibilities: Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance -Support exception investigations -Review and approval of production, QC, and AS and T records -MBR review -Support OpEx improvement projects Qualified Person - Executes batch release in compliance with registration -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) On-time and GMP-compliant release of dosage forms -No complaints about inspections by authorities in your own area of responsibility without these being noticed and communicated beforehand -Successfully support continuous improvement projects -Executes batch release in compliance with registration Minimum Requirements: Essential Requirements: Functional Breadth. QC/ QA in pharmaceutical ind./ biotech with environmental monitoring . Collaborating across boundaries. cleanliness zones. Skills: Continuous Learning. Dealing With Ambiguity. Gmp Procedures. Qa (Quality Assurance). Quality Control (Qc) Testing. Quality Standards. Self Awareness. Technological Expertise. Technological Intelligence. Languages : English.

Note: Candidates having below mentioned relevant skills should apply on the link. https://forms.gle/tyZf41YWk5QfcQnz8 Role & responsibilities Assist in the development and implementation of Environmental Management Plans for infrastructure projects. Monitor environmental parameters such as air quality, water quality, noise levels, and solid waste management on project sites. Ensure adherence to environmental laws, standards, regulations, and other applicable authorities. Conduct environmental audits and site inspections; recommend and follow up on corrective actions. Support in obtaining environmental clearances and liaise with environmental consultants and government authorities. Prepare periodic environmental monitoring and compliance reports. Promote sustainable construction practices and environmental awareness at the site level. Participate in risk assessments and propose mitigation measures for potential environmental hazards. Maintain documentation of environmental compliance for internal and external audits. Desired Candidate Profile Qualification: BE / B.Tech - Environmental Engineering, Civil Engineering, or Mechanical Engineering Experience: 2 to 7 years of experience Expertise: Underground Metro & Box Pushing Strong communication and interpersonal skills Person having a positive attitude and a self starter / go-getter approach. Excellent organizational and multitasking abilities.

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

Key Responsibilities (Performance Indicators) Analysis & Documentation at ETP, STP & RO plant. ETP, STP & RO Plant and Laboratory inventory management. Supervision of ETP, STP & RO operation & maintenance/ Management of ETP, STP & RO staffs. IMS & RC 14001 related documents preparation, Implementation, maintain & audit job. Hazardous waste management & disposal. Manifest & document preparation. Coordination with plants for effluent monitoring & receipt. Plant round from environment point of view, observation & action. Environmental monitoring & audit job. ETP daily report preparation, making of batches in BAAN-LN system. PR, Job orders, Issue slip preparation etc. BAAN related activities related to Environment function. Ensure the effective compliance and implementation of IMS/RC/EnMS standard and related activities. Regular updating of Environmental data information display board/ LED board at Main gate. Regular checking of online environmental parameters website of GPCB/CPCB. Environment compliances and documentation: Form 3, Form 4, Form 5 Environment Statement, EC compliance, E-waste return, Battery waste return etc. Environmental compliances on EY conformity tool. Monthly patrak update on GPCB XGN site. Environment Monthly report preparation. Environment Monthly review presentation preparation etc. Qualification & Experience B.E. Environment or B.E. Chemical or M.Sc. in environment / chemistry / bio-technology with min. 5 years of Environment/ ETP/ STP/ RO relevant experience. Competencies (Technical, Functional & Behavioral) Experience of ETP/STP/RO plant operation, Lab. Analysis, Hazardous waste management & Environmental Compliances & IMS/ ISO/ RC management system & documentation. Knowledge of environmental compliances, effluent treatment, trouble shooting, hazardous waste handling & lab. analysis. Hard working, positive attitude towards work & result oriented. ",

The Field Officer appointed will be responsible for conducting environmental sample collection, on-site monitoring, and field investigations. The role involves working in compliance with regulatory standards, ensuring quality assurance, and supporting laboratory analysis processes. Key Responsibilities: Conduct field sampling and monitoring of air, water, soil, noise, and other environmental parameters as per standard guidelines. Ensure proper handling, labeling, preservation, and transportation of collected samples to the Operate and maintain field monitoring instruments such as stack monitoring kits, air samplers, noise level meters, and water quality testing equipment. Adhere to standard operating procedures (SOPs) and regulatory guidelines set by MITCON, NABL and MoEFCC. Prepare field reports, data sheets, and documentation related to environmental sampling and Assist in environmental impact assessment (EIA) studies and compliance monitoring projects. Coordinate with laboratory analysts for sample analysis and reporting. Maintain accurate records of monitoring activities and ensure timely submission of reports. Follow safety protocols and environmental best practices while performing field activities. Provide technical support to clients on sampling procedures and regulatory compliance. Required Qualifications & Skills: 1-3 years of experience in environmental monitoring, field sampling, or a related role (Fresher s with relevant academic experience may also apply). Hands-on experience with environmental monitoring instruments is an advantage. Ability to travel extensively for fieldwork and work in various environmental conditions. Interested candidates are requested to send their updated resume along with a cover letter to [hr@mitconindia.com]. Only shortlisted candidates will be contacted.

Key Responsibilities (Performance Indicators) Analysis and Documentation at ETP, STP and RO plant. ETP, STP and RO Plant and Laboratory inventory management. Supervision of ETP, STP and RO operation and maintenance/ Management of ETP, STP and RO staffs. IMS and RC 14001 related documents preparation, Implementation, maintain and audit job. Hazardous waste management and disposal. Manifest and document preparation. Coordination with plants for effluent monitoring and receipt. Plant round from environment point of view, observation and action. Environmental monitoring and audit job. ETP daily report preparation, making of batches in BAAN-LN system. PR, Job orders, Issue slip preparation etc. BAAN related activities related to Environment function. Ensure the effective compliance and implementation of IMS/RC/EnMS standard and related activities. Regular updating of Environmental data information display board/ LED board at Main gate. Regular checking of online environmental parameters website of GPCB/CPCB. Environment compliances and documentation: Form 3, Form 4, Form 5 Environment Statement, EC compliance, E-waste return, Battery waste return etc. Environmental compliances on EY conformity tool. Monthly patrak update on GPCB XGN site. Environment Monthly report preparation. Environment Monthly review presentation preparation etc. Qualification and Experience B.E. Environment or B.E. Chemical or M.Sc. in environment/chemistry/bio-technology with min. 5 years of Environment/ ETP/ STP/ RO relevant experience. Key Competencies (Technical, Functional and Behavioral) Experience of ETP/STP/RO plant operation, Lab. Analysis, Hazardous waste management and Environmental Compliances and IMS/ ISO/ RC management system and documentation. Knowledge of environmental compliances, effluent treatment, trouble shooting, hazardous waste handling and lab. analysis. Hard working, positive attitude towards work and result oriented.

Job Summary: We are seeking a motivated and skilled QC Microbiologist to join our Quality Control team. The successful candidate will be responsible for performing microbiological testing on raw materials, in-process samples, finished products, water systems, and environmental monitoring to ensure compliance with GMP and regulatory standards. Key Responsibilities: Conduct microbiological testing of raw materials, in-process samples, finished products, and stability samples. Perform environmental monitoring of manufacturing areas including viable and non-viable particle counts, surface monitoring, and air sampling. Carry out water analysis (e.g., Total Microbial Count, Endotoxin, TOC). Execute Sterility testing, Microbial Limit Tests (MLT), Endotoxin testing (LAL method), and Growth Promotion Tests (GPT). Maintain proper documentation of all microbiological activities in compliance with cGMP and GLP. Participate in method validation, media preparation, and equipment qualification. Investigate microbiological deviations, OOS/OOT results, and support implementation of CAPA. Ensure calibration and maintenance of all microbiological instruments (e.g., incubators, autoclaves, particle counters). Support internal and external audits by regulatory authorities. Comply with all lab safety protocols and procedures. Exp.- Fresher or 1 year of experience in a pharmaceutical microbiology lab. Location-Por GIDC, Gujarat

locationsSHELL CENTRE CHENNAIposted onPosted 3 Days Ago time left to applyEnd DateMay 30, 2025 (13 days left to apply) job requisition idR177536 , India Job Family Group: Health, Safety, Security, and Environment Worker Type: Regular Posting Start Date: May 13, 2025 Business unit: Experience Level Early Careers About The Role About The Role Whats the role An Engineer in Carbon and Environment Reporting is responsible for comprehensive greenhouse gas emissions accounting and reporting. This includes reviewing process diagrams, supporting environmental programs, and using tools for frequent emissions monitoring. Daily tasks involve monitoring emissions, planning for reductions, and collaborating with teams to review fuel and flare reports. The role requires advanced knowledge of equipment and emission sources in oil and gas facilities, preparing monthly emission summaries, and managing operational issues to ensure compliance with standards. Additionally, the engineer reviews flare allocation reports, stays updated on greenhouse gas accounting rules, and supports external regulatory compliance, including ISO 14001 audits. Knowledge of sustainability and ESG reporting standards is also essential. What youll be doing Advanced Knowledge of Greenhouse gas emissions Accounting/ Reporting & calculation methodologies Process Engineering/ Modelling - Reviewing PFDs/PIDs, analyzing process parameters. Support the coordination of environmental monitoring programs and initiatives along with site environment teams. Experienced in Focused/ High frequency Emissions monitoring programs/ tools Daily operational Baseline monitoring for emission parameters and action management. Operational Planning Forecasting Emissions & abatement; Abatement Actuals Tracking Experience in working with hydrocarbon allocation team for reviewing flare, fuel volume report Advanced process knowledge of equipment and emission sources within oil and gas facility. Prepare Monthly Emission performance summary for assets. Monthly - diesel, venting, fuel gas, flaring, fugitives - in line with events in the asset events & provide supporting analysis. Manage and follow-up on operational issues, performance metrics, and determine root cause of the problems and implement sustainable corrective action Review Flare Allocation report, accommodate flare volume accounting methodology change/ transition. Advanced knowledge of environmental reporting - Waste, Water, Soil, Emissions, etc Knowledge of Sustainability/ESG reporting- CSRD, TCFD, GRI, ISSB External Regulatory compliance - ISO 14001 - External Assurance Audits. Support and coordinate audits and verification of environmental data. Manage and follow-up on operational issues, performance metrics, and determine root cause of the problems and implement sustainable corrective action Review Flare Allocation report, accommodate flare volume accounting methodology change/ transition. Prepare Monthly Emission performance summary for assets. Monthly - diesel, venting, fuel gas, flaring, fugitives - in line with events in the asset events & provide supporting analysis. External regulatory compliance - Support the environment team with queries from regulator and audits. What you bring Bachelors Degree in Chemical Engineering/Process Engineering/ Environmental Engineering/Petroleum Engineering/Carbon Management. At least 4 years of experience in Carbon & Environment management, preferably in process monitoring or carbon/environment reporting. Advanced knowledge of equipment and emission sources within oil and gas facility Advanced knowledge of existing and emerging global air / water regulatory reporting requirements Champion in process simplification and digitalization utilizing toolsPower Apps, PI, SEEQ, SAP EC, PI process book, PI Vision, Aspen Hysys, Unisim Serves as team resource in monitoring GHG accounting protocols, protocol changes, and interpretations of GHG accounting rules. Optimizing internal procedures that ensure alignment to external standards and guidelines. Identifying, obtaining, and maintaining credentials as the sustainability industry evolves and to meet asset and company needs. What we offer You bring your skills and experience to Shell and in return you work with talented, committed people on one of the most important challenges facing our planet. Youll have the opportunity to develop the skills you need to grow in an environment where we value honesty, integrity, and respect for one another. Youll be able to balance your priorities as you become the best version of yourself. Progress as a person as we work on the energy transition together. Continuously grow the transferable skills you need to get ahead. Work at the forefront of technology, trends, and practices. Collaborate with experienced colleagues with unique expertise. Achieve your balance in a values-led culture that encourages you to be the best version of yourself. Join an organisation working to become one of the most diverse and inclusive in the world. We strongly encourage applicants of all genders, ages, ethnicities, cultures, abilities, sexual orientation, and life experiences to apply. Grow as you progress through diverse career opportunities in national and international teams. Gain access to a wide range of training and development programmes. - An Inclusive & Progressive Place to Work To power progress together, we need to attract and develop the brightest minds and make sure every voice is heard. Here are just some of the ways were nurturing an inclusive environment one where you can express your ideas, extend your skills, and reach your potential. Were creating a space where people with disabilities can excel through transparent recruitment process, workplace adjustments and ongoing support in their roles. Feel free to let us know about your circumstances when you apply, and well take it from there. Were closing the gender gap whether thats through action on equal pay or by enabling more women to reach senior roles in engineering and technology. Were striving to be a pioneer of an inclusive and diverse workplace, promoting equality for employees regardless of sexual orientation or gender identity. Shell in India Shell is a diversified energy company in India with 13,000 employees, and presence in Integrated Gas, Downstream, Power, Renewable and Upstream. Additionally, we have deep capabilities in R&D, digitalisation, and business operations. Our global strategy, Powering Progress, is designed to generate value for our shareholders, customers, and the wider society, and focuses on creating more value with less emissions. The strategy supports our purpose of providing more and cleaner energy solutions, with the aim of profitably transforming Shell into a net-zero emissions energy business by 2050. As India moves towards its target of net-zero emissions by 2070, Shell India aims to play a leading role in securing vital energy for today, while investing in, and helping to build, the energy system of the future through strategic investments in the country. Our Lubricants business serves over 50,000 consumers through a strong network of over 200 distributors, and operates an end-to-end value chain that spans conceptualization, development, and production at a world-class blending plant at Taloja. Through our 350-plus retail stations, we offer an integrated mobility experience including fuels, cafes, and convenience stores, with a prominent network of EV recharging facilities. Shell owns and operates a LNG re-gasification terminal at Hazira, Surat, with a capacity of 5 MTPA and a LNG truck-loading unit that plays a crucial role in helping meet Indias growing demand for gas across sectors. In 2022, Shell acquired Sprng Energy in a $1.55 billion deal to build an integrated energy transition business in the country. Sprng is a leading renewable energy company in India which develops and manages solar, wind, and hybrid power generation facilities and infrastructure. Our three capability centres across Bangalore and Chennai serve as a technology and innovation powerhouse for Shell globally, working as a delivery engine for core technical, digital, and finance processespioneering digital innovation and cutting-edge technologies across the energy sector. We also have strong academic partnerships and collaborations with leading universities and technology institutes to accelerate decarbonization efforts within the energy sector. We are committed to positively contributing to the communities in which we operate through programmes on STEM Education, Skilling, and Livelihood across India. We nurture and invest in startups developing initiatives focused on accelerating energy innovation through programs such as Shell E4 and Shell Eco-marathon. We also have strategic investments in new energy companies such as Husk Power, d.light, Orb Energy, and Cleantech Solar. DISCLAIMER: Please noteWe occasionally amend or withdraw Shell jobs and reserve the right to do so at any time, including prior to the advertised closing date. Before applying, you are advised to read our data protection policy. This policy describes the processing that may be associated with your personal data and informs you that your personal data may be transferred to Shell/Shell Group companies around the world. The Shell Group and its approved recruitment consultants will never ask you for a fee to process or consider your application for a career with Shell. Anyone who demands such a fee is not an authorised Shell representative and you are strongly advised to refuse any such demand. Shell is an Equal Opportunity Employer.

Urgent Hiring: Microbiologists (47 Years Experience) Are you a skilled Microbiologist with a passion for quality and precision? Join our growing team in Moga and contribute to excellence in the spice industry! Position: Microbiologist Qualification: B.Sc in Microbiology Experience: 4 to 7 Years Industry: Spices & Food Manufacturing Location: Moga, Punjab Salary: 22,000 28,000 (based on experience) We're looking for professionals who are detail-oriented, passionate about microbiological testing, and eager to grow in a fast-paced industry. Interested or know someone who fits? Send your resume at mansi.sharma@manpower.co.in

We are urgently looking to hire EIA Manager for Surat & Ahmedabad location. Role & responsibilities To interact with PPs and get project complete details. To fill up Forms/applications for required approvals based on project details. To defend project proposals for obtaining approvals for TOR/EC/Amendment/CRZ/Corrigendum. To organize base line data generation as per TOR through laboratory. To present proposals to EAC/SEAC/SEIAA To write and submit draft EIA reports and Executive Summary translated in local language to statutory bodies for projects needing public hearing. To organize and attend Public Hearing. Working exp. with GPCB or Pollution Control board To compile Public Hearing proceedings and prepare Final EIA report. To assist client in obtaining Consent to Establish CTE/CTO from concerned GPCB. Prepare detailed EIA report that clearly outline findings, impact assessments, mitigation strategies, and potential alternatives Stay updated on relevant environmental regulations, policies, and best practices to ensure compliance and quality in assessments Candidate must be FE or having QCI knowledge will be preferred Preferred candidate profile B.E /B.Tech (Environment Science / Engineering /Chemical), M.Sc/M.E/M. Tech (Environmental Science/Engineering) In-depth knowledge and expertise of environmental concerns, environmental regulations, laws, and pertinent amendments. Strong communication (Verbal & Written), Presentation skills. Competency in proposal preparation, negotiation and departmental budgeting and analysis. Analytical skills for comparative analysis (cost, competitor, technology) Interested candidate can apply by clicking apply icon or send CV on hr@en-vision.in / WhatsApp on 7016006676

Role & responsibilities: Lead, manage, track, and ensure the timely completion of Quality Management System (QMS)-related documents, Standard Operating Procedures (SOPs), and other departmental paperwork. Ensure the facility operates in full compliance with GMP requirements. Ensure compliance with EHS (Environmental Health & Safety) standards. Lead all aspects of facility operations, including cleanroom maintenance, equipment qualification, and environmental monitoring. Ensure all systems (HVAC, BMS, water systems, etc.) are functioning within validated parameters. Work closely with QA, Validation, and Engineering teams to support new installations, expansions, or requalification efforts. Direct engineering and maintenance teams in preventative and corrective maintenance strategies. Facilitate effective communication between departments to address and resolve facility-related issues promptly. Ensure safety, training, and development of facility staff. Manage contractors, vendors, and service providers involved in facility design, maintenance, and upgrades. Lead site readiness for inspections, audits, and periodic reviews of facility systems. Build and foster a strong GMP and quality culture across the site. Preferred candidate profile Bachelors or Masters degree in Science (Mechanical, Electrical, Chemical, Biomedical) or related technical field. Approx 10 years of experience in facility and engineering management within GMP biopharma or cell therapy facilities. Strong working knowledge of GMP cleanroom requirements, HVAC/BMS/EMS systems, and utility validation. Familiarity with cell and gene therapy/biologics/biopharma manufacturing infrastructure (closed systems, modular cleanrooms, etc.) is a strong plus. Experience managing large teams and multi-disciplinary projects in regulated environments. Hands-on experience with quality systems, including documentation, investigations, and CAPA management. Proficiency in regulatory inspection readiness and hosting (FDA, EMA, local authorities).

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Role & responsibilities Exp : 4 to 8 years (Environmental Monitoring, MLT, Media Preparation & QMS activities etc.,) Qualification : B.Sc (Microbiology/ Biotechnology /Biology), M.Sc (Microbiology/Biotechnology) Preferred candidate profile Responsible for sampling, testing and documentation of MLT samples of finished and stability samples. Responsible for Handling of Instruments like LAF/BOD incubators/Autoclave/colony counter /Microscope/pH meter /Air sampler and Vitek etc. Responsible for monitoring and review of daily printouts of instruments like incubators, Autoclaves, refrigerators, hot air ovens and deep freezers. Responsible for ensuring the destruction of used media plates/tubes, product plates/tubes, monitoring plates, GPT plates/tubes and IND plates/tubes. Responsible for ensuring the handling, calibration of Instruments like pH meter and top pan balance. Responsible for ensuring external calibration review of standard weights used in Microbiology laboratory. Responsible for ensuring the receipt, storage and handling of ATCC cultures/cryovials/bio balls. Responsible for Preparation of SOPs and ensure that complies in microbiology laboratory. Responsible for ensuring verification of instrument preventive maintenance schedules for incubators, autoclaves, LAFs, air samplers, hot air oven, refrigerator and deep freezer, Colony counter and Vitek. Responsible for MLT, BET Analysis & method validations, and other validation studies. Responsible for Perform and verify Environmental monitoring at sterile and non-sterile production blocks. Responsible for QMS activities OOS, OOL, Deviations and incidents. Responsible for Data integrity compliance. Responsible to follow and implement the applicable Environment Health and safety procedures, practices in the plant premises Perks and benefits As Per the company Norms

Job Summary: HSE Manager The HSE Manager at Bondada group will oversee all safety, health and environment standards and practices across the site, supporting the Head of Quality & Safety. This role ensures compliance with national and international safety regulations, particularly in high-risk manufacturing and EPC environments. The Safety Manager will conduct regular safety audits, and lead safety training programs. They will collaborate with site heads and department leads to integrate safety requirements into all operations, drive continuous improvement, and ensure the availability of health, welfare, emergency, and rehabilitation services. Additionally, the Safety Manager will liaise with statutory bodies, ensure timely submission of environmental reports, and maintain up-to-date regulatory approvals and licenses. Key Responsibilities: Develop, implement, and oversee safety standards and practices across the site, ensuring all safety protocols are followed. Conduct regular safety audits and assessments to identify potential hazards and recommend corrective actions. Ensure compliance with all national and international safety regulations, specifically in a high-risk manufacturing environment. Collaborate with site heads, program managers, and department leads to ensure safety requirements are integrated into all operations. Lead and manage safety training programs to ensure staff are aware of safety protocols, emergency procedures, and safe operational practices. Monitor and manage digital safety systems, ensuring their effective use and integration across all site operations. Contribute to organizational team efforts in developing strategies, policies, and plans. Monitor organizational performance to ensure EHS policy objectives are achieved. Implement Environment, Health and Safety systems and best practices Develop local EHS policies and ensure compliance with all approved company SOPs. Engage with plants and project sites management to identify areas for safety improvements. Ensure all near misses and incidents are reported and thoroughly investigated. Implement Corrective and Preventive Actions (CAPA) and share lessons learned. Ensure the availability of health, welfare, emergency, and rehabilitation services. Conduct EHS internal audits, mock drills, and facilitate external audits. Implement recommendations for improvements. Monitor and ensure all fire protection systems are always operational and ready. Liaison with Statutory Bodies (through approved consultants) e.g. Pollution Control Board, Fire Department, Atomic Regulatory Board and Other statutory bodies on Safety & Environment. Ensure timely submission of environmental monitoring reports to statutory authorities. Keep all regulatory approvals, agreements, and licenses up-to-date. Develop, conduct, and implement EHS due diligence, audit, and risk reporting. Ensure all site operations comply with local regulations and the policies/standards Conduct energy audits, monitor energy KPIs, and identify high-impact saving opportunities. Develop and monitor implementation of ISO 14001 and ISO 50001 Energy Management Systems. Qualifications Education Qualifications: Bachelor s degree in Safety Management, Occupational Health and Safety, Engineering, or a related field. 6 plus years of experience as a Safety Officer in manufacturing sites or EPC related industries.

-Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems. Job Description Major accountabilities: Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance -Support exception investigations -Review and approval of production, QC, and AS and T records -MBR review -Support OpEx improvement projects Qualified Person - Executes batch release in compliance with registration -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Key performance indicators: On-time and GMP-compliant release of dosage forms -No complaints about inspections by authorities in your own area of responsibility without these being noticed and communicated beforehand -Successfully support continuous improvement projects -Executes batch release in compliance with registration Minimum Requirements: Work Experience: Functional Breadth. QC/ QA in pharmaceutical ind./ biotech with environmental monitoring &. Collaborating across boundaries. cleanliness zones. Skills: Continuous Learning. Dealing With Ambiguity. Gmp Procedures. Qa (Quality Assurance). Quality Control (Qc) Testing. Quality Standards. Self Awareness. Technological Expertise. Technological Intelligence. Languages : English. Skills Desired Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence

We are hiring for multiple position in Microbiology Dept. Contact person Mr. Srinivasa M, those who are unable to attend the interview are requested to forward their resumes to email id: naveenkumarp@microlabs.in, jonesnaveenrajp@microlabs.in Candidates are requested to carry their copies of Resume, Mark Sheets, Experience Certificates, Latest salary certificate, pay slips of three months and one photographs. MICROBIOLOGY Dept: Position: Sr.Officer/ Executive / Sr. Executive ( Only for male candidates) Qualification: B.Sc/ M.Sc- Microbiology/ BioTech Experience: 2-8 years experience in Sterile Manufacturing facility. Job Profile: Microbiology Analytical Activities (MLT, BET, Stability), Environmental monitoring, QMS activities in sterile manufacturing facility.

Maintain the microbiology laboratory as per regulatory requirements. Planning and coordination with cross functional team for timely release of the RM,FP, Stability samples. Handling of microbiology related OOS/OOT, Deviation, Lab event. Prepare the response and closure of audit observations. Change control management for revision of SOP s, Validation protocol. Ensure the availability of resources of microbiology laboratory. Ensure the microbiologist certification program of all microbiologist. Implementation of new projects for cost saving, compliance enhancement , work simplification. Having technical knowledge of following major test MLT of OSD products and MLT validation. Disinfectant efficacy test ( Disinfectant Validation) Maintenance of microbial cultures Maintenance of Microbiological media, Growth promotion test. Autoclave validation LAF, Biosafety cabinet, Incubators, pass box validation. Objectionability assessment of identified inhouse isolates. ALCOA++ Good knowledge of various guidelines like ISO14644, HTM 2010, EU Annex 1, 4, WHO, USP chapter 60, 61, 62, 1115, 1116, 1072, 21 CFR regulations Part 210, 211 Environment monitoring program design, risk evaluation, Location selection, Alert and action limit establishment. Purified water system validation. Chemical and microbial analysis of water. 10. Audit experience for FDA, MHRA. ANVISA, TGA etc. 11. Handling of software following but not limited: SLIMS, Lonza Moda, Equisoft, Vitek 2 compact software, High air flow, ICDAS, Trackwise, EDAMS, LMS, e residue , Lab X software, TOC software 12. Hands on experience of major instruments like: Vitek 2 system, TOC analyser, Autoclave, Conductivity meter, Air sampler, Digital Microscope, LAF, Biosafety cabinet.