1181 Microbiology Jobs

Responsibilities: * Conduct lab tests using DMLT skills * Collaborate with healthcare team on patient care * Perform blood collection via phlebotomy * Collect samples through sample collection methods

Must have skills required: Communication, Fluent in English, Real-time PCR, Microbiology, ELISA, computer skills Responsibilities: Perform accessioning verification by reviewing all Test Requisition Forms and specimen data to ensure information has been entered correctly. Issue discrepancy reports to the lab for corrective action. Perform Real-Time PCR analysis and interpretation of results using the Rotor-Gene software. Enter and verify all laboratory result reports including Real-Time PCR, Conventional PCR, Western blot, and ELISA. Evaluate lab results for repeat and/or reflex testing. Follow up on results pending. Maintain and communicate pending list with lab personnel. Perform batch processing of test results to be released. Perform weekly reporting of positive communicable disease results to state agencies as mandated. Requirements: Bachelor's and Master Degree in Medical Biotechnology, Biology, Microbiology REQUIRED. English / Literature as a curriculum a mandate Male candidates preferred

JOB DESCRIPTION :- Exeperience : - Required 2 -3 year Education :- MSC Microbiology Any Master's Degree We are seeking a highly skilled Medical Content Writer to join our team. As a writer, you will be responsible for: l Conducting in-depth research to gather reliable and up-to-date medical information from credible sources. l Creating clear, concise, and engaging content for blogs, manuscripts, abstracts, posters, info graphs, visual aids (VA), leave-behind literature (LBL), big reminder card (BRC), slide decks, and related creative’s l Content management on website l Proofreading documents to ensure accuracy and consistency l Collaborating with cross functional teams to enhance creative inputs (visuals, info graphics, videos, etc.) l Participating in meetings and project discussions with clients and internal teams l Pitch creative content ideas to attract and engage the target audience. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹35,000.00 per month Schedule: Day shift Work Location: In person

Responsibilities Develop and implement food safety and quality assurance programs Ensure compliance with regulatory and customer requirements Lead internal and external audits and manage corrective actions Train and supervise quality assurance staff Monitor production processes to ensure quality standards are met Analyze quality data and implement improvements Collaborate with suppliers to ensure raw material quality Maintain documentation and records for traceability Stay current with food safety regulations and industry trends Communicate quality issues and solutions across departments Requirements Bachelor’s degree in Food Science, Microbiology, or related field 5+ years of experience in food quality assurance or food safety Strong knowledge of HACCP, GMP, and food safety regulations Experience with third-party audits and certifications (e.g., SQF, BRC) Excellent leadership and team management skills Strong analytical and problem-solving abilities Effective communication and interpersonal skills Proficiency in Microsoft Office and quality management systems Detail-oriented with strong organizational skills Ability to work in a fast-paced, dynamic environment Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹20,000.00 per month Schedule: Day shift Work Location: In person Application Deadline: 27/06/2025 Expected Start Date: 01/07/2025

Who we are At Progenesis, we are a team of experts fighting against infertility issues that couples often face, ensuring a hurdle-free journey towards pregnancy. It was in 2014 when we first stepped into the area of healthcare with the sole motto of being companions in highs & lows of couples journey to parenthood. Company Website - www.progenesisivf.com What you will do | Job Responsibility ● Semen analysis. ● Semen Washing. ● IUI. ● Semen freezing and semen thawing. ● Lab cleaning. ● Documentation. ● Media aliquoting. ● Assisting in ET. ● E-mails and order to be placed. ● DFI. ● Stock. ● Consent forms. ● Machines. What you need to have | Job Specification Experience 2 Years of Relevant Experience Education Msc/Bsc Microbiology, BioTech, Msc in Clinical Embryology, MSc/Bsc in Zoology Language Marathi (Mandatory) Hindi and English Required Female Job Type: Full-time Benefits: Health insurance Provident Fund Schedule: Day shift Language: Marathi (Required) Location: Ratnagiri, Maharashtra (Required) Work Location: In person

Overview: The primary job function of the Field Application Specialist includes but not limited to: Provide pre and post sales technical application support to customers to achieve customer satisfaction and business objectives. Conduct product application trainings to customers and to internal team members. Manage product evaluation at customer site to meet business objectives Support sales personnel to achieve team objectives He/she needs to be independent, self-motivated, likes to work with different people and can work under pressure. He should be ready for frequent traveling as almost 75% traveling is required in this position. Possess positive attitude towards work, forthcoming, ability to multi-task, creative in handling technical application service matters/problems. He/she should possess exceptional verbal and written communication skills, excellent inter-personal skill, soft skill in customer relation management, organization skill, as well as excellent technical analysis and problem-solving skills. How You’ll Make an Impact: Provide pre- and post-sales technical application support Provide post-sales technical application support & training mainly for trouble shooting purpose to achieve customer satisfaction and meet business objectives Develop a systematic troubleshooting approach to diagnose common application problems to be shared among team members. Manage product evaluation and provide feedback on further evaluation needs at customer site as part of sales process and ensure it meets business objectives Conduct pre-sales product presentations and demonstrations. Create training / Demo module (training notes, equipment, consumables & checklist) to be used as reference for other FAS. Work with manager to devise the yearly application training plan Ensure that the Bio-Rad commitment to customer satisfaction is achieved and constantly improved. Log in all field visits in Salesforce (SFDC) and upload supporting reports Maintain internal documents for application trainings conducted Ensure all instruments used for evaluation are properly accounted for Collect reference/performance letters for different products from customers regularly Presentation on specific product applications Prepare materials required for workshop/exhibitions & seminars Manage relationships with key customers & develop reference/key seminars Managing products performance related complaints and replacement requests Submit product related complaints to Product team in timely fashion and do the evaluation Ensure that all relevant documentation is in order and traceable What You Bring: Experience of working in life science research laboratory for at least 2 years. Proactive and passionate to provide excellent support to meet customer satisfaction. Excellent written, oral communication and presentation skills. Must have proven track record of hands-on experience in conducting wet lab experiments for at least 2 of the techniques (preferably more) Protein Purification (FPLC) Chromatography SDS-PAGE, Western Blotting, Imaging (Protein/DNA gel & blot documentation) PCR, Electrophoresis, Real-Time PCR, Transfection Droplet Digital PCR (ddPCR) Flow cytometry, cell Imaging & cell culture ELISA, Multiplex Immunoassays and use of different antibodies Experience at managing evaluation and training Proven track record to meet customer satisfaction in a technical support environment Able to work independently and pro-actively Preferably Ph.D. in Life Sciences (Biotechnology, Biochemistry, Microbiology etc Minimum 2 years working experience in a life science research laboratory with strong technical understanding of laboratory procedures Superior technical application knowledge of diagnostic/research methodologies Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Recently voted a Best Place to Work, Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see. Benefits: Bio-Rad's biggest asset is its people, and the reason why our Total Rewards deliver programs that provide value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Our robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees through the various stages of an employee’s work and life cycle. We’re proud to offer a variety of options, including competitive insurance plans for you and your immediate family, Annual Health checkup , Marriage Leave, Paternity Leave ,Employee Assistance Programme , extensive learning and development opportunities, and more. EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with disabilities, and people of all races, ethnicities, genders, ages, and orientations are encouraged to apply. Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resum

Job Scope _ The Quality Assurance & Food Safety Specialist is responsible for ensuring that food products meet all safety standards and regulatory requirements. This role focuses on managing and maintaining food safety systems, conducting audits, and implementing quality control processes to ensure that food products are produced, processed, and distributed in compliance with food safety laws and regulations. Key Responsibilities: 1. Food Safety Management:  Develop, implement, and maintain food safety policies and procedures.  Monitor and ensure compliance with federal, state, and local food safety regulations (e.g., FDA, USDA, FSMA).  Oversee the HACCP (Hazard Analysis Critical Control Points) program and ensure its effectiveness.  Conduct routine inspections of food processing areas, ensuring adherence to sanitation and hygiene protocols. 2. Quality Assurance:  Ensure the implementation of product specifications, quality standards, and best practices in food manufacturing processes.  Perform routine checks on products to ensure they meet quality standards.  Oversee product testing (microbiological, chemical, sensory, etc.) and analyze results.  Review and approve food product labeling for compliance with regulatory standards.  Manage non-conformance reports (NCRs), corrective actions, and preventive measures. 3. Training & Development:  Train production staff in food safety practices, quality standards, and regulatory requirements.  Conduct training sessions on proper hygiene, sanitation, and food safety techniques.  Stay current on industry best practices and changes in food safety regulations to ensure ongoing compliance. 4. Documentation & Reporting:  Maintain accurate and up-to-date records of food safety inspections, audits, and tests.  Prepare detailed reports for management regarding food safety compliance and quality control activities.  Manage documentation for food safety certifications, including internal records and third-party audit results. 5. Continuous Improvement:  Identify areas for improvement in the food safety and quality systems and suggest corrective measures.  Collaborate with cross-functional teams to drive improvements in food quality, production processes, and food safety.  Participate in risk assessments and root cause analysis to resolve quality issues. 6. Audits:  Coordinate food safety audits (internal and external) and manage corrective actions. FSSI Audit.  Schedule, prepare checklist, review past findings, ensure resources pre audit.  Inspect key areas, facilitate external audits, interview staff, observe practices, document findings.  Summarize findings, review with management, create corrective actions, follow up post audit  Analyze trends, update training, collaborate on solutions for improvement  Ensure readiness for certifications and regulatory audits. 7. Guest Complaints Handling:  Address guest complaints related to food quality, safety, or other concerns.  Investigate complaints to identify the root cause and implement corrective actions.  Maintain documentation of complaints and resolutions for quality assurance purposes. JOB REQUIREMENTS: Qualifications: Education: Bachelor’s degree in Food Science, Food Safety, Microbiology, or related field. Equivalent work experience may be considered. 1. Experience: 1. 2+ years of experience in food safety or quality assurance in a food manufacturing or production environment. 2. Experience with HACCP, GMPs (Good Manufacturing Practices), and relevant food safety standards (e.g., ISO 22000, SQF, BRC). 3. Knowledge of food safety laws and regulations (FDA, USDA, FSMA). 2. Required Skills and Qualifications: 4. Strong analytical skills and attention to detail. 5. Excellent written and verbal communication skills. 6. Ability to conduct audits and inspections efficiently. 7. Proficiency in MS Office Suite and familiarity with food safety management software. 8. Strong problem-solving and decision-making abilities. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹30,000.00 per month Benefits: Cell phone reimbursement Health insurance Life insurance Provident Fund Schedule: Day shift Evening shift Morning shift Night shift Supplemental Pay: Yearly bonus Work Location: In person Application Deadline: 30/06/2025 Expected Start Date: 01/07/2025

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

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

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

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

Huron helps its clients drive growth, enhance performance and sustain leadership in the markets they serve. We help healthcare organizations build innovation capabilities and accelerate key growth initiatives, enabling organizations to own the future, instead of being disrupted by it. Together, we empower clients to create sustainable growth, optimize internal processes and deliver better consumer outcomes. Health systems, hospitals and medical clinics are under immense pressure to improve clinical outcomes and reduce the cost of providing patient care. Investing in new partnerships, clinical services and technology is not enough to create meaningful and substantive change. To succeed long-term, healthcare organizations must empower leaders, clinicians, employees, affiliates and communities to build cultures that foster innovation to achieve the best outcomes for patients. Joining the Huron team means you’ll help our clients evolve and adapt to the rapidly changing healthcare environment and optimize existing business operations, improve clinical outcomes, create a more consumer-centric healthcare experience, and drive physician, patient and employee engagement across the enterprise. Join our team as the expert you are now and create your future. Position Summary: Responsible for the day-to-day production and quality functions of a team of coders specializing in meeting client production goals and coding accuracy goals. Plans, directs, supervises and evaluates feedback workflows and coordinates activities across all coding staff assigned to the team. Excellent communication skills, attention to detail, and strong technical and problem solving skills are essential aspects of this role. JOB DETAILS: Perform a variety of activities involving the coding of medical records by ascribing accurate diagnosis and CPT codes as per ICD-10 and CPT-4 systems of coding Perform Coding for Outpatient and/or Inpatient records with a minimum of 96% accuracy and as per turnaround time requirements Exceeds the productivity standards for Medical Coding - as per the productivity norms for inpatient and/or speciality specific outpatient coding standards Maintains high degree of professional and ethical standards Focuses on continuous improvement by working on projects that enables customers to arrest revenue leakage while being in compliance with the standards Focuses on updating coding skills, knowledge, and accuracy by participating in coding team meetings and educational conferences Experience in specialties such as Inpatient, E&M, Acute, Ambulatory, Cardiology, Radiology, Pathology, Anesthesia, Emergency Room, Surgery, and others Exposure to CPT-4, ICD-9, ICD-10, and HCPCS coding Understand the client requirements and specifications of the project and code the charts accordingly Code records by following prescribed coding standards such as ICD-9/ ICD-10 and CPT Ensure patient information are correct and appropriate signatures on all medical records Assign appropriate medical codes to all diagnosis and services Follow client specific guidelines wherever applicable & working as per client updates and coding the charts accordingly Meet the productivity targets of clients within the stipulated time Ensure that the deliverables to the client adhere to the quality standards Prepare and maintain status reports QUALIFICATIONS: Graduate in Life Science, Pharmacy, Physiotherapy, Zoology, Microbiology discipline 2+ years of industry experience CPC – Certified Coding Professional or CCS - Certified Coding Specialist Responsible for the day-to-day production and quality functions of a team of coders specializing in meeting client production goals and coding accuracy goals. Plans, directs, supervises and evaluates feedback workflows and coordinates activities across all coding staff assigned to the team. Excellent communication skills, attention to detail, and strong technical and problem solving skills are essential aspects of this role. JOB DETAILS: Perform a variety of activities involving the coding of medical records by ascribing accurate diagnosis and CPT codes as per ICD-10 and CPT-4 systems of coding Perform Coding for Outpatient and/or Inpatient records with a minimum of 96% accuracy and as per turnaround time requirements Exceeds the productivity standards for Medical Coding - as per the productivity norms for inpatient and/or speciality specific outpatient coding standards Maintains high degree of professional and ethical standards Focuses on continuous improvement by working on projects that enables customers to arrest revenue leakage while being in compliance with the standards Focuses on updating coding skills, knowledge, and accuracy by participating in coding team meetings and educational conferences Experience in specialties such as Inpatient, E&M, Acute, Ambulatory, Cardiology, Radiology, Pathology, Anesthesia, Emergency Room, Surgery, and others Exposure to CPT-4, ICD-9, ICD-10, and HCPCS coding Understand the client requirements and specifications of the project and code the charts accordingly Code records by following prescribed coding standards such as ICD-9/ ICD-10 and CPT Ensure patient information are correct and appropriate signatures on all medical records Assign appropriate medical codes to all diagnosis and services Follow client specific guidelines wherever applicable & working as per client updates and coding the charts accordingly Meet the productivity targets of clients within the stipulated time Ensure that the deliverables to the client adhere to the quality standards Prepare and maintain status reports QUALIFICATIONS: Graduate in Life Science, Pharmacy, Physiotherapy, Zoology, Microbiology discipline 2+ years of industry experience CPC – Certified Coding Professional or CCS - Certified Coding Specialist Position Level Senior Analyst Country India

ALL VET DIAGNOTSTIC SOLUTIONS PVT LTD which is a company dedicated to providing comprehensive diagnostic solutions for the veterinary field under VETLAB a registered trade mark. They aim to support veterinarians with accurate and reliable diagnostic tools and services, ensuring the health and well-being of animals. Services : The company may provide advanced laboratory testing services, including blood tests, pathology, microbiology, and other diagnostic analyses. These services would be essential for diagnosing complex health issues in animals. The company also offers consultation services to veterinary professionals on how to use diagnostic tools and interpret results accurately. This support can include training and continuous assistance to ensure optimal use of their products. Vision: Vetlab India’s vision is to become a most Reliable and Respectable name in field of veterinary diagnosis, Mission: The mission of Vetlab India is likely to enhance veterinary care by providing top-notch diagnostic solutions. They aim to support veterinarians in making informed decisions, leading to better health outcomes for animals. The BDM need to visit the clinics to promote our services . The candidate should have good communication and interpersonal skills. We are looking for Business Development manager for our company. Male female both candidates can apply for this job. Manage field marketing team in product promotion and service activities. Develop field marketing plans for improving sbusiness and profitability. Assist the team in planning and scheduling marketing campaigns, tradeshows, conferences, industry meetings, etc. Recommend innovative and creative marketing approaches for revenue growth. Provide guidance to team for product positioning. Monitor and manage expenditures within allotted budget. Recommend marketing techniques and tactics based on changing business demands. Address customer concerns and issues in a professional and timely manner. Monitor field marketing programs regularly to evaluate the efficiency and effectiveness. Act as a primary contact to address questions and inquiries regarding market related activities. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹30,000.00 per month Schedule: Day shift Supplemental Pay: Performance bonus Education: Bachelor's (Preferred) Experience: Business development: 2 years (Preferred) total work: 3 years (Preferred) Language: English (Preferred) Work Location: In person

Location: BANGALORE Experience: 2-3 years Role and Responsibilities: Conduct food safety audit of Food Business Operator as per FSSAI requirement. Verify the compliance by the Food Business Operator of the provisions of the Act and the rules and regulations by FSSAI. Maintain confidentiality of food safety audit. Conduct customized audit across Catering/Base Kitchen Audits/ Live kitchen Audits. Follow up of NC closure for both external and internal audits. Ensure developed corrective action on nonconformities are implemented effectively. Analysis for the identified non-conformities or complaints. Verify the corrective action implementation effectiveness. Conduct training on food safety and hygiene practices. The role requires up to 90% travel within the city. Educational Qualification: Bachelor or Master Degree in food science, Food-technology, Microbiology, Bio-technology from recognized university Preference would be given if acquired Accredited Lead Auditor Course in food safety Management System(lS022000/FSSC22000). Have su cient Knowledge of FSS Act and regulation. Must have sector specific knowledge regarding Hygiene, Sanitary practices, process knowledge, Allergen management, etc. Certified internal auditor on ISO 22000 / HACCP. Knowledge in Quality and Food Safety Management System Job Type: Full-time Schedule: Day shift Application Question(s): How many years of experience do you have in Food Safety? Work Location: In person

Division VTC Mfg - MMR Job posted on Jun 23, 2025 Employee Type P-P8-Probationer-HO Executive Experience range (Years) 1 year - 6 years Walk In Interview for Vaccine Technology Center @ Pune Venue: Radisson Blu Pune Hinjawadi 136/1, Near Mahindra International School, Phase1, Hinjawadi, Pune. T: +91 020 69528000, M: +91 7888013458 Date: - 29.06.2025 (Sunday) Timing: - 9:00 AM to 5:00 PM Ø Education: - Post-Graduate M.Sc. in Biochemistry, Biotechnology, Microbiology, Lifesciences. Ø Experience: - 1-6 years of hands-on experience in relevant field, preferred Vaccine/Biotech background. Vaccine Manufacturing (Cell Culture) Responsible for cell revival, subculture, cell counting of MRC-5 cells. Preparation of MCB/WCB. Experience in Preparation of media and in process buffers in media mixing vessels. Experience in handling Roller bottles, Cell stacks, TCF’s. Experience in working in GMP conditions / production department of viral vaccines. Preparation of SOP, BMR’s, Protocols related to cell culture / virus culture. Experience in virus infection, virus harvesting procedures. Experience in working with Chicken embryo fibroblast cells, pooling of embryos, seeding of RB’s . Quality Control (Bacterial/Viral) Candidate should have good knowledge of Product testing techniques like : Biochemical, Chromatography, Electrophoresis, Immuno assay, Cell culture & Molecular techniques. Experience in handling HPLC, Dionex, UV-Spectrophotometer, Multimode plate reader and ELISA -Shall be well versed with Biochemical assays (Protein, O-acetyl) immuno-chemical assays and electrophoresis, -Knowledge in calibration and qualification of equipment and instruments. -To perform/ monitor activities in compliance with GMP/GLP/GDP and record keeping. -Experience in preparing SOPs, Specification, STPs and Study protocols -To prepare method validation protocol and execute method validation. -Experience in handling stability studies and maintaining records. -Role shall require to coordinate with engineering/ maintenance department or third party labs as and when required. -Should possess basic skills in MS-Office, LIMS & SAP -Analyst shall be well versed with cell based assays, Virus titration, RTPCR and immuno-chemical assays. ==Instrument knowledge on pH meter, Analytical balance, Karl Fischer, Real time PCR and ELISA ==Knowledge in calibration and qualification of equipment and instruments. ==Experience in handling QMS elements like OOS, OOT, change control and deviation are added advantage. ==To perform/Monitor activities in compliance with GMP/GLP. ==Experience in preparing SOPs, specification and study protocols ==To prepare protocol and execute method validation ==Experience in handling stability studies and maintaining Good documentation practice. ==Role shall require to coordinate with maintenance department or third party lab as and when required.

ENVIRONMENTAL HEALTH AND SAFETY RESEARCH & DEVELOPMENT CENTRE is looking for Microbiologist to join our dynamic team and embark on a rewarding career journey Microbial Research: Conduct research to investigate the growth, genetics, physiology, and behavior of microorganisms. Culturing Microorganisms: Grow and maintain cultures of microorganisms for various research and diagnostic purposes. Identification: Identify and classify microorganisms, often using techniques like DNA sequencing, microscopy, and biochemical assays. Disease Detection: Study and diagnose infectious diseases caused by microorganisms, which may involve clinical and diagnostic microbiology. Environmental Analysis: Evaluate the role of microorganisms in environmental processes, such as bioremediation, soil health, and water quality. Food and Beverage: Assess and ensure the safety and quality of food and beverages by monitoring for microbial contamination and spoilage. Pharmaceuticals: Work on the development and production of pharmaceuticals, including antibiotics, vaccines, and biologics. Biotechnology: Contribute to biotechnological processes, such as genetic engineering, fermentation, and the production of biofuels. Laboratory Testing: Perform a wide range of laboratory tests, including microbial culture, antimicrobial susceptibility testing, and molecular techniques. Quality Control: Monitor and maintain quality control in industries like healthcare, pharmaceuticals, and food production. Qualification : B Sc/M.Sc/M.Tech Experience require in NABL and BIS Audit ,FSSAI Documentation Validation,Preparation of SOP Familiar about protocol of Microbiology

Position: MLT Trainer Program : B.Sc. in Medical Laboratory Technology Location : Jaipur Gender - Female About the Role: We are seeking a dedicated and experienced academic professional to join our university campus in Indore as a Lecturer for our B.Sc. in Medical Laboratory Technology program. This role offers the opportunity to contribute to the education and development of future professionals in the field of Medical Laboratory Technology. Key Responsibilities: - Teach undergraduate and possibly postgraduate courses in Medical Laboratory Technology, Microbiology, and Biochemistry. - Develop and deliver engaging lectures, practical sessions, and seminars. - Design and evaluate curricula and assessment methods. - Conduct research and contribute to academic publications. - Provide academic guidance and mentorship to students. - Participate in departmental meetings and contribute to program development. - Educator will have to travel to different locations. Qualifications: - Master’s degree (M.Sc.) in Medical Laboratory Technology, Microbiology, Biochemistry, or a related field. - Bachelor’s degree (B.Sc.) in Medical Laboratory Technology or a closely related field. - 3 to 5 years of clinical and/or teaching experience in Medical Laboratory Technology or a relevant field. Skills and Competencies: - Strong knowledge of Medical Laboratory Technology, Microbiology, and Biochemistry. - Excellent teaching and presentation skills. - Ability to engage and inspire students. - Strong organizational and administrative skills. - Commitment to research and academic excellence. What We Offer: - A dynamic and supportive academic environment. - Opportunities for professional growth and development. - Competitive salary and benefits package. Application Process: Interested candidates should submit their CV, and demo video at kishan@crystalclearservices.in Job Type: Full-time Pay: ₹35,000.00 - ₹55,000.00 per month Education: Bachelor's (Preferred) Experience: Medical Laboratory Technology teaching: 2 years (Required) Work Location: In person

Job Title: Senior Manager/ Manager – Quality Assurance (QA) Department: Quality Assurance Location: Dewas (M.P) Reporting To: Operations Head / Director Role Summary: The QA Head will be responsible for establishing and maintaining strong quality assurance systems and processes to ensure that all products meet regulatory, company, and customer standards. The role involves overseeing raw material inspection, in-process quality control, finished goods evaluation, and compliance with food safety standards in a Soya processing environment. Key Responsibilities: Lead and manage the QA team across the manufacturing unit. Ensure compliance with FSSAI, HACCP, ISO 22000, GMP, and other food safety standards. Monitor quality control procedures for raw materials, intermediate products, and finished goods. Develop and implement SOPs for quality checks and documentation. Manage audits—internal, external (regulatory), and customer audits—and ensure timely closure of NCs (non-conformities). Handle customer complaints and implement corrective/preventive actions (CAPA). Coordinate with production and procurement teams for quality-related issues and improvements. Oversee laboratory functions including testing, analysis, calibration, and equipment maintenance. Lead training sessions on quality and food safety for cross-functional teams. Ensure traceability of all batches and maintain detailed quality documentation. Lead continuous improvement initiatives to enhance product quality and reduce wastage. Qualifications & Experience: M.Sc / B.Sc / B.Tech / M.Tech in Food Technology, Microbiology, Biotechnology, or related discipline. 10–15 years of QA experience in the food industry; prior experience in Soya or edible oil processing preferred. In-depth knowledge of food safety regulations and quality standards. Experience in managing audits and certification processes (ISO, HACCP, FSSC, etc.) Strong leadership, analytical, and communication skills. Key Skills: Food Safety & Hygiene Compliance Quality Management Systems (QMS) Analytical Testing & Lab Management Root Cause Analysis & CAPA Regulatory & Customer Audit Handling Documentation & SOP Development Team Leadership & Cross-functional Coordination Job Type: Full-time Pay: ₹924,528.74 - ₹1,200,716.59 per year Application Question(s): Do you have experience of audit handling? Work Location: In person

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com . Job Summary Reporting to the General Manager, QA 3rd Party Ops, India, this role is responsible for supporting the Quality Systems required to ensure that Apotex meets its regulatory and GMP compliance obligations for Apotex Suppliers. Support Managers with compliance activities for Third Party Organizations and Customer Operations. Responsible for executing GMP activities related to the corporate governance of Suppliers to global Apotex Manufacturing Sites. Job Responsibilities Negotiates with external suppliers on the provisions of the customer Quality Agreements. Makes decisions in consultation with the Manager, External Quality on the respective quality responsibilities to ensure both parties are compliant to GMP and meet Apotex internal standards. Responsible for ensuring that Quality Agreements are in place and current for vendors supplying to multiple Apotex Manufacturing Sites. Liaise directly with Apotex Suppliers in negotiating Supplier Quality Agreements and escalate to management when roadblocks occur. Monitor and track status of Quality Agreements. Provides support to External Quality Managers, in reviewing GMP Quality Documents that form part of Product Compliance Files. Reviews third party manufacturer’s Stability protocols and Summary Reports. Reviews and approves third party manufacturer’s Change Controls. Provides support to Customer Operations Manager, in processing customer requests for products manufactured by Apotex for Third Parties. Works as a member of a team to achieve all outcomes. Performs all work in accordance with all established regulatory and compliance and safety requirements. Performs all work in compliance with our Code of Conduct and Business Ethics, and related policies and with the legal and regulatory requirements that apply to our job activities. Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements. Performs all work in support of our Corporate Values: Collaboration, Courage, Perseverance, and Passion. All other relevant duties as assigned. Job Requirements Education Minimum B.Sc. in Biology, Microbiology, Chemistry, Pharmacy or a related science Knowledge, Skills and Abilities Must be familiar with overall pharmaceutical manufacturing and quality systems/process. Good knowledge of global GMPs and QA/QC systems associated with the manufacture of human drug products. Excellent written and verbal English communication skills. Excellent interpersonal skills and ability to relate well to internal and external customers. Experience Minimum 8 years experience in the pharmaceutical industry with relevant QA/QC/Mfg experience, preferably with multiple dosage forms. Experience with international regulations (e.g. Health Canda, US FDA, EU) is an asset. Must be detail oriented, accurate and reliable. Demonstrate personal leadership and accountability. Excellent organization skills and analytical thinking. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

The primary job function of the Field Application Specialist includes but not limited to: Provide pre and post sales technical application support to customers to achieve customer satisfaction and business objectives. Conduct product application trainings to customers and to internal team members. Manage product evaluation at customer site to meet business objectives Support sales personnel to achieve team objectives He/she needs to be independent, self-motivated, likes to work with different people and can work under pressure. He should be ready for frequent traveling as almost 75% traveling is required in this position. Possess positive attitude towards work, forthcoming, ability to multi-task, creative in handling technical application service matters/problems. He/she should possess exceptional verbal and written communication skills, excellent inter-personal skill, soft skill in customer relation management, organization skill, as well as excellent technical analysis and problem-solving skills. How You’ll Make An Impact Provide pre- and post-sales technical application support Provide post-sales technical application support & training mainly for trouble shooting purpose to achieve customer satisfaction and meet business objectives Develop a systematic troubleshooting approach to diagnose common application problems to be shared among team members. Manage product evaluation and provide feedback on further evaluation needs at customer site as part of sales process and ensure it meets business objectives Conduct pre-sales product presentations and demonstrations. Create training / Demo module (training notes, equipment, consumables & checklist) to be used as reference for other FAS. Work with manager to devise the yearly application training plan Ensure that the Bio-Rad commitment to customer satisfaction is achieved and constantly improved. Log in all field visits in Salesforce (SFDC) and upload supporting reports Maintain internal documents for application trainings conducted Ensure all instruments used for evaluation are properly accounted for Collect reference/performance letters for different products from customers regularly Presentation on specific product applications Prepare materials required for workshop/exhibitions & seminars Manage relationships with key customers & develop reference/key seminars Managing products performance related complaints and replacement requests Submit product related complaints to Product team in timely fashion and do the evaluation Ensure that all relevant documentation is in order and traceable What You Bring Experience of working in life science research laboratory for at least 2 years. Proactive and passionate to provide excellent support to meet customer satisfaction. Excellent written, oral communication and presentation skills. Must have proven track record of hands-on experience in conducting wet lab experiments for at least 2 of the techniques (preferably more) Protein Purification (FPLC) Chromatography SDS-PAGE, Western Blotting, Imaging (Protein/DNA gel & blot documentation) PCR, Electrophoresis, Real-Time PCR, Transfection Droplet Digital PCR (ddPCR) Flow cytometry, cell Imaging & cell culture ELISA, Multiplex Immunoassays and use of different antibodies Experience at managing evaluation and training Proven track record to meet customer satisfaction in a technical support environment Able to work independently and pro-actively Preferably Ph.D. in Life Sciences (Biotechnology, Biochemistry, Microbiology etc Minimum 2 years working experience in a life science research laboratory with strong technical understanding of laboratory procedures Superior technical application knowledge of diagnostic/research methodologies Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Recently voted a Best Place to Work, Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see. Benefits: Bio-Rad's biggest asset is its people, and the reason why our Total Rewards deliver programs that provide value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Our robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees through the various stages of an employee’s work and life cycle. We’re proud to offer a variety of options, including competitive insurance plans for you and your immediate family, Annual Health checkup , Marriage Leave, Paternity Leave ,Employee Assistance Programme , extensive learning and development opportunities, and more. EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with disabilities, and people of all races, ethnicities, genders, ages, and orientations are encouraged to apply. Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resum Legal Entity: (IND_3006)Bio-Rad Laboratories (India) Pvt Ltd

Walk-In Interview for Life Science Graduates in Medical Coding at Vee Healthtek, Salem on June 28 & 29, 2025 Eligibility : Graduates in Life Sciences Only (Candidates with non-life science degrees or diplomas or final year students/who has stand-in arrears are not eligible) Job Location : Salem- Work From Office Interview Schedule : June 28 & 29, 2025 at 10:00 AM Sharp (Late Comers won't be allowed) Interview Venue: Vee Healthtek Pvt Ltd (V5), Plot No:14, IT/ITES ELCOT SEZ (Salem Allotment), Salem to Bengaluru NH-7 Road, Jagir Ammapalayam Village, Suramangalam SRO, Salem - 636302 Compensation : CTC of 21,000 per month Shift Details : Rotational shifts as per business needs Interview Process : Two rounds (Technical Assessment & Final Oral Technical Interview) Joining Date : Immediate Required Documents for the Interview: Original 10th & 12th Mark Sheets and Resume Important Note : Candidates will be required to sign a minimum commitment of 18 months and submit the original 10th/12th Mark Sheets. Topics to Prepare for the Interview: - Human anatomy and physiology systems - General medical terminologies - Medical Coding, ICD, and CPT Contact Information: Ramesh- 9443238706 (Available on WhatsApp) ramesh.m@veehealthtek.com Important Note: Please be advised that only candidates who have successfully completed their studies and present original mark sheets will be permitted to attend the walk-in interview. Additionally, participation is limited to a maximum of 250 individuals per day, and entry will be granted on a first-come, first-served basis. Regards Ramesh- HRD

Who we are At Progenesis, we are a team of experts fighting against infertility issues that couples often face, ensuring a hurdle-free journey towards pregnancy. It was in 2014 when we first stepped into the area of healthcare with the sole motto of being companions in highs & lows of couples journey to parenthood. Company Website - www.progenesisivf.com What you will do | Job Responsibility ● Semen analysis. ● Semen Washing. ● IUI. ● Semen freezing and semen thawing. ● Lab cleaning. ● Documentation. ● Media aliquoting. ● Assisting in ET. ● E-mails and order to be placed. ● DFI. ● Stock. ● Consent forms. ● Machines. What you need to have | Job Specification Experience 2 Years of Relevant Experience Education Msc/Bsc Microbiology, BioTech, Msc in Clinical Embryology, MSc/Bsc in Zoology Language Marathi (Mandatory) Hindi and English Required Female Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Language: Marathi (Required) Location: Dhule, Maharashtra (Required) Shift availability: Day Shift (Required) Willingness to travel: 100% (Required) Work Location: In person

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

We require doctors for Medical Colleges & Hospitals Pan India Qualification : MD / MS / DNB (All Department ) 0-5 years of experience after MS/MD degree (any specialization) Position : Consultant , Senior Resident , Assistant Professor , Associate Professor , Professor Department : Clinical & Non Clinical Key-skills - Strong knowledge of Different Departments according to Qualification . Excellent communication skills for effective interaction with patients & colleagues. Ability to work efficiently under pressure during emergencies or critical situations Reema Call/Whatsapp : 9877677063 Email Id - weps.hrworld@gmail.com

Job Description Position: Medical Coder Ct: HR SRIMATHI 7358425167 Job Description:Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis (Medical Problems) and Procedure (Treatments) Codes using ICD-10 CM and CPT code books. Requirement: knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills No of vacancy: 500 Eligibility: Nursing GNM/DGNM Life science graduates Pharmacy Physician assistant Bio medical Engineers Bio chemistry Bio technology Bio informatics Micro biology Zoology and Advanced zoology Biology Botany Plant biotechnology Genetics Food and Nutrition Paramedical Physiotherapy M.Sc. Clinical Nutrition M.Sc. Human Genetics M.Sc. Medical Laboratory Technology M.Sc. Medical Sociology M.Sc. Epidemiology M.Sc. Molecular Virology M.Sc. Biostatistics M.Sc. Blood Banking Technology M.Sc. Rgnerative Medicine M.Optom. M.Sc. Genetic Counseling M.Sc. Radiolog & Imaging Technology M.Sc. Medical Biochemistry M.Sc, Medical Microbiology M.Sc. Clinical Care Technology M.Sc. Clinical Care Technology M.Sc. Medical Physics B.Sc. - Accident & Emergency Care Technology B.Sc. - Audiology & speech Language Pathology B.Sc. - Cardiac Technology B.Sc. - Cardio Pulmonary Perfusion Care Technology B.Sc. - Critical Care Technology B.Sc. - Dialysis Technology B.Sc. - Neuro Electrophysiology B.Sc. - M.L.T. B.Sc. - Medical Sociology B.Sc. - Nuclear Medicine Technology B.Sc. - Operation Theatre & Anaesthesia Technology Bachelor of Science in Optometry B.Sc. - Physician Assistant B.Sc. - Radiology Imaging Technology B.Sc. - Radiotherapy Technology B.Sc. - Medical Record Science B.Sc. - Respiratory Therapy B.Sc. - Fitness and Lifestyle Modifications Accident & Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre & Anaesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology & Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Salary 15K to 17K (fresher) To 50K (experienced) Pm (Incentives && Benefits as per Corporate Standards) 4K fixed hike after six months Other Benefit: 1. Pick Up & Drop Facility 2. Food Facility 3. Day Shift 4. Weekend Off Reach us : SRIMATHI 7358425167 Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology GNM DGNM Physician assistant Anesthesia technician Perfusion Technology Medical coder Freshers Medical coding Freshers jobs in chennai Medical coding openings in chennai Wanted Medical coder Freshers jobs Medical coding Medical coder Medical coding Freshers Jobs in chennai Jobs for Passed outs Freshers jobs in chennai Jobs for freshers Nursing jobs for freshers Pharma jobs for Freshers Biotechology Jobs Microbiology jobs Biomedical jobs Bioinformatics jobs Bsc/Msc Jobs Biochemistry jobs Life science jobs in chennai Paramedical jobs in chennai Jobs in Tamilnadu Jobs in Pharmacy Jobs in Hospital Perks and Benefits Incentives & Benefits as per Corporate Standards