185 Environmental Monitoring Jobs - Page 2

Division Department Sub Department 1 Job Purpose Execute analysis of allocated samples and Produce reliable and reproducible results in order to ensure their compliance to the microbiological quality parameters and predefined specifications and standards. Key Accountabilities (1/6) Analyse and review samples based on work allocation to meet the service level agreement Analyse samples as per priority and work allocation Review the data as per respective specification, Microbiological Methods and results obtained Prepare, review and submit reports to Team leader within stipulated timelines in order to support individual sample release within stipulated timelines to achieve SLA Key Accountabilities (2/6) Report errors, abnormal observations, non-compliances related to procedures, equipment and instruments, and deliver results promptly to facilitate timely action and avoid delay in releases Initiate investigations and take necessary corrective and preventive actions Investigate incidence & lab error on priority basis so that batch release timely and issues are not recurring Key Accountabilities (3/6) Document entries, raw data and findings concomitantly in relevant test data sheets so as to facilitate the lab QA to review the reports and avoid missed entries Review reports as per cGMP & GDP for compliance to GLP Ensure no GMP / regulatory concern are raised by adhering to SOPs and following procedures Key Accountabilities (4/6) Evaluate & document Instrument / equipment break down and suggest mechanisms to avoid the same Maintain equipment and instruments optimally to ensure no incidences or non-compliances occur due to malfunctioning of equipment/ instruments Key Accountabilities (5/6) Key Accountabilities (6/6) Major Challenges Availability of Validation records of analysis samples becomes a challenge in cases where validation is performed on other sites. Material and resource availability becomes a challenge due to conflicting priorities between labs and coordination between analysts which makes it tough to fulfil SLA Key Interactions (1/2) Units for receiving specification, documents, protocols, area availability etc. (daily) QA/QC for product sample release (daily) Stores for procuring materials (need basis) Communicate if any observation find on the specification. Key Interactions (2/2) CQA for procuring pharmacopial guidelines (need basis) Dimensions (1/2) Review and release approximate 15 MLT reports on daily basis to achieve the SLA. Review and release approximately 15 sterility batches on weekly basis and 15 bio load samples. 50 Water Samples analysis and release 10 Technical Information Sheets for swap analysis 6 Autoclave & DHS Operation 200 locations released on daily basis for Environmental monitoring Dimensions (2/2) Key Decisions (1/2) Daily Media and Plates requirement (to Team Leader Microbiology) Key Decisions (2/2) Education Qualification M. Sc (Microbiology) Relevant Work Experience 1-5 years experience for analyst and 3-7 years for reviewer in Microbiology Good knowledge of Microbiology, skill to perform assigned task, communication in English

Role & responsibilities To follows cGLP and cGMP in the laboratory. To ensure good housekeeping and maintenance of cleaning record. To execute the microbiological activities and related documentation. To perform the sampling & testing of water (chemical and microbial analysis). To perform the environmental monitoring of the microbiology lab and production area and related documentation. To procure and maintain microbial cultures. To prepare and document disinfectants used for regular cleaning and sanitization of microbiology laboratory. To execute the testing or operating procedure as per current and approved SOPs. To calibrate the Instruments and equipment’s like pH meter, Conductivity meter, Balance etc. To co-ordinate with microbiologist in routine analysis. To Intimate and handle the change control, deviation, out of specification & out of trend. To perform the MLT of raw material, finished product, semi-finished product, stability samples, packing material samples or any other samples. To perform the analytical method validation of the product and related documentation. To perform the Bio Assay & preservative efficacy test and related documentation. To maintain and review the documents and log books which are used in routine analysis. To prepare and standardize volumetric solutions, reagents and indicators. To perform the work given by head microbiologist. To ensure the implementation and compliance with GMP aspects as trained on. To uphold the requirements of data integrity in all activities performed and monitored. To ensure compliance with integrity of data as trained on.

Job Title: Microbiologist Experience: 01 - 03 Years Salary: 2 3.5 LPA Location: Gallops Industrial Park 2, Vasna Chacharvadi, Ahmedabad Job Summary: We are seeking a skilled and detail-oriented Microbiologist with 1 to 3 years of experience to join our quality and laboratory team. The ideal candidate will be responsible for conducting microbiological testing, ensuring compliance with industry standards, and maintaining proper documentation as per regulatory norms. Key Responsibilities: Conduct microbiological analysis of raw materials, in-process samples, and finished products. Perform environmental monitoring and hygiene audits within the production facility. Identify and isolate microorganisms using various culture techniques and instruments. Maintain and calibrate microbiology lab equipment as per SOPs. Prepare and maintain accurate test reports and lab records. Ensure compliance with GMP, GLP, and safety protocols. Coordinate with Quality Assurance/Quality Control and production teams on microbiological issues. Participate in internal audits and assist in regulatory inspections. Ensure proper storage, handling, and disposal of microbial cultures and biohazard materials. Desired Candidate Profile: Bachelor’s or Master’s degree in Microbiology or related life sciences. 1 to 3 years of relevant industrial experience in a microbiology laboratory (pharma/food/cosmetics preferred). Work Location: Gallops Industrial Park 2, Vasna Chacharvadi, Ahmedabad

Required Qualifications & Skills: 1-3 years of experience in environmental monitoring, field sampling, or a related role. Ability to travel extensively for fieldwork and work in various environmental conditions. [lab.nagpur@gogreenmechanisms.com] Provident fund

Job Summary: Responsible for managing day-to-day operations of the calibration lab, maintaining documentation, ensuring compliance with ISO/IEC 17025 and regulatory requirements, and overseeing calibration activities for thermal and biomedical devices. Acts as the coordinator equipment traceability, and calibration data management. Key Responsibilities: Maintain and control all calibration-related documents such as SOPs, calibration procedures, master equipment records, and logbooks. Review calibration results and ensure correctness before issuing certificates. Monitor the validity and performance of master equipment and arrange for their periodic calibration. Maintain equipment history cards and calibration status labelling Ensure compliance with ISO/IEC 17025, ISO 13485, and NABL documentation requirements. Manage environmental monitoring records (temperature, humidity) for thermal calibration setups. Qualifications and Skills: Experience in NABL Lab [Calibration discipline- Medical devices, Thermal etc, QA Testing]. Understanding ISO/IEC 17025. Preferably a person with thermal training certificate. Minimum 2-3 years of experience in calibration lab with exposure to medical and thermal disciplines. Document Control & Record Keeping, Verifying the calibration & QA report, Excel techniques etc. No. of positions: 1

Responsibilities: performing routine testing of raw materials, in-process materials, and finished goods, maintaining and calibrating laboratory equipment, documenting and reporting test results accurately Health insurance Provident fund Annual bonus

The job requires immediate joining and is specifically looking for female candidates. The location of the job is Ambegaon, Pune. The ideal candidate should have a qualification in Environmental, Chemical, or Civil engineering. As part of the job responsibilities, you will be required to understand customer requirements and prepare quotations for ETP, STP, RO, DM, etc. You should also have knowledge of Environmental monitoring and consent. Timely updates on orders forecast, target opportunity projects, and other marketing activities will be expected. You will attend Technical and Commercial clarification meetings with clients, generate leads, and coordinate with clients. Additionally, you will be responsible for tender filling, documentation work, and following up on submitted quotations. The candidate should have a minimum of 1 to 2 years of experience in a similar field. The job is full-time and follows a morning shift schedule. Yearly bonus is included in the benefits package. The ability to commute or relocate to Pune, Maharashtra (postal code: 411046) is required. Cell phone reimbursement is one of the benefits provided. The application deadline is 30/06/2025, and the expected start date is 01/07/2025.,

Eurofins is a leading provider of assurance and inspection services, covering a broad spectrum of sustainable supply chain practices, including the circular economy. Eurofins helps the customers to identify and mitigate risks in their supply chain and to ensure the benchmarking performance with operations, processes, systems, people, or capabilities. We hold accreditations for various industry standards and memberships, ensuring comprehensive service throughout the supply chain. Whether you are in the food, consumer products, healthcare, or cosmetics industries, we offer a full range of services including product inspection, auditing, certification, training, and consultation. Eurofins Assurance helps you mitigate compliance risks, enhance quality, and prevent safety failures early on, safeguarding your business from brand damage, product recalls, and other potential issues in the future. Sustain your business growth and commitment with Eurofins Assurance, a global network of assurance experts that you can trust. Manage accreditation activities. Oversee certification operations. Handle unannounced, semi-announced, and additional audits. Support the Coordinator for reviewing and accepting applications. Maintain auditor qualifications and plan related activities for all schemes. Provide technical support to the team. Address technical queries from clients. Compile scheme updates for clients. Act as the product owner of IT tools for operation management. Verify and submit all scheme data internally and externally (scheme owner and accreditation body). Ensure readiness and updates for dTrackit, eTrackit, GTB, and the BCI portal. Investigate complaints. Conduct technical reviews of audit reports and documentation. Make certification decisions. Conduct calibration, harmonization, and technical training sessions. Manage accreditation activities. Oversee certification operations. Handle unannounced, semi-announced, and additional audits. Support the Coordinator for reviewing and accepting applications. Maintain auditor qualifications and plan related activities for all schemes. Provide technical support to the team. Address technical queries from clients. Compile scheme updates for clients. Act as the product owner of IT tools for operation management. Verify and submit all scheme data internally and externally (scheme owner and accreditation body). Ensure readiness and updates for dTrackit, eTrackit, GTB, and the BCI portal. Investigate complaints. Conduct technical reviews of audit reports and documentation. Make certification decisions. Conduct calibration, harmonization, and technical training sessions. Qualifications Bachelor's Degree in Textile Engineering from a reputed institute (preference for Postgraduates). 12 years of professional experience in a technical capacity in the textile industry, with at least 6 years in a certification body. ISO 9001 Lead Auditor Training Course. ISO 14001 Lead Auditor Training Course. SA 8000 Auditor Training Course. High level of proficiency with standards, related documents, interpretations, and the latest updates. Detailed knowledge of norm requirements for GOTS, GRS, RCS, OCS, MMS, Better Cotton. Knowledge of production methods and processes applicable to textile, plastic, paper, leather, and metal industries. Ability to produce clear, accurate, and complete written audit reports and technical review reports. Experience conducting shadow audits for auditors. Bachelor's Degree in Textile Engineering from a reputed institute (preference for Postgraduates). 12 years of professional experience in a technical capacity in the textile industry, with at least 6 years in a certification body. ISO 9001 Lead Auditor Training Course. ISO 14001 Lead Auditor Training Course. SA 8000 Auditor Training Course. High level of proficiency with standards, related documents, interpretations, and the latest updates. Detailed knowledge of norm requirements for GOTS, GRS, RCS, OCS, MMS, Better Cotton. Knowledge of production methods and processes applicable to textile, plastic, paper, leather, and metal industries. Ability to produce clear, accurate, and complete written audit reports and technical review reports. Experience conducting shadow audits for auditors. Additional Information Impeccable proficiency in both written and spoken English. Knowledge of a foreign language is an added advantage. Highly organized with the ability to plan and prioritize work. Efficient time management. Working knowledge of Microsoft Office tools (Word, Excel, PowerPoint, SharePoint, Teams). Experience with IT tools used in certification or accreditation bodies.

1.Preparation of dilute disinfectants and ensure microbiology area cleaning. 2.Temperature, Relative humidity (RH) and Differential pressure (DP) monitoring in Microbiology Laboratory. 3.Sampling of water as per the schedule. 4.Execution of environmental monitoring activities in the microbiology laboratory and manufacturing facility as per the schedule. 5.Receipt, storage and Preparation of Microbiological media followed by growth promotion testing. 6.Gowning qualification of Personnel Involved in Aseptic Operations.

Sterilization and preparation of media, Media growth promotion test, Media fill validations. Analysis of Pathogenesis test, MET, Environmental monitoring. Hands on experience in Analyzing of ELISA techniques like Binding ELISAs, Impurity based Assays HCP, LPA. Analysis of electrophoresis methods such as SDS-PAGE, IEF. Analysis of In-Process, DS, DP and Stability samples. Exractable volume of final DP sample. Aliquoting of batch release, stability samples. Withdrawing of stability samples as per the protocol. Receiving, storage and Physical verification of Reserve samples

1. Receipt, storage and usage of medias, Microbial cultures, materials and documentation 2. Perform viable / non-viable monitoring activities, media plates observations and documentation in testing facilities. 3. Environmental monitoring, sampling, receipt, testing and documentation of all Microbiology samples. 4. Perform cleaning, fumigation and other activities in Microbiology laboratory. 5. Monitoring of temperature, DP and RH of the Microbiology laboratory. 6. Preparation of dilute disinfectants, reagents solutions / indicator solutions. 7. Responsible for compliance to cGLP. 8. Operation and usage of instruments. 9. Execution of method validations / method verification samples. 10. Receipt / testing of validation samples from manufacturing / other areas 11. Training and qualification of analysts in Microbiology department. 12. Responsible for handling of Bio-waste in Microbiology department. 13. Review, checking and verification Microbiology laboratory documents. 14. Responsible for implementation activities related to resource manager and sample manager of Laboratory information management System #40;LIMS#41;

1. Environmental monitoring in manufacturing facilities, Warehouse facilities, Microbiology laboratory and Bioassay area. 2. Instruments calibrations, validation / revalidation, operation and usage. 3. Preparation and sterilization of microbiological media, reagents and materials 4. Sampling and analysis of compressed gases and Drain monitoring in manufacturing facilities. 5. Documentation of the media consumption records and review of outside COAs. 6. Preparation of disinfectants and Swab analysis. 7. Involve in the execution of Media fill validations. 8. Performing area qualification and requalification of Manufacturing facilities, Warehouse facilities, Microbiology laboratory and Bioassay area. 9. Performing gowning qualification and requalification of Manufacturing facilities and Microbiology laboratory. 10. Performing environmental monitoring and nonviable particle count of manufacturing facilities, Warehouse facilities, Microbiology laboratory and Bioassay area. 11. Responsible for compliance to cGLP.

1. Receipt, storage and usage of medias, Microbial cultures, materials and documentation 2. Perform viable / non-viable monitoring activities, media plates observations and documentation in testing facilities. 3. Environmental monitoring, sampling, receipt, testing and documentation of all Microbiology samples. 4. Perform cleaning, fumigation and other activities in Microbiology laboratory. 5. Monitoring of temperature, DP and RH of the Microbiology laboratory. 6. Preparation of dilute disinfectants, reagents solutions / indicator solutions. 7. Responsible for compliance to cGLP. 8. Operation and usage of instruments. 9. Execution of method validations / method verification samples. 10. Receipt / testing of validation samples from manufacturing / other areas 11. Training and qualification of analysts in Microbiology department. 12. Responsible for handling of Bio-waste in Microbiology department. 13. Review, checking and verification Microbiology laboratory documents. 14. Responsible for implementation activities related to resource manager and sample manager of Laboratory information management System #40;LIMS#41;

Industry Type: IT Services & Consulting Department: Environment, Health & Safety (EHS) Employment Type: Full Time, Permanent Role Category: Occupational Health & Safety Your New Role: Challenging and Future-Oriented As a Chief Safety Officer at the Grid Transmission (Large Transmission Systems) Factory in Goa, you will play a critical role in ensuring the implementation of EHS (Environment, Health & Safety) management systems and legal compliance. This role is integral to building a Zero Harm Culture within the factory and project sites, supporting factory operations, contractors, and customers. Key Responsibilities Assist management in fulfilling legal EHS requirements and implementing the EHS management system. Support factory operations, contractors, and customer teams to foster a Zero Harm Culture and ensure compliance at project sites. Lead EHS planning with process owners for various operational activities. Inspect tools, equipment, and safety processes; ensure alignment with EHS guidelines. Prepare and periodically review: Risk assessments Method statements Training plans CAPA (Corrective and Preventive Actions) Oversee contractor EHS management: Support SCM and factory teams in contractor qualification, performance evaluation, and improvement planning. Mentor contractors and customers on safety practices. Conduct EHS training for employees and contractors. Support the Factory Manager in meeting: Goa Factory Rules GPCB (Gujarat Pollution Control Board) requirements EHS objectives, targets, and management programs Lead incident reporting, investigation, and compliance tracking. Compile and communicate EHS MIS reports as scheduled. Conduct internal audits and risk assessments in line with the audit plan. Recommend safety-related resources and solutions. Serve as the interface with internal and external stakeholders concerning EHS matters. Professional Competencies & Qualifications Mandatory: Diploma/Advanced Diploma in Industrial Safety or B.Tech/M.Tech in Safety At least 2 years of experience as an independent Factory EHS In-Charge Solid experience in: Contractor safety management Factory expansion/construction oversight Environmental protection initiatives Maintenance-related EHS compliance MIS preparation and presentations Desirable: NEBOSH IGC certification (added advantage) Certification from Chief Inspector of Factories and Boilers Degree/Diploma in Engineering or Science Graduate

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview We are seeking a highly skilled Cost Modeling Analyst to join the Digital Data Networks Business Unit at TE Connectivity India Pvt. Ltd. In this role, you will be responsible for developing and maintaining robust cost models that support new product development and drive cost improvement initiatives. The ideal candidate will have a strong background in should-cost modeling, data analytics, and manufacturing cost estimation, with hands-on experience in key connector industry processes such as stamping, plating, molding, and assembly. Required Skill & Responsibilities Required Skills : B.Tech in Mechanical, Electrical, or Electronics Engineering. 812 years of experience in cost modeling and analysis, preferably in the connectors or electronics manufacturing industry Proficiency in costing software (aPriori, TcPCM, Excel) Strong understanding of manufacturing processesstamping, molding, plating, and assembly. Solid foundation in cost estimation methodologies, data analytics, and reporting. Excellent analytical thinking, problem-solving, and communication skills.Proven ability to work in a collaborative, cross-functional environment . Cost Modeling Development: Develop and maintain should-cost models for connector and cable products using tools such as aPriori, TcPCM, and Excel. Build cost structures that include direct materials, labor, overhead, and other relevant cost components. Support design-to-cost and value engineering initiatives by providing cost insights during product development. Data Analysis and Validation: Analyze BOMs, supplier quotations, purchase history, and manufacturing process data to derive accurate cost estimates. Validate cost model assumptions through back testing, sensitivity analysis, and expert reviews. Ensure data integrity and consistency across cost modeling tools and reports. Cost Optimization and Collaboration: Identify cost drivers and recommend opportunities for cost reduction and efficiency improvements. Collaborate with engineering, procurement, finance, and operations teams to align cost models with business goals. Provide actionable insights to optimize product design and manufacturing processes. Reporting and Communication: Prepare and present cost analysis reports to stakeholders, highlighting key trends, risks, and recommendations. Communicate complex cost modeling concepts to non-financial audiences in a clear and actionable manner. Competencies

JOB DESCRIPTION Job Title: Lead - Tech support (LIMS/ELN-QCM) 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 Core Purpose of the Role : Static data creator/ reviewer for LIMS Validation of LIMS and ELN sheet Thorough knowledge on LIMS development, validation and GMP modules Knowledge on guidelines requirement for microbial analysis Ensure Microbial Method Validation, Method verifications Planning Microbiology analysis (Bioburden, MLT, Test for specified organisms, BET analysis) Sterility testing and validation Calibrations, Qualifications in Microbiology lab Handling QMS in Microbiology lab Role Accountabilities Documents preparation/review/validation for LIMS and ELN for microbiology Facing regulatory and client audits, ensuring audit compliance Leading team for Microbial analysis section Ensuring Microbiology lab maintenance Media and culture qualifications data review and planning Responsible for Ensuring Microbiological analysis, Sterility testing, Bacterial Endotoxin Test and analysis of different grades of water (PW/WFI/POW) as per the respective specification. Responsible for risk assessment documents preparations, Protocol and reports preparation Responsible for QMS related to microbiology - change controls, CAPA, deviations, incidents, OOS/OOT investigations Responsible for Area qualification, calibrations, equipment qualifications and requalification Responsible for sample management and coordination with team for smooth operation of samples release activity. Responsible to perform the Method verification activity for Sterility, BET, MLT and Bioburden test. Responsible for review of microbiology documents Responsible for review of specifications and STP. Responsible for review of protocols and reports Preparation and planning of sampling schedule Interaction with clients Ready to work in shifts and supervising the shift analyst activities Follow the required EHSS policies and Good hygiene practice. Undertake other responsibilities related to Microbiology as per requirement. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Accountabilities as a Syngene Leader 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. 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. Specific requirements for this role Experience : Demonstrated Capability : Education : Experience : 9-10 yrs YEARS Skills and Capabilities Microbial analysis of water, OSD products, Injectable products, Environmental monitoring 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 Education : M. Sc. Microbiology Equal Opportunity Employer .

JOB DESCRIPTION Job Title: QC Microbiology Reviewer 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 Core Purpose of the Role : Static data creator/ reviewer for LIMS Facing regulatory and client audits, ensuring audit compliance Microbial Method Validation, Method verifications Microbiology analysis (Bioburden, MLT, Test for specified organisms, BET analysis) Sterility testing and validation Environmental/Utility Monitoring data review Microbiology lab maintenance Calibrations, Qualifications Review of Microbiology data Media and culture qualifications data review and planning Handling QMS in Microbiology lab Role Accountabilities Responsible for Microbiological analysis, Sterility testing, Bacterial Endotoxin Test and analysis of different grades of water (PW/WFI/POW) as per the respective specification. Responsible for risk assessment documents preparations, Protocol and reports preparation Responsible for QMS related to microbiology - change controls, CAPA, deviations, incidents, OOS/OOT investigations Responsible for Area qualification, calibrations, equipment qualifications and requalification 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 Sterility, BET, MLT and Bioburden test. Responsible for ensuring environmental monitoring of clean rooms in Microbiology laboratory. Responsible for review of microbiology documents Responsible for preparation of specifications and STP. Responsible for preparation of protocols and reports Audit trail review Preparation and planning of sampling schedule Interaction with clients Ready to work in shifts and supervising the shift analyst activities Well versed with LIMS and electronic documents execution and review. Follow the required EHSS policies and Good hygiene practice. Undertake other responsibilities related to Microbiology as per requirement. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism 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. 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. Specific requirements for this role Experience : Demonstrated Capability : Education : Experience : 9-10 yrs YEARS Skills and Capabilities Microbial analysis of water, OSD products, Injectable products, Environmental monitoring 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 Education : M. Sc. Microbiology Equal Opportunity Employer .

Role & responsibilities 1. Responsible for Daily sampling and analysis of in-process and water samples as per procedure. 2. Responsible For Preparation and pouring of media plate. 3. To perform BET (Bacterial Endotoxin Test) test and Microassay. 4. To perform Sterility Test, Bioburden and MLT (Microbial Limit Test) or water and product. 5. To Perform Growth Promotion / Inhibitory / Indicative Property Test Of Media. 6. To report results of analysis in raw data sheet issued. 7. Entry and maintain all micro related logbooks. 8. To Follow the QMS (Quality Management System) system (Out of Specification, Deviation, Incident) 9. To participates in validation activity. 10. Observation and review of media fill container. 11. To perform environmental monitoring in clean room as per standard operating procedure. 12. To run the autoclave cycles and unload the loads as per SOP (Standard operation procedure). 13. To monitor incubator condition daily and record, to take print out and verify. 14. To maintain the GLP (Good laboratory practices) and follow GDP (Good documentation practices) in the laboratory. 15. To run washing and drying machine. 16. To raise Out of Specification if noticed. 17. Responsible to perform analysis of Analytical method Validation, Analytical method Transfer, reconstitute Solution stability, additional analytical test required as per party quarry reply. 18. Responsible for preparation Analytical method validation protocol, raw data, report. 19. Responsible for review of Analytical method validation protocol, raw data, report. 20. Responsible for preparation excel sheet preparation of analytical method validation, method transfer, Reconstitute Solution Stability study. 21. Responsible for planning of method validation activity. Requirement of sample, standard, reference standard, column, instrument provide to the analyst. 22. Responsible for training providing to the analyst for analytical method validation and method transfer SOPs (Standard operating procedures). 23. Responsible to control and maintain records like protocols, raw data, and report of method validation, method transfer and reconstitute solution stability. Analysis records, usage log books and status labels during day to day Analysis of validation. 24. Any other Responsibility assigned by HOD (Head of Department). 25. To assist HOD (Head of Department) for the preparation of regulatory inspection. Preferred candidate profile Candidate Should be From Pharma Background Good Verbal and Written Communication Willing to Relocate in Navsari , Gujarat Willing to Work in a Shift

Role & responsibilities 1 Assist F&E Section, HO during processing of Forest clearance for the following activities: Authentication of land schedule as on 25.10.1980 from Forest, Mining and Revenue official, DGPS map and other maps enclosed in Forest diversion proposal from Forest, Mining and Revenue officials. Persuasion at office of Collector, BDO and Panchayat office to conduct Gram Sabha and co-ordinate during Gram Sabha till obtaining of Certificate under FRA, 2006. Authentication of Enumeration report by Range officer and forwarded to DFO. Pursuance of Forest Diversion proposal at DFO and RCCF level during the processing of proposal, to get the different demand under Stage-I FC and recommendation of Stage-I FC compliance from DFO Level upto PCCF (N) level through RCCF. Pursuance at DFO Office, Tahasil Office, Sub-collector office and Collector office to complete the process of allotment & mutation. Recommendation of different schemes under Stage-I FC from DFO and persuasion at RCCF level for approval of schemes under Stage-I FC. 2 FC Compliance after grant of Stage-II for the following activities: Co-ordination of tripartite meeting between Forest, OMC and OFDC officials to initiate tree felling work. Follow up with Follow up Forest and OFDC officials to complete the tree felling work and get the working permission. 3 Assist F&E Section, HO during processing of Environmental Clearance (EC) for the following activities: Authentication of production since inception of mines by Mining Officer or DDM. Authentication of flora & fauna by concerned DFO. Co-ordinate with RO, OSPCB and ADM to conduct Public Hearing till finalization of pH proceedings. 4 During processing of Consent to Establish (CTE), Consent to Operate (CTO), Hazardous Waste Authorization (HWA), Biomedical Waste Authorization (BMWA), NOC Ground Water, Surface Water Permission (SWP). Co-ordinate during site inspection by RO, OSPCB. Presentation before OSPCB during processing of CTE/CTO. Pursuance with OSPCB till the grant of CTE/CTO/HWA/BMWA. Co-ordinate during site inspection by CGWB/CGWA for grant of NOC-GW 5 Vigilant monitoring of conditions stipulated in various statutory approvals. Verify the status of compliance once in a week. Communicate the compliance to Mines Manager. To design corrective & Preventive action (CAPA) with proper justification for the non-compliances observed by Jr. Professional (SPOC-F&E) for further processing of work order either at RM Level or HO. Verification of returns and reports. 6 Miscellaneous work To attend following meetings/Programmes at HO/RO/Mines site: IMS audit, Internal Audit, SDF work, Annual Safety week, MEMC week, EMC meeting, Regional review meeting, Weekly VC, World Environment Day, Vanmahotsava, National Pollution Prevention Day. Organize various trainings & Environment Awareness programs for various categories (skilled/unskilled). Co-ordinate Site inspection by Statutory Authorities for periodical compliance monitoring. Liasoning with Forest officials as and when required. Supervise the work assigned to SPOC F&E and ensure smooth implementation of compliance monitoring for all the projects under the concerned Region. Preferred candidate profile Academics Experience B.Tech, Env. Engineering/ * MSc. Env. Science/M.Sc in Forestry/M.Sc in Wild Life Science 3 years plus experience in Compliance Monitoring (F & E matters) * Only in case of non-availability of B.Tech. in Env. Engineering MSc. Env. Science/M.Sc in Forestry/M.Sc in Wild Life Science qualification to be considered.

Intersted candidates can send their CVs on career@scott-edil.com or can contact on 9805091898 We are seeking a dynamic and experienced Micro QC- Offcer/ Sr. Offcer/ Executive /Sr. Executive to join our Quality Control team. The ideal candidate will have 2 to 6 years of hands-on experience in microbiological quality control, with strong exposure to both Oral Solid Dosage (OSD) and Injectable formulations. The candidate must have practical knowledge of Environmental Monitoring (EM) and a solid understanding of GMP/GLP practices in a regulated manufacturing environment. Role & responsibilities Preferred candidate profile Perform routine microbiological testing of raw materials, finished products, and in-process samples. Conduct Environmental Monitoring (EM) in cleanrooms, including air sampling, surface sampling, and personnel monitoring. Handle microbial limit testing, sterility testing, BET, and water analysis. Manage and review microbiological documentation and records as per regulatory guidelines. Support validation activities for cleanroom qualification and water systems. Investigate and document any non-conformances or deviations. Coordinate with cross-functional teams including production, QA, and engineering for EM-related observations and improvements. Ensure compliance with cGMP, regulatory standards, and company SOPs.

We are looking for a Sales Engineer with 3+ 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.

Job Title: QC Microbiology Reviewer Location: Bangalore, KA, IN, 560099 Syngene is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is a top priority and is embedded in every aspect of our work. We emphasize safety guidelines, procedures, and SOPs to ensure a safe working environment for all. As a QC Microbiology Reviewer at Syngene, your core responsibilities include conducting microbiological analysis, sterility testing, bacterial endotoxin tests, and analysis of different grades of water according to specifications. You will be involved in preparing risk assessment documents, protocols, and reports, as well as managing QMS related to microbiology. Additionally, you will oversee area qualifications, calibrations, equipment qualifications, and sample management activities. Key Responsibilities: - Conduct microbiological analysis, sterility testing, and various microbiology tests - Prepare risk assessment documents, protocols, and reports - Manage QMS related to microbiology including change controls, CAPA, deviations, incidents, and investigations - Coordinate sample management activities for smooth operation - Perform environmental monitoring of clean rooms in the microbiology laboratory - Review microbiology documents and prepare specifications and STPs - Plan and execute sampling schedules - Interact with clients and supervise shift analyst activities - Ensure compliance with EHSS policies and good hygiene practices - Demonstrate a commitment to excellence, integrity, and professionalism Requirements: - Experience: 9-10 years - Education: M.Sc. Microbiology - Skills: Proficiency in microbial analysis, strong dedication, excellent communication skills, attention to detail, ability to work in a dynamic environment, meet deadlines, and collaborate in a team setting Syngene values excellence, integrity, and professionalism in all employees. As a leader, you will champion effective EHSS practices, promote a culture of safety and sustainability, and prioritize people management and talent retention. Syngene is an equal opportunity employer, providing a supportive and inclusive work environment for all employees. Join us in our commitment to innovation, safety, and scientific excellence.,

You will be responsible for ensuring line clearance for the start-up of the tablet section, including compression, coating, and capsule filling sections. Additionally, you will be in charge of filling logbooks for the Tablet section, manufacturing area, and grinding section. Your duties will also include in-process sampling of tablets and final sampling of tablets. You will be required to conduct online reviews of BPR for Tablet, Capsule, and Jawkut sections. Monitoring environmental conditions in the respective operational areas is a key part of the role. Issuing tablet excipients and empty capsules and checking online parameters of Tablet and Capsule are also among your responsibilities. This is a full-time, permanent position with benefits such as internet reimbursement, leave encashment, and paid sick time. The work schedule is during the morning shift. A background in pharmaceuticals or herbal medicine is preferred for this role. A Bachelor's degree is preferred for this position. The work location is in person.,

Rama Super Speciality Hospital is looking for CSSD Technician - Noida to join our dynamic team and embark on a rewarding career journeyOperating and maintaining sterilization equipment.Cleaning, inspecting, and assembling surgical instruments and equipment.Ensuring that all instruments and equipment are properly sterilized and packaged for use.Managing inventory and restocking supplies as needed.Maintaining accurate records and documentation of all sterilization procedures and equipment maintenance.Adhering to infection control policies and procedures to prevent the spread of infection.Collaborating with other departments, such as surgery and nursing, to ensure the timely delivery of sterilized equipment and instruments.

JD Of Microbiologist Job Title: Microbiologist Experience 3-5 years Location: Kala Amb Job Summary: We are seeking a motivated Microbiologist with xperience to conduct microbiological testing, analyze results, and support laboratory operations. The ideal candidate will have hands-on experience in microbial culture techniques, sterility testing, and environmental monitoring. Key Responsibilities: Perform microbiological testing on raw materials, in-process samples, and finished products Conduct environmental monitoring and sterility assurance Isolate and identify microorganisms using standard microbiological methods Maintain accurate laboratory records and ensure compliance