2539 Microbiology Jobs - Page 15

Role & responsibilities Identify, isolate, and characterize beneficial microbial strains for use in bio-fertilizer and bio-pesticide products Develop, test, and optimize microbial formulations to improve product performance and shelf life Manage end-to-end production pipeline. Lead quality control protocols to ensure microbial consistency and efficacy across production batches Conduct in-depth research on microbial-soil-plant interactions to support product development Collaborate with agronomists, R&D teams, and field experts to validate application practices Document experimental findings, maintain comprehensive lab records, and contribute to scientific publications or technical reports Preferred candidate profile Required Qualifications & Skills Postgraduate degree (M.Sc./Ph.D.) in Microbiology, Agricultural Microbiology, or a related discipline Minimum 12 to 15 years of hands-on experience in microbiological research, particularly in agriculture-related applications Expertise in microbial culturing, fermentation, and formulation techniques Familiarity with quality control standards and regulatory compliance for biological products Strong analytical, documentation, and English communication skills Ability to work collaboratively across functions and lead technical discussions

Job description Job Opening: Medical Coder (Fresher Opportunity) ISkills solution Are you a recent graduate in life science looking to kickstart your career in the healthcare industry Iskills solution is offering an exciting opportunity to join as a Medical Coder and grow in one of the most in-demand domains. Eligibility Criteria Education : B.Pharmacy (UG), M.Pharmacy ,Bsc Microbiology, Biotechnology,Biomedical,AHS Academic Performance : Minimum 60% in 10th, 12th, and UG Age Limit : Below 28 years Perks & Benefits Attractive Salary Among the best in the industry Certification Sponsorship Get trained and certified in medical coding Career Growth Fast-track your journey in the healthcare domain Location Work Mode : Work From Office (WFO) City : Chennai, Tamil Nadu How to Apply Interested candidates can reach out directly: Contact Person : KAVIYA (HR) Phone : +91 9087738811 Email : Campus@iskillssolution.com Role: Medical coder Department: Healthcare & Life Sciences Employment Type: Full Time, Permanent Role Category: Health Informatics Education UG: B.Pharma in Any Specialization, B.Sc in Optometry, Bio-Chemistry, Biology, Microbiology Key Skills Skills highlighted with are preferred keyskills

Should have knowledge in Clinical Data Management Should have good knowledge in edit checks crf design SAE Reconcilation crf annotation Clinical Data Management Trained Candidates Only Eligible Required Candidate profile Strong understanding of clinical data management and E2b Guidelines Excellent clinical assessment and Communication Skills

Key Responsibilities: Implement and maintain QA systems in compliance with GMP, ISO, and regulatory standards Review and maintain Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) Conduct internal quality audits and assist in regulatory inspections (e.g., FDA, ISO) Monitor manufacturing and packaging activities for adherence to SOPs Prepare and review quality-related documents like SOPs, change controls, deviations, and CAPAs Conduct line clearance before manufacturing/packing Handle product complaints and support investigation with the QC and Production teams Support in product stability studies, validation activities, and documentation Ensure proper documentation control and record keeping Provide training to staff on quality standards and GMP practices Key Requirements: B.Sc. / M.Sc. in Chemistry, Microbiology, Pharmacy, or related discipline 1–2 years of experience in a QA role, preferably in cosmetics, pharma, or food industries Strong knowledge of GMP, GLP, and regulatory guidelines (FDA, ISO, AYUSH, etc.) Excellent attention to detail, documentation, and analytical skills Familiar with quality management systems (QMS) and documentation practices Preferred Skills: Good communication and coordination skills Problem-solving and root cause analysis abilities Proficiency in MS Office and QA software tools Ability to work both independently and in teams Employment Type: Full-Time Location: Kothariya, Rajkot, Gujarat (Preferred) Work Location: In person Application Deadline: 30/07/2025 Job Type: Full-time Pay: ₹13,000.00 - ₹15,000.00 per month Schedule: Day shift Work Location: In person

Key Responsibilities: Perform in-process and final product quality checks as per defined SOPs Test raw materials, packaging materials, and finished goods for compliance Monitor and maintain quality control records and reports Ensure all products meet regulatory standards and internal specifications Conduct stability studies and validation of cosmetic/healthcare products Investigate quality-related issues and implement corrective actions Ensure compliance with GMP, ISO, and other relevant regulatory guidelines Coordinate with production and QA teams to resolve quality issues Assist in preparation and review of batch manufacturing records (BMR) and quality documentation Support audits and inspections (internal/external) Key Requirements: B.Sc. / M.Sc. in Chemistry, Microbiology, Pharmacy, or related field 1–2 years of experience in QC, preferably in cosmetics, personal care, or health products Sound knowledge of analytical techniques, product testing, and cosmetic regulations Familiarity with instruments like HPLC, UV, pH meter, viscometer, etc. Good documentation practices and attention to detail Knowledge of BIS/AYUSH/FDA norms is a plus Preferred Skills: Understanding of skin care, personal care, and wellness product formulations Strong communication and reporting skills Ability to work independently and in a team environment Problem-solving and analytical thinking Employment Type: Full-Time Location: Kothariya, Rajkot, Gujarat (Preferred) Work Location : In person Application Deadline: 30/07/2025 Job Type: Full-time Pay: ₹13,000.00 - ₹15,000.00 per month Schedule: Day shift Work Location: In person

Job Title: Quality Assurance Manager Location: [Manor-Wada Road, Waveghar Gaon, Kanchad - Mumbai 421303] Employment Type: Full-time Department: Quality Assurance / Operations Industry: Food Manufacturing (Preferred) Job Summary: We are seeking an experienced and proactive Quality Assurance Manager to oversee and maintain quality standards across raw materials, production processes, and finished products. The ideal candidate will have hands-on experience in implementing quality systems, conducting audits, managing internal and external non-conformances, and driving continuous improvement initiatives. A strong background in team leadership and stakeholder coordination is essential. Key Responsibilities: Conduct quality inspections and audits for raw materials, in-process checks, and final products. Establish, manage, and improve internal and external non-conformance reporting (NCR) systems. Handle customer complaints efficiently, ensuring proper documentation, root cause analysis, and corrective actions. Ensure maintenance and calibration of laboratory equipment and plant instruments in compliance with quality standards. Lead initiatives focused on continuous improvement, process optimization, and implementation of company policies and procedures. Conduct and support internal and external audits (e.g., ISO, FSSAI) and ensure compliance with regulatory standards. Train, mentor, and manage a team of QA professionals. Collaborate with cross-functional teams including Production, Procurement, R&D, and Sales to maintain quality standards. Monitor and manage inventory levels of raw materials (RM) and finished goods (FG) to ensure timely availability and quality compliance. Preferred Qualifications & Skills: Bachelor’s or Master’s degree in Food Technology, Microbiology, Chemistry, or a related field. Minimum 10 years of experience in Quality Assurance, preferably in a food manufacturing environment. Strong understanding of HACCP, GMP , and regulatory compliance in the food industry. Proven leadership experience in managing QA/QC teams. Excellent problem-solving, analytical, and communication skills. Proficiency in using QA tools, ERP systems, and reporting tools. Nice to Have: Experience with inventory and stock management of RM & FG. Certifications in ISO, FSSAI, or related food safety standards. Job Types: Full-time, Permanent Pay: ₹435,706.49 - ₹716,661.86 per year Ability to commute/relocate: Mumbai, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: QA: 5 years (Required) Shift availability: Day Shift (Preferred) Night Shift (Preferred) Work Location: In person

Job Summary: We are seeking a dynamic and self-motivated Area Sales Manager to lead and grow our sales operations in the Eastern Uttar Pradesh region , with a base in Varanasi . The ideal candidate will possess strong technical knowledge, a proven track record in B2B/B2C sales, and the ability to develop and maintain client relationships in the life sciences and chemical sectors. Key Responsibilities: Manage and grow sales within assigned territory (Eastern UP). Develop new business opportunities with institutions, research labs, pharmaceutical companies, and distributors. Build strong customer relationships to ensure long-term success and repeat business. Monitor sales performance, prepare monthly reports, and meet revenue targets. Conduct product presentations, technical discussions, and training sessions. Coordinate with internal teams (marketing, logistics, technical) for order processing and support. Analyze competitor activities and suggest strategies to maintain market leadership. Participate in trade shows, seminars, and conferences to enhance market visibility. Key Requirements: Bachelor’s degree in Science (Chemistry, Biotech, Microbiology or equivalent). 8–10 years of field sales experience in chemicals, lab reagents, pharma, or life sciences products. Excellent communication, negotiation, and interpersonal skills. Strong understanding of regional market dynamics and customer base in UP. Proficient in MS Office, CRM tools, and sales reporting. Willingness to travel extensively within the region.

Urgently hiring for Senior Executive or Assistant Manager - Micro. Location: Panchkula, Haryana Experience Required: 5+yrs Early joiners Preferred Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Schedule: Day shift Morning shift Application Question(s): Notice Period? Current Salary? Expected Salary? Current Location? Relevant experience in Microbiology? Work Location: In person

We are a prominent diagnostic laboratory chain with accreditation from the National Accreditation Board for Hospitals (NABH). Our branches in Pothencode, Kanyakulangara, Venjaramood, and Kallara offer a diverse range of affordable laboratory tests covering various medical disciplines such as Clinical Biochemistry, Haematology, Clinical Pathology, Microbiology, and specialized tests. We are seeking smart, adaptive, and confident candidates preferably with some experience in the medical field. Candidates should be willing to undergo an unpaid training period of at least one month if they lack prior experience. Responsibilities include participating in the day-to-day operations, demonstrating a willingness to learn, taking on additional responsibilities when required, and providing home collection services. Candidates should uphold safety standards and maintain quality registers. Prior experience of at least 1 year is preferred, and owning a two-wheeler with a valid license is advantageous. Applicants must be willing to commute to any of our branches, as we do not provide hostel facilities. This is a full-time position with benefits such as health insurance and leave encashment. The job involves working in day, evening, morning, and rotational shifts. Candidates must have a Bachelor's degree, fluency in Malayalam and English, and be willing to commute to any of our branches. Application Question(s): - University from which you have completed your Diploma/ Degree - Will you be able to commute to any of our branches (Shift timings: 6:30 a.m - 2:30 p.m & 11:30 a.m - 7:30 p.m). Education: Bachelor's (Required) Language: Malayalam & English (Required),

1.To perform cleaning of Visual inspection equipment in fill finish facility. 2.To Perform visual inspection of Vials, PFS and Cartridge along with documentation. 3.Making entries in log books, batch packing record and status labeling. Required Candidate profile 1. Looking for smart and dynamic pharma fresher candidate. 2. Candidate should be very good in to written and oral english communication 3. Candidate should be very dynamic.

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 meets the highest standards of safety and efficacy. What You Will Achieve In this role, you will: Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records. Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories. Support media preparation, Bio ball culture handling, and conduct microbiology-related investigations. Perform testing on various samples, manage Laboratory Information Management System builds, and review laboratory data. Serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and train junior colleagues. Here Is What You Need (Minimum Requirements) Master's degree in microbiology with minimum of 6 years relevant experience Strong technical skills in method validation and testing Experience in microbiological testing of water Deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations Detail-oriented with robust knowledge of quality systems Familiarity with research unit clinical and analytical laboratory environments Effective written and verbal communication, as well as interpersonal skills Bonus Points If You Have (Preferred Requirements) Relevant pharmaceutical experience Strong understanding of computer system hardware, infrastructure, and networks Experience with Laboratory Information Management Systems (LIMS) Proficiency in data analysis and interpretation Knowledge of regulatory requirements and guidelines Strong problem-solving abilities Effective time management and organizational skills Ability to mentor and train junior colleagues Work Location Assignment: On Premise 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

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 in microbiology with minimum of three years' experience Demonstrated technical skills in method validation and testing 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 using 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 Work Location Assignment: On Premise 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

Experience: 6-8 years of experience in Quality Assurance / Quality control of sterile dosage manufacturing facility. Core Competencies Change Management process Risk assessments principles and tools Validation of lab equipment’s Drug Product Process validations Regulatory requirements Compendial Changes Technical Skills Knowledge in validation principles and practices related to the Process validation, cleaning validation, Analytical Method validation, Water system, HVAC system, Equipment & Utility Qualifications. Knowledge of various Quality tools required for investigations Technical Writing- Ability to create documentation that is accurate, complete, unambiguous, and as concise as possible aimed to be understood by any level of organization Knowledge in change control assessment Knowledge on Chemical and Microbiology analysis. Basic idea on manufacturing operations, validation and engineering functions Experience in handling Regulatory agency inspections Behavioral/Any Other Skills Interpersonal Skills: Effective communication with all staff from different levels and builds constructive and effective relationship Managerial Skills: Persistent approach to resolving issues, Effective situation handling capabilities, strong time management skills. Acts Decisively: Makes decision in a timely manner based on available information Grows Self: Identify Individual development needs and create a plan and work towards achieving those objectives Self-accountable & Proactive approach Critical thinking and Compliance mindset Core Responsibilities Partially/fully independent, reviews critical change controls and protocols, trains others. Responsible for review & approval of documents as per current regulatory requirements. Assessment, approval & closure of change control and action items Site change review committee (SCRC) meeting with cross functional team to assess the change before initiation in gqts and present the critical change controls to the leadership team for its adequacy. Coordinating with CFT for addressing & resolving of Review Comments for timely Closure. Review & approval of Sops, Job aids, forms, Quality Risk Assessment (QRA), validation protocols, study protocols & summary reports. Review and approval of STP’s and specifications. Review and approval of stability compilation reports. Review and approval of APR’s. Review and approval of Environmental monitoring trends, Water monitoring trends, bioburden, BET, sterility trends, isolate trends and summary reports. Ensure manufacturing policies, procedures conform to Pfizer Report any non-compliance to the Manager Experience in handling regulatory, corporate and internal auditors/ inspectors. Work Location Assignment: On Premise 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

Vibonum Technologies Private Limted hiring Microbiologiest for its OSD Plant at Mysore. Technical Skills & Experience: Hands-on experience in water sampling and analysis Proficient in media preparation and microbial culture handling Skilled in environmental monitoring (EM) in controlled environments Exposure to Microbiological Limit Testing (MLT) and method validation Experience in disinfectant efficacy studies and validation Working knowledge of Quality Management Systems (QMS) , including documentation and compliance protocols Work Location: Nanjangud, Mysuru Note: Immediate joiners or candidates with a notice period of up to 1 month will be given high preference.

Company Name Aditi Foods Job Title QA & QC Executive Job Location: Maharashtra Description We’re Hiring! Join Our Quality Team at Aditi Foods At Aditi Foods, quality isn’t just a department — it’s a commitment to excellence in every product we deliver. As we continue to grow, we are looking for passionate and detail-oriented professionals to join our team! 🔍 Open Positions Quality Assurance (QA) Executive Quality Control (QC) Executive 📍 Location: Plant side. 📅 Experience Required: 1–3 years preferred 🎓 Qualification: B.Sc / M.Sc in Food Technology, Microbiology, or related field 💼 What You’ll Do Ensure adherence to food safety and quality standards Conduct inspections, audits, and lab testing Maintain documentation and regulatory compliance Collaborate with production for continuous improvement Join us in ensuring that every product from Aditi Foods meets the highest standards of taste, safety, and trust. Apply Here aditifoodsmktg4@gmail.com

🚀 Internship Opportunity – Sales & Market Research | Life Sciences | Jharkhand 📍 Location: Jharkhand (preference for locals) 🏢 Company: AIB Life Science (ALS) 🧪 Industry: Lab Equipment | Biotechnology | B2B Sales 📅 Duration: 3-6 Months | Full-time 🎓 Eligibility: Final year or recent graduates in B.Tech/M.Tech/M.Sc – Life Science/Microbiology/Biotechnology/Biochemistry or allied fields Are you passionate about life sciences and eager to kickstart your career in B2B technical sales and market strategy ? AIB Life Science (ALS) is offering an exciting internship for aspiring professionals to get hands-on experience in sales operations, client interaction, and market research in the thriving lab equipment sector. 🔧 What You’ll Work On: Assist in generating and qualifying sales leads in your assigned territory Support the sales team in client relationship management and follow-ups Collaborate with marketing and applications teams on local campaigns Perform secondary research and trend analysis to support sales planning Gain exposure to GeM and CPP tender platforms (eProcurement process) Learn sales forecasting and documentation processes 🎯 What We’re Looking For: Strong interest in technical sales or lab equipment industry Excellent communication & interpersonal skills Analytical mindset and basic understanding of market dynamics Willingness to travel locally when required Strong academic background in Life Sciences/Biotech/Microbiology ✅ Bonus if you have: Understanding of lab instruments or bioscience products Are from Jharkhand or looking to relocate back 💼 About AIB Life Science (ALS): Headquartered in Bangalore, ALS is a fast-growing lab equipment supplier representing leading global brands like Thermo, Leica, Beckman Coulter, and more. With a strong policy-driven culture and a presence across India, ALS is committed to nurturing talent passionate about science and sales. 🌱 Why Join Us? On-the-job training & mentorship High learning curve in a dynamic B2B sector Potential for full-time placement based on performance 📩 Apply Now if you're ready to grow in the intersection of science and sales . Tag or share with someone who’s a good fit! #Internship #LifeScienceJobs #SalesInternship #BiotechCareers #B2BSales #BiharJobs #LabEquipment #Biotechnology #GeM #JobOpening #LinkedInJobs Reach out - abhinav@aiblifescience.com

Division Department Sub Department 1 Job Purpose Execute analysis of allocated samples and Produce reliable and reproducible results in order to ensure their compliance to the microbiological quality parameters and predefined specifications and standards. Key Accountabilities (1/6) Analyse and review samples based on work allocation to meet the service level agreement Analyse samples as per priority and work allocation Review the data as per respective specification, Microbiological Methods and results obtained Prepare, review and submit reports to Team leader within stipulated timelines in order to support individual sample release within stipulated timelines to achieve SLA Key Accountabilities (2/6) Report errors, abnormal observations, non-compliances related to procedures, equipment and instruments, and deliver results promptly to facilitate timely action and avoid delay in releases Initiate investigations and take necessary corrective and preventive actions Investigate incidence & lab error on priority basis so that batch release timely and issues are not recurring Key Accountabilities (3/6) Document entries, raw data and findings concomitantly in relevant test data sheets so as to facilitate the lab QA to review the reports and avoid missed entries Review reports as per cGMP & GDP for compliance to GLP Ensure no GMP / regulatory concern are raised by adhering to SOPs and following procedures Key Accountabilities (4/6) Evaluate & document Instrument / equipment break down and suggest mechanisms to avoid the same Maintain equipment and instruments optimally to ensure no incidences or non-compliances occur due to malfunctioning of equipment/ instruments Key Accountabilities (5/6) Key Accountabilities (6/6) Major Challenges Availability of Validation records of analysis samples becomes a challenge in cases where validation is performed on other sites. Material and resource availability becomes a challenge due to conflicting priorities between labs and coordination between analysts which makes it tough to fulfil SLA Key Interactions (1/2) Units for receiving specification, documents, protocols, area availability etc. (daily) QA/QC for product sample release (daily) Stores for procuring materials (need basis) Communicate if any observation find on the specification. Key Interactions (2/2) CQA for procuring pharmacopial guidelines (need basis) Dimensions (1/2) Review and release approximate 15 MLT reports on daily basis to achieve the SLA. Review and release approximately 15 sterility batches on weekly basis and 15 bio load samples. 50 Water Samples analysis and release 10 Technical Information Sheets for swap analysis 6 Autoclave & DHS Operation 200 locations released on daily basis for Environmental monitoring Dimensions (2/2) Key Decisions (1/2) Daily Media and Plates requirement (to Team Leader Microbiology) Key Decisions (2/2) Education Qualification M. Sc (Microbiology) Relevant Work Experience 1-5 years experience for analyst and 3-7 years for reviewer in Microbiology Good knowledge of Microbiology, skill to perform assigned task, communication in English

About Us We are surrounded by the world's leading consumer companies led by technology - Amazon for retail, Airbnb for hospitality, Uber for mobility, Netflix and Spotify for entertainment, etc. Food & Beverage is the only consumer sector where large players are still traditional restaurant companies. At Rebel Foods, we are challenging this status quo as we are building the world's most valuable restaurant company on the internet, superfast. The opportunity for us is immense due to the exponential growth in the food delivery business worldwide which has helped us build 'The World's Largest Internet Restaurant Company' in the last few years. Rebel Foods' current presence in India, UAE & UK with close to 50 brands and 4500+ internet restaurants has been built on The Rebel Operating System. While for us it is still Day 1, we know we are in the middle of a revolution towards creating never seen before customer-first experiences. We bring you a once-in-a-lifetime opportunity to disrupt the 500-year-old industry with technology at its core. Position :: Executive Quality Assurance Reports to :: Manager/Assistant Manager Educational Qualification , Work experience & Key Competencies Qualification B.Sc Microbiology/M.S.C Microbiology/B Tech./MTech. Food Technology or equivalent Work Experience Min 1 year in food industry (FMCG/QSR) Key Competencies Good communication skills Good understanding of the domain of food safety, RCA & CAPA , quality standards Well versed with FSSAI regulations for catering industry Knowledge of MS Excel & Power Point Presentation Job Description Monitoring and continuously up keeping food safety and hygiene standards of the kitchen Giving training to the kitchen team on various SOPs, quality and food safety standards Prepping kitchen to comply to FSSAI standards and other internal audits Proactively checking the quality of raw ingredients/products through sensory and its documentation Handling customer complaints by doing RCA and sharing CAPA Analyzing data to understand regional performance on various metrics Ready to travel to different locations of the city

Mission: The mission of the position Consultant Pathologist is to provide qualitative pathology services, contribute to accurate diagnostic interpretations, and ensure the highest level of patient care. The person in this role will play a vital role in supporting the business commitment to delivering accurate and timely results, maintaining quality standards, and fostering a culture of excellence in diagnostics. Key Responsibilities: Diagnostic Operations: Perform and interpret diagnostic tests, including cytopathology, hematopathology, biochemistry, immunohistochemistry, and microbiology. Analyze and evaluate laboratory data, including tissue samples, blood smears, body fluids, and molecular analyses to provide accurate diagnoses. Collaborate with other healthcare professionals, including clinicians to provide comprehensive diagnostic reports and contribute to patient management. Quality Assurance and Compliance: Ensure compliance with NABL standards, laboratory policies, and procedures to maintain the highest level of quality and patient safety. Participate in quality control activities, proficiency testing, and external quality assurance programs to monitor and improve laboratory performance. Contribute to the development and implementation of quality improvement initiatives to enhance the efficiency and accuracy of pathology services. Consultation and Collaboration: Provide expert consultation to referring physicians, hospitals, and healthcare providers to assist in patient management decisions. Collaborate with other pathologists and laboratory staff to discuss complex cases, share knowledge, and contribute to the continuous professional development of the team. Actively participate in interdisciplinary meetings, and research activities to enhance diagnostic capabilities and contribute to laboratory advancements. Training and Education: Mentor and supervise laboratory staff in the principles and practices of diagnostics. Conduct educational sessions, seminars, and workshops to enhance the understanding of pathology concepts and promote professional growth within the organization. Stay updated with the latest advancements in pathology through continuous learning, attending conferences, and engaging in professional societies. Documentation and Reporting: Prepare accurate and detailed diagnostic reports, incorporating clinical and laboratory findings, in a timely manner. Maintain comprehensive patient records, including specimen information, test results, and interpretations, following NABL guidelines and regulations. Assist in the development and implementation of standardized reporting templates and guidelines to ensure consistent and meaningful pathology reports. ** This job description provides a general outline of responsibilities and qualifications and is not exhaustive. The role may be required to perform additional duties as necessary for the smooth functioning of the business. Requirements: Medical degree (MBBS) with specialization in Pathology (MD/DNB) from a recognized institution. Valid state medical license and registration to practice pathology. Significant experience in diagnostic pathology and proficiency in performing and interpreting complex laboratory tests and techniques. Strong knowledge of NABL regulatory and accreditation requirements related to pathology services. Excellent communication and interpersonal skills to collaborate effectively with healthcare professionals and patients. Ability to work independently, handle multiple priorities, and meet deadlines in a fast-paced environment. Commitment to quality, accuracy, and continuous professional development Compensation and Benefits: We offer a competitive salary package commensurate with experience, along with comprehensive benefits and opportunities for professional growth and development.

Today Secret Unspecified Unspecified Healthcare and Science GA (ON-SITE/OFFICE) Duties Responsible for performing all food safety and food handling /preparation and public facility sanitation inspections. With direction from the Bioenvironmental Public Health Office Chief, helps plan, organize, and conduct the activities of the office. Analyzes, evaluates, and coordinates various aspects of the base public health and occupational health programs, including Population Health, Epidemiology, Vector Disease Control and Prevention, Rabies Exposure Surveillance, Medical Intelligence, Bloodborne Pathogen Exposure Control, Disaster Response, Reproductive Hazard Assessment, Illness and Injury Investigation and Remediation programs, Occupational Health, Food Safety programs, Facility Sanitation programs, and Occupational Safety and Health Administration (OSHA) compliance. Assists the Bioenvironmental Public Health Office Chief with the development and administration of Public Health programs for wing organizations ensuring that office programs comply with legal and regulatory requirements. In absence of the Supervisor, may represent the Bioenvironmental Public Health Office withina variety of installation and functional area organizations. Requirements Conditions of employment U.S. Citizenship is required Males must be registered for Selective Service, see www.sss.gov If authorized, PCS will be paid IAW JTR and AF Regulations. If receiving an authorized PCS, you may be subject to completing/signing a CONUS agreement. More information on PCS requirements, may be found at: https://afciviliancareers.com/regulatory/ This position is subject to provisions of the DoD Priority Placement Program Disclosure of Political Appointments All federal employees are required to have direct deposit. May be required to work extended and/or irregular hours during exercises or contingency situations. Will be required to accomplish temporary duty (TOY) assignments in the performance of official duties and to travel by military or commercial aircraft or other modes of transportation. May act in place of the Bioenvironmental Public Health Office Chief as needed. A degree in Public Health or Allied Sciences is highly desired. Must obtain and maintain an appropriate security clearance. PCS paid by gaining unit. Must be a current civilian employee in the Air Force Reserve Command (AFRC) Qualifications In order to qualify, you must meet the specialized experience requirements described in the Office of Personnel Management (OPM) Qualification Standards for General Schedule Positions, Administrative and Management Positions, Public Health Program Specialist Series 0685 SPECIALIZED EXPERIENCE: Applicants must have at least one (1) year of specialized experience at the next lower grade GS-09, or equivalent in other pay systems. Examples of specialized experience includes Knowledge of organizational, operational, and programmatic concepts and practices applied by public, private, or nonprofit agencies and organizations engaged in public health or other health-related activities. Knowledge of the methods, processes, and techniques used to develop and deliver public health or health-related programs in State and local settings. Knowledge of a specialized public health program. Knowledge of, and skill in, the application of administrative or analytical methods and techniques necessary for working within the framework of a public health or related organization and carrying out specific program functions. Skill in oral and written communications, gathering and conveying information, making oral presentations, and preparing reports, correspondence, and other written materials. Note: Resume must show supporting details. OR EDUCATION: Successfully completed a Ph.D. or equivalent doctoral degree or 3 full years of progressively higher-level graduate education leading to such a degree with a major study in public health or other field of study with course work directly related of the position to be filled. NOTE: YOU MUST SUBMIT COPIES OF YOUR TRANSCRIPTS. OR COMBINATION OF EXPERIENCE AND EDUCATION: A combination of education and experience may be used to qualify for this position as long as the computed percentage of the requirements is at least 100%. NOTE: You must submit a copy of your transcripts with your application. FEDERAL TIME-IN-GRADE (TIG) REQUIREMENT FOR GENERAL SCHEDULE (GS) POSITIONS: Merit promotion applicants must meet applicable time-in -grade requirements to be considered eligible. One year at the GS-09 level is required to meet the time-in-grade requirements for the GS-11 level. TIG applies if you are in a current GS position or held a GS position within the previous 52 weeks. NOTE: Applicants applying as VEOA candidates who are current GS civil service employees or are prior GS civil service employees within the past 52 weeks must also meet time-in-grade requirements. KNOWLEDGE, SKILLS AND ABILITIES (KSAs): Your qualifications will be evaluated on the basis of your level of knowledge, skills, abilities and/or competencies in the following areas: 1. A Bachelor of Science degree or higher with emphasis in a biological science or Public Health is desirable, and at least (3) years related job experience in the Public Health career field. 2. Knowledge of the missions, organizations, programs, and requirements of health care delivery systems and the relationships of Public Health, Force Health Management, and Occupational Medicine within the Air Force and Air Force Medical Service; and of Air Force Customer Satisfaction Priorities to demonstrate sensitivity and responsiveness to needs and requirements of customers, employees, supervisors, and peers. 3. Knowledge of regulations and standards of regulatory and credentialing groups and directives including requirements for accreditation promulgated by The Air Force Occupational Safety and Health Program, the Food and Drug Administration (FDA), United States Department of Agriculture (and World Health Organization counterparts), Department of Defense Health Affairs, and HQ U.S. AirForce. 4. Knowledge of the principles, concepts, and methodologies of public health including communicable diseases, foreign diseases and their prevention, preventive medicine techniques, epidemiology, occupational safety and health, community environment, bacteriology, microbiology, laboratory techniques, diseases transmissible to man, biophysics, basic anatomy and physiology, medical administration, food and water safety and security, medical intelligence sources, biological warfare/terror agent detection and prevention, and disaster response. 5. Knowledge of AF/DeCA/AAFES/NAF, DOD, CDC state and local safety and security regulations, laws, practices, procedures, and investigative processes as related to public health and occupational standards and requirements. Knowledge of basic PC/small office computer skills and ability to learn new applications/programs used within the health care field. Ability to use word processing, spreadsheets, and presentation materials and charts/graphs is essential. 6. Skill in gathering and analyzing data, delivering briefings, and making recommendations based on complex and diverse data. PART-TIME OR UNPAID EXPERIENCE: Credit will be given for appropriate unpaid and or part-time work. You must clearly identify the duties and responsibilities in each position held and the total number of hours per week. VOLUNTEER WORK EXPERIENCE: Refers to paid and unpaid experience, including volunteer work done through National Service Programs (i.e., Peace Corps, AmeriCorps) and other organizations (e.g., professional; philanthropic; religious; spiritual; community; student and social). Volunteer work helps build critical competencies, knowledge and skills that can provide valuable training and experience that translates directly to paid employment. You will receive credit for all qualifying experience, including volunteer experience. Education IF USING EDUCATION TO QUALIFY: If position has a positive degree requirement or education forms the basis for qualifications, you MUST submit transcriptswith the application. Official transcripts are not required at the time of application; however, if position has a positive degree requirement, qualifying based on education alone or in combination with experience, transcripts must be verified prior to appointment. An accrediting institution recognized by the U.S. Department of Education must accredit education. Click to check accreditation. FOREIGN EDUCATION: Education completed in foreign colleges or universities may be used to meet the requirements. You must show proof the education credentials have been deemed to be at least equivalent to that gained in conventional U.S. education program. It is your responsibility to provide such evidence when applying. ********************ADDITIONAL INFORMATION FOR ACTIVE DUTY SERVICES MEMBERS******************** ACTIVE DUTY SERVICE MEMBERS: The VOW Act requires federal agencies to treat an eligible active duty service member as a veteran, disabled veteran, and preference eligible (as applicable) when applying for civil service positions before the effective release or discharge date. Appointment of military members before the release or discharge date is permissible if the member is on terminal leave. At the time the active duty member applies for a civil position, he or she must submit a "certification" memo in lieu of a DD-Form 214, Certificate of Release or Discharge from Active Duty . Active duty members applying for a civil service position without submitting a valid certification memo or DD-Form 214 with their application will render the member ineligible for the position. The certification memo must originate from the member's military service branch on official letterhead and contain the following: Name/Rank/Grade of Service Member Branch of Armed Forces Dates of Active Service (Start and End Date(s) Expected Date of Discharge/Release from Active Duty Terminal leave start date (if applicable) Expected character of service (honorable or general) and type of separation (i.e. separation or retirement) Must be certified within 120 days of anticipated discharge Signature by, or by direction of the adjutant, personnel office, unit commander, or higher headquarters commander. Note: The VOW Act provides tentative preference. If appointed, a DD Form-214 must be submitted upon receipt Additional information Interagency Career Transition Assistance Program (ICTAP): For information on how to apply as an ICTAP eligible click . To be well-qualified and exercise selection priority for this vacancy, displaced Federal employees must be rated well qualified or above for this position. You must submit a copy of the agency notice, your most recent performance rating, and your most recent SF-50 noting position, grade level, and duty location. Employed Annuitants (Reemployed Annuitants): Applicants in receipt of an annuity based on civilian employment in the Federal Service are subject to the DoD Policy on The Employment of Annuitants. Click for more information. 120-Day Register: This announcement may result in a 120-day register that may be used to fill like vacancies for 120 days after the closing date. Applicants may be referred for consideration as vacancies occur. Military Spouse Preference (MSP) Eligible: MSP applicants, if determined best qualified, must be selected and placed at the highest grade for which they applied. You must include a completed copy of the DD Form 3145-4, Military Spouse PPP Self-Certification Checklist dated within 30 days along with the documents identified on the checklist to verify your eligibility for MSP. Click to obtain/download a copy of the DD Form 3145-4, Military Spouse PPP Self-Certification Checklist. Priority Placement Program (PPP) Applicant Eligible: PPP Applicants, if determined well qualified and selected, will be placed at the at the full performance level. You must include the applicable completed copy of the PPP Self-Certification Checklist dated within 30 days along with the documents identified on the checklist to verify your eligibility as a PPP Applicant. Click to obtain/download a copy of the applicable PPP Self-Certification Checklist (DD3145-1 through DD3145-4, select the appropriate checklist for your claimed preference). To determine the applicable PPP Self-Certification Checklist required to substantiate the eligibilities you are claiming, refer to the AF Civilian Employment Eligibility Guide located in the Required Documents section of this vacancy announcement. is available to a Federal employee hired on/after 5 Nov 2016, who is a veteran with a service-connected disability rating of 30% or more. For more information, click . If you have questions regarding this announcement and have hearing or speech difficulties click . Tax Law Impact for PCS: On 22-Dec-2017, Public Law 115-97 - the "Tax Cuts and Jobs Act of 2017" suspended qualified moving expense deductions along with the exclusion for employer reimbursements and payments of moving expenses effective 01-Jan-2018 for tax years 2018 through 2025. When you perform a Civilian Permanent Change of Station (PCS) with the government, the Internal Revenue Service (IRS) considers the majority of your entitlements to be taxable. Visit GSA Bulletin FTR 20-04 for additional information. GROUP ID: DOAF

Biomend Life Sciences is seeking a proactive and driven Business Outreach Executive to lead client engagement efforts across Kerala. This role is central to expanding our presence in the genomics and microbiome diagnostics space. Success in this position means establishing strong relationships with healthcare professionals, identifying new opportunities, and effectively communicating the clinical value of our solutions. You’ll play a key role in building awareness of our personalized microbiome and genomics services, driving adoption in hospitals, clinics, and wellness centers. Responsibilities Build and maintain relationships with doctors, clinics, hospitals, and wellness institutions across Kerala. Conduct outreach visits, presentations, and discussions to promote our gut microbiome and genomics testing services. Identify business opportunities, gather market intelligence, and report insights to the strategy and marketing teams. Coordinate with internal teams to ensure timely support, kit delivery, and customer satisfaction. Participate in awareness campaigns, CME programs, and exhibitions to represent the brand. Maintain detailed records of outreach activities, leads, and follow-ups using CRM tools. Qualifications B.Sc. or M.Sc. in Life Sciences (Microbiology, Biotechnology, Genetics, or related fields). Minimum 1 year of experience in sales, business development, or marketing in healthcare, diagnostics, or life sciences (preferred). Strong verbal and written communication skills in English and Malayalam . Excellent interpersonal skills and the ability to build trust with healthcare professionals. Willingness to travel locally for field visits and client meetings. Self-motivated, target-driven, and eager to contribute to a growing organization. Job Types: Full-time, Permanent Work Location: In person Application Deadline: 26/07/2025

Job Title: Fermentation Executive – Vinegar Production The Fermentation Executive oversees the vinegar fermentation process, ensuring product quality and consistency. They lead production teams, optimize yields, and scale up processes as needed. Responsibilities include developing new product lines, ensuring food safety compliance, and analyzing market trends. They also collaborate with R&D and marketing teams to innovate and improve products. The role involves managing quality control, troubleshooting production issues, and maintaining regulatory standards. Strong leadership and expertise in fermentation processes are essential. Preferred Qualifications: MSc in Microbiology, Biotechnology, or an equivalent qualification in Food Technology; BTech or MTech in a related field, or other relevant qualifications that align with the responsibilities of the Fermentation Executive role. A minimum of 2-3 years of relevant experience is also required. Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Food provided Paid time off Provident Fund Schedule: Day shift Morning shift Rotational shift Supplemental Pay: Overtime pay Performance bonus Yearly bonus Education: Bachelor's (Preferred) Experience: Fermentation: 2 years (Preferred) Work Location: In person

Job Role: Quality Control Microbiologist Conduct microbiological testing of raw materials, in-process, and finished products. Monitor hygiene, sanitation, and environmental conditions in the processing unit. Ensure compliance with FSSAI, ISO, HACCP, and food safety standards. Maintain accurate laboratory records and test reports. Test water, air, equipment, and surfaces for microbial contamination. Investigate out-of-specification results and contamination sources. Support audit preparations and documentation requirements. Train plant staff on hygiene and microbiological safety. Perform routine swabbing and environmental monitoring. Suggest improvements in quality control procedures and preventive actions. ualifications: Education : B.Sc. / M.Sc. in Microbiology, Food Technology, Biotechnology, or related discipline from a recognized university. Experience : 1–3 years of hands-on experience in microbiological testing, preferably in the food or agro-processing industry. (Freshers with strong academic background may also be considered.) Job Type: Full-time Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Food provided Paid time off Provident Fund Schedule: Day shift Morning shift Rotational shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Roles and Responsibility Develop and maintain strong relationships with patients, families, and healthcare professionals. Provide excellent customer service and ensure patient satisfaction. Manage and coordinate patient appointments, scheduling, and communication. Collaborate with healthcare teams to develop and implement patient care plans. Maintain accurate and up-to-date patient records and reports. Identify and address patient concerns and issues promptly. Job Requirements Minimum 2 years of experience in patient relationship management or a related field. Strong knowledge of biotechnology, pharmaceuticals, or clinical research. Excellent communication, interpersonal, and problem-solving skills. Ability to work effectively in a fast-paced environment and prioritize tasks. Strong analytical and organizational skills with attention to detail. Experience with electronic health records (EHR) systems is an asset.

We are looking for a highly skilled and compassionate Nurse to join our team at Vijaya Diagnostic Centre Limited in the Biotechnology industry. The ideal candidate will have 2-5 years of experience in nursing, with a strong background in providing high-quality patient care. Roles and Responsibility Provide comprehensive nursing care to patients, including assessing, planning, implementing, and evaluating individualized care plans. Administer medications, perform medical procedures, and maintain accurate records of patient treatment and progress. Collaborate with interdisciplinary teams to develop and implement effective care strategies that meet patient needs. Monitor patient vital signs, administer medications, and perform routine diagnostic tests as needed. Maintain a clean, safe, and organized work environment, adhering to infection control policies and procedures. Develop and maintain relationships with patients, families, and healthcare professionals to ensure optimal communication and collaboration. Job Requirements Bachelor's degree in Nursing or related field required; Master's degree preferred. Minimum 6 years of experience in nursing, with a focus on patient care and satisfaction. Possess strong knowledge of nursing principles, practices, and protocols, along with excellent communication and interpersonal skills. Demonstrate the ability to prioritize tasks effectively in a fast-paced environment while maintaining attention to detail and accuracy. Familiarity with electronic health records (EHR) systems and other healthcare software applications is essential. Commitment to ongoing learning and professional development, staying current with best practices in nursing care.