17 Fluorescence Jobs

Duties and responsibilities Following are some of the key duties and responsibilities for this position • Follow all safety policies and guidelines during lab work and site visits • Ensures compliance with Ecolab corporate safety standards, policies and procedures and manages the lab and other processes • Independently operates, can develop methods and performs troubleshooting of advance analytical instruments related majorly to chromatography, spectroscopy, fluorescence, rheology, polymer, gravimetric analysis. • Ability to quickly learn processes, instruments, softwares as well as others like LIMS • Fostering, collaborating and continuous improvement for digitalization and automation of QA Process • Conduct water analysis/tests, performance studies of technologies, customer technical support and present the findings in meetings. • Develop and maintain ISO17025 excellence and compliance of the lab • Engage with internal customers to solve/support industry challenges through analytical studies • Provides solutions to a variety of problems which require collecting and analyzing data from diverse sources to solve problems • Be an advocate of the region for analytical during Global meetings/forums to provide the regional needs and highlight challenges and opportunities of the IMEA region Minimum Qualifications • Master’s Degree in Analytical Chemistry/Biotech or related discipline • 5+ years of industrial experience in handling analytical instruments like ICP, HPLC, TOC, XRF, GC, etc • Highly skilled in conducting water analysis like cations, anions, COD, BOD, Alkalinity, organic carbon, dissolved/suspended solids, etc • Profound knowledge of ISO17025 certification • Strong written and oral communication skills. • self-motivated, open minded team player • Focused and driven while at the same time agile and flexible with the approach and assignments • Strong problem-solving skills

University: Delft University of Technology (TU Delft) Country: Netherlands Deadline: 6 July 2025 Fields: Physics, Biophysics, Biochemistry, Nanotechnology, Materials Science The Caneva Lab at Delft University of Technology invites applications for a PhD position focused on the development of DNA origami nanoactuators for molecular diagnostics. This project aims to advance single-molecule biophysics by integrating DNA nanotechnology with ultraflat 2D materials, enabling the detection of rare circulating tumor DNA through innovative biosensor platforms. Requirements Master’s degree (MSc) in Physics, Biophysics, Biochemistry, Nanotechnology, Materials Science or a related field Experience with AFM imaging of biological samples, DNA origami nanotechnology, and/or fluorescence microscopy is highly desirable Demonstrated creativity, open-mindedness, and proactive research attitude Strong experimental and analytical skills Ability to work both independently and as part of a multidisciplinary team Fluency in spoken and written English Successful candidates will join the Dynamics of Micro and Nanosystems (DMN) section within the Precision and Microsystems Engineering Department, collaborating with leading experts in a vibrant, interdisciplinary environment. Access to state-of-the-art facilities at the Delft Kavli Institute of Nanoscience and other departments will support your research endeavors. Application Procedure Interested applicants should submit the following documents by 6 July 2025: – Cover letter detailing motivation for the position – Curriculum Vitae (CV) – Names and contact details of three references Please apply via: https://careers.tudelft.nl/job/Delft-PhD-Position-in-DNA-Origami-Nanoactuators-for-Molecular-Diagnostics-2628-CD/822273302/ For further information regarding this vacancy, contact: s.caneva@tudelft.nl Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/register Show more Show less

Overview Overview : Bruker is enabling scientists to make breakthrough discoveries and develop new applications that improve the quality of human life. Bruker’s high-performance scientific instruments and high-value analytical and diagnostic solutions enable scientists to explore life and materials at molecular, cellular and microscopic levels. In close cooperation with our customers, Bruker is enabling innovation, improved productivity and customer success in life science molecular research, in applied and pharma applications, in microscopy and nanoanalysis, and in industrial applications, as well as in cell biology, preclinical imaging, clinical phenomics and proteomics research and clinical microbiology. Today, worldwide more than 8500 employees are working on this permanent challenge at over 90 locations on all continents. Bruker continues to build upon its extensive range of products and solutions, its broad base of installed systems and a strong reputation among its customers. Being one of the world's leading analytical instrumentation companies, Bruker is strongly committed to further fully meet its customers’ needs as well as to continue to develop state-of-the-art technologies and innovative solutions for today's analytical questions. Bruker India is looking for an experienced Remote Support Engineer (Analytical Instruments) to be based in based in Bengaluru, India . Responsibilities Essential Functions : Work Remotely With Customers To Diagnose BAXS Instruments Like Xray Diffractometers, Fluorescence Spectrometers, Single Crystal Diffractometers, Optical Emission Spectrophotometers Including But Not Limited To Diagnose, test, develop, optimize, communicate, and execute the most efficient solution plan for complex electromechanical hardware/software instrument issues, operations and training related issues. Optimize instrument and/or accessory performance to meet specification. Create and maintain record of activity in support database Provide a great customer experience through the entire support process Ask customers targeted questions to quickly understand the root cause of their instrument issues. Effectively communicate with end-users to understand the technical issues or concerns via various channels (phone, email, Chat etc.) to identify and resolve them within short time. If the first level customer support is unsuccessful, using ticket management and transferring call will be pushed to second level remote support team If job demands for onsite support, engineer should travel and support customers within short notice. Experience in dealing with analytical instruments like spectrophotometers, X-ray based instruments or optical measuring systems is a must Leverage internal technical expertise, including peers, mentors, knowledge base, community forums and other internal tools, to provide the most effective solutions to customer issues. Build knowledge base to reduce reliance over time on other internal resources. Contribute to internal technical knowledge base and publish Frequently Asked Questions to enable customer self-support. Accurately document and update tickets in the tracking systems. Ability to maintain a personal queue of open requests. Maintain communication with the customers on the status of all open tickets. All responses should be professional, complete, well formatted, and consistent with prior communications and Corporate Identity. Future outbound activities as follow up possible (updates, surveys) Properly escalate unresolved issues to appropriate technical support teams Provide necessary information/observations/logs - all the required data to next level support or R&D team to diagnose a reported/escalated problem. Ability to describe incident and requests as part of a ticket management. Ability to create and update operational procedures and proposal of decision trees. (issues resolution, requests, and administration procedures) Perform other tasks as assigned by manager. The job demands to work in rotational shifts (Monday through Friday). 20% on field and 80% on office Excellent customer relation skills and the ability to make timely and effective decisions is a plus. Other duties as assigned Qualifications Knowledge, Skills and Abilities : Customer focused, passionate about science and technology, and eager to enable customers with Bruker technology. Demonstrated Excellent analytical capabilities and theoretical understanding of physics. Customer service-oriented working experience in technology-based instruments like XRD, XRF, OES to support various technical issues Working knowledge of electronics, mechanics, control systems, computers, networking. Able to use common electrical testing tooling like oscilloscopes, multimeters, etc. to be an effective problem solver of complex system, product user, and/or application issues. Demonstrated ability to provide clear, logical, and effective communication in English. Ability to communicate effectively in a professional and friendly manner with both internal and external customers. Experienced in use of Salesforce (CRM) and SAP preferred is a plus Should have worked on remote support tools, e.g., TeamViewers, Webex, any desk. The personality of a natural team player, willing and able to build confidence and to establish strong co-operative relationships with personnel throughout the company, customer base and with key individuals within the industry. A flexible attitude to working hours which are sometimes influenced by factors such as the need to complete the job or the availability of the client. For further development, engineer should be willing in general to travel up to 20% Students of Engineering & Science background are welcome. Start your service career with first step in making our clients happy. Language skills in addition to English are welcome. Education BE/BTech in Electronics/ Electrical/ Instrumentation, MSc in Physics, Chemistry and Material Science Should have a technical education and / or worked already as a technician. Experiences At least 1 year of previous service experience or hotline activity within electronic systems Technical expertise in electronics and mechanics Confident in handling all common PC operating systems and networks Bruker is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, national origin, disability, veteran status, and other protected characteristics. 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 looking for a skilled, enthusiastic and experienced Scientist to join our Immunogenicity team. This role supports the nonclinical development of complex generics and differentiated products from strategy and development to product approval, across all verticals and global markets. Roles & Responsibilities Immunogenicity Risk Assessment: Responsible to develop and implement strategies for in-vitro immunogenicity risk assessments, including literature surveillance, execution, and evaluation during development and submission stages. Assay Development and Execution: Responsible to independently design, optimize, and perform in-vitro cell-based assays, immunological assays, immune cell profiling, and biomarker analysis for API, complex generics, and differentiated products. Cytokine and T-cell Assays: Responsible to establish and validate cytokine release immunogenicity assays and T-cell proliferation assays using PBMCs to support product development. Study Coordination and Data Analysis: Responsible to plan, execute, and coordinate nonclinical in-vitro studies, manage test articles with cross-functional teams, conduct experiments, analyze data, perform statistical evaluation, and compile reports for internal review. Regulatory and Scientific Research: Responsible to continuously gather and analyze peer-reviewed literature, regulatory guidelines, and scientific reports related to immunogenicity, contributing to team discussions and decision-making. Documentation and Compliance: Responsible to prepare and maintain SOPs, STPs, study reports, and incident records, ensuring adherence to QMS and organizational safety standards. Cross-functional Collaboration: Responsible to engage with internal teams and external stakeholders to support immunogenicity assessments and ensure alignment with project goals and regulatory requirements. Qualifications Educational qualification: PhD in Biological Sciences/ M.Sc/ M.Tech in Biological Sciences/Pharmacology Minimum work experience: 3 years in Pharma Industry with M.SC/M.Tech or fresh PhD graduate Technical Skills: Cell Culture Handling: Proficiency in maintaining primary and established cell lines, handling PBMCs, and sterile culture techniques. Immunoassays: Expertise in ELISA, multiplex cytokine analysis, and in-vitro immunogenicity assays for immune response evaluation. Flow Cytometry (FACS): Skilled in immune cell phenotyping, fluorescence-based sorting, and multi-color panel design. MACS-Based Cell Isolation: Experience in magnetic bead separation for immune cell enrichment and functional assays is an added advantage. Data Analysis: Strong statistical analysis skills using GraphPad Prism and Excel for result interpretation, visualization, and reporting. Behavioural Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams. Ability to multi-task, prioritize and deliver effectively under stringent timelines Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. 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

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 This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent work collaboratively in the reference standard/ARM development program within the Global Biologics department. The incumbent will participate in the development of replacement and new reference standards /ARM in support of USP’s mission and core business. The incumbent will also focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in timely manner. 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. The Sr. Scientist -I (RSS) Has The Following Responsibilities Roles and Responsibilities Maintain smooth collaboration and works closely with key stakeholders across the globe to develop reference standards for biotechnology pharmaceutical products including proteins, peptides, heparins, antibiotics, and advanced therapies. Works to draft protocols, reports and address scientific and technical queries from internal and external stakeholders in timely manner pertaining to reference standards/ARMs Oversees and facilitates the development of standards and solutions to address analytical challenges associated with biological medicines. Supports day to day operations of the Stability (CSU) program covering the USP Biologics RS catalog inventory. Reviews RS testing history and drafts test protocols for collaborative studies and CSU studies and submits to labs based on designated testing requirements and schedules. Liaisons and Assists laboratories to ensure collaborative testing/CSU testing is completed accurately and in timely manner. Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use. Compiles current and historical Stability testing data assessment and prepare stability trend reports. Maintains and updates various databases documenting laboratory data and program determinations on suitability and Stability interval updates. Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Quality Assurance and Reference Standard Evaluation with investigation of unexpected stability testing results Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps. Prepare, present and discuss regular work updates with Team Lead and other team members Reviews protocols and/or reports of other Scientists as assigned by manager. Who is USP Looking For? Preferred Qualifications 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: Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc. Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development. Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays. Excellent technical writing, presentation and oral communication skills are required. Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders. Sr. Scientist I Ph.D. degree in Biochemistry, Analytical Chemistry or Biological Sciences . Minimum of 7 to 10 years of post-educational work experience in recombinant therapeutic proteins, peptides and carbohydrates. in Biochemistry, or Biological Sciences with minimum of 11 to 13 years of commensurate industrial experience. Additional Desired Preferences Knowledge of USP products and services is highly desirable. Operates collaboratively at all levels of the organization in a highly technical environment. Must be able to work in a fast-paced environment and respond to shifting priorities. Well-developed interpersonal, negotiation, conflict-resolution and listening skills. Must possess the ability to multi-task and to work effectively with a team. Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality. Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred. Supervisory Responsibilities No 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 Summary As Service Engineer, you will be responsible for the complete Customer Experience – right from the smooth installation of instruments, to training of users, to providing in-warranty support as well as post-warranty solutions (preventive and breakdown maintenance services) throughout the life of the instrument. You will also be responsible for commercial activities related to maintenance contracts, spares & consumables supplies. You will follow the company values, business ethics, compliance and processes. Technical Required Skills: You are a Solutions oriented person with enthusiasm to face technical challenges, to diagnose & solve problems and continuously improve customer satisfaction. Communication You are proactive in communicating with all customer stakeholders to schedule & execute service visits with punctuality. You also easily connect with internal colleagues and factory team with a sense of urgency to resolve issues. You are committed to attending breakdowns complaints even during off work hours and provide prompt responses, offer support remotely as and when required. You are extremely professional & courteous with your verbal and written communication. You have experience with basic email software, excel. You are a self-motivated technologist, with passion to travel widely, ability to work alone. You are interested in continuous learning and self-development to improve your technical skills and keen to attend all the training programs you are nominated to attend. Requirements Graduate or Diploma Engineer - Electronics / Electrical / Instrumentation Min 1 to 2 years of prior service experience with any industrial analytical technology provider is preferredMulti-tasking & Negotiation skills are preferred. The role requires working inside industrial manufacturing sites including shifting and lifting instrument. Travel is mainly within West region (Maharashtra, Gujarat, Madhya Pradesh) but you may also require to travel anywhere across India as and when required and to factory in Germany for training as and when nominated. About Us AMETEK SPECTRO, a business unit of AMETEK Inc, is one of the worldwide leading suppliers of analytical instruments, employing optical emission (stationary and mobile Arc/Spark OES, ICP-OES) and X-ray fluorescence spectrometry (XRF) technology, used for the elemental analysis of materials in industry, research and academia. AMETEK SPECTRO is a preferred technology partner for customers across India, for more than 40 years with our advanced technology as well as our dedicated service network which is the largest in our industry providing world class support to our customers. AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.0 billion. AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers’ most complex challenges. We employ 21,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK (NYSE:AME) is a component of the S&P 500. Visit www.ametek.com for more information. Show more Show less

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 This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent work collaboratively in the reference standard/ARM development program within the Global Biologics department. The incumbent will participate in the development of replacement and new reference standards /ARM in support of USP’s mission and core business. The incumbent will also focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in timely manner. 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. The Sr. Scientist -I (RSS) Has The Following Responsibilities Roles and Responsibilities Maintain smooth collaboration and works closely with key stakeholders across the globe to develop reference standards for biotechnology pharmaceutical products including proteins, peptides, heparins, antibiotics, and advanced therapies. Works to draft protocols, reports and address scientific and technical queries from internal and external stakeholders in timely manner pertaining to reference standards/ARMs Oversees and facilitates the development of standards and solutions to address analytical challenges associated with biological medicines. Supports day to day operations of the Stability (CSU) program covering the USP Biologics RS catalog inventory. Reviews RS testing history and drafts test protocols for collaborative studies and CSU studies and submits to labs based on designated testing requirements and schedules. Liaisons and Assists laboratories to ensure collaborative testing/CSU testing is completed accurately and in timely manner. Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use. Compiles current and historical Stability testing data assessment and prepare stability trend reports. Maintains and updates various databases documenting laboratory data and program determinations on suitability and Stability interval updates. Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Quality Assurance and Reference Standard Evaluation with investigation of unexpected stability testing results Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps. Prepare, present and discuss regular work updates with Team Lead and other team members Reviews protocols and/or reports of other Scientists as assigned by manager. Who is USP Looking For? Preferred Qualifications 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: Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc. Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development. Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays. Excellent technical writing, presentation and oral communication skills are required. Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders. Sr. Scientist I Ph.D. degree in Biochemistry, Analytical Chemistry or Biological Sciences . Minimum of 7 to 10 years of post-educational work experience in recombinant therapeutic proteins, peptides and carbohydrates. in Biochemistry, or Biological Sciences with minimum of 11 to 13 years of commensurate industrial experience. Additional Desired Preferences Knowledge of USP products and services is highly desirable. Operates collaboratively at all levels of the organization in a highly technical environment. Must be able to work in a fast-paced environment and respond to shifting priorities. Well-developed interpersonal, negotiation, conflict-resolution and listening skills. Must possess the ability to multi-task and to work effectively with a team. Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality. Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred. Supervisory Responsibilities No 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

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting, Office Job Title: Scientist-I, Protein Biology Job Location: India, Bangalore About Company: Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with an annual revenue of approximately $44 billion. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. About Team: Protein Biology The Protein Biology team is involved in large-scale functional validation of antibodies, with a deep focus on reagent quality and specificity. The core activities of the team include data mining and processing, Western blotting with state-of-art tools, high efficiency and high-resolution immuno-fluorescence imaging, immunohistochemistry, ChIP (Chromatin Immunoprecipitation), and gene-silencing to provide advance application tags to our antibody portfolio. The program's goal is high-quality product validation and product information creation to promote research use. Role & Responsibilities Purpose: Contribute to the antibody validation workflow. Understand target biology validation and validate antibodies for reproducibility using innovative methods and crafting data sets to enable market differentiation. The role of the successful candidate would entail demonstrating scientific proficiency in experimental planning and execution. Prior experience in working in a research team, with a proven track record of setting goals, handling work-related customer concerns, and ensuring timely delivery in alignment with the program goals. Proficiency in verbal and written communication of results in the workplace is helpful. Responsibilities: Knowledge of key aspects of protein biology, to deliver results on antibody validation and characterization. Meticulous experimental design to meet program goals. Excellent record keeping of results into data sheets and laboratory note-books. Regular mining of literature and keeping oneself up to date with developments in field of antibody validation. Compilation and presentation of data in written and oral formats; active participation in team meetings. Attention to detail and adherence to schedules. Candidate Requirement: Education & Experience levels: Applicants should have a Masters’ degree with 2-5 years of experience or PhD in molecular biology, immunology, biotechnology or biochemistry. Skills: Familiar with experimental workflow in cell and molecular biology, with experience in the design and development of protein assays. protein-protein interaction (using co-immunoprecipitation), or development of immunoassays. Proven experience in immunoassays such as Western blotting, Immunofluorescence, Immunohistochemistry, Flow cytometry or ELISA. Communication of research data and providing expert-level technical troubleshooting to resolve scientific problems. Good understanding of computation biology tools and basic knowledge of databases and programming languages. Thermo Fisher Scientific is an equal opportunity employer and value diversity at our company. All qualified applicants will receive consideration for employment without discrimination basis race, color, religion, sex, sexual orientation, gender, gender identity or expression, national origin, protected veteran status, age, genetics, pregnancy, disability or any other legally protected status. Thermo Fisher Scientific aligns with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer a company culture that stands for integrity, intensity, involvement, and innovation! Thermo Fisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Show more Show less

Role: Assay Biologist Department: Biology Location: Hyderabad About Us: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and follow equal opportunity practices across all levels. Summary of Job: Knowledge on biochemical and cell-based assays. Key Responsibilities : Execute assay optimization, validation, and compound screening in various in vitro biochemical and cell-based assays. For cell-based assays hands on following is desirable: Ø Media preparation Ø Cell culture (Suspension and Adherent) Ø Cell cryopreservation Ø Cell seeding using automated dispensers Ø Compound dilutions, manually or using Echo Ø Hands on multimode microplate readers such as Envision and FLIPR For cell free (biochemical) assays understanding of following is desirable: Ø Enzyme kinetics Ø KM Ø Assay optimization parameters Ø Different assay technologies for kinase assays Analyse and interpret the data from assay optimization, validation, and compound screening studies. Record the experimental data in prescribed format in LNB and or ELN Operate instruments for efficient, accurate and reproducible data. Use analysis software/s for data handling (GraphPad Prism). Familiar with the current assay techniques (HTRF, AlphaLISA, Luminescene, Fluorescence, Absorbance.) and assays (Reporter gene assays, FLIPR assay, CTG assay, ADP Glo kinase assay, etc) Execute compound management procedures, indenting process, receiving, maintenance of reagents and consumables stocks. Adhere to and follow Sai policies and company rules. Experience/Qualification: M.Sc/M.Tech/M.Pharm with 2-3 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioural): Technical: Multi-channel pipettes, Multimode plate readers, Western blot apparatus, operation of centrifuge, ELISA etc. Functional: Basic knowledge on biochemical and cell-based assays. Behavioural : Team player, ability to work with multidisciplinary teams. Strong analytical skills and ability to work under stringent timelines, good communication skills.

Role: Assay Biologist Department: Biology Location: Hyderabad About Us: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and follow equal opportunity practices across all levels. Summary of Job: Knowledge on biochemical and cell-based assays. Key Responsibilities : Execute assay optimization, validation, and compound screening in various in vitro biochemical and cell-based assays. For cell-based assays hands on following is desirable: Ø Media preparation Ø Cell culture (Suspension and Adherent) Ø Cell cryopreservation Ø Cell seeding using automated dispensers Ø Compound dilutions, manually or using Echo Ø Hands on multimode microplate readers such as Envision and FLIPR For cell free (biochemical) assays understanding of following is desirable: Ø Enzyme kinetics Ø KM Ø Assay optimization parameters Ø Different assay technologies for kinase assays Analyse and interpret the data from assay optimization, validation, and compound screening studies. Record the experimental data in prescribed format in LNB and or ELN Operate instruments for efficient, accurate and reproducible data. Use analysis software/s for data handling (GraphPad Prism). Familiar with the current assay techniques (HTRF, AlphaLISA, Luminescene, Fluorescence, Absorbance.) and assays (Reporter gene assays, FLIPR assay, CTG assay, ADP Glo kinase assay, etc) Execute compound management procedures, indenting process, receiving, maintenance of reagents and consumables stocks. Adhere to and follow Sai policies and company rules. Experience/Qualification: M.Sc/M.Tech/M.Pharm with 2-3 years of relevant industry experience. Key Competencies (Technical, Functional & Behavioural): Technical: Multi-channel pipettes, Multimode plate readers, Western blot apparatus, operation of centrifuge, ELISA etc. Functional: Basic knowledge on biochemical and cell-based assays. Behavioural : Team player, ability to work with multidisciplinary teams. Strong analytical skills and ability to work under stringent timelines, good communication skills. Show more Show less

Qualification: Ph.D./Master’s degree in Life Sciences with minimum 1-2 years of research experience. Required Skills: 1. Technical Skills: - Must be proficient in · Constituting Media & Fine pipetting · Cell staining protocols and biological assays · Good knowledge of bright-field microscopy · Immunofluorescence staining assays and Fluorescence microscopy · PCR and RT-PCR techniques 2. Data compilation and analysis: - Compilation and analysis of experiment data and give suggestions for the next experimentation plan 3. Troubleshooting: - Identify performance issues encountered in experiments and work to resolve them by analysing their underlying cause 4. Communication skills: - Must be proficient with communication in English & Hindi. Should also have exposure of using Microsoft Word and PowerPoint Remuneration: - As per industry standards. Work Location: - Faridabad Job Type: Full-time Pay: ₹340,331.91 - ₹700,000.00 per year Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting, Office Job Title: Scientist-I, Protein Biology Job Location: India, Bangalore About Company: Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with an annual revenue of approximately $44 billion. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. About Team: Protein Biology The Protein Biology team is involved in large-scale functional validation of antibodies, with a deep focus on reagent quality and specificity. The core activities of the team include data mining and processing, Western blotting with state-of-art tools, high efficiency and high-resolution immuno-fluorescence imaging, immunohistochemistry, ChIP (Chromatin Immunoprecipitation), and gene-silencing to provide advance application tags to our antibody portfolio. The program's goal is high-quality product validation and product information creation to promote research use. Role & Responsibilities Purpose: Contribute to the antibody validation workflow. Understand target biology validation and validate antibodies for reproducibility using innovative methods and crafting data sets to enable market differentiation. The role of the successful candidate would entail demonstrating scientific proficiency in experimental planning and execution. Prior experience in working in a research team, with a proven track record of setting goals, handling work-related customer concerns, and ensuring timely delivery in alignment with the program goals. Proficiency in verbal and written communication of results in the workplace is helpful. Responsibilities: Knowledge of key aspects of protein biology, to deliver results on antibody validation and characterization. Meticulous experimental design to meet program goals. Excellent record keeping of results into data sheets and laboratory note-books. Regular mining of literature and keeping oneself up to date with developments in field of antibody validation. Compilation and presentation of data in written and oral formats; active participation in team meetings. Attention to detail and adherence to schedules. Candidate Requirement: Education & Experience levels: Applicants should have a Masters’ degree with 2-5 years of experience or PhD in molecular biology, immunology, biotechnology or biochemistry. Skills: Familiar with experimental workflow in cell and molecular biology, with experience in the design and development of protein assays. protein-protein interaction (using co-immunoprecipitation), or development of immunoassays. Proven experience in immunoassays such as Western blotting, Immunofluorescence, Immunohistochemistry, Flow cytometry or ELISA. Communication of research data and providing expert-level technical troubleshooting to resolve scientific problems. Good understanding of computation biology tools and basic knowledge of databases and programming languages. Thermo Fisher Scientific is an equal opportunity employer and value diversity at our company. All qualified applicants will receive consideration for employment without discrimination basis race, color, religion, sex, sexual orientation, gender, gender identity or expression, national origin, protected veteran status, age, genetics, pregnancy, disability or any other legally protected status. Thermo Fisher Scientific aligns with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer a company culture that stands for integrity, intensity, involvement, and innovation! Thermo Fisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Show more Show less

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting, Office Job Title: Scientist-II, Protein Biology Job Location: India, Bangalore About Company : Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with an annual revenue of approximately $44 billion. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers. About Team: Protein Biology The Protein Biology team is involved in large-scale functional validation of antibodies, with a deep focus on reagent quality and specificity. The core activities of the team include data mining and processing, Western blotting with state-of-art tools, high efficiency and high-resolution immuno-fluorescence imaging, immunohistochemistry, ChIP (Chromatin Immunoprecipitation), and gene-silencing to provide advance application tags to our antibody portfolio. The program's goal is high-quality product validation and product information creation to promote research use. Role & Responsibilities Purpose: - Contribute to the antibody validation workflow. Understand target biology validation and validate antibodies for reproducibility using innovative methods and crafting data sets to enable market differentiation. The role of the successful candidate would entail demonstrating scientific proficiency in experimental planning and execution. Prior experience in working in a research team, with a proven track record of setting goals, handling work-related customer concerns, and ensuring timely delivery in alignment with the program goals. Proficiency in verbal and written communication of results in the workplace is helpful. Responsibilities: Acquire and utilize knowledge on key aspects of protein biology, to deliver results on antibody validation and characterization. Regular mining of literature and keeping oneself up to date with developments in field of antibody validation. Perform in a fast- paced environment towards antibody validation, with attention to detail and adherence to schedules. Informal leadership of team of scientists in matrix style operation, provide technical and operational supervision. Mentoring and training junior scientists in research, design and experimental execution, interpreting data and data presentation to collaborators and partners. Drive conceptualization within teams to enable development of successful protocols to address complex biological targets Partner with supporting functions such as product management, program management, and business development to meet program goals. Candidate Requirement : Education & Experience levels : Applicants should have a PhD in molecular biology, immunology, biotechnology or biochemistry with 2 to 3 years' experience, or Master's degree with 5 to 10 years of experience. Skills : Familiar with experimental workflow in cell and molecular biology, with extensive experience in the design and development of protein-assays, protein-protein interaction (using co-immunoprecipitation), or development of immunoassays. Proven and extensive experience in Flow cytometry and ELISA. Good working knowledge of western blotting and immunofluorescence is desirable. Communication of research data and providing expert-level technical troubleshooting to resolve scientific problems and develop new protocols/methods. Experience in antibody development platforms is desirable. Thermo Fisher Scientific is an equal opportunity employer and value diversity at our company. All qualified applicants will receive consideration for employment without discrimination basis race, color, religion, sex, sexual orientation, gender, gender identity or expression, national origin, protected veteran status, age, genetics, pregnancy, disability or any other legally protected status. Thermo Fisher Scientific aligns with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer a company culture that stands for integrity, intensity, involvement, and innovation! Thermo Fisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Show more Show less

Job Description Designation : HPLC Trainee Section : Training Qualification : Ph. D./ M. Tech./ M. Sc./ B. Tech./ B. Sc. Experience : Fresher Employment Type : Short Term / Long Term Location : Gurugram, Haryana Description High-Performance Liquid Chromatography (HPLC) is a widely used analytical technique for separating, identifying, and quantifying components in a mixture. Utilizing high pressure to force a liquid mobile phase through a stationary phase, HPLC effectively separates compounds based on their interactions with both phases. This method is highly versatile, allowing for the analysis of a wide range of substances, including pharmaceuticals, food additives, and environmental samples. HPLC is renowned for its speed, precision, and sensitivity, making it an essential tool in laboratories for quality control, research, and development across various industries. FARE Labs conducts a specialized training on High-Performance Liquid Chromatography (HPLC) tailored for various sample matrices following national/ international standard methodology. This training is aimed at laboratory professionals, researchers, and students interested in analyzing food additives such as antioxidants, synthetic colors, preservatives, artificial sweeteners etc. Objectives Provide a solid understanding of HPLC principles and applications in food safety. Equip trainees with practical skills for operating HPLC systems. Discuss the analysis of specific food additives using HPLC. Familiarize attendees with data analysis and interpretation techniques. What is to learn? Introduction to HPLC Overview of chromatography principles and HPLC components (pumps, injectors, columns, detectors) Instrumentation Pumps: Isocratic vs. gradient systems Injectors: Manual vs. automatic Columns: Selection criteria for food analysis Detectors: UV-Vis, fluorescence, ELSD, and mass spectrometry HPLC Method Development for Food Additives Identification And Quantification Of Various Target Analytes Such As Antioxidants: TBHQ, BHT, BHA etc. Synthetic Colours: eight permitted synthetic colours, banned colours Preservatives: benzoates, sorbates etc. Artificial Sweeteners: Aspartame, saccharin etc. Practical Applications Hands-On Training Instrument setup and calibration for food analysis Preparation and analysis of more than 500 samples of various matrices Running HPLC methods for food additives Data Analysis Understanding chromatograms and quantification methods Software tools for data processing and reporting Troubleshooting Common Issues Resolving baseline noise, peak tailing, and fronting Preventive maintenance tips for HPLC systems Responsibility Adherence to Safety Protocols: Strictly follow all laboratory safety guidelines and protocols to prevent accidents and ensure the well-being of all participants. Active Participation: Engage actively in all training sessions, discussions, and practical exercises. Complete all assigned tasks and projects on time. Respect for Equipment and Facilities: Handle all laboratory equipment and materials with care. Report any damages or malfunctions to the instructor immediately. Collaboration and Teamwork: Work collaboratively with fellow participants, sharing knowledge and supporting each other’s learning. Integrity and Accuracy: Maintain a high standard of integrity in all testing procedures and documentation. Ensure that all results are accurate and reliable. Requirements - Skills, Knowledge And Abilities Commitment to the Program: Participants must demonstrate a commitment to the training program by attending all scheduled sessions, completing all assignments, and actively participating in practical exercises. A signed commitment agreement may be required before the start of the program. Health and Safety Compliance: Participants must comply with health and safety regulations, including wearing appropriate personal protective equipment (PPE) and adhering to all safety protocols. A medical clearance or proof of immunizations may be required for certain training programs. Get in Touch Email at trainings@farelabs.com Show more Show less

Job Summary As Service Engineer, you will be responsible for the complete Customer Experience – right from the smooth installation of instruments, to training of users, to providing in-warranty support as well as post-warranty solutions (preventive and breakdown maintenance services) throughout the life of the instrument. You will also be responsible for commercial activities related to maintenance contracts, spares & consumables supplies. You will follow the company values, business ethics, compliance and processes. Technical Required Skills You are a Solutions oriented person with enthusiasm to face technical challenges, to diagnose & solve problems and continuously improve customer satisfaction. Communication You are proactive in communicating with all customer stakeholders to schedule & execute service visits with punctuality. You also easily connect with internal colleagues and factory team with a sense of urgency to resolve issues. You are committed to attending breakdowns complaints even during off work hours and provide prompt responses, offer support remotely as and when required. You are extremely professional & courteous with your verbal and written communication. You have experience with basic email software, excel. You are a self-motivated technologist, with passion to travel widely, ability to work alone. You are interested in continuous learning and self-development to improve your technical skills and keen to attend all the training programs you are nominated to attend. Desired Skills Multi-tasking & Negotiation skills are preferred. The role requires working inside industrial manufacturing sites including shifting and lifting instrument. Travel is mainly within Southern ( Tamilnadu, Kerala, Andhra Pradesh ) but you may also require to travel anywhere across India as and when required and to factory in Germany for training as and when nominated. Experience Level Min 1 to 2 years of prior service experience with any industrial analytical technology provider is preferred. Educational Qualification Graduate or Diploma Engineer - Electronics / Electrical / Instrumentation About Us AMETEK SPECTRO, a business unit of AMETEK Inc, is one of the worldwide leading suppliers of analytical instruments, employing optical emission (stationary and mobile Arc/Spark OES, ICP-OES) and X-ray fluorescence spectrometry (XRF) technology, used for the elemental analysis of materials in industry, research and academia. AMETEK SPECTRO is a preferred technology partner for customers across India, for more than 40 years with our advanced technology as well as our dedicated service network which is the largest in our industry providing world class support to our customers. AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.0 billion. AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers’ most complex challenges. We employ 21,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK (NYSE:AME) is a component of the S&P 500. Visit www.ametek.com for more information. Show more Show less

Amptek is a high technology company and a recognized world leader in the design and manufacture of state-of-the-art instrumentation for the satellite, x-ray and gamma ray detection, laboratory, analytical, and portable instrumentation industries. Location: Bangalore, India Key Responsibilities Create software user interfaces to control and monitor new products in development and production Write software development plans during early stages of development Identify and execute on user software deliverables for new products Present software deliverables at engineering design reviews Document software accomplishment summaries and user manuals Demonstrate functionality of software and compliance to requirements Work with IT to ensure adherence to corporate software security requirements, including evaluation, test, and documentation of findings Ensure product compatibility with operating system updates such as Windows 11 Work with electrical and FPGA engineers to understand firmware programmed into products while coordinating product interface to test software Responsible for USB ID and certification Manage tools, vaulting and recurring maintenance for software used in engineering development and production Automatic Test Equipment (ATE) Requirements Ability to clearly communicate problems, solutions, deliverables and progress Bachelor’s Degree in Computer Science, Engineering, or Software related field 5 years of professional experience writing software and supporting new production introductions Proficiency with C/C++ and Visual Basic (VB) Familiarity with USB, ethernet and RS232 communication interfaces Knowledge of SCPI protocols Driven for results and commitment to say-do Experience with software interfaces used in material analysis equipment such as X-Ray Fluorescence (XRF) preferred AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.0 billion. AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers’ most complex challenges. We employ 21,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK (NYSE:AME) is a component of the S&P 500. Visit www.ametek.com for more information. Show more Show less

Job Title: Cytogenetics Technologist / Staff Scientist – Diagnostic Lab Location: Panjarapol , Ahmedabad Department: Cytogenetics / Molecular Diagnostics Experience : 1 Year Qualifications: Education: M.Sc. in Cytogenetics, Genetics, Biotechnology, or related life sciences. Experience: Minimum 1 to 1.5 years of hands-on experience in a cytogenetics lab. Technical Skills: Proficient in karyotyping and chromosomal banding techniques (G-banding, etc.). Strong working knowledge of FISH procedures and probe interpretation. Familiarity with metaphase spread preparation, cell culture, and harvesting techniques. Skilled in using cytogenetics imaging and analysis software (e.g., MetaSystems, Applied Spectral Imaging). Job Summary: We are seeking a dedicated and detail-oriented Cytogenetics Technologist with an M.Sc. background and 1–1.5 years of experience in cytogenetics. The ideal candidate will have hands-on expertise in chromosomal analysis and FISH techniques , supporting high-quality diagnostic services in genetic testing. Key Responsibilities: Perform karyotyping and chromosomal analysis on various sample types (e.g., peripheral blood, bone marrow, amniotic fluid). Prepare and process samples for FISH (Fluorescence In Situ Hybridization) analysis, including probe hybridization and interpretation. Analyze metaphase and interphase cells using microscopy and imaging systems. Accurately record findings and prepare detailed cytogenetic reports under supervision. Assist in quality control and ensure compliance with laboratory SOPs and accreditation standards. Maintain and calibrate cytogenetics equipment and documentation logs. Follow all biohazard safety and infection control protocols during sample handling. Collaborate with genetic counselors, pathologists, and other laboratory personnel for integrated diagnostics. Maintain strict patient confidentiality and data security as per lab and ethical guidelines. Hemangi Gandhi 7069004878 Job Types: Full-time, Permanent Benefits: Cell phone reimbursement Leave encashment Provident Fund Schedule: Fixed shift Work Location: In person