1354 Microbiology Jobs - Page 5

Location: Goa Job ID: 00011 Department: Design Implementation Job Description We are looking for experienced candidate to carry out and end-to-end design implementation/technology transfer activities from conceptualization in R & D to production in Manufacturing. The candidate will also oversee and troubleshoot the manufacturing of Molbio’s PCR products, peripherals, and associated consumables. The major objective will be transfer of technology through appropriate design transfer and validation processes Responsibilities Collaborate with R&D to understand the technology of new product assembly, review the design transfer file and enable the introduction of the new products in the manufacturing lines. Identify and mitigate risk associated with design and implementation projects, such as technical feasibility and regulatory hurdles Planning and execution of product and process validation Validation activities such as Design file review, protocol design and review Validation of method, equipment, software, raw/packaging material, facility, user Troubleshooting of issues faced by production and quality department Work on the effective manufacturing strategy and scalability with executive team Keep abreast of latest manufacturing technologies and methodologies and implement appropriate solutions. Ensure data analysis of manufacturing to improve productivity, quality and maintenance of machines. Ensure compliance with local and international laws and regulations. Education PhD in Life Sciences (Molecular Biology, Chemical Engineering, Microbiology, Biotechnology, Biochemical Engineering, Biomedical Engineering, Medical Devices, Clinical Pathology, Pharmaceutical Sciences, etc.) domain. Master’s candidate with suitable industry experience. Experience for both Roles Sr. Executive - 2-5 years after PhD, 6-8 years after Masters Executive – Fresher PhD, 2-4 years after Masters in medical devices (preferably in POC IVD) industry with comprehensive understanding regulations such as CDSCO, ISO 13485, IVDR, MDSAP. Thorough understanding of the RTPCR related R&D processes and Design transfer activities. Requirements Thorough understanding and practice of Quality Management System (QMS), Quality Control, Quality Assurance, GMP, GLP, ISO, FDA, Risk Management Experience of carrying out feasibility studies for scale up manufacturing of new products before locking stage of design file by R&D. Develop detailed design specifications and documentation, ensuring clarity for manufacturing and regulatory submissions. Medical devices/IVD product development (ideation, design input, process, output, verification, validation) Process development, automation, product validation processes Lean six sigma, production management Statistical process control, data analysis and interpretation Strategic thinking, superior analytical skills, exceptional problem-solving ability and attention to detail Functional/domain knowledge in POC medical devices/IVDs Timely delivery, excellent technical communication skills Experience 2-5 Years after PhD, 6-8 Years after Masters

Position: Medical Coder Ct: HR Shanmugapriya - 8072891550 Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medial reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim. Eligibility: All (UG/PG) Life Science& Paramedical Graduates BDS BPT BHMS BAMS Siddha,Unani,Naturopathy {Dip Bsc Msc} Nursing/GNM {B.E M.E} Biomedical Engineering {B.tech,M.tech}Biotechnology Biochemistry Bioinformatics Microbiology Zoology and Advanced zoology Biology Botany Medical Lab Tech Plant biotechnology Pharmacy(B.Pharm M.pharm) Paramedical Physiotherapy Physician assistant Critical Care Technology Medical Biochemistry Medical Record Science Operation Theatre & Anaesthesia Technology {Bsc Msc Dip} Clinical Nutrition Human Genetics Medical Laboratory Technology Medical Sociology Epidemiology Molecular Virology Biostatistics Blood Banking Technology Regenerative Medicine Optom. Genetic Counseling Radiology & Imaging Technology Medical Biochemistry Medical Microbiology Clinical Care Technology Clinical Care Technology Medical Physics {Bsc Msc Dip} Accident & Emergency Care Technology Audiology & speech Language Pathology Cardiac Technology Cardio Pulmonary Perfusion Care Technology Critical Care Technology Dialysis Technology Neuro Electrophysiology Medical Sociology Nuclear Medicine Technology Operation Theatre & Anaesthesia Technology Optometry Physician Assistant Radiology Imaging Technology Radiotherapy Technology Medical Record Science Respiratory Therapy 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 Requirement: Knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills Benefits System based job Weekly 5 days duty Day shift with Sat and Sun off Food and Cab provided by company Incentives based on performance Starting salary 12k to 25k with increment in 6 months for experienced. Abroad opportunities available Bonus for referring friends Medical expenses covered by company Provident Fund will be provided Gratuity after 5 yrs of work experience. Job Location: Chennai, Coimbatore, Vellore, Trichy, Cuddalore, Pondi Salem, Erode, Namakkal, Thanjavur, Nagercoil, Theni,Dindokal Thiruvannamalai, Villupuram, Karur, Tirunelveli,Kanniyakumari Tirupati, Kerala, AP,Tamilnadu,Telangana Reach Us: HR Shanmugapriya - 8072891550 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 GNM STAFF NURSE ANM STAFF NURSE GNM FEMALE STAFF NURSE DGNM FEMALE STAFF NURSE GNM MALE NURSE MALE STAFF NURSE NURSING JOBS IN CHENNAI Perks and Benefits Incentives & Benefits as per Corporate Standards

Skill required: Clinical Data Operations - Clinical Database Testing Designation: Clinical Data Svs Associate Qualifications: Master’s in actuarial science Years of Experience: 1 to 3 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world s leading biopharma companies bring their vision to life and enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. The Clinical Testing Team is dedicated to conduct through validation of all clinical trial database components ensuring that database meets quality standards while remaining cost effective. Their responsibilities include reviewing requirement specification, developing test scripts for carious testing types, performing data entry according to these scripts, executing test steps, documenting results and maintaining comprehensive records of all tested components in compliance with regulatory requirements. Design and test EDC databases, create and maintain User Acceptance Testing (UAT) procedures for EDC systems, including the creation of test plans, verification of requirements for databases, eCRFs, edit checks, extractions, and reports. What are we looking for? Candidates who have completed Master s or Post graduate degree in Life Science domain (Biology, Genetics, Microbiology, Biochemistry, Biotechnology, and Ecology) in 2024 & 2025 (if all semester s results are available). Adaptable and flexible. Ability to perform under pressure. Problem-solving skills. Ability to establish strong client relationship. Agility for quick learning. Experience with Clinical testing, Understanding of clinical Trials, Phases and clinical domain. Familiarity with clinical data management concepts and terminologies, Knowledge of regulatory guidelines such as GCP, ICH, 21 CRF Part 11 and GDRP. Experience in test script development and strong documentation skills for test cases, validation reports and audit trials. Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Show more Show less

Skill required: Clinical Data Operations - Clinical Database Testing Designation: Clinical Data Svs Associate Qualifications: Master’s in actuarial science Years of Experience: 1 to 3 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world s leading biopharma companies bring their vision to life and enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. The Clinical Testing Team is dedicated to conduct through validation of all clinical trial database components ensuring that database meets quality standards while remaining cost effective. Their responsibilities include reviewing requirement specification, developing test scripts for carious testing types, performing data entry according to these scripts, executing test steps, documenting results and maintaining comprehensive records of all tested components in compliance with regulatory requirements. Design and test EDC databases, create and maintain User Acceptance Testing (UAT) procedures for EDC systems, including the creation of test plans, verification of requirements for databases, eCRFs, edit checks, extractions, and reports. What are we looking for? Candidates who have completed Master s or Post graduate degree in Life Science domain (Biology, Genetics, Microbiology, Biochemistry, Biotechnology, and Ecology) in 2024 & 2025 (if all semester s results are available). Adaptable and flexible. Ability to perform under pressure. Problem-solving skills. Ability to establish strong client relationship. Agility for quick learning. Experience with Clinical testing, Understanding of clinical Trials, Phases and clinical domain. Familiarity with clinical data management concepts and terminologies, Knowledge of regulatory guidelines such as GCP, ICH, 21 CRF Part 11 and GDRP. Experience in test script development and strong documentation skills for test cases, validation reports and audit trials. Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Show more Show less

Skill required: Clinical Data Operations - Clinical Database Testing Designation: Clinical Data Svs Associate Qualifications: Master’s in actuarial science Years of Experience: 1 to 3 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world s leading biopharma companies bring their vision to life and enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. The Clinical Testing Team is dedicated to conduct through validation of all clinical trial database components ensuring that database meets quality standards while remaining cost effective. Their responsibilities include reviewing requirement specification, developing test scripts for carious testing types, performing data entry according to these scripts, executing test steps, documenting results and maintaining comprehensive records of all tested components in compliance with regulatory requirements. Design and test EDC databases, create and maintain User Acceptance Testing (UAT) procedures for EDC systems, including the creation of test plans, verification of requirements for databases, eCRFs, edit checks, extractions, and reports. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Ability to establish strong client relationship Agility for quick learning Candidates who have completed Master s or Post graduate degree in Life Science domain (Biology, Genetics, Microbiology, Biochemistry, Biotechnology, and Ecology) in 2024 & 2025 (if all semester s results are available). Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Show more Show less

Company Description CRL Diagnostics Pvt LTD is a leading diagnostic network in India, committed to meeting the evolving needs of the medical community through advanced diagnostic testing, information, and services. In just four years, CRL has expanded to three regional labs and 1,500 collection points across the country. Our team of dedicated pathologists and scientific staff provide specialized diagnostic services in various disciplines, ensuring accurate and timely results. CRL strives to make every customer and patient experience positive, satisfying, and memorable by delivering facts with respect and dignity. Role Description This is a full-time on-site role for a Consultant Pathologist, located in West Delhi. The Consultant Pathologist will be responsible for analyzing laboratory samples, conducting diagnostic tests, providing diagnostic information to physicians, and contributing to the development of diagnostic protocols and procedures. The role involves daily interactions with a multidisciplinary team to interpret test results, ensure quality control, and maintain compliance with regulatory standards. Regular duties include participating in case reviews, attending multidisciplinary meetings, and staying updated with the latest advancements in pathology. Qualifications Experience in diagnostic testing, including Biochemistry, Hematology, Microbiology, Histopathology, Immunohistochemistry, and Molecular Pathology Skills in interpreting laboratory results and providing accurate diagnostic information Ability to maintain quality control and regulatory compliance Excellent communication and interpersonal skills for interacting with physicians and multidisciplinary teams Capability to work efficiently in a dynamic, fast-paced environment Subspecialty expertise in Dermatopathology, Gastrointestinal Pathology, or Gynecologic Pathology is an advantage Advanced degree in Pathology (MD/DNB) and relevant certifications Show more Show less

IQVIA (www.iqvia.com) is a global human data science company focused on the pharmaceutical and biotechnology industry. We are committed to providing solutions that enable healthcare companies to innovate with confidence, maximize opportunities and, ultimately, drive healthcare forward. We do this via breakthroughs in insights, technology, analytics, and human intelligence that bring the advances in data science together with the possibilities of human science. The Custom Research team within IQVIA provides rapid, convenient, and effective communication between pharmaceutical companies, healthcare professionals and patients. We conduct market research studies to address critical strategic and tactical business questions faced by our biopharmaceutical clients. We employ a wide variety of methodologies to best address client objectives. Outstanding strategic thinking, analytical skills, and communication skills are essential to our business. Job Summary: We are seeking bright and highly motivated candidates for a full-time Primary Market Research Consultant position. The Consultant will be responsible for timely and accurate delivery of client deliverables to internal stakeholders and assist in project execution. The ideal candidate should have primary market research experience with analytical skills, strong attention to detail, excellent communication skills, and desire to work in a fast-paced, high growth environment. Essential Duties and Responsibilities: Conduct in-depth research on potential clients, products, and therapeutic areas to build a strong understanding of client objectives and market dynamics. Contribute to the design and/or revision of market research tools, including screeners, questionnaires, and discussion guides, ensuring alignment with client and business goals. Ensure data accuracy through rigorous validation, sanity checks, and outlier adjustments. Develop clear, compelling, and insightful visualizations using PowerPoint and BI tools to effectively communicate findings and support client decision-making. Perform comprehensive quality control (QC) checks, including data verification, formatting reviews, proofreading, and comparison with previous deliverables to ensure high-quality, client-ready reports. Document internal and client meetings with detailed, insightful notes that summarize key discussion points and outline actionable next steps for the project team. Lead complex data analysis tasks, including applying statistical weights and other advanced analytical techniques as required. Manage end-to-end project execution, including survey design, fieldwork planning, data analysis, client delivery, and handling follow-up requests. Collaborate effectively with cross-functional teams to ensure seamless project execution and delivery of high-impact insights. Ensure all project activities comply with client specific and IQVIA’s internal compliance and regulatory standards. Qualifications/ Key Skills: Master's/ Bachelor’s in Pharma, Biochemistry, Medical Microbiology MBA with primary market research experience in healthcare domain Excellent analytical skills, written and verbal communication skills. Self-motivated, accountable, can be counted on to get the job done with integrity. Ability to draw insights and answer client business questions. Proficient skills in MS PowerPoint, Excel, and analytical tools Ability to exercise judgment and work in a fast-paced environment. Experience: Preferred: 4.5+ years of experience in Primary Market Research and Strategy within the healthcare domain. Expertise: Proven hands-on experience in conducting both Quantitative and/or Qualitative primary research studies, including Trackers/ ATUs, Demand Assessments, Segmentation, and Chart Audits. Project Management: Strong track record of effectively managing projects. Consulting Experience: Prior consulting experience is an asset. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com Show more Show less

Company Description Dr. B. Lal Clinical Laboratory, established in 1991, provides top-quality Pathological and Diagnostic solutions with advanced technology. Renowned for reliability over 31+ years, it operates a vast network with over 100+ Collection Centers throughout Rajasthan. The laboratory boasts a state-of-the-art Central Processing Laboratory and 11 Regional Laboratories in various locations. Offering more than 1500+ tests in Clinical Pathology & Biochemistry, Haematology, Microbiology, Serology, and Molecular Biology, it's a leader in the field. Role Description This is a full-time on-site role for a Business Development Manager, located in Jaipur. The Business Development Manager will be responsible for identifying and developing new business opportunities, building and maintaining client relationships, developing strategic plans to achieve sales targets, and conducting market research. The role includes overseeing marketing initiatives, managing sales processes, and contributing to business growth strategies. Qualifications Business Development, Sales, and Marketing skills Ability to build and maintain client relationships Strategic planning and market research skills Excellent communication and interpersonal skills Analytical and negotiation skills Ability to work on-site in Jaipur Bachelor’s degree in Business Administration, Marketing, or related field Experience in the healthcare industry is a plus Proficiency in MS Office and CRM software Show more Show less

At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world’s most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we’re working at the pace of change on diagnostic tools that address the world’s biggest health challenges, driven by knowing that behind every test there is a patient waiting. Learn about the Danaher Business System which makes everything possible. The Strategic Accounts Manager is responsible to drive a highly complex Diagnostic Labs sales in the identified key accounts: from introduction of new screening and diagnostic concepts through closure and implementation, working with physicians, laboratory personnels, Quality Assurance team and executive staff members from management team to identify needs, gain consensus, and close new assay and instrumentation business as rapidly as possible in assigned laboratory chains across India. This position is part of the Sales Function located in Gurgaon/ Delhi-NCR. You will be a part of the Sales function and report to the National Sales Head, Commercial Business, India. Your core area of responsibility is driving revenue within your defined/ identified key laboratories with National & Regional presence and build strategic partnerships with them. In this role, you will have the opportunity to: Manage and Grow business in the existing set of national lab accounts& Regional Lab accounts (NRL’s/RRLs)) . Achieve the annual Sales number along with timely collection of Accounts Receivable. Expand Menu utilization and Assay Maximization for additional revenue. Increase wallet share for the entire product portfolio including GX instrument placement. Driving the Funnel Management, daily SFDC reporting & ensuring right funnel is prepared and prospect are met at right frequency. Work with National Sales Head to develop sales strategies, customer Specific Plans and execute the plans to achieve agreed targets in the territory. Work closely with Field Application Specialists (FAS), Field Service Engineers (FSE) and Technical Support Specialists (TSS) to maintain customer satisfaction. Develop and deliver presentations, proposals and should be confident for assay demonstrations at customer sites Essential Job Requirements Include - Minimum Exp- 8- 10 Years Bachelor's/Master's in Science/Biotechnology/ Microbiology/MBA Proficient level language fluency in English. Work experience in CRMs like SFDC Agile and willing to travel 10-15 days in a month Ability to work independently and within a team Strong team player with excellent communication and negotiation skills with a scientific approach for the customers. 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 danaherbenefitsinfo.com. At Cepheid we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cepheid can provide. 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. Show more Show less

🩺 Faculty Required – Reputed Medical College (50 MBBS Seats) 📍 Location: Near Delhi, Uttar Pradesh 🏛️ Affiliated to: Atal Bihari Vajpayee Medical University 🧾 Vacancies: 24 Openings For 👨‍🏫 Professors 👩‍🏫 Associate Professors 👨‍⚕️ Assistant Professors 🧑‍⚕️ Senior Residents (SRs) 📚 Departments Anatomy | Physiology | Biochemistry | Pharmacology | Pathology | Microbiology | Forensic Medicine | General Medicine | Community Medicine | Anesthesiology | Psychiatry | Dermatology 💼 Employment Type ✅ Full-Time ✅ Part-Time ✅ Contractual Skills: forensic medicine,teaching,pathology,communication,anesthesiology,clinical skills,physiology,general medicine,community medicine,pharmacology,biochemistry,medical knowledge,dermatology,psychiatry,research,psychophysiology,anatomy,microbiology Show more Show less

Job Description Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of executed BMRs and BPRs. Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc.. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Review of Visual inspector qualification record. Qualifications BSc/MSc. Show more Show less

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physiotherapy, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM excluding Allowances

Position Overview: The Fitting Technician at will be responsible for managing the entire lab operations, ensuring precise fitting of spectacles according to customer orders, and coordinating with various teams to meet delivery timelines. The ideal candidate will be detail-oriented, with strong organizational skills and the ability to maintain high standards of quality and efficiency. Min 2 years of fitting experience required.

Profile Summary- The main goal of this role is to contribute to our organization's growth by conducting comprehensive research, writing research articles across various fields, and managing the publication process. Key Roles and Responsibilities- ● Research Article Writing: Conduct in-depth research across diverse fields and produce high-quality research articles for publication. Collaborate with subject matter experts to ensure accuracy and relevance in content. ● Publication Strategy: Demonstrate expertise in the research publication process, including selecting appropriate journals, understanding submission guidelines, and ensuring compliance with publication standards. ● Submission Follow-up: Take ownership of the submission process, ensuring timely follow-upon research articles submitted to journals. Communicate with editors, track submission progress, and address any queries or revisions requested by the editorial team. Knowledge and Skills- ● Education: PhD, Masters in streams like Pharmacy, Biotechnology, Bioinformatics, Zoology, Chemistry, Physics, Microbiology, Agriculture, Forensic Science, Engineering and Management. ● Experience: Fresher or Experience ● Knowledge of the research publication industry. ● Must have published 1-2 articles. ● Excellent communication (written &verbal) ● Interpersonal and problem-solving skills ● Research and Development skills and attitude- ● Adaptive to challenging environment ● Proactive, results-oriented and organized ● Willingness to collaborate and coordinate with different departments and team members Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹27,800.00 per month Benefits: Provident Fund Schedule: Day shift Ability to commute/relocate: Panchkula, Haryana: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): How many Articles have you published ? Are you comfortable with the offered CTC ? Work Location: In person

Job Title: Sr. Officer / Executive – QC DRA Department: Quality Control / Drug Regulatory Affairs (DRA) Reporting To: DRA Manager / QC Head Employment Type: Full-time Experience Required: Minimum 2 Years Qualification: M.Sc. / B.Sc. (Science/Pharmacy stream preferred) Job Summary: We are seeking a motivated and detail-oriented Sr. Officer / Executive for QC DRA to support the preparation, compilation, and review of regulatory documents required for product registrations and regulatory submissions. The ideal candidate should have experience working in QC or DRA functions within a pharmaceutical manufacturing setup and should be well-versed with regulatory compliance requirements (domestic and international). Key Responsibilities:1. Dossier Compilation & Review: Assist in preparation and review of CTD / ACTD / eCTD dossiers for domestic and international regulatory submissions. Compile and verify quality-related documents including specifications, STPs, validation protocols, and COAs for submission. Coordinate with internal teams (QA/QC/Production/R&D) to collect and organize required data for regulatory filings. 2. Regulatory Documentation: Prepare and maintain Product Master Files (PMFs) and Site Master Files (SMFs) . Support submission of Annual Product Reviews (APRs) , and DMFs (Drug Master Files) as per regulatory timelines. 3. Compliance and Coordination: Ensure all documentation aligns with current regulatory guidelines (e.g., WHO, USFDA, MHRA, EU, TGA). Coordinate with external consultants or agents for country-specific dossier submissions. 4. QC Interface: Liaise with the QC team to obtain data such as method validation, stability studies, and analytical results required for regulatory submissions. Review analytical data and reports to ensure correctness and readiness for regulatory review. 5. Audits & Queries: Assist in addressing regulatory queries and deficiencies. Support audit preparations and participate in internal and external audits as required. Candidate Requirements: Education: M.Sc. or B.Sc. (Chemistry, Microbiology, Biochemistry, or related disciplines) Experience: Minimum 2 years of experience in Quality Control or DRA in a pharmaceutical company. Skills: Good understanding of ICH guidelines, regulatory documentation structure , and technical writing. Hands-on experience in document review , dossier compilation , and data coordination . Proficiency in MS Office and regulatory software tools (if any). Soft Skills: Strong attention to detail and data accuracy. Good communication and coordination skills. Ability to meet deadlines and manage multiple priorities. Work Schedule: 6-day working week (as per company policy) Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹28,000.00 per month Benefits: Flexible schedule Food provided Health insurance Paid time off Provident Fund Schedule: Day shift Morning shift Weekend only Supplemental Pay: Overtime pay Performance bonus Yearly bonus Work Location: In person

Job Title: Officer – Quality Control (Microbiology) Department: Quality Control – Microbiology Reporting To: QC Microbiology Manager / Quality Head Employment Type: Full-time Salary: ₹20,000 per month Experience Required: Minimum 2 YearsQualification: M.Sc. / B.Sc. (Microbiology or related life sciences field) Job Summary: We are looking for a dedicated and detail-oriented Officer – QC Microbiology to join our Quality Control team. The selected candidate will be responsible for performing microbiological testing of raw materials, finished products, water, and environmental monitoring to ensure compliance with quality and regulatory standards. Key Responsibilities: 1. Microbiological Testing: Conduct routine microbiological analysis of raw materials, finished products , and in-process samples . Perform water testing (WFI, Purified Water, RO Water) for microbial limits. Execute sterility testing, BET (Bacterial Endotoxin Test) , and Microbial Limit Testing . 2. Environmental Monitoring: Carry out environmental monitoring of production and sterile areas , including air, surface, and personnel monitoring. Maintain and review EM records, trends, and reports. 3. Media Preparation & Validation: Prepare, sterilize, and validate media for microbiological testing. Perform growth promotion tests and media control checks. 4. Documentation & Compliance: Ensure timely and accurate documentation of all microbiological activities as per cGMP and GLP . Maintain logbooks, worksheets, test reports, and analytical records as per SOPs. 5. Instrument Handling: Operate and maintain laboratory equipment such as Incubators, LAF, Autoclave, pH meter, Conductivity meter, and Particle counter . Ensure instruments are calibrated and maintained as per schedule. Candidate Requirements: Education: M.Sc. / B.Sc. in Microbiology or Life Sciences Experience: Minimum 2 years in pharmaceutical QC microbiology Knowledge Required: Strong understanding of microbiological techniques and regulatory standards. Familiarity with GMP , GLP , and ISO guidelines. Skills: Good observation and documentation skills. Ability to follow SOPs and work in a sterile environment. Basic computer proficiency for record-keeping and reporting. Work Schedule: 6 days working Job Types: Full-time, Permanent Pay: ₹216,000.00 - ₹240,000.00 per year Benefits: Flexible schedule Food provided Health insurance Paid time off Provident Fund Schedule: Day shift Morning shift Weekend only Supplemental Pay: Overtime pay Performance bonus Yearly bonus Location: Baddi, Himachal Pradesh (Required) Work Location: In person

We're Hiring: Lab Technician – Bio-Input Analysis 📍 Location: Coimbatore 💼 Salary: ₹30,000 – ₹40,000/month (Based on Experience) Are you passionate about soil health, lab science, and sustainable agriculture? Join us as a Lab Technician – Bio-Input Analysis at our model farm in Coimbatore. You’ll support critical research and field initiatives that impact farming communities across India. 🔍 Key Responsibilities: Sample Preparation & Analysis Collect, label, and prepare samples (soil, compost, water, extracts) Conduct microbial assays and microscopy (protozoa, fungal networks) Instrument Operation & Maintenance Calibrate and operate pH meters, spectrophotometers, moisture analyzers Perform regular maintenance and basic troubleshooting Data Management Accurately record lab results in notebooks and digital tools (AppSheet, BigQuery) Generate summary reports and visuals for internal teams Quality Assurance Follow SOPs and lab safety protocols Manage lab inventory and storage conditions Field Support Assist with field sample collection and on-site testing as required 🎓 Qualifications: Bachelor’s in Soil Science, Microbiology, Chemistry, or related field 1–2 years of lab experience (academic or industry) Comfortable using basic lab tools and sterile techniques Strong analytical and teamwork skills 🌱 What We Offer: Training in cutting-edge, analysis-based farming Hands-on experience with impactful, field-driven research An opportunity to create real change for farmers If you’re a detail-oriented lab enthusiast eager to work at the intersection of science and sustainability, we’d love to hear from you! Mail your resumes to: kavitha.a@sadhguru.org Show more Show less

Who are we HaystackAnalytics is a HealthTech company creating clinical genomics products, which enable diagnostic labs and hospitals to offer accurate and personalized diagnostics. Supported by India's most respected science agencies (DST, BIRAC, DBT), we created and launched a portfolio of products to offer genomics in infectious diseases. Our genomics based diagnostic solution for Tuberculosis was recognized as one of top innovations supported by BIRAC in the past 10 years, and was launched by the Prime Minister of India in the BIRAC Showcase event in Delhi, 2022. Job Summary We are looking for a Fresher MD/PhD with a specialization in Microbiology to join our team as a Clinical Outreach / Scientific Outreach professional. This position requires active field engagement in collaboration with the sales team, including visits to hospitals and clinical institutions to interact with physicians and other healthcare professionals. The candidate will be responsible for effectively communicating the scientific, microbiological, and clinical aspects of our products, ensuring a clear and thorough understanding of their clinical relevance, applications, and value. The candidate will be participating in Continuing Medical Education (CME) programs and Round Table meetings (RTMs). What we want you to do Work closely with the sales team during client visits, primarily engaging with doctors and healthcare providers. Explain the microbiological and clinical aspects of our products in a clear and professional manner. Bridge the gap between scientific knowledge and clinical application to support the adoption of our products. Provide technical support and medical guidance during client meetings and product demonstrations. Help doctors understand how the product integrates into patient care, infection control, and diagnostic workflows. Share relevant case studies, clinical experiences, or infection trends to highlight product effectiveness. Maintain a strong understanding of emerging microbiological trends and technologies, including Next-Generation Sequencing (NGS). Collaborate with internal teams such as R&D, sales, and Operto ensure accurate communication and feedback. Actively participate in Continuing Medical Education (CME) programs and Round Table Meetings (RTMs) What are we looking in you Freshers - Fresher MD/PhD with a specialization in Microbiology Proven track record of effective communication and collaboration with interdisciplinary healthcare teams. Demonstrated understanding of infection control protocols and antimicrobial stewardship principles. Familiarity with molecular and sequencing (NGS) technologies and their applications in clinical microbiology is advantageous. Strong knowledge of clinical microbiology, infectious diseases, and diagnostic methods Excellent verbal communication and presentation skills. Ability to explain complex technical and medical concepts in a simple, clinician-friendly language. Comfortable with on-field client interactions. Must be willing to travel to PAN India for CME programs and RTMs. What you will gain Dynamic and collaborative work environment dedicated to making a meaningful impact in healthcare Experience in working with advanced sequencing technology in the diagnostic industry i.e. NGS, WGS, Nanopore, and Illumina. Opportunities for professional development and continued education Competitive salary commensurate with experience Comprehensive health benefits package Job Types: Full-time, Fresher Pay: ₹1,000,000.00 - ₹1,100,000.00 per year Benefits: Health insurance Provident Fund Schedule: Day shift Application Question(s): When did you complete your MD or PhD program (please specify the month and year)? Work Location: In person

We are looking for an Associate STEM Content Analyst to join GENESEQ team (Intellectual Property) in Hyderabad/ Chennai. This is an amazing opportunity to deliver value-add scientific information for GENESEQ™ Indexing product which is a proprietary database to easily search and identify biological sequences covered in patent. The team consists of 40 plus colleagues. We have a great skill set in biotechnology, genetics, and molecular biology concepts to curate biological sequence information and we would love to speak with you if you have skills in comprehensive knowledge in the respective technology domain. About You Should hold a Master’s degree in Genetics, Molecular Biology, Biochemistry, Bioinformatics, Microbiology, Biotechnology and equivalent skill set / B. Tech Biotechnology 0-2 yrs of experience. Having sound knowledge about biotechnology related concepts, techniques, molecular biology and genetic engineering concepts. It will be great if you also had…. Technical skills as defined for each technology area. Problem identification and solving skills. Attention to detail. Computer and internet literacy with good keyboard skills. Excellent English written and verbal communication skills. Ability to deal with complex and demanding issues. What will you be doing in this role? To apply biotechnology, genetics, and molecular biology concepts to curate biological sequence information. Ensure to meet the weekly production volume and quality targets are maintained as per the policy. No escalation from internal or external customers. Identify key developmental areas for process improvement. Maintain awareness of current developments in own technology areas Able to adapt to the changes as per customer delight. Effective personal planning and time management. To be a trusted resource to team and others/customers About the Team GENESEQ Team in IP Operations, curate biological sequence value-add information from patent documents in line with editorial policies and conventions. Record detail includes organism name, gene/protein name, sequence modification or other highlighted biologically significant regions of the sequence, and associated disease information Hours of Work (Permanent role) Full-time – 9 am to 6 pm IST At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.

Title of Project: Development of mouse and human organoids as alternative to laboratory animals in Biomedical Research. Qualifications: Master’s degree in Life Science (Virology, Biotechnology, Biochemistry, Microbiology, Zoology) from a recognized university with background of 3D cell culture, stem cell biology, molecular biology techniques, FACS, small animal handling etc., Job Types: Full-time, Temporary Contract length: 18 months Pay: ₹158,981.94 - ₹436,800.00 per year Shift: Day shift Fixed shift Work Days: Monday to Friday Weekend availability Language: English (Preferred) Work Location: In person

Job Title: Quality Control (QC) Executive – F&B (Bulk Catering) Location: Gurgaon Sector-63A Department: Quality Control / Food Safety Reports To: Quality Manager / Operations Head Experience Required: 2–5 years in large-scale or bulk food production/catering QC Education: B.Sc / M.Sc in Food Technology, Microbiology, or Hotel Management with food safety specialization Employment Type: Full-time Job Summary: The QC Executive for Bulk Catering is responsible for ensuring food quality, safety, and hygiene throughout the large-scale food preparation and dispatch process. This includes raw material inspection, process monitoring, hygiene audits, and final dispatch checks to meet both company and regulatory standards. Key Responsibilities:1. Raw Material Quality Check: Inspect all incoming raw materials (grains, vegetables, dairy, meat, etc.) for freshness, temperature, packaging, and expiry. Ensure materials meet vendor specifications and food safety norms. 2. Production Monitoring: Monitor large-scale cooking processes to ensure adherence to recipes, temperature control, cooking time, and hygiene. Ensure batch records and cooking logs are maintained. 3. Hygiene & Sanitation: Conduct daily kitchen and storage area hygiene inspections. Monitor staff hygiene (handwashing, PPE use, grooming). Check cleaning schedules, dishwashing, and sanitation logs. 4. Final Product Quality Control: Verify taste, texture, portioning, temperature, and packaging of food before dispatch. Conduct spot checks on tiffin boxes, bulk containers, and serving utensils. 5. Dispatch Monitoring: Ensure hot holding temperatures are maintained during loading. Verify food labels, container seals, delivery timing, and vehicle hygiene. 6. Documentation: Maintain checklists, daily QC reports, temperature logs, and non-conformance records. Report any deviations or potential hazards to the QC Manager immediately. 7. Pest & Waste Control: Ensure regular pest control and waste management practices are in place and documented. 8. Regulatory Compliance & Training: Ensure compliance with FSSAI, HACCP, and company standards. Assist in training kitchen staff on food safety and hygiene practices. Skills & Competencies: Strong understanding of food safety, HACCP, GMP, and FSSAI compliance Good knowledge of bulk cooking procedures and critical control points Keen observation, documentation, and reporting skills Ability to work during early hours or late shifts as per dispatch schedule Proficiency in MS Excel / digital logs / checklist formats Preferred Background: Experience in bulk or industrial catering (e.g., schools, hospitals, corporates, weddings, tiffin services) Certification in FSSAI/HACCP or ISO 22000 (preferred) To proceed, please fill out the following form or mail us on assistance@gourmerservices.com *Google Form* https://forms.gle/nb8Cu5S5FP7DKy7y9 Note: (If link not open then do it copy and paste on browser) Job Types: Full-time, Fresher Pay: ₹18,000.00 - ₹30,000.00 per month Benefits: Food provided Provident Fund Schedule: Day shift Work Location: In person

Quality Assurance Manager - Indore Calling all visionary Quality Assurance leaders! Golden Bansi is looking for a Quality Assurance Manager to join our team in Indore, Madhya Pradesh. If you're a hands-on leader who can drive quality culture, ensure regulatory compliance, optimize lab operations, and lead transformative quality initiatives aligned with international food safety standards, we want to hear from you! Here’s what you'll do: Lead and develop our QA/QC team. Supervise rigorous quality testing of durum semolina. Implement and uphold FSSC 22000 and BRC standards. Apply modern quality tools (RCA, FMEA, CAPA) for continuous improvement. Lead quality transformation strategies. Conduct audits of CMUs and critical suppliers. Handle customer feedback and complaints. You're a great fit if you have: B.Tech / M.Tech in Food Technology, Chemistry, Microbiology, or related field. Minimum 5 years of hands-on QA experience in food processing (durum milling/pasta ingredient manufacturing preferred). Strong leadership skills and deep familiarity with FSSC 22000, BRC, and global food safety norms. Ready to make an impact? Send your resume to hr@goldenbansi.com with the subject: Application – Quality Assurance Manager #QualityAssurance #QAManager #FoodSafety #IndoreJobs #Hiring #FoodProcessing #QualityControl #FSSC22000 #BRC #JobOpportunity #GoldenBansi#SKGMPL Show more Show less

We are looking for a Pharma Content Writer to join our editorial team and enrich our websites with new blog posts, guides and marketing copy. The candidate should be a Graduate of biotechnology, microbiology and any other pharma Related Experience- 6 Month To 1 Year > Research pharma-related topics > Write clear marketing copy to promote our products/services > Proofread and edit blog posts before publication > Submit work to editor for input and approval on time > Coordinate with marketing and design teams to illustrate articles > Promote content on social media > Identify customers’ needs and gaps in our content and recommend new topics > Ensure all-around consistency (style, fonts, images and tone) Job Type: Full-time Pay: ₹18,000.00 - ₹20,000.00 per month Schedule: Day shift Work Location: In person

Lab Technician – Honey Industry Company: Yieppie Internationals Location: Patiala, Punjab Qualification: Minimum B.Sc. in Microbiology, Chemistry, Food Science, Biotechnology, or Agriculture Experience: 1–3 years preferred (Freshers may apply) Job Types: Full-time, Permanent, Fresher Pay: From ₹15,000.00 per month Supplemental Pay: Overtime pay Yearly bonus Work Location: In person

Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible to perform the environment monitoring activities Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of executed BMRs and BPRs. Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc.. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Review of Visual inspector qualification record. Education: B.Sc./ M.Sc in Microbiology Total Experience - 2 - 4 Year inexperience in Environmental Monitoring for sterile manufacturing plant Note: Candidates who want to apply for internal jobs, must have completed atleast 2 years within existing role.