2539 Microbiology Jobs - Page 11

This position requires a sound knowledge of medical coding and the denial management process for multiple specialties. Applicants must be proficient in ICD-10 and CPT medical coding and have obtained a Certified Professional Coder (CPC) credential Required Candidate profile Should have strong knowledge In Medical Coding Anatomy Physiology and Medical Terminology Should have Good Communication Skills

Position: Quality Assurance Manager Organization: Bankai Agrifood Pvt Ltd. Function: QA/AC Website: www.bankaiagrifood.com Primary Purpose: We are seeking a highly skilled and experienced Quality Assurance Manager to join our Bankai Agrifood Team. As the Quality Assurance Manager, you will be responsible for ensuring the overall quality control and assurance activities in the production of dairy products. Your primary objective will be to establish and maintain quality standards. Key Accountabilities/Activities: Overall Planning and Execution of Quality Control and Assurance Activities: · Develop and implement strategies for maintaining and improving product quality and safety. · Establish quality control procedures, guidelines, and standards. · Ensure adherence to quality control processes throughout the organization. · Oversee the activities of the chemical and microbiological laboratories within the plant. · Ensure proper organization, calibration, and maintenance of laboratory equipment. · Coordinate testing procedures and quality control checks. · Develop and implement a calibration schedule for measuring instruments. · Coordinate the calibration process and ensure instruments are calibrated at regular intervals. · Plan and execute quality inspections of milk collection centers. · Ensure adherence to quality standards and guidelines. · Collaborate with milk producers and agents to address quality-related concerns. · Ensure the dispatch of milk and milk products according to standard operating procedures (SOPs). · Verify product quality and compliance before dispatch. · Verify the quality and adherence to specifications of incoming packaging material. · Conduct inspections and assessments as required. · Identify and implement statistical techniques in the quality control process. · Analyze data and trends to drive process improvements. · Coordinate pest control activities to ensure a pest-free environment within the facility. · Monitor and implement preventive measures against pests. · Oversee and ensure the overall housekeeping and hygiene of the factory. · Implement and maintain cleanliness standards and protocols. Liaison with Statutory Authorities: · Interact and maintain effective relationships with statutory authorities such as FSSAI, AGMARK, ISO, HACCP, EIA accreditation bodies, and consultants. · Stay informed about relevant regulations and standards and ensure compliance. · Coordinate inspections, audits, and certifications. Organization of RMRD Activities: · Organize and oversee the activities of the Research, Monitoring, and Development (RMRD) department. · Ensure research projects and development activities align with quality goals. Liaison with Milk Producers and Agents: · Maintain effective communication and collaboration with milk producers and agents. · Address quality-related issues and provide guidance on quality requirements. Preparation of Quality Control and Assurance MIS Reports: · Generate and analyze quality control and assurance management information system (MIS) reports. · Present reports to management, highlighting key findings and recommendations · Maintain all relevant records and documentation as per ISO and HACCP standards. · Ensure records are accurate, up-to-date, and easily accessible. · Identify and implement corrective and preventive actions based on quality issues and non-conformances. · Drive root cause analysis and implement effective solutions. · Facilitate and monitor the implementation of TQM principles and systems. · Drive continuous improvement initiatives based on TQM principles. · Implement processes to ensure proper quality of milk received from various sources. · Monitor and maintain quality standards throughout the milk supply chain. · Ensure strict adherence to approved test methods and procedures. · Verify that test reports are accurately prepared and forwarded to the designated authority. · Ensure that all required inspections and tests are carried out in accordance with established procedures and techniques. · Monitor and verify that quality assurance personnel perform necessary sampling using correct procedures. Compliance with Statutory Obligations: · Act as the nominated person under relevant regulations, such as PAF, 1954. · Ensure compliance with all statutory obligations related to the quality of the product. · Verify and monitor critical process parameters to ensure compliance with quality standards. · Implement corrective actions when deviations occur. Work Relations: Internal: · Reporting to COO for all Functional as well as administrative purposes. · Second level reporting to CEO · Interface with Production, Quality Control Team, Maintenance, Procurement teams · Interface with HR Teams- Global Head HR, Plant HRBP, AVP-Group HRBP for manpower planning, and all other employee life cycle issues · Interface with Accounts, Finance, and Facility management teams. External: · Interface with various suppliers, regulatory agencies, Service Providers, Customers · Interface with various industry associations - Participate in industry events, seminars, or forums to stay updated on the latest trends, technologies, and best practices in dairy production. Build professional networks and exchange knowledge with industry peers. Qualification Essential: M. Tech. / B. Tech (Dairy Technology) or B.Sc / M.Sc can be considered. Experience Essential: 10 to 15 Years in QA Department, Well versed with HACCP / FSMS / ISO / FSSAI etc · Proven experience in quality assurance management within the dairy industry. · Strong knowledge of regulatory standards and requirements, such as FSSAI, AGMARK, ISO, and HACCP. · Familiarity with quality management systems, such as ISO 9001 and ISO 22000. · Experience in organizing laboratory activities and coordinating testing procedures. · Knowledge of Good Manufacturing Practices (GMP) and quality control techniques. · Strong analytical and problem-solving skills. · Excellent communication and interpersonal abilities. · Leadership skills and the ability to effectively manage a team. · Attention to detail and a commitment to ensuring product quality and safety. · Ability to work in a fast-paced environment and manage multiple priorities. · Proficient with Microsoft Office (Word, Excel, PowerPoint) Work Environment: 24 X 6 (6 days a week) Shift Details: General Shift. (09:00 AM – 5:30 PM), Shift might rotate Job Type: Full-time Pay: ₹400,000.00 - ₹900,000.00 per year Benefits: Health insurance Life insurance Paid sick time Provident Fund Application Question(s): Do you have a Graduate or Postgraduate degree in Dairy Technology, Food Science, Microbiology, or a related field? Yes/No Are you experienced in both chemical and microbiological testing of dairy products? Yes/No Are you familiar with ISO, HACCP, FSSAI, and AGMARK compliance processes? Yes/No Are you experienced in preparing and presenting MIS reports for QC/QA? Yes/No Do you have experience liaising with milk producers and collection agents on quality issues? Yes/No Work Location: In person Speak with the employer +91 9925039044

Walk-In Interview for BDS/BHMS/BAMS/ BPT/ BSC/MSC( Nursing) Fresh Graduates For Medical Coding Non Certified Freshers Only Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology and CPT Exposure to CPT-4, ICD-9, ICD-10, and HCPCS coding

Reporting to: Coordinator, Biosciences Research Laboratory, School of Arts and Sciences Role Summary: Involved in conducting practicals of Integrated MS students About the School: The School of Arts and Sciences has five divisions: Humanities and Languages , Social Sciences , Mathematical and Physical Sciences , Biological and Life Sciences and Performing and Visual Arts . Biological and Life Sciences currently operates in the areas of nanotechnology, bioinformatics, cancer biology, ecology, microbiology, parasitology, plant biology, infectious disease and evolutionary biology. Responsibilities Assisting laboratory executive in the procurement of the laboratory supplies by contacting vendors, inventory maintenance, developing and improving laboratory protocols Conducting practical’s in various laboratories, assisting with experiments by logging details and setting up lab equipment for the students Recording and maintenance of students results and journal records Maintenance of laboratory equipment Perform regular lab disinfection and management of biohazard waste Any other laboratory task assigned by the Lab Coordinator/Lab Executive Key Skills Good knowledge of life science concentrated practicals Good and effective communication skills in English, Hindi and Gujarati Be able to conduct laboratory practicals independently Prior experience in teaching is desirable Qualification: MSc (any area of Biochemistry/Microbiology/Molecular biology/Biotechnology/Microbiology/Life Sciences/Plant Sciences) with minimum 55 per cent marks from a UGC recognised University. How to apply: The position is temporary and the appointment will be for one year only, extended based on performance. Shortlisted candidates will be informed through email. CV should include details of academic grades starting from 10th standard onwards with details of year of passing, university or college, etc and also work experience and nature of work if applicable. Incomplete applications will be rejected. Interested candidates can submit their application with their curriculum vitae to email info.artsandsciences@ahduni.edu.in with the following text in the subject of your email: Application for the position of Lab Associate by August 1, 2025. No TA/DA will be paid for attending the interview.

Should have knowledge in Clinical Data Management 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

Role & responsibilities Raw material sampling and testing Maintenance of Raw material testing records Preparation of RM Specifications ERP -sampling, testing and release of RM Third party testing of RM-records. Preparation of method validation Instrument qualification and calibration Skill Requirement Preferred candidate profile WHO-GMP, GLP knowledge Communication skills Basic computer knowledge Job Location : Kadi Gujarat (Bus facility are available)

Role & responsibilities Planning of day to day microbiological activities Drug substance and drug product related documentation Communication with Production & QA, Engineering for day to day update Stability study of drug substance & product BTR review Preferred candidate profile Knowledge of General Microbiological GMP/GLP awareness Current guidelines like D&C act or schedule M knowledge of FDCA requirements Job Location : Kadi Gujarat (Bus facility are available)

Role & responsibilities Preparation of SOP, STP and Protocols as per requirement. Perform the Instrument calibration/ verification as per SOP. Involving in analytical method validation /verification and technology transfer activity. Handling of equipment the UV Spectrophotometer, SDS PAGE, RT-PCR, ELISA. Implementing all documentation as per GMP, cGLP & WHO GMP guidelines. Follow the established procedures and policies of the company Pertaining to EHS management system. Preferred candidate profile Execution of biochemical analysis like total protein Content, mycoplasma testing and DNA content etc., Perform cell culture analysis and virus titration performing micro biological tests such as micro bio identification, micro biological testing of material/intermediate products, Sterility testing, BET, mycoplasma and mycobacterial testing Performing Environmental monitoring Perfuming water testing (bio Chemical & Microbiology) Job Location: Kadi, Gujarat ( Bus facilities are available)

Mega Walk in Drive at CorroHealth! Hello from CorroHealth! We are thrilled to announce a fantastic opportunity for 2024 Life Science graduates only to join us as Trainee Medical Coders at our Bangalore office. As a Medical Coder at CorroHealth, you will play a crucial role in accurately coding medical procedures and diagnoses to assist our healthcare clients. Here are the details: Eligibility Criteria: - Work Experience: Fresher - Designation: Trainee Medical Coder - Work Location: Bangalore - Graduation: Only those mentioned (Pharm D, M Pharm, B Pharm, Bsc/Msc-Microbiology/Biotechnology/Zoology) - Academic Requirement: Minimum 60% in all subjects - Medical Coding Certificate: Non Certified - Work Mode: On-Site Office Work Interested candidates can walk in directly on 26th July between 9 am to 11 am at: CorroHealth Bhartiya Centre of Information Technology (BCIT) block -1 7th Floor, Thanisandra Main Rd, Kannuru, Bengaluru, Karnataka 560064 Contact: - WhatsApp: 6363914170/9148894943 - Email: Soundarya.Nandakumar@corrohealth.com Join us at Corrohealth and contribute to the advancement of healthcare delivery through precise medical coding. We invite talented individuals to apply and become an integral part of our team!

Doctors Required in Varanasi, Uttar Pradesh A leading hospital in Varanasi is seeking dedicated and skilled doctors to join their team. Positions Available: Neurosurgeon MD General Medicine MD Pulmonary Medicine Required Candidate profile To apply or for more information, please contact: Mr. Mohit: 9216999555 Mr. Arnav: 7837780722 Doctors Placements

Job Summary: We are seeking a reliable and organized Store Supervisor to manage inventory and material handling for the Microbiology Division . The ideal candidate should be a graduate with at least 1 year of experience in store management or inventory control, preferably in a pharmaceutical, biotech, or chemical industry. Key Responsibilities: Manage inventory of microbiology raw materials, chemicals, consumables, and glassware. Ensure proper labeling, storage, and segregation of microbiology-specific materials as per SOPs. Monitor stock levels and initiate timely requisitions to avoid stockouts or overstocking. Receive, inspect, and document incoming materials and coordinate with quality control for clearance. Maintain daily stock records, GRNs (Goods Receipt Notes), and issue slips. Ensure compliance with safety, hygiene, and storage guidelines (e.g., temperature, humidity). Coordinate with procurement, microbiology, and QA/QC teams for smooth material flow. Perform periodic physical stock verification and audits. Requirements: Graduate (Science background preferred) Minimum 1 year of experience in stores/inventory management Basic knowledge of storekeeping procedures in a microbiology or laboratory setup Familiarity with ERP systems, MS Excel, and documentation Strong organizational skills and attention to detail Ability to follow SOPs and regulatory storage norms

Kenvue Is Currently Recruiting For A: Director, Analytical Chemistry and Microbiology R&D Operations What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role Reports To: Sr Director Mumbai R&D Center of Excellence Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Fully Onsite What You Will Do Kenvue is currently recruiting for: Director, Analytical Chemistry and Microbiology R&D Operations This position reports into Senior Director, R&D Center of Excellence and is based at Mumbai. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours. For more information, click here. What You Will Do The objective of this position is to deliver R&D Analytical and Microbiology services to Kenvue- Global R&D organization to enable targeted business growth through compliant laboratory operations and successful alliance with internal partners and external stakeholders. The scope of the role applies to multiple product categories under various segments such as Self Care (OTC drugs), Skin Health and Essential Health (Baby care, Oral Care, etc.) etc. Technical Deliverables: Lead overall Analytical, Stability and Microbiology operations for R&D/Innovation and lifecycle management projects executed from India R&D site for markets worldwide. This also includes oversight of facility, equipment, and Computerized system validation management program for GMP laboratories, shipment management program and implementation of Quality and Safety processes and systems Develop and implement long-term strategies that align with the organization’s vision and goals e.g. analyzing market trends, assessing risks, identifying opportunities and strategic outsourcing Drive informed decisions quickly, often with limited information. This includes weighing the pros and cons and considering the impact of decisions on organizational outcomes Responsible for overall financial activities/expense management related to scope of operations. Understanding of financial principles and metrics, enabling effective budgeting, resource allocation, and financial decision-making Responsible for resource management, lab efficiency and key performance and quality metrics for scope of work Stakeholder management: Partner with key stakeholders (R&D/Supply Chain/Quality) in support of project plans, technical discussions and or Regional/Global initiatives Partner with Quality team to drive laboratory compliance, implementation of standards and systems and developing site procedures Functional lead during internal inspections and external Health authority audits. Project Management: Facilitating group leads to manage projects inclusive of planning, execution, communication with regional/global teams and presentations to stakeholders Represent on cross functional project teams as technical expert to share technical requirements, timelines, risk assessments, decisions, compliance needs related to specific analytical deliverables Ownership of performance and Quality metrics Representation On Regional/Global Teams: Regional voice on Global teams for initiatives Representation on Leadership Teams to engage and drive assigned deliverables Develop new strategies, project charters or proposals and present to Senior leadership to drive innovative solutions, efficiencies, or related initiatives Leadership And Organizational Responsibilities: Encourage a culture of innovation, supporting new ideas, and being open to experimentation and learning from failures Commitment to developing talent within the organization, providing coaching and guidance to help team members grow in their roles Partner with Regional/Global teams to leverage best practices and behaviors to strengthen culture and collaboration Build and maintain relationships with key stakeholders, both inside and outside the organization, to facilitate collaboration and support Lead and manage change initiatives, helping the organization adapt to new challenges while minimizing resistance and maintaining morale What We Are Looking For Required Qualifications and Competencies Minimum Masters or Ph.D in Chemistry or equivalent stream with minimum 18-20 years of work experience and minimum 10 years of leading people Experience of working in a Global organization, preferred Experience of GMP operations, leading Health Authority audits, highly recommended Technical Competencies Deep technical expertise related to chemistry, analytical techniques, stability study assessment, microbiology operations and research technologies. Exceptional skills for proactive planning and prioritization Capable of applying diversified expertise in technical principles and practices in broad chemistry areas or technology. Excellent knowledge of current GMP, quality systems, SOPs, latest regulatory trends, and global regulations as appropriate Ability to learn and adapt to new and advanced technologies e.g. application of digital tools, problem solving abilities and data management. Ability to develop internal connects and external networks to drive new opportunities, improvements and scientific solutions Leadership Competencies Excellent oral and written communication and articulation skills Flexible mindset adaptable to changing needs of business and organizational ways of working Ability to leverage meaningful external relationships and partnerships outside of organization to solve problems to meet business needs Lead internal collaboration of teams and/or stakeholders across the enterprise, leveraging a broad range of cross-functional skills and perspectives to create innovative solutions Display inclusive mindset to promote a work environment that leverages diverse perspectives, backgrounds and talent to generate innovative ideas or solutions Experienced to conduct and engage in transparent and constructive conversations, contributing to high-performing teams and strong working relationships Strong decision-making skills and capable of driving actions with a global or enterprise-wide mindset in ambiguous or uncertain situations What’s In It For You Competitive Benefit Package* Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Kenvuer Impact Networks This list could vary based on location/region Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Role & responsibilities Handled Microbiology QMS Activities. Should have experience in OOS,OOT protocol review Preferred candidate profile Male Candidate Preferred

Job Title: Diabetes Educator – Mehsana Project Location: Gujarat (with travel to Mehsana District and/or Ahmedabad) Organization: The Diabesties Foundation Type: Full-Time/Hybrid Project: Comprehensive Care & Support for Type 1 Diabetes in collaboration with Mehsana DDO Office Reports To: Project Manager Number of positions: 2 About Our Organization: The Diabesties Foundation (TDF) is a non-profit pioneering Type 1 Diabetes care since 2018. Through various projects, we address health inequities by promoting access to insulin, education, and support—working with diverse stakeholders to drive sustainable, inclusive healthcare impact. Role Summary: We are seeking a committed and empathetic individual to serve as an Educator for our Mehsana Project. This role is critical in supporting and educating individuals impacted by Type 1 Diabetes (T1D) within the community. The ideal candidate should have good command on the Gujarati language, basic digital literacy, and preferably a lived experience or close connection to T1D. Key Responsibilities: · Conduct awareness and education sessions on Type 1 Diabetes in the community. · Support individuals and families with T1D through one-on-one and group interactions. · Collaborate with healthcare professionals and key stakeholders in the community. · Participate in meetings with government officials. · Maintain basic documentation and data related to the project. · Track progress through consistent monitoring and data collection · Support with research and evidence-based decision making. · Travel to Mehsana District and/or Ahmedabad as required. Qualification: B.Sc. in Nutrition, Food Science & Nutrition, Microbiology, Life Sciences/ B.Sc. Nursing/ Medical degree (MBBS, BDS, BAMS, BHMS, BUMS)/ Pharmacy (B. Pharm)/ Degrees in Occupational Therapy or Physiotherapy / Certified Diabetes Educator (CDE) Language Proficiency: Fluency in reading, writing, and speaking Gujarati is mandatory. Preferred Background: · Individuals living with Type 1 Diabetes (T1D) · Caregivers of someone with T1D · Healthcare professionals (HCPs) willing to undergo CDE training or already certified Skills: · Basic digital literacy, familiarity with MS Office Suite, Zoom and other · Research and Data analysis · Report writing · Government liasoning · Community organizing Other Requirements: Willingness and ability to travel within Gujarat Application Process: Interested candidates may apply below by 31 st July 2025.

Job Title: Diabetes Educator – Mehsana Project Location: Gujarat (with travel to Mehsana District and/or Ahmedabad) Organization: The Diabesties Foundation Type: Full-Time/Hybrid Project: Comprehensive Care & Support for Type 1 Diabetes in collaboration with Mehsana DDO Office Reports To: Project Manager Number of positions: 2 About Our Organization: The Diabesties Foundation (TDF) is a non-profit pioneering Type 1 Diabetes care since 2018. Through various projects, we address health inequities by promoting access to insulin, education, and support—working with diverse stakeholders to drive sustainable, inclusive healthcare impact. Role Summary: We are seeking a committed and empathetic individual to serve as an Educator for our Mehsana Project. This role is critical in supporting and educating individuals impacted by Type 1 Diabetes (T1D) within the community. The ideal candidate should have good command on the Gujarati language, basic digital literacy, and preferably a lived experience or close connection to T1D. Key Responsibilities: · Conduct awareness and education sessions on Type 1 Diabetes in the community. · Support individuals and families with T1D through one-on-one and group interactions. · Collaborate with healthcare professionals and key stakeholders in the community. · Participate in meetings with government officials. · Maintain basic documentation and data related to the project. · Track progress through consistent monitoring and data collection · Support with research and evidence-based decision making. · Travel to Mehsana District and/or Ahmedabad as required. Qualification: B.Sc. in Nutrition, Food Science & Nutrition, Microbiology, Life Sciences/ B.Sc. Nursing/ Medical degree (MBBS, BDS, BAMS, BHMS, BUMS)/ Pharmacy (B. Pharm)/ Degrees in Occupational Therapy or Physiotherapy / Certified Diabetes Educator (CDE) Language Proficiency: Fluency in reading, writing, and speaking Gujarati is mandatory. Preferred Background: · Individuals living with Type 1 Diabetes (T1D) · Caregivers of someone with T1D · Healthcare professionals (HCPs) willing to undergo CDE training or already certified Skills: · Basic digital literacy, familiarity with MS Office Suite, Zoom and other · Research and Data analysis · Report writing · Government liasoning · Community organizing Other Requirements: Willingness and ability to travel within Gujarat Application Process: Interested candidates may send their CV and a brief cover letter to contact@diabesties.foundation by 31st July 2025. Job Type: Full-time Benefits: Flexible schedule Work from home Work Location: In person

This position is no longer available. University: Polish Academy of Sciences Country: Poland Deadline: Not specified Fields: Immunology, Microbiology, Molecular Biology, Biomedical Sciences, Nutrition Science The Institute of Genetics and Animal Biotechnology at the Polish Academy of Sciences, under the supervision of Prof. Atanas G. Atanasov and Dr. Michel-Edwar Mickael, invites applications for a funded PhD student position to investigate the therapeutic potential of functional food supplementation in modulating gut microbiota and immune responses in the context of diabetes. The position is available from 1st September 2025 for a period of three years. Project Overview – Study the impact of functional food supplementation on gut microbiota composition, focusing on beneficial species such as Faecalibacterium prausnitzii and Bifidobacterium. – Assess the Th17/Treg balance and systemic inflammation in diabetic mouse models. – Evaluate liver function and metabolism following functional food intake via NRF2 pathways. – Employ metagenomics, immunophenotyping, animal models, and molecular biology techniques with translational relevance to metabolic and liver-related complications in diabetes. Key Responsibilities – Conduct in vivo and in vitro experiments, including dietary interventions in diabetic mice. – Perform metagenomic sequencing and microbiota data analysis. – Assess immune responses using flow cytometry and molecular profiling. – Analyze liver histology and metabolic function parameters. – Collaborate with internal and external project partners and contribute to scientific publications and presentations. Requirements – Strong background in immunology, microbiology, or molecular biology. – Experience with laboratory mice, including handling, injections, and tissue collection. – Familiarity with flow cytometry, qPCR, or RNA sequencing is an advantage. – Interest in gut microbiota research and host–microbe interactions. – Excellent communication skills in English (written and spoken). We Offer – A collaborative international research environment at a well-established institute near Warsaw, Poland. – Training in advanced microbiota and immune profiling methods. – Full-time funded position for three years with the possibility of extension. – Highly affordable accommodation provided by the institution. – Support for attending international conferences and workshops. Also See Fully Funded PhD Position in Cellular Mechanisms of RNA Localization in the Drosophila Brain… Industrial PhD Fellowship in Swine Nutrition & Metabolism Research Assistant Position in Human Stem Cell Biology and Neuroscience at Palo Alto… Fully Funded PhD Positions in Climate Disruptions and Food Systems Resilience Fully Funded PhD Opportunities at the University of Ferrara, Italy – 41st Cycle (2025/2026) Application Procedure Applicants should send the following documents in a single PDF file: – Cover letter outlining motivation and research interests. – CV with contact details of two referees (referee recommendation may be attached to the CV). – Copy of MSc certificate. Applications should be sent to Dr. Michel Edwar Mickael at m.mickael@igbzpan.pl. Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/register

Job Location : Delhi Reporting Manager : Manager Scientific Research/ Research Scientist Purpose of Position : The purpose of the position is to assist the HOD in the planning, organizing and conducting Research Analysis and to ensure timely completion of allotted assignment and projects. Job Responsibility : To work on the projects assigned. Meeting deadlines for the timely completion of projects/assignments. Calibration/Validation of lab equipment. Routine Lab work as assigned on different projects. Online Documentation. Skills : Good technical Knowledge of Immunological Techniques Qualification M. Sc. Biotechnology, M. Sc. Microbiology Experience Freshers

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Research & Development In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality. The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation. About The Role As an R & D Category Assistant at Reckitt, you will thrive in our fast-paced environment alongside a team of expert scientists dedicated to ensuring product safety and efficacy. Your meticulous attention to detail will be crucial in supporting technical dossier management and analytical lab compliance. Your responsibilities Knowledge or experience in sourcing, screening and selecting candidates is a bonus. Capability to manage projects, large and small, with diligence and efficiency. Strong communication skills, capable of providing advice and best practise guidance. Aptitude for innovative thinking and an entrepreneurial attitude within scientific realms. Experience working under pressure, prioritising quality while delivering on deadlines. The experience we're looking for Knowledge or experience in sourcing, screening and selecting candidates is a bonus. Capability to manage projects, large and small, with diligence and efficiency. Strong communication skills, capable of providing advice and best practise guidance. Aptitude for innovative thinking and an entrepreneurial attitude within scientific realms. Experience working under pressure, prioritising quality while delivering on deadlines. The skills for success R&D, Product Lifecycle Management, Commercial Awareness, Business Partnership, Collaboration, Partnership building, Collaborator, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Analytical, Formulation, Science, Chemistry. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.

Sales Executive Responsibilities: · Setting sales goals and developing sales strategies. · Researching prospects and generating leads. · Contacting potential and existing customers on the phone, by email, and in person. · Handling customer questions, inquiries, and complaints. · Preparing and sending quotes and proposals. · Managing the sales process through specific software programs. · Building and maintaining a CRM database. · Meeting daily, weekly, and monthly sales targets. · Participating in sales team meetings. Sales Executive Requirements: · Bachelor degree/ Master degree in Biotechnology/microbiology · 0-1 years of sales experience. · Excellent customer service and sales skills. · Strong verbal and written communicator. · Excellent phone and presentation skills. · Proficiency in Microsoft Office · Good negotiation and problem-solving skills. Job Types: Full-time, Permanent, Fresher Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Cell phone reimbursement Health insurance Ability to commute/relocate: Pune, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Application Question(s): Ready to travel and own two wheeler Require from Biotechnology/ Microbiology Degree or Master degree Education: Master's (Preferred) Language: English, Hindi, Marathi (Required) License/Certification: Driving Licence (Required) Willingness to travel: 75% (Required)

Kenvue is currently recruiting for a: Director, Analytical Chemistry and Microbiology R&D Operations What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. Role reports to: Sr Director Mumbai R&D Center of Excellence Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Fully Onsite What you will do Kenvue is currently recruiting for: Director, Analytical Chemistry and Microbiology R&D Operations This position reports into Senior Director, R&D Center of Excellence and is based at Mumbai. What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who we are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours. What you will do The objective of this position is to deliver R&D Analytical and Microbiology services to Kenvue- Global R&D organization to enable targeted business growth through compliant laboratory operations and successful alliance with internal partners and external stakeholders. The scope of the role applies to multiple product categories under various segments such as Self Care (OTC drugs), Skin Health and Essential Health (Baby care, Oral Care, etc.) etc. Technical Deliverables: Lead overall Analytical, Stability and Microbiology operations for R&D/Innovation and lifecycle management projects executed from India R&D site for markets worldwide. This also includes oversight of facility, equipment, and Computerized system validation management program for GMP laboratories, shipment management program and implementation of Quality and Safety processes and systems Develop and implement long-term strategies that align with the organization’s vision and goals e.g. analyzing market trends, assessing risks, identifying opportunities and strategic outsourcing Drive informed decisions quickly, often with limited information. This includes weighing the pros and cons and considering the impact of decisions on organizational outcomes Responsible for overall financial activities/expense management related to scope of operations. Understanding of financial principles and metrics, enabling effective budgeting, resource allocation, and financial decision-making Responsible for resource management, lab efficiency and key performance and quality metrics for scope of work Stakeholder management: Partner with key stakeholders (R&D/Supply Chain/Quality) in support of project plans, technical discussions and or Regional/Global initiatives Partner with Quality team to drive laboratory compliance, implementation of standards and systems and developing site procedures Functional lead during internal inspections and external Health authority audits. Project Management: Facilitating group leads to manage projects inclusive of planning, execution, communication with regional/global teams and presentations to stakeholders Represent on cross functional project teams as technical expert to share technical requirements, timelines, risk assessments, decisions, compliance needs related to specific analytical deliverables Ownership of performance and Quality metrics Representation on Regional/Global teams: Regional voice on Global teams for initiatives Representation on Leadership Teams to engage and drive assigned deliverables Develop new strategies, project charters or proposals and present to Senior leadership to drive innovative solutions, efficiencies, or related initiatives Leadership and organizational responsibilities: Encourage a culture of innovation, supporting new ideas, and being open to experimentation and learning from failures Commitment to developing talent within the organization, providing coaching and guidance to help team members grow in their roles Partner with Regional/Global teams to leverage best practices and behaviors to strengthen culture and collaboration Build and maintain relationships with key stakeholders, both inside and outside the organization, to facilitate collaboration and support Lead and manage change initiatives, helping the organization adapt to new challenges while minimizing resistance and maintaining morale What we are looking for Required Qualifications and Competencies Minimum Masters or Ph.D in Chemistry or equivalent stream with minimum 18-20 years of work experience and minimum 10 years of leading people Experience of working in a Global organization, preferred Experience of GMP operations, leading Health Authority audits, highly recommended Technical Competencies Deep technical expertise related to chemistry, analytical techniques, stability study assessment, microbiology operations and research technologies. Exceptional skills for proactive planning and prioritization Capable of applying diversified expertise in technical principles and practices in broad chemistry areas or technology. Excellent knowledge of current GMP, quality systems, SOPs, latest regulatory trends, and global regulations as appropriate Ability to learn and adapt to new and advanced technologies e.g. application of digital tools, problem solving abilities and data management. Ability to develop internal connects and external networks to drive new opportunities, improvements and scientific solutions Leadership Competencies Excellent oral and written communication and articulation skills Flexible mindset adaptable to changing needs of business and organizational ways of working Ability to leverage meaningful external relationships and partnerships outside of organization to solve problems to meet business needs Lead internal collaboration of teams and/or stakeholders across the enterprise, leveraging a broad range of cross-functional skills and perspectives to create innovative solutions Display inclusive mindset to promote a work environment that leverages diverse perspectives, backgrounds and talent to generate innovative ideas or solutions Experienced to conduct and engage in transparent and constructive conversations, contributing to high-performing teams and strong working relationships Strong decision-making skills and capable of driving actions with a global or enterprise-wide mindset in ambiguous or uncertain situations What’s in it for you Competitive Benefit Package* Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Kenvuer Impact Networks This list could vary based on location/region Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

We are looking for a Associate STEM content analyst to join our Biosis team in Chennai/Hyderabad . This is an amazing opportunity to work on Web of Science . The team consists of 23 Analysts and is reporting to the Team Manager . We have a great skill set in life sciences and we would love to speak with you if you have skills in biochemistry, microbiology, biotechnology, pharmacology or genetics . About You – Experience, Education, Skills, And Accomplishments Freshers to 1 year of experience Postgraduate in Biotechnology, Microbiology, Biochemistry, Genetics, Molecular biology, or any related Life Sciences field It would be great if you also had . . . 1+ years’ experience of content editing in a science-related field. 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. A good team player with the ability to work on their own initiative Well organized and disciplined with regards to policy, guidelines, and standards Excellent English written and verbal communication skills Ability to set priorities and be flexible in a changing environment Effective time management Self-motivated with the ability to deliver consistently What will you be doing in this role? Apply biotechnology, microbiology, pharmacology, molecular biology concepts to curate biology-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 Achieve and maintain consistent quality standards Adheres to editorial publishing schedules and quality standards. Maintain a flexible and adaptable approach towards process change Takes initiative by raising, discussing, and resolving subject matter and production issues Maintains and develops scientific knowledge and skills training as required to complete work and stay current on scientific trends and developments related to the employee’s editorial responsibilities To make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognized codes of practice provided or advised by management to ensure safe working practices. To undertake any other reasonable duties as requested by your line manager /Manager/Leadership team on a permanent or temporary basis About The Team The position is for Associate STEM content analyst in Biosis (Web of Science). This team is responsible for applying biotechnology, microbiology, pharmacology, molecular biology concepts to curate biology-related data from research articles in line with editorial policies The team consists of Senior STEM Content Analysts, STEM Content Analysts and Associate STEM content analysts working from different locations, such as Chennai, Hyderabad and Bangalore. Internal stakeholders – SIP team External Stakeholders – Customers Hours of Work 40 hrs – Hybrid (Permanent) Location - Chennai & Hyderabad 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.

We are looking for a Associate STEM content analyst to join our Biosis team in Chennai/Hyderabad . This is an amazing opportunity to work on Web of Science . The team consists of 23 Analysts and is reporting to the Team Manager . We have a great skill set in life sciences and we would love to speak with you if you have skills in biochemistry, microbiology, biotechnology, pharmacology or genetics . About You – Experience, Education, Skills, And Accomplishments Freshers to 1 year of experience Postgraduate in Biotechnology, Microbiology, Biochemistry, Genetics, Molecular biology, or any related Life Sciences field It would be great if you also had . . . 1+ years’ experience of content editing in a science-related field. 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. A good team player with the ability to work on their own initiative Well organized and disciplined with regards to policy, guidelines, and standards Excellent English written and verbal communication skills Ability to set priorities and be flexible in a changing environment Effective time management Self-motivated with the ability to deliver consistently What will you be doing in this role? Apply biotechnology, microbiology, pharmacology, molecular biology concepts to curate biology-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 Achieve and maintain consistent quality standards Adheres to editorial publishing schedules and quality standards. Maintain a flexible and adaptable approach towards process change Takes initiative by raising, discussing, and resolving subject matter and production issues Maintains and develops scientific knowledge and skills training as required to complete work and stay current on scientific trends and developments related to the employee’s editorial responsibilities To make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognized codes of practice provided or advised by management to ensure safe working practices. To undertake any other reasonable duties as requested by your line manager /Manager/Leadership team on a permanent or temporary basis About The Team The position is for Associate STEM content analyst in Biosis (Web of Science). This team is responsible for applying biotechnology, microbiology, pharmacology, molecular biology concepts to curate biology-related data from research articles in line with editorial policies The team consists of Senior STEM Content Analysts, STEM Content Analysts and Associate STEM content analysts working from different locations, such as Chennai, Hyderabad and Bangalore. Internal stakeholders – SIP team External Stakeholders – Customers Hours of Work 40 hrs – Hybrid (Permanent) Location - Chennai & Hyderabad 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.

Position Title: Sr. Manager QSE-Process and Technology Integration Job Description Summary: The Senior Manager will lead the integration and compliance of Quality, Safety, and Environmental (QSE) initiatives across water, aseptic, dairy, and other future emerging technologies while managing systems for reporting, program effectiveness, and adherence to standards. The role ensures effective communication of updated KORE requirements and local regulatory mandates to bottlers, supports capability building through webinars and discussions, and oversees robust market monitoring programs with data-driven insights. This role also includes managing QSE by design to ensure compliance is embedded in product and process development, while driving operational excellence by onboarding advanced technologies and systems. The incumbent will collaborate with global, regional, and local teams to lead critical compliance functions and ensure consumer safety, product quality, and alignment with Coca-Cola’s sustainability and regulatory commitments. Key Responsibilities: Integration and Compliance for Water, Aseptic, and Future Technologies Water Management: QSE Framework for Water Management: Develop integration frameworks for water treatment systems to ensure compliance with global KORE standards and local water quality regulations (e.g., BIS, FSSAI). Risk and Performance Oversight: Monitor water use efficiency, source vulnerabilities, and treatment facility performance while addressing quality, food safety, and safety risks in alignment with QSE standards and regulatory requirements. Aseptic and Dairy Operations: Develop and implement compliance frameworks for aseptic processing technologies, including risk assessments, validations, and adherence to food safety standards. Monitor dairy technology operations to ensure process hygiene, microbiological compliance, and product safety during formulation and packaging. Lead plant-level assessments to ensure readiness and compliance with quality systems for aseptic and dairy technologies. Emerging Technologies: Guide the adoption of new technologies within the Coca-Cola system by developing fit-for-purpose compliance frameworks. Conduct risk assessments and evaluate system readiness for advanced manufacturing processes, leveraging QSE strategies to ensure regulatory and corporate adherence. Partner with internal and external stakeholders to drive innovation without compromising quality, safety, or sustainability requirements. Communication and Collaboration with Bottlers KORE Updates: Act as the lead communicator of KORE, Coca-Cola’s global quality system, and regulatory requirement updates to bottlers. Draft and distribute technical bulletins, presentations, and compliance notices related to updated QSE requirements for water, aseptic technologies, and regulatory changes. Capability Building: Plan and conduct webinars, workshops, and interactive sessions with bottlers to align on updated KORE standards, new programs, and regulatory mandates. Lead targeted discussions with bottling teams to address implementation challenges, share best practices, and bridge compliance gaps. Develop tailored training materials for plant teams and compliance officers, focusing on new technological areas such as aseptic, dairy, and automation systems. Market Monitoring Programs Lead the design, integration, and reporting of key market monitoring programs: Product Integrity Program (PIP): Monitor marketplace products to ensure quality compliance with corporate guidelines and consumer safety requirements. Trade Sampling Program (TSP): Conduct quality assessments on trade samples to evaluate product condition across distribution and retail channels. Consumer Complaint Trend Monitoring (CCTM): Analyze consumer complaint trends, identify root causes, and implement corrective actions with relevant stakeholders. Establish KPIs for market monitoring programs and translate findings into actionable quality improvement plans. Present trends, risks, and outcomes from monitoring programs to bottler leadership, aligning on improvement strategies needed. Management Information System (MIS) and Reporting Data Management and Analytics: Leverage tools like Power BI to develop dashboards, track QSE metrics, analyze trends, and standardize reporting across bottlers, enhancing transparency and data-driven decision-making. Compliance and Action Planning: Ensure timely submission of GAPs/CAPAs, monitor compliance, and use analytics-driven insights from MIS to create actionable improvement plans during regular reviews. QSE by Design Embed Quality, Safety, and Environmental (QSE) considerations into the design process for new products, processes, and technologies. Collaboration with Global Teams & Analytics Function Audit and Compliance: Collaborate with GAO to resolve compliance gaps and align bottling plants with Coca-Cola’s quality standards. Analytics and Optimization: Partner with the Analytics team to enhance dashboards, automate MIS, and align systems with global quality priorities. Dispensed Beverage Program Management Oversee the onboarding of new key accounts within the Dispensed Beverage Program and ensure compliance during installations and business operations. Conduct compliance assessments for dispensed beverage equipment and implement corrective actions for non-conformances. Plan and execute QSE-related training programs for key account operational staff to ensure alignment with Coca-Cola operating standards. Generate insights and trend reports on dispensed beverage program compliance to identify risks and opportunities for improvement. Work Focus: System Integration: Drive compliance across water, aseptic, dairy, and new technologies by establishing robust compliance frameworks that adhere to KORE and local regulatory standards. Data and Insights: Leverage tools like Power BI to translate monitoring, audit, and operational data into actionable improvement strategies. Collaboration: Build strong partnerships with bottling teams to support compliance management and capability development through training, insights, and discussions. Capability Building: Conduct knowledge-sharing workshops and interactive sessions to reinforce compliance readiness for bottling teams. Education: Required Qualifications and Skills: Bachelor’s degree in Food Science, Microbiology, Chemistry, Engineering, or a related technical field. Certifications in Quality (HACCP, ISO 9001, FSSC 22000), with expertise in water treatment and aseptic systems preferred. Experience: 12+ years of experience in Quality, Food Safety, or Operations within the food and beverage industry. Expertise in complex QSE domains (e.g., water, aseptic, dairy) with a demonstrated track record in compliance management. Skills: Technical Compliance: In-depth knowledge of KORE and regulatory frameworks for food safety, water quality, and emerging technologies. Leadership: Proven experience driving initiatives among diverse teams, including plant teams, bottlers, and global stakeholders. Analytics Expertise: Proficiency in Power BI and analytics tools to create insights and reporting systems. Communication: Strong ability to disseminate technical updates, influence stakeholders, and conduct engaging training sessions. Problem-Solving: Demonstrated success in bridging compliance gaps and mitigating operational risks. Expected Travel: 40–50%, including visits to bottlers, plants, and onsite training/support. This Senior Manager role is pivotal to Coca-Cola’s QSE mission, ensuring seamless compliance, innovation integration, and the consistent delivery of world-class product quality and safety standards. Skills Packaging Engineering; Program Measurement (Inactive); Continual Improvement Process; Sustainability; Lean Manufacturing; Environmental Science; Measurement Verification (Inactive); Root Cause Analysis (RCA); Waterfall Model; Six Sigma; Communication; Food Safety and Sanitation; ISO 9001; Green Solutions; Environmental Regulatory Compliance Annual Incentive Reference Value Percentage:15 Annual Incentive reference value is a market-based competitive value for your role. It falls in the middle of the range for your role, indicating performance at target.

Position Title: Senior Manager- QFS Function: QSE- Quality and food Safety Job Description Summary As a Senior Manager in Quality and Food Safety, the individual’s primary focus is to ensure excellence in product quality, food safety, and regulatory compliance across the supply chain while driving governance, risk mitigation, and capability development within the Coca-Cola system. The role involves fostering a culture of quality and safety, engaging internal and external stakeholders to enhance QFS systems, and enabling efficient operations aligned with business goals. The work focus includes operational oversight, strategic initiatives, system effectiveness, and continuous improvement in QFS practices across bottling plants, co-packers, and supplier ecosystems, ensuring consumer trust in Coca-Cola products is sustained. Function-Related Work Priorities Quality and Food Safety Governance Establish Governance Protocols: Define and implement QFS policies, standards, and procedures in alignment with global Coca-Cola guidelines to ensure product quality, compliance, and food safety across plants and suppliers. Develop governance systems tailored to the adoption of new technologies, such as water treatment, aseptic processing, and other emerging technologies, ensuring proper integration into the QFS framework. Inspection and Compliance Monitoring: Conduct comprehensive plant and co-packer assessments to validate QFS processes, adherence to standards (e.g., KORE, ISO 9001, FSSC 22000, HACCP, and ISO 14001), and regulatory compliance. Incorporate specific assessments for water quality, aseptic processes, and new technologies to ensure compliance with requirements and their flawless operation within the context of product safety and overall quality standards. Audit Management: Ensure Corrective and Preventive Actions (CAPAs) are implemented following non-compliance issues during GAO, FSSAI or any 3rd Party assessment. Include specific audit protocols for specialized operations such as aseptic processing, water stewardship, and upcoming innovations to mitigate risks and ensure robust compliance mechanisms. Regulatory Engagement and Advocacy: Partner with Scientific and Regulatory Affairs (SRA) to interpret and influence local regulations (e.g., FSSAI, BIS, MOH) to ensure compliance and readiness for current and emerging requirements. Special focus should be placed on regulatory standards governing water quality, new technologies, and advanced production systems such as aseptic lines. Collaborate with regulatory teams to ensure that standards for water resources and filtration align with local and international guidelines. Risk Management QFS Risk Assessments: Lead risk assessments for raw materials, production processes, new equipment, and storage systems to identify, mitigate, and manage QFS risks across the value chain. Crisis Management and Incident Resolution: Act as a key decision-maker during quality and food safety incidents, implementing root cause analysis (RCA), containment measures, and systemic corrections. Post-Market Surveillance/Monitoring: Support post-launch monitoring programs such as Product Integrity Programs (PIP), Trade Sampling, and marketplace inspections to identify and resolve issues related to product safety or quality deviations. Process Excellence and Continuous Improvement Operational Efficiency: Collaborate with bottlers and corporate teams to identify and rectify inefficiencies in QFS systems, driving process standardization to ensure optimal operational performance. Data-Driven Decisions: Analyze real-time data and insights from quality metrics and reports (e.g., sensory, shelf-life, microbiological analysis) to identify trends, troubleshoot issues, and recommend strategies. Innovating QFS Practices: Explore and implement automation tools, digital platforms, and cutting-edge quality technologies (e.g., Quality 4.0) to drive compliance and operational resilience. Product and Packaging Compliance Shelf-Life and Stability Studies: Coordinate product and packaging stability tests, ensuring products meet shelf-life specifications under diverse market conditions. Labelling and Specifications Compliance: Work with integration tools (e.g., KO-Art for label approvals) to verify local regulatory compliance for labelling, storage instructions, and traceability requirements. Ingredients, Materials, and Cleaning Protocols: Maintain updated specifications for new and existing raw materials, packaging materials, and Cleaning-In-Place (CIP) protocols for extended compliance. Consumer Complaints and Issue Resolution Consumer Feedback Handling: Analyze all QFS-related complaints, identify trends, and collaborate with bottling teams to implement corrective actions. Root Cause Investigation: Lead cross-functional teams in investigating product-related complaints, developing preventive measures, and communicating findings with technical rationales to stakeholders. Systemic Improvements: Use feedback and data from complaints to drive quality improvement projects for products, packaging, and processes. Capability Building and Training Capability Development: Establish programs to train bottling plant teams, co-packers, and suppliers in key areas such as HACCP, problem-solving tools (RCA, FMEA), microbiology, and new quality technologies. Standardized Training Programs: Develop structured training templates and deliver regulatory- and industry-specific training, ensuring alignment with Coca-Cola’s global QSE priorities. Building QFS Culture: Foster a performance-driven culture by engaging plant leadership and associates on QFS fundamentals, ensuring quality and safety become integral parts of the production mindset. Co-Packer Governance: Implement fit-for-purpose QFS standards for co-packers to ensure product quality and compliance. Manage the authorization process for co-pack lines, plants, and ingredients. Strategic Partner Collaboration: Work with global and regional QFS teams to develop bottler capabilities, especially around analytical testing, stability studies, and new technologies. Stakeholder Collaboration Internal Stakeholders: Collaborate with Brand, Product Commercialization, Packaging, Supply Chain, Technical Operations, and other functions to align QFS initiatives with broader business goals. External Stakeholders: Build alliances with regulators, industry associations, NGOs, and external quality forums to ensure Coca-Cola’s leadership in quality, safety, and environment best practices. Cross-Functional Issue Resolution: Partner cross-functionally to address cross-domain QFS challenges (e.g., sourcing, logistics, customer complaints related to quality issues). Key Metrics For Success Achievement of Zero Quality Incidents (Zero Defect initiative). Reduced consumer complaints year-over-year (with Root Cause closure rates >90%). Successful audit performance (Internal/GAO/Third Party) with minimal corrective actions. Increased operational efficiency through QSE process optimization and innovation. Compliance with global and local QFS and regulatory requirements. Capability enhancement through training across the system. Summary This position centres on driving a culture of excellence in Quality and Food Safety by focusing on quality assurance, risk management, incident resolution, capability upgrades, and system-wide governance. The Senior Manager will serve as a critical enabler in ensuring that Coca-Cola’s products consistently meet consumer expectations, regulatory requirements, and the company's safety and sustainability priorities. Annual Incentive Reference Value Percentage:15 Annual Incentive reference value is a market-based competitive value for your role. It falls in the middle of the range for your role, indicating performance at target.

The Quality Control Analyst will be responsible for ensuring that all raw materials, in-process products, and finished goods meet the company's quality standards and regulatory requirements. You will be performing laboratory tests, maintaining documentation, identifying deviations, and coordinating with production teams to ensure consistent product quality. Conduct routine testing of raw materials, in-process samples, and finished products as per standard operating procedures (SOPs). Monitor and ensure compliance with quality standards (ISO, GMP, FSSAI, etc.). Document and analyze test results, maintain accurate records, and prepare quality reports. Identify quality issues, deviations, and recommend corrective actions. Assist in the calibration and maintenance of laboratory equipment. Support in audits and inspections conducted by internal teams and external agencies. Collaborate with production, R&D, and procurement teams to maintain product consistency. Ensure adherence to safety protocols and company policies within the lab and production areas. Qualifications & Skills: - Bachelors/Masters degree in Chemistry, Cosmetic Industry, Microbiology, or a related field. - 1-3 years of experience in a quality control or quality assurance role (freshers with relevant qualifications can also apply). - Knowledge of quality standards, testing methodologies, and regulatory compliance (ISO, GMP, FSSAI). - Strong analytical skills and attention to detail. - Good communication and documentation skills. - Ability to work collaboratively in a fast-paced environment. Job Types: Full-time, Permanent Benefits: - Cell phone reimbursement - Internet reimbursement Schedule: Day shift Performance bonus,