Job Title: Medical Writer Company : MS Clinical Location : Bangalore Job Type : Full-time Experience: 2-4 years About MS Clinical : MS Clinical is a dynamic and innovative company dedicated to advancing medical research and improving patient outcomes. We specialize in conducting clinical trials and providing comprehensive medical writing services to pharmaceutical, biotechnology, and healthcare organizations worldwide. Job Description : We are seeking an experienced Medical Writer to join our vibrant team. The successful candidate will be responsible for creating high-quality, scientifically accurate medical documents in support of our clinical trial activities and regulatory submissions. The ideal candidate will have a strong background in medical writing, excellent communication skills, and the ability to work both independently and collaboratively in a fast-paced environment. Responsibilities : Prepare and review clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and other clinical trial documents in accordance with regulatory guidelines and industry standards. Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and biostatistics, to ensure the accuracy and completeness of medical writing deliverables. Interpret and summarize clinical trial data from various sources, including study reports, statistical analyses, and scientific literature. Assist in the preparation of regulatory submissions, including INDs, NDAs, BLAs, and MAAs, by providing high-quality medical writing support. Participate in project meetings, provide updates on the status of medical writing activities, and contribute to project planning and timelines. Stay current with developments in the field of medical writing, regulatory requirements, and therapeutic areas relevant to our projects. Mentor junior medical writers and provide guidance on best practices for medical writing and document preparation. Qualifications : Bachelor's degree in life sciences, pharmacy, or related field; advanced degree (e.g., MD, PhD, PharmD) preferred. Minimum of 3 years of experience in medical writing within the pharmaceutical, biotechnology, or contract research organization (CRO) industry. Proficiency in interpreting and summarizing clinical trial data, including statistical analyses and safety reports. Strong understanding of regulatory guidelines (e.g., ICH, FDA, EMA) governing the preparation of clinical trial documents and regulatory submissions. Excellent written and verbal communication skills, with the ability to communicate complex scientific concepts clearly and effectively. Detail-oriented with exceptional organizational and time management skills. Ability to work independently and collaboratively in a multidisciplinary team environment. Proficiency in Microsoft Office Suite and familiarity with document management systems (e.g., SharePoint). Benefits : MS Clinical offers a competitive salary and benefits package, including health insurance, retirement plans, and opportunities for professional development and advancement. Show more Show less

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

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

He has to plan the internship and placement activities of the UG, PG and Ph.D students of Amrita School of Biotechnology, in consultation with the Dean, Amrita School of Biotechnology. He has to establish excellent rapport with companies through personal visits and other means of communication. He has to invite prospective recruiting companies to the campus as per priority that is based on the best interest of the students and the organisation. He is to ensure that the process of campus recruitment by each company is systematically carried out as per the standard procedure, i.e. to; Liaise with company authorities to get their travel plans in time. Carry out the following functions with respect to extending hospitality to company officials in co-ordination with the Dean, Amrita School of Biotechnology. Make arrangements for their pick-up & drop at required places. Ensure that rooms as per the requirement are booked well in advance at the campus guest house for the accommodation of company officials, if required. Take special care to ensure that the company officials have a comfortable stay at the campus. Arrangements are made for the smooth conduct of Pre-Placement Talk, Test & Evaluation, Group Discussion and Interview processes as required by the Company. Obtain first-hand information from company officials regarding performance of the students during the placement process and give this information to the respective heads and the concerned faculty for corrective action. He is to liaise with companies for getting the offer letters for the placed students, in time. He is to constantly maintain close interaction with students, so as to get first-hand information with respect to all activities under his purview. He is to ensure that the sanctity of the college premises is maintained during the entire process of campus recruitment. He will adhere to the campus placement policies, stipulated from time to time. He will be located at Amrita School of Biotechnology, Amritapuri and execute his functions by undertaking extensive travel and contact with relevant organisations. Being part of CIR, he will leverage his existing contacts and contacts of other managers of Corporate Relations, for the benefit of students of School of Biotechnology. He will submit reports of his performance to both Dean-School of Biotechnology and Director, CIR, every 15 days. Show more Show less

!! URGENT HIRING !! For more information call or WhatsApp - +919899 2828 11 (Amreen HR) Job Title: Pharmacist Locations: Toronto, Canada; Sydney, Australia; Singapore; London, UK; Dubai, UAE; Riyadh, Saudi Arabia Job Type: Full-time/Permanent Industry: Healthcare/Pharmacy About : There are reputable pharmacies and healthcare organizations are seeking experienced Pharmacists to join our teams in Canada, Australia, Singapore, London, and Gulf countries. We offer a dynamic and supportive work environment, with opportunities for professional growth and development. Responsibilities : - Dispense medications and provide patient counseling on medication use and side effects - Review prescriptions for accuracy and completeness - Collaborate with physicians and other healthcare professionals to optimize patient care - Participate in medication therapy management and disease management programs - Maintain accurate records and reports, including patient profiles and inventory management Requirements : - Bachelor's degree in Pharmacy or a related field - 1-2 years of experience as a licensed Pharmacist - Strong knowledge of pharmacology, pharmacy law, and regulations - Excellent communication and interpersonal skills - Ability to work effectively in a fast-paced and dynamic environment Preferred Qualifications : - Certification in a specialized area of pharmacy practice, such as pharmacotherapy or nuclear pharmacy - Experience with pharmacy management software and automated dispensing systems - Familiarity with quality improvement and patient safety initiatives - Strong analytical and problem-solving skills - Experience working in a multicultural and diverse work environment What They Offer : - Competitive salary and benefits package - Opportunities for professional growth and development - Collaborative and supportive work environment - Relocation assistance (if applicable) Specializations : - Clinical Pharmacy - Hospital Pharmacy - Community Pharmacy - Industrial Pharmacy - Regulatory Affairs How to Apply : If you're passionate about innovative software solutions, send your resume and cover letter to [[HIDDEN TEXT]] or call [+919899 2828 11] Benefits of Working with Us: - Access to exclusive job openings - Expert career guidance - Streamlined application process - Visa assistance (if required) Contact Information: [Name = Amreen Khan] [company = Dreamwide Immigration Solutions] [Mail =[HIDDEN TEXT]] [Mobile = +919899 2828 11]

Company Description Analytical Technologies Limited is a global brand with a presence in 96 countries, specializing in designing, manufacturing, and marketing analytical instrumentation. The company offers a wide range of products including HPLC systems, Spectrophotometers, Spectrometers, and analyzers for various applications. ATL is a multinational analytical group conglomerate, leading global manufacturer & exporter of Analytical, Chromatography, Spectroscopy, Biotechnology, Biomedical, Clinical Diagnostics and Material Science & General Laboratory Equipment. Main products includes HPLC, UHPLC, GC, GPC ( Gel permeation chromatography ), IC ( Ion chromatography ) , HSCCC, PREP HPLC,Production and Process HPLC Chromatography purification systems, DAC ( dynamic axial compression columns ), HbA1HPLC, Spectrophotometers, LCMS, LCMSMS, GCMS,GCMSMS, ICPMS, ICPMSMS, LCICPMS , LCICPMSMS, MALDI TOF MS, ICPTOF MS , TOC , liquid Particle counters, HpTLC, AAS, FTIR, SEM, XRD, Zeta particle Size Analyzers , MicroGC, XRF, Carbon Sulphur & cHNS analysers, ICPOES, OES, bomb calorimeters, DSC TGA STA THERMAL ANALYSERS, mass spectro leak detectors ( MSLD ), microwave digestion systems etc, & provides Labs setups solutions on turnkey basis. 🙏www.analyticalgroup.net Role Description This is a full-time hybrid role for a Products Managers for each product listed above at Analytical Technologies Limited for every major City across the country and globe. The Product Manager will be responsible for overseeing the Business development, marketing, and distribution of the company's analytical instruments manager for each special product named above Qualifications Product Management, Sales and Marketing skills Experience in the analytical instrumentation industry especially the product he/she choose to be. Strong analytical and problem-solving skills Excellent communication and presentation skills Ability to work independently and in a team Bachelor's degree in Chemistry, Engineering, or related field Knowledge of chosen product in chromatography, spectroscopy, Material Science , General Lab equipment or biomedical instrumentation Show more Show less

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level: - Assistant Manager/ Senior Executive Location: - Greater Noida Department: - EHS Key Responsibilities Implementing Environmental Policies and Practices Devising Strategies to meet targets and to encourage best practice Devising the best tools and systems to monitor performance and to Implement Strategies Ensuring compliance with Environmental Legislation Assessing, analyzing and collating environmental performance data and reporting information to internal staff, clients and regulatory bodies Confirming that materials, ingredients and so on are ethically or environmentally sourced Managing environmental strategy budgets. Liaising with internal staff including senior managers and directors Acting as a champion or cheerleader for environmental issues within organisation Providing environmental training to staff at all levels Writing plans and reports Keeping up to date with relevant changes in environmental legislation and initiatives including international legislation where applicable Producing educational or information resources for internal staff, clients or the general public Liaising with regulatory bodies such as the Environment Agency Ensure proper operation of ETPs / STPs Ensure air pollution control facilities are well maintained and performed Periodically monitoring of all the Environmental facilities Excellent communication and influencing skills. Person Profile Qualification: - B. tech / M.Sc. in Environment Certifications: Environment Management. Experience: - 5-7 years working Experience. Working in chemical or pharmaceutical industry Implementation of ISO 14001 Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. Show more Show less

Job Title: Editorial – Language Editor (Life Sciences / Medical Writing) Experience Required: 5 to 8 Years Location: Mumbai (Thane – Olympus Office) Job Summary: We are seeking a skilled and detail-oriented Language Editor with a strong background in life sciences, medical writing, or scientific communication. The ideal candidate will have extensive experience in editing academic manuscripts, research papers, and scientific content to improve readability, clarity, and accuracy. You will be responsible for ensuring that written materials meet high editorial standards and are publication-ready for global scientific and medical journals. Key Responsibilities: Perform comprehensive language editing of manuscripts in life sciences, medicine, biotechnology, and related fields. Ensure scientific content is clear, concise, and coherent , while adhering to journal-specific guidelines and formatting requirements. Edit for grammar, punctuation, style, tone, syntax, and consistency , maintaining the author’s original intent. Conduct structural and substantive editing , including sentence-level rewrites to improve logical flow and clarity. Collaborate with in-house editorial, quality assurance, and production teams to deliver high-quality content. Research and incorporate subject-specific terminology to maintain scientific accuracy. Provide constructive feedback to authors on improving content quality and structure. Ensure on-time delivery of edited content, maintaining quality benchmarks and tight turnaround timelines . Must-Have Competencies: Excellent command of written and spoken English ; proven ability to simplify complex scientific language. Hands-on experience in academic and scientific editing (life sciences, medicine, biotechnology, or pharmaceuticals). Proficiency in MS Office tools (Word, Excel, PowerPoint). Strong attention to detail , organizational, and multitasking skills. Ability to work independently and meet tight deadlines in a fast-paced editorial environment. Familiarity with scientific publishing standards, referencing styles (APA, MLA, Vancouver, etc.) , and peer-reviewed journal requirements. Preferred Qualifications: Experience in medical/scientific writing or editing for publishers, CROs, or academic institutions. Familiarity with editorial workflows, QA processes , and working with author queries. Prior recognition or certifications in editing or writing from recognized bodies (e.g., IGMPI, AMWA, BELS). Experience in freelance, contract, or full-time editorial roles for medical journals, life sciences publications , or educational content platforms . Educational Requirements: Ph.D. or Master’s Degree in Life Sciences, Biochemistry, Biotechnology, or related fields. Bachelor's in Medical Laboratory Technology or equivalent clinical/scientific degree is a plus. Certifications in medical writing or scientific editing (e.g., Executive Diploma in Medical Writing) preferred. Key Soft Skills: Strong interpersonal and communication skills Team player with an eye for detail Excellent time management and prioritization abilities Why Join Us? Join a purpose-driven editorial team working on high-impact global content in the scientific and healthcare space. Be part of an organization that values quality, precision, and continuous learning while collaborating with renowned authors and researchers. Show more Show less

Company Description: Established in 1951, Fermenta Biotech Limited (FBL) is a global Vitamin D3 manufacturer with state-of-the-art R&D and manufacturing facilities in Thane, Kullu, and Dahej. FBL also offers niche APIs, enzymes for antibiotic synthesis, and environmental solutions for wastewater management. www.fermentabiotech.com Summary: Fermenta Biotech Limited is looking for an experienced and highly motivated Jr. Executive / Executive to join our Biotech Division. The ideal candidate will have hands-on experience in both upstream and downstream processes, with specific expertise in fermentation and critical shift process handling. This role is integral to the production of high-quality pharmaceutical APIs, and the candidate must possess knowledge of cGMP standards, documentation practices, and sterilization processes. The successful candidate will play a key role in supporting the production team and ensuring the smooth operation of biotech manufacturing processes. Roles & Responsibilities: Upstream and Downstream Process Handling: Manage and monitor both upstream (fermentation) and downstream (purification, recovery, etc.) processes to ensure the smooth production of biotechnological products. Operate and maintain equipment involved in these processes. Fermentation Expertise: Operate fermentation systems, monitor fermentation parameters, and ensure optimal conditions for microbial growth and product yield. Handle fermentation media, inoculation, and harvest processes. Dry Heat Sterilization: Perform dry heat sterilization for equipment, media, and related items as per SOPs to ensure sterile conditions are maintained in the production environment. Critical Shift Process Management: Oversee critical shift operations during fermentation and other biotechnological processes. Ensure processes are running according to predefined protocols and handle any process deviations or issues during shifts. Compliance with cGMP & Documentation: Ensure all activities are conducted in compliance with current Good Manufacturing Practices (cGMP). Maintain and update necessary documentation, including batch records, process logs, and compliance reports. Troubleshooting & Process Optimization: Troubleshoot any issues or deviations in the production processes and provide solutions. Assist in process improvements and optimization activities to enhance production efficiency and yield. Safety & SOP Adherence: Ensure all safety protocols and standard operating procedures (SOPs) are strictly followed during biotech production activities. Participate in training sessions to stay updated on safety, regulatory, and technical advancements. Cross-functional Collaboration: Collaborate with other departments such as Quality Control (QC), Quality Assurance (QA), and Maintenance to ensure the production process runs smoothly and meets the required standards. Qualification & Skill Requirements: Graduate in Science (e.g., Biotechnology, Microbiology, Biochemistry, or related field). Minimum 3 years of proven experience in biotech production, specifically in fermentation and downstream/upstream processing within the pharmaceutical/API industry. Extensive experience in fermentation processes. Hands-on experience with downstream and upstream processing techniques. Thorough understanding of cGMP regulations and documentation requirements. Proficiency in dry heat sterilization and handling critical shift processes. Knowledge of relevant equipment and instrumentation. Strong analytical and problem-solving skills. Excellent communication and interpersonal skills. Ability to work effectively in a team environment. Strong attention to detail and accuracy. Ability to work under pressure and meet deadlines. Adaptability to changing priorities and tasks. Show more Show less

Dear Candidate, Currently we required Research Scientist for leading Medical device and Surgical Textile industry. Location - Nuh, Sohna , Haryana Working days - 6 Job Description : Research Scientist Job Responsibilities Planning and conducting experiments (Knowledge of cell culture facility and handling of primary cells and cell lines). Basic knowledge of animal handling and aware of working environment in animal house facility. Recording and analyzing data obtained from in-vitro studies. Experience in writing research papers, reports, reviews and summaries. Preparing research proposals and funding applications/bids. Ensuring that quality standards are met (GLP compliance). Liaising with research and/or production staff. Keeping up to date with relevant scientific and technical developments. Know and adhere to all safety and environmental regulations regarding experimentation on various life forms. Collect and analyze all pertinent data related to each research project in a manner that ensures the precision and accuracy of the results. Job Skills & Qualifications Required: Must hold a bachelors and master’s degree in biotechnology, biochemistry or another related life science field. 3+ years of working experience. Strong communication skills, including written and oral abilities in English. If Interested plz share your cv at hr.prathamsearch@gmail.com Regards, Khushi Asthana HR Manager Pratham Search Job Types: Full-time, Permanent Pay: ₹40,000.00 - ₹65,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person

Job ID R-227428 Date posted 06/10/2025 Job Title: Senior Scientist - In Vitro Secondary Pharmacology Career Level: D Introduction to role: Are you ready to make a significant impact in the world of drug discovery and development? Join AstraZeneca's Clinical Pharmacology & Safety Sciences (CPSS) department, where innovation meets collaboration. Our Safety Innovation team is at the forefront of advancing a diverse pipeline across therapeutic areas, delivering safety science from early discovery through clinical development. We are seeking a talented in vitro pharmacologist to join our Secondary Pharmacology team, contributing to the clinical advancement of new medicines. Accountabilities: In this pivotal role, you'll leverage your expertise in pharmacology, toxicology, and biology to collaborate with drug safety specialists and project safety pharmacologists. Your insights will shape drug design during the early phases of discovery, ensuring the selection of safer molecules and developing strategies to mitigate safety risks. You'll generate in vitro pharmacological profiling data at contract research organizations (CROs), identify off-target risks, and interpret pharmacological interactions. Your work will translate in vitro activity into pre-clinical and clinical adverse events, providing crucial guidance for project decisions. Essential Skills/Experience: PhD or Masters or equivalent experience in a relevant scientific field with 4+ years of industrial experience. A strong background in pharmacology (e.g., pharmacology, biology, biochemistry, toxicology, physiology) with a proven track record in driving innovative science, preferably in the pharmaceutical or biotechnology industry. Technical experience in in vitro pharmacological or biochemical assay development and screening (e.g., kinase profiling technologies, radioligand binding, enzyme activity, and functional cell-based systems) applied to various biological target classes. Excellent problem-solving and organisational skills, delivery focus, and outstanding communication skills. A true collaborator with highly effective networking skills and experience collaborating across scientific disciplines, cultures, and expertise. Desirable Skills/Experience: Experience with off-target profiling data and strategies in the pharmaceutical industry. Practical understanding of kinase profiling technologies. Experience working with CRO’s, commissioning requests and driving delivery processes. Experience with being entrepreneurial taking the initiative in projects. Demonstrated leadership in scientific projects or teams. Experience in regulatory interactions or safety assessments. Knowledge of emerging trends in drug safety and pharmacovigilance. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, we are driven by curiosity and courage, exploring what science can achieve. Our commitment to making a difference is unwavering as we fuse data and technology with scientific innovation to tackle some of the world's most complex diseases. We celebrate successes and learn from failures, creating an inclusive environment where diverse knowledge is leveraged for swift impact on disease. With opportunities for lifelong learning and career growth, AstraZeneca is where you can push boundaries and deliver life-changing medicines. Ready to make a difference? Apply now and be part of a team that transforms patient lives through groundbreaking science! AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. Senior Scientist - In Vitro Secondary Pharmacology Posted date Jun. 10, 2025 Contract type Full time Job ID R-227428 APPLY NOW Why choose AstraZeneca India? Help push the boundaries of science to deliver life-changing medicines to patients. After 45 years in India, we’re continuing to secure a future where everyone can access affordable, sustainable, innovative healthcare. The part you play in our business will be challenging, yet rewarding, requiring you to use your resilient, collaborative and diplomatic skillsets to make connections. The majority of your work will be field based, and will require you to be highly-organised, planning your monthly schedule, attending meetings and calls, as well as writing up reports. Who do we look for? Calling all tech innovators, ownership takers, challenge seekers and proactive collaborators. At AstraZeneca, breakthroughs born in the lab become transformative medicine for the world's most complex diseases. We empower people like you to push the boundaries of science, challenge convention, and unleash your entrepreneurial spirit. You'll embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. Here, diverse minds and bold disruptors can meaningfully impact the future of healthcare using cutting-edge technology. Whether you join us in Bengaluru or Chennai, you can make a tangible impact within a global biopharmaceutical company that invests in your future. Join a talented global team that's powering AstraZeneca to better serve patients every day. Success Profile Ready to make an impact in your career? If you're passionate, growth-orientated and a true team player, we'll help you succeed. Here are some of the skills and capabilities we look for. 0% Tech innovators Make a greater impact through our digitally enabled enterprise. Use your skills in data and technology to transform and optimise our operations, helping us deliver meaningful work that changes lives. 0% Ownership takers If you're a self-aware self-starter who craves autonomy, AstraZeneca provides the perfect environment to take ownership and grow. Here, you'll feel empowered to lead and reach excellence at every level — with unrivalled support when you need it. 0% Challenge seekers Adapting and advancing our progress means constantly challenging the status quo. In this dynamic environment where everything we do has urgency and focus, you'll have the ability to show up, speak up and confidently take smart risks. 0% Proactive collaborators Your unique perspectives make our ambitions and capabilities possible. Our culture of sharing ideas, learning and improving together helps us consistently set the bar higher. As a proactive collaborator, you'll seek out ways to bring people together to achieve their best. Responsibilities Job ID R-227428 Date posted 06/10/2025 Job Title: Senior Scientist - In Vitro Secondary Pharmacology Career Level: D Introduction to role: Are you ready to make a significant impact in the world of drug discovery and development? Join AstraZeneca's Clinical Pharmacology & Safety Sciences (CPSS) department, where innovation meets collaboration. Our Safety Innovation team is at the forefront of advancing a diverse pipeline across therapeutic areas, delivering safety science from early discovery through clinical development. We are seeking a talented in vitro pharmacologist to join our Secondary Pharmacology team, contributing to the clinical advancement of new medicines. Accountabilities: In this pivotal role, you'll leverage your expertise in pharmacology, toxicology, and biology to collaborate with drug safety specialists and project safety pharmacologists. Your insights will shape drug design during the early phases of discovery, ensuring the selection of safer molecules and developing strategies to mitigate safety risks. You'll generate in vitro pharmacological profiling data at contract research organizations (CROs), identify off-target risks, and interpret pharmacological interactions. Your work will translate in vitro activity into pre-clinical and clinical adverse events, providing crucial guidance for project decisions. Essential Skills/Experience: PhD or Masters or equivalent experience in a relevant scientific field with 4+ years of industrial experience. A strong background in pharmacology (e.g., pharmacology, biology, biochemistry, toxicology, physiology) with a proven track record in driving innovative science, preferably in the pharmaceutical or biotechnology industry. Technical experience in in vitro pharmacological or biochemical assay development and screening (e.g., kinase profiling technologies, radioligand binding, enzyme activity, and functional cell-based systems) applied to various biological target classes. Excellent problem-solving and organisational skills, delivery focus, and outstanding communication skills. A true collaborator with highly effective networking skills and experience collaborating across scientific disciplines, cultures, and expertise. Desirable Skills/Experience: Experience with off-target profiling data and strategies in the pharmaceutical industry. Practical understanding of kinase profiling technologies. Experience working with CRO’s, commissioning requests and driving delivery processes. Experience with being entrepreneurial taking the initiative in projects. Demonstrated leadership in scientific projects or teams. Experience in regulatory interactions or safety assessments. Knowledge of emerging trends in drug safety and pharmacovigilance. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, we are driven by curiosity and courage, exploring what science can achieve. Our commitment to making a difference is unwavering as we fuse data and technology with scientific innovation to tackle some of the world's most complex diseases. We celebrate successes and learn from failures, creating an inclusive environment where diverse knowledge is leveraged for swift impact on disease. With opportunities for lifelong learning and career growth, AstraZeneca is where you can push boundaries and deliver life-changing medicines. Ready to make a difference? Apply now and be part of a team that transforms patient lives through groundbreaking science! AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. APPLY NOW Explore the local area Take a look at the map to see what’s nearby. Reasons to Join Thomas Mathisen Sales Representative Oslo, Norway Christine Recchio Sales Representative California, United States Stephanie Ling Sales Representative Petaling Jaya, Malaysia What we offer We're driven by our shared values of serving people, society and the planet. Our people make this possible, which is why we prioritise diversity, safety, empowerment and collaboration. Discover what a career at AstraZeneca could mean for you. Lifelong learning Our development opportunities are second to none. You'll have the chance to grow your abilities, skills and knowledge constantly as you accelerate your career. From leadership projects and constructive coaching to overseas talent exchanges and global collaboration programmes, you'll never stand still. Autonomy and reward Experience the power of shaping your career how you want to. We are a high-performing learning organisation with autonomy over how we learn. Make big decisions, learn from your mistakes and continue growing — with performance-based rewards as part of the package. Health and wellbeing An energised work environment is only possible when our people have a healthy work-life balance and are supported for their individual needs. That's why we have a dedicated team to ensure your physical, financial and psychological wellbeing is a top priority. Inclusion and diversity Diversity and inclusion are embedded in everything we do. We're at our best and most creative when drawing on our different views, experiences and strengths. That's why we're committed to creating a workplace where everyone can thrive in a culture of respect, collaboration and innovation.

Job Opening: International Business Development Executive (Internship) Company: Unicrop Biochem Industry: Agriculture BioTechnology Established: 2018 Website: www.unicropbiochem.com About Us: Unicrop Biochem is a pioneering Agriculture BioTechnology company focused on developing innovative, organic, and sustainable agricultural inputs. Since 2018, we’ve been dedicated to empowering farmers through eco-friendly products that enhance crop productivity while preserving the environment. We are currently offering an exciting 6-month paid internship for the role of International Business Development Executive Intern . This is an excellent opportunity for fresh minds to gain real-time experience in international markets, client communication, regulatory processes, and market development strategies. Roles and Responsibilities: Lead Generation : Identify and research prospective international clients Quotation Management : Prepare and share quotations; manage timely follow-ups Client Communication : Interact professionally with international clients via email and virtual meetings Market Research : Analyze target countries, competitor trends, and product demand Supply Chain Coordination : Assist in export order tracking, shipping documentation, and logistics coordination Import-Export Documentation : Support with preparing documents like invoices, packing lists, COOs, etc. License & Regulatory Work : Help in managing registration, trade licenses, and compliance for exports Legal Coordination : Assist in handling agreements, NDA drafts, and export-import compliance checks CRM & Record Keeping : Maintain accurate client databases, communication logs, and sales documentation using tools like Google Drive and spreadsheets Required Skills and Qualifications:Educational Background: Pursuing or recently completed BBA / MBA Preference for students specializing in International Business Core Skills: Strong command over written and verbal English Familiarity with Google Workspace (Docs, Sheets, Drive) Basic knowledge of AI tools, ChatGPT, CRM platforms Understanding of international trade terms and export processes Personal Attributes: Organized, detail-oriented, and deadline-driven Quick learner and team collaborator Strong problem-solving and research abilities Interest in global business operations and documentation Key Result Areas (KRAs): Generate leads and explore international business opportunities Ensure timely and accurate client communication Assist in documentation and coordination for smooth export flow Support compliance, licensing, and legal paperwork Contribute to business growth through strategic research Why Join Us? This internship offers unique exposure to global trade practices , international licensing , and legal compliance in the Agriculture BioTechnology industry. Gain practical skills and grow your career with one of the most dynamic companies in the sector. Internship Details: Duration: 6 Months Type: Paid Internship Location: Vadodara, Gujarat (India Office) Contact Us: Email: hr@unicropbiochem.com Phone: +91 63510 57338 Website: www.unicropbiochem.com Office Address: 225, Orchid Plaza, Behind McDonald’s, New Sama Savli Road, Vadodara, Gujarat – 390008 Job Types: Full-time, Fresher, Internship Contract length: 6 months Pay: Up to ₹7,000.00 per month Schedule: Day shift Morning shift Supplemental Pay: Overtime pay Work Location: In person

JOB TITLE: Tea & Health Executive LOCATION: Bangalore REPORTS TO: One of the Beverages Program S&T Leaders About Unilever With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people – we believe that when our people work with purpose, we will create a better business and a better world. At Unilever, your career will be a unique journey, grounded in our inclusive, collaborative, and flexible working environment. We don’t believe in the ‘one size fits all’ approach and instead we will equip you with the tools you need to shape your own future. Business Context Delivering superior technologies and innovations to solve consumer relevant problems is very crucial for success in the area of plant-based beverages. Driven by this strong demand, Unilever intent to deliver cutting-edge technologies through fundamental understanding on various secondary metabolite pathways in tea and other botanicals through cross fertilization of ideas between biologists, chemists, chemical engineers. The biology/bioscience/biochemistry/biotechnology expertise is an integral part of other leading-edge expertise in Beverages S&T The role requires the following key skills: Key Skills Strong hands-on experience on key analytical techniques in biochemistry, biotechnology, life sciences, molecular biology, health and wellness. Good understanding of nutritional biochemistry and various biological process involved in metabolism and human health. Appreciation for of natural product chemistry and secondary metabolites from plants. Enthusiasm to carry out hands-on practical R&D experiments in the lab, pilot plant and factories Awareness on relevant latest science developments in the external scientific world and how it can be translated to pragmatic and cutting-edge technologies to deliver un-met need of consumers. Pro-active and self-motivated to engage with internal and external science leaders, to learn new skills in relatively shorter time frame. Main Accountabilities Will be working very closely under the guidance of program leaders in Beverages S&D on Elucidating metabolitic pathways for secondary metabolites in tea and thier application in health & wellbeing and end cup sensorials To develop cutting-edge technologies supported by risk-based assessment, consumer benefit to drive product superiority and savings Underpinning the science across processes, product chemistry/ key technologies/innovations via closely working with Global TPLs, ecosytem partners under the guidance of Senior Scientists To influence both Global and local R&D teams on implementing technological solutions in plant based beverages portfolio which are sustainably accretive Accountable prepare scientific substantiation and dossier preparation for nutritional claims for beverages & food products. Responsible for screening functional actives by reviewing scientific literature, clinical studies, Ayurveda. Key Requirement MSc Biochemistry, Biochemistry, Life Sciences, BE/Btech Biotechnlogy, Biochemistry with 6-12 months experience in FMCG or academia. Our commitment to Equality, Diversity & Inclusion Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity. Show more Show less

The Clinical Systems Specialist plays a critical role in the implementation, management and optimization of clinical trial systems, ensuring their functionality and alignment with study needs. They collaborate with the System Administrator & vendor on system configuration to deliver features, fixes, and updates in alignment with the system’s roadmap, ensuring efficient operation and compliance throughout the clinical trial lifecycle. Additionally, they assist with system maintenance activities and act as the primary point of contact for training, end-user technical support, and communications, to ensure operational efficiency and compliance with internal & external requirements. System Development & Implementation (10-20%) Support the System Administrator in performing key system development lifecycle (SDLC) activities including requirements analysis, configuration and validation, system updates, and change control. Collaborate with IT and clinical teams to improve system efficiencies and automation, supporting continuous improvement of system management. System Maintenance, Security & Compliance (30-40%) Support user account management and access controls for compliance with regulatory standards and assist with user access reviews. Support audit activities (sponsor audits, vendor audits and regulatory audits) to demonstrate compliance Coordinates & executes data governance initiatives such as identifying opportunities for data cleaning, training end-users or other system support staff on data governance activities, and conducting oversight on these activities. Assist with system-related assessments including vendor assessments, risk assessments, and validation reviews, and audit trail reviews. Support necessary data inputs, lead and support data governance efforts, and configure or generate required reports or dashboards for end users User Support & Training (40-50%) Provide technical support to end-users and troubleshoot system-related issues. Provide training to end-users and collaborate with System Administrator on creation and management of training materials. Provide study-related services for end-users including study setup and publishing reports & dashboards, to support study reporting and compliance related study activities. Oversee user onboarding to system including assignment to system roles & studies. Qualifications 4 - 6 years of related experience (Honors) Bachelor’s degree Additional Knowledge / Skills Education in IT, software or a related field is preferred but not required Strong problem-solving and analytical skills Excellent communication and stakeholder management skills Ability to work independently and as part of a team. A minimum of 4 years of experience in clinical systems management, technical support, or a related role within the pharmaceutical, biotechnology, or contract research organization (CRO) industry is preferred. Experience working with clinical trial platforms such as clinical trial management systems (CTMS), electronic data capture (EDC) systems, electronic trial master file (eTMF) systems, or other platforms is essential. Previous experience in system configuration, validation, and troubleshooting in a regulated environment is highly desirable. Understanding of clinical trial processes, regulatory requirements, including GxP, 21 CFR Part 11, and other relevant guidelines. Knowledge of system validation procedures, including user acceptance testing (UAT), configuration management, and compliance documentation, is essential. Familiarity with clinical data integrity standards and audit processes is also required. Strong analytical and problem-solving skills with the ability to identify and resolve complex system issues independently. Excellent communication skills, both verbal and written, to effectively interact with technical and non-technical stakeholders. The ability to prioritize tasks, manage multiple projects, and meet deadlines in a fast-paced environment. Attention to detail and a commitment to ensuring the accuracy and integrity of clinical data. Ability to work independently with minimal supervision while collaborating with cross-functional teams. Proactive approach to continuous learning and adapting to new technologies and industry trends PHISHING SCAM WARNING: Alimentiv is aware of the continued increase of phishing scams, leveraging various methods of attack via email, text, voice and social media. Please note that Alimentiv only uses company email addresses, which contain “@ alimentiv.com ”, to communicate with candidates via email. If you are contacted by someone about an open job at Alimentiv, please verify the domain of the sender’s email address and that they are asking you to apply on this website. If you believe you’ve been a victim of a phishing scam, please contact your local government cyber authority to report. Show more Show less

Software Proficiency: AutoCAD Plant3D (Must) Autodesk Mechanical (Must) Navisworks Manage (Preferred) BIM360 Collaboration (Preferred) Autodesk Inventor (Added Advantage) Autodesk Vault / Pro (Added advantage) Educational Background Diploma / Bachelor’s degree in mechanical engineering, or a related field. Certification in Piping Design, Stress Analysis, or 3D Modeling Tools (e.g., Autodesk Plant 3D) would be added advantage. Professional Experience 5+ years of experience in piping design and layout engineering, preferably in industries like dairy, food or beverage for Associate Engineer. 8+ years of experience in piping design and layout engineering, preferably in industries like dairy, food or beverages for Senior Engineer. Proven track record in designing hygienic and sanitary piping systems compliant with industry standards such as ASME BPE. Hands-on experience with 3D modeling and drafting tools, particularly Autodesk Plant 3D. Additional Requirements Willingness to work in multidisciplinary and multicultural environments across APAC and EMEA regions. Flexibility to travel to client sites for project execution, commissioning, or troubleshooting (may or may not be needed). Responsibilities / Tasks Develop piping layouts for sanitary and hygienic applications, including food, beverage, pharmaceutical, and biotechnology industries, ensuring compliance with relevant standards (e.g., ASME BPE). Ensure designs minimize dead legs and promote cleanability and sterilizability, supporting CIP (Clean-in-Place) and SIP (Sterilize-in-Place) operations. Incorporate industry-specific standards, such as ASME-BPE, into piping designs to ensure the system meets sanitary and hygienic regulations. Ensure all fittings, valves, and components adhere to hygienic standards to maintain product integrity. Design skids and valve manifolds for hygienic systems, ensuring compact layouts that meet operational, cleaning, and maintenance requirements. Work with process engineers to integrate piping systems into hygienic equipment such as tanks, pumps, and heat exchangers. Ensure seamless integration of hygienic piping with instruments like flowmeters, pressure sensors, and temperature transmitters. Develop piping designs that promote laminar flow, reduce turbulence, and prevent product stagnation, ensuring optimal process efficiency and hygiene. Analyze and address potential areas of contamination in the system design. Create and review 3D models tailored to hygienic piping systems using tools like Autodesk Plant 3D, ensuring precision in complex assemblies. Use clash detection software Navisworks to ensure clean and efficient piping layouts. Collaborate with process, mechanical, and instrumentation teams to align piping designs with broader system requirements. Software Proficiency: Your Profile / Qualifications AutoCAD Plant3D (Must) Autodesk Mechanical (Must) Navisworks Manage (Preferred) BIM360 Collaboration (Preferred) Autodesk Inventor (Added Advantage) Autodesk Vault / Pro (Added advantage) Educational Background Diploma / Bachelor’s degree in mechanical engineering, or a related field. Certification in Piping Design, Stress Analysis, or 3D Modeling Tools (e.g., Autodesk Plant 3D) would be added advantage. Professional Experience 8+ years of experience in piping design and layout engineering, preferably in industries like dairy, food or beverages for Senior Engineer. Proven track record in designing hygienic and sanitary piping systems compliant with industry standards such as ASME BPE. Hands-on experience with 3D modeling and drafting tools, particularly Autodesk Plant 3D Did we spark your interest? Then please click apply above to access our guided application process. Show more Show less

About Amgen Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. About The Role Role Description: The Compensation Senior Manager serves as a strategic advisor and business partner to deliver world class end-to-end support across all facets of compensation. This role blends deep subject matter expertise with business acumen to guide (HR) business partners on compensation-related decisions that drive attrition, motivation and retention of staff. Acting as a trusted partner, the Senior Manager will contribute to the design and implementation of new future – ready compensation programs and frameworks, using analytical rigor to turn insights into impactful recommendations. Key focus areas of this role will be on supporting the annual compensation cycle, holistic organizational design & job leveling, leveraging AI, automation & tech to drive continuous process improvement, and playing a leadership role in global rewards projects. With a continuous improvement mindset, and staying abreast of market trends & developments, it will also drive simplification, automation, and process enhancements to elevate the efficiency and effectiveness of the Total Rewards function. Roles & Responsibilities: Act as trusted compensation partner delivering high-quality consultative guidance and strategic support on all compensation-related topics to (HR) business partners. Support the seamless execution of the year-end cycle, including base, bonus, and equity planning, in close collaboration with (HR) business partners and the global Total Rewards team. Support compensation benchmarking initiatives by leveraging external survey data and internal analytics to ensure market competitiveness and internal equity. Provide strategic input and guidance on org design, role creation, job leveling, and internal mobility decisions for supported client groups. Drive or contribute to the execution of global compensation initiatives, such as M&A, pay equity & transparency analysis, compensation framework redesign, or job architecture development. Partner with global leadership to contribute to the design, rollout, change management, and refinement of future – oriented compensation programs & frameworks that align with business goals and market practices. Use strong analytical skills to translate complex data into insights and compelling narratives that influence decision-making and drive strategy. Identify opportunities to streamline & simplify processes, reduce manual effort, and enhance user experience through automation, technology and digital tools. Ensure compliance with labor laws, pay equity & transparency legislations, tax regulations, and corporate governance policies. Support the development and implementation of SOPs, knowledge bases, and training materials different audiences like (HR) business partners, Talent Acquisition, Tier 2 and Tier 3. Basic Qualifications and Experience: Master’s degree in Human Resources, Finance, Business, or related field 8+ years of progressive experience in compensation or Total Rewards, with experience supporting senior leadership in a consultative capacity Proven success managing complex compensation cycles and designing compensation programs in a matrixed, global environment Skills: Strong understanding of job architecture, market pricing, salary structures, incentive plan design, and equity compensation. Exceptional analytical skills with the ability to interpret data, generate insights, and tell compelling, data-driven stories. Experience with compensation tools (e.g., Workday, Radford, Mercer, WTW, MarketPay) and data visualization platforms (e.g., Visier, Tableau, Power BI) is a plus. Demonstrated ability to influence and collaborate effectively across HR, Finance, and business leadership. Adept at managing ambiguity and competing priorities while maintaining a focus on delivery and continuous improvement. Strong project management skills and comfort driving work from strategy through execution. Experience in continuous improvement methodologies (e.g., Lean, Six Sigma) is a plus. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation. Show more Show less

Healthcare Business Analyst M.Tech Biotechnology/ B.Tech Biotechnology/ MPharm/ BPharm/ Msc Biotechnology/ Bsc Biotechnology

Bhagwan Mahaveer Cancer Hospital & Research Centre is looking for Senior Resident Radiation Oncology to join our dynamic team and embark on a rewarding career journey. Patient Care: Provide comprehensive medical care to patients under the supervision of attending physicians Perform physical examinations, diagnose medical conditions, develop treatment plans, and monitor patient progress Clinical Supervision: Supervise and provide guidance to junior residents, interns, and medical students in their clinical duties Assist in their training, evaluation, and professional development Hospital Rounds: Conduct regular hospital rounds to assess patients, review test results, and discuss treatment plans with the healthcare team Coordinate and communicate patient care plans with nurses, specialists, and other healthcare professionals Medical Procedures: Perform or assist in various medical procedures, such as venipuncture, wound care, suturing, and bedside procedures Ensure adherence to sterile techniques, safety protocols, and best practices Medical Documentation: Maintain accurate and up-to-date medical records, including patient history, physical examination findings, treatment plans, and progress notes Ensure compliance with legal and regulatory requirements Patient Education: Educate patients and their families about their medical conditions, treatment options, and preventive measures Provide counseling on lifestyle modifications, medication management, and post-discharge care instructions Interdisciplinary Collaboration: Collaborate with other healthcare professionals, including nurses, pharmacists, therapists, and social workers, to ensure coordinated and holistic patient care Participate in interdisciplinary team meetings and contribute to care planning Continuity of Care: Facilitate smooth transitions of care between inpatient and outpatient settings Coordinate follow-up appointments, referrals, and discharge planning to ensure continuity of care and optimal patient outcomes Medical Research and Education: Stay updated with the latest medical advancements, evidence-based practices, and clinical guidelines Engage in research activities, present at conferences, and contribute to medical education and scholarly activities Quality Improvement: Participate in quality improvement initiatives to enhance patient safety, clinical outcomes, and healthcare delivery Identify areas for improvement, implement evidence-based practices, and contribute to quality assurance programs Professional Development: Engage in continuing medical education (CME) activities, attend conferences, and pursue opportunities for professional growth Maintain licensure and board certification requirements

Gujarat Biotechnology University is looking for Junior Research Fellow to join our dynamic team and embark on a rewarding career journey Research Support: JRFs work under the guidance of senior researchers or principal investigators on research projects They assist in conducting experiments, data collection, literature reviews, and data analysis Data Collection and Analysis: Collecting and recording data from experiments or research studies and using appropriate software or statistical tools for data analysis Literature Review: Conducting comprehensive literature reviews to understand the current state of research in the field and to inform the research design and methodology Experimental Work: Depending on the field, JRFs may perform laboratory experiments, fieldwork, surveys, or other research activities specific to their project Documentation: Keeping detailed records of research procedures, findings, and outcomes This documentation is critical for the research process and for publishing research results Research Proposal Writing: Assisting in the preparation of research proposals and grant applications to secure funding for research projects

Responsible for maintaining the product backlog change items, Prioritising the items as per the business need and maintain open communication with all the partners. Perform functional analysis of customer’s requirements and understand how insurance products will be integrated with proposed solution through collaborating with customer’s resources/requirements, workshop sessions. Perform impact analysis of the changes requested on the product functions and provide detailed analysis to evaluate the extend of changes, impacted areas of the system, Document the impact, provide walk-throughs and obtain sign-offs from the customer Facilitate/manage design sessions regarding business functionality and/or product logic with the customer. Ability to communicate and influence the Business/Design teams to achieve the Business benefit as per the agreed priorities of the requirement Required education Bachelor's Degree Preferred education Master's Degree Required technical and professional expertise Education Qualification - BE/Btech/MCA/M.Tech, 6-7 yrs Experience in Advises clients regarding products & solutions for solving problems in the Insurance Industry. Experience in Insurance industry and deep knowledge of clients' businesses and how it relates to specific Insurance segments. knowledgeable in the trends and directions of the industry, the marketplace, and the players. Respond to technical queries / requests from team members and customers Preferred technical and professional experience Ambitious individual who can work under their own direction towards agreed targets/goals. Ability to handle change and be open to it along with good time management and an able to work under stress Proven interpersonal skills while contributing to team effort by accomplishing related results as needed

Yokogawa Electric International Pte is looking for Service Engineer to join our dynamic team and embark on a rewarding career journey Technical Support: Respond to service inquiries, troubleshoot technical issues, and provide solutions Maintenance and Repair: Perform routine maintenance, inspections, and repairs on systems or equipment Installation and Setup: Install, configure, and set up new systems or machinery as required Testing and Diagnosis: Conduct tests, analysis, and diagnostic procedures to identify problems and recommend solutions Customer Interaction: Interact with customers, clients, or internal stakeholders to understand their needs and address concerns Documentation: Maintain accurate records of service activities, reports, and documentation Training and Guidance: Provide training and guidance to users or clients on the proper use and maintenance of equipment or systems Required Skills and Qualifications:Technical Knowledge: Proficiency in relevant technologies, systems, or machinery Problem-Solving Skills: Ability to diagnose and resolve technical issues efficiently Communication Skills: Strong verbal and written communication for interacting with clients and documenting procedures

Yokogawa Electric International Pte is looking for System Sales to join our dynamic team and embark on a rewarding career journey As a Sales Representative at our Personnel Network, you will play a critical role in connecting with potential clients, customers, or members of our network and promoting our products or services You will be responsible for developing and maintaining strong relationships, understanding the needs of clients, and achieving sales targets Responsibilities:Client Engagement: Identify and approach potential clients, customers, or members within our personnel network Product/Service Promotion: Educate clients on the benefits and features of our products or services, tailored to their needs Relationship Building: Cultivate and maintain strong relationships with existing and potential clients, demonstrating excellent customer service Sales Targets: Achieve or exceed sales targets and goals, including revenue and volume targets Needs Analysis: Understand the unique requirements and preferences of each client, tailoring solutions to meet their specific needs Sales Presentations: Prepare and deliver persuasive sales presentations and proposals Follow-up: Conduct post-sale follow-ups to ensure customer satisfaction and gather feedback Market Research: Stay informed about industry trends and competitors to adjust sales strategies accordingly Documentation: Maintain accurate and up-to-date records of client interactions, sales, and prospects in a CRM system Sales Reporting: Prepare regular sales reports and forecasts for management Networking: Actively participate in events, trade shows, or networking opportunities to expand your personal network and create leads

Job Description Visiting to manufacturing and warehouse facility to ensure that activities are being carried out by following GMP requirements and as per approved procedures. Line clearance for the process operation during manufacturing activity. To ensure that facilities are maintained to be GMP ready always. Follow-up to close the findings as per established procedures Review and initiation of QMS elements like change control, deviation, CAPA, Market complaint, Investigation etc. Preparation and review of APQR of manufactured products Ensure that process and cleaning validation activities are being carried out by following approved protocols Work Experience 3 to 6 Years Education Masters B. Tech in Biotechnology Competencies 1. Strategic Agility 2. Innovation Creativity 3. Customer Centricity 4. Developing Talent

Job Description Bachelor in instrumentation having 4 to 6 years experience in machine main of biotech , scada , bms , fms , conductivity , PH, DO sensor . calibration , validation software system knowledge , main of fermentor , bioreactor , tff , crom system etc Work Experience Bachelor in instrumentation having 4 to 6 years experience in machine main of biotech , scada , bms , fms , conductivity , PH, DO sensor . calibration , validation software system knowledge , main of fermentor , bioreactor , tff , crom system etc Education B. Tech Diploma in Instrumentation Competencies

Job Description Candidate should have good knowledge about all microbiological related activity, Environmental monitoring of classified areas, Water testing Bioburden BET and Sterility. Environmental monitoring of all classified areas of Drug product manufacturing. Media Preparation required for Utility and area monitoring. To execute Validation / Qualification / Re-qualification as per protocol. Sub culturing, serial dilution of standard cultures and GPT and Identification of isolate. To execute IQ/OQ/PQ of the new equipment installed in the Microbiology Section. Sampling, Testing of Water samples To perform Population Determination of Biological Indicators. Operation of Daily pH, Balance Calibration, Autoclave, DHS, Incubators, Air Samplers and particle counter. To report any Deviations/ Out of Specifications results and Safety risks to the supervisor as and when observed. Candidate should have good experience in the BET testing by using Gel clot and KTA method To perform Qualification of Equipment, Autoclave, DHS, Incubator, KTA, etc. The candidate should be familiar with cGMP requirements, Change Control, Deviations, Out of Specifications, Sample management, Stability Management and investigation tools. To perform Compressed air sampling and analysis To ensure cGMP compliance and maintain the laboratory in audit ready condition. The candidate should be familiar with SAP system. Work Experience 0 to 2 years Education Post Graduation in Microbiology or Biotechnology Competencies