2560 Microbiology Jobs - Page 29

Job Description Job Summary: The Quality Assurance Associate Director will support a technical team interfacing between our Company and External Partners in the Biologics Drug Substance and Drug product manufacturing area. This individual will be responsible for ensuring that all quality assurance processes, and compliance requirements are met during technical transfers to and from External Partners and throughout the continuous commercial manufacturing process at External Partner sites. Key Responsibilities: Quality Oversight: Report to the Quality lead (or delegate) and provide general direction on quality goals and objectives, functioning independently to ensure oversight of all quality-related issues at External Partner site. Regulatory Compliance: Ensure that all quality assurance activities comply with regulatory requirements (FDA, EMA, etc.) and internal quality standards throughout the product lifecycle, including during facility start-up and technical transfers. Manufacturing Support: Provide ongoing quality support to External Partners by resolving quality issues, performing proactive analysis of process performance, and developing plans to ensure compliance and quality meet capacity needs. Collaboration: Work collaboratively with Biologics Quality Operations and other relevant teams within the Focused Factory to support the product lifecycle and address quality-related matters. Validation Strategies: Support and oversee validation strategies for new and existing products, ensuring compliance with best practices in quality assurance. Technical Review: Conduct a calibrated technical review of External Partners’ process change requests, deviations, protocols, and Master Batch Record changes to ensure compliance with quality standards. Issue Resolution: Troubleshoot quality-related manufacturing issues and support investigations using scientific problem-solving methodologies. Efficiency Improvement: Work with Operations, Quality, and External Partners to develop more efficient methods to meet regulatory requirements while ensuring quality standards are upheld. Quality Management System: Ensure adherence to the highest quality, compliance, and safety standards by participating in and complying with our Manufacturing Division Quality Management System requirements. Partner Engagement: Collaborate with External Partners to achieve business goals while fostering a common culture that prioritizes quality and compliance for both organizations. Education Minimum Requirement: Bachelor’s or master’s degree (or equivalent) in Chemical/Biochemical Engineering, Biotechnology, Microbiology, Pharmaceutical Science, Life Sciences, or a related field. Required Experience and Skills: Proven experience in highly regulated manufacturing environments with a minimum of 15 years of experience in quality assurance within biopharmaceutical operations, particularly related to Drug substance and drug product manufacturing and validations. Strong knowledge of quality systems, regulatory compliance, and quality assurance practices in the biopharmaceutical industry. Familiarity with change management processes and regulatory support planning. Experience in process validations, cleaning validations, and the associated quality documentation requirements. Proficiency in large molecule manufacturing, in process controls, analytical testing, validations, batch records review and release. Ability to perform risk assessments and develop strategies for continuous improvement initiatives. Proficient in computer system validations, equipment validations, area qualification, Audits, batch release procedures. Effective communication skills for managing partnerships and addressing quality concerns. Preferred Experience and Skills: Familiarity with high-performance organizational tools and a strong understanding of digital manufacturing processes, computer system validation requirements, and quality management within biologics production and quality. Experience with quality management software and metrics analysis to drive performance improvements. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Required Skills: Adaptability, Adaptability, Biotechnology, Change Management, Cross-Cultural Awareness, Cross-Functional Teamwork, Digital Manufacturing, GMP Training, Good Distribution Practice (GDP), Immunochemistry, Inspection Readiness, IS Audit, Management Process, Manufacturing Compliance, Manufacturing Environments, Manufacturing Quality Control, Microbiology, Product Lifecycle, Quality Assurance (QA), Quality Auditing, Quality Management, Quality Management Standards, Quality Metrics, Quality Standards, Quality Systems Compliance {+ 2 more} Preferred Skills: Job Posting End Date: 08/11/2025 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. Requisition ID: R357786

Responsibilities: Follow inspection and testing protocols for materials, products and packaging. Follow SOP’s and conditions for handling, storage and preservation of samples. Implement plans and strategies to support provision of safe food products. Review reports and develop guidelines and standard practices for data documentations and analysis. Specify the protocols and laboratory infrastructure and equipment to be inspected and tested. Verify alignment of sampling documentation, testing activities and procedures with established protocols to identify issues. Reporting faulty packaging or problems on the machines to the relevant managers. Requirements: · Having Minimum Experience of 2 Years at any Food Industry with Lab & QA Executive profile. Bachelor's degree in food science, microbiology, chemistry, or a related field. Proven experience in quality assurance and quality control within the food industry, preferably as Executive role. A clear understanding of health and safety standards and protocols. Good communication and interpersonal skill. Ability to work well individually and as part of a team. Job Types: Full-time, Fresher Pay: ₹18,000.00 - ₹22,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person

Veterinary pathologist required for a diagnostic laboratory. investigating animal diseases by examining tissues, organs, and bodily fluids. Monitoring complete laboratory which includes molecular biology, microbiology and clinical pathology. Job Type: Full-time Pay: ₹14,255.99 - ₹24,474.04 per month Benefits: Provident Fund Ability to commute/relocate: Bengaluru, Karnataka: Reliably commute or planning to relocate before starting work (Preferred) Education: Master's (Preferred) Experience: 5year: 1 year (Preferred) Work Location: In person Expected Start Date: 21/07/2025

Senior Executive – Quality Control (Spices), 3-6 yrs exp, Chennai Location: Chennai, Ambattur Department: Quality Control (QC) Industry: Food Processing / Spices / FMCG Job Purpose: To ensure that all raw materials, in-process products, and finished goods are tested and meet predefined quality specifications. Responsible for daily laboratory testing, product decisions, process monitoring, and supporting food safety initiatives. Key Responsibilities:  Conduct physical, and chemical testing of raw spices, in-process samples, and finished products.  Monitor critical control points (CCPs) and maintain in-process quality controls during production.  Approve/reject raw materials and final products based on specification compliance.  Ensure sample retention and maintain sample reference libraries for traceability.  Perform routine laboratory analysis: moisture, ash content, volatile oil, microbial load, aflatoxin, pesticide residue, etc.  Maintain all test records, inspection reports, certificates of analysis (COAs), and batch-wise quality documentation.  Ensure timely reporting and communication of quality issues to the production and QA teams.Process and Compliance Monitoring  Supervise hygiene and GMP practices on the shop floor. Troubleshooting and Corrective Actions Team Support and Training Key Requirements: B.Sc. / M.Sc. in Food Technology, Microbiology, Chemistry, Agriculture, or relatedfield. 3–6 years in Quality Control within the spices , food ingredients, or FMCG industry. o Strong understanding of analytical techniques and laboratory operations. o Knowledge of food safety standards (FSSAI, HACCP, ISO 22000). o Familiarity with spice testing parameters (moisture, volatile oil, foreign matter, microbial load, etc.). o Experience in laboratory equipment handling (oven, moisture analyzer, HPLC, Spectrophotometer, GCMS preferred). Salary: 4-5 LPA Interested candidates are requested to share their updated resumes to mdjinitha@gmail.com Job Type: Full-time Schedule: Day shift Application Question(s): How many years o f experience in Quality Control within the spices Are you familiar to handle equipment like HPLC, Spectrophotometer, Experience: in Quality Control within the spices: 3 years (Preferred) Work Location: In person

Inviting Applications for Professor/Associate Professor/ Assistant Professor Positions Engineering: CSE, AI&DS, AI&ML, Cyber Security, EEE, ECE, Civil & Mechanical Arts & Science: Computer Science, Computer Applications, AI, Cyber Security, English, Mathematics, Microbiology, Biochemistry & Biotechnology Commerce & Management Law Agriculture: Agronomy, Entomology, Soil Science, Genetics, Plant Pathology, Extension, Horticulture & Agri Engg. Eligibility: Ph.D in relevant fields. Experience: 5+ years Job Type: Full-time Benefits: Provident Fund Work Location: In person

Job Summary We are seeking a detail-oriented and motivated Laboratory Assistant to join our dynamic team. The ideal candidate will support laboratory operations by performing a variety of tasks that contribute to the efficiency and accuracy of research activities. This role is essential in maintaining high standards of quality control and ensuring compliance with Good Laboratory Practices (GLP). The Laboratory Assistant will work closely with scientists and researchers, providing assistance in various laboratory techniques and data collection processes. Responsibilities Assist in the preparation of laboratory samples and specimens for analysis. Conduct routine laboratory tests and experiments under the supervision of senior staff. Maintain accurate records of experiments, observations, and results in compliance with GLP standards. Perform quality control checks on laboratory equipment and supplies to ensure reliability. Support data collection efforts by compiling results from experiments and tests. Utilize microbiology techniques to assist in research projects related to veterinary terminology or histology. Ensure cleanliness and organization of the laboratory workspace, adhering to safety protocols. Collaborate with team members to troubleshoot issues related to laboratory procedures or equipment. Skills Proficiency in laboratory techniques and methodologies relevant to microbiology and histology. Familiarity with veterinary terminology is a plus for effective communication within the team. Strong understanding of quality control processes and Good Laboratory Practices (GLP). Excellent math skills for accurate data analysis and calculations. Ability to collect, record, and interpret data effectively. Detail-oriented mindset with strong organizational skills to manage multiple tasks efficiently. Effective communication skills for collaboration within a research laboratory environment. Join us as a Laboratory Assistant where your contributions will play a vital role in advancing our research initiatives while gaining valuable experience in a professional laboratory setting. Job Types: Full-time, Part-time Pay: ₹20.65 - ₹22.09 per hour Expected hours: 48 per week Benefits: Work from home Schedule: Day shift Morning shift Supplemental Pay: Performance bonus Work Location: In person

Project Staff Walk-in-Interview (Advt. No.: MMP025302/WP02/DRC/2025/01) Total Number of Posts: 02 Interview Date: 24th July 2025; Thursday at 10.00 AM Post code: PAT-I Post Name: Project Associate I (PAT-I) Number of posts: 02 Essential Qualification: Master's degree (M.Sc.) in Microbiology/Biotechnology / Biochemistry Preferred experience: Basic knowledge of PGPRs, microbial community-NGS, metabolite profiling skills/ethics to execute/deal with the experimentations Emoluments: (a) ₹. 31,000/- + HRA for those candidates who have qualified CSIR-UGC / ICAR / ICMR NET including lectureship/assistant professorship or GATE or those who have qualified National level examinations conducted by Central Government Department like DBT/DST or equivalent and/or their Agencies/Institutions (b) ₹ 25,000/- + HRA for others who do not fall under (a) above Job description: Selected candidate will work in the CSIR-sponsored project entitled “ Bioresource Conservation and Prospection (MMP025302) ” in WP-02 “ Bio-prospection of Mangroves”. The candidates are expected to design/ execute the experiments as well as visit the mangrove growing sites to fulfill the project objectives. Age limit: 35 years as on the date of interview (age relaxation as per CSIR rule). Other details: Duration: This position is purely temporary, initially for one year and subsequently extendable based on work performance up to project duration, whichever is earlier. It does not confer any right or claim for absorption in CSIR-CSMCRI. This post is purely temporary and co-terminus with the project. The engagement of a project staff in different projects either in the CSIR - Central Salt & Marine Chemicals Research Institute, Bhavnagar or different Laboratories/Institutes of CSIR taken together shall not exceed 06 years in any case. It would, therefore, not confer any right/claim implicit or explicit for any candidate for claiming extension or absorption in CSIR-CSMCRI, Bhavnagar. Interview Details: Interested candidates should appear before the Selection Committee for an interview/written test at CSIR-Central Salt and Marine Chemicals Research Institute, G. B. Marg, Bhavnagar-364002 (Gujarat) on 24 th July 2025, Thursday at 10.00 AM in the institute. Required Documents: Please bring an application with full particulars, including: Full name and postal address with email and phone number (application form attached), Date of birth and recent photograph. Educational qualifications and experience (if any) with photocopies of certificates/testimonials. Also, bring the following original documents (compulsory): Certificates and mark sheets (Degree/Diploma, etc.) of educational qualifications and proof of date of birth mentioned in the application (degree certificate is compulsory). GATE/NET Score Card, validity of the score, and details of seminars/projects done in the Master’s course. Experience certificates and testimonials. "No Objection Certificate" from the present employer if employed in a Government/Semi-Government or Autonomous Organization. For queries, please email drchaudhary@csmcri.res.in. No TA/DA will be provided for attending the interview.

Title: Senior Manger - API Supply chain team Date: Jul 11, 2025 Location: Dewas API - Supplychain Company: Sun Pharmaceutical Industries Ltd Role: Senior Manger – API Supply chain team Qualification: B.E. (Chemical) – preferred OR M. Sc (Chemistry) / Biotechnology / Microbiology OR B.Sc.+ MBA (Operations) Experience: Chemical Engineer with 3-4 years of experience OR candidate from other educational background with 6-9 years of experience Department: API Supply chain team Industry Preference: Pharma, Chemical, Paint, Agro, Speciality Chemicals Job Location: Andheri, Mumbai Areas of responsibilities: Capacity Planning & Capacity Effective Utilization Campaign Planning Business Continuity – De risking Plan (OS to IH, IH to OS), AVD Plan Implementation Site Transfer- API & Intermediate Cost Reduction Batches – MRP -à Commercial Supply NPL, Filling & Query Batches Supply management SCM Process maturity - Norms Setting, Cost to Serve, Planning Master Data Controller Chronic Supply Issues Resolution Responsible for Team Development & people Management - Training/ capability development of team Internal Interactions (within the organization) - Plants, RA, Procurement, R&D , Quality, LCM

If you are someone who: 🔬 Has hands-on experience in routine and advanced lab testing (biochemistry, haematology, microbiology, etc.) 📊 Can manage day-to-day lab operations independently, including workflow, reporting, and quality control 🧠 Is adaptable, eager to learn, and open-minded (no mental blockage) 🤝 Has the confidence to interact with doctors and medical teams to explain test utilities and reports 🎯 Is goal-driven with a desire to grow professionally in a fast-paced, innovation-driven environment

Position: Medical Coder - Work from Home Ct: HR Kamatchi- 8925264660 Job Description:Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis (Medical Problems) and Procedure (Treatments) Codes using ICD-10 CM and CPT code books. Requirement: knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills No of vacancy: 500 Eligibility: Nursing GNM/DGNM Life science graduates Pharmacy Physician assistant Bio medical Engineers Bio chemistry Bio technology Bio informatics Micro biology Zoology and Advanced zoology Biology Botany Plant biotechnology Genetics Food and Nutrition Paramedical Physiotherapy M.Sc. Clinical Nutrition M.Sc. Human Genetics M.Sc. Medical Laboratory Technology M.Sc. Medical Sociology M.Sc. Epidemiology M.Sc. Molecular Virology M.Sc. Biostatistics M.Sc. Blood Banking Technology M.Sc. Rgnerative Medicine M.Optom. M.Sc. Genetic Counseling M.Sc. Radiolog & Imaging Technology M.Sc. Medical Biochemistry M.Sc, Medical Microbiology M.Sc. Clinical Care Technology M.Sc. Clinical Care Technology M.Sc. Medical Physics B.Sc. - Accident & Emergency Care Technology B.Sc. - Audiology & speech Language Pathology B.Sc. - Cardiac Technology B.Sc. - Cardio Pulmonary Perfusion Care Technology B.Sc. - Critical Care Technology B.Sc. - Dialysis Technology B.Sc. - Neuro Electrophysiology B.Sc. - M.L.T. B.Sc. - Medical Sociology B.Sc. - Nuclear Medicine Technology B.Sc. - Operation Theatre & Anaesthesia Technology Bachelor of Science in Optometry B.Sc. - Physician Assistant B.Sc. - Radiology Imaging Technology B.Sc. - Radiotherapy Technology B.Sc. - Medical Record Science B.Sc. - Respiratory Therapy B.Sc. - Fitness and Lifestyle Modifications Accident & Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre & Anaesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology & Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Salary 15K to 17K (fresher) To 50K (experienced) Pm (Incentives && Benefits as per Corporate Standards) 4K fixed hike after six months Other Benefit: 1. Pick Up & Drop Facility 2. Food Facility 3. Day Shift 4. Weekend Off Reach us : Ct: HR Kamatchi 8925264660 Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology GNM DGNM Physician assistant Anesthesia technician Perfusion Technology Medical coder Freshers Medical coding Freshers jobs in chennai Medical coding openings in chennai Wanted Medical coder Freshers jobs Medical coding Medical coder Medical coding Freshers Jobs in chennai Jobs for Passed outs Freshers jobs in chennai Jobs for freshers Nursing jobs for freshers Pharma jobs for Freshers Biotechology Jobs Microbiology jobs Biomedical jobs Bioinformatics jobs Bsc/Msc Jobs Biochemistry jobs Life science jobs in chennai Paramedical jobs in chennai Jobs in Tamilnadu Jobs in Pharmacy Jobs in Hospital Perks and Benefits Incentives & Benefits as per Corporate Standards

Ct: HR SRIMATHI:7358425167 Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis and Procedure Code using ICD-10 CM and CPT code Eligibility:Any lifescience,paramedical & medical UG/PG

FACULTY OF HEALTH AND LIFE SCIENCES INSTITUTE OF INFECTION, VETERINARY AND ECOLOGICAL SCIENCES DEPARTMENT OF VETERINARY ANATOMY, PHYSIOLOGY & PATHOLOGY This residency position provides an exciting opportunity for a veterinarian interested in a career in veterinary clinical microbiology and wishing to further develop their skills whilst studying for diploma level qualification. This clinical training position is based in the Veterinary Microbiology Diagnostic Laboratory (VMDL), within the Department of Veterinary Anatomy, Physiology and Pathology within the Institute of Infection, Veterinary and Ecological Sciences (IIVES) at the University of Liverpool’s Leahurst Campus on The Wirral. The VMDL is an Approved Training Centre of the European College of Veterinary Microbiology (ECVM) and you will receive a broad practical and theoretical training in veterinary clinical microbiology, hospital infection control, clinical teaching and research. Residents are expected to apply to register with the ECVM; after 36 months of continuous attendance, they will become eligible to take the qualifying examination (Dipl.ECVM). Please note that applicants must hold a veterinary qualification from the European Association of Establishments for Veterinary Education (EAEVE) and hold or be eligible for membership of the Royal College of Veterinary Surgeons. This post is fixed term until 14th August 2028. Commitment to Diversity The University of Liverpool is committed to enhancing workforce diversity. We actively seek to attract, develop, and retain colleagues with diverse backgrounds and perspectives. We welcome applications from all genders/gender identities, Black, Asian, or Minority Ethnic backgrounds, individuals living with a disability, and members of the LGBTQIA+ community. Closing date: 31 August 2025. For full details and to apply online, please click the APPLY button

Job Description Job Summary The Quality Assurance Associate Director will support a technical team interfacing between our Company and External Partners in the Biologics Drug Substance and Drug product manufacturing area. This individual will be responsible for ensuring that all quality assurance processes, and compliance requirements are met during technical transfers to and from External Partners and throughout the continuous commercial manufacturing process at External Partner sites. Key Responsibilities Quality Oversight Report to the Quality lead (or delegate) and provide general direction on quality goals and objectives, functioning independently to ensure oversight of all quality-related issues at External Partner site. Regulatory Compliance Ensure that all quality assurance activities comply with regulatory requirements (FDA, EMA, etc.) and internal quality standards throughout the product lifecycle, including during facility start-up and technical transfers. Manufacturing Support Provide ongoing quality support to External Partners by resolving quality issues, performing proactive analysis of process performance, and developing plans to ensure compliance and quality meet capacity needs. Collaboration Work collaboratively with Biologics Quality Operations and other relevant teams within the Focused Factory to support the product lifecycle and address quality-related matters. Validation Strategies Support and oversee validation strategies for new and existing products, ensuring compliance with best practices in quality assurance. Technical Review Conduct a calibrated technical review of External Partners’ process change requests, deviations, protocols, and Master Batch Record changes to ensure compliance with quality standards. Issue Resolution Troubleshoot quality-related manufacturing issues and support investigations using scientific problem-solving methodologies. Efficiency Improvement Work with Operations, Quality, and External Partners to develop more efficient methods to meet regulatory requirements while ensuring quality standards are upheld. Quality Management System Ensure adherence to the highest quality, compliance, and safety standards by participating in and complying with our Manufacturing Division Quality Management System requirements. Partner Engagement Collaborate with External Partners to achieve business goals while fostering a common culture that prioritizes quality and compliance for both organizations. Education Minimum Requirement Bachelor’s or master’s degree (or equivalent) in Chemical/Biochemical Engineering, Biotechnology, Microbiology, Pharmaceutical Science, Life Sciences, or a related field. Required Experience And Skills Proven experience in highly regulated manufacturing environments with a minimum of 15 years of experience in quality assurance within biopharmaceutical operations, particularly related to Drug substance and drug product manufacturing and validations. Strong knowledge of quality systems, regulatory compliance, and quality assurance practices in the biopharmaceutical industry. Familiarity with change management processes and regulatory support planning. Experience in process validations, cleaning validations, and the associated quality documentation requirements. Proficiency in large molecule manufacturing, in process controls, analytical testing, validations, batch records review and release. Ability to perform risk assessments and develop strategies for continuous improvement initiatives. Proficient in computer system validations, equipment validations, area qualification, Audits, batch release procedures. Effective communication skills for managing partnerships and addressing quality concerns. Preferred Experience And Skills Familiarity with high-performance organizational tools and a strong understanding of digital manufacturing processes, computer system validation requirements, and quality management within biologics production and quality. Experience with quality management software and metrics analysis to drive performance improvements. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Hybrid Shift Valid Driving License Hazardous Material(s) Required Skills Adaptability, Adaptability, Biotechnology, Change Management, Cross-Cultural Awareness, Cross-Functional Teamwork, Digital Manufacturing, GMP Training, Good Distribution Practice (GDP), Immunochemistry, Inspection Readiness, IS Audit, Management Process, Manufacturing Compliance, Manufacturing Environments, Manufacturing Quality Control, Microbiology, Product Lifecycle, Quality Assurance (QA), Quality Auditing, Quality Management, Quality Management Standards, Quality Metrics, Quality Standards, Quality Systems Compliance {+ 2 more} Preferred Skills Job Posting End Date 08/11/2025 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. Requisition ID R357786

Internship Opportunity – Food Tech & Microbiology (Production Level) – Frusome, MAK Foods Frusome, a brand by MAK Foods, is a fast-growing startup offering real fruit-based fruit creams as a healthier, cold-served dessert option. We are currently looking for enthusiastic interns from Food Technology or Microbiology backgrounds to join us at our production unit in Laxmi Nagar, East Delhi. This is a hands-on, production-level internship where selected candidates will work directly in the daily preparation and processing of our fruit cream. Responsibilities include assisting with mixing, filling, and sealing operations, maintaining hygiene and food safety standards, checking temperature and pasteurization cycles, performing basic quality checks like pH and microbial observations, and helping with new flavor trials and production documentation. The internship offers practical exposure to real-time batch production, cold-chain management, and compliance with food safety standards. Ideal candidates should be pursuing B.Tech/B.Sc. in Food Tech, Microbiology, or related fields, be physically fit for production floor work, and eager to learn startup-level multitasking. Duration of the internship is 1–3 months, and while it is unpaid or performance-based, interns will receive a certificate, letter of recommendation, and possible future placement opportunities.

The Center for Advanced Neurological Research at KS Hegde Medical Academy, a constituent college of NITTE (Deemed-to-be University) in Mangalore, Karnataka, is looking for a Scientist Grade 1. The research center, led by Professor Lekha Pandit, a renowned clinician researcher, focuses on autoimmune central nervous system disorders. Professor Pandit has patented two diagnostic live cell based assays for antibody mediated CNS demyelinating disorders. The current research at the center includes molecular biomarkers, microbial influences on CNS demyelinating disorders, and animal models of disease. This position offers the opportunity to enhance research abilities, translate clinical findings to basic science research, and collaborate on international studies. Candidates with expertise in microbiology/molecular biology, particularly in cell culture and flow cytometry, with a minimum of one year postdoc experience in India/Abroad and a proven track record of research publications are preferred. The ideal candidate should possess strong research skills and a commitment to teamwork in a disciplined environment. The salary for this position is as per norms. The qualification required is M.Sc and Ph.D. Interested and eligible candidates are invited to apply by sending their CV to lekhapandit@nitte.edu.in by October 31st, 2024.,

An Infection Control Nurse (ICN) plays a critical role in preventing and controlling infections within healthcare settings. As an Infection Control Nurse, you will be responsible for developing, implementing, and monitoring infection prevention and control programs within healthcare facilities. Working closely with healthcare teams, you will aim to prevent the spread of infections among patients, staff, and visitors while ensuring compliance with regulatory standards and best practices. Your key responsibilities will include developing and implementing infection control policies in collaboration with healthcare leadership, monitoring compliance with infection control protocols, guidelines, and regulations, educating staff on infection prevention measures, conducting surveillance of healthcare-associated infections (HAIs), leading outbreak investigations, and coordinating response efforts to contain and manage outbreaks effectively. Additionally, you will be involved in assessing and recommending appropriate resources for infection prevention activities, staying updated on emerging infectious diseases and best practices in infection prevention, collaborating with interdisciplinary teams to promote a culture of safety, and participating in research projects and quality improvement initiatives to enhance patient safety and outcomes. To qualify for this role, you should hold a Registered Nurse (RN) license, possess a Bachelor's or Master's degree in Nursing or a related field, and preferably have Certification in Infection Control (CIC). Experience in infection prevention and control, strong knowledge of epidemiology, microbiology, and infectious diseases, excellent communication, leadership, and problem-solving skills, as well as the ability to work collaboratively and independently in a fast-paced environment are essential. This is a full-time, permanent position with benefits such as health insurance, leave encashment, life insurance, paid sick time, paid time off, and Provident Fund. The work schedule is during the day shift with a yearly bonus offered. A Diploma is preferred for education, and at least 1 year of experience in nursing and a valid Nursing License are preferred qualifications. If you are looking to make a difference in infection prevention and control within a healthcare setting and possess the necessary qualifications and skills, we invite you to apply for the position of Infection Control Nurse.,

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 Manger - API Supply chain team Date: Jul 11, 2025 Location: Dewas API - Supplychain Company: Sun Pharmaceutical Industries Ltd Role: Senior Manger – API Supply chain team Qualification: B.E. (Chemical) – preferred OR M. Sc (Chemistry) / Biotechnology / Microbiology OR B.Sc.+ MBA (Operations) Experience: Chemical Engineer with 3-4 years of experience OR candidate from other educational background with 6-9 years of experience Department: API Supply chain team Industry Preference: Pharma, Chemical, Paint, Agro, Speciality Chemicals Job Location: Andheri, Mumbai Areas Of Responsibilities: Capacity Planning & Capacity Effective Utilization Campaign Planning Business Continuity – De risking Plan (OS to IH, IH to OS), AVD Plan Implementation Site Transfer- API & Intermediate Cost Reduction Batches – MRP -à Commercial Supply NPL, Filling & Query Batches Supply management SCM Process maturity - Norms Setting, Cost to Serve, Planning Master Data Controller Chronic Supply Issues Resolution Responsible for Team Development & people Management - Training/ capability development of team Internal Interactions (within the organization) - Plants, RA, Procurement, R&D , Quality, LCM Apply Now » Apply Now Start applying with LinkedIn Please wait...

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: Officer Date: Jul 11, 2025 Location: Baddi - Quality Control Company: Sun Pharmaceutical Industries Ltd Responsible for microbial analysis of Raw Material, Hold time samples and Finish Products & stability samples. Responsible for sampling & Microbial analysis of all types of water. Responsible for preparation of agar plates and planning for Environmental Air monitoring in Production Area, Dispensing Area, Sampling Area and in Microbiology laboratory. Responsible for microbial Assay (Antibiotic & Vitamins). Responsible for handling, operation and calibration Instruments used in Microbiology Laboratory. Responsible for online reporting/raw data compilation and completion of routine sample analysis in LIMS Responsible for preparation and Sterilization of Media and Sterilization of Glassware. Responsible for proper handling of microbial culture and ensure their sub culturing. Responsible for preparation of media as per requirements and maintain the log books and sterilization and verifying the proper sterilization by chemical indicator strips. Responsible for handling and Maintenance of all documents and records related to the routine work. Responsible for preparation the reports on time and giving to section in charge for checking and releasing on time. Responsible for daily verification of instruments. Responsible for maintenance of media and chemical reagents and to check their expiry and receiving. Responsible for monitoring of temperature, relative humidity and differential pressure. Responsible for fumigation of Microbiology Laboratory Responsible for monitoring the proper cleaning of micro lab including all the instruments inside the micro lab maintain the cleaning record or log books as per the SOPs. Apply Now » Apply Now Start applying with LinkedIn Please wait...

Job Description To ensure all the products manufactured and distributed by the bottling operation conform to the specifications through assurance of processes from supply to consumer. The QAE supports the identification, planning, documentation, and management of the practices, activities and resources needed to meet quality goals and objectives in a manner that enables management to assess quality performance. Job Responsibilities Responsibility for all quality management, and quality assurance activities in the bottling operation. Responsibility for adherence to Company guidelines and requirements in the supply, manufacturing and distribution processes. Responsibility for the conformance to specifications of the finished goods leaving the plant. Responsibility to monitor, assess and improve process capabilities in the plant Responsibility for conducting the required tests on raw materials, packaging materials, WIP and finished product at the specified frequencies. Responsibility for availability and calibration of inspection and testing equipment and chemical reagents. Responsibility for process control of the final syrup, water treatment Responsibility for raw material, ingredient and product identification and traceability. Responsibility for the implementation of GMP in the plant. Responsibility to document, implement and monitor a quality assurance system in accordance with the KORE Requirements. - Commitment to Development Commitment to Excellence Teamwork Planning and Execution Influencing Knowledge of the Business Job Requirement Minimum Education: Post Graduate in Microbiology. Minimum Experience: 2 - 3 years in a Microbiology in beverage industry.

Hello Candidate , We are #hiring for Project Research Scientist-I (Non Medical) ! Government Project Payroll company: - E Solutions Job role: - Project Research Scientist-I (Non Medical) ! Educational Qualification First Class M.Sc. In Life Sciences/Genetics/Clinical Research/Biostatistics from recognized University. Desirable Qualification Ph.D. in Life Sciences/Biotechnology/Microbiology with 2 years research experience, in immunology molecular biology techniques. No. of Vacancy :- 1 Age Limit: The upper age limit is 35 years Interested Candidate can share your CV on this Email ID :- anchal.g@esolglobal.com

Sales & Business Development Relationship Management Presentation & Counseling Skills Negotiation & Target-Driven Attitude Customer Service Orientation Team Collaboration Key Responsibilities: Educate pregnant women and families about stem cell preservation and its future health benefits. Counsel clients, answer their questions, and help them understand the scientific and emotional value of the service. Coordinate with doctors, gynecologists, and hospital staff to maintain smooth communication and support. Build Relationships with clients and hospital teams to promote awareness and trust in our services. Drive Enrollments by guiding and assisting parents through the decision-making and registration process Requirements Sales & Business Development Relationship Management Presentation & Counseling Skills Negotiation & Target-Driven Attitude Customer Service Orientation Team Collaboration Updated: 9 minutes ago

Educate pregnant women and families about stem cell preservation and its future health benefits. Counsel clients, answer their questions, and help them understand the scientific and emotional value of the service. Coordinate with doctors, gynecologists, and hospital staff to maintain smooth communication and support. Build Relationships with clients and hospital teams to promote awareness and trust in our services. Drive Enrollments by guiding and assisting parents through the decision-making and registration process Requirements Sales & Business Development Relationship Management Presentation & Counseling Skills Negotiation & Target-Driven Attitude Customer Service Orientation Team Collaboration

Sales & Business Development Relationship Management Presentation & Counseling Skills Negotiation & Target-Driven Attitude Customer Service Orientation Team Collaboration Key Responsibilities: Educate pregnant women and families about stem cell preservation and its future health benefits. Counsel clients, answer their questions, and help them understand the scientific and emotional value of the service. Coordinate with doctors, gynecologists, and hospital staff to maintain smooth communication and support. Build Relationships with clients and hospital teams to promote awareness and trust in our services. Drive Enrollments by guiding and assisting parents through the decision-making and registration process Requirements Sales & Business Development Relationship Management Presentation & Counseling Skills Negotiation & Target-Driven Attitude Customer Service Orientation Team Collaboration Updated: 2 minutes ago

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cepheid, one of Danaher s 15+ operating companies, our work saves lives and we re all united by a shared commitment to innovate for tangible impact. You ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher s system of continuous improvement, you help turn ideas into impact innovating at the speed of life. At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world s most complex health challenges. Together, we bring MORE change to the world. Learn about the Danaher Business System which makes everything possible. The Quality Control Analyst is responsible for ensuring inspection process as per MDR 2017, European regulations, ISO 13485 and Cepheid corporate quality system requirements. This position reports to the quality manager and is part of the quality and regularity compliance department located in Cepheid Manufacturing facility, Bengaluru and will be an on-site role. In this role, you will be responsible for: Perform inspections of incoming, in-process and finished products/stability testing and identify/troubleshoot product if non-conformance. Performs/monitor the laboratory equipment validation / calibration / maintenance and ensure quality control lab as per safety standards/GLP. Write/review SOP/WI, technical reports or documentation such as deviation reports, testing protocols, and trend analyses. Support for internal/external audit schedule, NC, CAPA for site. The essential requirements of the job include: Master s degree in Biochemistry, Molecular Biology, Microbiology, Biotechnology or related discipline and a minimum of 3+ years related to quality control experience. 2+ years experience in Vitro Diagnostics (IVD) is mandate. Need to act as competent technical staff for supervision the testing / analysis of diagnostic reagents & kits Business Schedule Requirement Must be flexible to work in shift-based time schedules (able to consistently maintain schedules and meet timelines). 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 Experience in leading continuous improvement efforts, in both quality systems and IVD products. Required strong interpersonal skills, effective communication skills / micro-soft word and excel knowledge / strong multi-tasking skill. Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. Join our winning team today. 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.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cepheid, one of Danaher s 15+ operating companies, our work saves lives and we re all united by a shared commitment to innovate for tangible impact. You ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher s system of continuous improvement, you help turn ideas into impact innovating at the speed of life. At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world s most complex health challenges. Together, we bring MORE change to the world. Learn about the Danaher Business System which makes everything possible. The Quality Control Analyst is responsible for ensuring inspection process as per MDR 2017, European regulations, ISO 13485 and Cepheid corporate quality system requirements. This position reports to the quality manager and is part of the quality and regularity compliance department located in Cepheid Manufacturing facility, Bengaluru and will be an on-site role. In this role, you will be responsible for: Perform inspections of incoming, in-process and finished products/stability testing and identify/troubleshoot product if non-conformance. Performs/monitor the laboratory equipment validation / calibration / maintenance and ensure quality control lab as per safety standards/GLP. Write/review SOP/WI, technical reports or documentation such as deviation reports, testing protocols, and trend analyses. Support for internal/external audit schedule, NC, CAPA for site. The essential requirements of the job include: Master s degree in Biochemistry, Molecular Biology, Microbiology, Biotechnology or related discipline and a minimum of 3+ years related to quality control experience. 2+ years experience in Vitro Diagnostics (IVD) is mandate. Need to act as competent technical staff for supervision the testing / analysis of diagnostic reagents & kits Business Schedule Requirement Must be flexible to work in shift-based time schedules (able to consistently maintain schedules and meet timelines). 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 Experience in leading continuous improvement efforts, in both quality systems and IVD products. Required strong interpersonal skills, effective communication skills / micro-soft word and excel knowledge / strong multi-tasking skill. Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. Join our winning team today. 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.