565 Chromatography Jobs - Page 9

JOB DESCRIPTION Job Title: Bioassay Analyst - Large molecules Job Location: Bangalore Department - BGRC Analytical About Syngene: Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines 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 Core Purpose of the Role: The candidate shall be responsible to perform the development, validation, and routine testing of bioassay/ELISA for Large Molecules (LMs), especially Monoclonal antibodies (mAbs) and other LMs. The candidate shall be responsible for method development, validation, and stability testing drug substance/drug product. The candidate shall be willing to work in shifts. Role Accountabilities: Shall develop and validate cell-based assays and binding assays (ELISA), SEC and CGE especially for monoclonal antibodies (mAbs), etc. Shall troubleshoot the problems for these methods. Must have strong knowledge of the development of cell-based bioassays for Monoclonal antibodies. Experience in Qualification and Validation of cell-based bioassays Shall have experience on Good documentation/laboratory practices such as ALCOA+ Broad knowledge on analysis of cell-based assays to derive relative potency software s (such as Softmax Pro and PLA) Basic cell culture technics and hands-on experience in maintaining of mammalian cells. Must have experience in handling various cell lines (adherent and suspension cell lines). Preparation of Mammalian cell banks for Bioassays. Experience in handling of primary and continuous cell lines like Revival, maintenance, cell bank preparation, and cryopreservation Shall prepare the raw datasheets, protocols, reports, and SOPs Handling of QMS (Incidents, deviations, Out of Specifications, change controls, etc.) for GMP activities Shall be responsible for procurement and inventory maintenance of Pharmacopeial Standards / Chemicals / Reagents / Consumables / Spares etc., required for the projects Shall adhere to the procedure of GxP/GMP/Safety and as per the procedure defined in the internal standard operation procedure Must have good hold on MS office (word, excel, ppt), outlook, and other essential tools required for routine activity Experience in developing and validating SEC, CGE methods is an added advantage especially for monoclonal antibodies (mAb) is an added advantage Experience in calibration and qualification of HPLC, UPLC, GC, and other QC laboratory instruments is added advantage Good communication and e-mail writing skills are required since the candidate needs to communicate with clients/external users situated overseas Commitment to safety Behavioral Skills Good Interpersonal skills Self-time management Good Team player Polite/Good Communication skills Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 2-6 years Skills and Capabilities: Development, validation, and routine testing of Bioassay /ELISA, SEC, CGE for Monoclonal antibodies (mAbs) and other Large molecules Qualification and validation of cell-based bioassays Able to follow instructions and perform the tasks under the supervision of the Team leader Preparation and Maintenance of all the documents Experience in developing and validating SEC, CGE and HPLC methods for mAbs is an added advantage Theoretical knowledge in Chromatography and spectroscopy technique Good documentation/laboratory practices such as ALCOA+ Good knowledge of MS-office (word, excel, ppt) and E-mail writing skills Education M. Pharm/ M. Tech/ M.Sc. / B.Sc. (Biotechnology/Biochemistry) with 2-6 years experience in GMP environment (QC) Equal Opportunity Employer:

Reference Number: R35331 Ahmedabad (India) Full time , Regular Services Service Engineer Chromatography System Service Engineer Required Qualifications for a Chromatography System Service Engineer Educational Qualifications 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. Ready to join Sartorius? 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.

Job Title : QC Executive – HPLC Department : Quality Control (QC) Location : Vatva Ahmedabad Company : Parshwanath Food Colour and Chemical Experience : 5–8 years in HPLC and QC laboratory operations Salary: 25000---35000 Employment Type : Full-Time Key Responsibilities Operate, calibrate, and maintain HPLC (High-Performance Liquid Chromatography) instruments as per SOPs Analyze raw materials, in-process samples, and finished goods using HPLC and related analytical techniques Review and validate HPLC data and ensure compliance with internal specifications and regulatory requirements Investigate and document Out-of-Specification (OOS) and non-conformance results Lead method development and method validation activities related to HPLC Prepare and maintain detailed records, chromatograms, and reports in accordance with GLP/GMP practices Train and mentor junior analysts in HPLC and other QC activities Coordinate with production and R&D teams to resolve analytical issues Ensure adherence to safety and quality protocols during lab operations Support regulatory audits and customer inspections by presenting analytical data and documentation Stay updated with new techniques and improvements in chromatographic analysis Key Skills and Competencies Strong hands-on expertise in HPLC operation, troubleshooting, and maintenance Experience with various detectors (UV, PDA, RI, etc.) Sound knowledge of GLP, GMP, ISO, and other quality system requirements Familiarity with software such as Shimadzu lab solution, Chromeleon, Empower, or similar chromatographic data systems Ability to interpret analytical results and identify trends or deviations Strong documentation and report-writing skills Good communication and coordination abilities Experience in food-grade or chemical/pharma industry preferred Educational Qualifications B.Sc./M.Sc. in Chemistry / Analytical Chemistry / Pharmaceutical Sciences or equivalent Interested candidates can send their updated CV to hr.parshwadyes@gmail.com with the subject: "Application for Senior QC Executive – HPLC" Job Types: Full-time, Permanent Schedule: Day shift Work Location: In person

Designation: Executive/Senior Officer/ Officer Department: Manufacturing - Antigens (Production) Educational Qualification: M.Sc/ B.Sc/ B. Pharmacy/ B.Tech (Biotechnology)/ Diploma (Any Life Sciences background) Experience: 1-7 years Location: Biological E. Limited (Vaccine Division), Kolthur, Hyderabad Roles & Responsibilities: Execution of Upstream & Downstream production batches. Focus on timely execution, to ensure that the process is carried out as per GMP and batch timelines. To execute planned Upstream & Downstream activities to ensure high degree of confidence that the process is delivering a product that meets its target specifications. Routine monitoring of the equipment, Facility and utilities for GMP compliance Execution of documentation activities of liaison with QA and QC for GMP compliance. Participate and execute compliance of validation/ Qualification documents. Participate in execution the various compliance from the different cross functional team for QMS compliance Interested candidates may walk-in with an updated CV, latest increment letter and the last 3 months' pay slips on Friday, 04th Jul'25 from 10:00 AM to 12:00 PM at Biological E. Limited (Vaccine Division). Address: Plot No.1, Phase-II, Near MN Park, Genome Valley, Kolthur (V), Shameerpet (M), Dt. Medchal Malkajgiri, Hyderabad Land Mark - A road opposite to Honey burg Resort on Karimnagar Highway. (Beside Venkateshwara Swamy Temple) Interested candidates unable to attend the walk-in can send in their CVs by mention subject as Applying for Department Name to "HR.Intern4@biologicale.com"

Date: 27 Jun 2025 Location: Kolthur Shamirpet, Medchal, TG, IN, 500078 Custom Field 1: Discovery Services Job Description Job title: Senior Research Associate Job location: Hyderabad Job grade: 9-II About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines 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 always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose Of The Role Personnel handling this profile will be working in Syngene reaction screening facility and responsible for setting library of reaction in small scale to optimize one reaction condition. The candidate should be good in data analysis and report making and metal catalyzed coupling reactions. Experience of handling glove box will be preferred. He or she should ensure that the experimental observations are recorded contemporaneously and in compliance with the Electronic Laboratory Notebook (ELN) policies of the project and Syngene. Role Accountabilities Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipments’. Ensure that the samples generated during 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. The candidate should be capable of meeting Syngene’s productivity expectations (# of compounds/month and # of steps/month) without compromising on safety and quality. The candidate should have excellent analytical interpretation and making report. Ensure that they know the SDS 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 Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety Attend all mandatory trainings and update training records as and when trainings are completed Always ensure confidentiality Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 4-6 years Skills And Capabilities Should have deeper knowledge with concepts of organic synthesis and reaction mechanism and metal catalyzed coupling reactions. Candidate should be capable of solving synthetic problems independently Should be excellent in purification and analytical interpretation, especially LCMS, UPLCMS skills. Familiar with operations of relevant apparatus - instrument / equipment. Glove-box uses experience will be preferred Handling small scale reaction Education M. Sc in general or organic chemistry

Dear Candidate , we are hiring for QC Jr Executive ,Down stream process executives & Operators. Open Positions-50 Down Stream Process Executives & Operators Required • Qualification: Bsc/Msc/ITI/B Pharmacy Experience in handling the following Equipment 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 PRODUCTION-DS M Pharmacy/Diploma/B tech/Any Degree 6 Expertise in documentation QMS/GMP Compliance / Process Awareness Biologics Company's only Preferable. • Experience: 2 to 6 years in Total Downstream CTC :up to 5.0 LPA. IMMEDIATE JOINERS ARE PREFERABLE" Interested candidates please reach out Manasa - 9502434725

Design and execute multistep organic syntheses under the supervision of senior scientists. Having knowledge of enzymatic reactions. Perform compound purification using techniques such as column chromatography, recrystallization, HPLC, etc. Characterize synthesized compounds using analytical techniques (NMR, LC-MS, IR, UV-Vis, etc.). Maintain accurate and detailed records of all experiments Participate in group meetings and contribute to scientific discussions. Ensure compliance with laboratory safety protocols and chemical handling guidelines. Assist in the preparation of reports, presentations, and research publications.

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 : NAMinimum 12 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- Expected to provide solutions to problems that apply across multiple teams- Lead the application development process effectively- Ensure seamless communication within the team and stakeholders Professional & Technical Skills: - Must To Have Skills: Proficiency in SAP for Oil & Gas Downstream- Strong understanding of application development processes- Experience in leading and managing application development projects- Knowledge of industry best practices in application design and configuration Additional Information:- The candidate should have a minimum of 12 years of experience in SAP for Oil & Gas Downstream- This position is based at our Hyderabad office- A 15 years full-time education is required Qualification 15 years full time education

A Trainee Analytical Chemist assists in the analysis of substances to determine their composition and properties. This role involves conducting experiments, analyzing data, and preparing samples under the guidance of senior chemists. They learn to use various analytical techniques and instruments to support research, quality control, or other scientific applications. Here's a more detailed breakdown:Key Responsibilities: Sample Preparation: Preparing samples for analysis by weighing, dissolving, diluting, or otherwise modifying them according to established procedures. Running Experiments: Performing a variety of analytical tests using techniques like spectroscopy, chromatography, or titration, and accurately recording the results. Data Analysis: Analyzing the data obtained from experiments, including calculations and interpretation of results. Maintaining Laboratory Equipment: Ensuring the cleanliness and proper functioning of laboratory equipment, including reporting any malfunctions. Following Procedures: Adhering to strict laboratory safety protocols and standard operating procedures. Essential Skills and Qualifications:. Laboratory Skills: Proficiency in basic laboratory techniques, such as solution preparation, weighing, and handling chemicals. Analytical Skills: Ability to analyze data, interpret results, and draw conclusions. Problem-Solving Skills: Ability to troubleshoot and solve problems that may arise during experiments. Communication Skills: Good written and verbal communication skills for reporting results and collaborating with others. Teamwork: Ability to work effectively as part of a team. Safety Awareness: A strong understanding of laboratory safety procedures and regulations. Job Type: Full-time Pay: ₹18,000.00 - ₹25,000.00 per month Benefits: Food provided Health insurance Schedule: Day shift Rotational shift Supplemental Pay: Yearly bonus Work Location: In person

Job Summary We’re looking for an experienced and detail-oriented professional to manage and oversee all QC lab activities. This role demands strong leadership, in-depth technical knowledge, and a commitment to regulatory excellence. The selected candidate will support the HOD, lead lab teams, and drive compliance with GMP, ISO, and global quality standards. Key Responsibilities Supervise daily QC lab operations and testing activities Act as HOD designee during their absence Ensure timely testing and release of RM, intermediates, and finished products Investigate and document deviations, OOS, OOT, and lab incidents Implement and maintain QMS in alignment with cGMP, ISO, FSSC, Halal & Kosher Review and update specifications and pharmacopeial methods Oversee validation and revalidation of analytical methods Train analysts on lab techniques, SOPs, GLP & GDP Monitor stability studies and ensure protocol adherence Manage instrument calibration, qualification, and maintenance Review analytical reports, calibration records, and lab documentation Lead/support internal and external audits Coordinate with Regulatory Affairs and QA teams Implement pharmacopeia updates and support regulatory readiness Contribute to continuous improvement and special quality initiatives Qualification : MSc Chemistry Experience : 4-8 Years Skills: cgmp standards,glp,high-performance liquid chromatography (hplc)

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 highly skilled Analytical Scientist to join our Research and Development team. The successful candidate will be responsible for developing, validating, and implementing analytical methods for the quantification and identification of genotoxic impurities in pharmaceutical products. This role will involve extensive use of chromatography techniques and adherence to regulatory standards. The ideal candidate should have a strong background in analytical chemistry, method development, and data analysis, with a keen eye for detail and a commitment to ensuring the highest quality standards. Roles & Responsibilities You will be responsible to ensure the quality and accuracy of reference standards and working standards used in analytical testing and method development.. You will be responsible to perform real-time analysis of samples during product development stages to ensure product quality and consistency. You will be responsible to evaluate the effectiveness of the product development strategy and identify any cross-functional issues affecting the process. You will be responsible to identify and plan for the developmental needs of the product, considering factors such as scale-up and potential process improvements. You will be responsible to source and manage the procurement of necessary chemicals, solvents, columns, and other laboratory equipment. You will be responsible to ensure proper maintenance of laboratory equipment as per Good Laboratory Practices (GLP) standards to guarantee accurate and reliable results. You will be responsible to calibrate instruments as per the calibration schedule and strictly follow Standard Operating Procedures (SOPs) to maintain consistency and accuracy. You will be responsible to maintain a clean and organized work area, and ensure that the laboratory environment is controlled at the required temperature for optimal analytical conditions. You will be responsible to keep all relevant documents well-maintained and organized for easy access and compliance with internal and external auditing requirements. Qualifications Educational qualification: Masters in Science/ Organic chemistry Minimum work experience: 5 to 7 years of experience in analytical method development Skills & attributes: Technical Skills Have work experience on Process scale up of Active Pharmaceutical Ingredients. Experience in instrumentation analysis (HPLC, GC, PSD). Experience in the development and regular analysis in Wet analysis-IR, Ultra Violet, Moisture analysis, Chromatographic techniques Strong understanding of regulatory guidelines and industry standards related to pharmaceutical product development and analysis. Proven experience in method validation and documentation in compliance with regulatory requirements. Behavioral Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams. 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/#!/

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting, Office About The Company Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. 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: Antibody team The antibody team is involved in engineering and development of antibodies, with a deep focus on reagent quality and specificity. The core activities of team include design, development, purification, conjugation and testing of antibodies in a variety of immunoassay applications using pioneering tools and technologies. The goal of the program is sophisticated product development and creation of product specific information to promote research use. Role & Responsibilities Role: To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, and cell biology methods. Responsibilities: Meticulous experimental planning and execution to meet program goals. Timely 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 development. 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 Masters with 0-3 years confirmed experience or a fresh PhD (submitted within last one year) in a life sciences field with a strong focus on protein design, protein purification, molecular biology, immunology, biotechnology or biochemistry. Nature of experience: Extensive experience in immunoassays such as Western blotting, Immunofluorescence, Immunohistochemistry, Flow cytometry or ELISA Experience with proteins, which could include but not limited to structure function or mutational analysis of proteins, and molecular biology expertise in handling nucleic acid extraction, PCR, and cloning. Familiarity with software for molecular biology such as Snapgene, CLC Workbench, or Geneious. Experience in single cell molecular biology or next generation sequencing will be considered a plus Experience and knowledge in protein purification and analysis technologies such as affinity or ion exchange chromatography, SEC, HPLC, and SDS-PAGE. Experience with protein affinity measurement desirable. Experience in cell culture, aseptic techniques, maintenance of cell lines and primary cells. Experience in sophisticated cell culture techniques such as stem cell technologies, differentiation or spheroid culture Theoretical or practical experience in antibody development platforms is desirable Project or work experience in support of relevant skills such as publications, project reports or thesis work Proficient in MS Office applications such as Word, Powerpoint, Excel and possess a strong statistical knowledge and familiarity with statistical software such as Prism The successful candidate will be self-motivated and a self-starter who is excellent at learning and applying new concepts for process or product improvements, possess excellent oral and written communication skills to connect to peers and leadership, and will be an excellent teammate with the ability to work with different colleagues. 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 driven 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 an exciting company culture that stands for integrity, intensity, involvement, and innovation! ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Title: Scientist I, Protein Biology Job Location: India, Bangalore About Company: About The Company Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. 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: Antibody team The antibody team is involved in engineering and development of antibodies, with a deep focus on reagent quality and specificity. The core activities of team include design, development, purification, conjugation and testing of antibodies in a variety of immunoassay applications using pioneering tools and technologies. The goal of the program is advanced product development and creation of product specific information to promote research use. Role & Responsibilities Role: To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, and cell biology methods. Responsibilities: Meticulous experimental planning and execution to meet program goals. Timely 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 development. 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 Masters with 0-3 years confirmed experience or a fresh PhD (submitted within last one year) in a life sciences field with a strong focus on protein design, protein purification, molecular biology, immunology, biotechnology or biochemistry. Nature of experience: Extensive experience in immunoassays such as Western blotting, Immunofluorescence, Immunohistochemistry, Flow cytometry or ELISA Experience with proteins, which could include but not limited to structure function or mutational analysis of proteins, and molecular biology expertise in handling nucleic acid extraction, PCR, and cloning. Familiarity with software for molecular biology such as Snapgene, CLC Workbench, or Geneious. Experience in single cell molecular biology or next generation sequencing will be considered a plus Experience and knowledge in protein purification and analysis technologies such as affinity or ion exchange chromatography, SEC, HPLC, and SDS-PAGE. Experience with protein affinity measurement desirable. Experience in cell culture, aseptic techniques, maintenance of cell lines and primary cells. Experience in advanced cell culture techniques such as stem cell technologies, differentiation or spheroid culture will be considered a plus Theoretical or practical experience in antibody development platforms is desirable Project or work experience in support of relevant skills such as publications, project reports or thesis work Proficient in MS Office applications such as Word, Powerpoint, Excel and possess a strong statistical knowledge and familiarity with statistical software such as Prism The successful candidate will be self-motivated and a self-starter who is excellent at learning and applying new concepts for process or product improvements, possess excellent oral and written communication skills to connect to peers and leadership, and will be an excellent teammate with the ability to work with different colleagues. 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 an exciting company culture that stands for integrity, intensity, involvement, and innovation! ThermoFisher 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.

Functional or Technical skills JOB DESCRIPTION Job Role : Analytical Chemistry-Analyst (NPD) Department : Analytical - BGRC Job Location : Bangalore About Syngene : Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines 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 Core Purpose of the Role: This role involves method development, method validation, method transfer and R&D stability studies by using laboratory instruments like Ultra performance liquid chromatography (UPLC), High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet (UV) spectrophotometer, Polarimeter, Particulate matter analysis using Malvern, PAMAS, HIAC and other relevant instrumentation techniques. etc. Role Accountabilities: Must have strong hands-on experience in development and validation of Assay & related substances methods for drug substance/drug product. Must have experience in handling HPLC, UPLC (Empower-3 software), GC, UV Visible spectrophotometer balances, Potentiometer, and stability chambers, Particulate matter analysis techniques. Shall have experience on Good documentation/laboratory practices such as ALCOA+. Experience in calibration and qualification of various analytical instruments HPLC, UPLC, GC, and other QC laboratory instruments Shall prepare and review the raw data sheets, instrument operating procedures, and standard operating procedures Shall have good experience in handling of QMS (such as incidents, Out of Specifications, Deviations, and Change control). Shall be responsible for procurement and inventory maintenance of Pharmacopeial Standards / Chemicals / Reagents / Consumables / Spares etc., required for the projects Shall adhere to the procedure of GxP/Safety and as per the procedure defined in the internal standard operation procedure Shall operate the MS office (word, excel, ppt), outlook, and other essential tools required for routine activity Must possess good communication and e-mail etiquettes. Behavioural Skills Good Interpersonal skills Self-time management Good team player Good communication skills Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 0-6 years Skills and Capabilities: Hands-on HPLC, UPLC/UHPLC, CG, UV-visible spectrophotometer, Potentiometer, Particulate matter analysis techniques and QC other analytical instruments Theoretical knowledge in Chromatography and spectroscopy technique Good documentation/laboratory practices such as ALCOA+. Able to follow work instructions and perform the tasks under the supervision of the Team leader Preparation and Maintenance of all the documents Good knowledge of MS-office (word, excel, ppt) Education M. Pharm/ M. Tech/ M.Sc. / B.Tech., B.Sc. (Analytical chemistry/Chemistry) Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Qualifications and education requirement The prospective candidate should be a PhD/Post Doc in Biochemistry with a minimum of 5-8 years of research in academia or industry. Should have experience in enzyme characterization, enzyme kinetics and enzymatic conversions Roles and responsibilities Identification and development of processes for the purification of proteins/ enzymes from bacterial and / or yeast expression systems Development of strategies for maximizing the protein yield by solubilization of IB and refolding • Complete characterization of enzymes like activity, specific activity, pH optima, temperature optima, substrate loading, inhibition studies etc Determination of kinetic parameters Km, Vmax, rate of reaction etc Development of assays for different enzymes and optimization of analysis protocols Process development for production of different products using purified enzymes Identification of matrices for enzyme immobilization with reduced activity loss Perform operational stability studies of enzymes at different temperatures Development of lab scale process for packed bed conversion Essential attributes • Ability to work and liaison with multi functional teams • Acumen for leading and guiding peers and subordinates • Prior experience in carbohydrates would be desired • Passion for doing science and creating value

About Immuneel Immuneel Therapeutics Private Limited is a pioneering start-up company leading the charge in cell therapy and personalized immunotherapy for patients in India. For more details, please refer www.immuneel.com We Pursue, with Purpose, to serve our Patients (3 Ps) by Connecting within, Collaborating globally and Creating (3 Cs) solutions. Our flexible, diverse, and vibrant team is bringing together best practices and innovations in the field of cell and gene therapy. Working at Immuneel promises the excitement of an agile startup on a critical mission. Proudly Indian in solutioning, yet global in outlook, we are keen to collaborate. We value diversity including in experience and perspectives. We value work-life balance and believe that having fun on the job is integral to achieving the right results. We pride ourselves on providing an open environment and our mission resonates with humanity everywhere. At Work, we are: Passionate in driving patient outcomes: We are passionately committed to doing the RIGHT thing to achieve the best outcomes for our patients through innovation, agility and performance orientation. We put the impact on the patient above all else. Responsible and accountable: We demonstrate ownership and accountability for our actions. We make timely and well-informed decisions, learning from our performance. Transparent, honest, and supportive in how we work together: We insist on integrity and respect for the individual. We demand excellence. Our performance management is focused on excellence through timely and constructive feed-forward. Inclusive and flexible: We are full of life and embrace all opportunities to collaborate and work together. We are excited about the collective knowledge and expertise that we share. “Being and thinking different” is valued. Immuneel prides itself as an organization that is keeping pace with best practices in organization design. Our role-based organization incorporates global trends in human capital that promote focus on work and greater nimbleness. Our role-based structure allows you to be cherished by the work you do and bring value to your work rather than designations, our organization is simplified into a flat, non-hierarchical, millennial, organization where you may fully inherit the role you play in the organization and are recognized by the accountability you take and the work you deliver. Immuneel’s employees are integral to our quest to develop and deliver high quality engineered cell therapies in India. We believe that our culture provides an environment for employees to excel and find purpose. The strength of our team is every bit as important as our cutting-edge technology and we invest in clear compensation and comprehensive benefits for our employees. People for us, are not resources, but our capital. If you are a talented professional, an out-of-box thinker with a zeal to help change, and passionate about healthcare, we invite you to join us and be a part of a historic initiative in India. Interested in being a part of the next revolution in cancer treatment? Send your resume to careers@immuneel.com 1. Role Title: Scientist - Research & Development (Downstream Process Development) 2. Department/Function: Research and Development 3. Reporting Structure: Reports to: Viral Vector Direct Reports: NA 4. Role Summary: Immuneel is looking for an Engineer/Scientist with experience in downstream process development for viral vectors. The said candidate must have a strong understanding of various downstream processes like chromatography, tangential flow filtration and normal flow filtration. Key deliverables will be to drive projects and programs through process development culminating in global IND applications. Knowledge of analytical method development, single use technologies and process automation is an added advantage. 5. Key Responsibilities: Experimental design and execution for downstream process development for viral vectors, small molecules and cell therapy products. Preparation, cross-functional review and training of MDRs, MTRs, MTPs and MQRs. Draft XOPs and other documents required for quality management system requirement. Compilation and recording of data in Lab Notebooks (paper based and digital) and preparation of plans and reports. Coordination with Application Scientists and Engineers for technical trouble shooting Process Development facilities and associated utilities. Resource management: ordering of reagents, consumables & inventory management. Support process development in the form of routine cell culture and associated experiments. Maintenance of laboratory equipment and instruments. 6. Primary Objectives: Outline the key objectives the role is expected to achieve. These should align with the company’s goals and strategic priorities. Downstream process development for viral vectors Technology transfer of downstream process as a part of technology transfer of the viral vector manufacturing process Associated documentation Enable MSAT function by leading experiments for ongoing programs and/ or in-licensed programs 7. Competencies Required: Technical Competencies: Downstream process development Bioprocess technology Filtration inclusive of depth filtration and tangential flow filtration Chromatography including ion exchange chromatography Sterile filtration and fill-finish Developed downstream process for viral vectors and/or mAbs Understanding of CQA and CPP, Process Verification and Validation CMC documentation experience Soft Skills: Project planning Resource management Data presentation Budget preparation Collaboration Team Player Willingness to Learn Challenge 8. Qualifications: M.Tech. or PhD (Engineering/Science) with 2-5 years of industry experience in biologics/viral vector process development 9. Working Conditions: Role Type: Full Time and Onsite Work Hours: 9:00 AM to 6:00 PM for the General Shift and 2:00 PM to 11:00 PM for the Post-Noon Shift (on a rotational basis). There will be two days off each week, which may not necessarily fall on a Saturday or Sunday. Travel Requirements: Depends Base Location: Immuneel Therapeutics Private Limited, 8th Floor, Mazumdar Shaw Medical Center, Narayana Health City, Bommasandra Industrial Area, Bangalore - 560099

Please call 9947350555 more details Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. Male candidate can apply Using chromatography, spectroscopy, and spectrophotometry techniques. Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods. Conferring with scientists and engineers to analyze, interpret, and develop tests. Introducing heat, light, energy, and chemical catalysts to chemical substances to induce reactions. Writing technical papers and reports, and preparing standards and specifications for processes, tests, and products. Maintaining laboratory instruments, troubleshooting malfunctions, and purchasing new laboratory supplies. Evaluating and ensuring compliance with laboratory safety procedures and standards. Job Type: Full-time Pay: ₹16,500.00 - ₹18,000.00 per month Benefits: Health insurance Provident Fund Schedule: Rotational shift Education: Bachelor's (Preferred) Language: Malayalam (Preferred) Work Location: In person Speak with the employer +91 9947350555

1. Understand the project requirements & deliverables from supervisor/manager 2. Carry out literature search by using SciFinder, Reaxys and other search engines 3. Comprehend and discuss the MSDS with supervisor/ team members. 4. Identify and mitigate any potential safety risk with the help of Manager 5. Plan, setup, monitor, and workup chemical reactions independently 6. Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) 7. Isolate product and Optimize reaction conditions for improved yields and output 8. Purify compounds by different methods using chromatography, distillation and crystallization etc. 9. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc 10. Ensure parallel execution of multiple reactions conducted both by self and the team 11. Scale up of R&D developed products to kg scale and then technology transfer to pilot plant 12. Troubleshoot as appropriate for successful execution with intimation to supervisor 13. Discuss research findings and work plan on daily basis with supervisor/ manager and Mentor junior lab personnel 14. Document reactions, research findings/ observations accurately in lab note books to ensure data integrity 15. Participate in project meetings and prepare daily, weekly and monthly reports and submit to Manager 16. Writing regular updates, final reports, PDR preparations and inter departmental communications 17. Regular lab duties including equipment maintenance, chemical inventory and lab clean-up Job Types: Full-time, Permanent Pay: ₹232,834.74 - ₹309,279.35 per year Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Education: Diploma (Required) Work Location: In person

Job Position: Downstream Processing We are seeking a dedicated Scientist/Engineer specializing in downstream processing and purification of biomolecules, including proteins, antibodies, and nucleic acids. The successful candidate will develop, optimize, and scale-up purification processes to ensure high product yield and quality while adhering to regulatory standards. This role involves hands-on work with chromatography systems, filtration techniques, and process analytical tools. Key Responsibilities Purification Process Development : Design and optimize purification workflows for biomolecules using techniques such as chromatography, ultrafiltration/diafiltration (UF/DF), and precipitation. Evaluate and implement scalable purification strategies for production processes. Chromatography Operations : Operate and troubleshoot chromatography systems (e.g., AKTA, TFF systems) for purification. Develop methods for ion exchange, size exclusion, affinity, and hydrophobic interaction chromatography. Filtration and Concentration : Perform tangential flow filtration (TFF), ultrafiltration, and diafiltration for biomolecule concentration and buffer exchange. Assess filtration parameters to improve recovery and throughput. Scale-Up and Technology Transfer : Optimize laboratory-scale processes for pilot and manufacturing scales. Collaborate with manufacturing teams to ensure seamless technology transfer and process scalability. Analytical and Process Monitoring : Utilize analytical tools such as SDS-PAGE, HPLC, ELISA, and spectrophotometry for in-process monitoring and final product characterization. Implement process analytical technologies (PAT) to ensure process consistency and quality. Documentation and Compliance : Maintain detailed records of experiments, protocols, and process development activities. Prepare standard operating procedures (SOPs), batch records, and regulatory documentation in compliance with GMP/GLP guidelines. Collaboration and Teamwork : Work with upstream processing, quality assurance, and regulatory teams to ensure end-to-end process integration. Mentor and train junior team members in downstream techniques and best practices. Innovation and Continuous Improvement : Stay updated on advancements in purification technologies and apply them to improve existing processes. Contribute to the development of novel purification strategies to enhance productivity and efficiency. Qualifications and Skills Education : Master’s or Ph.D. in Biotechnology, Biochemistry, Chemical Engineering, or a related field. Experience : 3–5 years of experience in downstream processing and purification of biomolecules, preferably in a biopharmaceutical or biotechnology setting. Hands-on experience with chromatography and filtration systems. Technical Skills : Expertise in chromatography techniques, filtration methods, and biomolecule characterization. Familiarity with regulatory guidelines (ICH, FDA, EMA) for biopharmaceutical production. Soft Skills : Strong analytical and problem-solving abilities. Effective communication and documentation skills. Team-oriented with the ability to manage multiple projects. Preferred Skills Experience with monoclonal antibodies (mAbs), recombinant proteins, or nucleic acids. Knowledge of high-throughput process development (HTPD) tools. Familiarity with single-use systems and continuous processing technologies.

Job description Role & responsibilities Operate and monitor bioreactors, fermenters, and processing equipment. Handle upstream processing (fermentation, cell culture, media preparation). Perform downstream processing (filtration, centrifugation, chromatography). Troubleshoot and resolve issues in bioprocess operations. Maintain GMP compliance and proper documentation. Collaborate with other teams like Quality and Engineering. Assist in equipment maintenance and calibration. Follow Standard Operating Procedures (SOPs). Support process optimization for better yields and efficiency. Report on production activities and suggest improvements. Skills Required: Hands-on experience in bioprocessing operations. Knowledge of GMP guidelines. Basic troubleshooting skills for process equipment. Teamwork and communication abilities.

Role & Responsibilities (Quality Control) HPLC Analysis of Solid Orals/Nasal Products You will perform High-Performance Liquid Chromatography (HPLC) testing on oral solid dosage forms (like tablets and capsules) and nasal products to ensure quality and consistency. Hands-on Experience in Quality Control (QC) Activities You should be actively involved in day-to-day QC operations like sampling, testing, and documentation. Key Sections (Work Areas) IPFP (In-Process & Finished Products ) Quality checks on products during and after manufacturing. Nasal Specialized QC testing and handling of nasal dosage forms. Raw Material Sampling and analysis of raw materials for identity, purity, and quality. LCMS (Liquid Chromatography-Mass Spectrometry) Advanced instrumental analysis technique—used for detailed compound identification and impurity profiling. Compliance with GMP/GLP Practices Work in strict adherence to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) to maintain regulatory and quality standards. Experience Required: 2 to 7 Years Candidate should have relevant industry experience within the pharmaceutical sector, specifically in Quality Control. Regulatory Plant Experience Prior work experience in plants approved by international regulators like USFDA (United States) or MHRA (UK) is preferred. This ensures familiarity with global standards and audit expectations.

Job Title -AM Research and Development Qualification: MSc (Organic Chemistry with first class), Experience: 4+ years in R&D Industry- Leading pharma, CRO (Contract research Organization), Agrochemicals JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) Plan, setup, monitor, and workup chemical reactions independently Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) Isolate product and Optimize reaction conditions for improved yields and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Ensure parallel execution of multiple reactions conducted both by self and the team Scale up of R&D developed products to kg scale and then technology transfer to pilot plant Troubleshoot as appropriate for successful execution with intimation to supervisor

Job Title - R&D Chemist Qualification: MSc (Organic Chemistry with first class), Experience: 4+ years in R&D Industry- Leading pharma, CRO (Contract research Organization), Agrochemicals JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) Plan, setup, monitor, and workup chemical reactions independently Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) Isolate product and Optimize reaction conditions for improved yields and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Ensure parallel execution of multiple reactions conducted both by self and the team Scale up of R&D developed products to kg scale and then technology transfer to pilot plant Troubleshoot as appropriate for successful execution with intimation to supervisor

1.Understand the project requirements & deliverables from supervisor/manager 2.Carry out literature search by using SciFinder, Reaxys and other search engines 3.Comprehend and discuss the MSDS with supervisor/ team members. 4.Identify and mitigate any potential safety risk with the help of Manager 5.Plan, setup, monitor, and workup chemical reactions independently 6.Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) 7.Isolate product and Optimize reaction conditions for improved yields and output 8.Purify compounds by different methods using chromatography, distillation and crystallization etc. 9. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc 10.Ensure parallel execution of multiple reactions conducted both by self and the team 11.Scale up of R&D developed products to kg scale and then technology transfer to pilot plant 12.Troubleshoot as appropriate for successful execution with intimation to supervisor 13.Discuss research findings and work plan on daily basis with supervisor/ manager and Mentor junior lab personnel 14.Document reactions, research findings/ observations accurately in lab note books to ensure data integrity 15.Participate in project meetings and prepare daily, weekly and monthly reports and submit to Manager 16.Writing regular updates, final reports, PDR preparations and inter departmental communications 17.Regular lab duties including equipment maintenance, chemical inventory and lab clean-up 18.Maintain strict IP Confidentiality and adhere to all related data privacy policies

UPLC Knowledge must Pharma Company Exp Required Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials Required Candidate profile Experience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC.