2560 Microbiology Jobs - Page 40

Ct HR Lavanya - 9566157632 Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medial reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim. Eligibility: All (UG/PG) Life Science& Paramedical Graduates BDS BPT BHMS BAMS Siddha,Unani,Naturopathy {Dip Bsc Msc} Nursing/GNM {B.E M.E} Biomedical Engineering {B.tech,M.tech}Biotechnology Biochemistry Bioinformatics Microbiology Zoology and Advanced zoology Biology Botany Medical Lab Tech Plant biotechnology Pharmacy(B.Pharm M.pharm) Paramedical Physiotherapy Physician assistant Critical Care Technology Medical Biochemistry Medical Record Science Operation Theatre & Anaesthesia Technology {Bsc Msc Dip} Clinical Nutrition Human Genetics Medical Laboratory Technology Medical Sociology Epidemiology Molecular Virology Biostatistics Blood Banking Technology Regenerative Medicine Optom. Genetic Counseling Radiology & Imaging Technology Medical Biochemistry Medical Microbiology Clinical Care Technology Clinical Care Technology Medical Physics {Bsc Msc Dip} Accident & Emergency Care Technology Audiology & speech Language Pathology Cardiac Technology Cardio Pulmonary Perfusion Care Technology Critical Care Technology Dialysis Technology Neuro Electrophysiology Medical Sociology Nuclear Medicine Technology Operation Theatre & Anaesthesia Technology Optometry Physician Assistant Radiology Imaging Technology Radiotherapy Technology Medical Record Science Respiratory Therapy Fitness and Lifestyle Modifications Accident & Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre & Anaesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology & Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Requirement: Knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills Benefits System based job Weekly 5 days duty Day shift with Sat and Sun off Food and Cab provided by company Incentives based on performance Starting salary 12k to 25k with increment in 6 months for experienced. Abroad opportunities available Bonus for referring friends Medical expenses covered by company Provident Fund will be provided Gratuity after 5 yrs of work experience. Job Location: Chennai, Tirumala,Tirupati,Hyderabad,Vizag,Eluru,Kakinada,Ongole,Anantpur,Bhimavaram,Coimbatore, Vellore, Trichy, Cuddalore, Pondi Salem, Erode, Namakkal, Thanjavur, Nagercoil, Theni,Dindokal Thiruvannamalai, Villupuram, Karur, Tirunelveli,Kanniyakumari Tirupati, Kerala, AP,Tamilnadu,Telangana Reach Us: Ct: HR Lavanya - 9566157632

Job Description This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance’s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Primary Responsibilities Include, But Are Not Limited To Regulatory Responsibilities Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic documentam based GMP systems Leadership Skills Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor’s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 10 – 12 yrs of Industry Pharmaceutical industry experience out of 6 years’ experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics. The candidate may be required to travel to other CMO sites on a need basis. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Hybrid Shift Valid Driving License Hazardous Material(s) Required Skills Adaptability, Adaptability, Animal Vaccination, Applied Engineering, Biochemistry, Biopharmaceutical Industry, Business, Business Management, Business Processes, Chemical Engineering, Communication Management, Detail-Oriented, Document Coordination, Electronic Common Technical Document (eCTD), Employee Training Programs, GMP Compliance, Immunoassays, Immunochemistry, Interpersonal Relationships, Management Process, Mentorship, Microbiological Analysis, Microbiology, Molecular Biology, Molecular Microbiology {+ 19 more} Preferred Skills Job Posting End Date 07/10/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R349215

Job Description This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance’s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Primary Responsibilities Include, But Are Not Limited To Regulatory Responsibilities Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic documentam based GMP systems Leadership Skills Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor’s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 10 – 12 yrs of Industry Pharmaceutical industry experience out of 6 years’ experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics. The candidate may be required to travel to other CMO sites on a need basis. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Hybrid Shift Valid Driving License Hazardous Material(s) Required Skills Adaptability, Adaptability, Animal Vaccination, Applied Engineering, Biochemistry, Biopharmaceutical Industry, Business, Business Management, Business Processes, Chemical Engineering, Communication Management, Detail-Oriented, Document Coordination, Electronic Common Technical Document (eCTD), Employee Training Programs, GMP Compliance, Immunoassays, Immunochemistry, Interpersonal Relationships, Management Process, Mentorship, Microbiological Analysis, Microbiology, Molecular Biology, Molecular Microbiology {+ 19 more} Preferred Skills Job Posting End Date 07/10/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R349215

Job Description This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance’s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Primary Responsibilities Include, But Are Not Limited To Regulatory Responsibilities Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic documentam based GMP systems Leadership Skills Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor’s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 10 – 12 yrs of Industry Pharmaceutical industry experience out of 6 years’ experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics. The candidate may be required to travel to other CMO sites on a need basis. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Hybrid Shift Valid Driving License Hazardous Material(s) Required Skills Adaptability, Adaptability, Animal Vaccination, Applied Engineering, Biochemistry, Biopharmaceutical Industry, Business, Business Management, Business Processes, Chemical Engineering, Communication Management, Detail-Oriented, Document Coordination, Electronic Common Technical Document (eCTD), Employee Training Programs, GMP Compliance, Immunoassays, Immunochemistry, Interpersonal Relationships, Management Process, Mentorship, Microbiological Analysis, Microbiology, Molecular Biology, Molecular Microbiology {+ 19 more} Preferred Skills Job Posting End Date 07/10/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R349215

The CSSD Technician is responsible for the effective sterilization and disinfection of surgical instruments and medical equipment. This role involves preparing, sterilizing, and ensuring the safe handling of instruments to maintain the highest standards of hygiene and safety within the hospital environment. The technician will also be responsible for the quality control of sterilization processes and will work closely with various departments to support surgical procedures. Roles and Responsibilities - Clean, decontaminate, and sterilize instruments and medical equipment using appropriate methods and technologies. - Ensure the proper functioning of sterilization equipment and report any malfunctions. - Monitor and maintain sterilization logs and quality assurance records. - Prepare and package instruments for surgery, following established protocols. - Collaborate with surgical teams to meet instrument and equipment needs during procedures. - Follow infection control standards and safety protocols to prevent contamination. - Conduct routine checks and maintenance of CSSD supplies and inventory management. - Participate in ongoing training and professional development related to sterilization techniques and infection control practices. Skills Required: - Knowledge of sterilization techniques, principles of infection control, and safety standards. - Familiarity with surgical instruments and medical equipment. - Attention to detail and strong organizational skills. - Ability to work under pressure and manage time effectively. - Excellent communication and teamwork skills. - Analytical skills to monitor sterilization processes and troubleshoot issues. Tools and Equipment: - Autoclaves and sterilization equipment. - Decontamination tools and instruments. - Personal protective equipment (PPE). - Inventory management software. - Quality control systems and logging tools.

To report and log OOS, OOT and EM Excursion To perform Environment monitoring of Laboratory. To Perform analytical validation, culture maintenance and GPT of media, recording observation and report generation. Perform microbiology laboratory tests such as Bioburden Analysis, MLT, Sterility, BET etc. in compliance with approved procedures. To maintain the media stock and its reconciliation record of media used in Analysis. To perform Water Sampling and analysis as per defined SOP/protocol and related documentation.

About Us We are a global leader in food & beverage ingredients. Pioneers at heart, we operate at the forefront of consumer trends to provide food & beverage manufacturers with products and ingredients that will delight their consumers. Making a positive impact on people and planet is all part of the delight. With a deep-rooted presence in the countries where our ingredients are grown, we are closer to farmers, enabling better quality, and more reliable, traceable and transparent supply. Supplying products and ingredients at scale is just the start. We add value through our unique, complementary portfolio of natural, delicious and nutritious products. With our fresh thinking, we help our customers unleash the sensory and functional attributes of cocoa, coffee, dairy, nuts and spices so they can create naturally good food & beverage products that meet consumer expectations. And whoever we re with, whatever we re doing, we always make it real . Main Purpose of the Job We are seeking a skilled and motivated Quality System Coordinator to support the implementation and oversight of quality management systems across multiple global sites. This role is part of the QMS Center of Excellence and reports directly to the Quality System Manager Key Responsibilities Project Coordination Collaborate with site teams across ofi to deploy global quality initiatives via the QuEST platform (including Document Management System, KPI tracking, internal audits, and Vendor Quality Management). Ensure timely and effective implementation. Data Management & Analysis Collect and upload site data into the QuEST KPI system. Assist in reviewing and analyzing data for accuracy and relevance. Reporting & Visualization Prepare monthly quality and food safety reports and dashboards. Ensure timely distribution to relevant stakeholders. Documentation Standardization Support efforts to harmonize system documentation across sites. Additional Assignments Contribute to other projects as assigned by the Quality System Manager Experience, Qualifications and Skills Bachelor s degree in Food Science, Chemistry, Microbiology, or Data Analytics . Minimum 4 years of experience in quality systems within the food industry. Intermediate proficiency in data analytics and visualization tools (PowerBI, Tableau). Working knowledge of database tools (MySQL, Power Query). Experience with programming languages (e.g., Python). Strong analytical and problem-solving skills. Excellent communication and interpersonal abilities. Ability to manage multiple projects simultaneously. A proactive and collaborative mindset aligned with ofi s culture. Comfortable working in a cross-functional, dynamic team environment. Positive outlook and professional demeanor. ofi is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, nationality, disability, protected veteran status, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law. Applicants are requested to complete all required steps in the application process including providing a resume/CV in order to be considered for open roles.

About Us We are a global leader in food & beverage ingredients. Pioneers at heart, we operate at the forefront of consumer trends to provide food & beverage manufacturers with products and ingredients that will delight their consumers. Making a positive impact on people and planet is all part of the delight. With a deep-rooted presence in the countries where our ingredients are grown, we are closer to farmers, enabling better quality, and more reliable, traceable and transparent supply. Supplying products and ingredients at scale is just the start. We add value through our unique, complementary portfolio of natural, delicious and nutritious products. With our fresh thinking, we help our customers unleash the sensory and functional attributes of cocoa, coffee, dairy, nuts and spices so they can create naturally good food & beverage products that meet consumer expectations. And whoever we re with, whatever we re doing, we always make it real . Main Purpose of the Job We are seeking an experienced and proactive Quality System Manager to join our Global QMS Center of Excellence (COE). This role is based in Bangalore and will play a key part in supporting the Global QMS COE Head in managing and enhancing quality management systems across multiple global sites. The ideal candidate will bring a strong background in food industry quality systems and advanced technical expertise in data analytics, visualization, and programming. Key Responsibilities Primary Contact for QuEST Act as the main point of contact for all communications related to the QuEST platform. Global Project Support Collaborate with site teams to implement global quality initiatives via QuEST (including Document Management System, KPI tracking, internal audits, and Vendor Quality Management). Provide hands-on support, training, and coaching to ensure successful adoption. Data Management & Analysis Ensure timely data submission from all sites. Review and validate data for accuracy, and conduct in-depth analysis to identify trends, generate alerts, and provide actionable insights to leadership. Audit Coordination Lead coordination efforts for internal, supplier, and vendor audits in collaboration with cross-functional teams. Reporting & Dashboard Development Drive the creation and optimization of dashboards and reports to support quality and food safety monitoring. Documentation & Training Support the standardization of system documents and develop training materials for deployment on the Learning & Development platform. Experience, Qualifications and Skills Bachelor s degree in food science, Chemistry, Microbiology, or Data Analytics; a Master s degree is an advantage. Minimum 7 years of experience in quality systems within the food industry. Advanced proficiency in data analytics and visualization tools (e.g., PowerBI, Tableau). Strong working knowledge of databases (e.g., MySQL, Power Query). Experience with programming languages (e.g., Python). Proven ability to lead data science projects, including data aggregation, modeling, and analysis of structured and unstructured data. Excellent project management and organizational skills. Strong analytical thinking and problem-solving capabilities. Effective communication and interpersonal skills. Ability to manage multiple priorities in a dynamic, cross-functional environment. High attention to detail and ability to work independently. ofi is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, nationality, disability, protected veteran status, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law. Applicants are requested to complete all required steps in the application process including providing a resume/CV in order to be considered for open roles.

The work involves development of technical documentation of various medical devices, and invitro diagnostics. Necessary training will be imparted from the company. Prefer post graduates in chemistry/microbiology/ biotechnology/biochemistry/pharmacy Skills expected: 1.Work/training experience in IVD manufacturing facilty (clinical chemistry reagents, rapid kits, molecular reagents etc) 2.Proficiency in MS word and Excel 3.Good English Language skills with grammatical accuracy 4. General understanding about basic concepts of biochemistry/ microbiology/biotechnology. Additional skills preferred: 1. Speaking knowledge in Hindi 2. Willingness to travel to client sites across India Job Type: Full-time Pay: ₹12,000.00 - ₹15,000.00 per month Schedule: Day shift Education: Master's (Required) Location: SEAPORT AIRPORT ROAD, THRIKKAKARA, Kochi - 682021, Kerala (Preferred)

Dear Sir/Madam, We are urgently looking for Doctors for various Medical Colleges and Hospitals across India. For Medical Colleges, we require the following in all Clinical & Non-Clinical Departments: * Senior Residents * Assistant professors * Associate Professors * Professors * Medical Superintendents * Dean/Principals For Hospitals: Consultants & Surgeons in All Clinical Departments *** Please reply at the earliest to avail the most suitable position *** WEPS is the Topmost Healthcare Recruitment Firm in India. We recruit healthcare professionals for a variety of the Medical Colleges & Hospitals in the country. For further information and to upload your resume, please visit Regards, Tanu Goyal WEPS SCO 12, LGF, Hollywood Plaza, VIP Road, Zirakpur, SAS Nagar, Punjab 140 603 Email: weps.careers@gmail.com Mob: 7015609544 whatsapp@87015609544

INSIDE SALES EXECUTIVE (Fresher - Biotech) | On-site at Cloudnine Hospital, Nallagandla Location : Cloudnine Hospital, Nallagandla, Hyderabad 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!) 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. Job Types: Full-time, Permanent, Fresher Pay: ₹23,000.00 - ₹26,000.00 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Schedule: Day shift Fixed shift Morning shift Application Question(s): When are you available to start working with us? Work Location: In person

About Vibcare Healthcare Vibcare Healthcare is a WHO-GMP certified contract manufacturer that supplies high-quality allopathic medicines across India and to export markets. Our modern plant makes tablets, capsules, liquids and topical products under strict quality standards. Role Overview The QC Manager will lead our Quality Control laboratory and ensure every raw material, in-process sample and finished product meets the required specifications and regulatory guidelines. You will manage a team of analysts, uphold cGMP practices and support regulatory audits. Key Responsibilities Lab Management : Plan and supervise daily testing of raw materials, bulk and finished goods (HPLC, GC, UV, wet chemistry, microbiology). Documentation : Review and approve analytical reports, COAs, SOPs and calibration logs. GMP Compliance : Maintain data integrity, good documentation practices and readiness for WHO, FDA and customer audits. Equipment & Calibration : Ensure timely qualification, calibration and preventive maintenance of all QC instruments. Stability & Validation : Oversee stability studies and analytical method validation/verification. Team Development : Train, guide and appraise QC chemists and technicians; promote a culture of continuous improvement. Change Control & CAPA : Investigate OOS/OOT results, implement corrective actions and monitor effectiveness. Cross-Functional Support : Coordinate with Production, QA and Regulatory Affairs for timely product release and dossier requirements. Requirements Experience : Minimum 5 years in pharmaceutical QC, with 2 years in a supervisory / manager role. Education : B.Pharm / M.Pharm / M.Sc (Chemistry, Pharmaceutical Sciences or equivalent). Technical Skills : Strong hands-on knowledge of HPLC, GC, dissolution, microbiology, cGMP, GLP, ICH guidelines and data-integrity principles. Soft Skills : Good leadership, problem-solving and communication abilities; proficiency in MS Office / LIMS / ERP. Personal Traits : Detail-oriented, disciplined, able to meet deadlines and comfortable facing audits. Benefits Competitive salary + performance bonus Medical & accidental insurance for self and dependants Professional training and skill-upgradation support Subsidised meals and company transport Friendly, growth-oriented work culture

Job Title: Senior Executive – Quality Assurance / Quality Control (QA/QC) Location: Vikasnagar, Uttarakhand Job Type: Full-Time, On-site About KIWI Kisan Window KIWI Kisan Window is an innovative and rapidly growing food brand committed to bringingHealthy Unique Flavours of India to every household. We connect farmers and consumersthrough sustainable sourcing, premium quality, and a mission to take handmade and authenticIndian produce to the world. Role Summary: We are looking for a detail-oriented and experienced Sr. Executive – QA/QC to ensure the highest quality standards across our fresh produce, grocery SKUs, packaging processes, and warehouse operations. The candidate will be responsible for monitoring, improving, and enforcing quality across raw materials, production, labeling, packaging, and dispatch processes, ensuring compliance with FSSAI, SOPs, and company protocols. Key Responsibilities:Quality Assurance Define and implement QA protocols for fresh, processed, and packaged food items. Ensure product quality meets internal standards and FSSAI regulations. Approve incoming raw materials by confirming specifications and conducting visual/physical checks. Conduct regular audits at vendors and internal processing units. Quality Control Perform and supervise quality checks across stages: receiving, processing, packaging, and dispatch. Monitor parameters like moisture content, microbial load (where relevant), packaging integrity, and label accuracy. Implement batch-wise QC reporting and traceability. Packaging &Label Control Check labeling compliance: MRP, date of packaging, batch no., expiry, nutritional info. Ensure correct packaging material usage as per SKU standards. Documentation & Compliance Maintain QA/QC documentation: checklists, batch records, test reports, and deviation logs. Support FSSAI, HACCP, and other regulatory audits. Drive adherence to SOPs and hygiene protocols (5S, GMP). Training & Team Coordination Train warehouse, processing, and packing staff on quality and hygiene standards. Work closely with procurement, production, and dispatch teams to resolve quality issues. Key Requirements: B.Sc./M.Sc. in Food Technology, Microbiology, or a related field. Minimum 3–5 years of hands-on experience in QA/QC in food processing, FMCG, agritech, or grocery brands. Strong knowledge of FSSAI regulations, shelf-life standards, food safety practices, and packaging QC. Experience with quality tools: checklists, RCA (Root Cause Analysis), 5 Why, and CAPA. Proficiency in MS Excel, Google Sheets, and basic data reporting. Good communication and team coordination skills. Ability to work in fast-paced, multi-SKU environments. What We Offer: Career Growth & Impact: Be part of a fast-growing brand making a mark in the food industry. Innovative Work Culture: Join a team that values creativity, collaboration, and customer-centric solutions. Performance-Based Incentives: Enjoy competitive bonuses and rewards for outstanding sales performance. Continuous Learning & Development: Gain access to mentorship, tools, and resources for career advancement. Who We Are: KIWI Kisan Window is a pioneering and innovative food brand committed to delivering the Healthy Unique Flavours of India to every household. As a bridge between farmers and consumers, we focus on sustainable practices, farmer empowerment, and offering premium, farm-fresh products that celebrate India’s diverse culinary heritage. Our journey has been fueled by a passion for redefining how people experience food—bringing fresh, authentic, and health-focused products to the forefront. Featured in Shark Tank India Season 4 , we take pride in our entrepreneurial spirit, commitment to excellence, and mission to take handmade to the world. How to Apply: Send your resume and cover letter to career@kisanwindow.com with the subject line “Application for Quality Assurance / Quality Control - KIWI Kisan Window.” We look forward to hearing from you! Job Types: Full-time, Permanent Pay: ₹14,000.00 - ₹25,000.00 per month Schedule: Day shift Morning shift Work Location: In person

🌿 We’re Hiring! Join Our Team at Eco Paryavaran Laboratories, Mohali 📌 Position: QA Executive | 🏢 Department: Quality Assurance 📍 Location: Mohali, Punjab Qualifications: Master’s degree in a scientific or technical field (e.g., Chemistry, Environmental Science, Microbiology, etc.). Minimum 2–3 years of experience in a NABL-accredited laboratory environment. Proven knowledge and hands-on experience with ISO/IEC 17025:2027 standards. Key Responsibilities: 1. Management System Implementation & Maintenance Establish, implement, and maintain the laboratory’s management system in compliance with ISO/IEC 17025:2027 . Ensure accurate documentation, version control, and accessibility of all quality-related policies, procedures, and records. 2. Quality Assurance & Compliance Monitor day-to-day laboratory operations to ensure compliance with ISO/IEC 17025 and requirements of accreditation/regulatory bodies. Plan, conduct, and report internal audits and management reviews. Track and manage nonconformities, corrective actions, and opportunities for continual improvement. Plan and execute Proficiency Testing (PT) , Inter-Laboratory Comparisons (ILC) , and Internal Quality Controls (IQC) ; maintain relevant documentation. 3. Document & Record Control Implement and manage document control systems ensuring up-to-date and accessible controlled documents. Ensure proper retention, security, and traceability of all quality assurance records. 4. Training & Competence Coordinate and monitor training programs related to quality systems and ISO 17025 compliance. Maintain up-to-date competence records for all staff involved in testing, calibration, and QA-related activities. Skills & Attributes: Strong attention to detail and excellent organizational skills. Effective communication and coordination skills across departments. Proficient in documentation and quality management systems. Analytical mindset and ability to troubleshoot and resolve quality issues.

Regulator Chemist Location: Chennai, India Required Language: English Employment Type: Full-Time Seniority Level : Associate Travel Mode: Moderate About Us : Buckman is a privately held, global specialty chemical company with headquarters in Memphis, TN, USA, committed to safeguarding the environment, maintaining safety in the workplace, and promoting sustainable development. Buckman works proactively and collaboratively with its worldwide customers in pulp, paper, leather, and water treatment to deliver exceptional service and innovative specialty chemical solutions to help boost productivity, reduce risk, improve product quality, and provide a measurable return on investment. Buckman is in the middle of a digital transformation of its businesses and is focused on building the capabilities and tools in support this. Purpose: The mission of the Regulatory Chemist Specialist (RAS) is to prepare and file demands for regulatory approval of the products of the company by preparing, coordinating, and supervising regulatory submissions and reviewing product conformance and assure compliance, Implementing different strategies in order to meet evolving regulatory initiatives, register products according to provincial guidelines and regulations of third party suppliers Keep current with regulations Participate in conferences and interdepartmental meetings. Qualifications & E xperience:  Degree in Chemistry / Microbiology or analytical chemistry discipline or relevant discipline.  Regulatory experience in Chemical industry  Understand Halal, Kosher requirement and application process  Familiar with REACH, FDA, GHS guidelines  Good document management skill and willing to spend more time on paper work  Experience with Asia Pacific regulatory processes and bodies  Detail-oriented and intrinsically motivated  Skilled user of Microsoft Office 365. knowledge on Intelligent Authoring will be a plus. Accountabilities :  Issue regulation compliance letter to the customer promptly and accurately when required.  Providing product-related regulatory information and knowledge to the stakeholder to make sure 100% compliance.  Obtain regulation information from the supplier  Maintain and update the regulation database  Assess regulatory requirements and develop regulatory strategies for the qualifications of new products in ASEAN, Australia, and New Zealand.  Compile technical files, test reports and documentations necessary for regulatory submissions.  Maintain up to date documentation and archival regulatory submissions and related documents according to the company’s documentation policies and procedures.  Work with the global regulatory affairs group and manage areas of regulatory risk to core business activities in Asia.  Maintain up-to-date knowledge and information related to product regulation.  Understand the product registration requirement in Asia countries and manage the product registration when required.  Stay updated on industry regulations, policies, trends, and opportunities by participating in industry associations and conferences.  Generate product SDS and make sure the SDS is up to date to the regulation requirement. #LI-SS1

Department MORAIYA QC Job posted on Jul 03, 2025 Employment type P-P7-Probationer-HO Staff Role name: QC - QMS - GLP Division - Moraiya Department - Quality Control Category - Staff Qualification - M.Sc./B.Pharma/M.Pharma Experience - 4 - 5 Years Zydus Experience - Must have completed at least two PMS cycle. Job Responsibilities: Main activities- related to Trackwise - Change control/ CAPA /NQ incident trend / Risk assessment (rarely) / IRA documents submission like, raw data/chromatogram etc. , Effective ness check of CAPA in track wise / SOP revision and Training) 1. To ensure day-to-day monitoring and compliance of the laboratory activities. 2. To ensure data integrity and good laboratory practices in the department. 3. To ensure global CAPA implementation within timeframe. / To comply the statutory compliance aspect. 4. To follow the Good Laboratory Practices. 5. To maintain interpersonal relationship and provide support to other functional group in the department. 6. To maintain data integrity and follow cGMP and GDP. 7. To ensure that training is acquired for each activity/instrument prior to its execution/operation and that it is as per respective TNI. 8. To maintain and ensure controlled laboratory practice in the quality control department. 9. To ensure laboratory inventory management. 10. To follow the SOPs of Quality control department and related area. 11. To prepare / revise the SOP's, related to QC in software except microbiology lab. 12. To impart the training after revision of SOPs as per the requirement. 13. To perform related documentation/transaction in the software (e.g. LIMS, Zytims/Trackwise/SAP) based on assigned user privileges. 14. To assist in the Qualification / Installation of instrument equipment with suitable documentation. 15. To perform the qualification of instruments as per the requirements 16.To co-ordinate with in-house service engineers and / or external service engineers as and when required. 17. To participate and provide appropriate feedback during failure investigation (if any). 18. To review the raw data of Raw material / Finish product /stability sample/ Validation sample / Exhibit sample analysis with respect to SOP and GDP. 19.To ensure the destruction of remainant samples after analysis as per applicable procedure. 20. To ensure the usage of required PPE’s during respective activities in the laboratory. 21.To ensure up-keeping of the instrument/equipment. 22.To inform section head about any OOS/ OOC/Incident on its immediate occurrence and for day to day activities. 23.To investigate OOS/OOC/Incident (if any) under consultation with the department head/section head. 24.To keep the things and work area clean and tidy and get involved for the routine trouble shooting (if any). 25. To execute the activities with maximum output with complete documentation. 26. To provide documentation of commercial batches to IRA. 27. Responsible for implementing company quality ethics policy for data integrity and inform management and responsible data integrity compliance head on any data integrity issues as per corporate data governance policy. 28. To prepare the audit response of internal/external customer/SME observation to QC. 29. To perform related documentation/transaction in the software (e.g. LIMS, SAP, Trackwise, DMS, Minitab, Zytims, Legatrix) based on assigned user privilege. 30. To initiate, track and closure of QMS event (CAPA, change control, incident, deviation, event, extensions etc, through Trackwise and in format-based system) and escalate it for completion. 31. Handling of laboratory information Management System (LIMS) system under the guidance of LIMS administrator, which includes preparation/modification/review and approval of specifications, worksheets, tests plans, stability protocols, Masters etc. as per requirement. 32. To assist Validation/Re-validation of LIMS modules as and when required. 33. To prepare validation protocol and report and co-ordinate for the validation of spread sheets as and when required. 34. Completion of Any other specific work or assignment as given by the section head/department head. 35. To report abnormalities (if any) to section head or designee. 33. To prepare Quality metrics and QI sheet, department level QRM data and to record action plan 34. To prepare trend data of QMS events. 35. To prepare analytical method verification/validation protocol/report. 36. To initiate the activity regarding New / revision of technical agreement / Quality agreement. 37. To initiate the Risk assessment / Gap assessment involving in the respective activity 38. To Make entry and verify the details in Zytimes. 39. To perform the required activities related to QUEST / SLIM programme. 40. To perform the required activities related to statutory requirements in Legatrix. 41. Management of column and other resources used in analytical activities. 42. To escalate the Issues related to the Process, Product, Quality, Cleaning process or documentation related activities to his/her immediate supervisor and take the appropriate action related to it. 43. To escalate any failures and overdue activity that can have a potential impact on product quality to his/her immediate reporting authority.

To perform and be responsible for all the activities and documentation of formulation and filling process development and should have strong knowledge of optimization of different vaccine formulations, stabilizer selection, excipient selection, selection and preparation of adjuvants such as aluminium salts, Oil-In-Water emulsions, Liposome-based adjuvants with TLR agonists and saponin, LNP formulation and preparation, aseptic filling and Lyophilization cycle designing for new vaccine products and troubleshooting for existing vaccines. To perform all the activities and documentation of the formulation and filling process, development and execution of clinical drug product manufacturing for the clinical batches, planning and execution of media fill activities Prepare and Maintain R/D lab documents, equipment and area qualifications as per GMP requirements and Responsible for preparation of process validation and technology transfer protocols as per GMP requirements and co-ordinates with QA, QC, Engineering department for viral vaccine development activities. Responsible to ensuring proper hygiene and entry exit procedures in the respective formulation and filling section and preparation of adjuvant, buffer solutions and other materials & ensuring proper arrangements for their preparation and supply. To coordinate with the central warehouse department for receipt and entry of RM and PM materials. Preparation / supervision of disinfectant solution, cleaning solution, integrity testing of hydrophobic and hydrophilic filters, sanitization and disinfection activities of R/D formulation department. Responsible for QMS such as deviations, MDD, investigation, observation and ensuring its timely closure. Preparation of standard operating procedure and Batch manufacturing records, QRM and protocol related to R/D formulation and filling section. To supervise washing, drying, packing and sterilizations 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), Masters Degree in Pharmacy or Engineering with biotechnology. Candidate should have experience in vaccine industry Candidate should be able to work on bench and this position has one reporting.

• Perform Manual Microbiological Testing including Streaking, Staining, Biochemical Tests, &Antibiotic Susceptibility Testing. • Microbial Identification, Colony Counting& Microscopy. • Serology, Haematology & Biochemistry. Required Candidate profile B.Sc. or M.Sc (Microbiology) with 3-5yrs of exp Manual Laboratory Work. Notice Period:Immediate Location: Thane(Mumbai)& Madanapalle (AP) Suitable candidates share CV to careers@lordsmicrobiotech.com

Company Description Perfect Poultry Products is a leading provider of comprehensive poultry solutions encompassing hatcheries, poultry farms, feed and nutrition, chicken processing plants, and frozen foods. With a wide array of brands such as Gruubb, WA-HA, Real Fresh, neatmeats.com, FnM Fish and Meat Market, and Sanctuary Equipment & Tools, we offer quality products for retail and e-commerce markets. Our commitment to excellence ensures we meet the highest industry standards. Job Summary: The Sr. Manager Quality will be responsible for ensuring that all raw chicken processing operations comply with internal quality standards, food safety regulations (FSSAI, HACCP, ISO), and customer specifications. This role involves managing the QA/QC team, driving continuous improvement, overseeing audits, and maintaining product safety and consistency. Key Responsibilities: Lead and manage the QA/QC function at the plant level. Ensure compliance with FSSAI, HACCP, ISO 22000, and other relevant food safety and quality standards. Monitor and control quality parameters across all processing stages: live bird receiving, slaughter, evisceration, chilling, packing, and dispatch. Implement and maintain plant-level SOPs, SSOPs, GMP, and hygiene practices. Coordinate internal and external audits (customer, regulatory, and third-party). Investigate quality deviations, customer complaints, and non-conformities; drive corrective and preventive actions (CAPA). Lead microbiological and residue monitoring programs in coordination with lab teams. Train staff and workers on food safety, hygiene, and quality protocols. Monitor performance metrics (KPIs) such as yield, rejection, rework, and customer complaints. Collaborate with Production, Maintenance, and Supply Chain teams for integrated quality improvements. Ensure traceability and documentation for all quality records. Desired Candidate Profile: Bachelor’s/Master’s degree in Food Technology / Microbiology / Veterinary Science / Poultry Science or related fields. 7–12 years of experience in quality assurance/food safety, preferably in raw chicken/meat/seafood processing plants. Strong understanding of Indian food safety laws (FSSAI), HACCP, ISO 22000, GMP, and other regulatory frameworks. Experience in managing audits, documentation, and plant hygiene programs. Leadership and team management skills. Strong communication, analytical, and problem-solving abilities.

About The Company Orange Health Labs is building India’s more futuristic diagnostic company that enables Indian consumers to get their diagnostic tests with ultimate convenience, reliability & speed. Launched in 2020, Orange Health Labs is now a top-10 diagnostic brand across India's 4 largest metro cities: Bangalore, Delhi, Mumbai, and Hyderabad. Founded by healthcare leaders, Dhruv Gupta & Tarun Bhambra, the Orange Health Labs team now consists of over 900 O-Rangers across our locations. Having served over 1 million customers, we are now also India’s highest-rated diagnostic lab, and we take extreme pride in the customer love that we get! We are backed by high-quality investors like Accel, Bertelsmann India, General Catalyst, Y Combinator, along with other marquee healthcare and global investors. Diagnostics is the starting point of most healthcare journeys, so it's a need for every family, and we want to be the brand of choice. Join us to make diagnostics 10x more convenient, 10x more accurate - 10x better! How will you make an impact? We are seeking an experienced MD Microbiologist to lead and enhance the microbiology function at Orange Health. The ideal candidate will bring deep domain expertise, ensure the accuracy and integrity of diagnostic results, and drive excellence in lab quality standards and clinical reporting. Why You Might Be Excited About Us We are on a mission to build the fastest diagnostic lab in India. We have a bunch of Talented folks who relentlessly work towards bringing a WOW customer experience. Rated currently at 4.9/5 Our team has a wide range of experience .Folks at OH have worked earlier with companies like Phonepe, Flipkart, Practo, Unacademy, Swiggy, Metropolis, Licious, cure.fit etc. and we are excited to learn from you too. We care for your career & growth and hence we will help you to shape a career you are excited about. We work hard and we party harder. Our People NPS is >90% and Glassdoor rating is also in the top 90% of companies. Competitive Pay + ESOPs What will you get to do? Conduct and supervise microbiological analysis and testing of clinical samples. Review and validate test results for accuracy and completeness. Implement and monitor compliance with standard operating procedures (SOPs) and quality assurance protocols. Work closely with cross-functional teams to streamline workflows and ensure rapid turnaround time (TAT). Supervise and train lab technicians and support staff in microbiological techniques. Assist in the evaluation and validation of new tests and technologies. Contribute to equipment maintenance, calibration, and troubleshooting. Ensure compliance with NABL, CAP, and other regulatory standards. Stay updated on advancements in microbiology, molecular techniques, and diagnostics best practices. Metrics for the role TAT (Turnaround Time) Result Accuracy Internal QC and External QA Compliance Audit Readiness and Error Rates Skills We Are Looking For MD in Microbiology from a recognized institution. Minimum 3 years of experience in a diagnostic or hospital laboratory. Strong knowledge of clinical microbiology, molecular diagnostics, and infection control protocols. Hands-on experience with both manual and automated microbiology instruments. Familiarity with quality standards (NABL/CAP/ISO) and lab information systems (LIS). Excellent documentation, reporting, and analytical skills. Strong interpersonal skills with the ability to lead and collaborate across teams. Flexibility to work rotational shifts, including weekends and holidays. Join our dynamic and dedicated team of professionals at Orange Health, where you can contribute to improving healthcare outcomes through accurate and reliable diagnostic testing. Get to know us even more :) Know more: Web | iOS | Android | Linkedin | Instagram | Twitter | Glassdoor So if you think you have that extra"orange"nary quality in you, we can't wait to welcome you. Skills: leadership,clinical microbiology,analytical reporting,md microbiology,reporting,md,infection control protocols,collaboration,interpersonal skills,md in microbiology,manual and automated microbiology instruments,analytical skills,documentation,team leadership,lab information systems (lis),molecular diagnostics,quality standards (nabl/cap/iso),nabl/cap compliance

Approved analytical chemist instrument and microbiology chemist

The Opportunity Avantor is looking for a Sales Application Support Specialist. The associate will be responsible for providing both pre- and post-sales technical support to customers and sales associates via telephone, email, and live chat. Our team comprises experts from various scientific fields within Life Sciences. What We’re Looking For Education: Graduate/Postgraduate Degree in Chemistry, Biology, Microbiology, Biotechnology, or an equivalent life science discipline. Experience 0-2 years of experience working in Life science-related industry (ex: molecular/ microbiology labs). Preferred Qualification Communication Skills: Excellent communication skills with telephone etiquette. Team Player: Strong team player with a drive for results. Customer-Centric Approach: Ability to provide accurate information in a user-friendly manner to both technical and non-technical purchasers. Sales Awareness: Understanding of the sales process and commercial aspects of the service, with attention to detail and accuracy. Analytical Skills: Ability to comprehend technical enquiries, analyze customer requirements, and ensure complete information before formulating responses. Competencies Analytical and Critical Thinking Collaboration & Teamwork Continual Improvement and Innovation Customer Focus Developing People Driving Results Adherence to Avantor’s policies, procedures, rules, and guidelines Upholding Avantor Culture and Values How You Will Thrive And Create An Impact Technical Support: Offer first-line technical information about our product range to customers via hotline or email. Enquiries are allocated among team members to leverage their technical expertise, with an emphasis on expanding knowledge and addressing diverse queries. Sales Enhancement: Maximize sales opportunities through technical assistance by: Providing product specifications and application support Checking product compatibility Identifying products based on end-user applications Suggesting alternatives for unavailable products Upselling products and services where feasible Database Maintenance: Maintain a comprehensive database of supplier product information, specifications, and certificates. Relationship Building: Foster strong relationships with Avantor sales staff and customer service associates to ensure seamless service delivery. Perform Under Pressure: Deliver results under pressure, adhering to agreed service levels and following through on all commitments. 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

I’m a dedicated and detail-oriented Medical Laboratory Technician with hands-on experience in clinical diagnostics, including blood analysis, microbiology, biochemistry, and pathology. I play a vital role behind the scenes, ensuring that every test is performed with precision and every result contributes to accurate diagnosis and effective treatment.

Dear Candidate , we are hiring for Fresher for the position Microbiologist . Job Description: Department:- Microbiology Exp: Fresher Des:- Jr Executive-Executive Qua:-MSc Microbiology Only Male Candidates Preferable Bio burden testing of in process samples as per the specification. BET testing of water samples, in-process samples, semi-finished and finished samples as per the specification. Sterility testing of finished product. Responsible to perform the MLT testing for raw materials and water samples. Maintenance and handling of Endotoxin indicators and biological indicators. Experience on culture maintenance and VITEK2 compact system To perform the method validations for MLT, BET, Bio burden and Sterility. Injectables or biologics experience is mandatory. Male candidates are preferable. Regulatory audits exposure is mandatory. IMMEDIATE JOINERS ARE PREFERABLE" Interested candidates please attach your CV here.

Assistant Manager - Quality Job Details | Tata Consumer Products Limited Search by Keyword Search by Location Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Assistant Manager - Quality Tata Consumer Products Limited Assistant Manager - Quality Assurance What are the Key Deliverables in this role? Financial Outcomes Proactively work with Tech-Ops & Planning team to ensure minimization of Material expiry at Plant level. Lunch of the NPD/EPD in their respective cluster with RFT, enabling the zero loss to Business Growth. Effectively Manage the QA budget approved for the Cluster. Customer Service Regular visit of Market and ensure Product Integrity (Product Quality Index & Packaging Quality index) at Consumer Level as per Design Quality. Collaborate with Supply-chain team in addressing the Internal Complaints with high sense of urgency. Collaborate with Procurement/Planning team in resolving the Incoming Materials Challenges with stipulated timeline. Collaborate with TechOps in reviewing the root cause analysis of consumer complaints and Prepare mitigation plan to ensure this does not repeat. Internal Processes Responsible for Implementation of the Corporate SOPs, Process and Practices across the cluster Co-Pack Units Responsible for periodic assessment and Improvement plan of the Co-Pack Operation quality (GMP, RFT, FSSAI/BIS, GLP, Drive the Food Safety Certification for the Co-Packs units Responsible for Managing the Daily Incidents and Deviations in the cluster across Supply-Chain Responsible for Training Program for the respective Cluster team Members (Co-Pack, Tech Ops, Supply-Chai & Sales) Innovation and Learning Responsible to drive the Statistical Process Control (SPC) Program for Continuous Improvements and Risk Assessment of the New Facility in the respective Cluster. Responsible for building the Process Engineering, Automation and digitalization in the respective Clusters. Responsible for New Plant/Line Qualification, Validation and Verification of Existing Product extension. What are the Critical success factors for the Role? B.Tech/M.Sc./M.Tech in Chemical Science/Chemical Engg/Food Process Engg/ Food Tech from a reputed Institute 7+ years of relevant work experience in Liquid Beverage/Food Processing/Flavour/Alcoholic Beverage Industry Technically sound in Water Treatment, Sanitation Program, Homogenization, Heat & Mass Transfer Technology etc Familiar with various Filling Technology (Cold Fill, Hot Fill, Aseptic, Carbonated etc) and Engineering aspects. Well versed with various packaging formats like PET, Cup, Tetra Pack, Glass, Pouch etc and Packing machinery. Rich understating of Calibration, Analytical Chemistry, Microbiology and Packaging Analysis. Good Knowledge in BIS/FSSAI regulations/FSSC/HACCP, ISO22000 and ISO 17025 in document/work Instruction preparation & Implementation. What are the Desirable success factors for the Role? Shall be Sig Sigma Certified, well acquainted with quality improvement tools and Digital Savvy. Knowledge of ISO certification related activities; GLP and GMP guidelines Good verbal and written communications with ability to manage multiple stakeholders (Co-Pack, Tech Ops, Innovation, Sales)