2524 Microbiology Jobs - Page 6

Job Description Job Title : HOD - Regulatory Affair Education : B.Sc. /M.Sc. (Agrochemicals, Chemistry) Location: Ahmedabad Roles And Responsibility:- Responsible for data generation of toxicology/ecotoxicology, microbiology studies according to OECD/CIPAC/SANCO/CDSCO international guidelines for the regulatory submissions of the agrochemicals in LATAM, Brazil, USA and other countries. Responsible for managing the regulatory process of agrochemical products and ensuring the compliance with international laws and regulations. Collaborate with R&D teams to develop new pesticide products or formulations. Monitor product performance, develop and execute sales strategies to achieve revenue. Establish relationship with customers across the globe and conduct business meetings with clients. Successfully manage the preparation and submission of regulatory dossiers, achieving timely approval and market access. Liase with global GLP laboratories to generate and interpret data for product registration. Also work closely with universities and research institutions to generate scientific data supporting product applications. Oversee the regulatory registration process for agrochemical products in multiple countries. Maintain up-to-date Toxicology, Chemistry, Packaging etc. plans for all projects/programs/products, including listings of studies, timelines, status and costs, update and refine as necessary to meet the committed timelines. Strengthening company relationships with government and regulatory bodies in order to ensure supportive political and regulatory environment for business growth. Developing regulatory strategies to obtain regulatory approvals with USA, EU, LATAM, AUSTRALIA and other International Agencies. Also working for Indonesia, Malaysia, Mexico, Philippines, Nepal, Bangladesh, Taiwan, Vietnam and African countries etc. Successfully manage the preparation and submission of regulatory dossiers, achieving timely approval and market access. Managed budget for regulatory activities ensuring cost effective use of resources.

Are you passionate about sustainable solutions and fascinated by the world of biotechnology and mycology? Join Mushloop, a leading startup dedicated to providing eco-friendly packaging alternatives to replace Styrofoam. About Us: Mushloop is a dynamic and growing company that specializes in innovative, sustainable packaging solutions. We are on a mission to revolutionize the packaging industry by harnessing the power of mushrooms to create eco-friendly products. Backed by IISc Bangalore, Bevisioneers by Mercedes Benz, Stanford Seed Spark, IIM Bangalore, and Kongu TBI. (Note: In line with our hiring process, selected candidates will undergo a three-month probation period before transitioning to full-time employment) Job Description: Are you a passionate mycologist with a deep love for fungi and a desire to make a positive environmental impact? We are seeking a talented Mycologist R&D to join our dynamic team and lead our research efforts in mycelium-based materials. Responsibilities: Identify novel mycelium strains for material production. Optimize mycelium growth conditions, substrates, and harvesting methods. Conduct experiments, collect and analyze data, and make data-driven decisions. Collaborate with biotechnologists and material scientists to advance products. Stay updated with the latest mycology developments and integrate new knowledge. Develop hybrid mushroom strains to improve product yield and quality. Research and improve mushroom growth processes. Maintain mushroom-growing facilities. Troubleshoot issues and actively contribute to team discussions. Pursuing or holding a Bachelor's/Master's in Microbiology or related field. Strong knowledge of mushroom growth processes and hybrid strain development. Familiarity with mushroom cultivation techniques. Excellent communication and problem-solving skills. Self-motivated and dedicated to learning and innovation. Qualifications: Master's degree in Mycology, Microbiology, Biotechnology, or related fields. Proven experience in mycological research and laboratory work. Strong analytical and problem-solving skills. Excellent communication and teamwork abilities. Passion for sustainability and a desire to contribute to a cleaner environment.

ILA BIOAMRINE founded in 2007 is purpose driven company, a leading marine biotech ingredients and formulation importer & distributor in personal care, health care, feed & agri input industry . With our Blue Biotechnology expertise, we offer the perfect combination of innovative, natural, organic & sustainable solutions to multiple leading personal care brands. Be part of ILA BIOMARINE – a purpose-led business as you work to impact the business and the world; we'll work to help you become a better you! Job Description: Marketing & Sales Executive – Personal Care Ingredients & Formulations Location: NCR, New Delhi Experience: 5–7years in B2B sales within personal care, cosmetics, or specialty ingredients sectors Education: B.Tech Cosmetics or B.Sc./M.Sc. in Microbiology, Biotechnology, Pharmacy or Chemistry Salary Range: ₹6–9 Lakhs per annum CTC (based on experience) Reporting To: Business Head / COO Key Responsibilities · Business Development: Identify and engage potential B2B clients in the personal care industry, including cosmetic brands, contract manufacturers and R&D labs. · Client Relationship Management: Maintain and nurture existing client relationships, ensuring high levels of customer satisfaction. · Technical Consultation: Provide clients with technical insights and recommendations on marine biotech ingredients and formulations. · Market Analysis: Monitor industry trends, competitor activities, and customer feedback to inform sales strategies. · Reporting: Prepare regular sales reports, forecasts, and market analysis for management review. Desired Skills & Attributes · Industry Knowledge: Familiarity with personal care ingredients, formulations, and industry standards. · Sales Acumen: Proven track record in B2B sales and client acquisition. · Technical Proficiency: Ability to understand and communicate complex technical information effectively. · Digital Savvy: Experience with digital marketing tools and platforms is a plus. · Communication Skills: Excellent verbal and written communication abilities. · Team Player: Collaborative mindset with the ability to work cross-functionally. . Ready to Travel extensively Job Types: Full-time, Permanent, Freelance Pay: ₹50,000.00 - ₹75,000.00 per month Benefits: Cell phone reimbursement Flexible schedule Internet reimbursement Work from home Supplemental Pay: Performance bonus Experience: B2B Marketing: 3 years (Required) Work Location: Remote

Job Title: Process Operations Scientist/Technologist – Dairy & Biogas Location: Shrimad Rajchandra JivaMaitridham (SRJMD), Baroliya, Dharampur, 396050 Gujarat Reporting To: SRJMD Manager Employment Type: Full-time Job Overview: We are seeking a qualified and dedicated Dairy and Biogas Process Operations Scientist/Technologist with a background in Chemistry, Microbiology, or a related science to oversee and manage the end-to-end processing of ghee and pasteurized milk , and ensure optimal process control in milk pasteurisation, ghee manufacturing, and biogas production . The candidate will also be responsible for daily operations, quality assurance, equipment hygiene, and regulatory compliance. Key Responsibilities: 1. Ghee & Milk Processing: Supervise the entire ghee manufacturing process including packaging. Oversee pasteurisation of milk, ensuring all parameters (temperature, time, flow, etc.) meet quality and safety standards. Implement and monitor process controls to ensure consistency in product quality and yield. 2. Quality Control & Assurance: Monitor microbial, chemical, and physical parameters during and after processing. Ensure compliance with FSSAI and other relevant safety, hygiene, and regulatory standards. Conduct regular testing in collaboration with lab technicians for both raw and finished products. 3. Biogas Plant Operations: Monitor the anaerobic digestion process, feedstock inputs, gas outputs, and digestate quality. Ensure safety measures and environmental compliance in gas handling and waste utilization. Maintain process logs and optimize performance through data analysis. 4. Equipment & Process Management: Ensure machinery is well-maintained and operated according to SOPs. Schedule and coordinate preventive maintenance with the engineering team. Maintain hygiene protocols for all food-contact equipment. 5. Operations & Team Supervision: Manage a small team of process operators and plant staff. Train staff on standard procedures, quality expectations, and safety. Maintain daily records, reports, and assist in inventory and procurement planning. Qualifications & Skills: Education: Bachelor’s Degree in Chemistry , Microbiology , Food Science , or equivalent. Experience: 2–5 years of experience in a dairy, food processing, or bioenergy plant (freshers with strong academic knowledge may be considered). Strong understanding of dairy processing technologies and basic microbiological testing. Familiarity with biogas plant operations and organic waste handling preferred. Knowledge of quality control systems like HACCP, ISO 22000, or GMP. Proficient in MS Office and basic data entry/reporting tools. Excellent organizational, problem-solving, and communication skills. Work Environment: Majority of time will be spent in production and processing units. Requires attention to detail, quick response to process deviations, and leadership in crisis handling. Compensation: Commensurate with experience and qualifications. If you're a detail-oriented professional with a scientific mindset and passion for process excellence in sustainable, ethical food production — we welcome your application! Please submit your CV to shahvp2000@gmail.com

u Conducting Research: Microbiologists design and execute experiments to investigate the behavior and properties of microorganisms. Analyzing Samples: They analyze various samples like blood, water, food, or soil to identify and classify microorganisms. Developing Experimental Protocols: They create and refine methods for studying microbial growth, interactions, and effects. Identifying Pathogens: A key task is identifying disease-causing microorganisms and assessing their resistance to antibiotics. Practical Applications: Developing Treatments: Microbiologists work on developing new medical treatments, vaccines, and other therapies based on their research. Ensuring Food Safety: They play a crucial role in ensuring food safety by analyzing food products for harmful microorganisms. Environmental Protection: Microbiologists may work on projects related to pollution control, biofuel production, or other environmental applications. Biotechnology: They contribute to various biotechnology applications, such as developing genetically modified crops or creating new industrial processes. Collaboration and Communication: Collaboration: Microbiologists collaborate with other scientists, healthcare professionals, and industry experts. Communication: They communicate their findings through reports, presentations, and other forms of communication. Mentoring: Senior microbiologists often mentor and train junior staff and laboratory technicians. Other Important Responsibilities: Ensuring Laboratory Safety: They are responsible for maintaining a safe and compliant laboratory environment. Quality Control: Microbiologists may be involved in quality control processes, particularly in the food and pharmaceutical industries. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹24,000.00 per month Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Overtime pay Performance bonus Education: Master's (Required) Experience: Microbiology: 2 years (Required) Work Location: In person

Lead the Quality Assurance department across both locations, ensuring compliance with FSSAI, ISO 22000, HACCP, and GMP standards. Develop, implement, and monitor quality control systems for raw materials, in-process checks, and finished goods. Conduct internal audits , prepare for external inspections, and ensure timely closure of non-conformities. Collaborate with production and procurement teams to resolve quality issues and improve product consistency. Maintain and update SOPs, quality manuals, and documentation as per regulatory and customer requirements. Train and mentor QA/QC staff on food safety protocols , hygiene standards, and best practices. Liaise with vendors and suppliers to ensure ingredient quality and traceability . Analyze customer complaints and implement corrective and preventive actions (CAPA) . Required Skills & Qualifications Bachelor’s/Master’s degree in Food Technology, Microbiology, or related field . Proven experience in food-grade QA systems , preferably in FMCG or food processing units. Strong knowledge of FSSAI regulations , ISO 22000, HACCP, GMP, and other food safety standards. Proficiency in MS Office, ERP systems , and quality reporting tools. Excellent leadership, communication, and analytical skills . Warmly Regards, Samir Kumar (MBA) Placenest Services Private Limited With 10+ years exp. In Talent Acquisition Mb. 9317955459 Job Types: Full-time, Fresher Pay: ₹60,000.00 - ₹91,189.69 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person

POST- Microbiologist EDUCATION-B. Sc.,/ M.Sc., Microbiology, Biotechnology EXP: Fresher salary: According to company norms Job Type: Full-time Pay: From ₹15,000.00 per month Benefits: Paid sick time Schedule: Day shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Bangalore, Karnataka: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Preferred) Work Location: In person

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Master's degree in microbiology with minimum of 3 year's experience Demonstrated technical skills in method validation and testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control #LI-PFE

As a Microbiologist with an MD degree, you will be responsible for supervising and conducting research on a variety of microbiological activities regularly. You will need to maintain a deep understanding of different research methods and execute manual operations on various supplies. It will be your duty to develop and uphold validation in all protocols related to environmental controls. Additionally, you will perform laboratory analysis on all materials post appropriate sterilization. This is a freelance position with work scheduled on weekends only. A shift allowance will be provided. The work location is in person. If you require further details or have any queries, please feel free to ask.,

As a Manager in the QC - microbiology laboratory, your primary responsibility will be to lead a team of analysts, senior analysts, and trainees. You will be responsible for managing a 12-member team and ensuring the smooth day-to-day operations of the laboratory. Your duties will include preparing plans, protocols, and reports related to microbiology laboratory activities. You will be expected to oversee the execution of these plans and ensure that the laboratory functions efficiently and effectively. In addition to your managerial responsibilities, a strong commitment to Diversity, Equity, and Inclusion is essential in this role. You will be expected to promote and uphold these values within the team and foster an inclusive work environment for all members. If you are looking for a challenging opportunity to lead a dynamic team in the field of microbiology laboratory management, this position may be the perfect fit for you. Join us in our commitment to excellence and make a difference in the world of quality control.,

You will be responsible for overseeing the production operations of the Microbiology Manufacturing unit, Real Time PCR Kit & Nucleic Acid extraction kits manufacturing unit in Visakhapatnam, Andhra Pradesh. Your primary focus will be to ensure strict control over the production schedule, maintain quality control standards, and adhere to all compliance regulations. To excel in this role, you should possess at least 5 years of experience in a relevant industry. Previous experience in managing operations related to medical devices will be highly advantageous. An educational background in Microbiology, Biotechnology, or a related field at the Masters level or equivalent experience is desired. Additionally, strong communication skills are essential for effective coordination with various stakeholders. If you believe you have the necessary skills and experience to contribute to our dynamic team, we encourage you to reach out to us at hr@dnaxperts.com and share why you are the ideal candidate for this position.,

Job Title: Flow Cytometrist – QC (Quality Control) Location: Vapi, Gujarat Employment Type: Full-time About the Role: We are seeking a highly skilled and detail-oriented Flow Cytometrist to join our Quality Control team at our state-of-the-art life sciences facility in Vapi. The ideal candidate will be responsible for performing flow cytometry analyses, ensuring compliance with quality standards, and supporting the release of critical biological products. Key Responsibilities: Perform flow cytometry assays to assess cell populations, viability, immunophenotyping, and other QC parameters. Prepare and handle samples, reagents, and controls in accordance with GMP/GLP guidelines. Operate, calibrate, and maintain flow cytometers (BD, Beckman Coulter, or similar platforms). Analyze data using flow cytometry software (FlowJo, FCS Express, etc.) and generate detailed QC reports. Develop, optimize, and validate flow cytometry-based analytical methods for new products. Support troubleshooting , instrument qualification (IQ/OQ/PQ), and routine maintenance. Collaborate with cross-functional teams including QA, R&D, and manufacturing to ensure product quality. Ensure compliance with regulatory standards (FDA, EMA, ISO, ICH) and maintain proper documentation. Train and mentor junior staff on flow cytometry techniques and QC processes. Qualifications & Experience: Master’s degree (M.Sc) or PhD in Life Sciences , Biotechnology, Microbiology, Immunology, or related field. 3–5 years of hands-on experience in flow cytometry within a QC/QA/biologics Strong understanding of GMP/GLP and regulatory requirements. Proficiency in flow cytometry software and data interpretation. Excellent analytical, documentation, and problem-solving skills. Ability to work effectively in a fast-paced, team-oriented environment. Preferred Skills: Experience with cell-based assays , immunoassays, and cytometric bead arrays. Knowledge of quality management systems (QMS) and audit processes. Familiarity with sterile techniques and biosafety practices.

The dental bond is looking for Dental Assistant to join our dynamic team and embark on a rewarding career journeyPatient Preparation: Dental assistants prepare treatment rooms by sterilizing and organizing dental instruments, tools, and equipment. They also ensure the comfort of patients by preparing them for procedures and explaining treatment plans.Chairside Assistance: During dental procedures, dental assistants work chairside to provide necessary instruments and materials to the dentist. They may also assist with procedures, such as handing instruments, aspirating saliva and debris, and retracting tissues.Radiography: Dental assistants may take and process X-rays (radiographs) of patients' teeth and jaws. They ensure that patients are properly shielded and follow safety protocols.Infection Control: Dental assistants maintain strict infection control practices, including sterilization of instruments and disinfection of equipment, to prevent the spread of infectious diseases.Dental Impressions: They may assist with taking dental impressions for creating crowns, bridges, and other dental prosthetics.Patient Education: Dental assistants explain dental hygiene and post-treatment care instructions to patients, including proper brushing and flossing techniques and dietary recommendations.Administrative Tasks: They manage patient records, schedule appointments, and handle billing and insurance claims. Dental assistants often handle administrative duties, such as maintaining patient files and updating records.Equipment Maintenance: They are responsible for maintaining and ordering dental supplies and ensuring that equipment is in good working condition.

p style="text-align:justify"> Oakridge Gachibowli is a premium international day school in India. We have the proud privilege of being the pioneers of IB schooling in South India and one of the largest providers of IB education in India. We have 150+ IB-trained teachers with years of experience, helping us consistently achieve outstanding results and seeing our students go on to study at some of the world s leading universities. Oakridge offers IB, CBSE, and Cambridge curricula, and is recognized as one of the best schools in Hyderabad, India. . Job Description Please write the Job Description. Job Responsibilities

Manager, Regulatory Affairs - CMC This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Your role at our organization is integral to helping the world meet new breakthroughs that affect generations to come, and we re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. Primary responsibilities include, but are not limited to: Regulatory Responsibilities: Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills: Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic document based GMP systems Leadership Skills: Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 5 7 yrs of Industry Pharmaceutical industry experience out of 4 years experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics The candidate may be required to travel to other CMO sites on a need basis. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we follow the science and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Required Skills: Adaptability, Adaptability, Applied Engineering, Biochemistry, Business Processes, Chemical Engineering, Communication, Communication Management, Compliance Investigations, Documentation Standards, Electronic Common Technical Document (eCTD), Employee Training Programs, Global Regulatory Submissions, Immunoassays, Immunochemistry, Management Process, Microbiology, Molecular Biology, Molecular Microbiology, Pharmaceutical Manufacturing, Policy Implementation, Records Retention Management, Regulatory Affairs Compliance, Regulatory CMC, Regulatory Communications {+ 4 more} Preferred Skills: Job Posting End Date: 07/26/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

A Position Overview Position Title Executive/ Sr. Executive Department Zonal Operations Level/ Band 201 / 251 -Executive/Senior Executive Role Summary: Underwrite cases allotted as per assigned underwriting authority matrix Underwrite new business / resolving average of 80 cases per day allocated Scrutinize documents for completeness and check supportings B Organizational Relationships Reports to Regional Processi ng Centre (RPC) In charge Supervises Individual contributor C Job Dimensions Geographic Area Covered Underwriting transactions for cases upto 15 L for Branches in 1 region at Zone (cluster of 25 - 35 branches) Stakeholders Internal Central Underwriting (technical underwriting) Central Issuance External CAMs unit Customers D Key Result Areas Underwrite cases allotted as per assigned underwriting authority matrix Underwrite new business / resolving average of 80 cases per day allocated Scrutinize documents for completeness and check supportings Carry out risk assessment and complete cases / raise pendings if incomplete / for additional information Liaise with Branch Operations for tracking of cases for underwriting at Zone Participate in risk mitigation plans, contingency planning, business continuity programs by executing and reporting within defined timelines. Highlight and recommend process gaps, flaws and process changes. E Skills Required Technical Good Knowledge of MS Office Behavioral Essential Desired Interpersonal skills Communication skills Creative thinking skills Supervising/Leadership skills Teamwork Skills Influencing skills Relationship Building skills Decision making skills F Incumbent Characteristics Essential Desired Qualification Graduate in relevant field ( Science / Pharmacy / Medicine / Life Science / Microbiology, etc), Knowledge on risk evaluation tools in Underwriting, Knowledge of basic medical terminologies Experience 2 - 4 years experience 1 - 2 years in Insurance - similar field, medical setups

Professor / Associate / Assistant, Tutor (Clinical/Non Clinical) Anatomy, Physiology, and Biochemistry, Pathology, Pharmacology, Microbiology, Forensic Medicine & Toxicology, General Medicine, Pediatrics, Gynecology, Community, Ophthalmology, ENT

Applications are invited from interested and motivated candidates for the post of Junior Research Fellow (JRF) in a time bound research project for a temporary period, purely on contractual basis in School of Advanced Sciences (SAS), at Vellore Institute of Technology (VIT), Vellore, T.N, India.as per the following details. Position Junior Research Fellow (JRF) Number of Vacancy One Project Title MULTIFUNCTIONAL SILICA COMPOSITE COATINGS ON TI-6AL-4V BY SPIN COATING AND IT’S OPTIMAL IMPLANT/SCAFFOLD FABRICATION FOR BIOMEDICAL APPLICATIONS Sponsoring agency Council of Scientific & Industrial Research (CSIR) CSIR-ASPIRE 01WS(030)/2023-24/EMR-II/ASPIRE Department Department of Chemistry, School of Advanced Sciences (SAS) Project Tenure 3 years Job Description Project aims to develop the usability of defect free coatings and nanofibous scaffolds of bioactive silica glass and it’s composite for biomedical applications. Knowledge about ceramic materials, coatings and corrosion knowledge is required. Strong communication and writing skills are desirable. Essential Qualification Integrated BS-MS/MSc, M.Sc in material science, chemistry, physics, M Tech in nanotechnology or equivalent degree, with 55% marks and with valid NET/GATE test. Upper Age Limit JRF-28Yrs. Age relaxation The upper age limit is relaxable up-to 5 years in the case of candidates belonging to scheduled castes/tribes/OBC, women and physically handicapped candidates. Fellowship Junior Research Fellow (JRF)- Rs.37,000/-p.m. Principal Investigator Dr. U. Vijayalakshmi Professor (Grade I) Department of Chemistry, School of Advanced Sciences (SAS), Vellore Institute of Technology, Vellore Tamil Nadu – 632014 Send your resume along with relevant documents pertaining to the details of qualifications, GATE/NET score card, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (10/08/2025) through online http://careers.vit.ac.in Please note that the CV should include contact details (address, mobile phone no., email ID), date of birth, qualifications mentioned clearly. Complete information regarding publications of research papers in SCOPUS Indexed Journals should be mentioned in the CV. Incomplete applications will be rejected. No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF Funded Project in the Department of Physics, School of Advanced Sciences (SAS), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : “Development of cost-efficient and scalable perovskite based colloidal nanoparticles for high performance plastic scintillators” Qualification : M.Sc./ M.Tech. in Physics/ Materials Science or related fields from recognized universities/institutes with a minimum of first class and with GATE / CSIR-UGC JRF / NET-LS qualification. Mandatory Skills : Candidates should have a strong research background in synthesis and characterization of nanomaterials. Experience with colloidal semiconductor nanomaterials and related photo physics is desirable. Stipend : Rs. 37,000 p.m. + 8% HRA for the first two years (JRF); Rs. 42,000 p.m.+ 8% HRA for the third year (SRF) will be as per Institute norms. No. of Vacancies : 01 Post (ONE) Age Limit (if any) : Not exceeding 30 years i.e. Age must be from 18 to 30 years Sponsoring Agency : ANRF, PMECRG program, New Delhi, India Duration : 36 Months Principal Investigator : Dr. Abhinav Anand, Assi stant Professor, Department of Physics School of Advanced Sciences, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Interested candidates with the above-mentioned qualifications can send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before ( 18/08/2025) through the website: http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

About us: At Satopradhan Private Limited , based in Amritsar , we’re on a mission to promote healthy, natural living. Since 2019, we’ve been offering organic, vegan, and eco-friendly products across India through our online store and are committed to sustainable, chemical-free living and believe in delivering only the best to our customers. To know more about us; visit our website: www.satopradhan.com Job profile: We are hiring a Quality Assurance Manager to lead the testing of Food Products' raw materials and finished products. You’ll be responsible for ensuring the highest product quality of our Food & Non-Food products through lab testing , chemical testing , and micro testing processes in our in-house facility. Key Responsibilities: Handle end-to-end quality assurance for food (grocery, nuts, teas,butters, wheats, pulses), natural cleaners, and personal care products. Carry out regular lab testing of raw materials and final products Supervise chemical and micro testing procedures for safety and shelf life Maintain proper documentation of all testing reports and quality logs Ensure compliance with company’s quality assurance protocols and hygiene standards Collaborate with production teams to resolve quality issues promptly Set up SOPs for regular testing , calibrations, and preventive checks Maintain cleanliness and safety of the lab testing space. Identify root causes of quality failures and suggest improvements Requirements: B.Sc./M.Sc. in Microbiology, Chemistry, Food Science, or related field 2+ years of experience in L ab testing and quality assurance Hands-on experience with chemical and micro testing techniques. Strong attention to detail and documentation Company Benefits: Calm and supportive work environment Be part of a fast-growing natural brand Skill-based growth opportunities, yearly increments. Leaves (EL, CL, FL) ESI Staff discounts on organic and vegan products. To apply reach us at 86992-92575 or hr@satopradhan.com Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Health insurance Leave encashment Paid sick time Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Ability to commute/relocate: Amritsar, Punjab: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: Quality assurance: 2 years (Required) Quality management: 2 years (Required) FMCG: 2 years (Required) Location: Amritsar, Punjab (Required) Work Location: In person

Position: QC Inward Executive (Food Industry) Role Summary The QC Inward Executive is responsible for inspecting, sampling, and testing all incoming raw materials and ingredients to ensure they meet defined quality, safety, and compliance standards. This role supports the seamless flow of the production line by verifying material quality at intake and flagging any deviations early. Key Responsibilities Raw Materials Inspection Conduct thorough visual inspections and quality checks on all incoming materials (ingredients, packaging) to ensure compliance with specifications. Measure parameters such as moisture, pH, purity, or contaminants. Sample Collection & Testing Collect random samples for testing (chemical, microbiological, physical) either in-house or via external labs. Compare against approved standards/specifications and document outcomes. Record Keeping & Reporting Maintain detailed logs of inspection results, test findings, and any deviations. Generate reports to inform higher QC levels, procurement, and production teams. Equipment Calibration & Maintenance Ensure measuring equipment (scales, moisture meters, pH meters, etc.) are calibrated regularly; coordinate repairs or replacements as needed. Supplier & Batch Verification Verify supplier credentials, batch compliance, certificates of analysis, and proper labeling. Work with procurement to update the approved supplier list. HACCP & GMP Adherence Follow critical control points (CCP) procedures as per HACCP standards. Ensure Good Manufacturing Practices and plant hygiene protocols for incoming materials are observed. Deviation Handling & Corrective Actions Highlight non-conformance issues, initiate corrective steps (quarantine, rejection, supplier feedback) and monitor resolution. Training & Awareness Educate warehouse and procurement staff on quality norms and best practices. Provide routine updates and training refreshers related to QC procedures. Continuous Improvement Recommend process enhancements to reduce defects or delays and improve efficiency in inbound QC workflows. Qualifications & Skills Bachelor’s degree (Food Technology, Microbiology, Chemistry, or related) Practical experience in QC/QC-inward roles within food manufacturing or FMCG Good knowledge of food safety systems: HACCP, ISO 22000, FSMS. Familiarity with GMP and relevant regulatory compliance Strong analytical skills; experience with lab testing and record-keeping Excellent communication abilities in delivering findings and collaborating with suppliers and internal teams Attention to detail and strong numerical/measurement proficiency Ability to work independently and maintain calm under production‑pressure conditions Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Schedule: Day shift

Job Description: Designation: Quality Control Manager Qualification: MSc in Biochemistry / Microbiology / MLT Experience: 5 years + Salary: Rs. 25,000 - Rs. 30,000 per month Location: Ganapathy, Coimbatore Job Type: Full-time Pay: ₹25,000.00 - ₹30,000.00 per month Schedule: Day shift Work Location: In person

Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of executed BMRs and BPRs. Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc.. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Review of Visual inspector qualification record. Activities other than defined in the Job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance. To perform aseptic behavior/practice monitoring of operators (while working inside aseptic process area) during each aseptic batch (GMP batch) as per SOP. Skills : Skills : Conducting sterility testing, endotoxin testing, and microbial contamination control. Monitoring and documenting environmental conditions (temperature, humidity, microbial contamination, airborne particulates).

Water testing Sterility Testing BET (LAL) Testing Media Preparation Sub- culturing Environment monitoring Serial dilution GPT testing Micro documentation working Handling of instrument as BOD Incubator Autoclave weighing Balance pH meter TDS meter Microscope

We’re Hiring: Microbiologist (Pharmaceutical Experience Required) Location: Kanpur | Full-Time Company: Varda Dios Healthcare Pvt. Ltd., Rania We are seeking a qualified Microbiologist with a minimum of 2 years’ experience in the pharmaceutical industry to join our team at Varda Dios Healthcare Pvt. Ltd., Rania (Kanpur). Key Requirements: Minimum 2 years of hands-on experience in pharmaceutical microbiology Knowledge of GMP, microbiological testing, and environmental monitoring Strong understanding of quality control protocols and documentation Bachelor’s or Master’s degree in Microbiology or related field Attention to detail and a strong work ethic Location Requirement: This is an on-site position based in Kanpur. Please apply only if you currently reside in Kanpur. What We Offer: Supportive and growth driven environment Competitive salary based on experience Opportunity to work with a dedicated, science focused team To Apply: Send your resume with the subject line “Application for Microbiologist – Kanpur” Job Type: Full-time Pay: ₹18,000.00 - ₹30,000.00 per month Benefits: Health insurance Life insurance Provident Fund Work Location: In person