567 Chromatography Jobs - Page 17

Quality Control Analyst – Chemical Industry Gait Naurish (I) Ltd. Location: Sector 155, Noida, Uttar Pradesh Salary: ₹300,000 – ₹400,000 per annum Experience: Minimum 1 years in a chemical/QC laboratory environment Company Overview Gait Naurish (I) Ltd. is a leading fine‐chemicals and flavour intermediate synthesis company, specializing in developing and manufacturing high‐purity compounds for the food, fragrance, and nutraceutical industries. We are committed to innovation, quality, and regulatory compliance, with state‐of‐the‐art laboratories and pilot‐plant facilities in Noida. Position Summary We are seeking a meticulous and proactive Quality Analyst Chemist to join our Quality Control team. The ideal candidate will perform routine and advanced analytical tests to ensure that all incoming raw materials, in‐process samples, and finished products meet predefined quality and regulatory standards. Key Responsibilities Analytical Testing Conduct and interpret chromatographic analyses using GC (Gas Chromatography) and HPLC (High-Performance Liquid Chromatography). Perform moisture determination via Karl Fischer titration. Execute TLC (Thin-Layer Chromatography) for rapid qualitative assessments. Method Development & Validation Assist in developing, optimizing, and validating new analytical methods in accordance with ICH and USP guidelines. Maintain method documentation, standard operating procedures (SOPs), and validation reports. Quality Assurance Support Review raw data and prepare analytical reports with clear interpretations. Investigate non‐conformities, deviations, and out‐of‐specification (OOS) results; propose corrective actions. Participate in internal and external audits; ensure compliance with GLP/GMP standards. Laboratory Maintenance & Safety Calibrate, maintain, and troubleshoot analytical instruments (GC, HPLC, Karl Fischer apparatus, TLC chambers). Monitor laboratory consumables, reagents, and standards; ensure proper storage and inventory control. Adhere to safety protocols, chemical handling procedures, and waste‐disposal guidelines. Qualifications & Experience Educational Background: Bachelor’s or Master’s degree in Chemistry, Analytical Chemistry, or a related discipline. Professional Experience: At least 1 years of hands‐on experience in a QC/analytical laboratory within a fine chemicals, pharmaceutical, or related industry. Technical Expertise: Proven proficiency in GC and HPLC operation, sample preparation, and data analysis. Demonstrated experience with Karl Fischer titration and TLC techniques. Familiarity with chromatographic software (e.g., Empower, ChemStation) and LIMS is a plus. Soft Skills: Strong attention to detail, analytical mindset, and problem‐solving ability. Excellent documentation, report‐writing, and communication skills. Ability to work both independently and collaboratively in a fast‐paced environment. What We Offer Competitive salary and performance‐based incentives Comprehensive health insurance and statutory benefits Opportunities for professional development and training A collaborative work culture in a cutting‐edge R&D and manufacturing environment Application Process Interested candidates may send their CV and a cover letter detailing relevant experience to hrm@fnni.in with the subject line “Quality Analyst Chemist – Sector 155, Noida” Job Type: Full-time Pay: ₹300,000.00 - ₹400,000.00 per year Benefits: Health insurance Paid sick time Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Application Deadline: 15/06/2025

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Executive Date: May 18, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Primary Responsibilities: Analytical Method development for API/NCE sample. Analysis of raw material, Intermediate, API/NCE samples on gas chromatography, liquid chromatography and chemical analysis. Method validation for API/NCE purity, impurity, excipients methods. Trouble shooting of various analytical issues for various products. Maintenance, calibration & trouble shooting of HPLC and GC. Preparation of SOP for related to instrument and system. Method transfer and method demonstration at other location as and when required. Documentation like ATP, Development report, Validation protocol, Validation report, STP preparation. To work as per cGMP/OECD GLP and to ensure its compliance. Basic understanding of ICH guidelines Candidate should have basic knowledge about handling of instruments like UV visible spectrophotometer High-performance liquid chromatography Ultra-performance liquid chromatography Karl-Fischer Titration Differential scanning calorimetry USP Dissolution Apparatus I and II Other minor equipment like analytical balance, pH meter, Sonicator and microcentrifuge. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Executive Date: May 29, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd GLP Bioanalytical To Access Study Plan and Standard Operating Procedures and to comply with instructions given in Study Plan and Standard Operating Procedures. To record raw data promptly and accurately and in compliance with the Principles of Good Laboratory Practice, review of raw data and are responsible for the quality of their data. Operation Maintenance and Calibration of Liquid Chromatography and Tandem Mass Spectrometer (LC/MS/MS). To perform the method Development, method validation and study sample analysis (non-clinical) for GLP Studies. Preparation of ATP (Method SOP), SOPs, Template for GLP Studies. Sample preparation for MD, MV and study analysis as per GLP guidelines. Pipette Maintenance and calibration assigned to the group. Other Job Responsibilities Assigned By Reporting Authority. Preparation of method validation/partial method validation reports and bioanalytical study reports for GLP studies in consultation with Study Director/Principal Investigator and in compliance with the Principles of GLP. Documentation of any type of Deviation in GLP study report & communicated directly to the Study Director and/or if appropriate, the Principal Investigator. Responding to QA observations for bioanalytical reports in consultation with Study Director/Principal Investigator and in compliance with the Principles of GLP. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Executive Date: May 10, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Primary Responsibilities: Analytical Method development for API/NCE sample. Analysis of raw material, Intermediate, API/NCE samples on gas chromatography, liquid chromatography and chemical analysis. Method validation for API/NCE purity, impurity, excipients methods. Trouble shooting of various analytical issues for various products. Maintenance, calibration & trouble shooting of HPLC and GC. Preparation of SOP for related to instrument and system. Method transfer and method demonstration at other location as and when required. Documentation like ATP, Development report, Validation protocol, Validation report, STP preparation. To work as per cGMP/OECD GLP and to ensure its compliance. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Work Schedule Standard (Mon-Fri) Environmental Conditions Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) What Makes This Opportunity Unique Join Thermo Fisher Scientific Inc., a company dedicated to scientific innovation, providing top-tier technical service. Responsibilities Support Thermo Fisher customers with technical service, installation, operation, training, and repair of Ion Chromatography (IC) and High-Performance Liquid Chromatography (HPLC) equipment. Undertake product installation on client premises, demonstrating features related to 21 CFR compliance under the CDS software. Provide training and technical advice on instrument usage, both in person and by phone, sharing standard methodologies for efficient performance of the IC & HPLC systems. Investigate and resolve operational difficulties and faults. Rectify problems, suggest solutions, or arrange for necessary repairs. Serve as an important link between customers and Sales and Marketing teams. Ensure effective service by maintaining communication between the customer and the company. Monitor repairs under service/warranty cover and suggest product improvements. Conduct planned maintenance and regular customer visits for the IC & HPLC product line. Recommend spare parts requirements and assist with equipment monitoring. Requirements Proven technical proficiency in Ion Chromatography and HPLC product lines. Outstanding problem-solving skills and the ability to determine and successfully implement solutions. Strong communication skills for effective customer training and support. Ability to collaborate and compete in a dynamic, fast-paced environment. Ambitious and meticulous approach to handling technical challenges and customer interactions. Join us in our mission to accelerate research, solve complex scientific challenges, and drive technological innovation! Show more Show less

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Phenomenex, one of Danaher s 15+ operating companies, our work saves lives and we re all united by a shared commitment to innovate for tangible impact. You ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher s system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Phenomenex isn t your typical scientific company. Founded nearly 40 years ago, Phenomenex is a global technology leader committed to developing novel analytical chemistry solutions that solve the separation and purification challenges of researchers, advancing the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. Be part of our global success and together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Learn about the Danaher Business System which makes everything possible. The Account Manager is responsible for maintaining and managing allocated territory by meeting and exceeding sales goals. Engaging with customers, providing them with sales and technical support, Build professional relations with key people at customer accounts. Work in cohesion with other functions of company to drive growth strategies and profit margins. This position reports to the District Sales Manager and is part of the Sales team located in Baroda and will be working remotely to cover the assigned territory. In this role, you will have the opportunity to: Ensure that assigned account territory meets sales and unit goals. Develop relationships with new and existing customers. Provide updates to Sales Manager regarding achievement of goals, trends and competition Implement account action plans, review performance and improve current account sales & support programs for the territory Manage and maintain information in customer database system (MSCRM) The essential requirements of the job include Bachelor s or Master s degree, in any Life Science stream required. At least 8 years of experience in Sales. Advanced knowledge of sales principles and methods of negotiation, and demonstrated advanced capability to identify business opportunities Good knowledge of Chromatography. Pharma & Non-Pharma Market & workflow understanding A proven track record of success in Sales/Customer Service type roles preferred Travel, Motor Vehicle Record & Physical/Environment Requirements: Willingness to travel as per customer engagement needs. It would be a plus if you also possess previous experience in: Laboratory with Hands on experience in chromatography using HPLC Phenomenex, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info . At Phenomenex we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Phenomenex can provide. Join our winning team today. Together, we ll accelerate the real-life impact of tomorrow s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Purpose: Personnel handling this profile will be responsible for performing reactions, documenting the observations in relevant lab note books or e-books and follow instructions from the supervisor and work in a group (or individually) to accomplish the tasks in a timely and efficient manner. They are also responsible for assisting the supervisor to alert shortfall of resources and train junior scientists to develop their technical skills Key Responsibilities: Perform synthetic chemistry reactions, reaction work-ups, purification of the compounds by column chromatography, , crystallization, re-crystallization techniques, preparative TLC and operating lab equipment s. Assist the supervisor to take stock of resources (raw materials, solvents, etc) in the project and report any shortfall and search literature using Reaxys Provide hands-on training and supervision to juniors while performing synthesis of compounds Ensure that the samples generated during the course of synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. Ensure that the instrument / equipment are calibrated, undergone preventive maintenance and are kept clean before use and in case of any breakdown, report to maintenance immediately Ensure that they know the MSDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms Follow EHS and quality system requirements at all times in the workplace ensuring individual safety and lab safety Attend all mandatory trainings and update training records as and when trainings are completed Ensure confidentiality at all times Prepare SOPs/IOPs/EOPs/OCPs when any new lab activity is identified or existing one requires updation Any other lab responsibilities as indicated by the EHSQ team member/ supervisor / group leader. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 3-12 years Skills and Capabilities: Should be familiar with concepts of chemical synthesis Familiar with operations of relevant apparatus - instrument / equipment. Education : M.Sc/ M.Pharm

Overview The Operational Excellence Manager will ensure the operational excellence & execution within the Global Capability Centre (GCC). This role will focus on optimizing processes, enhancing performance, and aligning operations with organizational goals. The ideal candidate will possess strong analytical skills, a strategic mindset, and a proven ability to lead & collaborate with cross-functional teams. The role involves overseeing & coordinating various processes and operations that are key and important for Waters GCC. It includes providing operational & tactical support to the Waters GCC Head in close collaboration with the stakeholders, GCC LT & support functions. T his position will follow a hybrid model work approach( 3 days a week working from GCC office, RMZ ecoworld, Bellandur, Bangalore) Responsibilities Operational Excellence: Drive continuous improvement initiatives to enhance efficiency and effectiveness of operations. Implement best practices in project management and operational processes. Monitor and evaluate operational performance, providing regular reports to stakeholders. Manage IT Supplier/Vendor Management, ensuring timely and efficient fulfilment of needs, SOW execution, and renewals Oversee and Track the Intake and Ideation processes at GCC Track and manage the SLAs/KPIs Oversee budgeting and financial management for operational activities, ensuring cost control and optimal resource allocation. Communication and Reporting: Prepare and present reports for senior leadership, highlighting key metrics, progress on initiatives, and areas of concern. Facilitate communication between the GCC and other departments, ensuring alignment and clarity on priorities. Draft internal communications, presentations, and strategic documents. People Engagement: Drive the People Engagement Initiatives at GCC and foster collaboration across Waters. Lead and mentor cross-functional teams, fostering a collaborative environment and ensuring staff motivation and engagement. Ensure optimal utilization of talent and technology across GCC. Co-ordinate and support University/Educational Institution tie-ups Co-ordinate with the Local GCC Ecosystems/Association & chapters Stakeholder Engagement: Build strong relationships with internal and external stakeholders to promote alignment and engagement. Act as a liaison between the GCC and other departments to ensure smooth operations and information flow. Engage with clients and partners to understand their needs and enhance service delivery. Co-ordinate any travel needs to and from GCC. Risk Management: Identify potential risks within operational processes and develop mitigation plan. Ensure compliance with relevant regulations and industry standards. Manage audits and coordination Prepare for and respond to operational challenges, ensuring business continuity. Performance Measurement: Establish key performance indicators (KPIs) to assess operational effectiveness and drive continuous improvement. Keep the GCC data and metrics up to date Utilize data analytics to drive decision-making and identify trends. Report on progress towards operational goals and make recommendations for improvement. Serve as a problem-solver, addressing challenges that arise during project execution. Analyse existing processes to identify opportunities and recommend improvements, utilizing industry proven methodologies. Qualifications Skills: Analytical Skills: Proficient in analysing data to inform decisions and track performance. Communication: Excellent verbal and written communication skills for engaging with stakeholders at all levels. Project Management: Strong organizational skills with the ability to manage multiple projects and deadlines. Proficiency in project management methodologies (e.g., Agile, Lean, Six Sigma). Adaptability: Capacity to adapt to changing business environments and priorities. Technical Proficiency: Familiarity with operational management software and tools. Familiarity with data analysis tools and software. Qualifications: Education: Master’s or Bachelor’s degree in business administration / engineering / computer applications/ Operations Management preferred. Expereince: Minimum of around 10 years of relevant Industry experience in IT Operations and management. A certified PMP from PMI preferred. Company Description Waters Corporation (NYSE: WAT), the world's leading specialty measurement company, has pioneered chromatography, mass spectrometry and thermal analysis innovations serving the life, materials, and food sciences for over 60 years. With approximately 8,000 employees worldwide, Waters operates directly in 35 countries, including 15 manufacturing facilities, with products available in more than 100 countries. Our team focuses on creating business advantages for laboratory-dependent organizations to enable significant advancement in healthcare delivery, environmental management, food safety, and water quality. Working at Waters enables our employees to unlock the potential of their careers. Our global team is driven by purpose. We strive to be better, learn and improve every day in everything we do. We’re the problem solvers and innovators that aren’t afraid to take risks to transform the world of human health and well-being. We’re all in it together delivering benefit as one to provide the insights needed today in order to solve the challenges of tomorrow. Diversity and inclusion are fundamental to our core values at Waters Corporation. It is our responsibility to actively implement programs and practices to drive inclusive behavior and increase diversity across the organization. We are united by diversity and thrive on it for the benefit of our employees, our products, our customers and our community. Waters is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, religion, sex, national origin, sexual orientation, age, marital status, disability, gender identity or protected Veteran status. Show more Show less

About PSC Biotech Who we are? PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients. ‘Take your Career to a new Level’ PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling points which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting. Employee Value Proposition Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met. Job Summary: The role is focused 100% on the supporting side Looking for candidates who is having primary experience in UiPath process automation. This position is responsible for equipment, facilities, and utilities automation qualification activities in a cGMP environment. The candidate should have a strong background in Automation Validation. This position will coordinate, validate, and manage projects related to equipment implementation and manufacturing process changes. The position will primarily focus on the validation needs of new implementations and changes, but will assist the users with equipment design documentation review and approval of User Requirement Specifications (URS), Functional Requirement Specifications (FRS), Software Design Descriptions (SDD), Configuration Specifications (CS), Factory Acceptance Testing (FAT), and Site Acceptance Testing (SAT)…), Automation Test Script (ATs), establishing acceptance criteria, and support regulatory agency assessments/reports. This position will be responsible for QA review of automation qualification documentation, serving clinical and commercial manufacturing facilities. Following validation, the position will assist with Regulatory document assessment and drafting, and with defending the work to regulatory agencies. The position organizes and performs qualification activities with minimal supervision. Requirements RESPONSIBILITIES Provide automation activities project management oversight for new equipment implementations and process changes. Coordinate with users to map out requirements and specifications. Coordinate with Engineering to ensure that validation activities are appropriately planned to coincide with the overall project implementation. Review and approve automation validation documentation for qualification of equipment (supporting new process changes or large novel equipment implementations) including bioreactors, autoclaves, chromatography equipment, pressure vessels, filling equipment, etc. as well as facilities and utility automation qualification packages. Review and approval of URS, FRS, SDD, CS, FAT, SAT and AT documentation. Assist with preparation of regulatory filings, with answering questions from regulatory agencies, and with presentation of materials in regulatory inspections. Create SOPs/Guideline documents for implementation of automation qualification for both new and existing process changes. Maintain current knowledge of industry standards and regulatory requirements for products developed or manufactured and validation approaches and systems utilized Represent Validation in multi-departmental meetings & project teams. Other duties as assigned. Requirements EDUCATION BS/MS in a technical discipline (physical, engineering or biological sciences preferred but not required). Training in project management preferred. Experience 5 + years' experience in a cGMP regulated environment, with exhibited knowledge or proficiency in validation and change control. Organizational and management skills to coordinate multi-discipline project groups Ability to speak, present data, and defend approaches in front of audiences and inspectors. Ability to comprehend technical information related to equipment, processes, and regulatory expectations. Experience with participation in regulatory inspections, with experience in presenting or defending departmental functions in audits and regulatory inspections. Proficiency with standard office software applications, including MS Word, MS Excel, MS Project, MS Power Point. Experience and proficiency with other applications (such as Power BI a plus). Understanding and familiarity with FDA & European regulatory requirements, guidelines, and recommendations for validation expectations. (Understanding of regulatory guidelines for other countries a plus). Show more Show less

Greetings, We are looking for an experienced and motivated Research Scientist to join our Downstream Fermentation team. The candidate should have hands-on experience in downstream processing of fermentation-based products in a biopharmaceutical or industrial biotechnology environment. Key Responsibilities: Lead and perform downstream processing of microbial fermentation products. Optimize purification processes (e.g., filtration, centrifugation, chromatography). Design and execute scale-up and pilot-scale studies. Collaborate with upstream, analytical, and quality control teams. Maintain accurate records and write technical reports. Ensure compliance with GMP/GLP and safety standards. Desired Candidate Profile: Strong knowledge of biotechnology/bioprocess engineering. Experience in purification of proteins, enzymes, or metabolites. Good communication and problem-solving skills. Prior experience in fermentation-based industries preferred. Interested candidate kindly share your cv to uma@bvrpc.om

Position Title: Bioprocess Engineer Department: Process Reports To: Director Job Overview: We are seeking a highly skilled Bioprocess Engineer to design, optimize, and scale up biotechnological processes for industrial applications. This role involves developing efficient bioprocessing workflows, troubleshooting technical challenges, and ensuring compliance with regulatory standards. The Bioprocess Engineer will collaborate with R&D, production, and quality teams to translate laboratory-scale processes into scalable manufacturing solutions. Key Responsibilities: 1. Process Development and Optimization: Design and execute experiments to develop, optimize, and validate bioprocesses (e.g., fermentation, cell culture, downstream purification). Analyze data to identify critical process parameters (CPPs) and optimize yield, efficiency, and product quality. Scale up processes from laboratory to pilot and commercial production scales. 2. Technical Collaboration: Work closely with R&D, manufacturing, and quality assurance teams to ensure seamless technology transfer and process validation. Provide technical support to resolve process deviations, equipment malfunctions, and production bottlenecks. 3. Compliance and Documentation: Ensure all processes comply with industry regulations, including GMP, FDA, ISO, and environmental/safety standards. Prepare and maintain detailed technical documentation, including SOPs, batch records, and validation reports. 4. Equipment and Technology Integration: Evaluate, select, and implement bioprocessing equipment and automation systems. Train operations staff on new equipment and process workflows. 5. Continuous Improvement: Identify opportunities for process innovation, cost reduction, and sustainability. Stay updated on emerging bioprocessing technologies and industry trends to drive continuous improvement. Required Qualifications: Ph.D. in Biotechnology, Biochemical Engineering, or a related field. Minimum 3–5 years of hands-on experience in bioprocess development, preferably in pharmaceuticals, biofuels, or biomanufacturing. In-depth knowledge of upstream (fermentation, cell culture) and downstream (purification, filtration) processes. Familiarity with bioreactor systems, chromatography, and process analytical technology (PAT). Desired Skills and Competencies: Excellent problem-solving skills with a focus on root-cause analysis and troubleshooting. Project management experience, including timeline adherence and cross-functional coordination. Ability to present technical data clearly to both technical and non-technical stakeholders. Personal Attributes: Innovative and analytical mindset with a strong attention to detail. Collaborative team player with excellent interpersonal skills. Self-driven and adaptable to fast-paced, dynamic environments. Committed to safety, quality, and ethical standards. Work Environment: Primarily lab and pilot plant settings, with occasional office work. Occasional travel to vendor sites or manufacturing facilities may be required. Application Instructions: Interested candidates should submit a resume on WhatsApp on +917888780061 detailing their relevant experience and qualifications for this role. Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Health insurance Life insurance Schedule: Day shift Morning shift Work Location: In person

Job Summary Are you passionate about service excellence? Would you love to work for a global organization that is doing more good for people and planet? IFF is a global leader in food, beverage, health, biosciences, and sensorial experiences. We are now seeking a highly motivated and results driven individual to join our Global Quality – ReADI Analyst function as specialized chemist working for manufacturing sites and creative centers around the world depending on the workload demand and customers' requirements, gathering efforts with R&D and the QC labs on the base of techniques such as Gas Chromatography and Mass Spectrometry and methodologies for Allergens and Phthalates determination Your Focus Assess and guarantee the quality of the raw material used to manufacture intermediate and finished products. Assure that the delivered products to the customers are within specifications, protecting IFF from liability cost effective on time. Supporting QC labs on the investigation of internal and external rejections and When needed, providing technical support worldwide The role reports to Supervisor Global ReADI How You Will Contribute Gas Chromatography evaluation of raw materials, intermediate and finished products from manufacturing plants and sample laboratories in accordance with internal specifications and external regulations, identifying deviations and/or abnormalities. In this point every analyst should be closing at least 25 UDs in SAP per day. Review the correct application of manual changes or reformulations or exceptions to the finished goods, on a timeline manner to assure the no impact on the OTP and/or any other KPI. Determine adjustments to turn the non-acceptable quality lots of finished products to Accepted quality, reducing rejection costs and avoiding any customer complaint and/or external rejection. Mass-spectrometry interpretation of allergenic agents and phthalates in raw materials and fine fragrances to assure the accomplishment of internal specifications and external regulations Daily communication of results and interfacing with the stakeholders requiring data. Prioritize work coming from different locations according to communicated needs Work together with Vendor Quality group on reviewing specifications of raw material, new quality of raw materials and / or new suppliers. Provide technical guidance when required for any QC lab around the world and support for resolving the root cause of some internal or external rejection. Generate GC documentation according to the customers' requirements. What You Will Need To Be Successful Bachelor’s degree in science Related Field (chemistry, chemical engineering or any related) preferred 2-3 years of experience. Broad knowledge of gas chromatography and mass spectrometry techniques (preferred 2 years) Broad understanding of Organic Chemistry Fluent English Knowledge on SAP (1 year) Data analysis and tools as SharePoint, Power Bi, Power automate, Phyton, SQL (is a plus) IFF is an Equal Opportunity Employer. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex or veteran status. We strive for inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more. I We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more Show more Show less

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description Job Summary We are seeking a skilled professional to serve as a specialist in upstream/downstream operations, specializing in processes like mammalian cell culture, perfusion technology, scale-up, single use technology, Bioreactor characterization, Chromatography, Ultrafiltration, and Virus Filtration. The role involves authoring validation protocols, conducting risk assessments, utilizing tools for process verification, and actively participating in technology transfers to ensure compliant, efficient, and continuously improved manufacturing processes. Roles & Responsibilities You will serve as a Subject Matter Expert (SME) and actively engage in hands-on operations involving processes like cell culture, tech-transfer from lab to manufacturing scale, Chromatography, Ultrafiltration, TFF, Virus Filtration, and handling drug substance. Your responsibilities include authoring process validation protocols and reports, conducting risk assessments, utilizing tools like Continued Process Verification (CPV), PAT Tools, and statistical analysis tools (e.g., JMP). You will be responsible for generating various documents related to process monitoring, investigating incidents for Deviations, and working with Quality Management Systems (QMS). Your role also involves active participation in technology transfers and implementing upstream/downstream processes including facility fit modelling based on process needs. You will build, modify, and utilize digital data storage, visualization, and analysis systems such as Minitab and/or JMP and custom web-based interfaces to enable site process monitoring and continuous process verification programs. You will be responsible for ensuring compliance, control, cost-effectiveness, and continuous improvement of manufacturing processes. Qualifications Educational qualification: A B.Tech. and a Master’s (M.Tech. or M.Sc.) or a Ph.D. Minimum work experience: 5-10 years (with Ph.D.) or 7-15 years (with Master’s) of experience in a Biopharmaceutical industry Skills & attributes: Technical Skills Thorough knowledge of Biosimilar, cell-culture, mAb purification processes, and current Good Manufacturing Practices (cGMP). Proficiency in scaling up manufacturing processes from laboratory-scale to larger production scales and transferring technology between different manufacturing sites at a clinical or commercial facility. Experience and understanding of Continued Process Verification. Familiarity and proficiency in using statistical software, particularly JMP, for data analysis, interpretation, and decision-making in the context of process optimization and control. Expertise in authoring documents related to cGMP and developmental processes, including process validation protocols and reports. Ability to identify, analyse, and resolve issues or challenges that may arise during the manufacturing process, ensuring continuous improvement. Skills in conducting risk assessments and comprehensive understanding and application of Quality Management Systems. Expertise in designing, optimizing, and implementing upstream and downstream processes in a manufacturing environment. Behavioural Skills Ability to convey complex upstream and downstream processes and technical information clearly to diverse audiences, including team members, management, and cross-functional teams. Good Interpersonal skills and capacity to work collaboratively with cross-functional teams, like R&D, manufacturing, SCM, quality assurance, regulatory affairs, and others. Strong analytical and problem-solving skills to address challenges. Demonstrates integrity by consistently following protocols, exhibiting trustworthiness and reliability. Takes responsibility and maintains a disciplined and agile approach to execution. Additional Information About the Department Biologics Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon. With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products. With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation. Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs. We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/ Show more Show less

Job Description Job Role: Lab Analyst Job Role ID SECTION I: BASIC INFORMATION ABOUT THE JOB ROLE Job Role Variant: Lab Analyst Manager Job Position Job Position ID: Value Stream: Asset Operations Job Family: Manufacturing Sub-Job Family: Trainee Grade/Level Location: SECTION II: PURPOSE OF THE ROLE To assist with various laboratory activities ensuring quality, safety, and compliance of Refinery, Petrochemical, Polymer, Elastomer, Polyester, New Energy products through meticulous testing and management of laboratory operations under the guidance of experienced lab personnel while ensuring accurate analysis, testing, and quality control of various products SECTION III: KEY RESPONSIBILITIES AND ACCOUNTABILITIES OF THE ROLE Responsibilities Laboratory Operations Assist in the collection and preparation of samples from various stages of production process including proper labelling, documentation, and sample handling and ensure integrity of samples for analysis. Perform routine tests and experiments on samples using laboratory instruments and equipments including chromatography, spectroscopy, titration and other analytical methods Record and document test results, observations and experimental data in raw data book, process register and in individual raw data book. Update analysed result in LIMS and inform supervisor to review and validate LIMS results. Detect exceptions or deviations in test results and highlight / report to concern Assist in the calibration, validation and maintenance of laboratory equipment and instruments to ensure validity of test results. Dispose left over samples safely as per laboratory practices and procedures. Conduct inspection of received routine samples and distribution of samples as per type of analysis to the different sections of the laboratory. Proactively communicate to shift in charge for any abnormal samples or non-receipt of routine sample as per schedule. Workplace Safety, Audit & ComplianceAdhere to laboratory safety protocols and guidelines at all times and ensure personnel as well the safety of assets Handle hazardous materials / chemical with outmost care and dispose as per the set guidelines/ protocols Keep self familiarized with the industry regulations, standards and protocols and ensure all lab activities comply with these requirements Policies, Processes and ProceduresConduct day to day activities in compliance with all relevant policies, processes, standard operating procedures (SOPs) and instructions so that work is carried out in a controlled and consistent manner. Keep self abreast with leading practices & trends in the industry and contribute in continuous improvement of systems, processes and procedures through LEAN six sigma methodology, DMAIC analysis, 5S adherence, QCC, Kaizen, etc. SECTION IV: SUCCESS METRICS (TOP 3-5 KPI's)Compliance to ISO 17025 Quality Management System Quality audit score Zero Penalty due to Non-Compliance of Health & Safety Regulations Reliability of reported results Awareness of LIMS and SAP-QM Awareness various standards and compliances (e.g. ISO 9001, ISO 18001, ISO 45001, AS9100D) SECTION V: OPERATING NETWORK Internal: Supervisor/ Manager, Lab Team, Quality Control/ Quality Assurance Team, Production Team, Research and Development Team, Health and Safety Team External: NA SECTION VI: KNOWLEDGE AND COMPETENCIES Education QualificationsBachelors of Science (Chemistry) or Master of Science (Chemistry); M.Sc. Candidates will be preferred. Experience (Must Have & Good to Have)0-2 years in QA/QC discipline Functional / Behavioral Competencies Required To Execute The Role FUNCTIONAL COMPETENCIES SECTION VII: CAREER MOVEMENTS Feeder Roles Possible Next Role Movement: Lab Analyst Show more Show less

Chromatography System Service Engineer Educational Qualifications Required Qualifications for a Chromatography System Service Engineer Bachelor’s degree in electrical engineering, Instrumentation, Biochemical Engineering, or a related field. Experience 2 - 5+ years of experience in industries, control systems, or a related field. Experience working in industries such as manufacturing, pharmaceuticals, automotive, or food processing Technical Skills & Experience Hands-on experience in servicing, troubleshooting, and maintaining chromatography systems Strong understanding of chromatographic techniques Knowledge of analytical instruments, pumps, detectors, and fluidic systems. Proficiency in calibration and validation of chromatography equipment. Familiarity with GMP, GLP, and FDA regulations for pharmaceutical/biotech environments. Experience with software and automation systems used in chromatography. Soft Skills Strong problem-solving and analytical skills. Ability to work independently and as part of a team. Good communication skills for customer interaction and technical support. Willingness to travel for onsite service and support. About Sartorius Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide. We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment. Join our global team and become part of the solution. We are looking forward to receiving your application. www.sartorius.com/careers Show more Show less

Dear Candidate, Please find job description below company: ICHOR biologics Location : Hyderabad Interview :Face to Face Responsiblities 1 Chromatography column and system handling. 2 Column Packing (BPG And Chromoflow) 3 TFF System 4 Centrifuge system 5 Filtration, Filter Integrity, Buffer Preparation, CIP_SIP 6 Expertise in documentation QMS/GMP Compliance/Process Awareness.  Pavan Kumar Associate –Talent Search | HRINPUTS Consulting Services 📞 +91-8688403001 | ✉️ pavankumarb@hrinputs.com 🌐 www.hrinputs.com | 📍 Hyderabad, India 🔗 Follow us: 🔹 Permanent Staffing | CXO Hiring | RPO | Project-based Hiring

Looking for Production Down Stream Process executives & Operators to handle following equipments. Candidates from Pharma/Bio tech companies background should only apply. Chromatography column and system handling Column packing (BPG and Chromoflow) TFF System Centrifuge system Filtration, Filter Integrity, Buffer preparation, CIP_SIP Expertise in documentation QMS/GMP compliance/ Process Awareness We have walk-in on 7 & 8 June at our client location, interested candidates can whats app your profile to 7075526597

Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP for Oil & Gas Downstream Good to have skills : No Function Specialty Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your day will involve overseeing the application development process and ensuring seamless communication within the team and stakeholders. Roles & Responsibilities: Expected to be an SME Collaborate and manage the team to perform Responsible for team decisions Engage with multiple teams and contribute on key decisions Provide solutions to problems for their immediate team and across multiple teams Lead the application development process Ensure effective communication within the team and stakeholders Professional & Technical Skills: Must To Have Skills:Proficiency in SAP for Oil & Gas Downstream Strong understanding of SAP modules specific to Oil & Gas Downstream industry Experience in configuring and customizing SAP applications for Oil & Gas Downstream sector Knowledge of integration with other systems and applications in the Oil & Gas industry Hands-on experience in leading application development projects in the Oil & Gas sector Additional Information: The candidate should have a minimum of 7.5 years of experience in SAP for Oil & Gas Downstream This position is based at our Pune office A 15 years full-time education is required Qualifications 15 years full time education

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities. Brief Job Overview The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients and dietary supplements manufactured, distributed, and consumed worldwide. USP’s drug standards are enforceable in the United States by the Food and Drug Administration, and these standards are used in more than 140 countries. This is a hands-on, non-supervisory individual contributor position in which the incumbent applies their knowledge and practical experience in execution of bioanalytical projects on collaborative testing of reference standards, documentary standards and characterization of biological products. Additionally, the incumbent will also actively engage and contribute in verification, international and national reference standard development programs as assigned. How will YOU create impact here at USP? In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments. Roles And Responsibilities Aligns with USP’s mission, goals and objectives and complies with USP’s guidelines and other requirements. Demonstrates laboratory skills and hands on expertise in analytical Chromatography (HPLC/UPLC/ Ion-chromatography), Capillary Electrophoresis, SEC-MALS, Circular-dichroism and Mass-spectrometry. Perform Intact Mass, Peptide mapping, Glycan profiling, HMW & LMW, HCP, Impurity Profiling studies & PTM analysis Plans and executes Compendial and R&D projects besides contributing in the new initiatives viz., proof of concept studies in Biologics for product classes such as proteins, enzymes, vaccines, monoclonal antibodies, peptides, antibiotics, raw material and any other biological products as assigned. Ability to plan, design, execute, and resolve technical issues within the scope. Evaluates and analyzes scientific reports, applies personal experience, academic training, and technical insights to troubleshoot and solve problems in the laboratory within the scope. Performs administrative responsibilities, mentors and trains team member/members as assigned. Actively engages in project coordination with cross-functional/global teams and aligns with Global Biologics objectives. Prepares and reviews project reports, SOPs, and other documents to ensure compliance to USP’s Quality Management System and contribute in Internal audits, ISO 9001 and ISO 17025 audits Assists and recommends improvements in laboratory/project management methods and processes. Performs other duties as assigned. Who is USP Looking For? The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience Ph.D. degree in Biochemistry, Analytical Chemistry or Biological Sciences . Minimum of 7 to 10 years of post-educational relevant work experience in either recombinant therapeutic proteins, peptides, mAbs and /or CGT and Vaccines areas. M.Sc./M.Tech./M.Pharm. in relevant stream of Biological Sciences with 11-13 years of industry experience working in Analytical R&D and QC department of Biopharmaceutical industry. Experience in method development, validation and technology transfer and analytical characterization for biomolecules. Must have experience include strong technical knowledge and practical experience of peptides and mAbs or CGT and Vaccines area. Work experience in cGLP/cGMP environment. Knowledge of reference standards development and collaboration related to biopharmaceutical products, reference materials manufacturing and development. Additional Desired Preferences Desired preferences are to showcase any additional preferred levels of expertise to perform the role. Reminder: any items listed in this section are not requirements nor disqualifies for candidate consideration. The candidate should be well-versed with operation and troubleshooting of all instruments used in performing the above-mentioned analytical techniques and should have sound knowledge of QMS systems. Previous experience working in biopharma cGLP/cGMP/QMS environment with practical experience in good documentation practices would be an advantage. The candidate should have strong competencies in technical writing, communication, and presentation skills. Good written and verbal communications skills Supervisory Responsibilities None Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time Show more Show less

Job Description Kenvue is currently recruiting for- Scientist, R&D Analytical This position reports into Principal Scientist, R&D Analytical and is based at Mumbai, India Who We Are At Kenvue , we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here . What You Will Do The Scientist, R&D Analytical is responsible for performing analytical and stability testing, conducting advanced research activities and utilizing technology and programs to enable Innovation projects- Key Responsibilities Lead and manage analytical research projects in R&D department Develop, optimize, validate and transfer analytical methods to support product development and life cycle management projects Execute developmental stability testing for Drug and Cosmetic products Collaborate with cross-functional teams to drive scientific advancements Provide technical expertise in analytical instrumentation and data analysis Ensure expertise in a wide range of analytical technologies and instrumentation for testing capabilities. Execute the assigned stability testing for shelf-life assessment of stability studies. Participate in method transfer process regarding testing activities. Work on specific research projects, if required. Stay current with industry trends and technologies to drive innovation Support process owners or subject matter experts for assigned responsibilities, critical laboratory processes and quality systems. Required Qualifications Minimum Masters in Chemistry or equivalent science (e.g. Biochemistry, Pharmaceutical Sciences) or Ph.D with 4-8 years of proven working experience in Analytical Chemistry and/or Medicinal chemistry, Quality Control or related functions in healthcare/pharma/FMCG sector with exposure to GMP and Quality environment preferred Proven track record of leading successful scientific projects Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health or Pharmaceutical environment Strong knowledge in UPLC, HPLC, and GC to execute Analytical test method development, validation and optimization in a cGMP environment Solid understanding of analytical and physical testing capabilities, technical skills related to instrumentation principles and working, basic troubleshooting, good documentation practices, data integrity aspects, etc. Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health environment Excellent communication and collaboration skills Strong experience with Empower chromatography data system, using electronic laboratory notebooks (ELN), and LIMS systems. Ability to grasp technical/compliance requirements and execute assigned work to meet the key performance indicators Excellent oral and written communication and articulation skills Challenges the status quo and brings innovative ideas and suggestions Displays technical curiosity and self-initiative to deliver beyond usual activities Good interpersonal skills to partner across functions, sites, and regions Kenvue is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Primary Location Asia Pacific-India-Maharashtra-Greater Mumbai Job Function Chemistry Job Qualifications What We Are Looking For Show more Show less

We( Sanzyme biologics, karakapatla unit )need executives, 2 in number with 2-3 years of experience in downstream operations for our recombinant proteins at PU 3. Qualification: B.Tech / M. Sc in Biotech / Biochemistry / Microbiology with 2-3 years of experience in downstream operations for recombinant proteins. Job Desciption: Handling TFF for micro and ultra filtration systems Handlng continuous centrifuge of varied capacities Handling Chromatography systems with audit trailing Column Packing and Un packing for the high scale BPG columns Buffer preparations as needed Sterilization of process materials Working in shifts is mandatory Aware of clean room procedures Hands on with the integrity testing Thorough with the documentation practices Aware of SOPs and the heirarchy... Interested can share their cv to my pw.. tq Show more Show less

Overview The Senior Analyst, Finance Transformation will apply advanced analysis, Project Management and Process Improvement methods and tools to prioritize, advise, or lead cross-functional, global projects, suggest/implement Finance transformation programs, create/deliver business cases and implement RPA. The position requires strong collaboration, financial acumen, willingness to challenge the status quo, communication, sense of urgency, ability to execute, leadership, and change management skills as well as experience driving business change projects. This position will follow a hybrid model work approach( 3 days a week (Tuesday, wednesday and Thursday) working from GCC office, RMZ ecoworld, Bellandur, Bangalore)). Responsibilities Apply advanced financial and operational analysis to assist with Finance Service Infrastructure and execute its design. Assist with process mapping, required standardization, data collection, and analysis. Drive RPA implementation projects. Develop and implement business cases that articulate the value propositions of a particular project/program. Successfully champion and drive the change. Leverage advanced financial acumen to analyze financial and operational data to problem solve and provide innovative and strategic solutions to the business that include a well-informed best practice perspective. Engage in strategic discussions and provide recommendations based upon analysis with quantified opportunities to drive business optimization. Synthesize results, drive conclusions, make recommendations to senior management, and implement change. Create and maintain Service Infrastructure KPI's and metrics. Create financial and operational reporting and assist with prioritization of the Finance Transformation portfolio. Plan, monitor, and manage global cross-functional projects and programs from initiation through completion including resourcing, staffing, progress reporting, and troubleshooting. Ensure effective communication between multiple organizations and regions by creating appropriate governance structures. Communicate with upper management and highlight key accomplishments, changes, and risks which may impact business results. Initiate risk management planning throughout. Ensure project results meet quality, reliability, milestones, and budget. Qualifications Bachelor's degree required; MBA preferred. Finance or related discipline. Approximately 5 years of experience in Finance, Business Operations, and Shared Services. Experience in a global, dynamic, and deadline driven environment. Exposure to Internal Controls and SOX/404 requirements Exposure to Process Mapping and Change Management. Experience creating KPI’s and benchmarking analysis. Ability to diagnose and solve problems that may be related to process, technology, or strategy. Demonstrated business acumen to learn other business disciplines Prior Robotic Process Automation experience or knowledge. Experience with implementation of technology programs that support global process improvement. Strong demonstrated experience in project management. Ability to analyze and address complex business situations and recommend solutions. Ability to present complex topics in an easy-to-understand manner. Ability to adjust approach and leverage creative thinking based on data availability Company Description Waters Corporation (NYSE: WAT), the world's leading specialty measurement company, has pioneered chromatography, mass spectrometry and thermal analysis innovations serving the life, materials, and food sciences for over 60 years. With approximately 8,000 employees worldwide, Waters operates directly in 35 countries, including 15 manufacturing facilities, with products available in more than 100 countries. Our team focuses on creating business advantages for laboratory-dependent organizations to enable significant advancement in healthcare delivery, environmental management, food safety, and water quality. Working at Waters enables our employees to unlock the potential of their careers. Our global team is driven by purpose. We strive to be better, learn and improve every day in everything we do. We’re the problem solvers and innovators that aren’t afraid to take risks to transform the world of human health and well-being. We’re all in it together delivering benefit as one to provide the insights needed today in order to solve the challenges of tomorrow. Diversity and inclusion are fundamental to our core values at Waters Corporation. It is our responsibility to actively implement programs and practices to drive inclusive behavior and increase diversity across the organization. We are united by diversity and thrive on it for the benefit of our employees, our products, our customers and our community. Waters is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, religion, sex, national origin, sexual orientation, age, marital status, disability, gender identity or protected Veteran status. Show more Show less

Overview Waters, the world's leading specialty measurement company that cares about inclusion and diversity is seeking for a Market Development Specialist to support the very successful growth of our businesses across Waters Central Region. Waters deliver benefits through innovation and people that enable customer success in the life, materials and food sciences. People create the Waters difference. By engaging with our talented and diverse workforce we continuously evolve, develop and enhance our products. We believe in delivering innovative technology and system solutions to our valued customers to enable their success. Our talented application teams have over the years delivered great and sustainable technical solution. As Market Development Specialist, this role will focus on sales supporting and marketing activities implementation. You will be required to team work with cross-functional departments such as Marketing, Service, Sales, ect. to boost Waters business in local territories. Your knowledge in technology and working experience in analytical chemistry lab are strongly expected to make Waters Customer Success. This position would cover the Central region specifficully Telengana, Andhra Pradesh, Chattisgarh and some part of Maharashtra. Responsibilities Sales supporting such as customer co-visiting, documents generation, solution presentation, etc. Provide application consultancy services and technical support to end users both in the area of liquid chromatography and Mass Spectrometer. Conduct or support local seminars, marketing events and solution demonstration on the customer sites. Plan, localize and implement diversified business development programs according to program codes in related industries. Work closely with sales to achieve and exceed business goals. Team work with Marketing, Service and Sales teams to collect, evaluate, and forecast the local business data. Qualifications Education: Bachelors Degree, Masters, or PhD in scientific area such as chemistry, biology, or biochemistry Experience: 10+ years chromatography experience. UPLC, Mass Spec, field sales and/or marketing experience is a plus Skills: Action oriented and eager to achieve results Sound communication and presentation skills Highly organized / well-prepared / time management skills Strong interactive skills and a good listener Matured disposition, positive attitude and strong sense of commitment Adaptive to a dynamic and ever-changing environment Strong technical background in analytical technologies, especially LC and MS Company Description Waters Corporation (NYSE: WAT), the world's leading specialty measurement company, has pioneered chromatography, mass spectrometry and thermal analysis innovations serving the life, materials, and food sciences for over 60 years. With approximately 8,000 employees worldwide, Waters operates directly in 35 countries, including 15 manufacturing facilities, with products available in more than 100 countries. Our team focuses on creating business advantages for laboratory-dependent organizations to enable significant advancement in healthcare delivery, environmental management, food safety, and water quality. Working at Waters enables our employees to unlock the potential of their careers. Our global team is driven by purpose. We strive to be better, learn and improve every day in everything we do. We’re the problem solvers and innovators that aren’t afraid to take risks to transform the world of human health and well-being. We’re all in it together delivering benefit as one to provide the insights needed today in order to solve the challenges of tomorrow. Diversity and inclusion are fundamental to our core values at Waters Corporation. It is our responsibility to actively implement programs and practices to drive inclusive behavior and increase diversity across the organization. We are united by diversity and thrive on it for the benefit of our employees, our products, our customers and our community. Waters is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, religion, sex, national origin, sexual orientation, age, marital status, disability, gender identity or protected Veteran status.

Overview The Biologics Business Unit Commercial Sales Organization is comprised of highly skilled, motivated, and customer focused professionals who are technical experts on the Wyatt Technology and SEC HPLC product suites. Focus spans nanoparticle and macromolecule applications across the Pharmaceutical & Life Sciences, Polymer, Food, Environmental, Academia and Government industries. The Field Service Applications Chemist is a technical expert for all Wyatt Technology and SEC HPLC and a key member of the Bio Business Unit sales team. Through high impact and proactive sales activities, this role ensures a team of Account Managers are successful and focused on selling Wyatt products. This role ensures that customers receive exceptional sales experience while purchasing and utilizing advanced scientific instrumentation and software. This is a remote position requiring you to work out of your home office when not traveling within the District. Up to 70% travel expected, with some overnight travel as needed. Responsibilities Proactively ensure assigned accounts/territory develops new sales opportunities collaborating with the local sales team through the provision of onsite seminars, technical consulting, application feasibility test, and demonstrations. Master technical application support during the sales process including pre-sales positioning and product introduction and support of existing customers on an ongoing basis with high level product training and application support technical partnership which leads to repeat sales. Set up and run live product demonstrations for SEC-MALS, FFF-MALS, CG-MALS, DLS, ELS, HPLC and provide data analysis support. Help mentor sales account managers through joint onsite activities. Build and present technical seminars about key applications at industry seminars, conferences, and symposiums. Identify and develop application solutions that provide high value to the biopharmaceutical and gene therapy markets. Advise the transfer of knowledge and data from application feasibility studies, industrial and academic applications and technical journals and publications to product management for development. Implementing programs following the annual business plan to develop business and achieve the target sales growth. Maintain and continue to develop an outstanding knowledge of our products, their applications, and our competitors’ offerings. Supervise competitive activity and industry trends, develops competitive solutions to meet sales goals. Timely submitting of weekly reports, monthly highlights, marketing intelligence, and other related reports for defined territory to supervisor. Continually work with your Regional Sales Manager to maintain accurate and current records of proposals, opportunities, accounts, contacts, leads and actions through CRM within defined territory. Capable of independently installing and providing hands-on training for Wyatt’s core (SEC-MALS and DLS) and advanced (FFF-MALS, CG-MALS, ELS) hardware and software products. Qualifications Post graduate Degree in Chemistry, Biochemistry or Life Science Degree. PhD in Chemistry, Three (3) years of hands-on experience with HPLC and Light Scattering instruments One year of light scattering experience Knowledge of polymer characterization techniques Strong communication and interpersonal skills, basic computer skills Valid Driver’s license in good standing is required Excellent written and verbal communication skills and an excellent familiarity with basic lab techniques, instrumentation, and software. Excellent organization, motivation, attention to detail, and communication skills are a must. Up to 70% travel for this role Company Description Waters Corporation (NYSE: WAT), the world's leading specialty measurement company, has pioneered chromatography, mass spectrometry and thermal analysis innovations serving the life, materials, and food sciences for over 60 years. With approximately 8,000 employees worldwide, Waters operates directly in 35 countries, including 15 manufacturing facilities, with products available in more than 100 countries. Our team focuses on creating business advantages for laboratory-dependent organizations to enable significant advancement in healthcare delivery, environmental management, food safety, and water quality. Working at Waters enables our employees to unlock the potential of their careers. Our global team is driven by purpose. We strive to be better, learn and improve every day in everything we do. We’re the problem solvers and innovators that aren’t afraid to take risks to transform the world of human health and well-being. We’re all in it together delivering benefit as one to provide the insights needed today in order to solve the challenges of tomorrow. Diversity and inclusion are fundamental to our core values at Waters Corporation. It is our responsibility to actively implement programs and practices to drive inclusive behavior and increase diversity across the organization. We are united by diversity and thrive on it for the benefit of our employees, our products, our customers and our community. Waters is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, religion, sex, national origin, sexual orientation, age, marital status, disability, gender identity or protected Veteran status.

Overview Waters, the world's leading specialty measurement company that cares about inclusion and diversity is seeking for a Field Service Engineer - Temp to support the very successful growth of our businesses across (Waters India - Hyderabad). Waters deliver benefits through innovation and people that enable customer success in the life, materials and food sciences. People create the Waters difference. By engaging with our talented and diverse workforce we continuously evolve, develop and enhance our products. We believe in delivering innovative technology and system solutions to our valued customers to enable their success. Our talented field sales/service and specialist teams have over the years delivered great and sustainable business results. With a constant focus on growth and by developing new markets we are able to increase the business even within very challenging economic circumstances. As Field Service Engineer - Temp, you are an ambassador of Waters and will bring to the market Waters’ products and services. The candidate will demonstrates a clear grasp of understanding the customers’ business and its growth plans and is able to take that knowledge and convert that into a solution and offering from Waters, with a primary aim of bringing “customer success”. This position brings a great degree of flexibility working in the field. The role will be designated to either a territory and/or markets. This is on contract role with 3rd Party payroll. Responsibilities Installation, performance maintenance, troubleshoot and support Waters' product suite (LC, HPLC/UPLC, Informatics) Establish and maintain effective relationships with external and internal customers ensuring their success Manage customer expectations, by communicating work performed and providing follow up plan if needed Ensure customer compliance regulations are followed Deliver system level training at customer sites Manage service inventory according to Waters policies Issue field service reports daily to document work performed Maintain sound knowledge regarding the technology and customers' application demands Work with Sales team in respect to identifying future business development opportunities and needs for service contract sales Ensure that quality system procedures and Health & Safety standards are adhered to at all times Qualifications Education: Bachelors/Masters Degree in Chemistry or Biology, engineering or other science related field is desired, will also consider applications with equivalent experience, training and education Experience: 2 years of experience with installation, performance maintenance, troubleshooting, support and/or end user utilization of scientific instrumentation, preference for previous Waters product suite (LC, HPLC/UPLC, Informatics) Ability to perform effective system level troubleshooting Understanding of the scientific application workflow along with the scientific software systems (CDS) Skills: Must possess a strong customer focus Strong communication skills; ability to communicate effectively to a diverse audience with specific customer needs Personal sense of integrity Effective time management skills System level approach to problem solving Analytical mindset with a strong drive to resolve open issues Excellent verbal and written communication skills Travel: This is a territory-based position with travelling within your designated territory, and occasional travels to other countries for activities such as governance of department, local business support, meetings and training. Company Description Waters Corporation (NYSE: WAT), the world's leading specialty measurement company, has pioneered chromatography, mass spectrometry and thermal analysis innovations serving the life, materials, and food sciences for over 60 years. With approximately 8,000 employees worldwide, Waters operates directly in 35 countries, including 15 manufacturing facilities, with products available in more than 100 countries. Our team focuses on creating business advantages for laboratory-dependent organizations to enable significant advancement in healthcare delivery, environmental management, food safety, and water quality. Working at Waters enables our employees to unlock the potential of their careers. Our global team is driven by purpose. We strive to be better, learn and improve every day in everything we do. We’re the problem solvers and innovators that aren’t afraid to take risks to transform the world of human health and well-being. We’re all in it together delivering benefit as one to provide the insights needed today in order to solve the challenges of tomorrow. Diversity and inclusion are fundamental to our core values at Waters Corporation. It is our responsibility to actively implement programs and practices to drive inclusive behavior and increase diversity across the organization. We are united by diversity and thrive on it for the benefit of our employees, our products, our customers and our community. Waters is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, religion, sex, national origin, sexual orientation, age, marital status, disability, gender identity or protected Veteran status.