Job Description Position - Clinical Microbiologist Location - Bangalore / Delhi Education - Freshers - MD Microbiologist Who are we HaystackAnalytics is a HealthTech company creating clinical genomics products, which enable diagnostic labs and hospitals to offer accurate and personalized diagnostics. Supported by India's most respected science agencies (DST, BIRAC, DBT), we created and launched a portfolio of products to offer genomics in infectious diseases. Our genomics based diagnostic solution for Tuberculosis was recognized as one of top innovations supported by BIRAC in the past 10 years, and was launched by the Prime Minister of India in the BIRAC Showcase event in Delhi, 2022. What we want you to do Integration of Microbiological Knowhow: Apply your expertise in microbiology to analyze and interpret clinical data, identifying trends and patterns relevant to infectious diseases. Bedside Versatility: Demonstrate proficiency in bedside care, understanding the clinical nuances of patient management, and effectively integrating microbiological insights into treatment plans. Effective Communication: Utilize your people skills to tactfully engage with senior clinicians, providing expert advice on microbiological matters and contributing to collaborative decision-making processes. Infection Control Leadership: Work closely with the infection control team and antimicrobial Stewardship Program (AMSP) champions to implement effective infection prevention and control measures within hospital environments. Experiential Knowledge Sharing: Communicate insights gained from practical experience to clients, demonstrating the value of experiential learning in the field of microbiology and infection control. NGS Technological Integration: Superimpose the minimum technological knowhow of Next-Generation Sequencing (NGS) to correlate with human infections, ensuring our solutions remain at the forefront of technological advancements in the field. What are we looking in you Freshers - MD Microbiologist / PhD. in Molecular Biology or Microbiology or Life Sciences or Biotechnology. Proven track record of effective communication and collaboration with interdisciplinary healthcare teams. Demonstrated understanding of infection control protocols and antimicrobial stewardship principles. Familiarity with molecular and sequencing (NGS) technologies and their applications in clinical microbiology is advantageous. What you will gain Dynamic and collaborative work environment dedicated to making a meaningful impact in healthcare Experience in working with advanced sequencing technology in the diagnostic industry i.e. NGS, WGS, Nanopore, and Illumina. Opportunities for professional development and continued education Competitive salary commensurate with experience Comprehensive health benefits package Skills: healthcare,clinical microbiology,ngs,next-generation sequencing (ngs),sequencing technologies,infection control,clinical data analysis,infection,collaboration,patient management,molecular technology,sequencing,microbiology,antimicrobial stewardship program (amsp),effective communication Show more Show less

Job description Key Responsibilities: * We are looking for a QC Technologist with an educational background in fisheries and relevant work experience in seafood and fishery processing. Conduct quality control checks at various stages of seafood processing, ensuring compliance with company and regulatory standards. Monitor raw material quality upon receipt, verifying freshness, texture, and compliance with specifications. Perform in-process quality inspections during production, processing, freezing, and packaging. Ensure adherence to food safety and hygiene standards, including HACCP, FDA, EU, and other export regulations. Maintain detailed records of inspections, test results, and non-conformance reports. Work closely with production teams to address quality issues and implement corrective actions. Oversee packaging integrity, labeling accuracy, and final product quality before dispatch. Assist in documentation for export quality certifications and audits conducted by regulatory authorities. Conduct training sessions for production staff on hygiene, quality standards, and food safety protocols. Collaborate with suppliers and procurement teams to improve raw material quality. Support continuous improvement initiatives to enhance product quality and minimize rejections. Requirements: Bachelor's degree in Food Technology, Microbiology, Fisheries Science, or a related field. 1+ years of experience in quality control, preferably in the seafood processing industry. Experience in quality audits, product sampling, and lab testing procedures. Familiarity with export documentation related to quality and regulatory compliance. Proficiency in MS Office and quality management software. Strong attention to detail, problem-solving skills, and the ability to work in a fast-paced environment. Job Types: Full-time, Permanent Pay: ₹10,000.00 - ₹15,000.00 per month Schedule: Day shift Ability to commute/relocate: Alipore, Kolkata, West Bengal: Reliably commute or planning to relocate before starting work (Required) Experience: total work: 1 year (Preferred) Work Location: In person Job Type: Full-time Pay: ₹10,000.00 per month Benefits: Paid sick time Schedule: Day shift Ability to commute/relocate: Alipore, Kolkata, West Bengal: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: QC: 1 year (Preferred) Work Location: In person Expected Start Date: 02/06/2025

Job Description: You will provide leadership in designing and implementing ground-breaking GPU computers that run demanding deep learning, high-performance computing, and computationally intensive workloads. We seek an expert to identify architectural changes and/or completely new approaches for accelerating our deep learning models. As an expert, you will help us with the strategic challenges we encounter, including compute, networking, and storage design for large scale, high-performance workloads, effective resource utilization in a heterogeneous computing environment, evolving our private/public cloud strategy, capacity modelling, and growth planning across our products and services. As an architect you are responsible for converting business needs associated with AI-ML algorithms in to a set of product goals covering workload scenarios, end user expectations, compute infrastructure and time of execution; this should lead to a plan for making the algorithms production ready Benchmark and optimise the Computer Vision Algorithms and the Hardware Accelerators for performance and quality KPIs. Optimize algorithms for optimal performance on the GPU tensor cores. Collaborate with various teams to drive an end to end workflow from data curation and training to performance optimization and deployment. Assign tasks to the team and monitor as well Skills Required MS or PhD in Computer Science, Electrical Engineering, or related field. A strong background in deployment of complex deep learning architectures . 7+ years of relevant experience in at least a few of the following relevant areas is required in your work history: Machine learning (with focus on Deep Neural Networks), including understanding of DL fundamentals; Experience adapting and training DNNs for various tasks; Experience developing code for one or more of the DNN training frameworks (such as Caffe, TensorFlow or Torch): Numerical analysis, Performance analysis, Model compression and Optimization & Computer architecture. Strong Data structures and Algorithms know-how with Excellent C/C++ programming skills. Hands-on expertise with PyTorch, TensorRT, CuDNN Hand-on expertise with GPU computing (CUDA, OpenCL, OpenACC) and HPC (MPI, OpenMP) In-depth understanding of container technologies like Docker, Singularity, Shifter, Charliecloud. Proficient in Python programming and bash scripting. Proficient in Windows, Ubuntu and Centos operating systems. Excellent communication and collaboration skills. Self-motivated and able to find creative practical solutions to problems. Good to have Hands-on experience with HPC cluster job schedulers such as Kubernetes, SLURM, LSF. Familiarity with cloud computing architectures Hands-on experience with Software Defined Networking and HPC cluster networking. Working knowledge of cluster configuration management tools such as Ansible, Puppet, Salt. Understanding of fast, distributed storage systems and Linux file systems for HPC workloads. About Company: AIRA Matrix provides artificial intelligence based solutions for Life Sciences applications. Our solutions improve efficiency, diagnostic accuracy, and turnaround times in pathology, microbiology and ophthalmology workflows across pharmaceutical and healthcare laboratories. We leverage machine and deep learning techniques to develop diagnostic, prognostic, and predictive solutions. Our solutions provide cost benefits in the pharmaceutical domain, by speeding up pre-clinical drug development timelines, and by enhancing the efficiency of environmental monitoring required in manufacturing. In healthcare applications, our solutions improve treatment outcomes by aiding disease stratification and enabling management protocols tailored to individual patients. Our clients and partners include leading hospitals, pharmaceutical companies, CROs, and research labs around the world. Our deep learning platforms with existing network models and pre-built AI applications provide the foundation for fast customizations and help tackle any unique challenges in your image analysis and study management workflows. Our flexible service model enables the swift deployment of these custom solutions with minimal resource and time commitment from your side. Our Application Development Team plays an important role in developing competent customer facing applications to access our AI solutions and enterprise-level image management systems in life sciences. -- Regards, Surya Prajapati Talent Acquisition Specialist Email : surya.prajapati@airamatrix.com Website : https://www.airamatrix.com Dosti Pinnacle, 801, Rd No. 22, Wagle Industrial Estate , Thane (W) Maharashtra, India - 400604. Show more Show less

Job Description: · The resource is expected to develop UI for digital pathology software that includes image viewers. · It would be desirable that candidates review the existing software and come up with new UX designs wherever required. · The resource is expected to be a self-initiator who can achieve challenging tasks independently. · Ability to test and debug for web developments. Functional and unit testing knowledge. Candidate Profile : Technical: · Primary skill sets required are JavaScript, TypeScript, AngularJS, Angular 2 to 8 (Angular10 Preferred), HTML 5 Canvas, Bootstrap, CSS (and related web UI development tools), AJAX, JSON · Good at basic problem solving and programming. · Hands on experience UX design is desirable Key Skills : · Angular8, Angular JS, Angular 2+,Responsive Web design (RWD), Html ,CSS, Java Script, jQuery, Bootstrap · Knowledge of Android and / or iOS is preferred. Academic background: · Bachelor’s degree in Computer Science or IT is a must and B.E is preferred · Prefer person with hands-on coding skills than any specific qualification. Experience : · Mid level : 5 - 10 years About Company: AIRA Matrix provides artificial intelligence based solutions for Life Sciences applications. Our solutions improve efficiency, diagnostic accuracy, and turnaround times in pathology, microbiology and ophthalmology workflows across pharmaceutical and healthcare laboratories. Our Application Development Team plays an important role in developing competent customer facing applications to access our AI solutions and enterprise-level image management systems in life sciences. It has successfully developed several innovative solutions, such as a one-of-a-kind image viewing platform for histopathology images enabled with digital collaboration, custom web applications with built-in workflows for microbial monitoring, and custom libraries for UI to support unique features and audit traceability across applications among other functionalities. With absolute flexibility to choose and use the latest technologies, our AppDev team comes up with best-in-class enhancements and feature upgrades which are highly appreciated by the customers. -- Regards, Surya Prajapati Deputy Manager - Talent Acquisition Email : surya.prajapati@airamatrix.com Website : https://www.airamatrix.com Dosti Pinnacle, 801, Rd No. 22, Wagle Industrial Estate , Thane (W) Maharashtra, India - 400604. Show more Show less

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. Show more Show less

Position - Clinical Microbiologist Location - Delhi Education - Freshers - MD Microbiologist.3 Who are we HaystackAnalytics is a HealthTech company creating clinical genomics products, which enable diagnostic labs and hospitals to offer accurate and personalized diagnostics. Supported by India's most respected science agencies (DST, BIRAC, DBT), we created and launched a portfolio of products to offer genomics in infectious diseases. Our genomics based diagnostic solution for Tuberculosis was recognized as one of top innovations supported by BIRAC in the past 10 years, and was launched by the Prime Minister of India in the BIRAC Showcase event in Delhi, 2022. What we want you to do ● Integration of Microbiological Knowhow: Apply your expertise in microbiology to analyze and interpret clinical data, identifying trends and patterns relevant to infectious diseases. ● Bedside Versatility: Demonstrate proficiency in bedside care, understanding the clinical nuances of patient management, and effectively integrating microbiological insights into treatment plans. ● Effective Communication: Utilize your people skills to tactfully engage with senior clinicians, providing expert advice on microbiological matters and contributing to collaborative decision-making processes. ● Infection Control Leadership: Work closely with the infection control team and antimicrobial Stewardship Program (AMSP) champions to implement effective infection prevention and control measures within hospital environments. ● Experiential Knowledge Sharing: Communicate insights gained from practical experience to clients, demonstrating the value of experiential learning in the field of microbiology and infection control. ● NGS Technological Integration: Superimpose the minimum technological knowhow of Next-Generation Sequencing (NGS) to correlate with human infections, ensuring our solutions remain at the forefront of technological advancements in the field. What are we looking in you ● Freshers - MD Microbiologist / PhD. in Molecular Biology or Microbiology or Life Sciences or Biotechnology. ● Proven track record of effective communication and collaboration with interdisciplinary healthcare teams. ● Demonstrated understanding of infection control protocols and antimicrobial stewardship principles. ● Familiarity with molecular and sequencing (NGS) technologies and their applications in clinical microbiology is advantageous. What you will gain ● Dynamic and collaborative work environment dedicated to making a meaningful impact in healthcare ● Experience in working with advanced sequencing technology in the diagnostic industry i.e. NGS, WGS, Nanopore, and Illumina. ● Opportunities for professional development and continued education ● Competitive salary commensurate with experience ● Comprehensive health benefits package Job Types: Full-time, Permanent Pay: ₹1,000,000.00 - ₹1,500,000.00 per year Education: Doctorate (Preferred) Work Location: In person

About Avam: Avam is an innovative biotechnology leader delivering cutting-edge solutions in molecular and microbiology technologies. Our products bridge scientific breakthroughs and real-world applications, serving a diverse customer base across research institutions, healthcare providers, pharmaceutical companies, and industrial laboratories globally. Position Overview: We are seeking an experienced and knowledgeable Product Specialist with expertise in molecular biology and/or microbiology techniques to join our dynamic team. This unique hybrid role combines deep product knowledge and technical communication skills, as you will engage directly with product support and customer training, while also drafting clear, accurate, and user-friendly technical documentation. Responsibilities: Provide specialized product support, training, and technical expertise to internal teams and external customers. Draft, maintain, and refine product technical documentation, including user manuals, application notes, protocols, technical datasheets, and troubleshooting guides. Collaborate closely with R&D, Quality Assurance, Regulatory Affairs, and Marketing teams to accurately translate product knowledge into effective documentation. Conduct technical demonstrations and webinars to educate customers and support sales efforts. Act as a primary resource for addressing technical questions, product applications, and resolving customer inquiries efficiently and effectively. Ensure accuracy, compliance, and consistency across all technical documentation, adhering to industry and regulatory standards. Qualifications: Bachelor’s or Master’s degree in Molecular Biology, Microbiology, Biotechnology, Life Sciences, or a related field. Demonstrated hands-on experience with molecular biology or microbiology laboratory techniques (PCR, qPCR, nucleic acid extraction, microbial culture methods, etc.). Proven experience in technical documentation, scientific writing, or related roles, preferably within biotechnology or life sciences sectors. Exceptional written and verbal communication skills, capable of translating complex scientific concepts into clear documentation. Fluent in English with strong English writing skills. Strong interpersonal skills, with experience in customer support or training roles being highly advantageous. Proficiency with documentation software and content management systems. Highly organized, detail-oriented, and capable of managing multiple tasks simultaneously. Benefits: Competitive salary and comprehensive benefits package. Opportunities for professional growth and career advancement. Collaborative and inclusive work environment. Flexible work arrangements. Why Avam? Contribute directly to innovative biotechnology solutions with global impact. Collaborative, supportive work environment that fosters professional growth and development. Competitive compensation package and benefits. Show more Show less

Location: On-site – Nalagarh, Himachal Pradesh Experience: 1–2 years (Mandatory) Qualification: B.Sc. in Chemistry / Microbiology / Biotechnology / Life Sciences About the Role: We are looking for a dedicated Quality Control (QC) Officer to join our pharmaceutical manufacturing team at our Nalagarh facility. The ideal candidate will have hands-on experience with laboratory testing and strong documentation practices in a GMP-regulated environment. Key Responsibilities: Conduct testing of raw materials, in-process samples, and finished products. Operate and maintain analytical instruments like HPLC, UV, IR, pH meter, etc. Ensure accurate and timely documentation as per cGMP and GLP guidelines. Perform stability studies and environmental monitoring (if required). Participate in lab audits, calibration, and equipment qualification. Maintain safety and hygiene in the lab environment. Desired Profile: B.Sc. in Chemistry / Microbiology / Biotechnology or relevant field 1–2 years of QC experience in a pharmaceutical formulation unit (mandatory) Sound knowledge of GMP practices and analytical techniques Attention to detail, good documentation habits, and strong analytical skills Mandatory Proficiency in written and verbal English Join a team committed to delivering high-quality, affordable medicines. Apply now to become part of our quality-driven organization! #QualityControl #PharmaJobs #ChemistryJobs #QCOfficer #PharmaceuticalIndustry #HimachalJobs #BScJobs #NalagarhJobs #PharmaCareers #GMPCompliance Job Type: Full-time Pay: From ₹30,000.00 per month Benefits: Commuter assistance Paid time off Schedule: Day shift Rotational shift Supplemental Pay: Performance bonus Work Location: In person

Pharmaceutical & Life Sciences Full-Time Job ID: DGC00473 Chennai, Tamil Nadu 1-2 Yrs ₹1.5 - ₹03 Yearly Job description Microbial Research: Conduct research on various microorganisms to understand their structure, behavior, growth patterns, and functions Microbial Identification: Use techniques like microscopy, DNA sequencing, and biochemical assays to identify and classify microorganisms Culturing Microorganisms: Cultivate and maintain microorganisms in the laboratory, ensuring that they have the appropriate growth conditions Disease Diagnosis: In clinical microbiology, microbiologists diagnose infectious diseases by identifying the pathogens responsible and conducting drug susceptibility testing Environmental Monitoring: Analyze water, soil, and air samples to assess microbial contamination, environmental impact, and safety Food Microbiology: Ensure the safety of food products by testing for the presence of harmful microorganisms and monitoring food production processes Pharmaceuticals and Biotechnology: Work on the development and production of antibiotics, vaccines, and biotechnology products Genetic Engineering: Engage in genetic engineering and genetic modification of microorganisms to develop new strains with specific characteristics Quality Control: Maintain quality control in various industries by conducting tests to verify product quality and safety Research and Development: Work on innovative research projects to advance scientific knowledge and discover new applications for microorganisms Public Health: Monitor and control infectious disease outbreaks, track microbial contamination in the environment, and contribute to public health policy Laboratory Safety: Ensure that laboratory safety protocols are followed to prevent the accidental release or exposure to dangerous microorganisms Reporting and Documentation: Maintain detailed records of experiments, findings, and laboratory procedures Prepare research reports and scientific publications

Skill required: Clinical Data Operations - Clinical Database Testing Designation: Clinical Data Svs Associate Qualifications: Master’s in actuarial science Years of Experience: 1 to 3 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world s leading biopharma companies bring their vision to life and enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. The Clinical Testing Team is dedicated to conduct through validation of all clinical trial database components ensuring that database meets quality standards while remaining cost effective. Their responsibilities include reviewing requirement specification, developing test scripts for carious testing types, performing data entry according to these scripts, executing test steps, documenting results and maintaining comprehensive records of all tested components in compliance with regulatory requirements. Design and test EDC databases, create and maintain User Acceptance Testing (UAT) procedures for EDC systems, including the creation of test plans, verification of requirements for databases, eCRFs, edit checks, extractions, and reports. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Ability to establish strong client relationship Agility for quick learning Candidates who have completed Master s or Post graduate degree in Life Science domain (Biology, Genetics, Microbiology, Biochemistry, Biotechnology, and Ecology) in 2024 & 2025 (if all semester s results are available). Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Master’s in actuarial science Show more Show less

Skill required: Clinical Data Operations - Clinical Database Testing Designation: Clinical Data Svs Associate Qualifications: Master’s in actuarial science Years of Experience: 1 to 3 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world s leading biopharma companies bring their vision to life and enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. The Clinical Testing Team is dedicated to conduct through validation of all clinical trial database components ensuring that database meets quality standards while remaining cost effective. Their responsibilities include reviewing requirement specification, developing test scripts for carious testing types, performing data entry according to these scripts, executing test steps, documenting results and maintaining comprehensive records of all tested components in compliance with regulatory requirements. Design and test EDC databases, create and maintain User Acceptance Testing (UAT) procedures for EDC systems, including the creation of test plans, verification of requirements for databases, eCRFs, edit checks, extractions, and reports. What are we looking for? Candidates who have completed Master s or Post graduate degree in Life Science domain (Biology, Genetics, Microbiology, Biochemistry, Biotechnology, and Ecology) in 2024 & 2025 (if all semester s results are available). Adaptable and flexible Ability to perform under pressure Problem-solving skills Ability to establish strong client relationship Agility for quick learning Experience with Clinical testing, Understanding of clinical Trials, Phases and clinical domain. Familiarity with clinical data management concepts and terminologies, Knowledge of regulatory guidelines such as GCP, ICH, 21 CRF Part 11 and GDRP. Experience in test script development and strong documentation skills for test cases, validation reports and audit trials. Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Master’s in actuarial science Show more Show less

JOB Description Job Title: Business Development (IVD Industry) Location: Netaji Subhash Place Company: Astam Diagnostics Department: Sales & Marketing Reporting to: Head – Business Development / Director – Sales About Astam Diagnostics Astam Diagnostics is a rapidly growing company specialising in the development, manufacturing, and marketing of high-quality diagnostic solutions, with a focus on enhancing healthcare outcomes. With a strong presence in the IVD sector, we are expanding our footprint and are looking for passionate professionals to join our journey. Key Responsibilities • Identify new business opportunities and develop strategies to increase sales in the IVD product segment (e.g., Rapid Tests, ELISA Kits, etc.) • Develop and manage strong relationships with distributors, hospitals, diagnostic labs, and healthcare providers. • Achieve revenue targets and market share growth in assigned territories. • Conduct market research to stay updated on competitor activities, pricing, and customer needs. • Collaborate with the marketing team to plan and execute promotional campaigns. • Prepare sales forecasts, reports, and business plans. • Ensure customer satisfaction through timely support, training, and communication. • Attend industry events, trade shows, and conferences to network and showcase Astam’s offerings. • Work closely with internal teams (Regulatory, QA, R&D) to align business development efforts. Requirements • Bachelor’s degree in Life Sciences, Biotechnology, Microbiology, or related field. An MBA in Marketing/Sales is an advantage. • 3+ years of proven experience in Business Development/Sales in the IVD diagnostics industry.• Strong understanding of IVD products and the diagnostics ecosystem in India. • Excellent communication, negotiation, and interpersonal skills. • Willingness to travel extensively within assigned regions. • Self-motivated, target-driven, and capable of working independently.

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances

Job Responsibilities JOB DESCRIPTION To handle and distribute various samples received for microbiological analysis. To maintain the logbook for the same. Maintain housekeeping of Microbiology lab. To maintain the inventory of various microbiological media, maintain log and status labels, media preparation, growth promotion test and reconciliation of media. Microbial culture handling and inoculum preparation. Water sampling and analysis of water samples as per schedule, with completion of all reports and records. Responsible for Sterility testing, Bacterial endotoxin testing, antibiotic microbial assay and bio burden testing of Raw material, in-process, finished products. Environmental monitoring of microbiology lab clean room area as per the defined schedule. Non-viable particle monitoring of microbiology lab clean room area as per the defined schedule. Responsible to identify and maintain data logging of EM Isolates. To perform disinfectant efficacy testing as per SOP. To perform microbial identification as per defined schedule. Responsible for handling and testing of biological indicator. To perform CCIT test of post media fill units. To perform observation of microbial plates exposed in manufacturing area. To perform media fill unit observation as per SOP. Responsible for reporting any OOS, Deviation to In-charge. Responsible for preparation of standard operating procedures of microbiology department. Responsible to co-ordinate with manufacturing, Engineering, and other QC personnel for respective Qualification / Validation / Re-qualification activity for timely completion of activities. Responsible to participate in perform qualification activities of manufacturing and Microbiology area. Responsible for Compressed air /nitrogen gas monitoring and Personnel monitoring. Preparation of indents as per the materials/product requirements. To initiate and review of a) Change controls b) Out of specifications c) Deviations. To attain and complete self- training record. Preparation of study protocols with respect to laboratory. Review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Preparation of COA. To keep neat and cleanliness at workplace and follow the good laboratory practices and safety related instruction in the laboratory. To perform water analysis and maintain daily water trend. Sampling, testing and release of Raw material, packing material, miscellaneous material samples and in process sample and maintain reserve sample as per SOP. Qualifications Qualification: M.Sc (Microbiology) / B.Pharm Experience: 4-7 years Show more Show less

Job Purpose As a Trainee Chemist, you will play a crucial role in supporting laboratory experiments, conducting field trials, gathering and analyzing technical data, and contributing to the design of performance-driven enzyme and yeast solutions. You will work closely with the technical, sales, and customer teams to bridge the gap between R&D and commercial implementation. Key Responsibilities Laboratory Work: Conduct day-to-day lab experiments related to enzyme and yeast applications. Record observations and maintain accurate lab notebooks and data logs. Field Trials & Customer Engagement: Attend and support on-site product trials at customer locations across India. Collect process samples during trials, conduct on-the-spot testing where required. Collaborate with the sales and technical team during field visits. Data Management & Reporting: Analyze samples and compile technical data into standardized lab/trial reports. Summarize trial outcomes, highlight performance parameters, and prepare conclusion reports outlining what worked and what didn’t. Present findings and reports to internal stakeholders and clients. Technical Collaboration: Assist in developing or modifying products based on market and trial feedback. Coordinate with the sales team to deliver customer-specific solutions. Support in market requirement identification through customer visits and research. Stakeholder Communication: Present and explain technical concepts and trial outcomes to both internal teams and external clients in a structured and professional manner. Continuous Improvement: Work on improving product applications and support services. Bring a proactive approach to troubleshooting and on-ground problem solving. Ideal Candidate Profile Education: B.Sc. / M.Sc. in Chemistry, Microbiology, Biotechnology, or related field. Experience: Freshers welcome. Internship or project experience in analytical work, fermentation, or enzyme technology is a plus. Skills: Strong interest in applied industrial chemistry or biotechnology. Good data handling, basic statistical understanding, and MS Excel skills. Comfortable with travelling for trials (25-50% travel as required). Strong written and verbal communication skills. Curious mindset with a willingness to learn and take initiative. Ability to work independently and collaboratively in a dynamic setup. What We Offer Hands-on experience with live industrial applications. Opportunities to work closely with global leaders in enzyme and yeast innovation. Exposure to diverse industries like ethanol, brewing, distilling, and more. A learning-driven, collaborative environment with mentorship from experienced professionals. Long-term growth path in technical, commercial, or innovation roles based on performance.

Type: Part-Time, Remote Perks: US organisation, handsome compensation Compensation: Starting at $12 to $25/hour (~Rs. 1400+ per hour) if you work an average of 3 hours a day - that could be upwards of Rs 1L per month if you choose to work average 8 hours a day - that could be upwards of Rs 2.2L per month Expected (minimum) Commitment: 10 hours/week Role Overview: A well-funded AI research company is looking for candidates with strong Food Science knowledge. What does day-to-day look like? You would evaluate and improve AI-generated content related to food chemistry, nutrition, food safety, and processing techniques. Example roles include: Food Safety Task: Review AI-generated guidelines for food storage and suggest improvements based on FDA/FSSAI standards. Nutritional Science Task: Assess AI-generated diet plans and refine them based on macronutrient and micronutrient balance. Food Technology Task: Evaluate AI-generated content on food preservation techniques and refine explanations based on scientific principles. Requirements: Strong understanding of food chemistry, microbiology, and nutrition. Familiarity with food regulations (e.g., FSSAI, FDA, Codex Alimentarius). Excellent analytical and communication skills. Preferred: Degree in Food Science, Nutrition, or Food Technology. Experience in food research, quality control, or product development. Prior experience in AI-driven food recommendation systems or nutrition apps. Benefits: Collaborate with globally renowned experts and build a network tailored to your career aspirations. Experience the flexibility of remote work while breaking away from traditional office setups. Receive industry-standard salaries in USD. Contribute to innovative projects pushing the boundaries of technology, keeping you at the forefront of advancements. Complete an online assessment! Join us in revolutionizing AI! ✅ Follow for more AI Jobs + Entrepreneurship Ayyush Sharma (Chhotapreneur) Growth, Strategy & Revenue Operations | A+ track record in scaling startups. Growth @ Outlier AI Show more Show less

Role & responsibilities Performing routine microbiological testing on raw materials, in-process samples, and finished products to ensure they meet quality and safety standards. Conducting environmental monitoring of clean rooms and other controlled environments Documenting and interpreting test results accurately and timely Ensuring adherence to Good Manufacturing Practices (GMP) and Hazard Analysis and Critical Control Points (HACCP) Monitoring and maintaining water systems for safety Assisting in achieving standards accreditation Validating and verifying cleaning and sanitation practices through microbiological testing Preferred candidate profile Qualification :- B.SC or M.SC (Microbiology) Work Experience :- 2-4 Years

Designation : Assistant Manager Quality Department : Coding Location : Airoli , Navi Mumbai Qualifications: Bachelor degree from a Life science stream (Biotech, Microbiology, Pharmacy, Physiotherapy, Zoology, Botany) or Equivalent Responsibilities Will be responsible for supervising and managing a team of 20-25 QAs Create an inspiring team environment with an open communication culture Design QA capacity planning Delegate tasks and set deadlines Manage Quality of ProFee EM Coding projects Quality control as per client SLA Ensure effective implementation of organization s Quality Assurance Management System Monitor team performance and report on metrics Performing random audit of auditor Perform RCA on audits observations. Identify knowledge gaps and develop an action plan with quality leads and operation managers Discover training needs and provide coaching to QAs Listen to team members feedback and resolve any issues or conflicts Recognize high performance and reward accomplishments Encourage creativity and business improvement ideas Suggest and organize team building activities Identify improvement opportunities and initiate action plans for improvement Experience Min 6-7 years coding experience in Physician Profee + Surgery or EM Coding in 1 or more areas of specialties with an AHIMA or AAPC certification. Preferably at least 2-3 years experience in a lead role with auditing, training, SME role and/or managing a team of QAs or coders. Should have hands on experience in the relevant specialty(s). Should have experience in prominent EMR(s) and Encoder(s). Should be very familiar with utilization of references from CMS sources, Coding Clinic, and CPT Assistant.

Join our team as the expert you are now and create your future. Responsible for the day-to-day production and quality functions of a team of coders specializing in meeting client production goals and coding accuracy goals. Plans, directs, supervises and evaluates feedback workflows and coordinates activities across all coding staff assigned to the team. Excellent communication skills, attention to detail, and strong technical and problem solving skills are essential aspects of this role. Responsible for the day-to-day production and quality functions of a team of coders specializing in meeting client production goals and coding accuracy goals. Plans, directs, supervises and evaluates feedback workflows and coordinates activities across all coding staff assigned to the team. Excellent communication skills, attention to detail, and strong technical and problem solving skills are essential aspects of this role. JOB DETAILS: Perform a variety of activities involving the coding of medical records by ascribing accurate diagnosis and CPT codes as per ICD-10 and CPT-4 systems of coding Perform Coding for Outpatient and/or Inpatient records with a minimum of 96% accuracy and as per turnaround time requirements Exceeds the productivity standards for Medical Coding - as per the productivity norms for inpatient and/or speciality specific outpatient coding standards Maintains high degree of professional and ethical standards Focuses on continuous improvement by working on projects that enables customers to arrest revenue leakage while being in compliance with the standards Focuses on updating coding skills, knowledge, and accuracy by participating in coding team meetings and educational conferences Experience in specialties such as Inpatient, EM, Acute, Ambulatory, Cardiology, Radiology, Pathology, Anesthesia, Emergency Room, Surgery, and others Exposure to CPT-4, ICD-9, ICD-10, and HCPCS coding Understand the client requirements and specifications of the project and code the charts accordingly Code records by following prescribed coding standards such as ICD-9/ ICD-10 and CPT Ensure patient information are correct and appropriate signatures on all medical records Assign appropriate medical codes to all diagnosis and services Follow client specific guidelines wherever applicable working as per client updates and coding the charts accordingly Meet the productivity targets of clients within the stipulated time Ensure that the deliverables to the client adhere to the quality standards Prepare and maintain status reports QUALIFICATIONS: Graduate in Life Science, Pharmacy, Physiotherapy, Zoology, Microbiology discipline 2+ years of industry experience CPC - Certified Coding Professional or CCS - Certified Coding Specialist Position Level Senior Analyst Country India

Fresher Hiring 2023 - 2025 Passouts only - All India Qualification - B.Pharm, M.Pharm, B.SC, M.SC, Life Sciences Graduates & Post Graduates Medical - BDS, BHMS, BAMS, MBBS Role & responsibilities Perform data reconciliation between different data sources and study documents to ensure data integrity and consistency across datasets. Generate data queries to address discrepancies, inconsistencies, and missing data identified during data review, ensuring timely resolution and documentation of data queries Communicate data queries to investigative sites, data managers, and study personnel, following up on query responses and resolving discrepancies in collaboration with relevant stakeholders Identify deviations from protocol-specified procedures, eligibility criteria, and data collection guidelines, escalating issues to appropriate personnel for resolution Perform quality checks and data validation procedures to ensure accuracy, consistency, and reliability of clinical trial data, adhering to data management standards and industry best practices Assist in the development and implementation of data validation plans, data review guidelines, and quality control procedures to maintain high standards of data quality and integrity. Assist in a variety of specialties including but not limited to primary care, orthopedics, rheumatology, etc. Updates patient history, physical exam, and other pertinent health information in the document as required. Complies with Compliance standards of the Organization as laid by HIPAA. Performs other duties and tasks to improve provider productivity and workflow as assigned by supervisors. Assist documenting the patients, electronic health record (EHR). Fresher Hiring - Pharma / Life Sciences / Medical Qualification - B.Pharm, M.Pharm, B.SC, M.SC, Life Sciences Graduates & Post Graduates Medical - BDS, BHMS, BAMS, MBBS Location - All India - Delhi, Mumbai, Pune, Bangalore, Kochi, Chennai, Hyderabad, Ahmedabad, Bhopal, Indore, Kolkata, Chandigarh

URGENTLY REQUIRED ANATOMY, PHYSIOLOGY, BIOCHEMSITRY, PHARMACOLOGY, RADIOLOGY, DERMATOLOGY, PSYCHIATRY, FORENSIC MEDICINE, MICROBIOLOGY. POST: DEAN, M.S., PROFESSOR, ASSOCIATE PROFESSOR. QUALIFICATION: MD/MS CONTACT: 7909992043 E: HR@BGCONSULTANCY.IN Perks and benefits ACCOMODATION IN COLLEGE OR HRA

Urgent Hiring – Senior Residents Location: Lucknow Joining: Immediate Departments Open: Clinical Non-Clinical Apply Now: Send CV to [effra@trimushr.com] **Contact:[8178692895]

JOB OPENING FOR INJECTABLES QC CHEMICAL 1. Experience: 6 to 7 years Education: M.Sc/B.Sc/M.Pharma Job Description: 1. Well versed knowledge of QC software (Chromeleon, Labsolution, Taimo etc). 2. Knowledge of QC documentation 3. Knowledge of analytical data review. 2. Experience: 3 to 5 years Education: M.Sc/B.Sc/M.Pharma Job Description: 1. Knowledge of laboratory instrument handling such as HPLC, GC, Autotitrator, UV, FTIR etc. 2. Well versed knowledge of GLP, GDP & Data Integrity PRODUCTION INJECTABLES 1. Lyo-Operator/ Officer Experience: 3 to 5 years Education: B.Pharma//M.Pharma Job Description: 1. Knowledge of Lyophilizer operation & troubleshooting 2. Handling of Automatic loading & unloading system 2. Aseptic Area Operator/Officer Experience: 3 to 5 years Education: B.Pharma//M.Pharma Job Description : 1. Knowledge of media fill & dry powder filing machine operation 2. Knowledge of aseptic area operation QC MICRO Experience: 3 to 5 years Education: B.Pharma//M.Pharma Job Description : 1. Preparation of trend data for water analysis & environment monitoring program. 2.Responsible for performing MLT of Water, Raw material and Bioburden Test of in process sample. 3.BET testing of finished products, raw material and stability sample. 4.Sterility Testing of finished products, raw material and stability sample. If interested, share your updated CV along with the below mentioned details on mail id: preeti.yadav@brookssteriscience.com 1. Current Organization 2. Total Experience: 3. Current Designation: 4. Current CTC: 5. Expected CTC: 6. Notice Period: 7. Availability for Interview: With Regards Team-HRA

Overview This role supports the global Specifications Management function by ensuring high-quality service delivery to Research & Development teams across regions. It involves leveraging technical expertise to develop and maintain clear and accurate Formula, Ingredient, and/or Packaging specifications. The role also includes collaborating with cross-functional teams and external partners, managing supplier relationships, and ensuring accurate documentation and tracking within relevant systems. Responsibilities Functional Responsibilities Leverage internal and external resources to develop or update existing ingredient and/or packaging specifications that are clear, concise, and accurate from spec readiness to supplier commercial qualification approval Learn, understand, and uphold Ingredient, Supplier, Third Party, Formula, and/or Beverage/Food Packaging Standards Dependent on team arrangement, may be mentored, take guidance and produce work to be checked by a Spec Writing Snr Analyst Maintain and foster relationships with in-market R&D spec teams, other spec GBS teams, and external suppliers Interact with and provide support to all disciplines to ensure complete and accurate specification. These stakeholders could include some or all of the following: Product Development (PD), Food Safety (FS), Regulatory Affairs (RA), Quality Assurance (QA), Procurement, Supplier Quality Assurance (SQA) Manage Supplier relationships and serve as point of contact to gather information/data needed to build specifications; complete timely follow-ups to keep the process moving to completion Collect supplier questionnaire and manage supplier alignment on spec details For certain Specifications (eg. Foods & Beverages) initiate material testing requests and validate specification quality parameters Maintain and update existing specs to ensure compliance with standards Upload all paperwork (re. Supplier Specs) and materials qualifications into the appropriate system (Product Vision / SAP) and track workflow For Packaging Specifications only: schedule and conduct Individual Component Specification (ICS) reviews, update documents, and manage supplier approval prior to internal review Ensure all requests are processed, documented, and delivered within defined SLAs (Service Level Agreements) Respond and escalate emerging business critical issues to avoid material supply shortages, outages and production delays Qualifications Bachelor’s degree in Food Science, Food Engineering, Food Chemistry, Microbiology, Biochemical Engineering or Chemical Engineering or equivalent relevant experience required. 1-2 years of experience on Regulatory, QA/QC, Food Analytical experience or other Food related FMCG in a technical role. Depending on talent and availability, this role could be filled by an exiting Intern. Ability to interpret technical information, escalate issues and seek alignment towards workable solutions Proficient with Microsoft Office Suite Ability to rapidly learn computer applications/programs & navigate systems For Formula and Ingredient Specifications: basic understanding of Food Safety, Microbiology and Regulatory Affairs Collaborative skills and strong interest in working with others across time zones; Ability to build relationships and work closely with both internal and external partners Good communication skills - oral and written (e.g. communication on telephone, external and internal to PepsiCo, managing with other support group functions, etc.) Ability to manage time effectively across multiple priorities and projects requiring a high degree of organizational and communication skills to ensure requests are delivered in a timely manner Exceptional data organizational and problem-solving skills with attention to detail and accuracy Self-motivated & demonstrated ability to take initiative on projects Fluent in English Show more Show less

Summary Lead, support and report independent GMP audits according to the Novartis Quality System and the current GMP regulations to assess compliance with applicable regulations, standards, and guidance documents. Review and approve corrective action plans in support of the audit observations. The audits performed include internal and external targets of manufacturing sites, development centers, quality systems, contract manufacturers, laboratories, warehouses, country organizations, and suppliers. Align strategic direction with senior leaders of Novartis and help establish programs to implement. Provide expert consultation to Novartis business units through risk based assessments. Act as SME for assigned areas of responsibility. Represent the company in external interactions with Health Authorities and industry groups. About The Role Expert GMP Auditor Location - Mumbai About The Role: Lead, support and report independent GMP audits according to the Novartis Quality System and the current GMP regulations to assess compliance with applicable regulations, standards, and guidance documents. Review and approve corrective action plans in support of the audit observations. The audits performed include internal and external targets of manufacturing sites, development centers, quality systems, contract manufacturers, laboratories, warehouses, country organizations, and suppliers. Align strategic direction with senior leaders of Novartis and help establish programs to implement. Provide expert consultation to Novartis business units through risk based assessments. Act as SME for assigned areas of responsibility. Represent the company in external interactions with Health Authorities and industry groups. Key Responsibilities: Contribute to establishing the strategic direction of an effective global risk-based audit strategy and program. Collect, collate, and incorporate input into the audit strategy and plan. Plan, lead, conduct, document, and follow-up of GMP audit according to the requirements specified in the respective Novartis Quality procedures as well as applicable regulations, standards, quality agreements, and guidance documents. For this expert role, the leader in this position is able to audit complex and high-risk sites and activities. The leader in this position is considered an expert and SME in one or more manufacturing areas, such as sterile manufacturing, combination products, biologics, etc. Provide technical guidance, mentoring, and training on audit activities. Provide regulatory guidance for timely remediation and recommendations regarding acceptability of the proposed filing. Prepare audit reports according to NVS requirements and timelines. Ensure appropriate escalation to responsible management in case of critical findings and support immediate follow-up measures according to NVS requirements on Management Escalations and other relevant procedures. Ensure adequate definition and recording of mitigation plans when applicable. Assess the adequacy of responses (CAPA plans) to audit findings in cooperation with the stakeholder QA representative and Auditee. Act as GMP compliance consultant for GMP trainings, task forces, continuous improvement projects as needed. Review and advise on relevant policies and procedures. Mentor junior GMP staff as required. Ability to perform training for non-certified and junior GMP staff. Maintain current, expert knowledge of regulations and elaborate best practices auditing guideline (when applicable). Support development/training of GMP auditors. Support HA commitments and global commitments/initiatives as an outcome of inspection findings. Essential Requirements: At least 15 years broad experience in Pharmaceutical or Medical Device Industry. The operational experience should include QA/QC management and manufacturing, or development or other relevant experience e.g. working at a regulatory health authority. At least 3+ years auditing experience, and excellent knowledge of regulatory requirements. Willingness to travel approximately 60% of the time. Expertise in at least one of the following areas: DP Manufacturing, Laboratories activities, Medical Devices, API, Excipients, Sterile, Biologics, Microbiology, Computer System Validation, Packaging activities, Quality Systems. Experience and/or interaction with local Health Authority and sporadically with other Health Authorities. Excellent interpersonal skills, including diplomacy and persuasion, used in obtaining cooperation and consensus with Novartis colleagues, vendors and customers. The Associate must be able to effectively represent the department both internally and externally. Sound and practical judgement in the interpretation and application of regulations and standards Ability to independently manage and objectively evaluate complex compliance issues with minimal supervision. Excellent leadership and facilitation skills Desirable Requirements: Degree in Chemistry, Pharmacy, Biology, Engineering or another related science Excellent oral and written English communication skills. Preferable: Good knowledge/mother tongue of an additional language (e.g. German, French, Italian, Chinese, or Spanish) is preferred. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Show more Show less