2560 Microbiology Jobs - Page 49

The Opportunity Avantor is looking for a Senior Associate for the Bids & Quotes NA team. It is an intermediate-level position. He/She is responsible for providing initial technical product support to customers by handling inquiries and troubleshooting basic technical product-related issues. Gather information to identify and assess nature of problem. Record incident in a tracking system to maintain log of product issues for escalation and product development teams. Typically refer to transcript or established process in training manuals and guides to recommend solutions. Escalate complex issues to higher-level technical product support specialists or management. They should be part of a multi-disciplinary team providing direct technical support to our customers and sales associates via call, chat, and email. The team consists of associates from a variety of scientific specialties, including Life Sciences (Microbiology, Molecular and cell biology, Biochemistry & Biotechnology) What We’re Looking For Education: Minimum of an Undergraduate/bachelor’s in science (Biotechnology & Industrial BT, Microbiology, Biochemistry, Applied/Advanced microbiology, Bioinformatics, Nanotechnology, Bio-Medical Eng/Instrumentation). Experience: Preferably with HPLC/chromatography/NGS experience. Preferred Qualifications Practical Laboratory experience is preferred. Excellent Communication Skills with telephone etiquette. Preferably with customer service experience. Proficiency in Microsoft Office - MS Word and MS Excel Positive attitude towards work, team, learning and taking up initiatives/tasks. Customer centric approach, with ability to provide accurate information in user friendly manner to both technical and non-technical purchasers. Awareness of the sales process and a commercial understanding of the service Eye for details and accuracy of information supplied. Ability to comprehend the technical enquiry, analyze, probe to understand thecustomer requirement and ensure complete information before formulating a response. Competencies Analytical and Critical Thinking Collaboration & Teamwork Continual Improvement and Innovation Customer Focus Developing People Driving Results Adhere to Avantor’s policies, procedures, rules, and guidelines. Always uphold Avantor Culture and Values. How Will You Thrive And Create An Impact Provide Pre & Post sales assistance relating to our product range to customers via Hotline/Live Chat or E-Mail. To make the greatest use of technical expertise and experience, team members divide up incoming inquiries, but they also should have a readiness to broaden their knowledge and address a range of inquiries. Maximize opportunity to achieve sales by; Identifying products based on end user’s specifications & application Suggesting alternatives to unavailable products Providing technical information about Avantor product ranges Providing first line troubleshooting for equipment & instruments Up selling of products and services where possible Maintain a database of supplier product information, specifications, and certificates. Build relationship with sales staff and customer service associates to ensure continuity of service provided. Ability to produce results in a pressurized environment, within agreed service levels and the ability to follow through on all commitments. Mentor team members and lead small groups within the team. Perform Quality Audits & Checks. Involve in Product & Process training for new hires. Perform Root Cause Analysis on customer complaints and take necessary actions. Disclaimer The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. 3rd Party Non-solicitation Policy By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation

Job Description Timely perform and plan for Calibration and maintenance of instruments. Preparation, sterilization and disposal of microbiological media and accessories. Planning and execution of Water sampling and testing (Microbial and Chemical) of OSD and Ophthalmic facility. Preparation of trend for water system and environmental monitoring. Perform the Environmental monitoring of Sterility area, Ophthalmic and OSD facility and participation in media fill activity. Planning and execution of Microbial analysis of raw material, packing material, intermediate / in-process samples, Finished Product and Stability samples for Sterility testing, Particulate matter testing, Bacterial Endotoxin testing, Antimicrobial effectiveness testing, Bio burden testing and Packing material testing. Planning and execution Growth promotion testing, Preparation of microbial culture suspensions, maintenance of microbial culture and Identification of microorganisms. Planning and execution of online documentation, Upkeep of housekeeping in laboratory. Preparation of method validation MET / Sterility / BET / other miscellaneous protocol for validation study. Proper arrangement of samples and analysis of samples performed within time line. Report any quality concerns or suggestions for improvements to Supervisors/managers. Handling of water, calibration and purchase activity through SAP. Ensure timely initiation and closure of QAMS documents such as lab incidence. Handling of all microbial testing and calibration of instrument/Equipment through LIMS. Responsible to person any other task/activity assigned by supervisor /Manager. Work Experience Experience :- 2 to 4 yrs. Education Masters in Microbiology Competencies

Job description Contact Number : 7892006386 Ø Interacts with physicians, nurses, department managers, supervisors, and occupational health and other professional/non-professional staff members to provide resource information, resolve infection control problems, and identify new opportunities to improve service and reduce costs. Ø Directs and assists in preparing reports and statistical data for the infection control committee, medical staff committees, medical executive committee and the facility's administration and other committees as needed. Ø Conducts rounds, discussing and monitoring infection control practices with staff; Ø Collects infection data from departments, maintaining records for each case. Ø Train staff on implementation of infection control practices. Ø Investigates incidents of infection and reports such incidents to the nursing Director. Ø Ensures availability of supplies required for infection control. Ø Daily rounds to all departments. Ø Post operative patients counselling. Ø Conducting infection control committee meeting and Formulating agenda and minutes of meeting. Ø Induction programme for all new joinee. Ø Initiate in cleaning and fumigation process within department and collection of swabs and send to microbiology department with approval of medical director. Ø Collecting data on infection rates related to VAP, CAUTI, CLASBI, SSI, VIE. Ø Monitoring of general cleanliness, bedside cleanliness, biomedical waste management in wards and ICCUs, equipment and instrument cleanliness Ø Participate in infection prevention/control and hygiene audits. Ø Managing and monitoring of housekeeping activities. Ø Maintaining of sterility of ETO and steam sterilised items. Ø Monitoring of nursing measures related to isolation/ barrier precautions. Ø Infection control bundle maintenance. Ø Infection control measures at bedside Job Type: Full-time Pay: ₹35,000.00 - ₹40,000.00 per month Benefits: Provident Fund Schedule: Rotational shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Req ID #: 227850 Hyderabad, IN 1st Full time For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. Job Summary Responsible for technical support for Endosafe® (including automated NEXUS system) and/or Celsis™ and their associated systems. Support customers on Endosafe® and/or Celsis™ instrument installation, qualifications and product validation. Provide on-site training, sample testing or troubleshooting for continued customer satisfaction of our clients. Manage activities to help meet revenue targets and goals for the business. ESSENTIAL DUTIES AND RESPONSIBILITIES: Understanding and application of one or more of the product lines under the Microbial portfolio (Endosafe® and/or Celsis™) Applies technical/scientific skills to develop existing accounts and compete for customers together with the Account Management team whether for products sales or services sales. Supports customer onboarding, provide customer training, qualify leads, perform test demonstrations and help close new business opportunities during customer start up and continued account management. Responsible for the initial training and validation/application development support for customers, ensuring full and continued utilization of Microbial Solutions products. Recommends or performs remedial actions to troubleshoot customer issues related to application, reagents and software for the assigned product line. Performs instrument qualification and installation for new customers. Establishes regular interface and communication with the Account Management and Field Services team to relay shared goals and targets; develop co-strategies to achieve defined targets; and work cohesively as a team to provide excellence in service to clients. Builds relationships with customers to influence the acceptance and use of Microbial portfolio. Input, manage and monitor cases on Service Cloud or SFDC.Ensures activities of the Technical Services team are continuously compliant to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate. GENERAL REQUIRMENTS Maintains confidentiality of all Client information according to internal SOPs, Quality Service Agreements, and regulatory requirements. Maintains appropriate records and documentation of activities to facilitate continuous compliance to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate. Actively seeks improvement within area of responsibility and takes necessary action to implement such improvements. Must be willing to travel domestically and internationally to customers’ sites. Adheres to Company Policies and Procedures, including Code of Ethics and to Health and Safety requirements. Performs all other related duties as assigned. Job Qualifications Education: Minimally M.Sc. or equivalent in Biology, Microbiology, Life Sciences, Biotechnology or any other related scientific discipline. Experience: 0-5 years of relevant industry experience, preferably involving customer-facing responsibilities. Salary range : 4 to 7 LPA. Understanding of Biology/Microbiology in the Pharma setting is an advantage. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Other: Must possess excellent communication and presentation skills. Proficient in the use of Microsoft Office applications. About Microbial Solutions Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

We are looking for a Pharma Content Writer to join our editorial team and enrich our websites with new blog posts, guides and marketing copy. The candidate should be a Graduate of biotechnology, microbiology and any other pharma Related Experience- 6 Month To 1 Year > Research pharma-related topics > Write clear marketing copy to promote our products/services > Proofread and edit blog posts before publication > Submit work to editor for input and approval on time > Coordinate with marketing and design teams to illustrate articles > Promote content on social media > Identify customers’ needs and gaps in our content and recommend new topics > Ensure all-around consistency (style, fonts, images and tone) Job Type: Full-time Pay: ₹15,000.00 - ₹22,000.00 per month Benefits: Health insurance Work Location: In person

IT Full-Time Job ID: DGC00817 Chennai, Tamil Nadu 4-5 Yrs ₹4.5 - ₹06 Yearly Job description Job Title: Emergency Department Clinical Documentation Improvement (ED CDI) Specialist Location: Chennai/Hyderabad Level: L2 Department : Clinical Documentation Improvement Reports To: Coding Manager Position Summary: The ED CDI Specialist is responsible for enhancing the quality and accuracy of clinical documentation in the Emergency Department to ensure compliance with regulatory standards, optimize reimbursement, and improve patient care outcomes. This role involves collaborating with coders, auditors, clients, physicians and other healthcare providers to ensure that documentation reflects the true clinical picture of patients' conditions and treatments. Key Responsibilities: Documentation Review: Perform regular audits of clinical documentation in the ED to identify areas for improvement, ensuring accuracy and completeness of report. Education and Training: Provide ongoing education and training to ED staff on best practices for clinical documentation, including coding guidelines and regulatory requirements. Collaboration: Work closely with Coders/QA staff/Leadership/Clients, ED physicians and clinical staff to clarify documentation issues and promote accurate coding and reporting. Data Analysis: Analyze documentation trends and outcomes to identify opportunities for improvement in clinical practices and documentation accuracy. Compliance Monitoring: Ensure adherence to CMS guidelines and other regulatory requirements related to clinical documentation. Feedback and Reporting: Develop and present reports on documentation improvement initiatives and outcomes to immediate supervisor, stakeholders and Senior leadership. Quality Improvement: Participate in quality improvement initiatives aimed at enhancing patient care and safety in the ED. Professional Development: Stay current with developments in clinical documentation and coding standards through continuing education and professional organizations. Qualifications: Education: Masters/bachelor s degree in any life science stream Medicine, Physiotherapy, Occupational Therapy, Physician Assistant, Nursing, Pharmacy, Biomedical, Biochemistry, Microbiology, health information management, or related field. Experience: Minimum of 4-5 years of clinical experience in an emergency department

Near Guindy, Wanted only Female candidates for Food Inspection Qualification: Masters in Microbiology, Chemistry, Biotechnology, Food Technology Experience : Minimum 4 years in Food Production/ Quality Sal: Rs.25,000 Contact:9941182838 Job Type: Full-time Pay: Up to ₹20,000.00 per month Schedule: Day shift Work Location: In person

Education : B.Sc ( Biotechnology,Microbiology,Chemistry and Similiar Life Sciences) Experience : 1-3 Years of experience Male candidates only Good oral and written communication Skills Role in Biotechnology and Biomedical domain Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹20,000.00 per month Schedule: Day shift Work Location: In person

Greetings from Shifa Hospitals ……… About Shifa: In the southern Tamilnadu, Shifa Hospitals, Tirunelveli , has in the past 51 years focuses its efforts to propagate the concept of well being through quality medical service . Shifa Hospitals is a 150 bedded multispecialty, tertiary and referral centre. We are looking for a professional, team player, reliable, dedicated person who can serve as a position Microbiologistour Growing Hospital. Pls find the job details below. Job Specification: Position Name: Microbiologist Qualification: Bachelor’s degree in Microbiology & Master of Microbiology Experience: 02 years experience in Multispecialty Hospital Salary: Attractive Salary Timings: General Timings Location: Tirunelveli, Southern Tamil Nadu No of Positions: 1 Job Type: Full-time Pay: From ₹15,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Overtime pay Yearly bonus Experience: total work: 1 year (Preferred)

Full job description MUST HAVE GRADUATION OR POST-GRADUATION IN BSC/MSC IN BIOLOGY OR MICROBIOLOGY, BIOTECHNOLOGY ROLES AND RESPONSIBILITES Identify new business opportunities. Generate leads through various channels. Build and maintain client relationships. Develop and execute sales strategies. Conduct market research and analysis. Collaborate with internal teams. Maintain accurate sales records. Achieve sales targets and revenue goals. Qualifications and Skills: Bachelor's degree in BSC, MSC in Biotechnology, Microbiology, Biology, B.TECH, Business Administration, Marketing, or related field. Proven track record of success in sales or business development roles. Strong communication, negotiation, and interpersonal skills. Ability to work independently and as part of a team. Proficiency in CRM software and Microsoft Office Suite. Knowledge of industry trends, market dynamics, and competitive landscape. These roles and responsibilities may vary depending on the company's industry, size, and specific business objectives. Benefits: Cell phone reimbursement Provident Fund Health Insurance Incentive Paid Leave Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹42,000.00 per month Job Types: Full-time, Fresher Pay: ₹18,000.00 - ₹32,000.00 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Quarterly bonus Yearly bonus Education: Bachelor's (Required) Experience: Pharma Sales: 1 year (Required) Work Location: In person

Job Overview We are seeking a dedicated Physics Teacher to join our educational institution. The ideal candidate will have a passion for teaching and a strong background in physics to inspire students in their learning journey. Responsibilities Develop and deliver engaging physics lessons to students Create and implement effective teaching strategies to enhance student understanding Utilize various instructional methods to cater to diverse learning styles Assess and provide constructive feedback on student progress Collaborate with colleagues to enhance the physics curriculum Manage classroom activities and ensure a conducive learning environment Skills Proficiency in physics concepts including Trigonometry and Biochemistry Ability to dissect complex scientific principles for student comprehension Strong communication skills to effectively convey information Experience in Higher Education teaching or Research Laboratory is a plus Knowledge of Curriculum Development and Behavior Management techniques Previous experience in Tutoring or Microbiology would be beneficial Job Type: Full-time Schedule: Day shift Education: Master's (Preferred) Experience: total work: 1 year (Required) teaching: 3 years (Preferred) Language: English (Preferred) Location: Visakhapatnam, Andhra Pradesh (Preferred) Work Location: In person Expected Start Date: 15/07/2025

Job Title: Lab Incharge Department: Laboratory Services Location: Apollo Spectra Hospitals Chirala Reports to: Pathologist / Medical Superintendent / Admin Head Job Summary: The Lab Incharge is responsible for overseeing the daily operations of the laboratory. This includes managing lab staff, ensuring accurate testing and reporting, maintaining quality standards, managing inventory and equipment, and ensuring compliance with safety and regulatory standards. Key Responsibilities: Supervise all laboratory staff and daily operations of the lab. Ensure timely and accurate processing of all lab tests (biochemistry, hematology, microbiology, etc.). Maintain and enforce quality control procedures and documentation as per NABH standards. Monitor equipment performance, coordinate calibration and maintenance. Ensure proper sample collection, labeling, processing, and storage protocols are followed. Oversee inventory of reagents, consumables, and supplies; raise purchase requisitions as needed. Coordinate with doctors, nurses, and other departments for test-related queries. Train and mentor junior staff and technicians. Ensure laboratory cleanliness, biosafety, and waste disposal protocols. Maintain documentation and records for audits and inspections. Implement and monitor infection control measures within the lab. Address and resolve any operational or technical issues in the lab. Qualifications: B.Sc / M.Sc in Medical Laboratory Technology (MLT) or equivalent. Minimum 5 years of laboratory experience with at least 2 years in a supervisory role. Knowledge of NABH, other relevant accreditation protocols preferred. Proficiency in lab management software is an advantage. Skills Required: Strong leadership and team management skills. Excellent communication and coordination abilities. Attention to detail and accuracy in test reporting. Ability to troubleshoot and resolve technical problems. Knowledge of biomedical waste management and lab safety protocols Note: laboratory staff also required for 3 Positions Job Type: Full-time Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Provident Fund Schedule: Day shift Work Location: In person

Department: Pharmacology and Toxicology (In-Vitro) We are hiring!!!!! Qualification: M.Sc. in life-science (Biotechnology and Microbiology Preferred). Experience: We are not hiring freshers for this role only preclinical experience candidate with - 3 to 15 years of experience in Pharmacology and Toxicology (In-Vitro) with OECD GLP , NABL (ISO/IEC 17025:2017). <<>>> Job description: Responsible for Cytotoxicity and Genotoxicity studies and their maintenance. Validated AMES and Cytotoxicity assays for medical devices according to ISO standards, ensuring accuracy and reliability in toxicological testing methodologies To act as a Study Director for in vitro studies as per the requirements of OECD GLP principle and ISO 17025. Should have performed Invivo Micronucleus assay, Ames assay & Chromosomal aberration. Authored comprehensive Standard Operating Procedures (SOPs) for laboratory activities Skills: Assays: AMES- bacterial reverse mutation assay, In vitro and In vivo micronucleus test and biochemistry parameters In vitro and In vivo Chromosome aberration test, Local Lymph Node Assay, Cell Gene Mutation assay Primary Cell lines handled. <<>>> Benefits : Large campus with leave facilities like Casual Leave, Privilege leave, Sick leave School/college fees deduction for employee's staff Yearly Annual Health Check Up Report. Gym facility Hostel and Canteen facility. Employee engagement activities, tours and training and much more. Salary: 30,000 to 1,50,000/-

Company Description Ipca Laboratories Limited, a consumer-led global pharmaceutical company, has been creating healthy doses of life since 1949. Operating in over 120 countries across six continents, Ipca is a fully-integrated pharmaceutical company that manufactures over 350 formulations and 80 APIs for various therapeutic segments. We are among the world's largest suppliers of over a dozen APIs, produced at fully-automated manufacturing facilities approved by top global regulatory authorities. Ipca maintains high-quality standards and prioritizes the safety and dignity of people and consumers. Role Description This is a full-time on-site role for a QC Microbiology Executive/Sr. Executive located in Gandhidham. The responsibilities include performing daily microbiological testing and analysis, ensuring compliance with regulatory standards, maintaining microbiological documentation, and conducting environmental monitoring. The role also involves participating in audits, reviewing SOPs, and coordinating with various departments to ensure quality control standards are met. Company: Ipca Laboratories Ltd. Department: Quality Control – Microbiology Location: Gandhidham Gujarat. Position: QC – Microbiology Executive / Sr. Executive Experience: 6 to 8 Years Qualification: B.Sc / M.Sc – Microbiology or related field Industry: Pharmaceuticals / Formulations Job Description: We are looking for experienced and motivated candidates to join our Quality Control – Microbiology team. The ideal candidate should have hands-on experience in: * Microbial analysis of raw materials, finished products, and water samples. * Environmental monitoring and handling of EM instruments. * Maintenance and calibration of microbiological instruments. * Documentation as per cGMP guidelines. * Knowledge of regulatory audits (USFDA, WHO, MHRA, etc.) will be an added advantage. Skills Required: * Strong microbiological technical skills * Good knowledge of cGMP and GLP * Attention to detail and strong documentation skills * Ability to work in shifts How to Apply: Interested candidates can share their updated resume at avneesh.patel@ipca.com with the subject line “Application for QC – Micro (6-8 Years)”. Thanks & Regard Avneesh patel Sr. Officer - HRD avneesh.patel@ipca.com Ipca Laboratories Ltd, - Gandhidham

Maintain the Laboratory's Quality System. , Perform analytical tests in the laboratory, Assist with laboratory administrative duties, Maintain smooth laboratory work flow, Obtain lab certifications and complete QA/QC assignments, Promote good customer Must have strong Knowledge ISO & Must have implemented the same in any Lab. Knowledge of GC, HPLC shall be an added advantage.

Amura’s Vision We believe that the most under-appreciated route to releasing untapped human potential is to build a healthier body, and through which a better brain. This allows us to do more of everything that is important to each one of us. Billions of healthier brains, sitting in healthier bodies, can take up more complex problems that defy solutions today, including many existential threats, and solve them in just a few decades. Billions of healthier brains will make the world richer beyond what we can imagine today. The surplus wealth, combined with better human capabilities, will lead us to a new renaissance, giving us a richer and more beautiful culture. These healthier brains will be equipped with deeper intellect, be less acrimonious, more magnanimous, and have a kinder outlook on the world, resulting in a world that is better than any previous time. We find this vision of the future exhilarating. Our hopes and dreams are to create this future as quickly as possible and ensure that it is widely distributed and optimized to maximize all forms of human excellence. Role Description We are seeking a highly motivated and socially intelligent Health Coach to join our dynamic team. As a Health Coach at Amura Health, you will play a crucial role in guiding our clients through their health crises and supporting them in achieving their wellness goals. Your ability to build genuine rapport, offer empathetic guidance, and facilitate meaningful conversations will be key to your success in this role. Responsibilities Client Engagement: Initiate and maintain regular, personalized interactions with clients, understanding their unique health needs and challenges. Health Guidance: Provide expert advice and support tailored to each client's specific health conditions and goals, utilizing a holistic and empathetic approach. Motivation and Support: Encourage and motivate clients to adhere to their health plans, overcome obstacles, and celebrate their progress. Education: Educate clients on health management strategies, lifestyle modifications, and wellness practices to promote long-term health improvement. Progress Tracking: Monitor and document clients' progress, adjusting plans as needed to ensure continued advancement towards health goals. Crisis Management: Assist clients in navigating and managing health crises, offering timely and effective support to alleviate concerns and facilitate recovery. Collaboration: Work closely with other healthcare professionals and team members to ensure a coordinated and comprehensive approach to client care. Requirements Education: PharmD, B.Sc / M.Sc. in Mind body Life Sciences,BDS, Biotech, Microbiology, Bio-Chemistry, Applied Microbiology, Bio-Informatics, Applied Psychology, Clinical Psychology, Medical Microbiology, Human Genetics, Clinical Immunology, or Molecular & Cellular Biology, B.Tech/M.Tech Biotechnology, M.Pharm, B. pharm Experience: Fresher; prior experience in health coaching or related fields is not required but is a plus. Languages: Fluency in English is a must. Strong interpersonal and communication skills with the ability to build rapport with clients. High level of empathy, patience, and a passion for supporting others in their health journeys. Ability to manage multiple tasks effectively and adapt to changing client needs. Basic knowledge of health management concepts and practices. Additional Information Shift Timing: This position requires your availability to working in rotational shifts: 6 AM to 6 PM for morning shift, 11 AM to 11 PM for afternoon shift. Flexibility to work in any shift is required. In-office reporting timings: 9 AM to 6PM for morning shift & 11 AM to 7 PM for afternoon shift. Here are answers to some questions you may have: Who is Amura? We are a health startup with a presence in multiple countries What is special about you? Our clients. The Amura protocol is an intensive health program to follow and execute and the clients who choose to go through the journey are the most special. Next comes our team. The Amura Team is one filled with brilliant minds, brimming with creativity be it at operations, medical or marketing. You can be one of them. Come and explore. What is special about working with you? You will grow crazy-fast. As a rule of thumb, you can expect 5 years of growth for every year you are with us. But beware, growth like that cannot be achieved with life as usual. / But beware, growth like that cannot be achieved by any ordinary person. What kind of people are you looking to add to your team? We are looking for people who, when given the opportunity to have a measurable impact on the world, will take it. Who values human life and is willing to work tirelessly on not only improving themselves for their own sake but for the benefit of everyone in the world. We work on the edge of our own best, striving to find what could come next in our growth. Is this a WFH role? We do not have a WFH option. The work done at Amura is very unique. In person interactions will help you understand the brand better and get creative in ways you never imagined possible. Where is your office? Chennai - Perungudi Do you have an online presence? https://amura.ai (we are @AmuraHealth on all social media) Perks I get when I join Amura? Health is the hardware of success. Amura has a one-of-its-kind performance health program. It has helped thousands of people to grow and flourish in dimensions that are important to them. Everyone in Team Amura, and their dependents, get all of our medical knowledge and services at no cost. This is very unique to Amura. Until you speak with one of us, you can never know what an unbelievable power-up it can be.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Account Manager will develop and drive the territory sales vision and strategy for the Madrid area. They will work to growth new business opportunities and drive profitable revenue through collaboration, business-acumen and sales focus. Key Responsibilities Account Management Planning – Conduct analysis of customer applications to assess the potential demands that clients may have. Develop short/medium- and long-term strategies that result in improving the opportunities to increase the sales (Territory planning activities). Be focus on sales execution! implementing action plans and delivering revenue growth and margin expansion, identifying innovative and creative ways to protect and grow the core business. Commercial Process Management – lead contractual processes including Confidentiality agreements, Preferred provider / Master Services agreements /pricing agreements and tender submissions. Responsible for the resolution of commercial issues. Be proactive and accountable in sales progression. Reporting – provide account status reports as required– integrate SFDC as part of daily work to ensure accurate reporting. Generate sales forecast and delivery monthly business reviews on the territory. Customer - be accountable and continuous as consultant, improving customer experience, networking activities and meeting Company expectations in terms of important metrics. Continuous improvement – find opportunities for standardized work, and improvement of quality and service with customer base. Formulate and implement action plans for continuous improvement. Experience Preferred commercial experience selling in similar technological areas. Good attitude to built strong relationship Education, Requirements A degree level education is needed, with preference given where degree subject has a strong relevance to our business (MIcrobiology, Biology, Biochemistry and related field with Biomedical Science Clinical Experience with Microbiology Product). Strong communications, both written and oral, and the self-confidence to use these skills to be able to deliver Company vision. English: good level (written and spoken) in addition to a local language. Strong interpersonal abilities and project ownership ethic with a “can do” personality. Travel minimum 75% extensively Demonstrates and drives the Thermo Fisher values – Integrity, Intensity, Involvement and Innovation (The Four I’s). Full clean driving license.

Company Description Perfect Poultry Products is a leading provider of comprehensive poultry solutions encompassing hatcheries, poultry farms, feed and nutrition, chicken processing plants, and frozen foods. With a wide array of brands such as Gruubb, WA-HA, Real Fresh, neatmeats.com, FnM Fish and Meat Market, and Sanctuary Equipment & Tools, we offer quality products for retail and e-commerce markets. Our commitment to excellence ensures we meet the highest industry standards. Job Summary: The Plant Quality Manager will be responsible for ensuring that all raw chicken processing operations comply with internal quality standards, food safety regulations (FSSAI, HACCP, ISO), and customer specifications. This role involves managing the QA/QC team, driving continuous improvement, overseeing audits, and maintaining product safety and consistency. Key Responsibilities: Lead and manage the QA/QC function at the plant level. Ensure compliance with FSSAI, HACCP, ISO 22000, and other relevant food safety and quality standards. Monitor and control quality parameters across all processing stages: live bird receiving, slaughter, evisceration, chilling, packing, and dispatch. Implement and maintain plant-level SOPs, SSOPs, GMP, and hygiene practices. Coordinate internal and external audits (customer, regulatory, and third-party). Investigate quality deviations, customer complaints, and non-conformities; drive corrective and preventive actions (CAPA). Lead microbiological and residue monitoring programs in coordination with lab teams. Train staff and workers on food safety, hygiene, and quality protocols. Monitor performance metrics (KPIs) such as yield, rejection, rework, and customer complaints. Collaborate with Production, Maintenance, and Supply Chain teams for integrated quality improvements. Ensure traceability and documentation for all quality records. Desired Candidate Profile: Bachelor’s/Master’s degree in Food Technology / Microbiology / Veterinary Science / Poultry Science or related fields. 7–12 years of experience in quality assurance/food safety, preferably in raw chicken/meat/seafood processing plants. Strong understanding of Indian food safety laws (FSSAI), HACCP, ISO 22000, GMP, and other regulatory frameworks. Experience in managing audits, documentation, and plant hygiene programs. Leadership and team management skills. Strong communication, analytical, and problem-solving abilities.

For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. Job Summary Responsible for technical support for Endosafe® (including automated NEXUS system) and/or Celsis™ and their associated systems. Support customers on Endosafe® and/or Celsis™ instrument installation, qualifications and product validation. Provide on-site training, sample testing or troubleshooting for continued customer satisfaction of our clients. Manage activities to help meet revenue targets and goals for the business. Essential Duties And Responsibilities Understanding and application of one or more of the product lines under the Microbial portfolio (Endosafe® and/or Celsis™) Applies technical/scientific skills to develop existing accounts and compete for customers together with the Account Management team whether for products sales or services sales. Supports customer onboarding, provide customer training, qualify leads, perform test demonstrations and help close new business opportunities during customer start up and continued account management. Responsible for the initial training and validation/application development support for customers, ensuring full and continued utilization of Microbial Solutions products. Recommends or performs remedial actions to troubleshoot customer issues related to application, reagents and software for the assigned product line. Performs instrument qualification and installation for new customers. Establishes regular interface and communication with the Account Management and Field Services team to relay shared goals and targets; develop co-strategies to achieve defined targets; and work cohesively as a team to provide excellence in service to clients. Builds relationships with customers to influence the acceptance and use of Microbial portfolio. Input, manage and monitor cases on Service Cloud or SFDC.Ensures activities of the Technical Services team are continuously compliant to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate. GENERAL REQUIRMENTS Maintains confidentiality of all Client information according to internal SOPs, Quality Service Agreements, and regulatory requirements. Maintains appropriate records and documentation of activities to facilitate continuous compliance to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate. Actively seeks improvement within area of responsibility and takes necessary action to implement such improvements. Must be willing to travel domestically and internationally to customers’ sites. Adheres to Company Policies and Procedures, including Code of Ethics and to Health and Safety requirements. Performs all other related duties as assigned. Job Qualifications Education: Minimally M.Sc. or equivalent in Biology, Microbiology, Life Sciences, Biotechnology or any other related scientific discipline. Experience: 0-5 years of relevant industry experience, preferably involving customer-facing responsibilities. Salary range : 4 to 7 LPA. Understanding of Biology/Microbiology in the Pharma setting is an advantage. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Other: Must possess excellent communication and presentation skills. Proficient in the use of Microsoft Office applications. About Microbial Solutions Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction. 227850

For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. Job Summary Responsible for technical support for Endosafe® (including automated NEXUS system) and/or Celsis™ and their associated systems. Support customers on Endosafe® and/or Celsis™ instrument installation, qualifications and product validation. Provide on-site training, sample testing or troubleshooting for continued customer satisfaction of our clients. Manage activities to help meet revenue targets and goals for the business. Essential Duties And Responsibilities Understanding and application of one or more of the product lines under the Microbial portfolio (Endosafe® and/or Celsis™) Applies technical/scientific skills to develop existing accounts and compete for customers together with the Account Management team whether for products sales or services sales. Supports customer onboarding, provide customer training, qualify leads, perform test demonstrations and help close new business opportunities during customer start up and continued account management. Responsible for the initial training and validation/application development support for customers, ensuring full and continued utilization of Microbial Solutions products. Recommends or performs remedial actions to troubleshoot customer issues related to application, reagents and software for the assigned product line. Performs instrument qualification and installation for new customers. Establishes regular interface and communication with the Account Management and Field Services team to relay shared goals and targets; develop co-strategies to achieve defined targets; and work cohesively as a team to provide excellence in service to clients. Builds relationships with customers to influence the acceptance and use of Microbial portfolio. Input, manage and monitor cases on Service Cloud or SFDC.Ensures activities of the Technical Services team are continuously compliant to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate. GENERAL REQUIRMENTS Maintains confidentiality of all Client information according to internal SOPs, Quality Service Agreements, and regulatory requirements. Maintains appropriate records and documentation of activities to facilitate continuous compliance to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate. Actively seeks improvement within area of responsibility and takes necessary action to implement such improvements. Must be willing to travel domestically and internationally to customers’ sites. Adheres to Company Policies and Procedures, including Code of Ethics and to Health and Safety requirements. Performs all other related duties as assigned. Job Qualifications Education: Minimally M.Sc. or equivalent in Biology, Microbiology, Life Sciences, Biotechnology or any other related scientific discipline. Experience: 0-5 years of relevant industry experience, preferably involving customer-facing responsibilities. Salary range : 4 to 7 LPA. Understanding of Biology/Microbiology in the Pharma setting is an advantage. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Other: Must possess excellent communication and presentation skills. Proficient in the use of Microsoft Office applications. About Microbial Solutions Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction. 227850

1. Supervisor (Production/Factory Supervisor)Role Objective: To oversee daily manufacturing operations, ensure smooth production, and maintain hygiene and safety standards. Key Responsibilities: Supervise and coordinate production staff and processes. Monitor raw material usage and wastage. Ensure timely production and packaging of products. Maintain cleanliness and compliance with FSSAI/food safety norms. Maintain daily production reports and shift schedules. Handle basic machine troubleshooting. Skills Required: Knowledge of food safety standards. Leadership and communication skills. Basic understanding of production machinery. Education/Experience: Diploma or Graduate in Food Tech/Production; experience in FMCG preferred. 2. AccountantRole Objective: To manage financial records, compliance, and ensure smooth accounting of transactions. Key Responsibilities: Maintain purchase, sales, ledger entries (manual and/or Tally/ERP). GST filing and TDS deductions. Handle daily expenses, bank reconciliation, petty cash. Assist in payroll processing. Prepare profit and loss reports, balance sheets. Skills Required: Proficiency in Tally/Busy/Zohobooks. Knowledge of GST and tax laws. Attention to detail and numeric skills. Education/Experience: B.Com or M.Com; 1-3 years of experience in manufacturing/FMCG industry preferred. 3. Quality Executive/Officer (Quality Control & Assurance)Role Objective: To ensure the products meet defined quality and safety standards throughout the manufacturing process. Key Responsibilities: Conduct quality checks for raw materials, WIP (work in progress), and finished goods. Monitor hygiene and cleanliness standards in the plant. Implement and maintain quality management systems (QMS, HACCP, ISO). Coordinate with production for corrective actions. Maintain quality documentation and audit records. Skills Required: Knowledge of FSSAI, HACCP, GMP. Lab testing knowledge for food products. Good analytical and observation skills. Education/Experience: B.Sc/M.Sc in Food Science, Microbiology or B.Tech in Food Technology; 1-3 years experience. 4. Graphic Designer (Packaging & Marketing Design)Role Objective: To create visual content and packaging designs that reflect brand identity and attract consumers. Key Responsibilities: Design product packaging, labels, and marketing materials. Work with sales and marketing teams for promotions. Create designs for social media, brochures, hoardings. Ensure compliance with packaging and labeling regulations (like FSSAI info). Skills Required: Adobe Illustrator, Photoshop, CorelDraw, Canva. Creativity and understanding of brand aesthetics. Knowledge of print formats and color theory. Education/Experience: Diploma or Degree in Graphic Design or related field; 1-3 years experience in FMCG preferred.

Job Description At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the worlds most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, were working at the pace of change on diagnostic tools that address the worlds biggest health challenges, driven by knowing that behind every test there is a patient waiting. Learn about the Danaher Business System which makes everything possible. The Customer Technical Support & Service Coordination Specialist is responsible for providing remote product support to customers requiring assistance with instrumentation, LIS, software, hardware components and Assays sold and distributed by Cepheid. As a member of the Technical Support Team, you provide product support to internal and external customers and provide a solution to the issues faced by Customer. This is done majorly remotely via phone, email and web serving as the technical expert in Cepheids Customer Care experience and log and maintain all customer queries/complaints in CRM. This role will also be responsible for supporting the coordination activities to facilitate on-site intervention by Field Service Engineer. This position is part of the APAC Customer Care Team and will be located in Gurugram, India. In This Role, You Will Have The Opportunity To Engage customers to collect and compile detailed information about customer complaints. Conduct data analysis and basic troubleshooting for instrument, hardware, assays, software, and operating system. Investigate and resolve first level customer complaints remotely through phone and email. Document complaints and resulting investigations in the Complaint Management System (SFDC). Adhere to Quality Management System procedures. Complete all assigned and required training satisfactorily and on time and keep the records data for any future audit(s). Complete all compliance and internal training within the stipulated timeline. Train internal associates and new hires on the technical support modules and CRM. Represent Technical Support on projects and operational teams, communicating findings back to Technical Support. Performs additional tasks as assigned by the Technical Support Manager or Supervisor. Coordinating with customers for all service-related activities (Contracts renewal, Engineer visit, Spare parts transfer, Defective parts return). Dispatch Field Service Engineers for service calls as appropriate and actively communicate with the FSE to confirm all logistics to ensure proper recording and communications. Process purchase orders for billable service activities, which relate to service calls and preventative maintenance events. Qualifications: Bachelors degree in engineering / electronics or experience working in Biological / Clinical Laboratory Science / Life Science / Medical Device Industry with minimum 5 years of relevant experience (or equivalent), preferably in a fast-paced Customer Support & Service, Order Management role. Masters Degree with minimum 3 Years of related work experience. Fluent English (written and oral). Laboratory or Remote Technical Support Experience in one or more of the following is a plus: PCR and Microbiology, Molecular Biology Oncology or Virology, Patient sample collection practices and workflow, Sample preparation practices and methodologies, Laboratory analytical diagnostic equipment, medical devices, and software. Customer oriented understands customer expectations and empathizes with customer & patient needs. Knowledge and use of commercial computer application packages (MS Excel), Familiarity with SalesForce.com (or similar CRM System) and SAP a plus. Able to follow complex procedures and processes. Works independently in a structured manner with the ability to prioritize critical tasks. Builds collaborative work relationships with different teams, including Field Service, Field Application, Sales, Marketing and Quality. Thrives in a dynamic and fast-paced environment. May include extended computer and telephone work involving repetitive arm/wrist motions. Cepheid, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether its a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com. When you join us, youll also be joining Danahers global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, youll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization. Danaher is committed to a diverse and inclusive culture where everyone feels they belong, and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why well empower you to push the boundaries of whats possible. If youve ever wondered whats within you, theres no better time to find out. Join our winning team today. Together, well accelerate the real-life impact of tomorrows 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.

Factory Operations Establishing and implementation of all standard food safety parameters mandated by the internal quality policy company and regulatory authorities. Manage product quality during entire process flow, verify that all process control parameters are being followed and always documented. Inspect products and follow process from beginning to end to ensure all products met safe quality food standards. Enforce all company GMP's policies and procedures. Support the on-time release of finished products and raw materials and provide compliance guidance during regulatory inspections and corporate audits. Evaluate and approve raw materials and finished products, ensuring organizational and industrial guidelines and specifications were followed. Maintain a culture of continuous improvement by identifying process improvement opportunities and work with the Quality Team to implement change. Will assist in conducting internal audits and manage audits by third-party inspectors. Will assist in data analysis and preparing reports on food quality status to relay to top management. Monitoring of all record keeping and retrieval of all records - tests, inspections, QC logs as per requirement. Managing quality executives/ trainees/ interns of the respective location. Customer Complaint Handling Will assist cs team in review and respond to customer complaints and feed back to respective departments Will be in charge of doing RCA & corrective action for the quality complaints for respected geos, record keeping. Hub And Retail Shop Operations hub inspection/audit and carry out routine inspection/audit of the all the hubs/retail shop in the city. Will assist/conduct regular scheduled training for hub/retail shop staffs. Procurement Operations documentation of all the suppliers and scheduling and conducting vendor audits. documentation of supplier performance evaluation. Will assist/conduct regular scheduled vendor improvement training for the approved suppliers Will assist in the implementation of food safety standards, quality programmes as mandated by the internal quality policy of the company and regulatory authorities with the supplier Laboratory Will assist in the monitoring the microbiology laboratory and chemical tests to ensure all the tests are being done according to internal laid manual and required FSSAI and / or other applicable standards. Other Requirements Work in shifts along with some travel required with occasional outstation travel for partner institution research programmes/ training field staff/ QA implementation/Vendor improvement program at different location or training purposes. Fieldtrip/Travel for the purpose of internal audits and supplier audit. Should be conversant in computer skills and Good English Language skills. Any other duties or deputation to meet the overall food safety and quality assurance objectives of the company.

Location: IIT-Bombay/Vikhroli Bioprocess Engineer- Upstream & Downstream R&D Day-to-day responsibilities include: Operating bench-scale bioreactor systems Perform reactor sample analysis (wet lab, GC, pH, moisture, ash) Evaluate reactor performance (conversion efficiency, mass balance, optimization) Operating and analyzing biological and chemical systems in batch and continuous mode. Compile and analyze data from process development, troubleshooting, and summarize in high-quality reports Assist the founding team in technology advancement Nice to have: 1. 2 -5 years of experience with operating a bench-scale bioreactor and wet-lab skills 2. Experience with analysis- pH, moisture, ash, and gas chromatography 3. Experience with operating bench and pilot scale distillation apparatus 4. Operating downstream process equipments 5. Experience with chemicals process design and simulation using ASPEN plus 6, Experience with process modeling and simulation using SuperPro Designer Must Have: 2-5 years of relevant experience BS / MS / PhD in relevant engineering or science fields (biotechnology, chemical, microbiology, biochemical, chemistry) with keen interest in waste to value technology development. Job Type: Full-time Salary: 15,000.00 - 50,000.00 per month Ability to commute/relocate: Mumbai, Maharashtra: Reliably commute to IIT Bombay, Powai & Vikhroli (Required)

Company Description EQUITRON MEDICA PRIVATE LIMITED (Formerly Medica Instrument Mfg Co) is an ISO 13485:2016 and ISO 9001:2015 certified Laboratory Equipment Manufacturer specializing in lab instruments for microbiology, organic chemistry, pathology, and Autoclaves. Their product range includes various lab equipment marketed under brands like EQUITRON, EQUIBATH, LAPIZ, and more, exported to countries worldwide. Role Description This is a full-time on-site Field Services Engineer role located in Kalyan. The Field Services Engineer will be responsible for providing technical support, troubleshooting, preventive maintenance, and exceptional customer service for a range of laboratory equipment including Autoclaves, Clean Benches, and other specialized instruments. Qualifications Field Service and Technical Support skills Troubleshooting and Preventive Maintenance abilities Excellent Customer Service skills Experience in laboratory equipment maintenance Strong problem-solving and analytical skills Ability to work independently and in a team Degree or certification in Engineering or related field