2560 Microbiology Jobs - Page 39

Job Description We are seeking a Scientist / Post Doctorate Fellow - Biological Sciences to join our Biologics - Product Development team in Hyderabad, India. In this role, you will contribute to cutting-edge research projects, supporting biosimilar – biotherapeutic drug development. Design and execute in vitro studies with an emphasis on modulation of the immune system using biotherapeutic or pharmaceutical approaches. Keep abreast with scientific literature and apply the knowledge appropriately to research projects. Interpret data, draw conclusions, and present data results at group meetings and other forums. Must think critically and creatively and be able to work independently. Analysis of samples, recording and reporting of data on time and submitting reports/data records for verification. Prepare protocol / report / manuscript as needed, including contributions to writing and reviewing content. Cell culture maintenance, preparation of master and working cell banks and their qualification. Collaborate with cross-functional teams to support development projects. Maintain accurate and detailed laboratory records, ensuring compliance with Good Documentation Practices (GDP). Laboratory equipment and inventory management. Ensure safe practices at workplace and participate in the organization-based safety and quality initiatives Execute the functional unit activities according to the need of the organization Qualifications Ph.D. in Immunology / Biotechnology/ Biochemistry/ Microbiology or related field Additional Information 0-1 years of experience in different types of complex immunological assays Strong attention to detail and ability to work in a fast-paced, collaborative environment. Excellent organizational and time management skills Ability to work independently and as part of a team

SHOULD HAVE SKILLS IN CHEMICAL LAB ACTIVITIES involving WATER , WASTE WATER, SOIL, AIR QUALITY, STACK, FOOD/MICROBIOLOGY TESTING ▪ Knowledge in LAB Compliance and Quality Procedures. ▪ Should have Knowledge Chemical Testing and Procedures. ▪ Ensuring compliance in all aspects. ▪ Assessing, analysing, and collating data and reporting test results. ▪ Attention to detail and systematic or methodical approach to work. ▪ Analysing Stack emissions report, Water Quality testing reports would be an added advantage ▪ Used to calibrate samples whenever require. ▪ Analysis of water, ores & minerals, and Industrial waste waters. ▪ Knowledge on Food Analysis & building material testing would be an added advantage. ▪ Knowledge on Instruments like AAS, ICP – OES, GC etc Job Type: Full-time Pay: ₹156,000.00 - ₹168,000.00 per year Schedule: Day shift Monday to Friday Weekend availability Supplemental Pay: Performance bonus Yearly bonus Experience: total work: 2 years (Required) Location: Iyyappanthangal, Chennai, Tamil Nadu (Required) Work Location: In person Application Deadline: 13/07/2025 Expected Start Date: 01/08/2025

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Master's degree with microbiology and minimum of 03 years of experience, Demonstrated technical skills in method validation and microbiology testing's Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control #LI-PFE

Company Description Hello, We're Doki. We are a brand focused on making healthy snacking easier and tastier by introducing Jerky, a dried and spiced meat snack, to the Indian market. Our products have high protein quantities and low-calorie counts, making them a unique and healthy snacking option. We prioritize social goals such as cruelty-free supply chains and carbon neutrality to ensure ethical business practices. Role Description This is a 2 months full-time on-site role as a Product Development Intern located in Delhi, India. The Product Development Intern will be responsible for market research, analytical tasks, communication with stakeholders, research and development (R&D), and product management. Qualifications Market Research and Analytical Skills Communication skills Research and Development (R&D) and Product Management skills Strong attention to detail and problem-solving abilities Knowledge of food industry trends and consumer preferences Ability to work in a fast-paced environment Currently pursuing or recently completed B.Tech/M.Tech/B.Sc/M.Sc in Food Technology, Food Science, Nutrition, Agriculture, Microbiology, or related disciplines

This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Master's degree with microbiology and minimum of 03 years of experience, Demonstrated technical skills in method validation and microbiology testing's Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

🔯 Position:- Site leader - Senior Microbiologist Quality Department 🔯 Location:- Kalamb Himachal 🔯 Salary:- 50 K 🔯 Experience:- Minimum [5-6] years of working experience in plant microbiology laboratory of a pharma, cosmetic or food industry, with at least [2-3] years of experience in leading plant micro control program 🔯 Qualification:- Master Degree in Microbiology Key Responsibilities ☀️Perform microbiological testing of raw materials, water, in-process, finished products, and environmental monitoring samples in accordance with approved test methods & SOPs. ☀️Oversee routine testing for microbial contamination and maintain aseptic practices in the laboratory. ☀️Supervise, train, and mentor junior microbiologists and lab technicians on microbiological testing, SOPs pertaining to microbiological laboratory, Reporting of micro data & other microbiology related work. ☀️Ensure micro compliance with applicable regulatory standards (e.g., FDA, ISO, HACCP, cGMP, EU regulations). ☀️Supervise/lead site Cleaning & Sanitization program, Identify & execute areas of improvement ☀️Develop and validate microbiological test methods (e.g., bioburden, endotoxin, sterility, pathogen detection). ☀️Investigate deviations, out-of-specification (OOS) results, and contamination incidents; participate in root cause analysis and CAPA implementation. ☀️Maintain and calibrate laboratory equipment and ensure availability of necessary supplies. ☀️Prepare and review technical documents including SOPs, reports, and protocols. ☀️Coordinate with cross-functional teams (Production, QA, R&D, Maintenance) to resolve microbiological issues and support continuous improvement. ☀️Manage microbiological data, trend reports, and present findings to management. ☀️Participate in internal and external audits and inspections. 👉🏻 Key Attributes 🔆 Certifications (preferred): Six Sigma, Lean, ISO Lead Auditor, ASQ Certified Quality Manager (CQM), or similar. 🔆 Technical Skills: Basic knowledge of quality tools and methodologies (FMEA, SPC, Root Cause Analysis, etc.) Hand on working experience in data management tools like LIMS, DMS, ERP & MES Systems 🔆 Regulatory Knowledge : Basic knowledge of industry regulations and standards relevant to IP, BP, USP, WHO GMP guidelines 🔆 Soft Skills : Leadership, communication, problem-solving, result oriented with good interpersonal skills. Computer knowledge & proficiency in Microsoft tools like Word, Excel, Powerpoint is essential. Skills: regulatory compliance,technical documentation,training and mentoring,plant microbiology,microbiology,microbiological testing,method development and validation,plant micro control program,cleaning and sanitization,root cause analysis,food industry,,data management tools (lims, dms, erp, mes)

Job Vacancy: MD Microbiologist Location: Almas Hospital, Kottakkal Almas Hospital, Kottakkal – a leading multi-specialty healthcare institution committed to clinical excellence and patient-centric care – is inviting applications for the position of MD Microbiologist to join our dedicated team of healthcare professionals. Position : MD Microbiologist Department : Laboratory / Microbiology Experience : Minimum 2-5 years preferred (Freshers with strong academic background may also apply) Qualification : MD in Microbiology from a recognized medical institution Registration : Must be registered with the Medical Council of India / Kerala Medical Council Key Responsibilities : Supervise and ensure quality control of microbiological diagnostic services Interpret microbiological results and provide clinical correlation Guide infection prevention and control measures in the hospital Collaborate with clinicians for antimicrobial stewardship programs Maintain NABL / NABH standards in microbiology laboratory practices Participate in internal training and CMEs Skills Required : Strong diagnostic acumen in clinical microbiology Expertise in infection control and hospital epidemiology Familiarity with molecular techniques and advanced diagnostics Excellent communication and teamwork skills Job Type: Full-time Pay: ₹100,000.00 - ₹101,000.00 per month Schedule: Day shift Morning shift Night shift Rotational shift Work Location: In person

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Master's degree with microbiology and minimum of 03 years of experience, Demonstrated technical skills in method validation and microbiology testing's Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

Company Overview At Sid’s Farm, we are a dedicated D2C brand committed to delivering 100% pure dairy products of the highest quality. Every drop of milk and product we offer embodies our promise of purity, quality, and safety. Founded in 2013 and named after our founder’s son, Sid, our company reflects a father’s commitment to providing the best for families and future generations. What began as a service to a few families has grown into a proud community, now serving over 25,000 families. Our employees are our greatest Cheerleaders and Assets, and we are committed to fostering a culture of Growth and Development. We provide ample opportunities for professional advancement, ongoing training, and mentorship to help our team members reach their full potential. At Sid’s Farm, we are passionate about ensuring that every product we create meets the highest standards for you and your loved ones. We also create a workplace where our employees can thrive and contribute meaningfully. We are growing like never before, expanding our horizons in Hyderabad, Bangalore, and a few more locations soon. We are a solid family of 500+ employees looking forward to more Culture Champions to enable every individual’s growth story. Role Summary Experience: 0 - 1.5 Years Position: Quality Executive Location: Vijayawada Plant Reporting to: Plant Manager Key Responsibilities Monitor raw milk quality from procurement to processing. Conduct quality checks at different production stages (pasteurization, homogenization, packaging). Ensure compliance with FSSAI, ISO, HACCP, and GMP standards. Implement microbiological, chemical, and physical testing for dairy products. Maintain records of quality control tests and corrective actions. Investigate and resolve customer complaints related to quality issues. Train production staff on hygiene, safety, and quality control procedures. Collaborate with procurement to ensure supplier quality compliance. Conduct internal audits and support external audits from regulatory bodies. Work with R&D to enhance product shelf-life, taste, and texture. Requirements Education: B.Sc../M.Sc. in Dairy Technology, Food Science, Microbiology, or related field. Knowledge of FSSAI regulations, ISO 22000, and HACCP principles. Strong analytical skills and experience in laboratory testing. Proficiency in MS Office and quality management software. Good communication and problem-solving skills. Why Sid’s Farm? Working at a Farm is fun, but you have to see it for yourself. But here we go with all the reasons to help you choose Sid’s Farm as your preferred workplace. Innovative Culture - With a commitment to quality and innovation, you’ll be part of a forward-thinking team that values fresh ideas and approaches with a new vision to act upon. If you’re passionate about high-quality dairy products and ideas, working at Sid's Farm allows you to be part of a team that shares that commitment and creativity. Sustainability Focus: Sid's Farm prioritizes sustainable practices, allowing employees to contribute to environmentally friendly initiatives and feel good about their impact. Visit our Farm to gain a deeper understanding of what we do. Growth Opportunities - As a growing company, there are ample chances for career advancement and professional development, allowing you to evolve alongside the business as you would be handling every nerve of the business. Working in a growing D2C Brand just elevates your learning curve by leaps and bounds. Community Engagement - Sid's Farm actively engages with local communities, providing employees with opportunities to participate in outreach programs and make a difference. Strong Values - The company emphasizes transparency, integrity, and customer satisfaction, fostering a positive and ethical work environment. Doing what you love - Here you will always end up doing what you love and in a more liberal way. Ideas and actions have no boundaries here as long as you have figured it all out. How to Apply? If this role excites you to join our Evolving Journey at Sid’s Farm, we look forward to your addition to our Sid’s Farm family. Interested candidates should submit their resume to careers@sidsfarm.com In the meantime, we invite you to dive into our world by following us on Instagram and LinkedIn.There, you can explore our vibrant community, get a behind-the-scenes look at our farm, and stay updated on all the exciting things happening at Sid's Farm. Stay updated by checking out our exciting Career Opportunities.

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

Interested candidates share resume to sanjay.behera@thyrocare.com or whatsapp to 8928285213 Eligibility Requirements: The candidate should be capable of independently managing the lab. Should be able to supervise and manage a small team of 23 technicians. Should be proficient in performing microscopy, particularly in Hematology and Clinical Pathology. Should have a basic understanding of laboratory quality assurance practices.

About Us: Continental Hospitals stands out as one of the best hospitals in Hyderabad, distinguished by its commitment to adhering to national and international guidelines while offering an extraordinary aesthetic ambience and safe design. Continental Hospitals is India’s first LEED qualified super specialty hospital. With 800 beds and more than 60 specialties, the healthcare institution is a Joint Commission International (JCI) accredited Tertiary care facility, spread across 18 floors (1.3 million sq. ft). Continental Hospitals is built on international standards redefine healthcare in India by providing quality patient care with integrity, transparency, a collaborative approach, and evidence-based medicine. Position: Consultant – Infectious Diseases Location: Continental Hospitals, Financial District, Nanakraguda Qualification: MD General/Internal Medicine with DM/Fellowship in Infectious Diseases Experience: Minimum 5 years post-specialization, preferably in a multi-specialty hospital setting Key Responsibilities: Diagnose and manage complex infectious diseases across OPD, IPD, and ICU settings Lead and oversee infection prevention and control protocols across the hospital Drive antimicrobial stewardship programs in alignment with global best practices Initiate and supervise clinical trials and contribute to clinical research within the department Collaborate with microbiology, pathology, and pharmacy teams for integrated patient care Actively engage in academic and research initiatives , case reviews, and publications Provide expert consultation for immunocompromised, transplant, and post-operative patients Ensure compliance with NABH/JCI standards regarding infectious disease management Required Skills & Profile: Proven experience in conducting and initiating clinical research and clinical trials Strong background working in multi-specialty or tertiary care hospitals Deep knowledge of emerging infectious disease patterns, public health responses, and WHO/CDC protocols Excellent communication, leadership, and collaborative skills across departments

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

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

Required a scientific sales officer for a hygiene solutions company. The company is into novel Enzyme based cleaning solutions. The ideal candidate should be a graduate in lifesciences, chemistry with or without experience. Candidate should be willing to travel inside Kerala and develop business. Institutional sales to be done, in places like airport, leading hotels, corporates, hospitals etc. Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Commuter assistance Compensation Package: Performance bonus Schedule: Morning shift Application Question(s): Are you a graduate in Microbiology or Life sciences? Are you willing to work in sales? Education: Bachelor's (Preferred) Language: English (Required) Work Location: In person Expected Start Date: 01/08/2025

Job description Horizon Biolabs Pvt Ltd. is a GLP compliant Pharmaceutical Testing Laboratory located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices and packaging Industries . Candidates with Msc in Microbiology having minimum 6 years of experience in any reputed Pharma Testing Lab/ CRO /Pharmaceutical Industry . To be responsible for planning and organizing daily activities of the Microbiology laboratory functions to ensure the quality of products /test items in compliance with Quality and as per various regulatory requirements. Should be familiar with : Development and validation of Microbial enumeration test and test for specified microorganisms (MLT), Antimicrobial Effectiveness Test (AET/PET), Sterility, Bacterial Endotoxin Test (BET by Gel Clot & Kinetic methods) and Microbiological Assays. Water System Validations. Disinfectant Efficacy Test. Hand Sanitizer Efficacy Evaluation. Environmental Monitoring. Facility Qualifications (Water and Area) General responsibilities of Job includes: -To ensure that microbiological testing is performed as per guidelines. To ensure shifts and tests are scheduled so that required tests are performed on time and the results are provided on time. - To be on top of compliance with respect to regulatory requirements, to interpret applicable quality and regulatory requirements and develop associated policies for the laboratories operations. - To continuously investigate and trend invalid and Out-of-Specification results. - To ensure appropriate and timely corrective actions are implemented. - To evaluate external audit observations and develop responses and oversight for related action plans. - To ensure all established laboratory, regulatory, safety, and environmental procedures are followed. - To adhere to the standards of quality as per GMP, company Quality Policies and site SOPs standards. - To ensure good documentation practices in all aspects and phases of the work; provide reports for review in a timely manner; work with other lab personnel on projects and participate in (OOS) Out-of Specification and failure investigations. - To maintain the safety and orderliness of the lab; apply knowledge of cGMPs and GLPs on a daily basis. Others : - To provide training on laboratory methods and the team members. - To ensure documentation and data trending activities. Team Management : - To guide and mentor the associates. - To review their performance on regular basis and provide feedback for improvement Job Type: Full-time Schedule: Day shift Education;MSC/BSC(Microbiology) Location: Hyderabad(Required) Requirment: Candidates having experience in any reputed Pharma Testing Lab/ CRO /Pharmaceutical Industry need apply . Experience: total work: 6-8 years (Required) Job Type: Full-time Pay: ₹45,000.00 - ₹60,000.00 per year Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Application Question(s): You have knowledge in Microbial enumeration test and test for specified microorganisms (MLT), Antimicrobial Effectiveness Test (AET/PET), Sterility, Bacterial Endotoxin Test (BET by Gel Clot ), Sterility, Environmental Monitoring and Microbiological Assays, Water validation.Are you residing in Hyderabad? Are you from Hyderabad?Are Immediate Joiner(7-10 days) candidates applied previously need not apply again and those applications will not considered. Experience: Pharma Testing Lab/ CRO /Pharmaceutical Industry : 5 years (Preferred) Location: Hyderabad, Telangana (Required) Work Location: In person

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)

We are looking for a Pharma Content Writer to join our editorial team and enrich our websites with new blog posts, guides and marketing copy. The candidate should be a Graduate of biotechnology, microbiology and any other pharma Related Experience- 6 Month To 1 Year > Research pharma-related topics > Write clear marketing copy to promote our products/services > Proofread and edit blog posts before publication > Submit work to editor for input and approval on time > Coordinate with marketing and design teams to illustrate articles > Promote content on social media > Identify customers’ needs and gaps in our content and recommend new topics > Ensure all-around consistency (style, fonts, images and tone) Job Type: Full-time Language: Hindi (Preferred) English (Preferred) Work Location: In person Application Deadline: 07/07/2025

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 Indias 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 its 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 cant wait to welcome you.

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 Indias 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 its 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 cant wait to welcome you.

Seed Lab Management: Manage master and working culture maintenance (bacteria, yeast, fungi, or actinomycetes). Oversee inoculum scale-up: shake flask → seed fermenter → production fermenter. Prepare and sterilize growth media, buffers, and equipment as per SOP. Monitor and optimize microbial growth parameters (pH, DO, OD, viability). Perform contamination checks at all stages of inoculum development. Maintain traceability records of inoculum batches, deviations, and test results. Upstream Inoculation: Coordinate microbial inoculation into pilot or production-scale bioreactors. Execute or oversee the transfer of seed culture into fermenters under sterile conditions. Optimize inoculum size and timing to match fermentation process requirements. Collaborate with process development and production teams to improve yield and productivity. Qualifications: Educational Background: M.Sc./M.Tech./Ph.D. in Microbiology, Biotechnology, Industrial Biotechnology, Bioprocess Engineering, or related fields. Experience: Executive: 2–5 years in microbial inoculum/fermentation operations. Manager: 6–12+ years with leadership experience in fermentation seed lab and upstream inoculation. Interested candidates can reach out to jai.mirchandani@symbiotec.in

Position Title : Senior Scientific Officer/Scientific Officer- USP Educational Qualification : M.Sc. - Microbiology/Biotechnology Experience : 3 to 7 years Job Summary: Senior Scientific Officer/ Scientific Officer shall be responsible for ensuring the quality and efficacy formulations at Vaccine Drug Substance Plant, Lalru (Punjab). This position will be responsible for Equipment handling i.e. Fermenters, Centrifuges, Process Vessels, TFF Systems, Weighing balances etc. Shift Operations and Production Activities Oversee and manage day-to-day production operations during assigned shifts, ensuring smooth workflow and adherence to production schedules. Ensure the completion of assigned tasks with optimum output and minimal downtime. Equipment Handling and Operations Operate and monitor fermenters (up to 1500L scale), centrifuges (e.g., CSC-15, CSC-20), process vessels (up to 1000L), TFF systems. Handle large-scale weighing balances (up to 500 kg) and perform filter integrity tests. Ensure all laboratory equipment is in good working condition, conducting routine checks to prevent disruptions. Quality Assurance and Compliance Conduct regular checks to ensure production quality, process consistency, and regulatory adherence. Liaise with Quality Assurance (QA) to address deviations, non-conformances, and ensure the release of high-quality products. Maintain compliance with regulatory requirements and documentation standards. Ensure online documentation in real-time, adhering to Good Documentation Practices (GDP). Maintain records for consumables, solutions, and other production-related items to ensure proper inventory control. Cleaning, Sterilization, and Culture Handling Perform and supervise Clean-in-Place (CIP) and Sterilization-in-Place (SIP) operations. Manage inoculations and transfers of cultures with strict aseptic techniques. Manpower Management and Shift Planning Allocate manpower effectively during shift operations to achieve maximum productivity. Develop and implement shift plans to ensure optimal utilization of available personnel. Calibration and Maintenance Calibrate and maintain instruments such as pH meters, conductivity meters, and other critical equipment. Coordinate with the engineering team for regular maintenance and upkeep of production equipment. Monitor the quality and quantity of consumables and solutions, ensuring timely delivery to meet production demands. Minimize waste and optimize the usage of materials. Competencies Required : Aseptic Handling and Behavior : Deep understanding of aseptic techniques and behavior in a cleanroom environment. Ability to teach and enforce aseptic practices among team members to prevent contamination. Quality Management System (QMS) : Proficiency in managing QMS aspects, including: Handling Events (deviations, non-conformances). Managing Change Controls effectively to ensure compliance with regulatory requirements. Implementation and tracking of Corrective and Preventive Actions (CAPA) . Sterile Operations and Scientific Practices : Thorough knowledge of sterile manufacturing processes and critical scientific practices in vaccine production. Understanding the critical control points and process parameters to ensure product quality and sterility. SAP Operations : Proficiency in SAP or equivalent systems for real-time posting of materials, tracking inventory, and handling final bulks. Leadership Competencies Team Motivation and High Performance : Ability to motivate team members and foster a high-performance culture. Encourage ownership, accountability, and collaboration within the team. Effective Team Management : Lead, manage, and allocate tasks to team members to ensure efficient operation during shifts. Build a cohesive team, resolve conflicts, and maintain morale in high-pressure environments. Performance Reviews and Training : Conduct regular and constructive performance reviews for team members. Identify skill gaps and implement targeted training programs to enhance team capabilities and ensure compliance with operational standards.

Job description Horizon Biolabs Pvt Ltd. is a GLP compliant Pharmaceutical Testing Laboratory located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices and packaging Industries . Candidates with Msc in Microbiology having minimum 6 years of experience in any reputed Pharma Testing Lab/ CRO /Pharmaceutical Industry . To be responsible for planning and organizing daily activities of the Microbiology laboratory functions to ensure the quality of products /test items in compliance with Quality and as per various regulatory requirements. Should be familiar with : Development and validation of Microbial enumeration test and test for specified microorganisms (MLT), Antimicrobial Effectiveness Test (AET/PET), Sterility, Bacterial Endotoxin Test (BET by Gel Clot & Kinetic methods) and Microbiological Assays. Water System Validations. Disinfectant Efficacy Test. Hand Sanitizer Efficacy Evaluation. Environmental Monitoring. Facility Qualifications (Water and Area) General responsibilities of Job includes: -To ensure that microbiological testing is performed as per guidelines. To ensure shifts and tests are scheduled so that required tests are performed on time and the results are provided on time. - To be on top of compliance with respect to regulatory requirements, to interpret applicable quality and regulatory requirements and develop associated policies for the laboratories operations. - To continuously investigate and trend invalid and Out-of-Specification results. - To ensure appropriate and timely corrective actions are implemented. - To evaluate external audit observations and develop responses and oversight for related action plans. - To ensure all established laboratory, regulatory, safety, and environmental procedures are followed. - To adhere to the standards of quality as per GMP, company Quality Policies and site SOPs standards. - To ensure good documentation practices in all aspects and phases of the work; provide reports for review in a timely manner; work with other lab personnel on projects and participate in (OOS) Out-of Specification and failure investigations. - To maintain the safety and orderliness of the lab; apply knowledge of cGMPs and GLPs on a daily basis. Others : - To provide training on laboratory methods and the team members. - To ensure documentation and data trending activities. Team Management : - To guide and mentor the associates. - To review their performance on regular basis and provide feedback for improvement Job Type: Full-time Schedule: Day shift Education;MSC/BSC(Microbiology) Location: Hyderabad(Required) Requirment: Candidates having experience in any reputed Pharma Testing Lab/ CRO /Pharmaceutical Industry need apply . Experience: total work: 6-8 years (Required) Job Type: Full-time Pay: ₹45,000.00 - ₹60,000.00 per year Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Application Question(s): You have knowledge in Microbial enumeration test and test for specified microorganisms (MLT), Antimicrobial Effectiveness Test (AET/PET), Sterility, Bacterial Endotoxin Test (BET by Gel Clot ), Sterility, Environmental Monitoring and Microbiological Assays, Water validation.Are you residing in Hyderabad? Are you from Hyderabad?Are Immediate Joiner(7-10 days) candidates applied previously need not apply again and those applications will not considered. Experience: Pharma Testing Lab/ CRO /Pharmaceutical Industry : 5 years (Preferred) Location: Hyderabad, Telangana (Required) Work Location: In person

University: Helmholtz Centre for Infection Research (HZI) Country: Germany Deadline: 2025-07-30 Fields: Chemistry, Biochemistry, Pharmacology, Molecular Biology, Microbiology The Chemical Biology Department at the Helmholtz Centre for Infection Research (HZI), under the leadership of Prof. Brönstrup, is seeking applications for a PhD researcher in the field of Bioanalytical Chemistry / Metabolomics. HZI is a member of the Helmholtz Association of German Research Centres, the largest scientific organization in Germany, and is dedicated to advancing strategies for the prevention, diagnosis, and treatment of infectious diseases. Research at HZI focuses on both bacterial and viral pathogens, their interactions with the immune system, and the discovery of novel therapeutic compounds. The Chemical Biology Department is committed to the discovery and characterization of new anti-infective agents through screening, mode of action studies, and chemical synthesis. Requirements For Application – Cover letter outlining your motivation and suitability for the position – Curriculum vitae (resume) – Employment references and certificates – Work samples or reference projects (if available) – Please do not include a photograph Application Procedure Applicants should submit all required documents, quoting the reference number 076/2025, to the Human Resources Department, Helmholtz Centre for Infection Research GmbH, Inhoffenstr. 7, 38124 Braunschweig, Germany. Applications may also be submitted by email as a single PDF document to jobshzi@helmholtz-hzi.de. Further information about the position can be found at: https://www.helmholtz-hzi.de/en/career/job-portal/job/076-2025-phd-researcher-f-m-d-in-bioanalytical-chemistry-metabolomics/ 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/position-alert-service/ We’re an independent team helping students find opportunities. Found this opportunity helpful? Support us with a coffee! Also See Postdoctoral Position in Chrononutrition at the German Institute of Human Nutrition Graduate Teaching & Research Assistant Position in Medicinal Chemistry and/or Chemical Biology Doctoral Scholarship in Immunoparasitology and Vaccine Development PhD Opportunities in Plastic Pollution and Climate Sustainability PhD Position in Gut Microbiota, Immune Regulation, and Liver Health in Diabetes

Job Title Asst. Manager- Production Reports To Head- Production CTC Budget Fixed Position Type 8 to 12 years of experience Location Bhiwandi, Maharashtra- Production Job Overview Work in area of Biopesticide production Responsibilities and Duties  Planning and execution of activities during running of solid state fermentation (SSF) batches for different fungal strains.  Timely delivery of production target and achieving the target and product quality  Monitoring of Powder processing steps (harvesting, drying, fungal spore extraction, sifting & blending) critically to avoid any market complaints.  Issuance of documents (BMR, Checklists, Equipment list, History card, Calibration records, etc.)  Ensure all documents of plant are online. BMR, Checklists, Equipment list, History card, Calibration records, etc.)  Maintaining batch wise data of SSF in soft copy form and submitting hard copies to higher authority whenever required.  Raw material planning as per batch plan and requisition in time.  Assisting Dept. Head in Training to the staff and helping training to workers.  Ensure proper housekeeping of the entire Production area.  Ensure Zero batch failure.  To ensure effective implementation of the Safety Management System.  To ensure continual improvement is facilitated using quality tool, Quality Management System, Total Productive Management, Safety policy. Soft Skills Good communication & leadership skills. Specific Skills  Manpower planning and controlling  Excellent knowledge and experience in biofertilizers, biopesticides product development. Experience 8 to 12 years of experience Education Qualification & Necessary education background &; MSc in Microbiology/Biotechnology/Agricultural/Life Sciences Salary up to 10 lpa