2560 Microbiology Jobs - Page 35

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

Medical college Jobs _ SR, Assistant Location : Hyderabad, Chennai, Bangalore MD/DNB or MS Microbiology biochemistry Community Medicine Anatomy Physiology Contact :Venu - 9642384567 hrdmedicoplacements@gmail.com Required Candidate profile part time jobs - Associate professors

Wondering what’s within Beckman Coulter Diagnostics? Take a closer look. At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In this role, you will have the opportunity to: Lead and manage the sustaining engineering activities for Electro-Mechanical products. Assist in the design and development of innovative mechanical solutions to improve performance, safety, reliability, throughput and cost-effectiveness (Knowledge of Should costing and estimation), in Design Change Project. Act as design change lead and ability to handle entire Design change process independently. Handle multiple projects with proper project planning and minimal guidance. Mentor and guide junior engineers and technicians provide technical leadership and actively transfer knowledge/expertise. Conduct root cause analysis and implement corrective actions for product issues. Collaborate with cross function teams, manufacturing, quality, and supply chain teams to resolve production and field issues. conduct feasibility studies, risk assessments, and design reviews to ensure project success and validate designs through analysis and testing. The essential requirements of the job include: Bachelor’s degree in mechanical engineering or a related field with 7+ years of experience and working with global teams. Strong knowledge of mechanical design principles, materials, manufacturing processes and Proficiency in SolidWorks CAD software and simulation tools. Knowledge of Tear down analysis and Reverse engineering, dFMEA/pFMEA, DFX, Tolerance Stack-up Analysis and GD&T, Create and maintain detailed engineering documentation, including CAD models, drawings, specifications, test plans. Experience with medical device regulations (FDA, ISO 13485, ISO 14971, IEC 60601) and Ensure compliance with industry standards, regulations, and company policies. Basic knowledge of metals and materials, its application knowledge on mechanical parts fabrication, Rapid prototyping and testing. Thorough knowledge on Selection of mechanical Off-the shelves components. Manage interactions with suppliers to ensure quality and timely delivery of components. Strong communication, interpersonal skills and Stakeholder management. Should have good Analytical skills, Excellent problem-solving skills and attention to detail. Ability to work effectively in a fast-paced, dynamic environment. Understand technical operations and make efficient decisions on routine engineering matters. Able to swiftly adapt to changes in project direction from management. It would be a plus if you also possess previous experience in: Experience in medical device design & development is a plus Experience in IVD instrumentation, such as clinical chemistry, immunoassay, hematology, urinalysis, molecular, microbiology or flow cytometry systems is a plus Advanced certification in CAD tools Familiarity with lean manufacturing and Six Sigma principles. Prior work experience in Electro-Mechanical products, Robotics and Automation Join our winning team today. Together, 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.

Company Name Fresh to Home Job Title QA- Sr. Executive Job Location: Karnataka Description Fresh it´s a new, simple and practical way to do groceries. We are an online supermarket decided to impose a positive change in the way we experience groceries. Job Description The Quality Assurance Executive/ Senior Executive is responsible for overseeing and ensuring the consistent application of quality assurance protocols and food safety standards within a designated food manufacturing plant. This role acts as an impartial third-party, providing expert oversight, independent verification, and continuous improvement recommendations to enhance product quality, safety, and regulatory compliance. The ideal candidate will possess a strong background in food science, quality assurance, and a thorough understanding of relevant food safety regulations (e.g., FSSAI, HACCP, GMP, ISO 22000). Open Positions: 1 Skills Required: FSMS, Food Safety, FSSAI regulations, HACCP, GMP, ISO 22000), Auditing, Training Skills Key Responsibilities Quality Assurance and Food Safety Oversight: * Conduct regular, unannounced inspections of production lines, raw material storage, finished product warehousing, and all operational areas to ensure adherence to established quality and food safety standards. * Verify the implementation and effectiveness of the plant’s HACCP (Hazard Analysis and Critical Control Points) plan, PRPs (Prerequisite Programs), and OPRPs (Operational Prerequisite Programs). * Monitor and verify critical control points (CCPs) and ensure appropriate corrective actions are taken when deviations occur. * Review and approve incoming raw materials, packaging materials, and finished products against specifications. * Oversee the calibration and maintenance of quality testing equipment. * Ensure proper sanitation procedures are followed throughout the plant. Auditing and Compliance: * Perform internal audits (product, process, system) to identify non-conformities and areas for improvement against client specifications, internal standards, and regulatory requirements (e.g., FSSAI regulations, local health codes). * Assist the plant in preparing for and participating in external audits (e.g., regulatory, customer, certification audits). * Ensure compliance with all applicable national and international food safety regulations and standards. * Maintain thorough and accurate documentation of all audits, inspections, and quality records. Data Analysis and Reporting: * Collect, analyze, and interpret quality data (e.g., sensory analysis, microbiological testing, physical attributes, complaint data). * Generate detailed reports on quality performance, non-conformances, and corrective actions for the premises. * Identify trends, root causes of quality issues, and recommend preventative measures. * Present findings and recommendations to plant management and stakeholders. Corrective and Preventive Actions (CAPA): * Investigate customer complaints, internal non-conformances, and quality deviations thoroughly to determine root causes. * Collaborate with plant personnel to develop and implement effective corrective and preventive actions. * Follow up on the effectiveness of implemented CAPAs to ensure sustained improvement. Training and Development: * Provide guidance and support to plant personnel on quality assurance and food safety best practices. * Identify training needs and potentially assist in the delivery of training programs related to food safety, GMPs, and quality control. Continuous Improvement: * Proactively identify opportunities for process optimization and quality enhancement within the plant. * Work collaboratively with plant management and production teams to implement improvement initiatives. * Stay updated on industry best practices, emerging food safety risks, and regulatory changes. Relationship Management: * Maintain a professional and collaborative working relationship with all levels of staff at the food plant. * Act as a liaison between [Your Company and the 3P Vendor to ensure clear communication and alignment on quality objectives. Qualifications Education: Bachelor’s degree or Master’s degree in Food Science, Food Technology, Microbiology, Chemistry, or a related scientific field. Experience Minimum 3-5 years of progressive experience in Quality Assurance/Food Safety within the food manufacturing industry. Experience working in a 3rd party auditing or consulting role is highly desirable. Strong understanding of various food processing technologies Certifications (Preferred) FSSC 22000 Internal auditor HACCP Certification Internal Auditor training for food safety management systems. Skills Good knowledge of food safety principles, quality management systems, and regulatory requirements (FSSAI, etc.). Strong analytical and problem-solving skills with attention to detail. Good communication (written and verbal) and interpersonal skills. Proficient in using quality management software and Microsoft Office Suite (Excel, Word, PowerPoint). Ability to work independently, make sound decisions, and manage multiple priorities. Strong ethical conduct and integrity. Ability to travel as needed (if applicable, e.g., to different plant locations). Apply Here https://careers.fresh2home.com/fresh2home/jobview/qa-sr-executive-karnataka-2025070511541696?source=linkedin

shroffsfoundation is looking for Lab Technician to join our dynamic team and embark on a rewarding career journeyAssist with testing and calibrating lab equipment in preparation for specific tasksAnalyze retrieved data and prepare reports for laboratory managementExperience in data collection and interpretation as well as the storage and retrieval of samples in a laboratory setting.

About HCP Wellness At HCP Wellness Private Limited , we are committed to delivering safe, effective, and high-quality skin care, cosmetic, and oral care products. Our culture thrives on scientific excellence, GMP compliance, and sustainable innovation. We believe in empowering our team to lead quality-focused solutions that help build trusted personal care brands. Job Overview We are looking for a Microbiologist to join our Quality & R&D division in Ahmedabad. The ideal candidate will be responsible for ensuring microbiological safety and compliance of all raw materials, bulk, and finished goods used in cosmetic and personal care product manufacturing. Your insights will directly impact product integrity, consumer safety, and regulatory compliance. Key Responsibilities Perform microbiological testing of raw materials, in-process samples, water systems, packaging, and finished goods. Conduct environmental monitoring of cleanrooms and production areas (air, surface, and personnel hygiene). Validate disinfectants, preservative efficacy, and microbial limits as per pharmacopeial standards (IP/BP/USP). Maintain and calibrate laboratory equipment and ensure proper documentation (SOPs, logbooks, test records). Support product stability studies, contamination investigations, and root cause analysis. Coordinate with QA and R&D for batch release, deviation handling, and process improvements. Ensure adherence to GMP, ISO, and regulatory compliance for cosmetic and oral care formulations. Qualifications & Skills Education / Certifications: B.Sc / M.Sc in Microbiology, Biotechnology, or Life Sciences Hard Skills: Expertise in microbial testing techniques (TPC, Yeast & Mold, Pathogens) Hands-on experience with colony counters, autoclaves, incubators, and laminar airflow Familiarity with preservative efficacy testing (PET), D-value & Z-value analysis Knowledge of regulatory guidelines BIS, FDA, ISO, and cosmetic-specific standards Soft Skills: Detail-oriented and accurate in documentation and reporting Strong analytical and problem-solving skills Team player with good communication across departments Ability to handle audits and provide scientific justifications Preferred Experience: 3+ years of hands-on experience in microbiology testing within a cosmetics, pharma, or personal care manufacturing setup Why Join Us? Be part of a growing and future-focused company where your scientific contributions directly shape the quality and safety of consumer products. We offer a collaborative and innovation-driven work culture, aligned with global best practices in personal care manufacturing. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

About HCP Wellness Private Limited: HCP Wellness is a GMP-certified, innovation-led contract manufacturer specializing in skin care, cosmetic, and oral care products. We believe in quality, consistency, and customer satisfaction fueled by science, safety, and sustainability. Join a growing team where quality meets innovation. Job Overview: We are seeking an experienced QC Microbiologist to support our quality control operations by performing microbiological testing on raw materials, bulk, and finished goods. The ideal candidate will ensure that all products meet regulatory, safety, and quality standards. Key Responsibilities: Conduct routine microbiological testing (TPC, yeast & mold, pathogens) on raw materials, in-process, and finished products. Perform environmental monitoring and maintain hygiene compliance across production areas. Validate sterilization methods and efficacy of preservatives in formulations. Calibrate and maintain laboratory instruments and microbial media as per SOPs. Document and report results accurately in line with cGMP and regulatory requirements. Coordinate with QA, production, and R&D teams for troubleshooting and investigations. Participate in internal audits and assist in regulatory inspections as needed. Required Qualifications: Education: B.Sc./M.Sc. in Microbiology or Biotechnology Hard Skills: Microbial limit testing, preservative efficacy testing, and identification techniques Use of laboratory instruments like autoclaves, incubators, laminar airflow cabinets Knowledge of pharmacopeial methods (IP, USP, BP) Proficient in documentation as per cGMP and SOP protocols Soft Skills: Detail-oriented with strong analytical and observational skills Team collaboration and good communication across departments Ability to manage lab timelines and troubleshoot independently Strong organizational and reporting ability Preferred Experience: Minimum 3 years of hands-on experience in a microbiology laboratory, preferably within a cosmetic, personal care, or pharmaceutical manufacturing setup. Why Join Us? Be part of an R&D-driven, future-focused manufacturing company Collaborative culture that values quality, innovation, and personal growth Competitive compensation, learning opportunities, and a cleanroom-grade work environment Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

Mynvax is a clinical-stage vaccine biotechnology company headquartered in Bangalore, India, developing novel, recombinant, and thermostable vaccines against respiratory viral infections, including influenza and RSV. With a pipeline of promising candidates and multiple ongoing collaborations, Mynvax offers a unique opportunity to work at the cutting edge of vaccine development. Role Perform gene cloning using various strategies including restriction/ligation, Gibson Assembly, and Golden Gate. Carry out site-directed mutagenesis and construct verification. Design and run PCR assays for amplification and screening. Prepare and submit samples for Sanger sequencing; analyze sequencing results. Express recombinant proteins in E. coli or other expression systems. Run SDS-PAGE and Western blotting for protein expression and analysis. Maintain accurate and detailed lab records; ensure reproducibility and quality of experimental data. Collaborate with team members involved in antigen production and vaccine R&D. Required Qualifications M.Sc. or M.Tech. in Molecular Biology, Biotechnology, Microbiology, or related field. 0-3 years of hands-on experience in molecular biology techniques. Experience with cloning methods including restriction/ligation, Gibson Assembly, Golden Gate, and site-directed mutagenesis. Basic understanding of recombinant protein expression workflows. Familiarity with PCR, gel electrophoresis, and gel-based detection methods. Desirable Skills Experience in bacterial transformation, plasmid preparation, and cloning troubleshooting. Experience with mammalian and insect cells expression systems. Knowledge of protein purification techniques such as Ni-NTA affinity chromatography. Familiarity with software tools for primer design and sequence analysis. What Mynvax offers: A dynamic research environment with exposure to cutting-edge vaccine development. Mentoring by senior scientists and opportunity for career growth. Competitive salary and full-time employment benefits. Location: Bangalore, India Company: Mynvax Private Limited Position Type: Full-Time Start Date: Immediate How to Apply: Email your CV and a brief cover letter to careers@mynvax.com Subject line: "Application-Research Associate Molecular Biology" Apply on LinkedIn: Research Associate-Molecular Biology

About HCP Wellness Private Limited At HCP Wellness , we are committed to delivering high-quality, innovative, and safe cosmetic and personal care products. Rooted in scientific excellence and a customer-first approach, we combine tradition and technology to craft skincare, oral care, and cosmetic solutions that people trust. Our culture is built on integrity, continuous learning, and a passion for wellness. Job Overview We are seeking a detail-oriented and quality-focused Microbiologist to join our dynamic Quality Assurance & R&D team. The ideal candidate will play a vital role in ensuring microbiological safety and compliance of our cosmetic and oral care products, supporting regulatory requirements and brand integrity. Key Responsibilities Perform microbiological testing on raw materials, in-process samples, and finished goods (TPC, Yeast & Mold, Pathogens etc.) Maintain and calibrate microbiology lab instruments and ensure timely documentation. Prepare and standardize culture media as per ISO, BIS, and GMP standards. Conduct environmental monitoring (air sampling, surface swabs, personnel hygiene monitoring). Investigate microbial contamination and implement corrective & preventive actions (CAPA). Work collaboratively with QA/QC, production, and R&D teams to ensure product safety and compliance. Stay up to date with relevant cosmetic microbiology standards and regulatory guidelines (e.g., IS 14648, ISO 22716, FDA, BIS). Qualifications & Skills Hard Skills Strong knowledge of microbiological testing methods and GMP/GLP practices. Proficiency in working with microbiological instruments (Incubators, Autoclaves, Laminar Flow, etc.). Understanding of regulatory requirements specific to cosmetics and personal care manufacturing. Ability to handle and interpret microbial limit tests (MLT), preservative efficacy test (PET), etc. Soft Skills High attention to detail and accuracy. Strong analytical and problem-solving skills. Excellent communication and documentation skills. Team-oriented, self-motivated, and adaptable to a fast-paced environment. Education & Certifications B.Sc. / M.Sc. in Microbiology or related Life Sciences field. Preferred Experience 3+ years of hands-on experience in a microbiology role within a cosmetic, pharmaceutical, or personal care manufacturing environment. Why Join HCP Wellness? Be part of an innovative and ethical company committed to wellness and sustainability. Work in a GMP & ISO-certified facility with a strong quality-centric culture. Grow with a team that values integrity, scientific rigor, and continuous improvement. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

Research Associate, Cell Culture and Bioassays About Mynvax Mynvax is a clinical-stage vaccine biotechnology company headquartered in Bangalore, India, developing novel, recombinant, and thermostable vaccines against respiratory viral infections, including influenza and RSV. With a pipeline of promising candidates and multiple ongoing collaborations, Mynvax offers a unique opportunity to work at the cutting edge of vaccine development. Role Maintain and passage mammalian cell lines under sterile conditions. Support in vitro bioassays such as ELISA, virus neutralization assays, and cytopathic effect-based assays. Perform RNA isolation, cDNA synthesis, and qPCR for viral load estimation. Assist in the preparation and handling of BSL-2 viruses under appropriate biosafety protocols. Process animal sera or tissue samples for immunological analysis. Maintain laboratory notebooks and electronic records with high attention to detail. Assist with assay optimization, reagent preparation, and documentation for preclinical studies. Ensure compliance with biosafety and quality standards during laboratory operations. Required Qualifications M.Sc. or M. Tech in biotechnology, microbiology, immunology, or related life science fields. 0-3 years of hands-on laboratory experience in academic or industrial settings. Familiarity with mammalian cell culture, ELISA, and virus-based neutralization assays. Knowledge of BSL-2 biosafety practices and handling of infectious materials. Good understanding of basic laboratory techniques and experimental design. Desirable Skills Experience with in vivo sample collection or processing from preclinical models. Exposure to data analysis tools and statistical interpretation of assay results. Prior work in a regulated or GLP/GMP-compliant environment. What Mynvax offers: A dynamic research environment with exposure to cutting-edge vaccine development. Training and mentorship in immunology, virology, and preclinical research. Collaborative environment with growth opportunities and skill development. Competitive salary and full-time employment benefits.

About Us: At HCP Wellness Private Limited , we are committed to delivering premium-quality skincare, cosmetic, and oral care products through innovation, safety, and compliance. Our values emphasize integrity, scientific excellence, and customer-centric solutions across every aspect of manufacturing. We are currently seeking a QC Microbiologist to join our Skin Care & Oral Care Division and ensure our products meet the highest microbiological standards. Role Overview: The QC Microbiologist will play a critical role in maintaining microbiological quality standards across the production of skin care and oral care products. This includes routine sampling, microbial testing, environmental monitoring, and compliance with GMP standards. The ideal candidate will have hands-on lab experience and a proactive approach to product safety and process hygiene. Key Responsibilities: Conduct microbiological testing of raw materials, bulk, and finished products (e.g., TVC, yeast & mold, pathogen testing) Perform environmental monitoring (air sampling, surface swabs, water testing) in production and QC areas Validate and maintain aseptic techniques and microbial limits Investigate microbial contamination and assist in root cause analysis and CAPA implementation Maintain detailed documentation and test records in compliance with GMP and GLP Ensure all QC microbiological equipment is calibrated and maintained Collaborate with QA, production, and R&D teams for continuous improvement in quality standards Stay updated with regulatory guidelines such as BIS, ISO 22716 (GMP for Cosmetics), and FDA Required Qualifications: Education: B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life sciences field Hard Skills: Proficiency in microbial testing (TVC, MPN, Pathogen Detection, etc.) Experience with autoclaves, laminar flow hoods, incubators, and related lab equipment Familiarity with regulatory documentation and SOPs Working knowledge of ISO, GMP, and microbiological quality systems Soft Skills: Attention to detail and strong observational skills Effective communication and reporting skills Analytical thinking and problem-solving attitude Team player with a quality-first mindset Preferred Experience: 3 to 4 years of hands-on experience in QC Microbiology in the cosmetics, skin care, or oral care industry Prior exposure to contract manufacturing or third-party testing labs is a plus Why Join HCP Wellness? Work in a GMP-certified, innovation-driven facility Be part of a growing cosmetic manufacturing leader in India Opportunity to grow with a culture that fosters scientific excellence and quality leadership Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

About Us: HCP Wellness Private Limited is a leading name in the manufacturing of high-quality skincare, cosmetics, and oral care products. As a GMP-certified and innovation-driven company, we are committed to product safety, quality, and excellence. Our work culture promotes integrity, collaboration, and continuous improvement. Position Overview: We are seeking a detail-oriented and quality-focused Microbiologist to support our Quality Control and R&D teams. The ideal candidate will ensure all cosmetic and personal care products meet microbiological safety and compliance standards in line with national and international regulatory guidelines. Key Responsibilities: Perform microbiological testing of raw materials, bulk, and finished cosmetic products. Conduct environmental monitoring of production and packaging areas. Validate and monitor water systems (RO/DM/Water for Injection) for microbial contamination. Prepare and maintain microbiological documentation, reports, and SOPs. Carry out microbial limit tests (MLT), preservative efficacy testing (PET), and pathogen identification. Ensure adherence to GMP, ISO, and cosmetic regulatory norms. Support QA/QC investigations in case of non-compliance or contamination. Coordinate with the R&D and production teams for product formulation safety. Required Qualifications: Education: B.Sc./M.Sc. in Microbiology, Biotechnology, or related life sciences field. Experience: Minimum 3 to 4 years in microbiological testing within cosmetics, personal care, or pharmaceutical manufacturing. Hard Skills: Strong knowledge of microbial limit tests, preservative efficacy testing, and aseptic techniques. Proficient in operating microbiology lab equipment (incubators, autoclaves, laminar flow, etc.). Familiar with regulatory standards (GMP, ISO 22716, BIS, FDA guidelines). Technical writing and documentation skills for lab reports and audits. Soft Skills: Attention to detail with strong analytical thinking. Good communication and team collaboration abilities. Problem-solving mindset with a focus on root cause analysis. Ability to work under pressure and meet tight deadlines. Why Join HCP Wellness? Opportunity to work with a leading third-party cosmetic manufacturer. Culture of innovation, integrity, and continuous learning. Safe and compliant work environment with career growth opportunities. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

Job Description Position: Medical Coder Ct: HR Shanmugapriya -8072891550 Job Description: Position: Medical Coder. . Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medical 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

Kenvue Is Currently Recruiting For A: Manager, R&D Analytical What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role Reports To: Director - Analytical Chemistry Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Fully Onsite What You Will Do Kenvue is currently recruiting for: Manager, R&D Analytical This position currently would report to the Director, R&D Analytical and Microbiology Operations and is based at Mumbai. Who We Are At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role reports to: Director, R&D Analytical and Microbiology Operations Location: Mumbai Travel %: 10 What You Will Do The Manager, R&D Analytical, would be responsible for leading the analytical activities for the Kenvue product portfolio such as defining the analytical strategy, execution planning, timing, resource requirements and interdependencies to complete the innovation and lifecycle management project deliverables. The role shall be responsible for delivering projects which deploy advanced analytical technologies and data interpretation tools and thus needs to be expert in these techniques. In addition, the role includes contributing to digital and data driven tools, lab automation and optimization of analytical processes to drive efficiencies through application of such advanced tools. The ideal candidate will be a subject matter expert in the Analytical domain and will have strong communication skills to partner with business partners independently lead projects. This is a people leader role, and hence specific skills related to people leader capabilities would be expected. Key Responsibilities Management of people, projects, lab systems and processes applied to Analytical R&D for the Innovation Pipeline in support of the portfolio. Deliver project milestones, excellence in execution of analytical studies (raw material and finished product) and documentation in compliance with requirements from internal policies and applicable regulations. Planning and executing the analytical strategy for new product development such as Test Method Development, Test Method Validation and Transfer to Quality Control Labs (internal and external) and CRO’s, Stability Studies, Impurity and degradation pathway assessments, etc. Advanced Analytical solutions (e.g. but not limited to Elemental impurities, Extractable and Leachable, Nitrosamines, etc.) and assessments using hi-tech instrumentation Technical documentation: protocols, reports, change controls, specifications, etc. Communicate the project progress to management, business partners, and team members. Attend and/or facilitate project and technical meetings. Assessment of internal processes identifying opportunities and implementing improvements such as organization of activities, redistribution of tasks, reduction of lead time and rework. Active participation in internal and external audits, from the preparation for the audit to responses to observation and closing out of action plans/commitments. Lead and manage team of scientific professionals: performance, development and coaching Representation on Global functional teams for specific assignments to lead future focused analytical strategies and solutions. Required Qualifications What we are looking for PhD preferred or Minimum Masters in Chemistry or with related field with minimum 12 to 15 years of experience. Work experience preferred in a consumer health or pharmaceutical industry, with at least 5 years in GMP working environment Strong knowledge and hand-on experience of advanced Analytical quantitative and qualitative techniques applied to finished products and raw materials e.g. MS, ICP-OES/MS, LC-MS/MS, NMR, etc. Deep knowledge and hands-on experience of lab operational and quality excellence tools to facilitate smart lab operations, workflows and data management. Experience of application of AI, data analytics, automation in Analytical domain highly preferred. Have strategic and operational skills to prioritize and complete projects based on business and compliance needs. Strong communication and presentation skills to effectively convey complex data insights Display of specific leadership attributes which indicate next level potential to take up higher roles Experience with change control processes and providing technical assessments and documentation to support changes for Finished Products Specifications, Raw Material, and/or Test Methods used at Internal and External Manufacturing sites. Strong and effective communication skills across different layers of the organization, as this role requires consistent, frequent collaborations with global sites, through virtual meetings and email correspondences. Strong knowledge in current compendia, industry standards, product registrations Experience in leading without follow-ups and frequent guidance assigned projects to meet business objectives Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

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 Sheetal Call/Whatsapp : 7814536255 Email Id - Email:weps.recruit@gmail.com

We are seeking to hire an innovative and highly motivated Research Associate for our Biologics RD team for our Mangalore lab. The qualified individual will have at least 1-3 years of relevant industry working experience in developing parenteral formulation, solid and liquid oral dosage forms for use in first-in-human studies. This is a highly collaborative role, that provides support to multiple project and senior scientist in a given day. The Research associate will be a lab-based role, will be working in pre-formulation, formulation, characterization, and analytical development of therapeutic proteins including monoclonal antibodies, virus-like particles, RNA therapeutics, and subunit-based vaccines. Since most of our clients are based out of USA and Europe, it is desirable that candidates to have some exposure working on international projects. Major Duties and Responsibilities Performing sample preparation steps which may include sample pipetting with a high degree of accuracy and precision Performing reagent and material preparation for testing Calibrating and maintaining all assigned laboratory equipment and instruments according to standard operating procedures to ensure quality results Maintain adequate inventory of supplies, reagents and materials needed for testing Document remedial action, troubleshooting, quality assurance activities and instrument maintenance Adhere to established processing timelines Perform cleaning and maintenance duties for laboratory spaces and instrumentation Retrieve and catalog samples for testing Properly store samples for short term and long-term storage Adhere to all quality and safety standards, as well as ensuring compliance with all applicable regulatory agencies Adhere to policies and protocols in the lab Disposes of bio hazardous materials, chemical waste, sharp and other potentially hazardous materials according to regulations Review daily run documentation for completeness and accuracy with provided reviewer guidelines Work closely and communicate with other lab associates to complete daily activities efficiently Other duties as assigned by reporting manager. Required Qualification Masters in Biotech/Biochemistry/ any related. Minimum of 1-3 years of experience working in similar field. Self-motivated, attention to details, excellent oral/written skills.

K.K. Patel Super Speciality Hospital is looking for Cathlab Technician to join our dynamic team and embark on a rewarding career journey Assist cardiologists and medical staff in cardiac catheterization procedures. Prepare and maintain cath lab equipment and supplies. Monitor patient vital signs during procedures. Operate imaging and monitoring equipment to visualize and record cardiac activity. Assist in the insertion and removal of catheters. Ensure adherence to sterile techniques and infection control protocols. Collaborate with healthcare teams to provide patient care and support. Document procedure details and patient outcomes.

Role & responsibilities The infection control Nurse is responsible for Surveillance: Conduct environmental rounds in all inpatient and outpatient care areas. Collect data on the incidence of selected device use in identified intensive care units. Participate in investigations of unusual hospital infection outbreaks utilizing the microbiology laboratory, Evaluate the effectiveness of the surveillance plan and modifies as necessary. Participating in quality/performance improvement activities by assessing, monitoring, and measuring HAIs and evaluating outcomes on a continuous basis. Assisting in the organization of regularly scheduled Hospital Infection Control meetings and dissemination of recommendations hospital-wide policies. Plan, organize, develop and implement educational programs for all hospital employees including administrative and ancillary services which convey specialized knowledge and skills to increase employee awareness of existence of HAIs, techniques for avoidance and preventive measures to provide a safe environment for hospital employees and patients. Develop appropriate informational materials at appropriate level of understanding and need. Serve as a knowledgeable and available resource on infection control practices and policies to patients, families& staff. Develop isolation techniques and procedures in accordance with current standard staff to improve practice. Routinely monitors compliance with set policies and protocols on the Isolation of patients with community acquired or hospital associated infections which require special care. Detects and investigates suspected hospital associated infections on a systematic and current basis and collects relevant information. Investigates all significant Infection Control problems. Interested Candidates can share their CV at hr@alchemisthospital26.com or can call directly at 9416376023/ 9582405923. Regards, Richa -HR Ojas Hospital,Panchkula Job Type: Full-time Pay: ₹25,573.58 - ₹38,096.93 per month Benefits: Health insurance Leave encashment Provident Fund Schedule: Rotational shift Supplemental Pay: Overtime pay Work Location: In person Application Deadline: 14/07/2025 Expected Start Date: 21/07/2025

Key Skills Required: · In-depth knowledge of ISO 13485, EN 13795, ASTM and BIS standards · Strong experience in in-process and final QC for sterile products · Exposure to EO sterilization and microbiological monitoring · Thorough knowledge of inspection method · Familiarity with applicable standards · Proficient in sampling and AQL techniques · Expertise in test procedures · Calibration and verification of measuring instruments · Record maintenance and documentation skill · Deviation and non-conformance management · Deviation and non-conformance management · Cleanroom inspection and hygiene monitoring · Environmental monitoring awareness · Basic microbiological testing understanding · Knowledge of ERP and QC software tools · Leadership and team supervision · Training skills · Effective communication and coordination · Audit readiness and compliance monitoring · Understanding of GMP and safety practices · Strong problem-solving and decision-making ability Location: Kerala Department: Quality Control Experience: 2– 5years (Medical Device Industry preferred) Qualification: · B.Sc/ M.Sc in Microbiology, Biotechnology, Chemistry ,or Diploma /B. Tech · B.Tech in Textile / Biomedical Engineering Job Type: Full-time Pay: ₹20,000.00 - ₹26,000.00 per month Schedule: Day shift Work Location: In person

Role & Responsibilities Complete all routine lab tasks as assigned Maintain records and paperwork required for lab analysis Perform method validations and submit job spreadsheets, raw data, and supporting documents Forward confirmed results for report preparation Follow laboratory safety protocols in chemical and microbiology labs Work flexible hours or additional shifts when required Ensure documentation aligns with Quality System standards Review audit documentation for completeness Record activities as per lab specifications Required Competencies Understanding of microbiological analysis techniques as per test procedures Experience in microbiology and biochemistry testing for food, water, and agricultural products Familiarity with ISO 17025 and relevant regulatory standards Ability to support biological testing operations for lab accreditation Team collaboration skills with adaptability and quality focus Experience working in microbiology labs aiming for NABL certification, EIC, and BIS approvals

Company: Heritage Vision Education Trust Position: Assistant Professor - Microbiology Requirements: Educational Qualification: M. Sc. In Microbiology Experience: Min 2-3 Years of Teaching (preferred) (*Preference will be given to Phd & NET candidates) *Candidates must have 55% marks in PG level for teaching position Location: Odisha Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹35,000.00 per month Schedule: Day shift Education: Master's (Preferred) Experience: Teaching: Min. 2-3 years (Preferred) Job Types: Full-time, Permanent, Fresher Pay: ₹25,000.00 - ₹35,000.00 per month Schedule: Day shift Work Location: In person

Job Title: New Medical Product Development Intern B-Arm Medical Technologies is a pioneering medical technology company dedicated to revolutionizing healthcare solutions. Committed to innovation and patient care, we strive to develop cutting-edge medical devices that improve the lives of patients worldwide. Position Summary: We are seeking a motivated and enthusiastic New Medical Product Development Intern to join our innovative team. This internship provides a unique opportunity to gain hands-on experience in the development of breakthrough medical devices. The intern will collaborate with cross-functional teams, contribute to research efforts, and participate in various stages of new product development. Key Responsibilities: · Researching and identifying unmet medical needs and potential opportunities for new product development. · Conduct research using relevant and qualified sources such as search engines, social media, web scrapping, etc. · Collaborate with engineers, clinicians, and designers in brainstorming and ideation sessions. · Contribute to the creation of detailed product specifications, requirements, and design documentation. · Participate in prototyping, testing, and validation of product concepts to ensure they meet safety, efficacy, and regulatory standards. · Collaborate with regulatory and quality teams to ensure products are developed in compliance with relevant medical regulations and standards. · Support the development of user interface and user experience designs for medical devices. · Participate in design review meetings, providing constructive feedback and ideas for improvement. · Assist in the preparation of project plans, timelines, and progress reports. · Contribute to the development of marketing materials and product launch strategies. · Stay informed about advancements in medical technology and relevant regulatory changes. · Contribute innovative ideas to enhance the overall product development process. Qualifications: · Strong passion for medical innovation and improving patient outcomes. · Excellent problem-solving and analytical skills. · Ethical mindset and commitment to patient safety. · Excellent oral/written communication skills. · Comfortable with both technical and business discussions · Expertise in Microsoft Suite. · Self-starter who enjoys working in a fast-paced, collaborative, and innovative hi-growth environment Education: BE/ME–Biomedical/Biotechnology/Microbiology/any Medical Related background/ E-Commerce/Marketing/ECE/EEE Salary: INR 10,000 Per Month Job Type: 6 Months Internship. Salary after 6 Months: 3-4 Lakhs PA (Performance-based) Job Types: Full-time, Internship Contract length: 6 months Pay: ₹10,000.00 per month Schedule: Day shift Evening shift

Key Responsibilities: Conduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain accurate records and documentation of environmental conditions Communicate findings and recommendations to stakeholders and management Participate in environmental remediation and restoration projects Ensure compliance with environmental regulations and standards Qualification: M.Sc (Microbiology) Experience: 2-7 years

Role Description This is a full-time role for an Academic Writer at NerdyTurtlez located in Kolkata. The Academic Writer will be responsible for writing high-quality academic content such as essays, research papers, and dissertations, following the specific guidelines, and meeting the deadlines. Key responsibilities: 1. Working on academic projects/research papers/dissertations/case studies of foreign university students based on an individual's subject expertise and genre 2. Submitting the solutions to the assignments within the deadline 3. Reading the requirements very carefully before working on assignments or case studies 4. Delivering plagiarism-free assignments Skill Requirements: Excellent knowledge of the subject. Ability to deliver plagiarism free assignments. Good writing and analytical skills. Efficiency with internet browsing and internet researching skills. Submitting the solutions of the assignments within deadlines. Reading the requirements very carefully before working on assignments. Eligibility and Criteria: Bachelors or Masters in Microbiology, Biotechnology, Zoology, Food and Nutrition, Botany, ENVS, Food Technology, Biochemistry Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Schedule: Day shift Morning shift Supplemental Pay: Performance bonus Work Location: In person

Role - Assistant Professor Qualification - MSc Microbiology / Biochemistry Experience - 2 to 5 yrs Location - Indore Job Types: Full-time, Permanent Pay: From ₹360,000.00 per year Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person