2539 Microbiology Jobs - Page 5

Department of Biotechnology, GLA University, Mathura The eligible candidate (appearing personal) are requested to send their CV along with scanned copies of the original documents only through email mentioned below by 31.07.2025. JOB DETAILS: 1) Name of Post: Junior Research Fellow (JRF)/Project Associate -1 2) Qualifications: M. Tech (any branch of life sciences) or M. Sc (any branch of life sciences) or equivalent with minimum 60% marks and with valid GATE / NET qualification. Candidate without NET/GATE can also apply. 3) Desirables: Research experience in microbiology and molecular biology or Research publications. 4) Age limit: As per DBT guidelines. 5) Contact details: shoorvir.singh@gla.ac.in (Mob: +91 9719072856), neeraj.gautam@gla.ac.in (7302644327) 6) Duration of Post: Upto Feb 2026 7) Emolument's: Rs 31,000/- + 16% HRA (with GATE/NET) and candidates without GATE/NET will get Rs. 25000/- + 16 HRA. 8) Name of the project: “Prevalence, Characterization and Molecular Epidemiology of Mycobacterial Infections in free ranging Kashmir Stag (Hangul) and captive Double-humped Camel, Mithun and Yak of Eastern and Western Himalayas.” Other Terms and Conditions: 1. No separate letter for the interview will be issued. No TA/DA will be paid for the interview. 2. Candidates will be shortlisted based on their qualifying academic performance as per an assessment criterion. These shortlisted candidates will undergo a panel interview 3. The appointment of the selected candidates will be subject to the condition that he/she is declared medically fit for the service by the prescribed medical authority. 4. The position is purely temporary, time-bound, co-terminus with the project, and on a purely contractual basis. The engagement of JRF will be liable for termination at any point in time in case of unsatisfactory performance. There will be no provision for absorption/re-employment/regular employment in GLA University during the duration of the project and after the termination of the time-bound projects. 5. Selected candidate have to join within one week of issuing date of offer letter. Candidates should report for interview latest by 10:00 AM on 02.08.2025 along with a copy of CV with photograph & original documents.

About the Job: FutureX Global Learning is hiring a highly qualified and experienced Subject Matter Specialist to join our team in Kochi, Kerala, with a focus on training students in the field of Microbiology, Food Technology, Biotechnology, or Life Sciences. As a Subject Matter Specialist, you'll play a key role in designing, developing, and delivering high-quality training programs that equip students with the knowledge and skills required to excel in their chosen field. Key Responsibilities: - Train and mentor students in the subject area through workshops, hands-on sessions, and interactive learning modules - Design, develop, and deliver high-quality training programs for students in Microbiology, Food Technology, Biotechnology, or Life Sciences - Develop and curate high-quality content, training programs, and solutions for various audiences - Create engaging and interactive learning experiences that cater to diverse student needs - Conduct research and stay up-to-date with industry trends and developments - Collaborate with internal stakeholders to design and deliver training programs - Work with instructional designers to develop engaging and effective learning experiences - Provide subject matter expertise and support to various teams - Stay current with industry developments to ensure training programs remain relevant and effective Requirements: - Master's degree in Microbiology, Food Technology, Biotechnology, or Life Sciences - Industrial experience in a related field - Strong knowledge and expertise in the relevant field - Excellent research and analytical skills - Ability to work independently and collaboratively - Strong communication and interpersonal skills - Experience in developing and delivering training programs or content - Familiarity with instructional design principles and adult learning methodologies - Familiarity with Microsoft Office - Immediate Joiners are preferred Why Join Us: - Competitive compensation package - Opportunity to work with a dynamic global team and contribute to innovative learning solutions - Professional development and growth opportunities - Collaborative and supportive work environment Position Type: Full Time / Morning Shift Resume Receipt: Accumulate Online Automatic Packet Generation: Yes Job Function: Subject Matter Specialist

Job Position: Medical Coder HR SRIMATHI 7358425167 Job Description Candidates should have Good Communication Analytical Skills and should be Good at Medical Terminology (Physiology Anatomy). Should be a good team player with good attitude. Should be flexible to work in rotational shifts whenever required Ready to Join with us immediately. Placement Locations: Chennai Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medial reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim. Eligibility All (UG/PG) Life Science Paramedical Graduates BDS BPT BHMS BAMS Siddha,Unani,Naturopathy {Dip Bsc Msc} Nursing/GNM {B.E M.E} Biomedical Engineering {B.tech,M.tech}Biotechnology Biochemistry Bioinformatics Microbiology Zoology and Advanced zoology 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. Reach Us: Ct HR SRIMATHI 7358425167 Contact Details Achievers Spot 13, Ramanathan Street,2nd Floor, T.Nagar, Chennai 600017 Landmark: Adjacent to Ranganathan Street Email: hr@achieversspot.com Website: www.achieversspot.com Achievers Spot This job is provided by Shine.com

Position: MLT Trainer (Senior Faculty) Program : M.Sc. in Medical Laboratory Technology Location : Hubli (Karnataka) 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: ₹30,000.00 - ₹65,000.00 per month Education: Bachelor's (Preferred) Experience: Medical Laboratory Technology teaching: 2 years (Required) Work Location: In person

Job Opportunity: Medical Coder 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. Qualification & Specifications : MBBS, BDS, BHMS, BAMS, BSMS, PHARMACY B.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDICAL, B.Tech (Biotechnology/Bio Chemistry). 2020-2025 passed out Skills Required: * Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy). Role: To review US medical records Initial file review for identifying merits Subjective review and analysis to identify instances of negligence, factors contributing to it To review surgical procedures, pre and post-surgical care, nursing home negligence To prepare medical submissions To prepare the medical malpractice case Regards Contact: HR Anu: + 91 9500408540

Company Description With a presence in more than 125 countries, HiMedia is among the top three brands in microbiology worldwide. Established by professionals and technologists, HiMedia specializes in manufacturing high-quality culture media for microbiology. Over the years, the company has built a rich portfolio of exemplary quality products, continuously focusing on innovation and excellence. Role Description This is a full-time on-site role located in the Mumbai Metropolitan Region. The Sales Marketing Coordinator will be responsible for supporting the marketing and sales teams in day-to-day tasks. This includes coordinating events, managing projects, and writing marketing materials. The individual will also be involved in sales activities, customer communication, and maintaining relationships with clients. Qualifications Strong Communication and Writing skills Experience in Sales and Event Planning Proficiency in Project Management Ability to work collaboratively with diverse teams Strong organizational and multitasking abilities Previous experience in the microbiology or life sciences industry is a plus Bachelor's degree in Marketing, Business Administration, or a related field

Job Description Able to perform independent sampling and analysis of water, compressed air. To perform microbiological environmental monitoring of clean area and compressed air with relevant records. Able to perform Microbiological limit test/method suitability testing and relevant data. Able to prepare media and perform GPT of media. Should have awareness of Caliber LIMS system operation. Should have knowledge of regulatory requirements and guidelines. Qualifications Should be M.Sc. in Microbiology or Biotechnology About Us Minimum experience of 1-3 Years in relevant department. Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion. About The Team The Human Resources team partners with all aspects of the organization, driving success through the effective and innovative management of people for both current and future business needs. Key Roles That The Human Resources Team Performs Executive Role: Specialists in all aspects of people management. High-level input at strategic level into all key business decisions. Audit Role: Ensures all areas of the organization are compliant with legal requirements AND best practice employment policies and procedures. Facilitator Role: Close partnership to support, advise and extend the ability of all areas of the organization to meet their objectives through implementation of highly effective employment practices in areas such as Talent Acquisition, Learning and Development, Reward systems, Performance Management, Health and Wellbeing. Consultancy Role: Provide expert advice to the organization and it’s managers on any aspect of workforce management and employee relations and performance. Service Role: Ensure the organization is fully aware of and is equipped to deal with developments impacting employment matters, such as changes in legislation, changes in the characteristics of the labor market.

Job Description Manager, Regulatory Affairs - CMC This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance’s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Your role at our organization is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. Regulatory Responsibilities Primary responsibilities include, but are not limited to Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic document based GMP systems Leadership Skills Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor’s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 5 – 7 yrs of Industry Pharmaceutical industry experience out of 4 years’ experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics The candidate may be required to travel to other CMO sites on a need basis. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Hybrid Shift Valid Driving License Hazardous Material(s) Required Skills Adaptability, Adaptability, Applied Engineering, Biochemistry, Business Processes, Chemical Engineering, Communication, Communication Management, Compliance Investigations, Documentation Standards, Electronic Common Technical Document (eCTD), Employee Training Programs, Global Regulatory Submissions, Immunoassays, Immunochemistry, Management Process, Microbiology, Molecular Biology, Molecular Microbiology, Pharmaceutical Manufacturing, Policy Implementation, Records Retention Management, Regulatory Affairs Compliance, Regulatory CMC, Regulatory Communications {+ 4 more} Preferred Skills Job Posting End Date 08/2/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R359084

Job Description Manager, Regulatory Affairs - CMC This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance’s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Your role at our organization is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. Regulatory Responsibilities Primary responsibilities include, but are not limited to Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic document based GMP systems Leadership Skills Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor’s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 5 – 7 yrs of Industry Pharmaceutical industry experience out of 4 years’ experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics The candidate may be required to travel to other CMO sites on a need basis. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Hybrid Shift Valid Driving License Hazardous Material(s) Required Skills Adaptability, Adaptability, Applied Engineering, Biochemistry, Business Processes, Chemical Engineering, Communication, Communication Management, Compliance Investigations, Documentation Standards, Electronic Common Technical Document (eCTD), Employee Training Programs, Global Regulatory Submissions, Immunoassays, Immunochemistry, Management Process, Microbiology, Molecular Biology, Molecular Microbiology, Pharmaceutical Manufacturing, Policy Implementation, Records Retention Management, Regulatory Affairs Compliance, Regulatory CMC, Regulatory Communications {+ 4 more} Preferred Skills Job Posting End Date 08/2/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R359084

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description Job Summary We are seeking an individual to test samples and release results within Turnaround Time (TAT) for commercial and stability batches, adhering to GMP (Good Manufacturing Practices). This role involves calibrating and maintaining assigned equipment within departmental and organizational guidelines, processes, and procedures. The primary objective is to ensure accuracy in results provided within timelines. Roles & Responsibilities • Your responsibilities encompass testing assigned samples and releasing data within defined timelines, ensuring absence of executional errors against established procedures. You will be responsible for preparing required reagents and buffers in alignment with the testing plan and ensuring the availability of equipment for analysis. • Your role involves documenting activities contemporaneously, adhering to Good Documentation Practices and compliance expectations, and conducting self-checks post-analysis to ensure accuracy. • You will promptly inform the supervisor about risk actions, providing necessary data and analysis to support the investigation process. You will adhere to QMS (Quality Management systems) and closure timelines, actively participate in laboratory investigations and discrepancy closures, fulfilling defined roles in audits. • Your responsibilities also include ensuring lab cleanliness, proper sample storage, chemical labeling, removal of expired material, usage of calibrated equipment, equipment calibration, maintenance, and qualification. • You will address instrument-related issues and conduct root cause analyses (RCAs) for unknown problems, and play a crucial role in training new team members on analytical techniques. Qualifications Educational qualification: An M.Sc., M.Tech. or B.Tech. in Microbiology, Biochemistry, or Biotechnology Minimum work experience: 2 years Skills & attributes: Technical Skills • Basic understanding of the Biologics/Biosimilar industry, including processes, regulations, and trends. • Hands-on experience in High-Performance Liquid Chromatography (HPLC) techniques, including Size Exclusion, Reverse Phase, Ion Exchange chromatography, and Peptide mapping analysis, especially within the context of Analytics. • Hands-on experience in Biochemical analysis techniques, specifically Electrophoresis, Enzyme-Linked Immunosorbent Assay (ELISA), and Polymerase Chain Reaction (PCR), with a focus on Analytics. • Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). • Basic knowledge in protein chemistry, including an understanding of protein structure, function, and relevant analytical techniques. • Basic knowledge and hands-on exposure to Microbiology techniques, particularly relevant for individuals working in Microbiology Labs. • Basic knowledge and hands-on exposure to cell culture techniques, specifically for working in Bioassay (BA) Labs. Behavioural skills • Prioritizes effective communication and demonstrates a performance-oriented mind-set. • Effective verbal and written communication skills. • Performance-oriented approach, consistently striving for high standards. • Demonstrates flexibility in working shifts and a clear understanding of team dynamics. Additional Information About the Department Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Who are we HaystackAnalytics is a HealthTech company creating clinical genomics products, which enable diagnostic labs and hospitals to offer accurate and personalized diagnostics. Supported by India's most respected science agencies (DST, BIRAC, DBT), we created and launched a portfolio of products to offer genomics in infectious diseases. Our genomics based diagnostic solution for Tuberculosis was recognized as one of top innovations supported by BIRAC in the past 10 years, and was launched by the Prime Minister of India in the BIRAC Showcase event in Delhi, 2022. Job Summary We are looking for a Fresher MD/PhD with a specialization in Microbiology to join our team as a Clinical Outreach / Scientific Outreach professional. This position requires active field engagement in collaboration with the sales team, including visits to hospitals and clinical institutions to interact with physicians and other healthcare professionals. The candidate will be responsible for effectively communicating the scientific, microbiological, and clinical aspects of our products, ensuring a clear and thorough understanding of their clinical relevance, applications, and value. The candidate will be participating in Continuing Medical Education (CME) programs and Round Table meetings (RTMs). What we want you to do Work closely with the sales team during client visits, primarily engaging with doctors and healthcare providers. Explain the microbiological and clinical aspects of our products in a clear and professional manner. Bridge the gap between scientific knowledge and clinical application to support the adoption of our products. Provide technical support and medical guidance during client meetings and product demonstrations. Help doctors understand how the product integrates into patient care, infection control, and diagnostic workflows. Share relevant case studies, clinical experiences, or infection trends to highlight product effectiveness. Maintain a strong understanding of emerging microbiological trends and technologies, including Next-Generation Sequencing (NGS). Collaborate with internal teams such as R&D, sales, and Operto ensure accurate communication and feedback. Actively participate in Continuing Medical Education (CME) programs and Round Table Meetings (RTMs) What are we looking in you Freshers - Fresher MD/PhD with a specialization in Microbiology Proven track record of effective communication and collaboration with interdisciplinary healthcare teams. Demonstrated understanding of infection control protocols and antimicrobial stewardship principles. Familiarity with molecular and sequencing (NGS) technologies and their applications in clinical microbiology is advantageous. Strong knowledge of clinical microbiology, infectious diseases, and diagnostic methods Excellent verbal communication and presentation skills. Ability to explain complex technical and medical concepts in a simple, clinician-friendly language. Comfortable with on-field client interactions. Must be willing to travel to PAN India for CME programs and RTMs. What you will gain Dynamic and collaborative work environment dedicated to making a meaningful impact in healthcare Experience in working with advanced sequencing technology in the diagnostic industry i.e. NGS, WGS, Nanopore, and Illumina. Opportunities for professional development and continued education Competitive salary commensurate with experience Comprehensive health benefits package Job Types: Full-time, Fresher Pay: ₹800,000.00 - ₹1,000,000.00 per year Benefits: Health insurance Provident Fund Schedule: Day shift Application Question(s): When did you complete your MD or PhD program (please specify the month and year)? Work Location: In person

We are seeking ambitious publishing professionals to join our growing team supporting the peer review process. As a Reviewer Selection Editor, you will be responsible for efficiently managing peer review administration procedures, utilizing tools like Scholar One Manuscripts and PubMed Central to identify international experts suitable for reviewing cutting-edge medical research. Reporting to the Reviewer Selection Lead, you will work alongside a team of Reviewer Selection Editors. The ideal candidate will hold a postgraduate qualification in MTech/M.Sc. in areas such as Electrical and Electronics (ECE, EEE, VLSI, Embedded Systems, Power systems, Communication systems), Life Science (Biotechnology, Biochemistry, Microbiology, Molecular biology), Economics (Business Economics, Financial Economics, Applied Economics), Agriculture, or Horticulture. You should have a solid understanding of the journal peer review process, a keen interest in academic publishing, and knowledge of current market trends. Proficiency in English grammar, experience with process-driven workflows, and a background in customer-facing roles are essential. Your responsibilities will include managing the peer review process for journals, selecting appropriate reviewers through database research, ensuring compliance with ethical publication practices, communicating with reviewers, analyzing data for process improvements, maintaining records, and collaborating with international editorial teams. Strong organizational skills, the ability to handle multiple tasks efficiently, effective communication, and a commitment to excellent customer service are key qualities we are looking for. Flexibility, familiarity with Microsoft Office, and a willingness to adapt to changing work plans are also important. The selection process will involve an online assessment, technical discussion, and final HR-level discussion. This position requires working from our office in Chennai or Puducherry. Prior experience with platforms like Scholar One Manuscripts or Editorial Manager is advantageous but not mandatory, as full training will be provided.,

Job Summary: We are seeking a highly motivated and detail-oriented Quality Assurance Professional to join our laboratory team. This role is crucial in ensuring the continuous implementation, maintenance, and monitoring of our quality management system, adhering to national and international standards. The ideal candidate will play a pivotal role in upholding regulatory compliance, driving continuous improvement, and ensuring the integrity of all laboratory operations. Key Responsibilities: Quality System Management: Actively participate in and support all quality assurance-related activities. Implement, maintain, and monitor the effectiveness of the Quality Management System (QMS) in compliance with ISO/IEC 17025:2017, NABL guidelines, FSSAI, EIC, APEDA, AYUSH, GLP, Commodity Boards (e.g., Tea Board), and other relevant regulatory body requirements. Ensure systematic control and management of all QMS documents and records, including preparation, review, issuance, revision, and updates. Training & Development: Identify, plan, and execute internal and external training programs for laboratory personnel. Review and compile comprehensive training records. Corrective & Preventive Actions (CAPA): Monitor the effective implementation and verification of corrective actions (CA) and preventive actions (PA). Systematically resolve complaints and non-conforming work, actively participating in complaint closure actions. Technical Review & Oversight: Review and maintain records for method development, validation, and verification. Review test reports, calibration, and validation certificates for accuracy and compliance. Vendor & Equipment Management: Perform qualification and ongoing evaluation of vendors providing products and services to the laboratory. Plan, conduct, and monitor equipment calibration, validation, intermediate checks, and maintenance activities. Quality Control & Proficiency Testing: Plan, conduct, and participate in inter-laboratory comparison (ILC), proficiency testing (PT), and internal quality check (IQC) programs, ensuring meticulous record maintenance. Audits & Compliance: Assist and actively participate in the execution of internal and external audits, as well as Management Review Meetings (MRM). Support the preparation for and participation in customer and regulatory audits, visits, and inspections, ensuring successful closure of any non-conformances raised. Customer & Information Management: Review, assess, and evaluate customer feedback to drive improvements. Assist in LIMS (Laboratory Information Management System) operation and ensure its compliant implementation. Circulate critical regulatory and laboratory information, circulars, notices, newsletters, and recent updates/guidelines to all relevant company personnel. Risk Management & Continuous Improvement: Identify, assess, and mitigate risks, while also developing and verifying the implementation of opportunities for system and process improvement. General Support: Perform other duties as assigned by the Lab Head or Management. Qualifications: Education: Master's degree in Biotechnology/Microbiology/Food Technology/Chmeistry or a related discipline. Experience: 3-6 of progressive experience in Quality Assurance within a NABL accredited. Technical Knowledge: In-depth understanding and practical experience with ISO/IEC 17025:2017. Familiarity with NABL guidelines, FSSAI, EIC, APEDA, AYUSH, GLP, and other relevant regulatory requirements (e.g., specific to food, pharma, tea, etc.). Proficiency in laboratory quality control principles, method validation, and equipment calibration. Experience with LIMS operations is highly desirable. Skills: Strong analytical and problem-solving skills. Excellent communication (written and verbal) and interpersonal skills. Ability to conduct effective training programs. Meticulous attention to detail and strong organizational skills. Proficient in Microsoft Office Suite (Word, Excel, PowerPoint). Ability to work independently and collaboratively within a team.

Who We Are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. How You’ll Spend Your Day Shall have FDA approval in Microbiology To carry out Microbiological testing of various products like in-process, finished products, pre-formulation study samples and stability samples etc Review of analytical results and suggest further course of action To carry out Microbial method development, method validation and transfer activity Preparation and updation of STP and analytical related SOPs Regulated market experience (US/EU/Canada etc) Laboratory resources management To execute Microbial method validation as per the protocol and to complete the required documentation Callibration and maintenance of analytical instruments. Maintenance includes activities such as Qualification, keeping track of AMC, History, Spares, Usage records etc. To ensure that all activities undertaken are executed in the framework of good laboratory and documentation practices and the existing quality systems are adhered to. To ensure safe practices are followed during the execution of activities and strict adherence to the EHS systems of the site Any other activity assigned by the line manager. Your Experience And Qualifications M.Sc. in Microbiology or Biotechnology Basic computer skills (MS Excel, Word) Shall be a Microbiologist with at least 6 to 10 years’ experience in any pharma company. FDA approval in Microbiology. Regulated market experience (US/EU/Canada) Experience in Routine Micro Analysis Sound knowledge of Microbiology and Microbial analysis, Microbial method development and method validation. Microbiological testing of various products like in-process, finished products, pre-formulation study samples and stability samples etc. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

As a skilled professional in the field of laboratory science, you will be responsible for conducting advanced diagnostic tests in various areas such as hematology, biochemistry, microbiology, and immunology. Your expertise will be vital in accurately analyzing samples and providing crucial insights for patient care. In this role, you will play a key part in troubleshooting and resolving technical issues that may arise with lab equipment and procedures. Your problem-solving skills will be utilized to ensure smooth operations and accurate test results. Ensuring the safety of the laboratory environment is of utmost importance. You will be expected to implement and monitor laboratory safety protocols and hygiene standards to create a secure and efficient work environment for yourself and your colleagues. Attention to detail is crucial in maintaining detailed records of test results, quality control data, and laboratory processes. Your meticulous record-keeping will contribute to the accuracy and reliability of the work conducted in the laboratory. Additionally, part of your responsibilities will involve supervising junior laboratory staff. Your role as a mentor and guide will be essential in providing support and fostering professional growth among your team members. This is a full-time position that requires a minimum of 1 year of relevant work experience. The work location for this role is in person, where your skills and expertise will directly contribute to the successful operation of the laboratory and the quality of patient care provided.,

You will be responsible for providing strong leadership and managing all aspects of the Microbiological production facility in Visakhapatnam, Andhra Pradesh. This includes overseeing quality, costs, P&L, market development, performance, employee engagement, and technical development. The ideal candidate should have 10+ years of experience and a background in handling operations of medical devices. Experience in the field of Microbiology, Biotechnology, or related areas is preferred. A Master's degree, PhD, or equivalent experience is desired. Additionally, excellent communication skills and prior experience in leading a large team of more than 25 people are essential for this role. If you believe you possess the skills and experience we are looking for, we encourage you to reach out to us at hr@dnaxperts.com and share why you are the best fit for this position. We are always seeking to collaborate with top talent in the industry.,

Company Description We suggest you enter details here. Role Description This is a full-time on-site role for a Microbiologist located in Palampur. The Microbiologist will be responsible for conducting microbiological experiments, analyzing samples, and identifying microorganisms. The role involves managing laboratory activities, maintaining laboratory equipment, ensuring quality control and assurance, and documenting findings. The Microbiologist will also collaborate with other departments and adhere to safety protocols and regulatory requirements. Qualifications Proficiency in Microbiology and Laboratory Skills Experience with Quality Control and Quality Assurance processes Familiarity with Laboratory Equipment and procedures Strong analytical and problem-solving skills Excellent attention to detail and documentation skills Bachelor&aposs degree in Microbiology or a related field Ability to work on-site in Palampur Previous experience in a pharmaceutical or healthcare setting is a plus Show more Show less

BDE (Business Development Executive) Great opportunity for someone looking for growth their career and is looking to enhance their knowledge in U.S. Business Development Job description: Role: Business Development Executive (Finance) Education: B.Sc, M.Sc, Biotechnology, Microbiology, BBA, BA, Bpharma Experience: 0-2 Years ( Freshers can also Apply ) Job Location: Phase 8 Industrial Area, Mohali, Punjab Shift: Night Shift (US Shift) Timings: 8:00 PM to 5:00 A Interview : F2F *2025 PASS OUTS CAN ALSO APPLY* Notes: Cab facility to and from work is available for all female employees. One time Meal for all the employees Requirements: 0-2 year of experience in lead generation . Excellent communication and interpersonal skills. Ability to work independently and as part of a team. Creative thinking and problem-solving skills Impeccable Communication Skills (written and verbal both) Should understand US market Job Description Conducting market research to identify potential industries. Developing and executing lead generation strategies across multiple channels, including email, social media, and cold calling. Identifying and qualifying leads through research, outreach, and communication. Managing and updating customer and prospect databases. Analyzing lead generation data and metrics to improve strategies and tactics continually. Creating and delivering reports and updates to senior management. Staying up to date with the latest lead generation trends and technologies.

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Priya 9600450980 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Pharmacy, Bpt, Nursing Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM Staff Nurse GNM Perks and benefits Incentive Up to 5k Insurance Provident Fund

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Rubini-9600405840 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Pharmacy, Bpt, Nursing Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM Staff Nurse GNM Perks and benefits Incentive Up to 5k Insurance Provident Fund

Division Department Sub Department 1 Job Purpose To execute the activities that are related to microbiology laboratory, Key Accountabilities (1/6) Involvement in all quality related activities Maintenance of all the area and the equipment, To ensure and monitor compliance with GLP and cGMP as per requirements of the respective authority, Key Accountabilities (2/6) Environment monitoring Monitoring of area to be carried out as per allocated schedule, Release and transfer within the timeframe mentioned in SOP, Follow the written procedure for Execution of aseptic process validation and testing of Aseptic process validation sample, Involvement in process Simulation, Key Accountabilities (3/6) III Media, PST management Stock of media and presterilized items to be maintained, Issuance to be done as per requirement Key Accountabilities (4/6) Water and MLT Water Analysis to be carried out as per schedule MLT to be carried out as per planning, Pathogen Continuation and releases should be on time Should ensure completeness of entries of all the tests performed and compilation of relevant data before submission for review, Disposal of balance samples after completion of analysis and review Key Accountabilities (5/6) Training To be present in any arranged scheduled training by the trainer, LMS training to be caried out before due date, Key Accountabilities (6/6) Major Challenges Releases of all the activities carried out should be on time, Maintenance of stock in the laboratory, Decontamination of material should be on time, Key Interactions (1/2) Internal Interaction with team members for all related activities including handover during shift changeover, Key Interactions (2/2) External Interaction with service engineers during AMC and laboratory visits, Interaction with external party during external calibration and validation of equipment, Dimensions (1/2) Should have basic knowledge of microbiology and relevantly qualified, Dimensions (2/2) Key Decisions (1/2) Decisions Suggestions and ideas for work simplification, Connecting with external Subject Matter Experts/ senior leaders within Cipla, Key Decisions (2/2) Education Qualification Educational Qualifications Post Graduate in Microbiology Relevant Work Experience Relevant experience: 2 5 years in pharma, microbiology, Good Knowledge about pharma process 2-5 years (Quality section) Good knowledge about computer (Excel, PPT and word file) Show

Maintain media stock and reconcile records of media used in analysis. Perform water sampling and analysis following defined SOPs/protocols and ensure proper documentation. Report and log OOS (Out of Specification), OOT (Out of Trend), and EM (Environmental Monitoring) excursions. Conduct environmental monitoring of the laboratory. Perform analytical validation, culture maintenance, and growth promotion testing (GPT) of media; record observations and generate reports. Carry out microbiology laboratory tests such as Bioburden Analysis, MLT (Microbial Limit Test), Sterility Testing, BET (Bacterial Endotoxin Test), etc., in compliance with approved procedures. Skills and Proficiency: Microbiology Instrumentation Handling Expert Good Laboratory Practices (GLP) & Documentation Accuracy Practitioner Data Integrity & Documentation Practitioner Regulatory Compliance Practitioner SOP Preparation & Revision Practitioner BET & Sterility testing expertise and evaluation skills Expert Interpretation of Resulting Data Trend Practitioner Laboratory Instrument qualification, Calibration & Maintenance Practitioner Quality Control & Compliance Practitioner QMS Documentation (OOS, OOT, Deviation & Incident) Beginner CAPA, Deviation, and Change Control Management Beginner

Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible to perform the environment monitoring activities Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of executed BMRs and BPRs. Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc.. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Review of Visual inspector qualification record. Skills: Environmental Monitoring (EM) - Expert In-Process Quality Controls (IPQC) & Sampling - Practitioner Aseptic Process Simulation (Media Fill) Monitoring - Expert Line Clearance & Batch Record Review - Practitioner Good Documentation Practices (GDP) - Practitioner Regulatory & Compliance Knowledge - Practitioner

Job description: Eligibility Criteria: Designation: Trainee Medical Coder Qualification: B.Pharma & M.Pharma (No Standing Arrears) Should have 60% in all the academics Work From Office only Work Location: Kochi, Kerala Shift: Day Age limit: 28 Yrs Salary: As Per Industry Interested Candidates share your resume durgadevi.chandrasekaran@corrohealth.com Durga HR 8248059972

Resource Engimech (India) Pvt. Ltd is looking for QC Assistant to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes