2539 Microbiology Jobs - Page 23

Hi Connections! CorroHealth Hiring Fresher's 2024 (Batch) *Work Experience - Fresher *Designation - Jr.Executive - Coding Services *Work Location - Chennai *Graduation - Paramedics (B. pharm, M. pharm) , Non Paramedics (BSC biotech, B.sc microbiology, BE - Bio medical engineering) Note - Not Eligible for Nursing / No BPT *Graduation Percentage - Minimum 60% and above *Medical Coding Certificate - Not Mandatory *Work Mode - Work From Office *Screening Process - 1 -Online Assessment , 2- L1 Technical, L2 Technical & Final HR Interview *Preferably looking for IN & Around Tamil Nadu Interested Can Connect to below mentioned Contact number & Email Contact - 9176418460 Email - Madhumitha.mohan@corrohealth.com

Job Title: Team Lead – Biotechnology Patent Research Wing Location: Mohali Department: Patent Research 💡 About TT Consultants TT Consultants is a global leader in IP and innovation support services. Leveraging our AI-powered platform XLSCOUT and deep human expertise, we provide cutting-edge solutions across IP Research, Biotechnology Patent Analysis, Technology Analytics, Litigation Support, and Competitive Intelligence. Our work enables Fortune 500 companies, law firms, and research institutions to stay ahead in technology and innovation. 📆 About the Role Are you a biotechnology or life sciences expert with a passion for patents and innovation? Do you want to lead high-impact IP projects with global clients? Join us as a Team Lead – Biotechnology Patent Research Wing and be part of our dynamic team in Mohali. 🚪 Roles and Responsibilities Lead and mentor a team of analysts working on biotechnology patent projects. Conduct and review patent landscape analysis, validity/invalidity searches, and FTO assessments. Analyze patent claims and scientific literature to assess novelty and inventive step. Map scientific disclosures with patent content and identify technical relevance. Prepare and review high-quality technical and analytical reports. Collaborate with patent attorneys, researchers, and cross-functional domain experts. Stay current on biotechnology advancements and patenting trends. 🔍 What We Are Looking For Strong background in biotechnology, molecular biology, microbiology, biochemistry, or a related field. Leadership experience with prior team or project management responsibility. In-depth understanding of patent databases (Orbit, PatBase, Derwent, etc.). Excellent analytical, comprehension, and technical writing skills. 👨‍🎓 Qualifications B.Tech/M.Tech or higher in Biotechnology, Life Sciences, Biochemistry, or related disciplines . 4–8 years of experience in IP/patent research, preferably in biotechnology or life sciences. 🚀 Why Join Us? Lead global biotech and pharmaceutical patent projects. Exposure to AI-driven patent intelligence platforms like XLSCOUT. Work with a highly skilled and motivated IP analytics team. A collaborative environment with learning and leadership growth. 👤 Who You Are A self-starter with a deep interest in biotech innovations and intellectual property. Strong leadership and mentoring skills. Detail-oriented and capable of handling scientific and legal content. A team player with excellent communication and problem-solving abilities. 📅 Ready to Join? Be part of our growing team that's shaping the future of innovation and IP strategy. If leading biotech patent analysis excites you, apply today and lead the change!

Job Summary The position is responsible for heading the Quality Assurance function in NOSD Parenteral Block at Sun Pharma laboratories Limited, Guwahati Responsible to set the team goals and objectives for the NOSD Quality at Guwahati site in alignment with goals of Cluster Quality and other business function(s). Responsible to collaborate and support to functional heads of QA, QC, Microbiology, Production, IT, Regulatory Affairs and commercial department to align organizational goal and business strategies for achieving overall quality. Responsible for providing guidance to ensure achievement of targeted completion of tasks and execution of team. Responsible for facilitate harmonization and consistent implementation or Quality Systems and procedures (Pertaining to parenteral), in alignment with Global Quality Policies, Standards and applicable SOPs. Essential Job Functions: Primary Responsibility: Review and monitoring of Quality operations at Parenteral Block. To execute, monitor, review, and approval of Quality management systems i.e. Change control, Deviation, and CAPA management as per requirements. To review and approve Standard Operating Procedure etc. To ensure the compliance of documentation at various stages of the process i.e. (Manufacturing, Filtration, Filling, Visual Inspection, Labelling and Packing operations). To review, approve the Master and executed BMR, BPR, Validation, Qualification and other GMP documents. To evaluate and monitor the Aseptic process simulation (Media Fill) activities with respect to the APS planner, Trending of intervention protocol & reports. To facilitate harmonization and consistent implementation of the quality systems and procedures at the site in alignment with corporate quality policies /procedures. To review, update, respond to GQS/Regulatory audit observations within the stipulated time frame. To participate in the review & approval of investigation in case of Non- conformance events i.e. Process Deviation, OOS, OOT & Product Quality Complaint. To ensure release, approval, or rejection of Raw Material, Packing Material, Intermediate, Finished products as per approved specifications. To ensure completion and implementation of CAPA as per established procedure and follow up to verify the effectiveness of CAPA. Responsible for the batch disposition (Batch release or reject). To ensure compliance of electronic systems such as manufacturing equipment/instruments etc. To ensure equipment /instrument, qualification/calibration and prevent maintenance are performed as per approved planner. To ensure that processing and storage area are qualified as per the approved procedure and GMP requirements. To impart training to the plant personnel as per requirement and ensure the effectiveness. To be part of self-inspection and or quality audits that regulatory appraises the effectiveness and applicability of the quality system as per schedule. To ensure and perform work as per established approved procedure, regulatory norms and its compliance as per the current regulatory requirement. Facilitate/support the implementation of new initiatives of Corporate functions at site. Secondary Responsibility Specific emerging projects as applicable. Perform any other responsibility assigned by the Quality Head/Management.

Job Description Position: QA Sterile Manager Department: Quality Assurance Designation: Manager - I Education Qualification: M.Sc. in Biotechnology / Microbiology / Chemistry Total years of Experience: 10+ Years Job Role: Management of Quality Assurance functions of Manufacturing Block – P. Responsibilities Ensure that manufacturing and packing of the batch is executed and records are completed and reviewed in accordance with established SOPs and cGMP regulations. Conduct certification of batch production records for compliance and stage-wise completion. To release / reject the Batch after complete review of batch and related quality documentation. Tracking and monitoring of QMS system. Ensure logical closure of deviations and investigations of related product before release. Conduct thorough investigations along with production for any complaints / deviations/ OOS / stability failure for products manufactured at the site and logical / timely closure of Complaints. To ensure contamination controls implemented and followed at site as per contamination controls strategy (CCS) and respective procedures. Work directly with planning, QC, other QA functions, and Regulatory Affairs to ensure Batches are released to meet supply chain requirements. Participate in self-audits of facility and equipment in partnership with Manufacturing and Engineering to ensure readiness for operations. Participate in Aseptic simulation (Media Fill) activity, Monitoring and Implementation for PENEM DF. Identify continuous improvement opportunities to improve compliance, process clarity, and operational efficiency. Review and approve master batch production records (Manufacturing / packing) and SOPs. Review and approve equipment qualification & process validation protocols and reports for accuracy, completeness, and traceability as well as adherence to protocol / procedures. Review and approve Annual Product Review (APR) reports for the products as per the schedule. Stability sample management of finished goods. Management of control sample pertaining to collection, review, storage and destruction. Management of line clearance, in-process check, coding approval and water sampling. Review and approval of IPQA instrument calibration record. Management of IPQA activities for Block-Penem. Review and approve artwork of Packaging material, STP and Specification. Provides appropriate training and development to support staff to meet their respective job responsibilities. Work in partnership with Manufacturing, Engineering, and QC to increase knowledge and understanding of cGMPs and improve practices and procedures. Review activities related to the Microbiology Laboratory. Review activities related to the beta-lactam containment monitoring. Compliance with Quality Policy of the organization. Improvement of System and procedures, Quality of products manufactured and delivered.

Job Description Position : Microbiology Head Reports to: Quality Head Department: Quality Grade: G8 Functional Area: QC - Microbiology Location: Dewas Position Summary Manage overall site microbiology department wrt sampling, testing, planning, qualifications, media fill program ( for sterile manufacturing),compliance and upgrades of facilities and procedures. Conduct effective review of team and portfolio, provide direction and guidance to the team and develop team competence with the objective of ensuring the quality of products released with adherence to GMP norms and timelines The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, Standard and Procedures. Key Responsibilities Provide leadership and direction to achieve all quality goals. Manage & Organize timely microbiological sampling, testing and release of raw materials, finished product, commercial stability, Exhibit stability, miscellaneous samples. Manage & Organize timely Microbiological sampling, testing and release of water and Utility samples. Manage & Organize timely Microbial Environmental Monitoring of passive air/active air/ Compressed air/equipment surfaces /personnel monitoring & Drain points of manufacturing blocks, warehouses & Microbiology lab etc. Monitoring effectiveness of the disinfectants used at the site and make appropriate timely change to the ineffective proved disinfectants. Manage & Organize timely handling & maintenance of microbial cultures. Isolation & identification of microbial isolates from various sources. Manage & Organize timely laboratory investigation of out of specification results /Out of trends/Out of limit, root cause analysis and Risk assessment and Health hazard evaluation of identified microorganisms. Participate in internal, external and/or regulatory inspections of Microbiology operations at the site. Learn from external regulatory audit observations and implement Global CAPA and local CQA observations CAPA in micro lab Ensure trend and annual summary reports of water/microbial environmental monitoring/Microbial isolates etc. Ensure calibration, validation and qualification of laboratory equipment/instrument. Ensure timely availability of laboratory Chemicals, media/ stationary/ gloves and Consumable. Ensure consistency in Microbiology lab operations and drive continuous improvements in laboratory performance. Ensure compliance to cGMPs and applicable safety standards in the Microbiology laboratory. Train microbiologist about the microbiological techniques, aseptic practices, critical quality management skills, including decision-making, handling of quality exceptions, staff development, personnel and planning, etc. Managing people on a day-do-day basis. Preparation of annual capex & revenue budget for microbiology section. Ensure adherence to approved budget work plan. Oversee that the cost of testing is controlled in microbiology lab. Liaison with Corporate Micro team to implement microbial risk assessment program and work to mitigate effective CAPA’s to prevent failures. Minimum Education/Experience Requirements Microbiology Graduateor Equivalent Minimum 15years With Microbiology Work Experience Preferred REQUIRED SUCCESS ATTRIBUTE Knowledge Of GxP’s, CGMP And Other Regulatory Requirements. Compliance Collaboration Accountability Customer service orientation Planning and prioritization Secondary Success Attributes Attention to detail People connect Emotional control Effective communication Problem solving Roles

Experience from major pharma industries in Non-oral Products: Topical product and transdermal product. Experience in end-to-end topical product development activities for generic product development ANDA (Cream, ointment, gel, solution, lotion, foam, patch etc.) as well as NDA 505(b)(2), 505(b)(1). Experience in execution of lab scale manufacturing, reverse engineering, analytical know-how, plant level manufacturing activities; scale-up and exhibit batches based on quality principles QbD, QTPP, CQA, CMA, CPP, RA, FMEA. Experienced scientist to perform experiments for development of optimum prototypes (generic, non-infringing composition and robust manufacturing process) with diverse class of drugs & prodrugs (sensitive to pH, acid, base, temperature, oxygen, humidity). Experience in regulatory documentation CMC, MF, BMR, PDR, controlled correspondence for CMC, Biowaiver & Dossier preparation for US-FDA, EU-EMA, AU-TGA & DCGI through successful filing. Experience in working with cross-functional teams (ADD, MSTG, production, QC, QA, RA, IPC, PMO, BD, Microbiology, Pharmacology etc.) to achieve project goals - Filings and subsequent approvals. Knowledge and develop continuous understanding on competitive intelligence, due diligence, US-FDA quality concepts, statistics and global pharma trend analysis to support new product evaluation & introduction. Job Responsibilities To design, conduct and verify/review experiments to develop a robust formulation . To do literature search, patent search, prepare summary report and review. To prepare product development reports and protocols. To do product scale-up, exhibit batches and prepare reports for product filing and regulatory queries including post filling and post approval market queries. To prepare documents (i.e. PDR, CPD etc.) for regulatory submission Group work co-ordination. Project status report preparation. Experimental result review, interpretation and conclusion. To prepare technology transfer documents. To procure raw materials (API / excipients), packaging materials, innovator samples in consultation with packaging/purchase department. To do product validation, site transfer/change activities of products. To write Laboratory Notebook to enter details related to drug product manufacturing. To prepare test request for analysis of raw materials (API/Excipients) and Drug product.

Job Title Manager / Sr.Manager – Micro Lead Job Grade G10 / G9B Function Global API Business Sub-function Manager’s Job Title: Skip Level Manager’s Title Function Head Title: Location: Ahmednagar No. of Direct Reports (if any) Areas of Responsibility To plan, review and monitor overall activities in Microbiology and lead the department. Co-ordination with other departments for priorities and provide the timely support/testing to avoid delay due to analysis. Review of all departmental related documents and review results in LIMS system in microbiology section. Ensure all documents are complete in time. To review the lysate sensitivity test, Bacterial endotoxin test of WFI and API products. To check method validation of bacterial endotoxin test and microbial quality of products. To procure, receipt, storage, maintenance, its use and reconciliation of biological indicator, media, reagents standard cultures and bioball etc. To ensure and check calibration and Operation of TOC analyzer Execute breakdown (If any) in consultation with vender. To ensure environmental monitoring activities performed as per schedule and to check the environmental monitoring reports. To review qualification, Calibration of all instruments in microbiology laboratory as per SOP/Schedule. To participate in investigation and to review of deviations/OOS/OOT/OOC/Lab Event / & review of SOPs as per revision date in micro section online in track wise system. To highlight observations, rejection / failure, quality related concern in time and contribute in troubleshooting To ensure and review all logbooks and registers are maintained on line and available at designated place. Preparation and review of GMP documents related to activities. To review and ensure fumigation activity and its verification as per SOP/Guidelines. To prepare / review trends for water and environment monitoring, Summary report of water and environment monitoring. Responsible to follow online good documentation practices for data recording and monitoring. To ensure and review validation of autoclave, Dry heat sterilizer (DHS), Incubators, Laminar Air flow, HVAC. To ensure and review preparation of reagents and volumetric solution and its standardization as per specification / SOP. To ensure and review inventory and stock record of media/reagents/culture/lysate/CSE/LRW. To ensure to follow the GLP as per current practice in the laboratory. To ensure safety and use of personnel protective equipment’s during day to day activities Responsible for carrying out any other responsibilities assign from time to time orally or in writing by Quality head, however related training imparted to concerns. To support for review and compliance activity in quality function and to support for any time readiness as well as enhancement of system and practices. To Coordinate with corporate functions with respect to microbiology activity. Travel Estimate Job Requirements Educational Qualification M.Sc (Microbiology) Specific Certification Skills Experience 15 to 18 Yrs

Job Description Title: Micro Lead API Location: Ahmednagar Grade: G9B- Sr. Manager 2 Job Responsibilities To plan, review and monitor overall activities in Microbiology and lead the department. Co-ordination with other departments for priorities and provide the timely support/testing to avoid delay due to analysis. Review of all departmental related documents and review results in LIMS system in microbiology section. Ensure all documents are complete in time. To review the lysate sensitivity test, Bacterial endotoxin test of WFI and API products. To check method validation of bacterial endotoxin test and microbial quality of products. To procure, receipt, storage, maintenance, its use and reconciliation of biological indicator, media, reagents standard cultures and bioball etc. To ensure and check calibration and Operation of TOC analyzer Execute breakdown (If any) in consultation with vender. To ensure environmental monitoring activities performed as per schedule and to check the environmental monitoring reports. To review qualification, Calibration of all instruments in microbiology laboratory as per SOP/Schedule. To participate in investigation and to review of deviations/OOS/OOT/OOC/Lab Event / & review of SOPs as per revision date in micro section online in track wise system. To highlight observations, rejection / failure, quality related concern in time and contribute in troubleshooting To ensure and review all logbooks and registers are maintained on line and available at designated place. Preparation and review of GMP documents related to activities. To review and ensure fumigation activity and its verification as per SOP/Guidelines. To prepare / review trends for water and environment monitoring, Summary report of water and environment monitoring. Responsible to follow online good documentation practices for data recording and monitoring. To ensure and review validation of autoclave, Dry heat sterilizer (DHS), Incubators, Laminar Air flow, HVAC. To ensure and review preparation of reagents and volumetric solution and its standardization as per specification / SOP. To ensure and review inventory and stock record of media/reagents/culture/lysate/CSE/LRW. To ensure to follow the GLP as per current practice in the laboratory. To ensure safety and use of personnel protective equipments during day to day activities Responsible for carrying out any other responsibilities assign from time to time orally or in writing by Quality head, however related training imparted to concerns. To support for review and compliance activity in quality function and to support for any time readiness as well as enhancement of system and practices. To Coordinate with corporate functions with respect to microbiology activity. Education : Graduates - Microbiology/ Equivalent ( experience In Micro testing / leading )

On-site at Cloudnine Hospital Location: Delhi Company: Cryoviva Biotech Pvt Ltd Type: Full-time | On-site Eligibility: B.Sc / M.Sc in Biotechnology, Microbiology, Biochemistry or related life sciences (Freshers welcome!) Tasks Key Responsibilities: Educate pregnant women and families about stem cell preservation and its future health benefits. Counsel clients, answer their questions, and help them understand the scientific and emotional value of the service. Coordinate with doctors, gynecologists, and hospital staff to maintain smooth communication and support. Build Relationships with clients and hospital teams to promote awareness and trust in our services. Drive Enrollments by guiding and assisting parents through the decision-making and registration process Requirements Sales & Business Development Relationship Management Presentation & Counseling Skills Negotiation & Target-Driven Attitude Customer Service Orientation Team Collaboration Job Types: Full-time, Permanent, Fresher Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Application Question(s): When are you available to start working with us? Work Location: In person

🚨 We’re Hiring: Head Quality Assurance 🚨 📍 Location: Murtuza Foods, Mahuva (Onion & Garlic Dehydration Manufacturing Unit) 💼 Position: QA & Check Head 💰 Salary: ₹5–7 LPA (Based on Experience) 🏠 Accommodation Provided by Company 🕒 Experience: 4–5 Years 🚚 Immediate Joining | Relocation to Mahuva Required 🔍 Key Responsibilities: Lead and supervise QA and Final Checking processes for production Ensure implementation and compliance of FSSAI, HACCP, ISO, and customer-specific quality standards Oversee raw material inspection, in-process quality checks, and final product inspection Handle customer audits and documentation conduct internal audits Maintain traceability and ensure corrective/preventive actions for non-conformities Coordinate with Production & Dispatch teams for quality approvals Train and manage QA/checking team and ensure hygiene & GMP practices are followed ✅ Candidate Profile: Bachelor's or Master’s in Food Technology / Microbiology / Chemistry or related field Strong experience in the dehydrated food industry, specifically onion and garlic Proven team management and leadership abilities Comfortable relocating to Mahuva and ready to join immediately 📩 Interested? Send your CV to hr@murtuzafoods.com or call us at +91 7861853566 🧄 Join us at Murtuza Foods – where quality meets commitment!

Position: Microbiologist Organization: Bankai Agrifood Pvt Ltd. Function: QA/QC Website: www.bankaiagrifood.com Primary Purpose: We are seeking a highly skilled and dedicated Microbiologist to join our team. As a Microbiologist, you will play a critical role in ensuring the quality and safety of our products through the testing and analysis of microbiological samples. Key Accountabilities/Activities: Microbial Testing: · Conduct microbial testing of incoming, in-process, and finished products to assess microbiological safety and quality. · Conduct microbial testing of water, process section environment, pipelines, equipment, and personnel working in the section. Preparation and Materials: · Prepare media, cultures, chemicals, and other necessary materials for microbial testing. · Issue materials from the stores as needed for microbiological testing. Compliance and Quality Assurance: · Perform quality clearance of in-process and finished products based on established microbiological criteria. · Determine the release or hold status of process equipment and activities after microbial testing. · Ensure compliance with ISO/HACCP standards and maintain relevant records accordingly. · Implement all HACCP points and closely monitor critical points, providing suggestions and reporting on improvements. Documentation and Records: · Maintain records of laboratory chemicals, glassware, and equipment to ensure availability and proper functioning. · Ensure all required inspections and tests are carried out according to established procedures and techniques. · Verify the cleaning and sanitation of all process equipment, pipelines, machines, etc., to prevent microbiological contamination. · Coordinate pest control activities to maintain a pest-free environment. · Facilitate and monitor the implementation of introduced systems and Total Quality Management (TQM) practices. Coordination and Communication: · Complete assigned tasks by seniors promptly and efficiently to contribute to the smooth functioning of the department. · Coordinate and arrange for medical testing of personnel as required. · Coordinate with other related departments to ensure effective communication and collaboration. Work Relations: Internal: · Reporting to Quality Assurance Officer for all Functional as well as administrative purposes. · Second level reporting to COO · Interface with Production, Quality Control Team, Maintenance, and Procurement teams · Interface with HR teams. External: · Interface with various suppliers, regulatory agencies, Service Providers, Customers Qualification Essential: M. Sc. / B. Sc. (Microbiology) / Biotechnology Experience Essential: Min 1 Year experience in microbial testing of Milk & Milk Products · Proven experience in microbiological testing and analysis, preferably within the food or dairy industry. · Strong knowledge of microbiological techniques, media preparation, and culture methods. · Familiarity with ISO/HACCP standards and their application in a laboratory setting. · Attention to detail and accuracy in conducting tests and interpreting results. · Excellent organizational and record-keeping skills. · Strong communication and teamwork abilities to collaborate effectively with cross-functional teams. · Knowledge of relevant regulations and guidelines related to microbiological testing and food safety. · Ability to work independently and handle multiple tasks simultaneously Work Environment: 24 X 6 (6 days a week) Shift Details: General Shift. (09:00 AM – 5:30 PM), Shift might rotate Job Types: Full-time, Fresher Pay: ₹15,000.00 - ₹25,000.00 per month Benefits: Health insurance Life insurance Paid sick time Provident Fund Application Question(s): Do you have at least 1 year of experience in microbiological testing of food or dairy products? Are you experienced in media and reagent preparation for microbiological tests? Are you familiar with ISO 22000, HACCP, or other food safety standards? Have you maintained laboratory records, logs, and inventories? Location: Karjan, Vadodara, Gujarat (Preferred) Work Location: In person

On-site at Cloudnine Hospital 📍 Location: Delhi 🏢 Company: Cryoviva Biotech Pvt Ltd 🕒 Type: Full-time | On-site 🎓 Eligibility: B.Sc / M.Sc in Biotechnology, Microbiology, Biochemistry or related life sciences (Freshers welcome!) Tasks Key Responsibilities: Educate pregnant women and families about stem cell preservation and its future health benefits. Counsel clients, answer their questions, and help them understand the scientific and emotional value of the service. Coordinate with doctors, gynecologists, and hospital staff to maintain smooth communication and support. Build Relationships with clients and hospital teams to promote awareness and trust in our services. Drive Enrollments by guiding and assisting parents through the decision-making and registration process Requirements Sales & Business Development Relationship Management Presentation & Counseling Skills Negotiation & Target-Driven Attitude Customer Service Orientation Team Collaboration

**READ THE JD CAREFULLY BEFORE APPLYING!!! VACANCY :RESEARCH ANALYST INTERN (R&D) LOCATION : BHUBANESWAR, Bangalore(if full time) Job Summary: We are seeking a dynamic and detail-oriented R&D Research Analyst to join our team. The ideal candidate will have a strong technical background and be capable of conducting in-depth research, writing high-quality technical papers, and preparing impactful presentations (PPTs) for internal and external stakeholders. Key Responsibilities: Conduct comprehensive research and analysis on emerging technologies, market trends, and scientific advancements. Write technical research papers, whitepapers, case studies, and journals that reflect high standards of scientific and industry relevance. Collaborate with engineers, product teams, and domain experts to extract and articulate complex ideas in a clear and concise manner. Prepare and design compelling PowerPoint presentations for R&D updates, stakeholder meetings, and academic/industry conferences. Maintain documentation of research findings, methodologies, and results. Stay updated with academic and industry publications to contribute to innovation and ideation. Support in patent documentation and technical grant proposals, if required. Participate in brainstorming sessions and innovation forums. Qualifications: Master’s in Science, Technology, or a related field. Proven experience in technical writing and academic publishing. Strong understanding of R&D processes, scientific methodologies, and data analysis. Proficiency in Microsoft PowerPoint, Word, and Excel. Excellent written and verbal communication skills. Preferred Skills: Experience publishing in peer-reviewed journals or conferences. Design skills (Canva, Adobe Illustrator, or Visme) for enhanced presentation quality. Strong analytical, problem-solving, and critical-thinking abilities. =========>>> FULL TIME JOB OFFER AFTER INTERNSHIP BASED ON PERFORMANCE ENCOURAGING FINAL YEAR STUDENTS TO APPLY (M.sc Biotechnology,microbiology,fisheries) * **CANDIDATES AIMING FOR HIGHER EDUCATION OR PHD CAN WORK WITH OUR PROJECTS THAT WILL HELP THEM SECURING GOOD RANK (SCHOLARSIPS)IN REPUTED UNIVERSITIES(INDIA OR OUTSIDE) Job Types: Fresher, Internship Contract length: 2 months Pay: ₹5,000.00 - ₹6,000.00 per month Benefits: Flexible schedule Leave encashment Paid time off Provident Fund Ability to commute/relocate: Patia, Bhubaneswar, Orissa: Reliably commute or planning to relocate before starting work (Required) Application Question(s): when can you come for interview? when can you join us if selected? Education: Master's (Preferred) Work Location: In person Application Deadline: 28/07/2025 Expected Start Date: 28/07/2025

You will be responsible for performing and documenting all activities related to the formulation and filling process development. Your role will involve optimizing different vaccine formulations, selecting stabilizers and excipients, as well as preparing adjuvants such as aluminium salts, Oil-In-Water emulsions, Liposome-based adjuvants with TLR agonists and saponin, LNP formulation, aseptic filling, and Lyophilization cycle designing for new vaccine products. Additionally, you will troubleshoot existing vaccines as needed. You will execute the clinical drug product manufacturing for clinical batches, plan and carry out media fill activities, and maintain R&D lab documents, equipment, and area qualifications in compliance with GMP requirements. Furthermore, you will be responsible for preparing process validation and technology transfer protocols as per GMP requirements and collaborate with QA, QC, and Engineering departments for viral vaccine development activities. Ensuring proper hygiene and entry/exit procedures in the formulation and filling section will be part of your responsibilities. You will also prepare adjuvants, buffer solutions, and other materials, and coordinate with the central warehouse department for the receipt and entry of raw materials and packaging materials. Supervision of disinfectant solutions, cleaning solutions, integrity testing of filters, and sanitization activities in the R&D formulation department will also be under your purview. Managing QMS processes such as deviations, MDD, investigations, observations, and ensuring timely closure will be crucial. You will also be involved in preparing standard operating procedures, batch manufacturing records, QRM, and protocols related to the R&D formulation and filling section. In addition, you will oversee the washing, drying, packing, and sterilization of materials required for R&D development and GMP clinical batch preparation. Preferred Candidate Profile: - Ph.D./M.Sc. in science (Biotechnology, Biochemistry, and Microbiology) or Masters Degree in Pharmacy or Engineering with biotechnology. - Experience in the vaccine industry. - Ability to work at the bench level, and this position involves one reporting relationship.,

Candidates should posses lifesciece back ground either Biotechnology, Microbiology, Biochemistry, Genetics, Zoology and Botany. Willing to travel to customer place and promote our lifesciece products in and around Bangalore, Mysore, Mangalore and Dharwad Should have basic knowledge about the molecular, Immunology and cell culture products Willing to travel and should have two wheeler Willing to take sales target and achieve

Position: Field Application Specialist (Marketing – IVD) Location: Kolkata, West Bengal Are you passionate about diagnostics and ready to make a meaningful impact in the healthcare industry? Join Imperial Biotek, one of the leading IVD solution providers in Eastern India. We’re looking for a dynamic and knowledgeable Application Specialist with: ✔ 2–3 years of experience in the IVD domain ✔ A background in B.Sc / M.Sc – Life Sciences, Biotech, Microbiology, or related fields ✔ Strong clinical understanding of diagnostic platforms (coagulation, hematology, immunoassay, etc.) ✔ Excellent communication and training skills ✔ Experience in customer support, product promotion & clinical marketing In this role, you’ll work closely with our marketing and technical teams to drive product adoption, support end-users and build scientific engagement across laboratories and hospitals. Apply now and be part of a team that’s driving innovation in diagnostics. Contact: 📌 Nisha Raha (HR-Executive) 📞 ‪+91 8017560524‬

You will be part of a leading expert organization specializing in assurance and risk management. With a commitment to safeguarding life, property, and the environment, you will play a crucial role in empowering customers and stakeholders with reliable insights to make confident decisions. Being a trusted entity for top global organizations, your expertise will contribute to advancing safety and performance, setting industry benchmarks, and innovating solutions to address global challenges. Your responsibilities will involve conducting audits and assessments related to In-Vitro Diagnostic Medical Devices. As an Assessor, you will perform assessments according to established procedures, ensure effective customer communication, and review Technical Files for specific products. Your role will also include completing projects related to IVDR procedures and making certification decisions within stipulated timeframes. In the role of an Auditor, you will be responsible for auditing manufacturers" quality management systems and suppliers/subcontractors when necessary. Conducting surveillance audits, maintaining strong customer relationships, and managing auditing teams efficiently will be key aspects of your job. Additionally, you will undertake projects related to IVDR procedures and contribute to certification recommendations within defined timelines. Required qualifications for Assessors and Auditors include a technical college degree in relevant areas such as Biology, Chemistry, Medical Technology, Human Physiology, Nursing, or related fields. Candidates must possess a minimum of 4 years of full-time work experience in the In-Vitro diagnostic medical device industry, academia, or hospital settings, with at least 2 years focused on device design, manufacturing, testing, or usage. Practical experience in quality management systems, production processes, and performance evaluation data related to In-Vitro diagnostic medical devices is essential. Preferred qualifications include a strong understanding of medical device management systems, standards, compliance auditing techniques, and risk management practices. Experience with Harmonized medical device standards, EN ISO 14971, and technical writing skills are advantageous for this role. Candidates with a Ph.D. in a relevant field related to in-vitro diagnostic medical devices may substitute work experience requirements with appropriate expertise. In addition to competitive compensation, you will enjoy flexible work arrangements, generous paid leaves, medical benefits, pension schemes, training assistance, and various additional benefits. The company values work-life balance, career development, and employee well-being, offering a supportive and rewarding work environment. Join us in our mission to drive trust, transparency, and sustainable results in the assurance industry, contributing to global transformations and making a positive impact on society.,

You are invited to join Karpagam Faculty of Medical Sciences & Research in Coimbatore for the following faculty positions: Anatomy - Senior Resident/Tutor Biochemistry - Associate Professor Pharmacology - Associate Professor Microbiology - Assistant Professor Community Medicine - Senior Resident/Assistant Professor General Medicine - Professor/Associate Professor Psychiatry - Associate Professor Orthopedics - Assistant Professor Ophthalmology - Senior Resident To be eligible, you must possess an MD/MS or DNB degree in the relevant specialty from an NMC recognized medical institution. Additionally, you should hold a valid medical license (State or Country) and demonstrate proven experience in clinical practice, teaching, and research. Strong interpersonal skills and the ability to work collaboratively in a team environment are essential qualities for this role. The ideal candidate will have 0 to 8 years of experience in the medical field. The salary offered for these positions ranges from 1 lakh to 3.5 lakhs, and accommodation facilities (2BHK/3BHK) inside the campus are provided as part of the perks and benefits package.,

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

Role & responsibilities Perform proper maintenance of equipment including daily, weekly, and monthly maintenance Processing the samples. Segregation of Samples Escalating identified issues to the designated supervisor. Timely processing of Sample Tests as per TAT. Recording results of samples tested Following proper quality control protocol and corrective action. Maintaining proper inventory of the Equipment. Maintaining all documentation of bench work. Maintenance of run records, kit literature, Quality control data, and instrument data. Responsible for operation of BD BACTEC FX40 and BD PHOENIX M50 machines. Media preparation and QC SOP and quality control step to be taken Assist in writing of Standard operating procedures. • In case of machine breakdown timely troubleshooting and escalating the issue. Preferred candidate profile Certificate/degree in MLT is mandatory should be available for face to face interview

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview We are seeking a highly skilled Cost Modeling Analyst to join the Digital Data Networks Business Unit at TE Connectivity India Pvt. Ltd. In this role, you will be responsible for developing and maintaining robust cost models that support new product development and drive cost improvement initiatives. The ideal candidate will have a strong background in should-cost modeling, data analytics, and manufacturing cost estimation, with hands-on experience in key connector industry processes such as stamping, plating, molding, and assembly. Required Skill & Responsibilities Required Skills : B.Tech in Mechanical, Electrical, or Electronics Engineering. 812 years of experience in cost modeling and analysis, preferably in the connectors or electronics manufacturing industry Proficiency in costing software (aPriori, TcPCM, Excel) Strong understanding of manufacturing processesstamping, molding, plating, and assembly. Solid foundation in cost estimation methodologies, data analytics, and reporting. Excellent analytical thinking, problem-solving, and communication skills.Proven ability to work in a collaborative, cross-functional environment . Cost Modeling Development: Develop and maintain should-cost models for connector and cable products using tools such as aPriori, TcPCM, and Excel. Build cost structures that include direct materials, labor, overhead, and other relevant cost components. Support design-to-cost and value engineering initiatives by providing cost insights during product development. Data Analysis and Validation: Analyze BOMs, supplier quotations, purchase history, and manufacturing process data to derive accurate cost estimates. Validate cost model assumptions through back testing, sensitivity analysis, and expert reviews. Ensure data integrity and consistency across cost modeling tools and reports. Cost Optimization and Collaboration: Identify cost drivers and recommend opportunities for cost reduction and efficiency improvements. Collaborate with engineering, procurement, finance, and operations teams to align cost models with business goals. Provide actionable insights to optimize product design and manufacturing processes. Reporting and Communication: Prepare and present cost analysis reports to stakeholders, highlighting key trends, risks, and recommendations. Communicate complex cost modeling concepts to non-financial audiences in a clear and actionable manner. Competencies

Job Summary: We are looking for a detail-oriented and organized Biological Lab Technician to support laboratory experiments and research activities. The ideal candidate will assist in preparing specimens, maintaining lab equipment, and ensuring that all testing is conducted accurately and safely in compliance with standard protocols. Key Responsibilities: Prepare biological samples (e.g., blood, tissue, cultures) for laboratory analysis. Set up, operate, and clean laboratory instruments and equipment. Perform basic laboratory tests and experiments under supervision. Record observations, test results, and other data accurately. Maintain and update laboratory logs, reports, and inventories. Sterilize equipment and maintain a clean and safe work environment. Assist in quality control and assurance processes. Follow proper safety and biosafety procedures in handling biological materials.

Job Summary: We are looking for a dedicated and detail-oriented Biochemist to join our research and development team. The ideal candidate will be responsible for conducting experiments, analyzing biological processes, and contributing to the development of new products, drugs, or diagnostic tools. The role requires strong analytical skills, laboratory expertise, and a passion for scientific discovery. Key Responsibilities: Conduct biochemical experiments and analyze the chemical composition of living organisms. Study the effects of substances such as drugs, hormones, and nutrients on biological systems. Develop and validate laboratory tests, procedures, and protocols. Operate and maintain laboratory equipment such as spectrophotometers, chromatography instruments, and electrophoresis systems. Record and interpret experimental results and present findings in reports or research papers. Collaborate with cross-functional teams including microbiologists, pharmacologists, and clinical researchers. Assist in the development of pharmaceutical compounds, diagnostic tools, or biotechnological products. Ensure compliance with safety standards, regulatory guidelines, and ethical practices in laboratory settings.

Job Summary: We are looking for a dedicated and detail-oriented Biochemist to join our research and development team. The ideal candidate will be responsible for conducting experiments, analyzing biological processes, and contributing to the development of new products, drugs, or diagnostic tools. The role requires strong analytical skills, laboratory expertise, and a passion for scientific discovery. Key Responsibilities: Conduct biochemical experiments and analyze the chemical composition of living organisms. Study the effects of substances such as drugs, hormones, and nutrients on biological systems. Develop and validate laboratory tests, procedures, and protocols. Operate and maintain laboratory equipment such as spectrophotometers, chromatography instruments, and electrophoresis systems. Record and interpret experimental results and present findings in reports or research papers. Collaborate with cross-functional teams including microbiologists, pharmacologists, and clinical researchers. Assist in the development of pharmaceutical compounds, diagnostic tools, or biotechnological products. Ensure compliance with safety standards, regulatory guidelines, and ethical practices in laboratory settings.

Job Summary: We are looking for a detail-oriented and organized Biological Lab Technician to support laboratory experiments and research activities. The ideal candidate will assist in preparing specimens, maintaining lab equipment, and ensuring that all testing is conducted accurately and safely in compliance with standard protocols. Key Responsibilities: Prepare biological samples (e.g., blood, tissue, cultures) for laboratory analysis. Set up, operate, and clean laboratory instruments and equipment. Perform basic laboratory tests and experiments under supervision. Record observations, test results, and other data accurately. Maintain and update laboratory logs, reports, and inventories. Sterilize equipment and maintain a clean and safe work environment. Assist in quality control and assurance processes. Follow proper safety and biosafety procedures in handling biological materials.