2560 Microbiology Jobs - Page 30

About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About the role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturers quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* About you Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology In addition to a relevant educational degree, candidates must have a minimum 4 years work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About the role DNV Product Assurance AS is one of the leading Notified Bodies for IVD medical devices. The unit is entitled to carry out tasks related to conformity assessment of IVD medical devices with Regulation (EU) 2017/746 In Vitro Medical Devices before such products are placed on the market. The role of Clinical Assessor is to assess performance data supporting safety and performance of IVD medical devices. Main tasks in this role are: Performing assessment and preparing reports of clinical performance aspects of legal manufacturers technical documentation according to the requirements given in the Regulation (EU) 2017/746. Evaluation of the summary of safety and performance reports for high-risk IVD medical devices. Review and approval of performance evaluation report and other relevant performance documentation for accuracy and compliance with the requirements in the Regulation (EU) 2017/746. Education and Competencies required: Clinical Assessors shall have a technical college degree in a relevant product or medical area, as described below. Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology What we offer A competitive compensation and benefit package DNV training and qualification program A professional community in a prestigious technological company Possibilities to work with interesting and challenging projects Access to an extensive competence network Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. About you Candidates must have a minimum 4 years work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the Assessment of Performance evaluation data, including Scientific Validity and Clinical Performance, or conducting performance evaluation studies for IVD devices. A PhD in a relevant area for IVD medical devices can substitute 3 years of work experience provided that it includes 2 years experience in Performance evaluation. Personal Qualities: Analytical approach. Strong communication skills. Customer focus. Excellent reporting skills. Ability to work independently and efficiently. Ability to form recommendations on certification in complex cases.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cepheid, one of Danaher s 15+ operating companies, our work saves lives and we re all united by a shared commitment to innovate for tangible impact. You ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher s system of continuous improvement, you help turn ideas into impact innovating at the speed of life. At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world s most complex health challenges. Together, we bring MORE change to the world. Learn about the Danaher Business System which makes everything possible. The Quality Control Analyst is responsible for ensuring inspection process as per MDR 2017, European regulations, ISO 13485 and Cepheid corporate quality system requirements. This position reports to the quality manager and is part of the quality and regularity compliance department located in Cepheid Manufacturing facility, Bengaluru and will be an on-site role. In this role, you will be responsible for: Perform inspections of incoming, in-process and finished products/stability testing and identify/troubleshoot product if non-conformance. Performs/monitor the laboratory equipment validation / calibration / maintenance and ensure quality control lab as per safety standards/GLP. Write/review SOP/WI, technical reports or documentation such as deviation reports, testing protocols, and trend analyses. Support for internal/external audit schedule, NC, CAPA for site. The essential requirements of the job include: Master s degree in Biochemistry, Molecular Biology, Microbiology, Biotechnology or related discipline and a minimum of 3+ years related to quality control experience. 2+ years experience in Vitro Diagnostics (IVD) is mandate. Need to act as competent technical staff for supervision the testing / analysis of diagnostic reagents & kits Business Schedule Requirement Must be flexible to work in shift-based time schedules (able to consistently maintain schedules and meet timelines). It would be a plus if you also possess previous experience in: Experience working with medical device quality systems in compliance with MDR and ISO 13485 Experience in leading continuous improvement efforts, in both quality systems and IVD products. Required strong interpersonal skills, effective communication skills / micro-soft word and excel knowledge / strong multi-tasking skill. Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. Join our winning team today. Together, we ll accelerate the real-life impact of tomorrow s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The ideal candidate should have 1-3 years of experience in the field of Microbiology QC. The candidate should have a good understanding of the principles and practices of Quality Control and should be able to work independently. The candidate should have excellent communication and interpersonal skills, and should be able to work in a team environment. The candidate should have a good understanding of the principles and practices of Microbiology and should be able to work independently. The candidate should have good problem-solving skills and should be able to work under pressure. The candidate should be able to perform the following tasks: Monitor and maintain the quality of the products manufactured Ensure that the products are manufactured as per the set standards Monitor and maintain the quality of the raw materials used Ensure that the products are manufactured as per the set standards Monitor and maintain the quality of the finished products Ensure that the products are manufactured as per the set standards Monitor and maintain the quality of the packaging materials used Ensure that the products are manufactured as per the set standards Monitor and maintain the quality of the environment in the production area Ensure that the products are manufactured as per the set standards Monitor and maintain the quality of the equipment used in the production process Ensure that the products are manufactured as per the set standards Monitor and maintain the quality of the laboratory tests conducted Ensure that the products are manufactured as per the set standards Monitor and maintain the quality of the documentation related to the production process Ensure that the products are manufactured as per the set standards The candidate should have a degree in Microbiology or a related field.

JOB DESCRIPTION Medical Coding is the process of taking a patient's health care information like medical procedures, diagnosis, necessary medical equipment and medical services information from the Physician's Notes Following strict coding guidelines within established productivity standards. Addressing coding related inquires for providers as needed, U.S. only. Attending meetings and in-service training to enhance coding knowledge, compliance skills, and maintenance of credentials. Maintaining patient confidentiality. Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy). * Should be a good team player with good attitude. * Should be flexible to work in rotational shifts whenever required *Ready to Join with us immediately. Medical Coding is the fastest-growing profession in the healthcare industry today. IT is a niche specialization and the demand for trained and certified medical coders is increasing exponentially and bound to increase in upcoming years, especially in India. You have at least a Diploma/Degree in any field. This role is open to fresh graduates with excellent English communication skills. You pay strong attention to details and are capable of delivering top-quality work You are goal-oriented and thrive in fast-paced environments Contact Us: HR Lavanya 9566157632

JOB DESCRIPTION Job Title: Sr Executive Sourcing Partner (Costing) Job Location: Bangalore Reporting to: Associate General Manager Job Grade: 9-II About Syngene : Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role : Responsible for achievement of business objectives by ensuring timely supply of requisite input materials i. e. raw materials, consumables, solvents, glass wares, reagents, stationeries etc; Periodic follow ups with all the stakeholders, service both internal and external customers to meet the organization standards as well to meet the requirements of regulatory authorities. Role Accountabilities Submitting RFQ with vendors and updating Rawmaterials cost sheet To track the purchase request (PR) in SAP / request for quote for key rawmaterials and Maintain tracker for the quotes submitted with operations team for proceeding for orders Sourcing right vendors globally for all raw materials, reagents, consumables and choosing competitive vendors. Support of vendor safety audits and Annual Rate contract finalisation Good negotiation with vendor for Pricing, Quality, INCOTERM, delivery turnaround time (TAT) etc. , Analysing spend data Monthly MIS support Finding opportunities for executing annual rate contracts Coordination with cross function team for licensing requirements for restricted materials Vendor Rating Fulfil end user requirements of emergency cases for quotes and delivery of materials on day to day basis Regular updates to the end users Experience Should have Strategic sourcing with Minimum of 4-7 years experience in Pharma in Pharma / CRO with same domain Sound knowledge on Chemicals, API, Impurities, Working Standard, Excipients, Cell culture media, glass wares and Packing materials etc Technical/functional Skills: SAP MM module Good knowledge on Import regulations for licensed and restricted products. Knowledge on Customs and Excise procedures Negotiation skill and vendor development Effective communication skills both written and verbal Behavioral Skills: Effective communication skills both written and verbal Time management Customer centric, empathy and determination Positive attitude, Ethics and Code of Conduct Education B. Sc, . Chemistry / Microbiology / Biotechnology (Chemistry as one of the subject in Degree ) Diploma in Materials Management from any reputed institute is an added advantage

Key Responsibilities Review and verify accompanying documentation for regulatory samples received from authorities. Coordinate with officials for any clarifications required. Categorize samples upon receipt and assign relevant testing parameters in accordance with FSSR, surveillance plans, or specific instructions from regulatory bodies. Ensure that all testing procedures are performed strictly in accordance with approved protocols and regulatory standards. Conduct verification and authorize final reports as per the requirements of FSSR, clearly indicating compliance or non-compliance with applicable food standards. Oversee proper handling, storage, retention, and timely disposal of regulatory samples in line with SOPs. Ensure turnaround times (TAT) are met as per requirements for import, legal, and surveillance samples. Manage timely uploading of completed reports onto the Infolnet portal following analysis. Collaborate with Microbiology and Instrumentation teams to ensure timely testing and integrated reporting. Participate in the submission of regulatory data, including monthly testing summaries, feasibility responses, and other official communications as required by FSSAI or FDA. Supervise laboratory personnel engaged in food testing activities and ensure adherence to quality protocols. Review test results generated by junior analysts and technicians for completeness and accuracy. Train and mentor team members on regulatory testing methodologies and best practices. Stay updated with changes in FSSAI guidelines, methods, and relevant national/international food laws to ensure continuous compliance. Qualifications Educational Background: Master’s degree in Chemistry (Analytical, Organic, or Inorganic), B.Tech in Food Technology, or any other degree with specialization in Food Technology. Experience: 3-5 years of relevant experience of working as a FSSAI Food Analyst Required Skills Analytical Skills: Proficiency in conducting chemical and microbiological analyses. Time Management: Ability to manage multiple tasks efficiently and meet deadlines. Attention to Detail: Meticulous in documentation and adherence to protocols. Team Collaboration: Effective communication and teamwork abilities Preferred Skills Familiarity with laboratory instruments such as HPLC, GC-MS, and ICP-MS. Knowledge of food safety standards and regulations (e.g., FSSAI guidelines). Experience with Laboratory Information Management Systems (LIMS).

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. The opportunity Join our mission in TAPI: Advancing health from the core. TAPI will soon continue as a standalone organization, fully dedicated to API & CDMO services. Join us on our standalone journey! Are you ready to make a significant impact on our company's future? We are seeking a Site Quality Head to lead our quality assurance and control efforts at our production site in Malanpur, India. In this pivotal role, you'll be the architect of our quality management framework, ensuring we maintain the highest standards in production and product excellence. As the leader of our site quality function, you'll collaborate closely with our production and operations teams to create a seamless and consistent experience for our customers. Your influence will extend beyond strategy; you'll be a key player in nurturing growth within our quality community. Additionally, we need someone who can roll up their sleeves and be a hands-on quality partner for our site teams, bringing your expertise directly to the heart of our operations. You'll also be responsible for designing and implementing quality systems, driving continuous improvement and high performance across our organization. Join us and be a driving force in shaping a future of excellence for our team! How You'll Spend Your Day Lead the Quality organization, including Quality Control, Microbiology, Compliance, Systems, and Assurance Operations Ensure and continuously improve the Quality Management System Guarantee products meet cGMP requirements and registered specifications Serve as the senior authority on product quality and market actions Identify and mitigate quality risks to ensure product safety and effectiveness Collaborate with Site GM and Global Quality to design and implement the site quality program Oversee quality data management and delivery to stakeholders Direct laboratory activities, including testing and approval of materials Foster a culture of quality and encourage open communication and innovation Maintain strong partnerships with the site leadership team Act as a strategic partner to ensure project timelines and objectives are met Provide leadership during inspections by internal, customer, and Health Authorities Ensure Quality KPIs meet targets and monitor CAPA commitments Manage the annual Quality Operations budget and resources Assist the Head of Quality function TAPI and approve related documents Perform additional responsibilities as assigned by the Head of Quality function TAPI Reporting to the VP Quality directly and incumbent will be part of site leadership team under the lead of the General Manager Your Experience And Qualifications The ideal candidate will possess a degree in Chemistry, Science, Chemical Engineering, or a related scientific field They should have over 10 years of experience in the pharmaceutical or API production industry, specifically in India Proven experience in leading a Site Quality Head role The candidate must have extensive experience in preparing for and managing inspections and audits from global authorities such as the FDA, local and European authorities, and Japanese regulatory bodies They should have in-depth knowledge and hands-on experience in deviation management, Corrective and Preventive Actions (CAPA), quality systems, and handling complaints Additionally, a solid background in Quality Control processes and practices is required The ideal candidate is an experienced leader with a proven track record of managing teams You will be responsible for leading Quality Assurance (QA), Quality Control (QC), and Quality Systems (QS) teams You possess excellent communication skills, capable of conveying complex ideas clearly and effectively You have the ability to build strong relationships and foster collaboration across teams You are passionate about inspiring and motivating team members to achieve their best You are comfortable making decisions under pressure, with a strong sense of integrity You demonstrate empathy and understanding, creating a supportive and inclusive work environment Reports To Direct reporting line to Head of Quality with a dotted line to the Site General Manager Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Role: Senior Manger – API Supply chain team Qualification: B.E. (Chemical) – preferred OR M. Sc (Chemistry) / Biotechnology / Microbiology OR B.Sc.+ MBA (Operations) Experience: Chemical Engineer with 3-4 years of experience OR candidate from other educational background with 6-9 years of experience Department: API Supply chain team Industry Preference: Pharma, Chemical, Paint, Agro, Speciality Chemicals Job Location: Andheri, Mumbai Areas Of Responsibilities Capacity Planning & Capacity Effective Utilization Campaign Planning Business Continuity – De risking Plan (OS to IH, IH to OS), AVD Plan Implementation Site Transfer- API & Intermediate Cost Reduction Batches – MRP - à Commercial Supply NPL, Filling & Query Batches Supply management SCM Process maturity - Norms Setting, Cost to Serve, Planning Master Data Controller Chronic Supply Issues Resolution Responsible for Team Development & people Management - Training/ capability development of team Internal Interactions (within the organization) - Plants, RA, Procurement, R&D , Quality, LCM

Responsible for microbial analysis of Raw Material, Hold time samples and Finish Products & stability samples. Responsible for sampling & Microbial analysis of all types of water. Responsible for preparation of agar plates and planning for Environmental Air monitoring in Production Area, Dispensing Area, Sampling Area and in Microbiology laboratory. Responsible for microbial Assay (Antibiotic & Vitamins). Responsible for handling, operation and calibration Instruments used in Microbiology Laboratory. Responsible for online reporting/raw data compilation and completion of routine sample analysis in LIMS Responsible for preparation and Sterilization of Media and Sterilization of Glassware. Responsible for proper handling of microbial culture and ensure their sub culturing. Responsible for preparation of media as per requirements and maintain the log books and sterilization and verifying the proper sterilization by chemical indicator strips. Responsible for handling and Maintenance of all documents and records related to the routine work. Responsible for preparation the reports on time and giving to section in charge for checking and releasing on time. Responsible for daily verification of instruments. Responsible for maintenance of media and chemical reagents and to check their expiry and receiving. Responsible for monitoring of temperature, relative humidity and differential pressure. Responsible for fumigation of Microbiology Laboratory Responsible for monitoring the proper cleaning of micro lab including all the instruments inside the micro lab maintain the cleaning record or log books as per the SOPs.

Job Purpose: To lead and manage the audits (internal & external) and compliance programs in accordance with BRC Global Standard for Food Safety Issue 9 , FSSAI regulations , customer specific (third party / second party) and other applicable Indian food laws. This role ensures certification readiness, regulatory compliance, and continuous improvement in food safety and quality systems by proactively identifying non-conformances, driving corrective actions, and fostering a culture of operational excellence. Key Responsibilities: Plan, schedule, and conduct internal audits to verify compliance with BRC Issue 9, FSSAI, and organizational food safety protocols. Coordinate and facilitate external audits (certification, customer, regulatory) and inspections, ensuring preparedness and timely closure of non-conformities. Prepare and maintain audit documentation including audit plans, checklists, audit reports, and corrective action logs. Ensure all operations, processes, and documentation are consistently aligned with BRC, FSSAI, and customer-specific standards . Lead root cause analysis (RCA) for non-conformities and ensure implementation and verification of effective Corrective and Preventive Actions (CAPA) . Monitor CAPA effectiveness on the shop floor through verification audits and follow-ups. Conduct training and awareness programs on food safety, BRC standards, regulatory updates, and audit readiness for cross-functional teams. Drive a compliance-first culture by promoting awareness, ownership, and continuous improvement in food safety and quality. Maintain audit records, CAPA tracking logs , compliance dashboards, and traceability documentation as per BRC documentation requirements. Prepare management review reports summarizing audit outcomes, compliance trends, and key improvement opportunities. Act as a key resource in maintaining BRC certification , including gap assessments and readiness checks for recertification. Liaise with cross-functional teams to ensure timely implementation of new requirements introduced under BRC Issue 9, FSSAI amendments or customers’ end . Identify and propose process improvements in the audit and compliance framework to enhance system robustness and reduce risk. Qualifications & Experience: Bachelor’s degree in Food Technology, Microbiology, Quality Assurance, or a related field . Postgraduate will be preferred. 3 to 5 years of experience in food industry audits, in a BRC-certified or GFSI-recognized environment. Certified Internal or Lead Auditor (preferably IRCA or equivalent) for BRC / FSSC 22000. Strong knowledge of BRC Global Standard for Food Safety Issue 9 , FSSAI regulations , HACCP , and other applicable Indian food safety legislation. Proficiency in MS Office , ERP , and document control systems. Strong written and verbal communication skills , with the ability to interface effectively across departments. Core Competencies: Deep understanding of food safety management systems , regulatory compliance, and risk-based auditing. High attention to detail, analytical thinking , and problem-solving capabilities. Ability to influence, train, and engage cross-functional teams in a structured audit and compliance program. Strong commitment to regulatory compliance , ethical conduct , and continuous improvement .

Qualifications  Graduate/ Post Graduate in Food Science/ Technology, Microbiology, Chemical or Process Engineer or any related field. Experience  Minimum 5 years at Assistant Manager level or equivalent in R&D having exposure on Frozen Foods, Ready to Eat, Snacks and Baking.  Experience & Technical Know How in Frozen Food industry will be desirable.  Requisite multi product technology and multi location/ cultural experience (Production, Quality etc Technical / Functional  Good know how of ingredients / processes and technologies involved in Frozen Foods, Ready to Eat, Snacks and Baking.  Good Know how on FDA, EU & FSSAI regulations and know how in SAP.  Good commercial & operational understanding, - Financial, Marketing and Consumers. Job Types: Full-time, Permanent Pay: ₹40,000.00 - ₹80,000.00 per month Schedule: Rotational shift Supplemental Pay: Yearly bonus Work Location: In person

Job Title: Lab Technician Job Summary: We are seeking a detail-oriented and skilled Lab Technician to join our team. The ideal candidate will be responsible for conducting laboratory tests, maintaining lab equipment, and ensuring accurate data recording to support research, diagnostics, or quality control. Key Responsibilities: Perform laboratory tests and experiments following standard procedures. Prepare samples, reagents, and equipment for analysis. Record and interpret test results with accuracy. Maintain and calibrate laboratory instruments and equipment. Ensure compliance with safety and hygiene regulations. Assist in research and development projects as required. Manage and store laboratory data and reports properly. Collaborate with scientists, researchers, and other technicians. Handle chemical and biological waste disposal safely. Qualifications & Requirements: Education: Diploma/Bachelor’s degree in Medical Laboratory Technology, Biology, Chemistry, or a related field. Strong knowledge of lab equipment, procedures, and safety protocols. Proficiency in using lab software and data analysis tools. Good organizational and multitasking abilities. Strong attention to detail and problem-solving skills. Preferred Skills: Experience with microbiology, hematology, or clinical chemistry techniques. Knowledge of Good Laboratory Practices (GLP). Ability to work independently and in a team environment. Job Type: Full-time Pay: ₹25,000.00 - ₹27,000.00 per month Benefits: Provident Fund Supplemental Pay: Yearly bonus Education: Bachelor's (Required) Experience: total work: 1 year (Preferred) Location: Delhi, Delhi (Required) Work Location: In person

Food Safety Lead Job ID 228843 Posted 10-Jul-2025 Role type Full-time Areas of Interest Facilities Management Location(s) Coimbatore - Tamil Nadu - India Job Summary: The Food Safety Lead is responsible for overseeing and ensuring food safety compliance across multiple office locations. This role involves developing and standardizing food safety protocols, conducting audits, managing vendor compliance, and leading a team of food safety executives or coordinators. The ideal candidate will have strong leadership skills, a deep understanding of food safety regulations, and experience managing multi-site operations. Key Responsibilities: Develop, implement, and monitor food safety policies and procedures across all office locations. Lead and coordinate food safety audits, inspections, and risk assessments at each site. Ensure compliance with local and international food safety standards (FSSAI, HACCP, ISO 22000, etc.). Manage and mentor a team of food safety executives or coordinators across different sites. Liaise with catering vendors and facility partners to ensure adherence to food safety protocols. Analyze audit findings and implement corrective and preventive actions (CAPA). Conduct training sessions and workshops for staff and vendors on food safety and hygiene practices. Maintain centralized documentation and reporting systems for all food safety activities. Collaborate with cross-functional teams including housekeeping, pest control, and maintenance to ensure a safe food environment. Stay updated on regulatory changes and industry best practices and update internal policies accordingly. Qualifications: Bachelor’s or Master’s degree in Food Technology, Microbiology, Public Health, or a related field. Certification in HACCP, ISO 22000, or FSSAI is mandatory. 5+ years of experience in food safety or quality assurance, with at least 2 years in a leadership or multi-site role. Strong knowledge of food safety laws, audit procedures, and vendor management. Excellent communication, leadership, and organizational skills. Willingness to travel across office locations as required.

Food Safety Executive Job ID 228841 Posted 10-Jul-2025 Role type Full-time Areas of Interest Facilities Management Location(s) Bengaluru - Karnataka - India, Chennai - Tamil Nadu - India, Cochin - Kerala - India, Coimbatore - Tamil Nadu - India, Madurai - Tamil Nadu - India Job Summary: The Food Safety Executive is responsible for ensuring that all food handling, preparation, and storage within the facility comply with local, national, and international food safety standards. This role involves conducting audits, training staff, and implementing hygiene and safety protocols to maintain a safe and compliant food environment. Key Responsibilities: Monitor and enforce compliance with food safety regulations (FSSAI, HACCP, ISO 22000, etc.). Conduct regular hygiene inspections and internal audits of food service areas, kitchens, and storage facilities. Develop and implement food safety policies and standard operating procedures (SOPs). Train facility staff on food safety practices, personal hygiene, and sanitation protocols. Investigate food safety incidents and implement corrective and preventive actions (CAPA). Maintain documentation and records related to food safety audits, inspections, and training. Coordinate with vendors and caterers to ensure food safety compliance in outsourced services. Stay updated on changes in food safety laws and best practices. Support pest control and waste management programs in food service areas. Collaborate with the housekeeping and maintenance teams to ensure cleanliness and equipment hygiene. Qualifications: Bachelor’s degree in Food Science, Microbiology, Nutrition, or a related field. Certification in HACCP, ISO 22000, or FSSAI preferred. 2–4 years of experience in food safety or quality assurance, preferably in a facilities management or hospitality environment. Strong knowledge of food safety regulations and standards. Excellent communication, training, and documentation skills. Attention to detail and strong problem-solving abilities.

Key Responsibilities: Environmental Monitoring: Conduct routine environmental monitoring of Quality Control, Production, and Warehouse areas, including but not limited to, viable and non-viable particle counting, surface sampling, and air sampling, all in strict adherence to approved procedures. Sampling: Perform accurate and timely sampling of Active Raw Materials (ARMs) and Inactive Raw Materials (IRMs), as well as final lot samples of finished products, according to established protocols. Microbiological Analysis: Execute microbiological analysis of various samples, including environmental swab samples and compressed air samples, utilizing validated methods. Trend Analysis & Reporting: Prepare and submit comprehensive monthly and annual microbiological trend summary reports for environmental monitoring procedures, identifying any deviations or critical trends. Documentation & Compliance: Maintain meticulous logbooks within the Quality Control department, review generated reports for accuracy and completeness, and actively participate in the preparation and revision of Standard Operating Procedures (SOPs). Media Fill Support: Participation in media fill, sample incubation and perform diligent vial observation to assess aseptic processing performance. Team Collaboration: Collaborate effectively with cross-functional teams and proactively take on any additional responsibilities assigned by the Head of Department to support overall QC operations. Qualifications: Bachelor's or Master's degree in Microbiology, Biotechnology, or a related scientific discipline. 1-5 years of experience in Quality Control Microbiology, preferably within a pharmaceutical, vaccine, or sterile manufacturing environment. Proficient in environmental monitoring techniques, microbiological testing, and aseptic practices. Strong understanding of cGMP guidelines and regulatory requirements for pharmaceutical manufacturing. Excellent data analysis, report writing, and documentation skills. Ability to work independently and as part of a team in a fast-paced environment. Detail-oriented with a strong commitment to quality and compliance.

Job Title: Production Manager – Food Industry Location: [Ecotech 1 , Greater noida] Annual CTC: 9 to 10 Lakhs Reporting To: Plant Head / Operations Manager Profile Summary: We are seeking a young, dynamic male professional , around 30 years of age , with strong leadership and production management skills in the food industry . The ideal candidate will bring at least 5 years of hands-on experience in managing production operations, ensuring product quality, and maintaining food safety standards. Key Responsibilities: Oversee daily production operations to ensure optimal output and efficiency. Monitor quality control standards, hygiene, and compliance with FSSAI and GMP norms. Coordinate with procurement, maintenance, and quality teams for smooth production flow. Implement and maintain SOPs and work instructions for production processes. Manage and train the production workforce, ensuring adherence to safety protocols. Analyze production data and reports to identify improvement opportunities. Manage inventory of raw materials and production inputs. Eligibility Criteria: Education (any one): B.Tech / B.E. in Food Technology B. Pharm M.Sc. in Food Science / Microbiology / Biotechnology Experience: Minimum 5 years of experience in the food processing or food manufacturing industry . Exposure to regulated production environments and process improvement initiatives preferred. Age: Around 30 years (30–32 years preferred) Gender Preference: Male candidates only (due to job nature and shift requirements) Job Types: Full-time, Permanent Pay: ₹65,000.00 - ₹70,000.00 per month Benefits: Food provided Work Location: In person

Job Description: Sales Manager – Enzyme and Probiotic Manufacturing Position Title: Sales Manager – Enzymes & Probiotics Department: Sales & Business Development Location: [Company Location] Reporting To: Director – Sales & Marketing / Managing Director ✅ Job Purpose: The Sales Manager will be responsible for driving sales growth of enzyme and probiotics across target industries such as Food & Beverages, Pharmaceuticals, Textiles, Detergents, and Agriculture. The role includes business development, client relationship management, revenue generation, and market expansion. This person will play a critical role in achieving monthly and annual sales targets. Key Responsibilities: 1. Sales Target Achievement: Develop and implement strategic sales plans to meet company targets. Drive B2B sales in both domestic and international markets (if applicable). Manage key accounts and maintain healthy business relationships. 2. New Business Development: Identify and acquire new customers across target industries. Conduct cold calls, client meetings, and industry networking. Convert leads into sales with an effective pitch. 3. Client Relationship Management: Build long-term relationships with customers. Provide technical support in coordination with the R&D team. Address and resolve customer complaints quickly. 4. Sales Pipeline Management: Maintain sales funnel through lead generation, prospecting, and closure. Track leads, follow-ups, and negotiations using CRM software. 5. Pricing & Negotiation: Prepare quotations and negotiate pricing, terms, and conditions. Work with finance and production teams on costings and delivery schedules. 6. Market Intelligence: Monitor competitor activities, market trends, and customer preferences. Provide regular feedback to the R&D and management teams for product and market strategy. 7. Reporting & Documentation: Submit weekly, monthly, and quarterly sales reports. Update sales pipeline and revenue forecasts. Ensure documentation of contracts, orders, and client communications. 8. Exhibitions & Industry Events: Represent the company in industry exhibitions, conferences, and trade shows. Organize and participate in customer workshops and seminars. Qualification & Experience: Education: B.Sc. / M.Sc. in Biotechnology, Chemistry, Microbiology, or MBA in Marketing preferred. Experience: Minimum 3-4 years of industrial sales experience, preferably in enzymes and probiotics or B2B Pharma and Nutraceutical ingredient segment. Job Type: Full-time Pay: ₹50,000.00 - ₹100,000.00 per month Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Language: English (Required) Work Location: In person Expected Start Date: 01/08/2025

Position Title: Quality Assurance (QA) Manager – Enzyme Manufacturing Department: Quality Assurance Location: [Company Location] Reporting To: Head – Operations / Managing Director Job Purpose: The QA Manager will be responsible for implementing, monitoring, and continuously improving the quality management systems (QMS) for enzyme production. The role will ensure that all products meet regulatory, customer, and internal quality standards from raw material procurement to final product dispatch. Key Responsibilities: 1. Quality Management System (QMS) Implementation: Establish and maintain ISO, FSSC, GMP, and other regulatory standards applicable to enzyme manufacturing. Develop, review, and implement SOPs (Standard Operating Procedures) across departments. 2. Product Quality Assurance: Oversee incoming raw material inspections, in-process quality checks, and final product release. Ensure adherence to defined product specifications, batch records, and quality protocols. 3. Regulatory Compliance: Ensure compliance with national and international quality standards (e.g., FSSAI, ISO, Kosher, Halal, etc.). Coordinate with external auditors, certification bodies, and regulatory agencies. 4. Customer Complaint Handling: Investigate customer complaints related to quality issues. Conduct root cause analysis (RCA) and implement Corrective and Preventive Actions (CAPA). Maintain a Customer Complaint Log. 5. Internal Audits and Continuous Improvement: Plan and conduct internal quality audits. Lead continuous improvement projects to minimize deviations, defects, and non-conformities. Monitor KPIs like rejection rate, customer complaints, and process deviations. 6. Supplier Quality Management: Evaluate and audit critical suppliers and raw material vendors. Maintain supplier quality records. 7. Documentation and Reporting: Maintain all QA-related documentation including batch records, COAs (Certificates of Analysis), and deviation reports. Submit monthly QA performance reports to management. 8. Team Management: Lead and mentor QA officers, QC analysts, and lab assistants. Provide regular training on GMP, SOP adherence, and safety protocols. Qualification & Experience: Education: B.Sc. / M.Sc. in Microbiology, Biotechnology, Biochemistry, Chemistry, or related fields. Experience: Preffered with 2 years of experience in QA/QC, preferably in enzyme manufacturing, biotech, or specialty chemicals. Skills Required: Strong knowledge of quality standards (ISO, FSSC, GMP, etc.). Expertise in regulatory documentation and internal auditing. Problem-solving and decision-making ability. Good understanding of enzyme production processes and application requirements. Excellent leadership and team management skills. Strong communication and reporting skills. Job Type: Full-time Pay: ₹30,000.00 - ₹40,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Speak with the employer +91 9978178140 Expected Start Date: 01/08/2025

Department VTC R&D Job posted on Jul 10, 2025 Employment type P-P6-Probationer-R&D Executive Qualification: PhD/MSc in science (Biotechnology, Biochemistry and Microbiology), master’s degree in pharmacy or engineering with biotechnology To perform and be responsible for all the activities and documentation of formulation and filling process development and should have strong knowledge of optimization of different vaccine formulations, stabilizer selection, excipient selection, selection and preparation of adjuvants such as aluminium salts, Oil-In-Water emulsions, Liposome-based adjuvants with TLR agonists and saponin, LNP formulation and preparation, aseptic filling and Lyophilization cycle designing for new vaccine products and troubleshooting for existing vaccines. To perform all the activities and documentation of the formulation and filling process, development and execution of clinical drug product manufacturing for the clinical batches, planning and execution of media fill activities Prepare and Maintain R/D lab documents, equipment and area qualifications as per GMP requirements and Responsible for preparation of process validation and technology transfer protocols as per GMP requirements and co-ordinates with QA, QC, Engineering department for viral vaccine development activities. Responsible to ensuring proper hygiene and entry exit procedures in the respective formulation and filling section and preparation of adjuvant, buffer solutions and other materials & ensuring proper arrangements for their preparation and supply. To coordinate with the central warehouse department for receipt and entry of RM and PM materials. Preparation / supervision of disinfectant solution, cleaning solution, integrity testing of hydrophobic and hydrophilic filters, sanitization and disinfection activities of R/D formulation department. Responsible for QMS such as deviations, MDD, investigation, observation and ensuring its timely closure. Preparation of standard operating procedure and Batch manufacturing records, QRM and protocol related to R/D formulation and filling section. To supervise washing, drying, packing and sterilizations of materials required for R/D development and GMP clinical batch preparation.

We require doctors for Medical Colleges & Hospitals PAN India Qual: MD/MS, DNB, (All Dept) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Vishakha Call/Whatsapp: 9041008939 weps.services17@gmail.com

Position: Microbiologist Organization: Bankai Agrifood Pvt Ltd. Function: QA/QC Location: Kurali, Karjan, Vadodra, Gujarat – India, 391240 Website: www.bankaiagrifood.com Primary Purpose: We are seeking a highly skilled and dedicated Microbiologist to join our team. As a Microbiologist, you will play a critical role in ensuring the quality and safety of our products through the testing and analysis of microbiological samples. Key Accountabilities/Activities: Microbial Testing: Conduct microbial testing of incoming, in-process, and finished products to assess microbiological safety and quality. Conduct microbial testing of water, process section environment, pipelines, equipment, and personnel working in the section. Preparation and Materials: Prepare media, cultures, chemicals, and other necessary materials for microbial testing. Issue materials from the stores as needed for microbiological testing. Compliance and Quality Assurance: Perform quality clearance of in-process and finished products based on established microbiological criteria. Determine the release or hold status of process equipment and activities after microbial testing. Ensure compliance with ISO/HACCP standards and maintain relevant records accordingly. Implement all HACCP points and closely monitor critical points, providing suggestions and reporting on improvements. Documentation and Records: Maintain records of laboratory chemicals, glassware, and equipment to ensure availability and proper functioning. Ensure all required inspections and tests are carried out according to established procedures and techniques. Verify the cleaning and sanitation of all process equipment, pipelines, machines, etc., to prevent microbiological contamination. Coordinate pest control activities to maintain a pest-free environment. Facilitate and monitor the implementation of introduced systems and Total Quality Management (TQM) practices. Coordination and Communication: Complete assigned tasks by seniors promptly and efficiently to contribute to the smooth functioning of the department. Coordinate and arrange for medical testing of personnel as required. Coordinate with other related departments to ensure effective communication and collaboration. Work Relations: Internal: Reporting to Quality Assurance Officer for all Functional as well as administrative purposes. Second level reporting to COO Interface with Production, Quality Control Team, Maintenance, and Procurement teams Interface with HR teams. External: Interface with various suppliers, regulatory agencies, Service Providers, Customers Qualification : Essential: M. Sc. / B. Sc. (Microbiology) / Biotechnology Experience : Essential: Min 1 Year experience in microbial testing of Milk & Milk Products Proven experience in microbiological testing and analysis, preferably within the food or dairy industry. Strong knowledge of microbiological techniques, media preparation, and culture methods. Familiarity with ISO/HACCP standards and their application in a laboratory setting. Attention to detail and accuracy in conducting tests and interpreting results. Excellent organizational and record-keeping skills. Strong communication and teamwork abilities to collaborate effectively with cross-functional teams. Knowledge of relevant regulations and guidelines related to microbiological testing and food safety. Ability to work independently and handle multiple tasks simultaneously Work Environment: 24 X 6 (6 days a week) Shift Details: General Shift. (09:00 AM – 5:30 PM), Shift might rotate

Company Description We suggest you enter details here. Role Description This is a full-time role for a Junior Microbiologist at CAPITAL AGRI TECHNOLOGIES PRIVATE LIMITED, located in Mansa, Gandhinagar. The Junior Microbiologist will be responsible for conducting microbiological tests and assays, maintaining laboratory equipment, performing quality control checks, and ensuring compliance with quality assurance protocols. The role includes sample preparation, data collection, and result analysis to support research and development activities. Qualifications Proficiency in Laboratory Skills and handling Laboratory Equipment Strong background in Microbiology Experience in Quality Control and Quality Assurance Attention to detail and accuracy in data collection and analysis Bachelor's degree in Microbiology, Biology, or related field Good communication and teamwork skills Prior experience in the agricultural technology or biotechnology sector is a plus

Experience in quality control within the Ayurveda or pharmaceutical industry Proficiency in analytical skills and laboratory skills Bachelor's degree in Chemistry, Microbiology, Pharmacy, or related field 1-3 years of experience in quality control Must be located in commutable distance to Bavla, Gujarat, India Job Type: Full-time Pay: ₹200,000.00 - ₹300,000.00 per year Benefits: Provident Fund Schedule: Day shift Education: Master's (Required) Location: Bavla, Ahmedabad, Gujarat (Required) Work Location: In person

Summary: Home Health Coder is responsible for coding using ICD-10 all diagnoses and applicable procedures of outpatient service visits. The position is also responsible for reviewing OASIS, Plan of Care and abstracting visit data for billing and data collection purposes. Job Description: Accurately assign ICD-10-CM codes to diagnoses from the care plans and documentation submitted by the client. Prospectively reviews OASIS assessments and Plan of Care to ensure appropriateness, completeness and compliance with federal and state regulations and organization policy. Probe clients’ clinicians when code assignments are unclear or when documentation is inadequate or ambiguous. Act as a subject matter expert regarding Coding and OASIS questions by clients and key stakeholders Review and identify errors and report them to supervisor or department manager for follow-up. Identifies trends in clinical documentation and/or potential problems and works with quality team to develop action plans to address opportunities for improvement. Maintains daily productivity and turnaround times. Assists with initial orientation and education/training of staff. Reads and reviews coding guidelines, Medicare updates, professional journals, etc. to maintain an up-to-date working knowledge of coding and reimbursement principles. Requirements /Qualification: Graduates / Post-Graduates in Life Science (MBBS, BDS, BHMS, BAMS, BUMS, Nursing, Pharmacy, Biotechnology, Microbiology, Biochemistry Pharmacy, Physiotherapy, Zoology, Microbiology, BAMS, BHMS, BUMS Exceptional knowledge of Anatomy, Physiology, Pharmacology and Medical Terminologies. BCHH-C certification is mandatory. Proficient Computing and Logical Reasoning skills. Excellent communication skills, both verbal and written. Who should not apply? If you want to work from home, Please do not apply. If you don't have BCCHH-C certification, Please do not apply. Freshers kindly do not apply (This position is only for experienced Home Health Coders) If you don't have more than 2 years of experience in Home Health Coding, Please do not apply. Salary/Compensation: This is purely based on your experience and your performance in the Interview. Job Type: Full-time Pay: ₹25,000.00 - ₹60,000.00 per month Benefits: Health insurance Life insurance Work from home Schedule: Day shift Monday to Friday Ability to commute/relocate: Pune, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Experience: Home Health Coding: 2 years (Required)