Location : Trichy City : Trichy State : Tamil Nādu (IN-TN) Country : India (IN) Requisition Number : 38796 Business Title: Senior Executive - Research & Development Global Job Title: Anl II Product Development Global Function: Research and Development Global Department: Product Development Country/Region: India Role Purpose Statement : Undertake Innovation projects in the area of Product and Process development related to Edible Oils, Fats, and Margarine. Main Accountabilities: Ensure food safety & quality of Bunge products and in compliance to all food laws. Develop new products and optimize existing products on quality, application, cost and delivery. Plan, conduct and monitor progress of pilot scale trials in line with innovation pipelines. Lead a team of junior management in new product and process developments, renovations, pilot plant & scale up operations, cost reduction exercises etc. Carry out competition benchmarking time to time and come up with continuous improvement opportunities. Liase with application, operations etc. on new product development & delivery, cost reduction, scale ups, operations etc. Provide oils & fats support to bakery ingredient portfolio teams Knowledge and Skills: Behavior Use knowledge of Bunge’s business, structure and strategy to develop innovative solutions to improve results or eliminate problems. Build partnerships, appropriately influence to gain commitment, foster talent and coach others to grow in current or future roles.. Drive results through high standards, focus on key priorities, organization, and preparing others for change. Technical Sound knowledge of basic sciences & engineering Well versed with analytical testing & handling of analytical equipment’s such as GC, HPLC, IR, UV etc Experience in handling pilot / plant operations. Basic Knowledge of food applications (baking, frying, culinary etc.), food laws (FSSAI, FPO etc.), Microbiology, process control aspects, functional & protective packaging Special features of job: Ability to manage product & process development and identify synergies among various operations & food applications. Other requirements: Good at computers & presentation skills. Travel to factories, markets etc Education & Experience: Educational qualifications: First Class Graduate in Chemical Engineering / Oil & Fats Technology / Food Technology / master's in science from a Premier Institute Experience: Above 4 years in Chemical Process / Oils & Fats / Food Industries Personality requirements: Good Analytical & Problem Solving ability Effective Communication Skills Entrepreneurial Spirit Ability to see synergies For behavior competencies please refer to the Bunge Leadership Model Bunge (NYSE: BG) is a world leader in sourcing, processing and supplying oilseed and grain products and ingredients. Founded in 1818, Bunge’s expansive network feeds and fuels a growing world, creating sustainable products and opportunities for more than 70,000 farmers and the consumers they serve across the globe. The company is headquartered in St. Louis, Missouri and has 25,000 employees worldwide who stand behind more than 350 port terminals, oilseed processing plants, grain facilities, and food and ingredient production and packaging facilities around the world. Bunge is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, transgender status, national origin, citizenship, age, disability or military or veteran status, or any other legally protected status. Bunge is an Equal Opportunity Employer. Minorities/Women/Veterans/Disabled Show more Show less

Job Title: QA/QC Executive Location: Jigani Industrial Area, Bangalore Company: Bonaiyu Health Pvt. Ltd. Salary: ₹30,000 per month Experience: 3–4 years Industry: Pharmaceutical / Nutraceutical About Bonaiyu Health Bonaiyu Health is a forward-thinking nutraceutical company known for its innovation in advanced delivery formats such as mouth-dissolving strips and functional shots. We are committed to upholding the highest standards of quality, safety, and regulatory compliance across both domestic and international markets. Role Overview We are seeking a detail-oriented QA/QC Executive with a strong analytical mindset. This role requires not only execution of routine quality activities but also critical evaluation of data trends, root cause analysis , and active participation in continuous improvement initiatives . Key Responsibilities Quality Assurance & Control Implement and monitor QA/QC protocols across manufacturing, packaging, and warehousing. Perform data-driven quality checks for raw materials, in-process materials, and finished goods. Analyze deviations and trends to identify patterns and recommend corrective actions . Ensure timely and accurate documentation for batch release and QA metrics. Water & Microbial Analysis Oversee monthly water testing (physicochemical and microbial parameters); interpret results and escalate as needed. Maintain and audit water testing records; ensure alignment with statutory and global standards . Conduct or coordinate microbiological analysis of environment, materials, and products; track recurring issues using trend analysis. Regulatory Compliance & Documentation Verify label and product compliance with FSSAI, HACCP, and international regulatory standards . Review and validate label claims, nutritional panels , and ingredient declarations, especially for export markets (UK/EU/US). Support preparation of regulatory dossiers and technical documentation for global submissions. SOP & Record Management Develop, update, and standardize SOPs , QA checklists, and CAPA reports. Implement Good Documentation Practices (GDP) and maintain traceable records for audits. Support internal and external audit readiness through data-backed QA documentation. Cross-Functional & Analytical Support Collaborate with R&D, Production, and Packaging teams to ensure product compliance from concept to execution . Participate in stability, validation, and shelf-life studies , using findings to influence process improvements. Use analytical tools or methodologies (Pareto, Fishbone, 5-Why, etc.) for problem-solving and risk mitigation . Qualifications & Skills Degree: B.Pharm / B.Sc / M.Sc in Chemistry, Microbiology, Food Science, or Pharmaceutical Sciences Experience: 3–4 years in QA/QC in pharmaceutical or nutraceutical manufacturing Working knowledge of: FSSAI, HACCP, GMP , and international regulatory frameworks Water and microbial testing methods with root cause analysis Label validation and export documentation Strong documentation, analytical, and audit-handling skills Proficient in data interpretation and report preparation Excellent communication and cross-functional coordination skills Work Details Full-Time , On-Site at Jigani Industrial Area , Bangalore To Apply Please email your CV to bhavna@bonaiyuhealth.com Subject Line: Application – QA/QC Executive – Bonaiyu Health, Jigani Show more Show less

Role & responsibilities Understand the Expectations and Deliverables of the Project and Ensure Proper Planning for delivering the same. Demonstrate Good Knowledge about Ingredients and their functionalities. Identify & Suggest vendors for Ingredients to Procurement team Investigate different Formulation combinations and Processing techniques to develop and optimize the product and establish product, process & sensory parameters Supervise/Conduct lab trials and internal sensory. Ensure Proper recording of Data & Results. Delegate activities to Product Development Associate (PDA) and monitor their work and productivity. Ensure timely documentation of all reports as per Organization requirements. Identify & Evaluate Third Party Manufacturers and Conduct trials at their Factory for Commercialization of the Product. Possess basic knowledge in Regulatory (FSSAI) & Legal compliances and ensure all developed products comply within those regulations. Coordinate with NABL accredited External Labs for analysis of developed Products and results Ability to frame Product labelling requirements such as Ingredients list, Nutritional Information, etc Preferred candidate profile 3-5 years Research & Development work experience in Beverages Qualification - B. Tech or M. Tech Food Technology/Food Science/Food Process Engineering or related Demonstrated experience in developing new products at Lab level and scaling up to Industrial level Demonstrated experience in understanding market trends and developing innovative products Good Project Management skills with experience in managing Client projects Possess Good communication and Presentation skills. Ability to build Strong Business Relationships.

M.Sc Microbiology candidate required for teaching microbiology to allied health science students. M.Sc in Medical / Clinical Microbiology preferred. Excellent atmosphere in a fast-growing campus. Food and accommodation will be provided to outstation candidates. Job Type: Full-time Pay: ₹14,000.00 - ₹20,000.00 per month Schedule: Day shift Experience: total work: 1 year (Preferred)

Job Title: Microbiology Lab Technician Experience: 2 to 5 Years Location: Perungudi ,Chennai. Key Responsibilities: Perform microbiological tests using LISA , Serology , and Bacteriology methods Prepare media, samples, and reagents Identify and analyze microorganisms in various sample types Maintain lab equipment, records, and ensure hygiene standards Support in audits, documentation, and quality control Requirements: B.Sc. in Microbiology / MLT or equivalent 2–5 years of lab experience Proficient in LISA, Serology, and Bacteriology Strong knowledge of lab practices and safety protocols Good communication and teamwork skills Interested can share resume to Priya-6383907434 or Direct walkin to Neuberg Diagnostics,7a, Rajiv Gandhi Salai, Industrial Estate, Perungudi, Chennai, Tamil Nadu 600096 Job Type: Full-time Pay: ₹18,000.00 - ₹30,000.00 per month Benefits: Provident Fund Schedule: Day shift Rotational shift Work Location: In person Application Deadline: 03/06/2025 Expected Start Date: 04/06/2025

Job Title: Territory Development Manager – Routine Division Location: Ahmedabad, Surat, Mehsana, Bhuj Department: Sales – Routine Diagnostics Reports To: Area Sales Manager Company: Unipath Specialty Laboratory Limited Industry: Healthcare / Diagnostics / Pathology Services Key Responsibilities:  Develop and execute a territory-wise sales strategy to meet and exceed revenue targets.  Identify and onboard new clients including clinics, hospitals, and diagnostic centers.  Build and maintain strong relationships with existing clients to ensure repeat business  Promote Unipath’s routine diagnostic services and explain their clinical benefits to healthcare professionals.  Monitor competitor activities and market trends to identify opportunities and threats.  Coordinate with internal teams (logistics, customer service, operations) to ensure seamless service delivery.  Organize and conduct promotional activities such as CMEs, health camps, and awareness drives.  Maintain accurate records of sales calls, client meetings, and follow-ups using CRM tools.  Provide regular reports and updates to the Area Sales Manager on performance metrics, market developments, and customer feedback. Job Types: Full-time, Permanent Pay: ₹400,000.00 - ₹600,000.00 per year Benefits: Health insurance Provident Fund Schedule: Day shift Application Question(s): Bachelor’s degree in Life Sciences, Microbiology, DMLT/BMLT Education: Bachelor's (Required) Experience: Healthcare/ Diagnostic sales: 2 years (Required) Pathology or Laboratory services: 2 years (Required) Healthcare Management: 2 years (Required) B2B sales: 2 years (Required) Language: English (Required) License/Certification: 2 Wheeler Licence (Required) Work Location: In person

Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc.. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. B.Sc. /M.Sc.

We are looking for a Lab QA to join our company. Qualification : B.Pharm / M.Sc. Experience : 3-5 Years Job Profile : Audit Trail Raw Data Review Chromatograph Review Spec, STP, Protocol Review Sound Knowledge of GLP & GDP Data Integrity Review in QC Stability Data Review IP,FP Raw Data Review Before Batch Release Microbiology Lab Documents Review Job Type: Full-time Pay: ₹19,654.44 - ₹34,360.94 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Overtime pay Performance bonus Work Location: In person Speak with the employer +91 9016463181

Req ID: 323217 NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now. We are currently seeking a Software Development Senior Specialist to join our team in Noida,Pune,Bangalore, Uttar Pradesh (IN-UP), India (IN). The EHR Support Specialist should be highly proficient with the electronic health record software (Meditech) or have a strong clinical background and a strong aptitude for computer systems. This role requires a strong working knowledge of Windows-based systems, excellent customer service skills, the ability to train and support doctors, nurses, support staff, and clinical administrators. This role also works closely with other members of the I.S. Department and I.T. roles supporting the computing infrastructure and desktop computers. Role Responsibilities Manage operational and service Level agreement compliance Follow ITIL practices for Level-2 Support In a timely manner, capture, track, and solve level 1 and 2 Production Support tickets. Escalate level 3 help requests to EHR vendors, or server and network administrators, as appropriate. Provide explanations and instructions about complex EHR topics to non-systems staff members in clear and understandable terms. Effectively and diplomatically communicate within and across teams, departments, and organizations. Investigate and resolve software problems/performance and proactively identify potential issues Prioritize, coordinate, expedite, and escalate help requests for the help desk team, balancing workload, skills, personnel development, quality, service levels, and customer needs/expectations Perform root cause analysis and implement corrective measures Identify areas of the environment that need improvement and develop solutions to address Adhere to and comply with all client and NTTDATA policies Provides weekly status reports of completed and ongoing activities to management Diagnose and troubleshoot EHR software issues Operate as a liaison between onshore technical SMEs and the end-user department Provide business systems and technical analysis to support the applications. Includes evaluation, analysis, documentation of requirements, and creation of system specifications. Classifies problems such as system, training, or process and recommends corrective actions Must understand business systems, applications and industry requirements Mentor and train juniors to support business growth and a high quality of service. Ensure secure, reliable access to data by users according to company standards and industry regulations and protect data from risks Flexibility to work on shifts Requirements: Must have hands on experience in Clinical Applications of EHR systems including- Meditech. Meditech Applications -(Magic, Client Server (CS),6.X, Expanse) Application & workflow Knowledge in Administrative Modules- (ABS - Abstracting,ADM - Admissions,MRI - Medical Records.MRM - Medical Records Management,MIS - Management Information Systems,SCH (CWS/OR) - Community-Wide Scheduling, Operating Room Management,HUB (EMR) - Enterprise Medical Records,UNV - Universe), Clinical Modules-(EDM - Emergency Department Management,LAB (also BBK/MIC/PTH) - Laboratory, Bloodbank, Microbiology, Pathology, Instruments,NUR (PCS) - Patient Care System,OE - Order Entry,PCM - Physician Care Manager,PHA - Pharmacy,RAD (ITS) - Radiology/Imaging and Therapeutic Services,RXM (AOM) - Ambulatory Order Management), Financial Modules-(AP - Accounts Payable,BAR - Billing/Accounts Receivable,GL - General Ledger,PP - Payroll/Personnel,PBR - Physician Billing and Receivables), Interfaces Meditech Report Writer (NPR Report writer, Report Designer, Data Repository,SQL, SSRS, Automation Tools) Preferences Masters in Hospital Administration Proficiency in various programming and clinical application reporting tools About NTT DATA NTT DATA is a $30 billion trusted global innovator of business and technology services. We serve 75% of the Fortune Global 100 and are committed to helping clients innovate, optimize and transform for long term success. As a Global Top Employer, we have diverse experts in more than 50 countries and a robust partner ecosystem of established and start-up companies. Our services include business and technology consulting, data and artificial intelligence, industry solutions, as well as the development, implementation and management of applications, infrastructure and connectivity. We are one of the leading providers of digital and AI infrastructure in the world. NTT DATA is a part of NTT Group, which invests over $3.6 billion each year in R&D to help organizations and society move confidently and sustainably into the digital future. Visit us at us.nttdata.com NTT DATA endeavors to make https://us.nttdata.com accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact us at https://us.nttdata.com/en/contact-us. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. NTT DATA is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click here. If you'd like more information on your EEO rights under the law, please click here. For Pay Transparency information, please click here.

Job Description : Job Title: Manager Cluster Quality About the Function: Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo’s 30,000+ people work in Supply Chain and Manufacturing. It’s an intricate and sophisticated operation that’s the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We’re committed to realising our ‘Society 2030: Spirit of Progress’ goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we’ll help you to thrive in our inclusive culture. Role Responsibilities: Position Name: Executive – Manager Quality Level : L5-B – Manager Quality Reports to: Manufacturing Unit Head PURPOSE OF THE ROLE: The purpose of the role is to collaborate with the unit team to improve and sustain quality systems and capability development at the unit level and ensure end to end quality of raw material, packaging material, liquids and finished goods. TYPICAL ROLE REQUIREMENTS Qualification: Post Graduate caliber or equivalent - preferably in Chemistry/Microbiology/Bio-chemistry/Bio-technology/Food technology/DIFAT Experience: 6-8 years of experience in the areas of Quality Assurance and Quality Systems on Food Processing / FMCG –Distillery, Brewery and Beverage Industry Knowledge & skills: • Hands on experience and in depth knowledge of quality management systems, developing quality related SOPs and its control • Experience in handling quality improvement projects • Knowledge of Microsoft Office package • Certified lead auditor for ISO 9001, ISO 22000, etc. Best Suited for Someone who • Experience in working across functions with various stakeholders • Excellent coaching, influencing and communication skills AREAS OF RESPONSIBILITY PERFORMANCE MEASURES (QUANTITATIVE / QUALITATIVE) 1 Quality Operations © Diageo India Highly Confidential • Play a pivotal role as unit quality manager in collaboration with unit team to improve and sustain quality systems and capability development at unit level • Carry out end of the line inspection of all finished goods at the unit as per UFPS standards • Conduct RM/PM inspection as per standards and sensory evaluation of samples • Lead root cause problem solving investigations for issues that occur on quality at units • Responsible for capability development of unit quality team on quality standards • Engage unit quality teams for the implementation of quality standards • Ensure all regulatory requirements to be complied without any deviations • Responsible for planning and conducting periodic Internal Audit, MRM for FSMS • Take appropriate action/approval for QC hold/under deviation/reworked material • Ensure MIS report submission to Unit Head, Cluster QA & QA-HO as & when required • Support all inter-departmental teams for ensuring smooth production in line with adherence to quality standards • End of line defects (PPM) • L1 audit score • Liquid quality compliance • Customer complaint closure (Lead time & CAPA verification © Diageo India Highly Confidential ) • Adherence to quality standards 2 Training • Develop Training calendar and impart trainings on quality related topics to unit team • Responsible for certification/implementation of ISO 9000/22000 as per organization requirements. • Ensure training of unit team for skills such as cross functional, quality etc. 3 CAPA • Ensure CAPA to all quality issues including customer complaints if any • Drive improvements in areas where targets are not met using RCPS methodology • Responsible for working-out and verification of CAPA with process owners © Flexible Working Statement: Flexibility is key to our success. From part-time and compressed hours to different locations, our people work flexibly in ways to suit them. Talk to us about what flexibility means to you so that you’re supported from day one. Diversity statement: Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this. We embrace diversity in the broadest possible sense. This means that you’ll be welcomed and celebrated for who you are just by being you. You’ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more. Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world. Feel inspired? Then this may be the opportunity for you. If you require a reasonable adjustment, please ensure that you capture this information when you submit your application. Worker Type : Regular Primary Location: Alwar Unit Additional Locations : Job Posting Start Date : 2025-05-28

Job Description Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc.. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Qualifications B.Sc. /M.Sc. Show more Show less

Biocon Biologics is a fully integrated ‘pure play’ biosimilars organization globally committed towards transforming patient lives through innovative and inclusive healthcare solutions. It is engaged in developing high-quality, affordable biosimilars aimed at expanding patient access to cutting-edge class of therapies across the world. Biocon Biologics is a subsidiary of Biocon Ltd, an innovation led-global biopharmaceuticals company and India's first publicly listed biotech enterprise. Biocon Biologics has one of the largest biosimilars portfolios, a wide global footprint, state-of-the-art manufacturing facilities, world-class R&D ecosystem, and high quality & compliance standards, enabling it to fulfil unmet needs of patients across the globe. Job Description. 1. Handling of OOS and OOL Investigation related to Environmental excursions and ensure closure of report on time and before batch release as applicable (report preparation, report review and closure). 2. Initiation of CAPA related to OOS and OOL for Environmental excursions and ensure its closure. 3. Keeping online tracking sheet for OOS/OOL. 4. Training of manufacturing personnel on relevantSOP's.5. Ensuring audit Compliance for Fill Finish Production. 5. Ensure the microbial events related to product (Deviations, OOS/OOTs), and microbial water excursion (OOS) investigations are timely conducted, and root cause analysis is identified out and appropriate CAPAs are identified to avoid repeat occurrence. 6. Timely assess the impact due to microbial excursion on the ongoing batches and subsequent batches and propose recommendation to the site. 7. Review of Investigation reports for data furnished for correctness of statements, evidence-based review and ensure no errors in the data and conclusions derived. 8. Involve in management review meetings to present the microbial excursions and status of closures. 9. Provide inputs during trending of microbial related deviations, OOS and propose recommendations and aseptic practise review. 10. Ensure oversight on microbial related investigations, to ensure consistency of global standards, harmonization, sharing of best practice. 11. Drive continuous improvement in microbial investigations to meet and sustain compliance with internal and external regulatory requirements. Qualifications and Experience BSc/MSc Microbiology or biotechnology or equivalent experience. 13 + Years Relevant Experience. Microsoft Office (Outlook, Excel, Word, PowerPoint, etc.) Organized Strong leadership skill Show more Show less

We are hiring for multiple position in Microbiology department, Below are the details Note: Contact person Mr. Srinivasa M, those who are unable to attend the interview are requested to forward their resumes to email id: naveenkumarp@microlabs.in, jonesnaveenrajp@microlabs.in Candidates are requested to carry their copies of Resume, Mark Sheets, Experience Certificates, Latest salary certificate, pay slips of three months and one photographs. Date & Time: 31st March,2025 (Saturday). Time: 9.00 AM TO 2.00 PM. STERILE - PRODUCTION, PACKING, MICROBIOLOGY, IT & QUALITY CONTROL 1. Microbiology Position: Sr.Officer/ Executive / Sr. Executive (freshers can apply) Qualification : B.Sc/ M.Sc- Microbiology/ BioTech Experience: 2-8 years experience in Sterile Manufacturing facility. Job Profile: Microbiology Analytical Activities (MLT, BET, Stability), Environmental monitoring, QMS activities in sterile manufacturing facility.

Plan and execute advanced microbiological research to develop new products and optimize existing processes. Conduct microbial culturing, isolation, identification, and characterization using classical and molecular biology techniques.

The candidate will undergo a self-financed job-oriented patent analyst training at the Indian Institute of Patent and Trademark. On successful completion of the training, they will be placed for full-time patent analysis in the pharmaceutical domain. Required Candidate profile Scientific and Analytical Thinking Eager to work in drugs and formulation Candidates must have sound knowledge about the subjects they study in Graduation

Immediate Hiring !! Designation: Medical Coder . Salary: Upto 20k PM + Incentives. Shift : General, Day. Skills: Anatomy, Physiology, Pathology. Location: Chennai, Coimbatore, Bangalore. Required Candidate profile Eligibility: UG or PG or Diploma ( 3 Years) Specialization: Life Science, Non - Life science , Para-Medical & Medical Studies. Passout: 2020- 2025

Hiring to conduct patent searches, analyze the latest technologies, and create detailed patent reports on inventions. Selected candidates will undergo training with skills in patent analysis, candidates will work as Analyst Required Candidate profile Strong knowledge of biotechnology Proficiency in MS Excel for data analysis and reporting Excellent writing and communication skills Provide a minimum of two references along with their resume.

Hiring to conduct patent searches, analyze the latest technologies, and create detailed patent reports on inventions. Selected candidates will undergo training with skills in patent analysis, candidates will work as Analyst Required Candidate profile Strong knowledge of biotechnology Proficiency in MS Excel for data analysis and reporting Excellent writing and communication skills Provide a minimum of two references along with their resume.

Hiring to conduct patent searches, analyze the latest technologies, and create detailed patent reports on inventions. Selected candidates will undergo training with skills in patent analysis, candidates will work as Analyst Required Candidate profile Strong knowledge of biotechnology Proficiency in MS Excel for data analysis and reporting Excellent writing and communication skills Provide a minimum of two references along with their resume.

Job Title: Head (VP) – Quality (Formulations) Location: Bangalore, India Experience Required: Minimum 20 years Function: Corporate QA Industry: Pharmaceutical Formulations Reporting To: Site Head / Corporate Quality Head Job Summary: We are seeking a highly experienced and dynamic Head of Quality to lead the Quality Assurance (QA), Quality Control (QC), and Microbiology functions across two state-of-the-art formulation manufacturing plants based in Bangalore. The ideal candidate must have strong expertise in regulatory audits, QMS, and laboratory operations, with a proven track record of successfully leading international regulatory audits (such as USFDA, UKMHRA, and EU QP audits). The incumbent must have at least 5 years of recent experience handling both QA and QC functions and should possess excellent leadership and compliance management capabilities. Key Responsibilities: Lead and manage the Quality Assurance , Quality Control , and Microbiology functions for both formulation plants. Ensure full compliance with global regulatory requirements including USFDA, UKMHRA, EU, and other international authorities. Oversee the development, implementation, and continuous improvement of Quality Management Systems (QMS) . Lead the preparation and handling of regulatory inspections and customer audits; ensure timely closure of audit observations (CAPA). Ensure effective documentation, data integrity practices, and adherence to cGMP guidelines across all quality functions. Provide strategic guidance to QA and QC teams to ensure the release of raw materials, in-process materials, and finished products as per specifications. Review and approve quality-related documentation such as SOPs, protocols, specifications, and validation reports. Drive laboratory excellence in QC and Microbiology with a strong focus on analytical accuracy and regulatory compliance. Collaborate closely with cross-functional teams including Manufacturing, Regulatory Affairs, and R&D to ensure alignment with business and compliance goals. Mentor, develop, and lead a team of quality professionals across both sites. Candidate Profile: Educational Qualification: M. Pharm / M.Sc. / B. Pharm or equivalent (higher qualifications preferred). Experience: Minimum 20 years of experience in Quality functions in pharmaceutical formulations. At least 5 years of recent experience leading both QA and QC functions . Strong track record in handling international regulatory audits such as USFDA, UKMHRA, EU QP , etc. Deep understanding of QMS , ICH guidelines , cGMP , and data integrity principles. Experience in managing multiple manufacturing sites will be an added advantage. Strong leadership, analytical, and communication skills with the ability to work cross-functionally. Compensation: Competitive and commensurate with experience. Location Flexibility: Candidate must be willing to be based full-time in Bangalore . Show more Show less

Position Overview We are seeking a dynamic and experienced professional to lead the Food Safety and Quality Assurance (FSQA) function at our flagship manufacturing site in Hathras. As the Head of Food Safety & Quality, you will be responsible for the overall leadership, strategic direction, compliance, implementation, and continuous improvement of all food safety and quality management systems. This role will serve as a key member of the factory leadership team, ensuring that all processes and products meet regulatory, customer, and internal quality standards. Key Responsibilities Leadership and Strategy - Define the long-term FSQA strategy aligned with Mahaan’s commitment to quality, innovation, and sustainability. - Lead the Quality Assurance (QA), Quality Control (QC), and Food Safety teams across functions. - Drive a culture of quality excellence, continuous improvement, and regulatory compliance. Compliance and Risk Management - Ensure full compliance with FSSAI, HACCP, GFSI, cGMP, FSMA, and other international standards and certifications. - Lead site preparedness for internal and third-party audits including customer audits, statutory audits, and certifications. - Implement, monitor, and review all prerequisite programs, CCPs, SSOPs, RM/PM controls, and validation protocols. Process & Product Quality Oversight - Oversee and enhance quality systems across raw material intake, production, packaging, warehousing, dispatch, and returns. - Review SOPs, deviations, CAPAs, market complaints, and product quality metrics on a regular basis. - Collaborate with cross-functional teams including Production, R&D, Procurement, and Sales to ensure quality throughout the product lifecycle. Technical Development and Systems - Develop technical quality parameters for RM/PM (Physical, Chemical, Microbial) with the R&D team. - Ensure documentation and validation of product dossiers, manufacturing instructions, and specification sheets. - Lead the implementation of a modern digital QMS system and data-driven decision-making. Supplier and Vendor Quality - Approve and audit vendors, including new vendor onboarding, performance assessment, and compliance. - Establish and maintain a robust Supplier Quality Assurance Program with procurement and R&D. Customer & Regulatory Interface - Handle customer queries related to product quality, certifications, and compliance. - Act as the site representative for food safety-related statutory and regulatory bodies. Required Qualifications - Bachelor’s/Master’s degree in Dairy Technology / Food Science / Microbiology. - Minimum 10+ years of progressive experience in food safety and quality, ideally in dairy/FMCG environments. - In-depth knowledge of Indian and global food regulations, certifications, and quality systems. - Experience working in or with USFDA/FSMA compliant facilities is an advantage. Key Skills and Competencies - Strong leadership and team management capabilities. - Excellent knowledge of HACCP, GFSI, FSSC 22000, ISO 9001, and GMP standards. - Exceptional problem-solving, analytical thinking, and risk assessment skills. - High proficiency in technical documentation, reporting, and root cause analysis. - Excellent communication, negotiation, and cross-functional collaboration. Why Join Mahaan? Impact Drive quality excellence that impacts the health and well-being of consumers across India. Culture Join a team of passionate food professionals fostering innovation, transparency, and excellence. Growth Direct exposure to senior management and the opportunity to influence large-scale transformation in a legacy company. Show more Show less

Job Title: QC Data Analyst Shift Timing: 7AM-4PM IST or 8AM-5PM IST (flexible) Role Overview: We are seeking a QC Data Analyst to analyze and interpret food sample data, ensuring compliance with quality standards. This role involves verifying data accuracy, investigating non-compliant results, and collaborating with production teams to resolve issues. The analyst will also prepare reports and perform statistical analysis to assess product quality. Key Responsibilities: Review test results, generate COAs, and verify data Perform calculations and investigate discrepancies Initiate investigations and recommend corrective actions Record data in LIMS Identify trends, assess data quality, and communicate findings Required Skills: Strong analytical and problem-solving abilities Attention to detail and accuracy Excellent communication and documentation skills Knowledge of quality standards Education: Bachelor / Master / Ph.D degree in food science, microbiology, chemistry, or related field Show more Show less

About Executive - HSEQ: The Executive - HSEQ will play a critical role in ensuring that our food vendor partners and cafeteria operations comply with all food safety regulations and standards. This position involves implementing, monitoring, and improving food safety protocols to maintain the highest levels of hygiene and safety in all food handling processes. Roles & Responsibilities: • Execute Food Safety audit as per FSSAI requirement. • Conduct customized audit across Catering/Base Kitchen Audits/ Live kitchen Audits. • Reports to be submitted within 2 working days. • Follow up of NC closure for both external and internal audits. • Ensure developed corrective action on nonconformities are implemented effectively. • Supporting for the preparation of external audits. • Involved in root cause analysis for the identified non-conformities or complaints. • Verify the corrective action implementation effectiveness. Prerequisites: • Educational Qualification – Bachelor’s Degree in food science and technology or Microbiology or Hotel management or catering technology from recognized university. • Preference would be given if acquired Accredited Lead Auditor Course in food safety Management System (ISO22000/FSSC22000). Have sufficient Knowledge of FSS Act and regulation. Must have sector specific knowledge regarding Hygiene, Sanitary practices, process knowledge, Allergen management, etc. • Certified internal auditor on ISO 22000 / HACCP. • Knowledge in Quality and Food Safety Management System Show more Show less

Job Title: Microbiology Lab Technician Experience: 2 to 5 Years Location: Perungudi ,Chennai. Key Responsibilities: Perform microbiological tests using LISA , Serology , and Bacteriology methods Prepare media, samples, and reagents Identify and analyze microorganisms in various sample types Maintain lab equipment, records, and ensure hygiene standards Support in audits, documentation, and quality control Requirements: B.Sc. in Microbiology / MLT or equivalent 2–5 years of lab experience Proficient in LISA, Serology, and Bacteriology Strong knowledge of lab practices and safety protocols Good communication and teamwork skills Interested can share resume to Priya-6383907434 or Direct walkin to Neuberg Diagnostics,7a, Rajiv Gandhi Salai, Industrial Estate, Perungudi, Chennai, Tamil Nadu 600096 Job Type: Full-time Pay: ₹18,000.00 - ₹30,000.00 per month Benefits: Provident Fund Schedule: Day shift Rotational shift Work Location: In person Application Deadline: 03/06/2025 Expected Start Date: 04/06/2025

Job Description You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise. Officer - Store Company: Ahlcon Parenterals IN Ltd Job Posting Location: IN-Bhiwadi Functional Area: Supply Chain Management Working Model: Onsite Requisition ID: 4929 Are you a Store Officer passionate about Physical verificationa, dispensing and documentation of Raw Material in Store? If so, this opportunity could be for you! Join us in Bhiwadi at Ahlcon Parenterals, a pioneer in medical devices, where your skills and experience will be recognized and celebrated. Take the next step in your career with us and help shape the future of healthcare! As a Store Officer at B. Braun Group you will play a vital role in efficient dispensing, physical verification, RM Store temperature monitoring as per SOP. Your key responsibilities: Dispensing of Raw Material as per BMR. Physical verification of Raw materials. Maintain clean record, temperature monitoring of RM Store and Dispensing area. Issuance of material as per FEFO and calculation of material. Maintaing dispensing and raw material store clean and presentable for audit. What you will bring to the team: Strong knowledge of receipt and dispensing of raw material in Store. Experience in inventory management, documentation, and Audit related to store activities. A Bachelor's degree in Pharmacy or a Bachelor of Science or a Master of Science in a relevant scientific discipline (e.g., Chemistry, Biology, Microbiology, Pharmacology) provides a strong foundation for the role. With 2-5 years of experience, you bring valuable hands-on knowledge of industry processes and best practices. What sets B. Braun apart? Ahlcon Parenterals (India) Limited is a B. Braun group company, located at Bhiwadi, Rajasthan. We are a major pharmaceutical formulation manufacturer of both Large and Small Volume Parenterals (LVP and SVP) for domestic and export markets. Our core values of Innovation, Efficiency, Sustainability, Trust, Accountability, and Diversity foster a performance-driven culture where we challenge each other constructively to grow personally and professionally. Recognized through awards such as 'Dream Companies to Work For' and 'Great Place to Work,' we invite you to join our team driven by a shared vision - to protect and improve the health of people around the world. What can we offer you? Convenient transport and subsidized canteen services. Mediclaim and Life Insurance. Learning programs and workshops to drive your development. Mental Wellness Support with counselling and mindfulness sessions. Paternity & Birthday Leave for life’s special moments. Fun activities and team building events. What’s next? Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you’ll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary! We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here Check us out on social media! B. Braun Group LinkedIn B. Braun India Facebook B. Braun Group YouTube