2560 Microbiology Jobs - Page 28

Job description Horizon Biolabs Pvt Ltd. is a GLP compliant Pharmaceutical Testing Laboratory located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices and packaging Industries . Candidates with Msc in Microbiology having minimum 6 years of experience in any reputed Pharma Testing Lab/ CRO /Pharmaceutical Industry . To be responsible for planning and organizing daily activities of the Microbiology laboratory functions to ensure the quality of products /test items in compliance with Quality and as per various regulatory requirements. Should be familiar with : Development and validation of Microbial enumeration test and test for specified microorganisms (MLT), Antimicrobial Effectiveness Test (AET/PET), Sterility, Bacterial Endotoxin Test (BET by Gel Clot & Kinetic methods) and Microbiological Assays. Water System Validations. Disinfectant Efficacy Test. Hand Sanitizer Efficacy Evaluation. Environmental Monitoring. Facility Qualifications (Water and Area) General responsibilities of Job includes: -To ensure that microbiological testing is performed as per guidelines. To ensure shifts and tests are scheduled so that required tests are performed on time and the results are provided on time. - To be on top of compliance with respect to regulatory requirements, to interpret applicable quality and regulatory requirements and develop associated policies for the laboratories operations. - To continuously investigate and trend invalid and Out-of-Specification results. - To ensure appropriate and timely corrective actions are implemented. - To evaluate external audit observations and develop responses and oversight for related action plans. - To ensure all established laboratory, regulatory, safety, and environmental procedures are followed. - To adhere to the standards of quality as per GMP, company Quality Policies and site SOPs standards. - To ensure good documentation practices in all aspects and phases of the work; provide reports for review in a timely manner; work with other lab personnel on projects and participate in (OOS) Out-of Specification and failure investigations. - To maintain the safety and orderliness of the lab; apply knowledge of cGMPs and GLPs on a daily basis. Others : - To provide training on laboratory methods and the team members. - To ensure documentation and data trending activities. Team Management : - To guide and mentor the associates. - To review their performance on regular basis and provide feedback for improvement Job Type: Full-time Schedule: Day shift Education;MSC/BSC(Microbiology) Location: Hyderabad(Required) Requirment: Candidates having experience in any reputed Pharma Testing Lab/ CRO /Pharmaceutical Industry need apply .Candidates applied previously applications will not considered. Immediate Joiners only(7-10 days) Experience: total work: 6-8 years (Required) Job Type: Full-time Pay: ₹45,000.00 - ₹60,000.00 per year Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Application Question(s): You have knowledge in Microbial enumeration test and test for specified microorganisms (MLT), Antimicrobial Effectiveness Test (AET/PET), Sterility, Bacterial Endotoxin Test (BET by Gel Clot ), Sterility, Environmental Monitoring and Microbiological Assays, Water validation.Are you residing in Hyderabad? Are you from Hyderabad?Are Immediate Joiner(7-10 days) candidates applied previously need not apply again and those applications will not considered. Experience: Pharma Testing Lab/ CRO /Pharmaceutical Industry : 5 years (Preferred) Location: Hyderabad, Telangana (Required) Work Location: In person

Company Description Transasia Bio-Medicals Ltd., headquartered in Mumbai, India, is recognized as India’s largest In-vitro Diagnostic Company, offering solutions in various fields including Biochemistry, Hematology, Coagulation, ESR, Immunology, Urinalysis, Critical Care, Diabetes Management, Microbiology, and Molecular Diagnostics. Leading the way in accurate and quality diagnostics since 1979, Transasia provides a broad spectrum of diagnostic products in Clinical Chemistry, Hematology, Immunology, Blood Banking, among others. The company has built a reputation for innovation and trust over four decades, with 60% of sales coming from repeat customers. Best-in-class hospitals and lab-chains rely on Transasia's solutions to optimize clinician productivity and improve patient care. Role Description This is a full-time, on-site role for a Senior Application Specialist-IVD at Transasia Bio-Medicals Ltd., located in Kolkata. The Senior Application Specialist-IVD will be responsible for providing technical and application support, troubleshooting issues, and offering training and demonstrations to clients. Day-to-day tasks include ensuring proper functioning of diagnostic systems, addressing customer inquiries, and collaborating with the technical and sales teams to enhance customer satisfaction. Qualifications Strong Analytical Skills and capability to perform troubleshooting Proficiency in Application Support and Technical Support Excellent Communication skills Bachelor's degree in Biomedical Engineering, Biotechnology, Medical Laboratory Technology, or related field Experience in the In-vitro Diagnostics (IVD) industry is a plus Ability to work independently and as part of a team Availability to travel as required

Profile Mahatma Gandhi Medical Advanced Research Institute (MGMARI), Sri Balaji Vidyapeeth, Pondicherry, invites applications for its two-year M.Sc. program in Medical Biotechnology and Bioinformaticsa unique opportunity to train in a research-driven environment with cutting-edge laboratories, expert faculty, and world-class academic resources. Rooted in a strong foundation of science, medicine, informatics, and engineering, the program is designed to nurture curious minds and welcomes applicants from diverse academic and professional backgrounds, including industry. Join a campus that thrives on innovation, collaboration, and academic freedomand take the next step in your scientific journey. More details about the program and admission process can be found at: https://sbvu.ac.in/mgmari/admi Apply now and become part of the next generation of biomedical innovators! Qualification Bachelors degree in an appropriate field of science such as B.Sc. in Life Sciences / Bioscience / Botany / Zoology / Biochemistry / Microbiology / Biotechnology / Bioinformatics / Biomedical Sciences / BE / B.Pharm / MBBS / BDS / BAMS or any other allied health science discipline with a background in biology related subjects with a minimum of 50 PERCENT marks. To Apply For more details click here.

Job Description Wondering whats within Beckman Coulter Diagnostics? Take a closer look. At first glance, youll see that for more than 80 years weve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. Were building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and youll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, were working at the pace of change to improve patient lives with diagnostic tools that address the worlds biggest health challenges. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru BDC and will be an on-site role. In This Role, You Will Have The Opportunity To Lead and manage the sustaining engineering activities for Electro-Mechanical products. Assist in the design and development of innovative mechanical solutions to improve performance, safety, reliability, throughput and cost-effectiveness (Knowledge of Should costing and estimation), in Design Change Project. Act as design change lead and ability to handle entire Design change process independently. Handle multiple projects with proper project planning and minimal guidance. Mentor and guide junior engineers and technicians provide technical leadership and actively transfer knowledge/expertise. Conduct root cause analysis and implement corrective actions for product issues. Collaborate with cross function teams, manufacturing, quality, and supply chain teams to resolve production and field issues. Conduct feasibility studies, risk assessments, and design reviews to ensure project success and validate designs through analysis and testing. The essential requirements of the job include: Bachelors degree in mechanical engineering or a related field with 7 years of experience and working with global teams. Strong knowledge of mechanical design principles, materials, manufacturing processes and Proficiency in SolidWorks CAD software and simulation tools. Knowledge of Tear down analysis and Reverse engineering, dFMEA/pFMEA, DFX, Tolerance Stack-up Analysis and GD&T, Create and maintain detailed engineering documentation, including CAD models, drawings, specifications, test plans. Experience with medical device regulations (FDA, ISO 13485, ISO 14971, IEC 60601) and Ensure compliance with industry standards, regulations, and company policies. Basic knowledge of metals and materials, its application knowledge on mechanical parts fabrication, Rapid prototyping and testing. Thorough knowledge on Selection of mechanical Off-the shelves components. Manage interactions with suppliers to ensure quality and timely delivery of components. Strong communication, interpersonal skills and Stakeholder management. Should have good Analytical skills, Excellent problem-solving skills and attention to detail. Ability to work effectively in a fast-paced, dynamic environment. Understand technical operations and make efficient decisions on routine engineering matters. Able to swiftly adapt to changes in project direction from management. It would be a plus if you also possess previous experience in: Experience in medical device design & development is a plus. Experience in IVD instrumentation, such as clinical chemistry, immunoassay, hematology, urinalysis, molecular, microbiology or flow cytometry systems is a plus. Advanced certification in CAD tools. Familiarity with lean manufacturing and Six Sigma principles. Prior work experience in Electro-Mechanical products, Robotics and Automation. Join our winning team today. Together, well accelerate the real-life impact of tomorrows 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.

Job Category Job Type: Job Location: Salary Years of Experience: Position Overview This position plays a vital role within the Payment Integrity team by contributing to the development, enhancement, and maintenance of medical policy content. The role is responsible for converting healthcare guideline-driven concepts into system-readable configurations and performing comprehensive testing to ensure accuracy. Responsibilities include configuration and testing, ensuring adherence to industry standards, and collaborating with cross-functional teams to validate outputs and maintain quality. This role needs passionate people with good interpersonal, analytical & problem-solving skills. Having hands-on expertise in one or more of the following areas is an added advantage. Payment Integrity. Clinical Coding. Medical Coding. Denials Management. Key Responsibilities Analyze and interpret concepts to ensure accurate configuration in line with medical coding, billing, and reimbursement guidelines. Analyze medical coding, reimbursement guidelines and configure logic to support accurate concept execution. Conduct in-depth reviews of contracts, policies, and federal/state regulations to formulate edit requirements. Apply industry coding guidelines to claims processes effectively. Demonstrate experience in analyzing and resolving coding issues for payment integrity purposes. Analyze, develop, and implement system configurations. Collaborate with subject matter experts (SMEs) and technical teams to translate regulatory and policy requirements into functional edit specifications. Translate editing logic into platform configurations with support from SMEs, and stakeholders to ensure clear understanding and configuration of concepts. Collaborate with cross-functional teams to assess configuration needs and implement appropriate solutions. Assist in developing and maintaining payment integrity policies and procedures. Review configurations to ensure completeness and accuracy based on the medical coding and billing guidelines. Troubleshoot and perform root-cause analysis for edit logics not functioning as intended. Effectively pinpoint configuration discrepancies and ensure concepts are deployed successfully and on schedule. Audit and validate concepts against healthcare guidelines; identify and address gaps with upstream teams. Conduct rigorous testing to verify concept accuracy and performance across outpatient, professional, and inpatient claim scenarios adhering to the coding guidelines. Perform acceptance testing to validate configuration accuracy. Stay updated with industry regulations and compliance requirements to ensure the configuration process adheres to relevant standards. Perform duties independently with a high level of accuracy and professionalism. Exhibit detail-oriented mindset with a focus on quality and accuracy in concept configuration & testing. Familiarity with AI tools and prompt engineering to support medical content development, automation of policy logic, and Concept generation. Design and optimize prompts for large language models (LLMs) to generate accurate and clinically relevant medical content. Experience in utilizing AI tools (e.g., Gemini, NotebookLLM, ChatGPT, Claude, Perplexity, Grok, Bard, or custom LLMs) to assist in ideation, content creation, review, summarization, and validation. Key Skills Domain Expertise in US Healthcare Medical Coding, Medical Billing, Payment Integrity, Revenue Cycle Management (RCM), Denials Management. Codeset Knowledge like CPT/HCPCS, ICD, Modifier, DRG, PCS, etc. Knowledge on policies like Medicare/Medicaid Reimbursement, Payer Payment Policies, NCCI, IOMs, CMS Policies etc. Proficiency in Microsoft Word and Excel, with adaptability to new platforms. Excellent verbal & written communication skills. Excellent Interpretation and articulation skills. Strong analytical, critical thinking, and problem-solving skills. Willingness to learn new products and tools. Strong time management skills and ability to meet deadlines. Qualifications: Education & Certification (one of the following required): Bachelor of Science in Nursing (B.Sc. Nursing). Pharmacist Degree (B.Pharm, M.Pharm or PharmD). Life science Degree (Microbiology, Biotechnology, Biochemistry, etc). Medical Degree (e.g., MBBS, BDS, BPT, BAMS etc). Other Bachelors Degree with relevant experience. Certification Requirements Candidates with certifications like CPC, CPMA, COC, CIC, CPC-P, CCS, or any specialty certifications from AHIMA or AAPC will be given preference. Additional weightage will be given for AAPC specialty coding certifications. Experience 0-1 years of experience in Payment Integrity, Medical Coding, Denial Management. Experience in payment integrity, claims processing, or related functions within the US healthcare system. Experience in denial management, retrospective payment audits, or medical coding. Familiarity with Medical coding guidelines, such as ICD, CPT, Modifiers, Medicare, Medicaid, or commercial payer guidelines. Work Location: Jayanagar Bangalore. Work Mode: Work from Office. Benefits Best-in-class compensation. Health insurance for Family. Personal Accident Insurance. Friendly and Flexible Leave Policy. Certification and Course Reimbursement. Medical Coding CEUs and Membership Renewals. Health checkup. And many more!

JOB DESCRIPTION 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 Danahers 15 operating companies, our work saves livesand were all united by a shared commitment to innovate for tangible impact. Youll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danahers 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, youll 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 worlds 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: Masters 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 / Microsoft 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 its 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, well accelerate the real-life impact of tomorrows 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.

Rylaq is at a pivotal growth stage, launching our new vertical for natural astaxanthin production from Haematococcus pluvialis. We are seeking an visionary and results-driven Director of Cultivation & Extraction to lead this critical new venture from concept to commercial scale. This is a unique, ground-floor opportunity for an experienced leader to build a world-class operation and participate directly in the company's success. What You Will Do: Strategic Leadership: Define and execute the end-to-end strategy for Haematococcus pluvialis cultivation in closed photobioreactors (PBRs), specifically leveraging bubble column bioreactor technology for optimal growth and astaxanthin induction. R&D and Optimization: Lead ongoing research and development efforts to optimize Haematococcus strains, nutrient media, light regimes, temperature control, CO2 supply, and stress induction protocols for maximum astaxanthin yield and quality. Facility Design & Setup: Oversee the design, procurement, installation, and commissioning of state-of-the-art PBR systems, harvesting equipment, and initial extraction facilities within our 2000 sq ft dedicated microalgae cultivation space. Process Development & Scaling: Develop, standardize, and scale up robust cultivation protocols from pilot to commercial production levels. Extraction & Downstream Processing: Implement and optimize efficient, cost-effective methods for biomass harvesting, cell disruption, and astaxanthin extraction to ensure high purity and recovery. Quality Assurance & Control: Establish stringent QC/QA protocols for all stages, from inoculum to final product, ensuring compliance with relevant industry standards (e.g., FSSAI, GMP where applicable). Team Building & Management: Recruit, train, and mentor a high-performing team of scientists, engineers, and technicians. Innovation & IP: Drive continuous innovation and contribute to the company's intellectual property portfolio related to Haematococcus cultivation and astaxanthin extraction. Sustainability & Efficiency: Ensure all processes adhere to Rylaq's commitment to sustainability, resource efficiency, and circular economy principles. Cross-Functional Collaboration: Work closely with the R&D, operations, and business development teams to align production with market needs. What We Are Looking For: Educational Background: Ph.D. or Master's degree in Biotechnology, Chemical Engineering, Microbiology, Algal Biotechnology, or a related field. Experience: Minimum 8-12 years of hands-on, progressive experience in microalgae cultivation, with at least 3-5 years specifically focused on Haematococcus pluvialis and astaxanthin production at a significant scale (pilot to commercial). Proven expertise in designing, operating, and optimizing closed photobioreactors (PBRs), particularly bubble column systems. Demonstrable experience in microalgae harvesting techniques (centrifugation, filtration) and downstream processing for biochemical extraction (cell disruption, solvent/solvent-free extraction of astaxanthin). Strong understanding of algal physiology, biochemistry, and bioprocess engineering. Leadership: Proven track record of leading and mentoring technical teams, managing complex projects, and driving innovation in a dynamic environment. Problem-Solving: Exceptional analytical and problem-solving skills with a practical, hands-on approach. Regulatory Knowledge: Familiarity with quality standards and regulatory requirements for nutraceuticals or food ingredients in India. Pioneering Spirit: Highly self-motivated, adaptable, and thrives in a fast-paced, startup environment. Location: Remote initially and Willingness to travel to to Palakkad, Kerala, for on-site presence. Compensation: This is an equity-only position designed for a visionary leader passionate about pioneering the future of sustainable biotechnology. You will receive a significant equity stake in Rylaq Private Limited, directly aligning your success with the company's growth and value creation. Full details of the equity vesting schedule and terms will be discussed with qualified candidates. Why Join Rylaq? Impact: Play a foundational role in building a cutting-edge, sustainable industry from the ground up in India. Ownership: Direct ownership in the company's success through substantial equity. Innovation: Work at the forefront of microalgae technology with a focus on high-value products. Mission-Driven: Be part of a team committed to environmental sustainability and health. Growth: Immense personal and professional growth potential within a rapidly expanding startup. If you are a bold innovator, a hands-on leader, and believe in the power of microalgae to transform industries, we invite you to be a part of Rylaq's journey. Rylaq is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Job Title: Lecturer – Microbiology (Part-Time) Department: Department of Graduate Studies offering PG Diploma in Hospital Administration, B.Voc. degree programms in MLT & CSSD and certificate programme in Phlebotomy . Location: Wellcaza School of Health Sciences, Elamakkara, Kochi, Kerala Mode: Offline (On-campus) Engagement Type: Part-Time (3 hours/week, up to 3 weeks/month or may be more depending upon module completion or may be decided by the Dean of the institute as required ) Job Summary: Wellcaza School of Health Sciences invites applications for the position of Part-Time Lecturer in Microbiology to support its undergraduate allied health sciences programs and postgraduate diploma programmes. This role is ideal for recently retired faculty members or early-career postgraduates with a strong passion for teaching. The appointed lecturer will be responsible for delivering high-quality offline (on-campus) classes in medical microbiology, particularly focusing on diagnostic and medical microbiology subjects taught in B.Voc and B.Sc. MLT or allied health programs. Key Responsibilities: Conduct in-person theory classes in microbiology for undergraduate students enrolled in B.Voc and allied health science programs. Deliver content aligned with curriculum covering general, clinical, and diagnostic microbiology topics. Prepare and administer academic content including lecture notes, presentations, and class assessments. Assist in curriculum enhancement and practical's planning or clinical posting related to the microbiology subject area. Eligibility Criteria: Essential Qualifications: M.Sc in Microbiology (Medical / Clinical / Diagnostic / General) Experience Requirements: For General Microbiology Degree Holders (Non-medical): Minimum 6 months of hands-on experience in a diagnostic clinical microbiology laboratory of NABL accredited lab in India or a Hospital, OR Teaching experience in allied health science colleges/universities handling courses like B.Sc MLT, B.Sc Microbiology, or equivalent. For All Other Candidates: Recently retired faculty from medical colleges holding MD Microbiology / allied health science colleges are strongly encouraged to apply. Current faculty members in any allied health sciences colleges may also apply if willing to take weekend or Friday classes. Preferred Candidate Profile: Early-career professionals with a flair for teaching and solid subject knowledge. Retired faculty with demonstrated teaching experience and subject expertise. Working Schedule & Commitment: Maximum Commitment: 3 hours/week Teaching Period: Up to 3 weeks per month Teaching Days: Preferably Fridays or weekends (negotiable) Mode: Fully offline (No online classes allowed) Remuneration: Competitive honorarium based on qualifications and experience. Details will be shared during the interview process. How to Apply: Interested candidates may send their updated CV, along with a cover letter and relevant experience/qualification certificates, to: institute@wellcaza.com/job platforms. Job Type: Part-time Pay: Up to ₹1,000.00 per hour Expected hours: No more than 3 per week Benefits: Flexible schedule Schedule: Day shift Morning shift Supplemental Pay: Overtime pay Work Location: In person Application Deadline: 15/08/2025 Expected Start Date: 15/09/2025

Date: 7 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Essential Functions Job Description Job Title: QC Microbiology Reviewer Job Location: Bangalore About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene’ s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose Of The Role Static data creator/ reviewer for LIMS Facing regulatory and client audits, ensuring audit compliance Microbial Method Validation, Method verifications Microbiology analysis (Bioburden, MLT, Test for specified organisms, BET analysis) Sterility testing and validation Environmental/Utility Monitoring data review Microbiology lab maintenance Calibrations, Qualifications Review of Microbiology data Media and culture qualifications data review and planning Handling QMS in Microbiology lab Role Accountabilities Responsible for Microbiological analysis, Sterility testing, Bacterial Endotoxin Test and analysis of different grades of water (PW/WFI/POW) as per the respective specification. Responsible for risk assessment documents preparations, Protocol and reports preparation Responsible for QMS related to microbiology – change controls, CAPA, deviations, incidents, OOS/OOT investigations Responsible for Area qualification, calibrations, equipment qualifications and requalification Responsible for sample management and coordination with team for smooth operation of samples release activity. Responsible to perform the Bioburden and Microbial Limit Test. Responsible to perform the Method verification activity for Sterility, BET, MLT and Bioburden test. Responsible for ensuring environmental monitoring of clean rooms in Microbiology laboratory. Responsible for review of microbiology documents Responsible for preparation of specifications and STP. Responsible for preparation of protocols and reports Audit trail review Preparation and planning of sampling schedule Interaction with clients Ready to work in shifts and supervising the shift analyst activities Well versed with LIMS and electronic documents execution and review. Follow the required EHSS policies and Good hygiene practice. Undertake other responsibilities related to Microbiology as per requirement. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Accountabilities as a Syngene Leader (only for Leadership Hires) Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities. Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance. Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority. Specific requirements for this role Experience : Demonstrated Capability : Education : Experience : 9-10 yrs YEARS Skills And Capabilities Microbial analysis of water, OSD products, Injectable products, Environmental monitoring Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team Good speaking-listening-writing skills, attention to details, proactive self-starter Ability to work successfully in a dynamic, ambiguous environment Ability to meet tight deadlines and prioritize workloads Ability to develop new ideas and creative solutions Should be able to work in team and flexible for working in shifts Should be a focused employee Good documentation capability Education : M.Sc. Microbiology Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

We are a leading diagnostic laboratory chain with accreditation from the National Accreditation Board for Hospitals (NABH). Our branches are located at Pothencode, Kanyakulangara, Venjaramood, and Kallara. We offer a wide range of laboratory tests at affordable prices, covering over 650 individual tests across various medical disciplines. We are seeking smart, adaptive, and confident candidates who are nearby and can commute to any of our branches. Candidates should have some experience in the medical field or be willing to undergo an unpaid training period of at least 1 month. Responsibilities include participating in day-to-day operations, learning new tasks, taking up additional responsibilities as needed, conducting home visits as part of our collection facility, and maintaining safety and quality standards. Preferred qualifications include at least 1 year of experience, a valid 2-wheeler license, and proximity to our branches. The job type is full-time, with benefits such as health insurance and leave encashment. The work schedule includes day, evening, morning, and rotational shifts. Applicants are required to have a Bachelor's degree and be proficient in Malayalam and English. Additionally, candidates should be able to answer questions about their university and commuting preferences to our branches. Please note that we do not provide hostel facilities, and our shift timings are 6:30 a.m. to 2:30 p.m. and 11:30 a.m. to 7:30 p.m.,

Basic Qualification : Graduate or Post Graduate in Science (Life Sciences, Microbiology, Biotechnology, Pharmacy, BDS, BHMS, BAMS, MBBS etc) Additional Qualification : Post Graduate Diploma in Clinical Research Experience: Prior experience particularly in clinical research, is preferable Skills: Strong organizational and time management skills with excellent communication (written and verbal). Proficiency in data management, medical terminology, and regulatory knowledge is also crucial. Job Roles and Responsibilities: Trial Management Participant Recruitment and Enrolment Data Management - Maintaining Study Documents,analysis Ensuring Data Quality Communication and Collaboration: with principal investigators, research team members, sponsors, and regulatory agencies. Adverse Event Reporting May also be involved in managing the trial budget and tracking expenses. Report Preparation Following Study Protocols Maintaining Study Documents Ensuring Data Quality Ensuring adequate supplies are available for study procedures.

Overview of the role: Alvotech is currently seeking a Quality Control scientist in the Microbiology Lab to join our Microbiology team in Reykjavik. QC Microbiology scientist is responsible for various microbiological testing, ensuring that the testing related to microbial analysis are conducted accurately, efficiently, and in compliance with regulatory standards, particularly Good Manufacturing Practices (GMP) to support manufacturing operations and shows thorough understanding of various techniques and microbial processes. Scope and responsibility: Performs routine microbial testing with advanced techniques to support manufacturing during 24/7 operations (shift-based work schedule). Execute endotoxin and bioburden testing Plate reading activities Sampling Environmental and Utility monitoring samples Execution of method and product verifications Management of identifications, microbial cultures and maintenance Performing routine cleaning, verification, reviews, stock checks, and upkeep of laboratory and equipment Participate as required in Aseptic Process Simulation Activities Support quality events such as CAPAs, Deviations, Change controls and laboratory investigations. Participation in the creation and maintenance of quality documents within Alvotech. Contributes to other documentation reviews and/or updates within the Quality management system, as Subject matter expect. Job requirements: BSc or M.Sc in Microbiology or relevant scientific discipline 1-5 years of experience in Pharmaceutical or Biopharmaceutical industry and a direct experience in the field of Microbiology. Strong understanding of microbial processes and regulatory compliance Good conceptual, problem solving, and organizational skills - must be detail-oriented, well organized, and able to work independently and in teams Knowledge of Good Manufacturing Practices (GMP) and documentation Rules is an asset. Proficient in using a PC and common Microsoft packages such as Word and Excel. Ability to work on a shift-based pattern work schedule What we offer: An inspiring challenge to work with great co-workers on ambitious projects that change peoples lives. The chance to be a part of a global and fast-growing company. An international work culture that encourages diversity, collaboration, and inclusion. Positive, flexible, and innovative work environment. Support for personal growth and internal career development. Company social events and milestone celebrations. Excellent in-house canteen and coffee house. Exercise and well-being support for full-time employees. On-site shower facility. Transportation grant towards eco-friendly modes of travel for full-time employees. Internet at home for full-time employees. Why Alvotech We at Alvotech are passionate about improving lives by increasing access to affordable biologics. We re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity, and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work, and empowered to succeed in an agile environment. True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds, regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let s create a healthier world together through affordable biologic medicines.

Overview of Role Alvotech is currently seeking a Quality Control senior scientist in the Microbiology Lab to join our Microbiology team in Reykjavik. QC Microbiology senior scientist is responsible for various microbiological testing, ensuring that the testing related to microbial analysis are conducted accurately, efficiently, and in compliance with regulatory standards, particularly Good Manufacturing Practices (GMP) to support manufacturing operations and shows thorough understanding of various techniques and microbial processes. Additionally senior scientist supports variosu projects with new product introduction, laboratory investigations and overall improvement projects within the team. Scope and responsibility Performs routine microbial testing with advanced techniques to support manufacturing during 24/7 operations (shift-based work schedule). Execute endotoxin and bioburden testing Plate reading activities Sampling Environmental and Utility monitoring samples Execution of method and product verifications Management of identifications, microbial cultures and maintenance Performing routine cleaning, verification, reviews, stock checks, and upkeep of laboratory and equipment Aseptic practices Participate as required in Aseptic Process Simulation Activities Support and lead quality events such as CAPAs, Deviations, Change controls and laboratory investigations. Creation of testing protocols and reports Participation and leading in creation and maintenance of quality documents within Alvotech. Training of personele Contributes to other documentation reviews and/or updates within the Quality management system, as Subject matter expect. Job requirements M.Sc in Microbiology and/or other relevant scientific discipline 5+ years of experience in Pharmaceutical or Biopharmaceutical industry and a direct experience in the field of Microbiology. Strong understanding of microbial processes and regulatory compliance Good conceptual, problem solving, and organizational skills - must be detail-oriented, well organized, and able to work independently and in teams Knowledge of Good Manufacturing Practices (GMP) and documentation Rules is an asset. Proficient in using a PC and common Microsoft packages such as Word and Excel. Ability to work on a shift-based pattern work schedule What we offer: An inspiring challenge to work with great co-workers on ambitious projects that change peoples lives. The chance to be a part of a global and fast-growing company. An international work culture that encourages diversity, collaboration and inclusion. Positive, flexible, and innovative work environment. Support for personal growth and internal career development. Company social events and milestone celebrations. Excellent in-house canteen and coffee house. Exercise and wellbeing support for full-time employees. On-site shower facility. Transportation grant towards eco-friendly modes of travel for full-time employees. Internet at home for full-time employees. Why Alvotech At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment. True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let s create a healthier world together, through affordable biologic medicines.

Company Description At Tricusp Diagnostics, we are dedicated to delivering accurate, timely, and high-quality diagnostic services to support better healthcare outcomes. As a leading pathology lab, we combine advanced medical technology with a patient-first approach to ensure reliability, transparency, and excellence in every test we perform. Our services include routine blood and urine tests, biochemistry, hematology, immunology, microbiology, serology, and specialized diagnostic testing. We pride ourselves on our modern lab infrastructure, certified and experienced medical professionals, strict quality control protocols, and fast turnaround times with digital report access. Role Description This is a full-time on-site role for a Senior Sales Executive located in Patna. The Senior Sales Executive will be responsible for identifying and developing new business opportunities, maintaining and expanding relationships with existing clients, and meeting sales targets. The role involves regular field visits, conducting presentations and demonstrations of Tricusp Diagnostics' services, and working closely with the marketing team to execute sales strategies. Additional responsibilities include providing excellent customer service and support, preparing sales reports, and staying updated on industry trends and competitor activities. Qualifications Proven experience in Sales, preferably in the healthcare or diagnostics industry Strong business development and client relationship management skills Excellent verbal and written communication skills Ability to conduct presentations and demonstrations Knowledge of diagnostics and pathology services is a plus Proficiency in Salesforce or similar CRM software Strong analytical and problem-solving skills Bachelor’s degree in Business, Marketing, or a related field Willingness to travel within the region as required

Applications are invited for the Post of Project Technical Support-III for the ICMR Funded Project in the School of Bio Sciences and Technology (SBST), at Vellore Institute of Technology (VIT), ( IIRP-2023-3019 dated 04-04-2025) Title of the Project : Preparation and Evaluation of Wound Dressing Material and Topical Ointment Using Magnetosome Conjugated Lemon Grass Extract (MLGE) Qualification : First Class Post-Graduate (PG) Degrees (M.Tech., M.Sc.,) degrees in Biotechnology /Botany /Microbiology or equivalent Describe if any Candidates having knowledge and hands-on experience in the area of animal work/herbal formulations / nanoformualtions / cell culture work will be preferred. Publication records relevant to the field. Fluent in English, both written and spoken. Stipend : Rs. 28,000/- + 10% HRA of Rs. 2800/- Total Rs. 30,800/- per month Sponsoring Agency : ICMR Duration : 11 Months or till the completion of project Principal Investigator : Dr. K. Suthindhiran , Professor, Department of Biomedical Sciences, School of Bio Sciences and Technology Vellore Institute of Technology (VIT), Vellore - 632 014, Tamil Nadu. Co-Principal Investigator : Dr. M. A. Jayasri, Associate Professor, Department of Biomedical Sciences, School of Bio Sciences and Technology Vellore Institute of Technology (VIT), Vellore - 632 014, Tamil Nadu. 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 ( 16/04/2025) through online 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.

Designations Available: Assistant Professor, Associate Professor and Professor Desired Skillset: Applicants should preferably hold a Ph.D. in the relevant subject from reputed Institutions. Should have sufficient experience in Teaching, Industry & Research with reputed Institutions. Should have research papers published in International / National Journals. Should have books published and Scholars awarded / currently working for. Applicants with patents registered / consultancy works carried out will be given preference. Exposure in handling high-value funded projects will be an added advantage Preferred Qualifications: Ph.D. in relevant streams with good academic records Areas of Specialization: Clinical Microbiology and Clinical Pathology Responsibilities: Academics: Classroom presentation Laboratory Instructions Development Learning of Resource Materials & Laboratory Development Student Assessment & Evaluation including Examination work of University. Participation in Co-curricular & extracurricular activities Student s guidance, counseling & helping in their personal, ethical, moral, and overall character development Keeping abreast of new knowledge and skills, help to generate new knowledge and help dissemination of such knowledge through books, publications, seminars, handouts, etc Continuing Education Activities Self-development through upgrading qualifications, Experience & Professional activities Research Consultancy: Research development activities & Research guidance Industry sponsored projects Providing consultancy and testing services Promotion of industry-institution interaction and R & D Academic / Administration: Academic and Administrative management of the institution Policy planning, monitoring & evaluation, and promotional activities; both at the department level and institution level Design and development of a new programme. Preparing projects for funding in areas of R&D work, laboratory development, modernization, expansion, etc Administration both at departmental & institutional levels Development, administration, and management at Institutional levels Monitoring and evaluation of academic and research activities Participation in policy planning at the Regional / National level for the Development of Technical Education Helping mobilization of resources for the Institution Develop, update and maintain MIS Plan and implement Staff Development activities, conduct Performance Appraisal Maintain Accountability Extension / Industrial Connectivity Interaction with Industry and Society Participation in Community services Providing R&D support and consultancy services to Industry and other user agencies Providing non-formal modes of education for the benefit of the Community Promotion of Entrepreneurship and Job rotation Dissemination of knowledge Providing Technical support in areas of social relevance Apart from the above duties, any other relevant work is assigned by the Dean of the respective schools

Role & responsibilities 1.1 To perform the media preparation, sterilization, disposal and record maintenance. 1.2 To transfer & Maintenance of all microbial pure cultures & record maintenance. 1.3 To perform a growth promotion test for microbiological media and observation. 1.4 To prepare the disinfectant solutions. 1.5 To perform microbial monitoring of classified areas of QC and production areas. 1.6 To perform the microbial analysis as per the method of analysis. 1.7 To operate and maintain the equipment/instruments as per respective SOP. 1.8 To monitoring and recording of differential pressure, temperature and humidity of the microbiology laboratory. 1.9 To receipt and handling of microbial media, cultures, biological or chemical indicator and accessories. 1.10 To perform the microbial analysis and method validation as per protocol (as and when required). 1.11 To maintain and check the cleaning of the micro lab and instruments. Preferred candidate profile

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.

Dear Candidate , we are hiring for Biologics for the Position JR Executive . Bio burden testing of in process samples as per the specification. BET testing of water samples, in-process samples, semi-finished and finished samples as per the specification. Sterility testing of finished product. Responsible to perform the MLT testing for raw materials and water samples. Maintenance and handling of Endotoxin indicators and biological indicators. Experience on culture maintenance and VITEK2 compact system To perform the method validations for MLT, BET, Bio burden and Sterility. Injectables or biologics experience is mandatory. Male candidates are preferable. Regulatory audits exposure is mandatory. Department:- Microbiology . Exp:-2-5 Years. Des:- Jr Executive-Executive . Qua:-MSc Microbiology . NOTE : Only Male Candidates Preferable for more details please reach out Venkat -9381915043 or please share your CV to venkateswara.k@talent21.in

Company Name Bharatiyam Job Title Quality Manager Job Location: Odisha Description Welcome to Bharatiyam Beverages Private Limited! Bharatiyam Group has a rich legacy in manufacturing, distributing, and retailing food products, sparkling beverages, juices, and packaged water across the Indian subcontinent. With 3 decades of experience, we have established ourselves as a trusted name in the industry. We are excited to announce the establishment of a world-class manufacturing facility in Uttar Pradesh. This cutting-edge facility will produce juices, aerated beverages, and mineral water, making us India’s first major homegrown beverage brand to challenge international corporations. With high-speed bottling lines, we will produce 60 crore units annually, ensuring wide distribution across Northern India. Looking ahead, Bharatiyam Beverages aligns with the Make In India campaign and Atma Nirbhar Bharat Abhiyaan. We are committed to building sustainable communities, reducing our environmental footprint, and supporting a self-reliant India. WE ARE HIRING QUALITY MANAGER OPEN POSITIONS: 2 LOCATION: Purquazi plant, Muzaffarnagar, Uttar Pradesh Food tech park – Khurdha plant, Odisha Role And Responsibility Ensure supplier quality and timely rmpm (raw material & packaging material) delivery. Oversee finished goods quality and compliance to set standards. Coordinate with manufacturing teams for process controls, startup verification, and early care systems. Implement and support total quality management (tom) practices. Build a strong shop-floor quality culture through pdca, quality circles, and real-time monitoring. Lead risk mitigation through change management and robust validation processes. Establish quality command centers for continuous stakeholder and customer engagement. Upgrade measurement systems and digitize data capture across plants. Ensure full compliance with FSSC 22000 and iso 9001 standard. Qualifications Bachelor’s degree in food science, microbiology, chemistry, or a related field (master’s preferred) 15+ years of experience in qaiqc in beverage or food manufacturing Strong knowledge of haccp, gmp, fssai, and iso/fssc standards Certification in sqf, six sigma, pcqi, or similar is preferred Excellent leadership, communication, and analytical skills Proficiency in MS office and quality data management tools Apply Here HR@Bharatiyambeverages.com

Job description Greetings from Indira IVF!!! Position- Lab Asst - Andrology Qualification- B.Sc. - Biotechnology/ Microbiology Experience- 1 to 4 Years Job Timing - 9 am to 6 pm Salary- Best in the industry

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

Responsible to collect the Sample, environmental monitoring Programme, Packaging,in process samples & finished product samples as per sampling plan & conduct the test as per FSSAI,Responsible for compositing the Finished Product & RM as per method

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.

Collect and prepare specimens (blood, urine, tissue) for laboratory testing Conduct tests in microbiology, hematology, immunology, and clinical chemistry Operate and maintain lab equipment, ensuring calibration and quality control Analyze results and report findings to physicians and healthcare professional Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Schedule: Day shift Supplemental Pay: Commission pay Overtime pay Performance bonus Shift allowance Work Location: In person