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.

Role & responsibilities 01 Quality Control Functions: 1.1 To ensure that the laboratory carrying out its testing, calibration, validation and all other technical activities in such a way to meet GLP requirements. 1.2 To carry out all technical activities and implementation of documented quality system. 1.3 To plan, schedule and monitor analysis of Raw Materials, Premix, Packing Materials, In-process materials, Finished products, Microbiological analysis, Water analysis and ensure that they meet defined relevant quality standards. 1.4 Periodically review logbooks, reports and test protocols related to Raw Materials, Premix, Packing Materials, Microbiological analysis, In-process and Finished products for proper entries, accuracy and completeness and ensure that they meet defined relevant quality standards. 1.5 To handle Quality management events according to SOP and complete its documentation with corrective and preventive actions. 1.6 To ensure that updated Specifications, Standard Testing Procedure, Test protocol and documents are available for use. 1.7 To review the resources of Manpower, Instruments, Equipment, Material and advise Management on the provision with justification. 1.8 To train the personnel in the department regarding Chemical Testing, Instrument qualification & current regulatory guidelines. 1.9 To establish effective communication systems with other departments including Commercial departments to achieve effective and efficient service from Quality Control Department. 1.10 To ensure implementation of cGMP in laboratory. 1.11 To ensure Qualification, Annual Maintenance and Calibration of QC instruments. 1.12 To ensure Management of Standards, Chemicals, Reagents and Glasswares. 1.13 To Review and approval of new or revised SOPs. 1.14 To handle instrument troubleshooting and interact with service Engineer in case of instrument breakdown. 1.15 To ensure compliance of Laboratory safety practices and firefighting devices. 2.0 General function 2.1 To provide compliance of Audit observations. 2.2 To take adequate measures to ensure updating of information and knowledge of the key people in the Quality control. 2.3 To provide support to planning, production, finish product for timely release of the goods for dispatch. 2.4 To monitor the microbiological analysis and ensure that all testing is carried out. 2.5 To create SOP awareness by continuous training. 2.6 To ensure good housekeeping of laboratory and up-keep of laboratory. 2.7 Self-updation of current regulatory guidelines. 2.8 Self inspection of other departments, as and when scheduled. . 2.9 Take necessary measures to prevent accident/incident and help in accident/incident Investigation. 3.0 Adherence and compliance to cGMP requirements. 3.1 Undertaking any other work, either for this department or any other department which the organization, which may be requested by the Plant Manager, for which training and/or an explanation has been provided and understood.

Prasad Group of Institutions is looking for Laboratory instructor to join our dynamic team and embark on a rewarding career journey Guide students in performing lab experiments Ensure lab safety and proper equipment use Evaluate student performance and provide feedback Maintain laboratory inventory and records

Long Description Execution of production batches in the Upstream process area as per approved BPR and timely documentation of the same. Operating of Upstream equipment for process and CIP/SIP as per SOP e. g. 100 L fermenter, Centrifuge, High Pressure homogenizer, spectrophotometer, Autoclave, DHS, Cold room, Integrity Machine etc. Preparation of process and equipment related SOPs. Raising change control and deviations in the QA approved format and working with concern departments for closure of the same. Timely instructions to engineering team in case of facility or equipment breakdown. Coordination for PM/AMC of manufacturing equipment. To Assist in Technology transfer from R&D to Manufacturing To attend on Job, cGMP and Safety trainings To ensure safety at workplace Competencies Strategic Agility Process Excellence Collaboration Innovation & Creativity Result Orientation Stakeholder Management Customer Centricity Developing Talent Education Masters in Biotechnology or Microbiology Post Graduation Work Experience 0 to 5 years of relevant experience in Fermentation/Biosimilar fermentation.

Job Title: QC Analyst I At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world s most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we re working at the pace of change on diagnostic tools that address the world s biggest health challenges, driven by knowing that behind every test there is a patient waiting. Learn about the Danaher Business System which makes everything possible. This position is part of the Quality Organization and will be in India. Reporting directly to the Quality Control lead or site lead, the Quality Control Analyst is responsible for managing the day today activities quality control function at Cepheid India Private Ltd. Ensure compliance of quality control procedures as per MDR 2017, European regulations, ISO 13485, Cepheid corporate quality system requirements. In this role, you will have the opportunity to: Conducts routine and non-routine analysis of raw materials, in-process and finished formulations under supervision and according to Standard Operating Procedures (SOPs). Competent technical staff for supervision the Testing/ analysis of diagnostic reagents & kits. Perform inspections of incoming, in-process and finished products. Performs and calibration and maintenance of lab equipment as per requirements. May perform special projects on analytical and instrument problem solving. Ensure that lab cleanliness and safety standards are maintained. Qualify test methods as part of new product development activities. Serve as a technical liaison between quality control and other departments Write technical reports or documentation such as deviation reports, testing protocols, and trend analyses & Write or revise standard quality control operating procedures. Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines. Follow documentation procedure (filling out Data History Records (DHRs), reading and understanding instructions from Work Release (WR), Planned Deviation Report (PDR) or Non-Conformance Report (NCR). Read and follow Standard Operating Procedures (SOPs) and Manufacturing Work Instructions. Review records and documents for completeness and compliance with company policies and procedures. Support for internal audit schedule, NC, CAPA for site. Review production batch records, QC test results and release product. Education and Experience: Master s degree in Biochemistry, Molecular Biology, Microbiology or related discipline and a minimum of 3+ years related Quality Control experience. 2+ years experience with in Vitro Diagnostics (IVD) is mandate Experience with in Vitro Diagnostics (IVD) is very beneficial and highly desirable Quality competent technical person approved as per D&C act if any Knowledge and skills: Hands on Experience on IVD product testing. Working Knowledge of current GxP regulations for Invitro Medical Devices and ISO 13485 QMS. Must be flexible to work off-shifts and weekends as per production Schedule. Schedule orientated (able to consistently maintains schedules and meet timelines) Strong interpersonal skills, Effective organization and Communication skills are essential. Good skills in English language Knowledge of Microsoft Word and Excel Strong multi-tasking and attention to details skills. It would be a plus if you also possess previous experience in: Experience working with medical device quality systems in compliance with MDR and ISO 13485 Able to interpret quality problem and establish practical solutions within a dynamic business environment. Experience in leading continuous improvement efforts, in both quality systems and products. Knowledge of the process of establishing facility QMS certifications. Cross functional experience with products and manufacturing processes to influence change at all levels within the organization Visio and Project knowledge desirable. When you join us, you ll also be joining Danaher s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here . We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. . Together, we ll accelerate the real-life impact of tomorrow s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

About the role: Communicates in a clear, open, active and honest manner (verbal and written) and seeks understanding of other views Actively contributes to the success of the team and collaborates to create results Builds good personal and professional relationships Is creative and takes initiatives Recognizes the need for and adapts well to change Able to have independent communication with customers professional staff Shows understanding of both customers needs and able to explain rational of decisions Cares for customer and provide solutions that improve their business. Proactively seeks to identify real customer needs and manage customer expectations accordingly Demonstrates proactive approach towards market and sales activities Receives positive feedback from customers and acts on feedback Able to reach and communicate decisions even under stressful situations Able to contribute actively with market intelligence Plans and executes work with required quality and within agreed schedule and budget Delivers according to DNV methodology Demonstrates continuous improvement Can work as PM for smaller projects based on clearly defined framework. Executes such projects according to relevant processes and procedures. Takes responsibility for own competence and career development Understands and follows relevant DNV systems, tools, work processes and methodology Demonstrates the ability to apply knowledge and skills in the work Shares information and professional knowledge with colleagues Understands relevant international standards and practices Systematically builds up and maintain/acquire auditor and trainer registration Travel to places including abroad for audits / assignments /Trainings and Customer Meet Major Duties as Lead Auditor Food Safety and IMS: Perform Food Safety / Quality / other management system audits according to specific client requirements or international recognized GFSI / ISO schemes and perform value added training. Reporting audit results accurately and timely manner in compliance to the scheme / Organizational requirements. Cooperation with sales and planning team for smooth delivery of projects. Demonstrated experience in managing key accounts and client relationships in business development situations Market input to regional tactical plans Developing new and large project opportunities Member of Key account team for relevant Key customers Opportunity portfolio management; ensure good processes that keep track on BA activities toward customers, prospects and order backlog. What we offer: Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About you: Masters or Graduate in Food Technology/ Food Science / Bio-Technology / Microbiology / Dairy Technology / Agriculture / Science / Fisheries Science / Aquaculture or Equivalent discipline from a reputed institute. Minimum 5 years of work experience in Food Industry or food supply chain, out of which minimum 3 years has to be in Quality or Production function. Further, minimum 3 years experience in Auditing, Inspection and Training in a recognized Certification body Qualified Lead Auditor for FSMS/FSSC 22K and IMS Qualification to BRCGS / IFS is preferable. Deep knowledge of FSSAI regulations Understanding of Food factory operations and Quality Assurance Demonstrated proficiency in Microsoft Office Ability to communicate directly with clients at all levels of an organization including senior management Ability to read/interpret audit protocols and work instructions Ability to write thorough audit reports

Psychiatrist Required Azamgarh UP Salary 2.5 Lakhs + Accommodation Varanasi UP Salary 1.5 to 2 Lakhs *Benefits:* - Doctor couples can be placed at the same location. - Assistance in finding suitable jobs based on preferred locations.

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.

Job Description Responsibilities: Sterility and BET Testing: Perform sterility and Bacterial Endotoxin Testing (BET) for raw materials and products. Validation Activities: Execute validation activities. Prepare and review Microbiology-related SOPs, STPs, validation protocols, and reports. Equipment Qualification and Calibration: Conduct equipment qualification (IQ/OQ/PQ/RQ and PV). Perform calibration activities related to the Microbiology department. Change Control, Deviation, and CAPA: Initiate and manage Change Control, Deviation, and Corrective and Preventive Actions (CAPA). Bioburden Testing: Perform bioburden tests for water, raw materials, and products. Population Determination of Biological Indicators: Conduct population determination of biological indicators. Cell Bank Testing: Perform cell bank testing. Work Experience 5 to 8 year experience Education Post Graduation in Microbiology or Biotechnology Competencies Innovation Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence

Inspection & Certification Division: FARE Labs Pvt Ltd, Gurgaon Job Title: Empanelled Auditors – Catering Sector Job Description: Education Qualification: Master degree in Food or Dairy or Fisheries or Oil Technology or Biotechnology or Agriculture or Veterinary Sciences or Bio-chemistry or Microbiology or Chemistry or Hotel management or Catering technology from a recognised university. Essential Requirements: Successful completion of Accredited Lead Auditor course in Food Safety Management System (ISO 22000). Professional Experience: Applicants should have a minimum of 4 years of relevant professional experience in the following areas: Conducting audits and inspections in accordance with international standards such as ISO/IEC 17020, ISO/IEC 17021-1, and other applicable quality or regulatory frameworks. Demonstrating in-depth knowledge of catering operations, processes, and food safety standards. Implementing or assessing HACCP systems within the catering and hospitality environment. A minimum of 10 man-days of audit experience in hotels or catering establishments under ISO 22000 standards. Knowledge & Skills: 1. Excellent communication and interpersonal skills. 2. Ability to produce clear, well-structured, and professional audit reports and supporting documentation. Salary: As per industry norms. Kindly share your CV at: hr@farelabs.com Show more Show less

PATH current employees - please log in and apply Here PATH is a global nonprofit dedicated to achieving health equity. With more than 40 years of experience forging multisector partnerships and with expertise in science, economics, technology, advocacy, and dozens of other specialties, PATH develops and scales up innovative solutions to the world’s most pressing heath challenges. About The Project The Ministry of Health and Family Welfare (MoHFW) has launched a dedicated Metropolitan Disease Surveillance Strengthening component under the Pradhan Mantri Ayushman Bharat Health Infrastructure Mission (PM-ABHIM). Covering 20 cities across India, this initiative is supported by the World Bank through the Transforming India’s Public Health Systems for Pandemic Preparedness Program (PHSPP). PATH has been selected as a key partner in establishing a Technical Support Unit (TSU) to provide expert guidance in the design and implementation of this initiative. The TSU will provide strategic direction and technical support for the initial two years of the program, leveraging global experience and best practices to strengthen metropolitan disease surveillance. The primary objective is to facilitate operationalization, address challenges, and promote innovations as global public goods. Position Overview PATH is seeking for Public Health Laboratory Expert on Third Party Payroll- (Randstad). The Public Health Laboratory Expert will play a pivotal role in guiding the strategic implementation, monitoring, and enhancement of the metropolitan disease surveillance program. This role involves close collaboration with national health authorities, stakeholders, and technical partners to ensure the success and sustainability of the program. The Consultant will lead efforts to improve public health laboratory infrastructure, enhance quality assurance processes, and strengthen laboratory-based surveillance across metropolitan cities. Duty Location : National Centre for Disease Control, Delhi Key Roles And Responsibilities Laboratory Infrastructure Assessment: Conduct assessments of public health laboratory infrastructure, staffing, and capabilities across selected metropolitan cities. Draw on the global best practices to provide recommendations for improvement and modernization. Private Sector Engagement: Develop strategies to enhance private sector participation in laboratory-based disease surveillance, including options for integration with public health systems and improving collaboration between stand-alone laboratories, hospital-attached laboratories, and national networks. Quality Assurance and Standards: Evaluate existing laboratory quality assurance systems and develop actionable plans to address critical gaps. Introduce global best practices to strengthen laboratory standards, protocols, and accreditation processes. Training and Capacity Building: Design and implement training programs for laboratory personnel to ensure adherence to national and international standards, with a focus on quality control, biosafety, and emerging disease diagnostics. Coordination and Technical Support: Work closely with state and national health agencies, including the Integrated Disease Surveillance Program (IDSP) unit of the National Centre for Disease Control (NCDC), to provide technical support and strategic direction for laboratory surveillance initiatives. Data Integration and Reporting: Support the integration of laboratory data into national surveillance systems, ensuring timely reporting and the use of laboratory data for public health decision-making. Policy and Advocacy: Contribute to the development of national policies and guidelines for laboratory-based disease surveillance, ensuring alignment with global standards and promoting sustainability. Qualifications And Experience Education: Master’s degree in microbiology, Molecular Biology, or a related field. A PhD in Microbiology or an MD in Microbiology would be preferred. Experience: Minimum of 10 years of experience in public health laboratory systems, with a strong background in disease surveillance, antimicrobial resistance (AMR), and infectious diseases, particularly in urban settings. Expertise: Proven expertise in public health infrastructure, laboratory quality assurance, and private sector engagement in laboratory-based surveillance. Partnerships: Experience working with national and state health agencies, including NCDC, IDSP, and NACO as well as with international partners such as WHO and CDC. Essential Skills Communication: Exceptional verbal and written communication skills in English and Hindi, with the ability to convey complex technical information clearly and effectively. Project Management: Strong organizational and project management skills, with a proven ability to manage multiple tasks and deadlines efficiently. Technical Proficiency: Proficiency in MS Office (Word, Excel, PowerPoint, Outlook) and familiarity with laboratory information management systems (LIMS) and digital tools for data analysis. Stakeholder Engagement: Demonstrated ability to work collaboratively with government counterparts, donors, and development partners at both national and state levels. Health Systems Knowledge: Deep understanding of India’s health system, particularly in the context of disease surveillance initiatives such as IHIP, IDSP, and key national programs like NHM, Ayushman Bharat, PM-ABHIM (specifically IPHL and BPHU component), and the XV-FC. Flexibility: Willingness to travel up to 30% of the time for program-related activities. Location: Delhi Show more Show less

Job Summary: We are seeking experienced and passionate faculty members to teach and mentor students in various paramedical and healthcare-related degree programs. The ideal candidate will have a strong academic background and practical knowledge in healthcare, combined with a dedication to teaching and student development. Key Responsibilities: Deliver lectures, practical sessions, and clinical demonstrations as per the academic schedule. Prepare lesson plans, academic materials, and assessment tools in line with the curriculum. Guide students in academic projects, seminars, and clinical postings. Conduct internal assessments, evaluate performance, and maintain academic records. Ensure compliance with accreditation standards and institutional policies. Participate in academic planning, curriculum development, and faculty meetings. Mentor students in both academic and career development matters. Engage in professional development and stay updated with industry trends. Assist in organizing workshops, conferences, and student development activities. Courses/Subjects May Include: Medical Laboratory Technology Radiology & Imaging Technology Operation Theatre Technology Dialysis Technology Physiotherapy Nursing Assistance Anatomy, Physiology, Pathology, Microbiology, etc. Qualifications: Essential: Master’s or Bachelor’s Degree in a relevant Paramedical/Health Science discipline (e.g., M.Sc./B.Sc. MLT, Radiology, etc.) Desirable: M.Phil./Ph.D./NET/SET-qualified candidates preferred (as applicable) Minimum 1–3 years of teaching or industry experience in the respective field. Strong communication skills and command of both theoretical and practical subjects. Job Type: Full-time Pay: ₹18,000.00 - ₹25,000.00 per month Benefits: Paid time off Schedule: Day shift Work Location: In person

We are hiring an MSc/Postgraduate professional in Microbiology/Chemistry/Product Development for our Faridabad-based team! Key Responsibilities: 1. Conduct microbiological & chemical analysis of raw materials, in-process, and finished products. 2. Perform microbial testing (e.g., TVC, pathogens), media prep, and aseptic sampling. 3. Support new product development, improve formulations & perform stability, efficacy & shelf-life studies. 4. Maintain lab records, perform data logging (LIMS), statistical analysis & reporting. 5. Ensure QC/QA compliance with ISO, GMP, GLP; troubleshoot lab issues. 6. Operate & maintain lab instruments (pH meter, spectrophotometer, autoclave, etc.). 7. Follow lab safety & regulatory protocols; manage waste disposal. 8. Stay updated with research trends & share knowledge. ✅ Requirements: 1. MSc in Microbiology/Chemistry/Biotech/Biochem with 1+ yrs experience 2. Strong lab skills, product development exposure, and data analysis proficiency Location: Faridabad Apply now: vikas@triindia.org Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹30,000.00 per month Benefits: Health insurance Leave encashment Provident Fund Schedule: Day shift Fixed shift Weekend availability Work Location: In person

Microbiologist (Mushroom/Vermicomposting) Job Description About Us: Since 2012 “Tru Prime Pvt. Ltd” has operated Punjab’s largest 2000 head dairy farm, mostly HF, at Majara about 32km from and 8 km from Ahmedgarh. The company now seeks to diversify into growing chamber multi-tier organic mushroom cultivation using captive cow manure as the principal substrate component. The venture will consist of multiple growing chambers cultivating a variety of mushrooms, including button, oyster, paddy straw and shiitake using internally generated spawn and industry leading practices. The company will also develop and cultivate medicinal mushrooms. Spent mushroom substrate (SMS) will be processed in an accompanying vermicomposting facility. The company will service both domestic and international markets, with exports dominating from year 3. Company products will be both packaged / branded and bulk for institutional customers. The company will develop partner farms with the supply of turnkey facilities and inoculated substrate and the buyback of SMS and bulk mushrooms. RECRUITMENT The company is seeking professionals with experience in organic multi-chamber multi-tier mushroom cultivation at all levels including production, quality control, R&D, management, sales and marketing, finance. On-site single and family accommodation is available. Come join India’s most integrated organic farming venture. Job Title: Microbiologist (Mushroom/Vermicomposting ) Job Summary: We are seeking a skilled Microbiologist to join our team, focusing on mushroom cultivation, vermicomposting, and related microbiological processes. The ideal candidate will have a strong background in microbiology, mycology with experience in research and development. Key Responsibilities: 1. Conduct research and development on mushroom cultivation, vermicomposting, and related microbiological processes. 2. Design, develop, and implement experiments to optimize mushroom growth, vermicomposting, and microbial consortia. 3. Analyze and interpret data to identify trends, patterns, and correlations. 4. Collaborate with cross-functional teams to develop new products, processes, and technologies. 5. Develop and maintain standard operating procedures (SOPs) for microbiological testing and analysis. 6. Identify and troubleshoot microbiological issues in mushroom cultivation and vermicomposting systems. 7. Develop and implement quality control measures to ensure consistency and quality. 8. Stay up-to-date with industry trends, research, and developments. 9. Research and improve mushroom growth processes. 10. Strong knowledge of mushroom growth processes and hybrid strain development. 11. Familiarity with mushroom cultivation techniques. 12. Maintain mushroom-growing facilities. Requirements: 1. Graduate in Microbiology, Mycology, Agriculture or related field. 2. Experience in mushroom cultivation, vermicomposting, or related areas. 3. Strong knowledge of microbial ecology, mycology. 4. Excellent analytical and problem-solving skills. 5. Ability to work in a team environment and communicate effectively. 6. Strong organizational and time management skills. Desired Skills: 1. 5 years experience with microbial culturing, isolation, and characterization. 2. Familiarity with vermicomposting, mushroom cultivation, or related processes. 3. Familiarity with laboratory information management systems. 4. Experience with Good Laboratory Practices and Good Manufacturing Practices. Industry: 1. Agricultural biotechnology 2. Environmental science 3. Food science What We Offer: 1. Competitive salary and benefits package. 2. Opportunities for professional growth and development. 3. Collaborative and dynamic work environment. 4. Paid time leave. 5. Opportunities for professional growth and advancement. How to Apply Interested candidates are invited to submit their resume and a cover letter detailing their relevant experience via email manish.kumar@primemilk.in or Whatsapp +91 9915929067. Please state the following on the subject line " Microbiologist ." Only suitable candidates will be contacted Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹50,000.00 per month Benefits: Food provided Internet reimbursement Leave encashment Paid sick time Paid time off Provident Fund Schedule: Day shift Evening shift Morning shift Night shift Rotational shift Weekend availability Work Location: In person Expected Start Date: 16/06/2025

QUALIFIED AND EXPERIENCED TO HANDLE FULLY AUTOMATED VITEC MICROBIOLOGY CULTURE MACHINE, RT PCR , CBNAAT MACHINE , ABLE TO DO CULTURE PLATES AND OTHER BASIC LAB TECHNIQUES Job Types: Full-time, Permanent, Fresher Pay: ₹12,000.00 - ₹20,000.00 per month Benefits: Flexible schedule Food provided Work Location: In person

Please Read Carefully Before Apply. Role: Academic Content Writer Industry Type: Academic Content Writing Employment Type: Full Time, Permanent Salary: 13,000-20,000(in hand) + Incentives Office Timing: 10.30 am to 6.30 pm.( Fixed timing) Work mode: Hybrid Mode (3 days Work from home & 3 days’ Work from office, Saturday half day ) Responsibilities Conducting deep research on industry-related topics to develop authentic content. Creating Technology, Civil Engineering related content Editing and proofreading academic content to ensure accuracy and clarity. Following proper citation and referencing guidelines. Collaborating with the team to develop and refine academic content. Microbiology, Nursing MBA Finance and Masters in Commerce Produce 2500-3000 words fresh words daily without plagiarism. Preferred Candidate Profile Bachelor's degree or Master Degree in (Computer Science, Information Technology, Civil Engineering, Law, MBA Management and Finance). (This is the major eligibility criteria). Fresher from the above mentioned educational background are also eligible for this job role. Ability to work independently and as part of a team. Work within deadline. Nursing and Medical MBA Management, Project Management MBA Finance/MCom Must have PC or Laptop at home. Skills Excellent research and writing skill in English . Have knowledge of MS word, MS Excel and PowerPoint. Have knowledge of Matlab, CSS, Java Script, Python, React JS,SQL,DBMS, AutoCAD, Revit (Preferable) Nursing and Medical MBA Finance/MCom MBA in Management courses Send your resume to: hrkolkata.ges@gmail.com Contact Us: 8013546537, 7003668326 Job Type: Full-time Pay: ₹13,500.00 - ₹24,000.00 per month Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

Job description Role & responsibilities :- 1. We are looking for energetic freshers with B.Sc./M.Sc. microbiology/ Biotechnology eager to start a career with an Agrochemical company. 2. Applicant must have basic knowledge of organic/inorganic chemistry along with chemical product testing procedures. 3. Perform routine and specialized microbiological analyses using a variety of techniques, including culturing, staining, and molecular methods. 4. Ensure compliance with quality control standards and protocols. 5. Implement and adhere to safety procedures in the laboratory. 6. Strong theoretical knowledge of microbiological principles and techniques. Required Candidate profile: - 1. B.Sc./ M.Sc in Microbiology 2. B.Sc./ M.sc in Biotechnology 3. Freshers Are Preferred. 4. Able to Immediately join 5. Ready to relocate to Raisen. Interested candidates share resumes at arindixit@katyayaniorganics.com Thanks and Regards HR Executive. Job Type: Full-timePay: ₹5,000.00 - ₹10,000.00 per monthBenefits: Food provided Schedule: Day shift Night shift Work Location: In person Job Type: Full-time Pay: ₹10,000.00 - ₹15,000.00 per month Schedule: Day shift Work Location: In person

Req ID: 323217 NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now. We are currently seeking a Software Development Senior Specialist to join our team in Noida,Pune,Bangalore, Uttar Pradesh (IN-UP), India (IN). The EHR Support Specialist should be highly proficient with the electronic health record software (Meditech) or have a strong clinical background and a strong aptitude for computer systems. This role requires a strong working knowledge of Windows-based systems, excellent customer service skills, the ability to train and support doctors, nurses, support staff, and clinical administrators. This role also works closely with other members of the I.S. Department and I.T. roles supporting the computing infrastructure and desktop computers. Role Responsibilities Manage operational and service Level agreement compliance Follow ITIL practices for Level-2 Support In a timely manner, capture, track, and solve level 1 and 2 Production Support tickets. Escalate level 3 help requests to EHR vendors, or server and network administrators, as appropriate. Provide explanations and instructions about complex EHR topics to non-systems staff members in clear and understandable terms. Effectively and diplomatically communicate within and across teams, departments, and organizations. Investigate and resolve software problems/performance and proactively identify potential issues Prioritize, coordinate, expedite, and escalate help requests for the help desk team, balancing workload, skills, personnel development, quality, service levels, and customer needs/expectations Perform root cause analysis and implement corrective measures Identify areas of the environment that need improvement and develop solutions to address Adhere to and comply with all client and NTTDATA policies Provides weekly status reports of completed and ongoing activities to management Diagnose and troubleshoot EHR software issues Operate as a liaison between onshore technical SMEs and the end-user department Provide business systems and technical analysis to support the applications. Includes evaluation, analysis, documentation of requirements, and creation of system specifications. Classifies problems such as system, training, or process and recommends corrective actions Must understand business systems, applications and industry requirements Mentor and train juniors to support business growth and a high quality of service. Ensure secure, reliable access to data by users according to company standards and industry regulations and protect data from risks Flexibility to work on shifts Requirements: Must have hands on experience in Clinical Applications of EHR systems including- Meditech. Meditech Applications -(Magic, Client Server (CS),6.X, Expanse) Application & workflow Knowledge in Administrative Modules- (ABS - Abstracting,ADM - Admissions,MRI - Medical Records.MRM - Medical Records Management,MIS - Management Information Systems,SCH (CWS/OR) - Community-Wide Scheduling, Operating Room Management,HUB (EMR) - Enterprise Medical Records,UNV - Universe), Clinical Modules-(EDM - Emergency Department Management,LAB (also BBK/MIC/PTH) - Laboratory, Bloodbank, Microbiology, Pathology, Instruments,NUR (PCS) - Patient Care System,OE - Order Entry,PCM - Physician Care Manager,PHA - Pharmacy,RAD (ITS) - Radiology/Imaging and Therapeutic Services,RXM (AOM) - Ambulatory Order Management), Financial Modules-(AP - Accounts Payable,BAR - Billing/Accounts Receivable,GL - General Ledger,PP - Payroll/Personnel,PBR - Physician Billing and Receivables), Interfaces Meditech Report Writer (NPR Report writer, Report Designer, Data Repository,SQL, SSRS, Automation Tools) Preferences Masters in Hospital Administration Proficiency in various programming and clinical application reporting tools About NTT DATA NTT DATA is a $30 billion trusted global innovator of business and technology services. We serve 75% of the Fortune Global 100 and are committed to helping clients innovate, optimize and transform for long term success. As a Global Top Employer, we have diverse experts in more than 50 countries and a robust partner ecosystem of established and start-up companies. Our services include business and technology consulting, data and artificial intelligence, industry solutions, as well as the development, implementation and management of applications, infrastructure and connectivity. We are one of the leading providers of digital and AI infrastructure in the world. NTT DATA is a part of NTT Group, which invests over $3.6 billion each year in R&D to help organizations and society move confidently and sustainably into the digital future. Visit us at us.nttdata.com NTT DATA endeavors to make https://us.nttdata.com accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact us at https://us.nttdata.com/en/contact-us . This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. NTT DATA is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click here . If you'd like more information on your EEO rights under the law, please click here . For Pay Transparency information, please click here . Show more Show less

Role & responsibilities Responsibilities: - Oversee and manage quality control processes and procedures within the organization - Develop and implement quality control standards and guidelines - Conduct regular inspections and audits to ensure compliance with quality standards - Analyze data and trends to identify areas for improvement and implement corrective actions - Collaborate with cross-functional teams to address quality issues and drive continuous improvement - Train and mentor QC staff to ensure adherence to quality control protocols - Prepare and maintain documentation related to quality control activities - Participate in regulatory inspections and audits as needed

Operate the FESEM in SE and BSE mode with EDS and EBSD. Performs routine maintenance on the microscope. Explains and demonstrates how to operate instruments to students, faculty, etc. Keeps records on instrument usage, service repairs and maintenance manuals. Essential: M. Sc. in Physics/Chemistry/Nano Technology or B. E/ B. Tech in Engineering Streams. Minimum two years’ experience on handling of FESEM, EDS with other possible attachments of FESEM.

Designation: Engineer - Technical Skill Development Education Qualification: B Tech (Biotechnology), BSc (Biotechnology), MSc (Microbiology) Years of Experience: 2-4 yrs Job Profile Overview: A Creative, Patient and Enthusiastic individual who in addition to his / her experience is driven to further learn the technical details about the DDE products and the industries that we operate in. Eventually, shall impart technical knowledge to applicable roles, both Freshers and experienced, in a lucid, structured and easily understood teaching format that would leave a lasting impact on the taught. An effective Public Speaker who is fluent-&-comfortable in English such that practical-yet-dry Technical Information / Data / Drawing are presented and communicated in a manner that would be fun to learn and easy to remember. Accountable and Responsible for: Can carry out the Learning Need Analysis activity under guidance for specific topics. Under guidance can perform the process of gathering training requirements from the target audience, convey to the SME / vendors, ensure that the same are covered in content / during sessions. Under guidance should Develop, Prepare and Document the Training Course Content (TCC), subject-wise, in a Presentation format that is concise and well-defined. Worksheets, Technical-Drawings, Graphics, Photos and Pictures should be presented in formats that shall be visibly presentable. Can conduct trainings on basic topics for trainees as part of technical induction during the onboarding process. Developing evaluation questionnaire to enhance training effectiveness under guidance and perform evaluation Can understand the parameters for taking the training feedback, maintain feedback forms , track and implement measures based on the feedback as part of continuous improvement, under guidance. Assist in the process of making annual training calendar , ensure further execution as per the schedule Keeping Track and raising timely flags regarding - 1. The completion of feedback sessions with the Trainees and/or their HODs. 2. The Evaluation Tests upon completion of respective subject-wise TCC as per the annual training calendar. Ensure training programs comply with company policies and regulatory requirements. Run the Employee Skill Development tool for routine processes like employee management, survey runs, co-ordinate with employees / managers for completion of assigned tasks under guidance. Maintain and manage training records and documentation for audits and inspections of all the planned as well as unplanned trainings. Assist in the development of SOPs, work instructions, and training manuals in collaboration with QA. Facilitating trainings Coordinate / collaborate with vendors, internal Subject Matter Experts (SMEs), stakeholders and getting things done for the entire training and evaluation process. Scheduling meetings / sessions including venue booking, sending invitations and equipment setup. Sourcing of external trainers / agencies, getting quotation. Make a repository of relevant online courses across departments. Functional Skills : Managing multiple training initiatives and deadlines simultaneously. Prioritizing urgent compliance training alongside regular skill development sessions. Effective written and verbal communication tailored as per the target audience needs. Behavioral Skills : Eye for Detailing A good listener A heightened sense of accountability Strong organizational, coordination, and documentation skills Excellent interpersonal skills Show more Show less

Job Description Job Description of Sr.Quality Executive - QA: Candidate shall be Graduate/Post Graduate in Science, Food technology/ Microbiology/DIFAT, Shall have min. 2 years of experience in FMCG i.e. distilleries/Breweries /Beverages/Food industries. Hands on experience in analysis techniques, lab instruments calibration and maintenance Knowledge on QMS and FSMS Knowledge on word, Excel and power point. To control quality defects in incoming and finished goods so as to get customer satisfaction by applying high quality standards in the product and the process. Capability to build and promote food safety and quality culture in unit. Responsible for end to end Quality monitoring in incoming and online checks. Responsible for Quality Control and other control activities in the factories and material. Responsible for checking raw material used in production, packaging material and in process material and finished goods- accept or reject as per set quality standards. Responsible for record maintaining and SAP records updation. Undertake training and development of shop floor workmen. To conduct internal quality audits for GMP, GRMS and SQIP. Deal with the Government authorities like FSSAI , LMR and Excise for audit and compliance. Ensuring that samples of all products are sent to external laboratory and calibration of equipment’s done as per requirement. To conduct analysis of raw materials and packaging materials and report in time. To visit market whenever new product / product quality survey / complaint samples collection is required. Should be street smart. Implement GMP/ GLP , GSP and GHP in premises at all times and 5S. Good oral and written communication skills and to maintain MIS data. Vendor communication for rejection and its handling on time and development in co-ordination with site QA team. Quick learning and initiative attitude in working. Diversity statement Celebrating our inclusive and diverse culture is core to Diageo’s purpose of “celebrating life every day everywhere”. This purpose is, in itself, inclusive in nature, as it values everybody irrespective of background, disability, religion, gender identity, sexuality or ethnicity. We know that for our business to thrive and for Diageo to realize its ambition, we depend on having diverse talent with a range of backgrounds, skills, and capabilities in each of the 180 countries in which we operate and to reflect our broad consumer base. We view diversity as one of the key enablers that helps our business to grow and our values, purpose and standards set the conditions for us to respect the unique contribution each person brings. Worker Type Regular Primary Location: Aurangabad Unit Additional Locations : Job Posting Start Date 2024-08-07 Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Executive- Microbiologist Date: Jun 5, 2025 Location: Mohali - Quality Control Company: Sun Pharmaceutical Industries Ltd 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. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Manager - QA Date: May 11, 2025 Location: Guwahati - Quality Assurance Company: Sun Pharma Laboratories Ltd Job Summary: The position is responsible for heading the Quality Assurance function in NOSD Parenteral Block at Sun Pharma laboratories Limited, Guwahati Responsible to set the team goals and objectives for the NOSD Quality at Guwahati site in alignment with goals of Cluster Quality and other business function(s). Responsible to collaborate and support to functional heads of QA, QC, Microbiology, Production, IT, Regulatory Affairs and commercial department to align organizational goal and business strategies for achieving overall quality. Responsible for providing guidance to ensure achievement of targeted completion of tasks and execution of team. Responsible for facilitate harmonization and consistent implementation or Quality Systems and procedures (Pertaining to parenteral), in alignment with Global Quality Policies, Standards and applicable SOPs. Essential Job Functions: Primary Responsibility: Review and monitoring of Quality operations at Parenteral Block. To execute, monitor, review, and approval of Quality management systems i.e. Change control, Deviation, and CAPA management as per requirements. To review and approve Standard Operating Procedure etc. To ensure the compliance of documentation at various stages of the process i.e. (Manufacturing, Filtration, Filling, Visual Inspection, Labelling and Packing operations). To review, approve the Master and executed BMR, BPR, Validation, Qualification and other GMP documents. To evaluate and monitor the Aseptic process simulation (Media Fill) activities with respect to the APS planner, Trending of intervention protocol & reports. To facilitate harmonization and consistent implementation of the quality systems and procedures at the site in alignment with corporate quality policies /procedures. To review, update, respond to GQS/Regulatory audit observations within the stipulated time frame. To participate in the review & approval of investigation in case of Non- conformance events i.e. Process Deviation, OOS, OOT & Product Quality Complaint. To ensure release, approval, or rejection of Raw Material, Packing Material, Intermediate, Finished products as per approved specifications. To ensure completion and implementation of CAPA as per established procedure and follow up to verify the effectiveness of CAPA. Responsible for the batch disposition (Batch release or reject). To ensure compliance of electronic systems such as manufacturing equipment/instruments etc. To ensure equipment /instrument, qualification/calibration and prevent maintenance are performed as per approved planner. To ensure that processing and storage area are qualified as per the approved procedure and GMP requirements. To impart training to the plant personnel as per requirement and ensure the effectiveness. To be part of self-inspection and or quality audits that regulatory appraises the effectiveness and applicability of the quality system as per schedule. To ensure and perform work as per established approved procedure, regulatory norms and its compliance as per the current regulatory requirement. Facilitate/support the implementation of new initiatives of Corporate functions at site. Secondary Responsibility Specific emerging projects as applicable. Perform any other responsibility assigned by the Quality Head/Management. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Hiring SR/AP, Professor Pediatrician Medicine Surgeon Orthopedic Gynecology Emergency Anesthesia Community Radiology Pharmacology Forensic Biochemistry Anatomy Physiology Microbiology In Medical College in Allahabad & Varanasi MBBS & MD 8423159700