Job Information Job Opening ID ZR_1781_JOB Date Opened 24/03/2023 Industry Technology Job Type Work Experience 5-8 years Job Title Sr. Engineer (Microbiologist) City Gurgaon Province Haryana Country India Postal Code 201303 Number of Positions 1 May support in the development, review and approval of sterilization process and equipment validation/qualifications (IQ, OQ & PQ). Be the point of contact for suppliers/development engineers for new process development, quality issues and process improvements for assigned projects. Participate in the development and improvement of the manufacturing processes for existing and new products. Support product transfers to other plants/facilities. Review/approve nonconforming material and system documentation. Review/approve product and process change control documentation and specifications. Actively participate on teams to support new product development activities. Support design verification and validation test requirements that ensure appropriate objective evidence is available to support acceptance criteria. Specific Job Skills: Must understand the fundamentals of at least one of the following sterilization techniquesgamma irradiation, ethylene oxide (preferred), hydrogen peroxide gas plasma, moist heat, or dry heat and be an expert in one of the techniques. Demonstrated knowledge about a variety of microbiological concepts, practices, and procedures. Ability to use ISO, AAMI, USP, ANSI, EPA, EU and related guidelines toward the design, manufacturing, development, and launch of initiatives. Experience with ISO 17025, Lab Quality Management System. Desired Profile EducationM.Sc. in Microbiology ExperienceMin 5 years of experience in applied device or pharmaceutical microbiological or biological testing, research and development, or sterility assurance experience. check(event) ; career-website-detail-template-2 => apply(record.id,meta)" mousedown="lyte-button => check(event)" final-style="background-color:#2B39C2;border-color:#2B39C2;color:white;" final-class="lyte-button lyteBackgroundColorBtn lyteSuccess" lyte-rendered=""> I'm interested

Greeting from UnoPath (A Unit of Axiom Pathology & Diagnostics.) We are looking for a Full Time Consultant Pathologist (MD/DNB - Pathology) in our Gorakhpur path Lab. Experience of NABL Accredited lab set up will be an added advantage Role & responsibilities Job Location : Barhalganj, Gorakhpur, Uttar Pradesh

Micro section independently,knowledge of bacterial identification Knowledge of lab instrument,practical Knowledge of handle the typhoid and disease causing acteria knowledge of sterilization of culture media and culture,disinfectant test procedure

Greetings!!!! We are seeking a skilled and motivated Microbiologist Fermentation to join our Microbiology department. The candidate should have solid hands-on experience in microbial fermentation processes, aseptic techniques, and culture handling. Key Responsibilities: Conduct microbial fermentation experiments and process optimization Handle pure culture maintenance, strain development, and inoculum preparation Operate and monitor bioreactors and fermentation systems Maintain lab hygiene and ensure sterile working conditions Prepare reports and maintain documentation per regulatory standards Desired Candidate Profile: Good understanding of fermentation microbiology Practical experience in aseptic handling and bioprocess equipment Strong analytical and communication skills Prior experience in pharma/biotech industry preferred Interested Candidates Kindly Share your updated to uma@bvrpc.com

Greetings, We are looking for an experienced and motivated Research Scientist to join our Downstream Fermentation team. The candidate should have hands-on experience in downstream processing of fermentation-based products in a biopharmaceutical or industrial biotechnology environment. Key Responsibilities: Lead and perform downstream processing of microbial fermentation products. Optimize purification processes (e.g., filtration, centrifugation, chromatography). Design and execute scale-up and pilot-scale studies. Collaborate with upstream, analytical, and quality control teams. Maintain accurate records and write technical reports. Ensure compliance with GMP/GLP and safety standards. Desired Candidate Profile: Strong knowledge of biotechnology/bioprocess engineering. Experience in purification of proteins, enzymes, or metabolites. Good communication and problem-solving skills. Prior experience in fermentation-based industries preferred. Interested candidate kindly share your cv to uma@bvrpc.om

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

The Opportunity Avantor is looking for a dynamic, forward-thinking, and experienced Associate - Cross Reference EU, who will be responsible for delivering results against some of the most complex business and technology initiatives. This role will be a full-time position based out of IND- Coimbatore. If you are passionate about solving complex challenges and driving innovation – let’s talk! Our organization is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We are looking for an associate who can work on data management strategies by investigating and resolving data quality issues in enterprise applications via deletion and merging, while safeguarding against data loss. Major Job Duties & Responsabilities Adhere to the workflow instructions/standard operating procedure provided by the business. Extract, analyze, update data, and implement of process improvement. Liaise with both internal and external customers and provide resolution with a customer centric approach. To provide alternatives through Branding Strategy promoting sales of Private label products. To enrich the SAP database by providing alternatives for Competitor codes. Responsible for the content of the cross-reference data in SAP. Building up knowledge of our product portfolio and know the preferred suppliers in different segments. Works with large amounts of data and regularly audits, research, analyzes, makes modifications to, and communicates about all the above tasks. Maintains accurate tracking of open and closed requests to ensure smooth workflow and accurate reporting. Perform other duties as assigned. Skills, Knowledge & Experience Results oriented and works with a sense of urgency. Assertive, responsible for his/her own work and has a strong affinity for defining work in deliverables and is willing to commit to deadlines. Focused and versatile team player that is comfortable under pressure. Knowledge of distribution, project management skills, critical thinking, data analysis. Experienced level in MS Excel & knowledge of MS Access, SAP, SQL & basic VBA skills are a plus. Excellent communication skills, oral and written. Results driven, self-sufficient and highly motivate. Must be able to work effectively with all levels of the organization. Must be able to develop excel reports as well as PowerPoint presentations. Knowledge of Avantor systems. Logical thinking and ability to analyse, standardize and improve fragmented processes. Independent thinker Affinity with large data sets and analytics Educational Qualifications Education: Bachelor's /master’s degree preferably in Biology, Chemistry / Life Science (Microbiology, Biotechnology, Biochemistry) or an equivalent subject. Experience: 0 to 5 years of experience in manufacturing and distribution environment preferred. Disclaimer The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. 3rd Party Non-solicitation Policy By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation Show more Show less

Job Description To handle and distribute various samples received for microbiological analysis. To maintain the logbook for the same. Maintain housekeeping of Microbiology lab. To maintain the inventory of various microbiological media, maintain log and status labels, media preparation, growth promotion test and reconciliation of media. Microbial culture handling and inoculum preparation. Water sampling and analysis of water samples as per schedule, with completion of all reports and records. Responsible for Sterility testing, Bacterial endotoxin testing, antibiotic microbial assay and bio burden testing of Raw material, in-process, finished products. Environmental monitoring of microbiology lab clean room area as per the defined schedule. Non-viable particle monitoring of microbiology lab clean room area as per the defined schedule. Responsible to identify and maintain data logging of EM Isolates. To perform disinfectant efficacy testing as per SOP. To perform microbial identification as per defined schedule. Responsible for handling and testing of biological indicator. To perform CCIT test of post media fill units. To perform observation of microbial plates exposed in manufacturing area. To perform media fill unit observation as per SOP. Responsible for reporting any OOS, Deviation to In-charge. Responsible for preparation of standard operating procedures of microbiology department. Responsible to co-ordinate with manufacturing, Engineering, and other QC personnel for respective Qualification / Validation / Re-qualification activity for timely completion of activities. Responsible to participate in perform qualification activities of manufacturing and Microbiology area. Responsible for Compressed air /nitrogen gas monitoring and Personnel monitoring Preparation of indents as per the materials/product requirements. To initiate and review of a) Change controls b) Out of specifications c) Deviations. To attain and complete self- training record. Preparation of study protocols with respect to laboratory. Review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Preparation of COA. To keep neat and cleanliness at workplace and follow the good laboratory practices and safety related instruction in the laboratory. To perform water analysis and maintain daily water trend. Sampling, testing and release of Raw material, packing material, miscellaneous material samples and in process sample and maintain reserve sample as per SOP. To keep update of instruments logbooks and to record the data in Laboratory Notebook / and respective software. To monitor and plan the activities of various glassware and items required for microbiological analysis with respect to their cleaning, sterilization, and dehydrogenation. To maintain log and status labels for all such items and reconciliation record. Responsible for Pure culture handling and maintenance. To maintain daily logs of area with respect to temperature, humidity, differential pressure, area cleaning, disinfectant preparation, etc.. To record such reading in the respective records and logs. Qualifications B.Sc. / M.Sc. Show more Show less

Overview About Bruker: Bruker is enabling scientists to make breakthrough discoveries and develop new applications that improve the quality of human life. Bruker’s high-performance scientific instruments and high-value analytical and diagnostic solutions enable scientists to explore life and materials at molecular, cellular and microscopic levels. In close cooperation with our customers, Bruker is enabling innovation, improved productivity and customer success in life science molecular research, in applied and pharma applications, in microscopy and nano analysis, and in industrial applications, as well as in cell biology, preclinical imaging, clinical phenomics and proteomics research and clinical microbiology. Today, worldwide more than 9700 employees are working on this permanent challenge at over 90 locations on all continents. Bruker continues to build upon its extensive range of products and solutions, its broad base of installed systems and a strong reputation among its customers. Being one of the world's leading analytical instrumentation companies, Bruker is strongly committed to further fully meet its customers’ needs as well as to continue to develop state-of-the-art technologies and innovative solutions for today's analytical questions. Bruker India is seeking for a Senior Administrator, Office & Facility to be based in Bengaluru, India. He/she is responsible for overseeing and hands-on execution of the management, maintenance, and smooth operation of the office buildings of Bruker India across various locations, facilities, and related services. This role ensures that the office environment is safe, efficient, and conducive to employee productivity. He/ she will manage day-to-day operations, lead facility-related projects, and maintain relationships with vendors and contractors. He/ she will also ensure compliance with safety regulations and company policies. Responsibilities Office Administration: Oversee day-to-day office administration tasks, including managing office supplies, equipment, and other office-related services. Ensure smooth office operations by maintaining inventory, ordering office supplies, and managing vendor relationships for office materials. Support HR and IT departments in managing the onboarding and offboarding processes for employees (e.g., preparing workstations and managing access). Serve as the point of contact for internal employee inquiries related to office resources and administrative services. Assist in scheduling and coordinating meetings, events, and other office-related activities to support business needs. Assist in organising overseas guest hotel reservations, local transportation arrangements, etc. Facility Operations & Maintenance Oversee the daily operations of the office building(s) including HVAC, electrical, plumbing, janitorial services, and other facility systems. Ensure all systems and equipment are operating efficiently and safely. Conduct regular inspections of the facilities to identify areas requiring maintenance or improvements. Manage facility-related budgets, including forecasting expenses and managing costs. Coordinate and oversee preventive maintenance programs for all building systems. Vendor & Contractor Management Liaise with external contractors, service providers, and vendors to ensure quality service delivery and compliance with contracts. Negotiate contracts and oversee the work of contractors for construction, maintenance, and other facility-related projects. Ensure vendors meet performance standards and adhere to safety regulations and timelines. Space Planning & Office Layout Oversee space planning and office layout to maximize utilization and efficiency. Manage office moves, renovations, and redesigns to support business needs and employee satisfaction. Collaborate with BRKR division managers, Finance, IT, and other departments to optimize the office environment. Safety, Security & Compliance Develop and implement facility safety programs in compliance with local laws and company policies. Ensure the office building complies with all relevant regulations (OSHA, fire codes, building codes, etc.). Oversee building security, including access control, surveillance systems, and employee safety procedures. Lead emergency preparedness and disaster recovery planning. Budget & Financial Management Prepare and manage facility budgets, ensuring cost-effectiveness while maintaining high standards of quality. Monitor and report on facility-related expenses and implement cost-saving measures where possible. Employee Engagement & Support Address employee facility-related concerns and ensure a high level of satisfaction with the workplace environment. Serve as a point of contact for building-related issues and resolve them promptly. Provide ongoing communication regarding office policies, changes, and improvements. Qualifications Qualifications: Bachelor's degree in Facility Management, Business Administration, or a related field (or equivalent work experience). Minimum 3-5 years of experience in facility management, office management, or related roles. Strong knowledge of building systems, operations, and maintenance procedures. Familiarity with health, safety, and environmental regulations. Experience with budget management and cost control. Excellent communication, organizational, and problem-solving skills. Proficiency with facility management software and MS Office Suite. Ability to manage multiple projects simultaneously and prioritize tasks effectively. Strong leadership abilities and the ability to work independently and as part of a team. Experience with corporate office environments and multi-location management. Knowledge of sustainability practices in facilities management. Bruker is an equal-opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. Show more Show less

Overview At Bruker, we enable scientists to make breakthrough discoveries and develop new applications that improve the quality of human life. Bruker’s high-performance scientific instruments and high-value analytical and diagnostic solutions enable scientists to explore life and materials at molecular, cellular, and microscopic levels. In close cooperation with our customers, Bruker is enabling innovation, improved productivity, and customer success in life science molecular research, in applied and pharma applications, in microscopy and nanoanalysis, and in industrial applications, as well as in cell biology, preclinical imaging, clinical phenomics and proteomics research and clinical microbiology. Today, worldwide more than 8,500 employees are working on this permanent challenge at over 90 locations on all continents. Bruker continues to build upon its extensive range of products and solutions, its broad base of installed systems, and its strong reputation among its customers. Being one of the world's leading analytical instrumentation companies, Bruker is strongly committed to further fully meeting its customers’ needs as well as to continuing to develop state-of-the-art technologies and innovative solutions for today's analytical questions. Bruker India is looking for enthusiastic and motivated individuals to join our Apprenticeship Training Program under the National Apprenticeship Program . The Apprenticeship Trainee/s (Internship) will be based in various locations (Bengaluru, Hyderabad, Kolkata, Mumbai, New Delhi) in India. This is a unique opportunity to kick-start your career with hands-on training in cutting-edge technologies and business operations. The duration for the apprenticeship program is 12 months . There are various opportunities within the different functions. These include : Helpdesk (Bengaluru) Order Management (Bengaluru) Business Analyst (Mumbai) Field Service (Hyderabad, Kolkata, New Delhi) Technical Sales Support / Sales Process Associate (SPA) (Bengaluru) Importantly, please indicate the following points in your resume : State your function/s of interest (Eg. Field Service/ Order Management etc) and reason for the selection Describe your career vision in less than 100 words Where is your base location Responsibilities As an Apprenticeship Trainee at Bruker India, you will: Learn and Grow: Gain hands-on experience and receive guidance from industry experts in a supportive learning environment. Contribute to Projects: Participate in real-world assignments that align with Bruker’s mission to drive innovation and discovery. Develop Skills: Enhance your technical and professional competencies through structured training and mentorship. Collaborate: Work with cross-functional teams to understand end-to-end processes in Bruker India’s operations. Why Join Us? Industry Exposure: Get trained on advanced technologies and real-world business processes. Career Development: Build a strong foundation for your future career in a globally renowned organization. Mentorship & Training: Receive structured training and guidance from experienced professionals. Qualifications Bachelor Degree - Engineering/ Chemistry/ Bio-medical/ Business Management. Fresh graduates / post graduates are welcome to apply. If you are eager to learn and want to work in a dynamic, innovative, and collaborative environment, apply now! Bruker is an equal-opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. Show more Show less

Should have knowledge in Clinical Data Managemen Should have good knowledge in edit checks crf design SAE Reconcilation crf annotation Good knowledge in Startup conduct phase and close out phase Required Candidate profile Strong understanding of clinical data management and E2b Guidelines Excellent clinical assessment and Communication Skills

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us. Your Role In this role, the hire will engage in activities related to Large Data handling, including data maintenance, updates, reporting, and more MDGM Data maintenance, PRM/PRP updates, Back-order reporting, Sales reporting, and more Training to be on site, 3 days work from office Who You Are Conduct data Analysis, management & visualization. Advance knowledge of MS Office especially in MS Excel & Access Proficient in SAP & ERP system navigation Utilize tools like Power BI and Palantir for reporting and data visualization. Problem Solving ability - Identifying and resolving data related issues and discrepancies. Strong verbal and written communication skills Planning, time management, organization, and attention to detail Work with stakeholders to define and set priorities, deadlines, and deliverable schedules. Basic/ Minimum Qualifications Proficient in navigating SAP: PRE, PRD. Excellent Excel skills. Knowledge of Master data management. Preferred Qualifications Education: University post-graduate degree: MSc in Life science, Biology or related fields Biotechnology, Biochemistry, Microbiology, Genetics, Molecular Biology, Zoology, Botany. Experience: 3-5 years of experience in Product management Operations, Master Data, Supply chain. Note Based on the experience and skills of the candidate, we are open to offering a higher role as well. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! Show more Show less

Teaching: Instructing undergraduate and graduate students in their subject area. Designing courses, creating syllabi, and delivering lectures. Developing and assessing student learning through exams, papers, and other assignments. Providing guidance and support to students on academic and career goals. Research: Conducting research in their field and publishing scholarly articles. Developing and presenting research findings at conferences and workshops. Seeking funding for research projects through grant proposals. Service: Participating in department meetings and university committees. Mentoring and advising students. Contributing to curriculum development and assessment. Collaborating with colleagues on research projects and interdisciplinary initiatives. Providing academic support to students and colleagues. Role & responsibilities Preferred candidate profile

We are inviting applications for two research positions under a Ministry of Earth Sciences (MoES), Government of India funded Deep Ocean Mission project in the Department of Marine Biotechnology at AMET University, Chennai. 🔬 Project Title: Exploring Marine Bioresources as Potential Natural Antifoulants: An In-depth Study on Secondary Metabolites of Marine Actinomycetes 🧪 Open Positions: Senior Project Associate – Ph.D. in Life Sciences – Experience in microbiology, biofilm, and antifouling studies – Fellowship: ₹42,000 + 24% HRA Project Associate-I – M.Sc. in any Life Science discipline – Preference for those with experience in marine-related fields – Fellowship: ₹25,000 + 24% HRA 📅 Last Date to Apply: 15 June 2025, 5:30 PM 📧 Apply via email: jayaprakashvel.m@ametuniv.ac.in 📍 Interview will be conducted in physical mode only. The selected Project Associate may also enroll in the Ph.D. program as per University norms. Interested and eligible candidates are encouraged to apply. For further details, feel free to reach out. 🔹 Dr. M. Jayaprakashvel Principal Investigator, MoES–DOM Project Professor, Department of Marine Biotechnology AMET University, Chennai #DeepOceanMission #MarineBiotechnology #MoES #ResearchOpportunity #LifeSciences #PhD #HiringNow #MarineEcology #BiofilmResearch #Actinomycetes #ProjectPositions #ChennaiJobs #AcademicJobs #ResearchCareers Show more Show less

Responsible for in process Quality Assurance activities Responsible for In process Quality Assurance checks during Manufacturing, packing operations. Responsible for line clearance of manufacturing, Packing and dispensing activities. Responsible for assurance of cleaning, sterilization and aseptic manipulations of components Responsible for Sampling of Cleaning Validation & Compilation of the records. Responsible for sampling and coordination during validation studies (process / cleaning validation). Responsible for routine monitoring of Manufacturing Areas. Responsible for Review of Batch Manufacturing Record (BMR) & Batch Packing Records (BPRs). Responsible for the routine GMP Inspection & review of Quality Records of other departments. Responsible for monitoring in Aseptic process simulation study. Responsible for Preparation and Compilation of Media Fill Protocol , Report Involve in Initiation of Change Control ,Deviation and Participate in Failure Investigation. Responsible for environmental monitoring (Viable) in liquid, lyophilized and dry powder manufacturing areas Responsible for preparation and implementation of SOP's Good Documentation recording and updation Responsible for Preparation and Implementation of SOP's. Viable monitoring in clean area of manufacturing and warehouse as per the defined schedule. Responsible for personnel monitoring. Responsible to participate in qualification, requalification, area qualification activities. Responsibilities other than defined in the JD are to be done as per instruction of HOD Bachelor's Degree in Pharmacy, Microbiology, Biotechnology, Chemistry, or a related field. Master's Degree in Quality Assurance, Regulatory Affairs, or a related field (preferred but not mandatory). 3-5 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry. Hands-on experience with GMP inspections , environmental monitoring , and aseptic process simulations . Proven track record in sampling . Experience in reviewing Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) . Familiarity with SOP preparation and implementation . Involvement in change control , deviation management , and failure investigations .

Overview T he R&D Manager is responsible for driving the organization's technological advancements and ensuring that its products and services meet the highest standards of quality and innovation. The manager is expected to oversee research and development activities, lead a team of scientists, ensure regulatory compliance, manage the quality department and collaborate with other departments within R&D budgets. Additionally, the manager should possess strong technical expertise, leadership skills, and a focus on innovation to achieve the overall business unit leading and lagging indicators. Responsibilities Driving Innovation: Developing and implementing strategies to foster a culture of innovation and creativity. Identifying and pursuing new product or process opportunities. Ensuring the organization stays ahead of industry trends and competitors. Improving Existing Products Overseeing the optimization of existing products to enhance performance, reduce costs, or address customer needs. Conducting research to identify opportunities for product improvement to meet customer unmet needs/pain points and industry gaps Ensuring Regulatory & Quality Compliance Ensuring that all Regulatory activities comply with relevant industry regulations and standards. Ensuring quality control tests and inspections to maintain product safety of raw materials and finished goods Customer service mindset on managing customer complaints Managing Department Resources Effectively Developing and managing the R&D budget. Allocating resources efficiently to support research projects. Monitoring expenditure and identifying cost-saving Ensure year on year continuous improvements in department ways of workings to improve productivity – doing more for less by improving efficiencies Leading and Developing the team Recruiting, hiring, and training team members. Providing leadership and mentorship to foster a collaborative and innovative work environment. Evaluating team performance and providing feedback. Collaborating With Other Departments Working closely with marketing, sales, production, procurement and finance to ensure successful product development and launch. Building relationships with external partners, suppliers, and academic institutions. In collaboration with the Leadership team, provide strategic directions for Kemin Food Technologies Asia to achieve the business unit leading and lagging indicators. Qualifications A PhD in Food Nutrition/Biochemistry/Microbiology or other related discipline, from a recognized university. Innovation: Demonstrates a track record of developing and implementing innovative solutions that drive business growth Tech Savvy: Stays up to date on emerging technologies and can effectively apply them to business challenges Resourcefulness: Efficiently secures and allocates resources to achieve project goals, even in resource-constrained environments Operational Excellence, Stakeholder Balancing, Action Orientation People Leadership: Talent Development, Accountability Working Conditions: The position will operate from Singapore/India and is expected to spend <20% travelling regionally within Asia / internationally to USA. The position is considered 40 hours per week and requires flexibility to take evening calls between Americas, Europe and Asia. Show more Show less

Qualification: R elevant diploma or certificate program in Medical Laboratory Technology (MLT) or a related field, A Bachelor of Science (B.Sc.) in MLT Both experienced and fresh candidates are eligible. Salary :12k Gender: Females are preferred. Job Description: We want a smart and enthusiastic Lab Assistant who is responsible for Medical Laboratory plays a crucial role in healthcare by performing laboratory tests to aid in diagnosing and treating diseases. They analyze samples, operate equipment, and ensure quality control of results. Key responsibilities and duties: Collecting and preparing patient samples: This includes drawing blood, collecting urine, and preparing tissue samples for analysis. Performing laboratory tests: MLTs conduct a variety of tests, including hematology, microbiology, clinical chemistry, and immunology tests. Analyzing test results: They interpret test results and provide information to healthcare providers for diagnosis and treatment. Operating and maintaining laboratory equipment : MLTs are proficient in using various laboratory instruments, including microscopes, centrifuges, and automated analyzers. Ensuring quality control: They perform quality control procedures to ensure the accuracy and validity of test results. Maintaining a safe and clean laboratory environment: MLTs adhere to safety protocols and ensure proper handling of samples and chemicals. Communicating with healthcare staff: They discuss test results and findings with physicians and other healthcare professionals. Keeping accurate records and reports: MLTs document test results and maintain detailed records. Job Type: Full-time Pay: Up to ₹12,000.00 per month Schedule: Day shift Education: Diploma (Required) Work Location: In person

We're Hiring! Technical Assistant- (Male Candidates Only) Location: Cochin Experience: 0-6 Months (Freshers welcome!) Education: MSc in Microbiology or Biotechnology Shift: Rotational shifts (Day, Mid, Night) | 6 days working with rotational week off Join Haystack Analytics, an IIT Bombay-based HealthTech company revolutionizing clinical genomics. Be part of a team advancing infectious disease diagnostics with cutting-edge sequencing technologies. Role Highlights: Work with diagnostic lab partners for smooth test operations Ensure timely upgrades and technical support for partners Liaison and document technical activities What We’re Looking For: Experience in DNA Extraction & RT-PCR Strong analytical, documentation & communication skills Ability to prioritize and execute tasks efficiently What You Will Gain: Exposure to advanced sequencing technologies (NGS, WGS, Nanopore, Illumina) Experience in troubleshooting during sequencing Work with a leading company in genomics & diagnostics Apply now and be part of the future of healthcare! #Hiring hashtag#TechnicalAssistant hashtag#Microbiology hashtag#BiotechJobs hashtag#Genomicshashtag#HealthTech hashtag#CareerOpportunity Job Types: Full-time, Permanent, Fresher Pay: ₹250,000.00 - ₹275,000.00 per year Schedule: Day shift Night shift Rotational shift Weekend availability Experience: DNA extraction: 1 year (Preferred) Work Location: In person

About You – Experience, Education, Skills, And Accomplishments Educational Qualification: M.Sc. Zoology or related life science streams. Fresher or experience of content analysis/ content editing in a science-related field or in related publication domain. Freshers preferred only if done Masters in Zoology Knowledge on animal classification, systematic taxonomy & Nomenclature will be added advantage. Knowledge in performing end of production cycle completeness, and accuracy tasks as assigned. Good scientific research and analytical skills, with attention to detail General computer proficiency (MS Office) and ability to quickly learn new software tools Good oral and written communication skills, with excellent command of English A good team player with the ability to work independently Ability to set priorities and be flexible in a changing environment Effective time management Self-motivated with the ability to deliver consistently It would be great if you also had . . . A PhD or postgraduate background in zoology would be beneficial. What will you be doing in this role? Apply zoology, systematic taxonomy, ICZN Nomenclature, microbiology, genetics and molecular biology concepts to curate animal and its biological related data from research articles in line with editorial policies Achieve weekly production volumes and consistently meet quality targets Take active role within the team to ensure targets are met Maintain a flexible and adaptable approach towards process change Take initiative by raising, discussing, and resolving subject matter and production issues Maintain and develop scientific knowledge and skills training as required to complete work and stay current on scientific trends and developments related to your editorial responsibilities Product you will be developing Zoological Records products About The Team It is an international team based in India and UK that works mainly for the Zoological Record product. It is part of the Selective indexed product team that is responsible of the selection and indexing of relevant academic items for inclusion in several Clarivate products such as Zoological Record, Derwent Drug File or the International Pharmaceutical Abstracts, within others Hours of Work This is a full-time permanent position At Clarivate, we are committed to providing equal employment opportunities for all persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations. Show more Show less

We are seeking a motivated Content Editor to join our talented Zoological Records (ZR) team in Chennai/Hyderabad. This is the team of 11 member. As a Content editor in the ZR team you will select, analyze and interpret, and summarize scientific research and, as such, you should have comprehensive knowledge in a life sciences subject. Your role will require you to be target-driven and to meet defined quality standards. About You – Experience, Education, Skills, And Accomplishments Work experience (Fresher or at least 1 year of experience in content editing in a science-related field Knowledge on animal classification, systematic taxonomy & Nomenclature will be added advantage. Education M.Sc. Zoology or related life science streams Knowledge in performing end of production cycle completeness, and accuracy tasks as assigned. Good scientific research and analytical skills, with attention to detail General computer proficiency (MS Office) and ability to quickly learn new software tools Good oral and written communication skills, with excellent command of English A good team player with the ability to work independently. Ability to set priorities and be flexible in a changing environment. Effective time management Self-motivated with the ability to deliver consistently. It would be great if you also had . . . Fresher or 1 year of experience Masters in life science (Zoology, Microbiology, Biotechnology). Knowledge on animal classification, systematic taxonomy & Nomenclature will be added advantage. What will you be doing in this role? Apply zoology, systematic taxonomy, ICZN Nomenclature, microbiology, genetics and molecular biology concepts to curate animal and its biological related data from research articles in line with editorial policies Achieve weekly production volumes and consistently meet quality targets. Take active role within the team to ensure targets are met Maintain a flexible and adaptable approach towards process change Take initiative by raising, discussing, and resolving subject matter and production issues Maintain and develop scientific knowledge and skills training as required to complete work and stay current on scientific trends and developments related to your editorial responsibilities About The Team ZR is a comprehensive source of animal information with mainly related animal classification, systematic taxonomy & Nomenclature coming from academic literature and covers all aspects of animal biology. As an Content editor in the ZR team you will select, analyse and interpret, and summarize scientific research and, as such, you should have comprehensive knowledge in a life sciences subject. Your role will require you to be target-driven and to meet defined quality standards. In addition, this team and its processes and workflows are about to undergo huge transformation which will offer opportunities to rethink how the team operates and identify synergies with similar teams so the ideal candidate will be comfortable with change and someone able to offer ideas and think creatively. Hours of Work Full-time Permanent role Team working hours – 9 am to 6 pm IST At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations. Show more Show less

Job Title: QC Analyst I At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world’s most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we’re working at the pace of change on diagnostic tools that address the world’s biggest health challenges, driven by knowing that behind every test there is a patient waiting. Learn about the Danaher Business System which makes everything possible. This position is part of the Quality Organization and will be in India. Reporting directly to the Quality Control lead or site lead, the Quality Control Analyst is responsible for managing the day today activities quality control function at Cepheid India Private Ltd. Ensure compliance of quality control procedures as per MDR 2017, European regulations, ISO 13485, Cepheid corporate quality system requirements. In this role, you will have the opportunity to: Conducts routine and non-routine analysis of raw materials, in-process and finished formulations under supervision and according to Standard Operating Procedures (SOPs). Competent technical staff for supervision the Testing/ analysis of diagnostic reagents & kits. Perform inspections of incoming, in-process and finished products. Performs and calibration and maintenance of lab equipment as per requirements. May perform special projects on analytical and instrument problem solving. Ensure that lab cleanliness and safety standards are maintained. Qualify test methods as part of new product development activities. Serve as a technical liaison between quality control and other departments Write technical reports or documentation such as deviation reports, testing protocols, and trend analyses & Write or revise standard quality control operating procedures. Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines. Follow documentation procedure (filling out Data History Records (DHRs), reading and understanding instructions from Work Release (WR), Planned Deviation Report (PDR) or Non-Conformance Report (NCR). Read and follow Standard Operating Procedures (SOPs) and Manufacturing Work Instructions. Review records and documents for completeness and compliance with company policies and procedures. Support for internal audit schedule, NC, CAPA for site. Review production batch records, QC test results and release product. Education and Experience: Master’s degree in Biochemistry, Molecular Biology, Microbiology or related discipline and a minimum of 3+ years related Quality Control experience. 2+ years’ experience with in Vitro Diagnostics (IVD) is mandate Experience with in Vitro Diagnostics (IVD) is very beneficial and highly desirable Quality competent technical person approved as per D&C act if any Knowledge and skills: Hands on Experience on IVD product testing. Working Knowledge of current GxP regulations for Invitro Medical Devices and ISO 13485 QMS. Must be flexible to work off-shifts and weekends as per production Schedule. Schedule orientated (able to consistently maintains schedules and meet timelines) Strong interpersonal skills, Effective organization and Communication skills are essential. Good skills in English language Knowledge of Microsoft Word and Excel Strong multi-tasking and attention to details skills. It would be a plus if you also possess previous experience in: Experience working with medical device quality systems in compliance with MDR and ISO 13485 Able to interpret quality problem and establish practical solutions within a dynamic business environment. Experience in leading continuous improvement efforts, in both quality systems and products. Knowledge of the process of establishing facility QMS certifications. Cross functional experience with products and manufacturing processes to influence change at all levels within the organization Visio and Project knowledge desirable. When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation. If you’ve ever wondered what’s within you, there’s no better time to find out. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. Show more Show less

Title: Executive- Microbiologist Date: Jun 5, 2025 Location: Mohali - Quality Control Company: Sun Pharmaceutical Industries Ltd Responsibility : Ensure compliance to cGMP and safety standards in the QC laboratory Conduct calibration and cleaning of laboratory equipment and instruments as per SOP. Culture Media preparation and sterilization. To perform growth promotion test of culture media. Maintenance of microbial culture. Document analytical data and calculate results. Maintain laboratory equipment, inventory and supplies. Ensure integrity, accuracy and adequacy of the analysis performed. Follow GLP activities and ensure their compliance. Conduct microbiological sampling and testing of sample. Conduct environmental monitoring. Identification of microorganism through Vitek 2 system. Daily Laboratory Monitoring including Temperature/Humidity and Testo Printout. Management of issuance and archival of log books and formats. Maintenance of various documents and records in Microbiology Lab. To assist in validation/Qualification exercise and any other assignment given by Lab. In charge / Mgr. Quality Control from time to time.

**READ THE JD CAREFULLY BEFORE APPLYING!!! Key Responsibilities and Tasks: Data Analysis and Interpretation: Analyzing large datasets, identifying patterns, and drawing meaningful conclusions from the data. Research and Experimentation: Conducting experiments, collecting data, and analyzing results. Report Writing and Presentation: Preparing detailed reports and presentations for internal and external stakeholders. Collaboration: Working with cross-functional teams, including researchers, scientists, and other analysts. Staying Current: Keeping up-to-date with the latest advancements and trends in the biotechnology field. Regulatory Compliance: Ensuring adherence to regulatory standards and company policies in research methodologies. Model Development: Developing and maintaining statistical models to predict outcomes and trends. Industry Knowledge: Understanding the dynamics of the biotechnology industry, including market trends, company performance, and competitive landscape. Skills and Qualifications: Strong analytical and problem-solving skills: Ability to analyze data, identify trends, and draw meaningful conclusions. Excellent communication skills: Ability to communicate research findings effectively through written reports and presentations. Knowledge of biotechnology principles: Understanding of key concepts and techniques in molecular biology, cell biology, and other relevant areas. Data analysis and statistical software proficiency: Familiarity with tools like Excel, R, Python, or other statistical software. Scientific writing skills: Ability to clearly and concisely communicate research findings in scientific reports. Proficiency in relevant software and tools: Familiarity with software and tools used in data analysis, modeling, and research. Strong communication and presentation skills: Ability to effectively communicate research findings and insights to both technical and non-technical audiences. =========>>>please note: FULL TIME JOB OFFER AFTER INTERNSHIP BASED ON PERFORMANCE ENCOURAGING FINAL YEAR STUDENTS TO APPLY (B.sc/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: 3 months Pay: ₹5,000.00 - ₹6,000.00 per month Benefits: Flexible schedule Leave encashment Paid time off Provident Fund Schedule: Day shift Fixed shift Supplemental Pay: Performance bonus Quarterly bonus Yearly bonus 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? What is your aim in Life? Education: Bachelor's (Preferred) Location: Patia, Bhubaneswar, Orissa (Preferred) Work Location: In person Application Deadline: 28/06/2025 Expected Start Date: 28/06/2025

Assistant Professor - Microbiology Experience 1 - 5 Years of teaching / industry / research experience Qualification Ph.D. / PG with 55% of marks and NET / SET Expectations The applicant should have expertise framing syllabus / industry exposure / and strong subject knowledge to contribute to the development of the department Excellent Communication, leadership, interpersonal, computational, organizational skills. Strong track record of research and publication in the respective field Responsibilities · Teach undergraduate and graduate courses in the respective discipline. · Conduct research in areas related to your subject and publish quality papers in Scopus/ SCI/ Web of Science. · Supervise graduate students and undergraduate research projects. · Submit proposals for get grants for research project. · To train the students to participate in Hackathons/ technical events. · Develop and deliver high-quality lectures, seminars, and practical sessions in the assigned courses. · Employ innovative teaching methodologies to engage and inspire students in active learning and critical thinking. · Provide mentorship and academic guidance to students, including advising on research projects, coursework, and career development. · Assist in curriculum development, review and evaluation to ensure alignment with the latest educational standards and practices. · Participate in departmental meetings, committees, and other administrative responsibilities as assigned. Job Location : Eachanari, Coimbatore. Pay Scale : As per Norms Job Type: Full-time Benefits: Food provided Paid time off Provident Fund Schedule: Day shift Work Location: In person

The Opportunity: Avantor is looking for a dynamic, forward-thinking, and experienced Associate - Cross Reference EU, who will be responsible for delivering results against some of the most complex business and technology initiatives. This role will be a full-time position based out of IND- Coimbatore. If you are passionate about solving complex challenges and driving innovation – let’s talk! Our organization is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We are looking for an associate who can work on data management strategies by investigating and resolving data quality issues in enterprise applications via deletion and merging, while safeguarding against data loss. MAJOR JOB DUTIES & RESPONSABILITIES: Adhere to the workflow instructions/standard operating procedure provided by the business. Extract, analyze, update data, and implement of process improvement. Liaise with both internal and external customers and provide resolution with a customer centric approach. To provide alternatives through Branding Strategy promoting sales of Private label products. To enrich the SAP database by providing alternatives for Competitor codes. Responsible for the content of the cross-reference data in SAP. Building up knowledge of our product portfolio and know the preferred suppliers in different segments. Works with large amounts of data and regularly audits, research, analyzes, makes modifications to, and communicates about all the above tasks. Maintains accurate tracking of open and closed requests to ensure smooth workflow and accurate reporting. Perform other duties as assigned. SKILLS, KNOWLEDGE & EXPERIENCE: Results oriented and works with a sense of urgency. Assertive, responsible for his/her own work and has a strong affinity for defining work in deliverables and is willing to commit to deadlines. Focused and versatile team player that is comfortable under pressure. Knowledge of distribution, project management skills, critical thinking, data analysis. Experienced level in MS Excel & knowledge of MS Access, SAP, SQL & basic VBA skills are a plus. Excellent communication skills, oral and written. Results driven, self-sufficient and highly motivate. Must be able to work effectively with all levels of the organization. Must be able to develop excel reports as well as PowerPoint presentations. Knowledge of Avantor systems. Logical thinking and ability to analyse, standardize and improve fragmented processes. Independent thinker Affinity with large data sets and analytics EDUCATIONAL QUALIFICATIONS : Education: Bachelor's /master’s degree preferably in Biology, Chemistry / Life Science (Microbiology, Biotechnology, Biochemistry) or an equivalent subject. Experience: 0 to 5 years of experience in manufacturing and distribution environment preferred. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. 3rd party non-solicitation policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation