2096 Hplc Jobs - Page 23

About The Role o Responsible for personal discussion of cases as per the laid down policies & procedures and maintain strict adherence to quality. o Adhere to agreed SLAs and timelines in completing the activities assigned. o A skill set of underwriting, disbursements, collateral, coordination with cross function sales operation function o Responsible for protecting company assets through proper evaluation of all credit requests, establishing credit limits and ensuring that all loans granted are adequately documented and secured by the appropriate collateral o Ensure proper communication of credit decisions to Stakeholders. o Responsible for improving underwriting efficiencies while ensuring adequate risk management Responsible for Loan Account Verification, Cross Verification (Member House Visit), KYC Check, Bank Passbook and other Document Check, Income and Expense Assessment, Check on Influence of Middleman, Negative Area Check, CPC Checklist Verification, Loan Card Check of other Lending Institutions, Bucket Monitoring, Death Case Verification, Branch Compliances and ICQ Observation Closure

Skills Required : Upstream, Microbiology, fermentation, Microscopy, Able to work in shift Roles and Responsibilities : 1) Operate fermenters and related equipment as per Standard Operating Procedures. 2) In-process sampling and real-time data entry in logbooks/annexures. 3) To perform microbial testings/Assays/Microscopic Observation. 4) Parameter Monitoring and compilation of data. 5) Adherence to Good Laboratory Practices, Good Documentation Practices and Safety. 6) Work in shifts (Days/Night).

Date: 12 Aug 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Essential Functions Job Description Job Title: Senior Analyst Job Location: Syngene International Limited, Bengaluru 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 companys 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 is an exciting opportunity to play a role in the Quality control department of Syngene. The role will provide several responsibilities of Analysis, documentation, Lab safety requirements, Compliance as per Syngene policy and EHSS requirement. It provides an opportunity to handle overall analysis of QC and Stability samples. Role Accountabilities Analysis of Raw Material/ In process samples/ cleaning samples/ Intermediate samples/Finished product/water sample/ Packaging materials/ Formulation finished products and management/traceability of Reserve samples and Visual inspection samples. Maintenance of sampling tools as per the standard operating procedure. Packing and Maintenance of reserve samples and visual inspection samples as applicable Carry out the analysis on the qualified techniques as per the approved specification/protocol/procedures and Interpret the data from analytical instruments and report the results and submit the completed documents for review promptly. Preparation of Certificate of analysis Recording of analytical observations/ findings, reporting of data and results in observation data sheets, forms, logbooks, LIMS and ELN application softwares. Reporting of any abnormal observation identified during analysis to reporting manager/Group leader/HOD immediately. Calibration of Instruments and perform HPLC lamp intensity test as per schedule, hot water flushing of HPLC and general preventive checks for laboratory instruments. Creation/ preparation of documents, master data/ static data creation in LIMS, ELN and LMS Softwares as applicable. Initiation of QMS elements and other documents in Trackwise and EDMS application softwares. Record updation for Outsourcing of sample testing based on requirement and updating respective Logbooks. Coordination with engineering & maintenance and external vendor for preventive maintenance and calibration activity. Initiation of Change control, CAPA, deviation, Laboratory Incident, OOS, OOT, Non-Conformity as applicable. Disposal of left-over Sample after review/approval of analytical report /Release. To indent the chemicals, glassware, document, instrument, and accessories required for performing analysis as per the plan. Archive and retrieve documents related to the section. Adherence to Good Laboratory Practice and Good documentation practices. Cleaning of workplace and following Good Laboratories Practices while working in QC Laboratory. Individuals working in the GMP environment are responsible for documenting/record the activities contemporaneously and accurately as per Good documentation practices. Handling of LMS, LIMS, ELN, TrackWise and EDMS Softwares for routine activities as applicable. Responsible for taking any other job allocated by Head QC / Group Leader /Section Head/ Section In-Charge. In addition, the responsibility of the standard management team as; Receipt, Inventory management, Qualification, Labeling, Dispensing of Analytical standards, removal and disposal of expiry standards and Storage of standards as per the appropriate storage condition used in Quality Control Laboratory. Review the status of Pharmacopoeial reference standards and their validity periodically. Preparation of Standard Qualification protocol, Report and COA as applicable. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience: 3-6 years Skills And Capabilities Expertise in handling multiple Instruments/ equipment like HPLC, Dissolution tester, KF, and GC. Capable of thinking scientifically to address complex problems and develop solutions. Work as a team and have a collaborative mindset. Good communication skills. Education: MSC/ B. Pharma 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. Show more Show less

Conduct Schedule and Surprise Visits for 8 branches as per schedule given by HO Gather market intelligence on MFI business in the area Maintain a record of Collection quality in the catchment and advice branches of caution areas Support field teams in difficult cases of collections Conduct investigation into special situation if need arises Location - mumbai,delhi,pune,bangalore,hyderabad,chennai

Dear All, We are seeking a highly motivated and talented Analytical R&D Scientist( Oral Solid Dosages ) to join our innovative team. The ideal candidate will have a strong foundation in Analytical development and you will play a crucial role in developing new and improved formulations, ensuring product quality, and meeting regulatory requirements. Location: Hyderabad(Dulapally) Required Experience: 2-7 Years Job Responsibilities: 1. To follow the departmental SOPs 2. To ensure the error free and online documentation. 3. To ensure only calibrated instrument /equipment's are used for analysis. 4. To coordinate with supervisor in developing the methods for dissolution, assay by UV/HPLC and RS by HPLC. 5. To coordinate with supervisor in developing the methods for peptide mapping, peptide sequencing, circular dichroism spectroscopy (CD), Fluorescence spectroscopy, SEC-GPC/MALS, NMR and peptide/ proteins sameness study. 6. To perform analysis of development samples for Dissolution, Assay by UV/HPLC and RS by HPLC as per test method. 7. Perform validation of test procedures like Dissolution, Assay, Related substances, Residue and Chiral purity etc., 8. To ensure the instruments/equipment are cleaned after completing the analysis. 9. Receipt and storage of samples/standards. 10. Labeling of standards, chemicals and reagents. 11. Receipt of log books and SOPs from QA. 12. To ensure the GLP compliance in laboratory. 13. Supporting for the installation of instruments and equipment's. 14. To ensure the reference, working standards and impurities are maintained as per GLP. 15. To ensure the archival of completed files and LNB. 16. Assist and/or perform analysis of development samples for water content by KF, LOD and Identification tests as per Analytical Test Method/Standard Test Procedure. 17. Coordinate and assist for timely completion of Instrument calibration and preventive maintenance. Note: Interested candidates can share their resumes to raghuveera.vutla@aizant.com and Immediate joiners are more preferable

1. Analytical method development by HPLC for KSM, In-process, Intermediates and Finished products. 2. Review of complete analysis, Method developments, Qualification data. 3. Maintain analytical instruments calibrations as per schedule. 4. Maintain analytical instruments logbooks. 5. Determining Moisture Content, Melting Range and Assay of samples. 6. Performing LOD, Heavy metals and Sulphated Ash.

Job description Position: ARD Officer/ Sr. Officer, Wet, GC, HPLC (API) Note: Candidate should be working in Pharma API industry In ARD Department in Wet, GC and HPLC section. Interested one can share updated resume on anuverma@sauravchemicals.com or WhatsApp/ call at 9875994190/9988339860 Role & responsibilities Position: ARD Officer Wet lab (API Plant)- No. of positions :10 Role & responsibilities Perform routine analytical tests and analyses on incoming raw materials, intermediates, and finished products using various wet chemistry techniques and instrumentation. Maintain accurate records of all testing procedures, results, and observations in accordance with Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs). Assist in the development and validation of new analytical methods and procedures to improve efficiency and accuracy of analytical processes. Calibrate and maintain laboratory equipment to ensure proper functioning and accuracy of test results. Participate in laboratory investigations and root cause analyses for quality incidents, implementing preventive measures to mitigate recurrence. Adhere to safety protocols and guidelines to maintain a safe working environment for yourself and others in the laboratory. Position: ARD - HPLC and GC (API Plant)- No. of positions :10 Role & responsibilities Perform routine maintenance and calibration of HPLC and GC. Prepare and maintain accurate records of all test results and instrument maintenance activities. Troubleshoot and resolve any issues or deviations in HPLC and GC analyses to maintain data integrity and reliability. Collaborate with cross-functional teams to ensure that the analytical methods are compliant with regulatory guidelines and company standards. Assist in method development and validation studies for HPLC and GC analyses as needed. Maintain a clean and organized work area, including the safe disposal of hazardous waste generated during testing. Proven experience in performing HPLC and GC analyses in a analytical laboratory.

Role Purpose The purpose of the role is to source and hire the right talent against the requirements shared by the business and ensuring a positive employer brand experience for the candidate throughout the hiring process. Do 1. Hire the required talent from the different sourcing channels Understand business projections and urgency of talent requirements across order and cadre demands, skill type (type A/B/C), volume vs. niche etc. As per the talent requirements shared by the business, Create sourcing plan as per hiring channel mix and cost considerations Utilize job portals, consultants, employee referral to find the right fit from the industry/ within Wipro For the shortlisted candidates, facilitate the selection process with the technical panel As per the requirement by the business, facilitate different selection tests like technical programming language skills Conduct HR evaluation round and negotiate with the candidate(s) on the salary, position etc Take necessary approval from the tower lead/ head ensuring, hiring is strictly as per Wipros salary range, minimizing exceptions to meet average cost per candidate target Formally roll out the job offer to the selected candidate(s) and coordinate with him/ her for offer acceptance Motivate, engage and maintain relationship with the selected candidate(s) from time to time till their joining Coordinate with the HRSS team for background verification of the selected candidate Communicate with Business Teams and Managers to from time to time on the status of joining etc 2. Manage Candidate Experience throughout the recruitment process Conduct candidate connect and pre-hiring candidate engagement activities to ensure healthy joining ratio Adherence to Wipro guidelines, processes and protocols with respect to responsiveness, clarity, compensation structure, SLAs, quality and auditability in all candidate communication, and deliver Zero valid escalation on hiring process Resolve candidate concerns and manage candidate escalations, turnaround slightest negative experience Daily maintain the data on the recruitment tool (Synergy) and upload all the candidate documents from time to time Ensure the weekly/ monthly/quarterly dashboards are updated and readily available for the management review Conduct meetings with WMG teams to update on the progress, risk and issues involved in hiring for a position and seek help if necessary Follow checks and balances placed by the recruitment team and conduct regular reviews with the management to ensure reliability, quality and integrity of recruitment data in the system

Develop and optimize analytical methods (HPLC, UPLC, GC, UV, Dissolution, KF, IR, etc.) for oral solid and oral liquid formulations. Perform analytical method validation and transfer to Quality Control / manufacturing sites.

Key Skills: Hands-on experience in HPLC handling . Proficiency in Empower3 software . Strong knowledge and practical exposure to instrument analysis . This is a walk-in post. Even then candidates are encouraged to share their resumes in advance at talenthire-unit4@metroapi.com with the subject line Profile for Quality Control . This will help our team connect with you beforehand and guide you about the position. We warmly welcome candidates who are currently working in Visakhapatnam and nearby areas. Note: Candidates with relevant skills in the Quality Control department are requested to apply for this position. .

We are looking for a skilled Senior Analyst to join our team at eClerx Services Ltd., with 6-10 years of experience in the IT Services & Consulting industry. The ideal candidate will have a strong background in analysis and problem-solving, with excellent communication skills. Roles and Responsibility Conduct thorough analysis of complex data sets to identify trends and patterns. Develop and implement effective analytical processes to drive business growth. Collaborate with cross-functional teams to provide insights and recommendations. Design and maintain databases and spreadsheets to track key performance indicators. Create reports and presentations to communicate findings to stakeholders. Stay up-to-date with industry trends and emerging technologies. Job Requirements Strong understanding of analytical principles and methodologies. Excellent communication and interpersonal skills. Ability to work in a fast-paced environment and meet deadlines. Proficiency in Microsoft Office and other analytical tools. Strong problem-solving and critical thinking skills. Experience working with large datasets and performing data analysis.

Department: Material engineering department Reports To: Head 2013 Material engineering department 1. Scope of the role 1)Role primarily involves handling basic chemical techniques, preparing samples and reagents, conducting routine quality checks, and ensuring that all tests comply with regulatory and company standards. 2)Providing necessary support in the day-to-day operations of the laboratory. 2. Job Profile Testing Assist in conducting routine chemical tests on raw materials, electroplated and Ion plated products. Prepare reagents, standard solutions, and samples for analysis. Operate basic laboratory instruments such as pH meters, titration setups and analytical balances. Record and maintain test results and ensure accurate documentation. Maintain 5S and orderliness in the lab. Precious metal recovery Assist in chemical leaching, filtration, and metal precipitation processes. Collect, weigh, and label samples for lab analysis. Operate basic equipment such as furnaces, fume hoods, filtration units, and balances. 3. Key Deliverables Execution of routine analytical tests and reporting. Support in maintaining test records, logs, and calibration reports. Effective collaboration with QA/QC teams. 4. Skills required Strong knowledge in chemistry & attention to detail. Ability to work in chemical-handling environments. Proficiency in MS Office (Word, Excel) is an advantage.

Job Description: We are seeking a detail-oriented and skilled Analytical Scientist (Five Batch Analysis) with hands-on experience in conducting Phy-Chem and validation studies for agrochemicals and pharmaceutical compounds. The ideal candidate will have strong knowledge of global regulatory guidelines and be capable of preparing study-related documentation while maintaining audit readiness at all times. Key Responsibilities: Conduct Physico-Chemical studies for agrochemical compounds in accordance with regulatory requirements. Act as Study Director for Five Batch Analysis studies in accordance with CRO and GLP regulatory requirements. Develop study plans, protocols, and schedules for analytical method validation and sample analysis. Review raw data, analytical reports, and ensure accurate documentation for regulatory submissions. Perform method validation studies for agrochemical products as per SANTEE/SANCO guidelines. Execute validation studies for pharmaceutical compounds as per ICH guidelines. Carry out dose formulation analysis to support toxicological and regulatory studies. Prepare and maintain Standard Operating Procedures (SOPs) for newly initiated studies. Develop study plans and compile final study reports as per relevant regulatory guidelines. Ensure all studies are conducted in compliance with GLP, OECD, OPPTS, CIPAC, SANCO, and SANTEE guidelines. Maintain effective communication with Quality Assurance (QA) personnel throughout the study lifecycle. Utilize Microsoft Excel for accurate calculations, data analysis, and result interpretation. Remain audit-ready at all times for sponsor audits, NGCMA inspections, or other regulatory reviews. Key Skills: Study Direction & GLP Compliance Five Batch Analysis & Regulatory Submissions Analytical Method Development & Validation HPLC, UPLC, LC-MS/MS Expertise Data Integrity & Quality Assurance Client and Sponsor Interaction Leadership & Team Mentoring Qualifications & Experience: Masters/PhD in Analytical Chemistry / Pharmaceutical Chemistry / Life Sciences or related discipline. 4-8 years of experience in Analytical R&D, QC, or CRO environment with exposure to GLP studies. Hands-on experience with HPLC, UPLC, LC-MS/MS, and other advanced analytical techniques. Prior experience as a Study Director for GLP studies, specifically Five Batch Analysis (mandatory). Regards NagaSravani G nagasravani.g@virinchi.com

Looking for a skilled Analyst to join our team at eClerx Services Ltd., an IT Services & Consulting company. The ideal candidate will have a strong background in analysis and problem-solving, with excellent communication skills. Roles and Responsibility Conduct thorough analysis of complex data sets to identify trends and patterns. Develop and implement effective analytical processes to drive business growth. Collaborate with cross-functional teams to provide insights and recommendations. Design and maintain databases and spreadsheets to track key performance indicators. Prepare detailed reports and presentations to communicate findings to stakeholders. Stay up-to-date with industry trends and emerging technologies to improve analytical capabilities. Job Requirements Strong understanding of analytical principles and methodologies. Excellent communication and interpersonal skills. Ability to work in a fast-paced environment and meet deadlines. Proficiency in Microsoft Office and other analytical tools. Strong problem-solving and critical thinking skills. Ability to adapt to changing priorities and requirements. About Company eClerx Services Ltd. is a leading provider of IT Services & Consulting solutions, committed to delivering exceptional results and exceeding client expectations.

Responsibilities: Collaborate with cross-functional teams on product development Ensure compliance with regulatory standards Conduct method validations and HPLC analysis Monitor QMS procedures and document changes

You are currently recruiting for a Principal Scientist, R&D Analytical at Kenvue. At Kenvue, you understand the extraordinary power of everyday care and are built on a rich heritage of over a century, rooted in science. As the house of iconic brands like NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSONS, and BAND-AID, science is your passion and care is your talent. The global team at Kenvue consists of approximately 22,000 brilliant individuals, fostering a workplace culture where every voice is valued, and each contribution is recognized. Passionate about insights and innovation, you are dedicated to delivering top-notch products to customers. As a Kenvuer, you have the power to impact millions daily, prioritizing people, demonstrating care, building trust with science, and approaching challenges with courage. Exciting opportunities await for you to shape both the company's and your future. The role of Principal Scientist, R&D Analytical at Kenvue is based in Asia Pacific, India, Maharashtra, Greater Mumbai, and requires full onsite presence. In this role, you will be responsible for supporting New Product Development and Life Cycle Management projects for the Asia Pacific market. Your tasks will include performing chemical analysis, guiding staff, conducting advanced research programs, and developing research proposals to achieve exploratory objectives in product discovery. Key responsibilities of the role include leading and managing analytical research projects, developing, optimizing, validating, and transferring analytical methods, collaborating with cross-functional teams to drive scientific advancements, providing technical expertise in analytical instrumentation and data analysis, staying abreast of industry trends and technologies, and offering expert guidance to staff members on analytical test evaluations and analyses, among other projects. To qualify for this role, you must hold a minimum BA/BS in Chemistry or equivalent science (e.g., Biochemistry, Pharmaceutical Chemistry) with at least 8 years of proven working experience in Analytical Chemistry and/or Medicinal Chemistry. You should have a track record of leading successful scientific projects, a strong knowledge of Asia Pacific Analytical and Stability requirements, experience in UPLC, HPLC, and GC, and familiarity with EP, ChP, USP compendia requirements and ICH guidelines. Desired qualifications for the position include experience in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health environment, excellent communication and collaboration skills, proficiency with Empower chromatography data system, electronic laboratory notebooks (ELN), and LIMS systems, and a Masters or PhD in chemistry or a closely related field with a profound understanding of medicinal chemistry principles. Total Rewards at Kenvue encompass salary, potential bonuses, and benefits. During the recruitment and hiring process, your Talent Access Partner will provide more information on total rewards offerings and the specific salary range for the relevant location(s). If you are an individual with a disability, refer to the Disability Assistance page for details on requesting accommodations.,

At USP, inclusive scientific collaboration is highly valued, recognizing the importance of diverse expertise in strengthening the development of trusted public health standards. The organizational culture at USP supports equitable access to mentorship, professional development, and leadership opportunities, reflecting the belief that broad participation in scientific leadership leads to more impactful global health outcomes. As an equal employment opportunity employer, USP is committed to fair, merit-based selection processes that enable the best scientific minds, regardless of background, to contribute to advancing public health solutions worldwide. Reasonable accommodations are provided to individuals with disabilities, and policies are in place to create an inclusive and collaborative work environment. This non-supervisory position at USP involves supporting the process development and scale-up of Active Pharmaceutical Ingredient (API) and related materials. The successful applicant will work on projects, including Analytical Method Development and evaluation for in-process samples in synthetic chemistry. Responsibilities also include performing a variety of routine and non-routine analytical tests, maintaining safety and GLP environment in the lab, development/validation of methods, stability studies, and research projects in analytical chemistry. The role requires directing, troubleshooting, and sharing insights on complex projects, collaborating closely with other scientists and/or USP personnel. As part of the mission to advance scientific rigor and public health standards, the individual in this position will contribute significantly to increasing global access to high-quality medicines through public standards and related programs. USP emphasizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure that health systems worldwide can rely on strong, tested, and globally relevant quality standards. The People and Culture division at USP, in collaboration with the Equity Office, invests in leadership and workforce development to equip all employees with the skills necessary to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Scientist IV at USP will have responsibilities including supporting reaction monitoring, scale-up, and final analysis of samples, preparing development reports, executing projects as per specifications, timelines, and budget, reviewing SOPs, protocols, reports, and more. Collaboration with the synthetics team, evaluation and implementation of Process Analytical Technologies (PAT) capabilities, planning and completion of projects, participation in ISO-9001 certification, maintenance of GLP, and safety procedures in the lab are key aspects of the role. The successful candidate will have a Master's degree in Analytical Chemistry/Organic Chemistry/M. Pharm with 8-10 years of experience or a Ph.D. with 4-7 years of experience in Analytical Research and Development. Hands-on experience with chemical methods and various instruments, understanding of process analytical technology, analytical testing and development, technical writing, communication skills, and the ability to function in a team-oriented environment are essential qualifications. USP welcomes applications from individuals holding historically marginalized and/or underrepresented identities. Desired preferences include hands-on experience with PAT instruments and techniques, knowledge of API manufacturing and product testing, expertise with USP compendial methods and requirements, pharmaceutical laboratory experience, strong project management skills, and proficiency in data evaluation and problem-solving. USP provides benefits to protect the personal and financial well-being of employees and their families. USP, the U.S. Pharmacopeial Convention, is an independent scientific organization collaborating with top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. With a core value of Passion for Quality, USP aims to strengthen the supply of safe, quality medicines and supplements worldwide. In building an inclusive organizational culture, USP affirms the value of Diversity, Equity, Inclusion, and Belonging to ensure confidence in health and healthcare quality for all.,

As an in-vitro Bioanalytical Scientist at Syngene, your core purpose will be to provide expert DMPK support to multidisciplinary integrated Drug Discovery projects. Your responsibilities will include defining and implementing the DMPK strategy to expedite project progression, participating in capability building projects as per business requirements, and providing input into the design of experimental protocols and Bioanalytical procedures for the analysis of drug candidates in biological samples. Additionally, you will be expected to deliver scientific presentations in departmental journal clubs and write official project reports. Your role accountabilities will involve planning and supervising routine Bioanalytical workflow to ensure deliverables and productivity, verifying analytical study data for accuracy and integrity, mentoring and supervising fellow scientists for method development and troubleshooting, and playing a key role in evaluating and interpreting bioanalytical results. Troubleshooting LC-MS/MS based bioanalytical methods, having a basic understanding of interpreting Mass/UV Spectra, and ensuring preventative maintenance and calibration schedules of HPLC & mass spec will also be part of your responsibilities. In terms of leadership capabilities, you are expected to demonstrate skills in people management, strong communication, team building, problem-solving attitude, and interpersonal skills. You should consistently align with Syngene's core values of Excellence, Integrity, and Professionalism. As a Syngene leader, you will champion effective Environment, Occupational Health, Safety, and Sustainability (EHSS) practices for the company, oversee compliance within the Biologics business, and foster a corporate culture that promotes an EHSS mindset, quality, integrity, and compliance. People management, career planning, and talent retention will be key areas where you will provide clear, active leadership. Specific requirements for this role include a minimum of 10-15 years of experience in the relevant industry, with demonstrated capabilities in collaboration, leading teams, and Bioanalytical Excellence. The educational background required is an M. Pharm in Pharmaceutical sciences or Pharmaceutical Analysis with a minimum of 10 years of experience in handling ADME assays and HPLC and LCMS/MS, or a fresh Ph.D. in similar disciplines. Syngene is an Equal Opportunity Employer, and all employees are expected to uphold the company's values of Excellence, Integrity, and Professionalism in their daily work.,

As a Chemist at HEPL, a Group company of a 35-year-old FMCG Brand, you will be responsible for conducting various analytical tests and quality control activities in industries such as FMCG, Cosmetics, Foods, and Pharmaceuticals. You should hold an M.Sc. degree in Chemistry, Food Science, or Life Sciences with 0 to 5 years of relevant experience. Your primary responsibilities will include operating, calibrating, and maintaining various laboratory equipment such as UV-Vis spectrophotometer, K.F. Titrator, Conductivity meter, Viscometer, FT-IR, Tinto meter, Analytical balance, pH meter, GC, and HPLC. You should also have hands-on experience in handling Kjeldahl digestion and Distillation Unit, as well as in the preparation and maintenance of reference standards and volumetric standard solutions. In addition, you will be involved in quality control and quality assurance activities, including testing retained samples, spiked samples, and participating in inter-laboratory comparisons and proficiency testing programs related to skincare, hair care, hair color, specialty products, foods, snacks, dairy products, beverages, and bakery products. Furthermore, you will be responsible for preparing Standard Testing Procedures (STPs), validation documents, raw material, and product specifications. Good documentation and adherence to Good Laboratory Practices are essential aspects of this role. You should possess strong communication skills to effectively convey analytical results to both scientific and non-scientific stakeholders. The ideal candidate should have excellent written and oral communication skills in English and be able to join immediately. Prior experience in Research, NABL, and Laboratory settings will be preferred. The role is based in Ekkatuthangal, Chennai, and involves working full-time on day shifts from Monday to Friday. HEPL offers benefits such as health insurance and Provident Fund, along with yearly bonuses. If you meet the qualifications and requirements mentioned above and are keen on contributing to a renowned FMCG brand, we encourage you to apply for this position.,

As the leading supplier of active pharmaceutical ingredients (APIs), TAPI is dedicated to advancing global health. With a legacy of over 80 years and a diverse portfolio of more than 350 products, along with custom CDMO services, we are shaping the future of the healthcare industry worldwide. Our team of over 4,200 professionals across 13 state-of-the-art facilities in various countries collaborates to innovate, problem-solve, and deliver excellence. By joining us, you will become part of a mission that transforms lives. Key Responsibilities: - Perform analysis of stability samples and working standard qualification following defined procedures and pharmacopeial monographs. - Operate and maintain analytical instruments, ensuring smooth function and troubleshooting in accordance with GLP standards. - Maintain accurate documentation of methods, specifications, logbooks, certificates, and stability reports, including data archiving. - Monitor stability studies based on ICH Q1 guidelines. - Conduct analytical method validation activities as per ICH Q2 standards. - Initiate LIR/OOS investigations for any deviations or gaps related to SOPs or monographs during routine operations. - Ensure qualifications and calibrations of all analytical instruments within the stability section. - Strictly comply with laboratory safety procedures during daily activities. Minimum Required Skills: - Solid understanding of Quality Control procedures. - Strong knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices). - Hands-on expertise with HPLC, GC, KF, Auto titrator, and Vacuum oven operations. - Ability to handle instrument troubleshooting and follow documentation protocols. Qualifications: - Experience Level: 4+ Years - Industry Experience: API Experience is required - Qualification: B.Sc. / M.Sc. in Chemistry or B. Pharmacy Join TAPI and embark on a journey to leave a lasting impact on global health. If you are prepared to lead, innovate, and inspire, we are thrilled to have you on our team. Lets together shape the future of pharmaceuticals. Apply on top of this page, and our talent acquisition team will reach out to you soon!,

As a candidate for this role, you will be responsible for working in accordance with organizational compliance requirements. Your main tasks will include developing methods for various quality attributes for complex injectable drug products such as Liposomes and Ophthalmic Drug products. You will also be in charge of performing method validation and verification, as well as analyzing drug products using a variety of analytical techniques including HPLC, GC, UV, and other relevant methods. In addition, you will be tasked with identifying, investigating, and troubleshooting issues as they arise. Your responsibilities will also involve conducting chemical analyses such as Extraction, Refluxing, Residue on ignition, Centrifuging, and Evaporation. Furthermore, you will be expected to prepare study templates, analytical method validation and verification reports, as well as protocols to support your findings. Overall, this role will require a high level of attention to detail, strong analytical skills, and the ability to work effectively within a regulated pharmaceutical environment.,

As an Analyst or Senior Analyst in Bioanalytical Research at Veeda Lifesciences, you will play a crucial role in conducting bioanalytical research activities. This includes method development, validation, and sample analysis utilizing a variety of techniques such as HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Your responsibilities will also involve developing and validating methods for bioanalysis of biologics and biosimilars in compliance with regulatory requirements, such as those set by the USFDA. Collaboration with cross-functional teams will be essential to ensure the timely delivery of high-quality results. Additionally, you will be tasked with performing stability testing of biological products under different conditions. Troubleshooting issues related to instrument calibration, maintenance, and operation will also fall within your scope of duties. The ideal candidate for this role should hold a Bachelor's degree in Pharmacy (B.Pharm) or a Master's degree in Pharmacy (M.Pharm) from an accredited institution, or alternatively an M.Sc. degree. Previous experience ranging from 0 to 4 years is preferred. A strong understanding of analytical instruments like HPLC, UPLC, GC, MS, ICP-MS, and wet analysis is highly desirable for this position.,

Rubicon Research Limited is a rapidly growing pharmaceutical formulation company focused on developing, manufacturing, and marketing branded specialty and generic prescription pharmaceutical products in regulated markets. With a diverse product portfolio of over 250 SKUs spanning more than 70 product families, we have established marketing, sales, and distribution platforms in the US through our subsidiaries AdvaGen Pharma and Validus Pharmaceuticals. Our US FDA-inspected R&D facilities in India and Canada, along with manufacturing facilities in Maharashtra, India, equipped with various drug development and manufacturing capabilities, demonstrate our commitment to quality and innovation. As a Manager in Analytical Method Validation at Rubicon Research Limited, you will play a crucial role in overseeing end-to-end activities related to validation and documentation for various regulatory markets. Your responsibilities will include ensuring accurate documentation for analytical method validation, planning daily validation activities, coordinating with the Analytical Development team, reviewing protocols and reports, managing incidences, investigations, and change control processes, and ensuring compliance with quality management systems. Additionally, you will be responsible for training and supporting the Analytical Method Validation team, providing technical input for analytical data generation, addressing analytical issues, and preparing material budgets. Key Qualifications & Experience: - M. Pharm/M. Sc in Organic or Analytical Chemistry - Proficiency in handling instruments such as HPLC, GC, KF, IC, PSD, etc. - Familiarity with US, UK, EU, and ROW regulatory bodies - Experience with GDP and regulatory query handling In this role, you will need to demonstrate a strong understanding of regulatory guidelines, ensure compliance in the laboratory, provide technical training to team members, and review documents through the Document Management System (DMS) following the Quality Management System (QMS). Your expertise will be crucial in maintaining GLP standards, meeting regulatory and quality expectations, and ensuring that all analytical work is audit-ready to meet FDA standards. Please note that the candidate is expected to work in various shifts as required and may need to visit external sites based on project requirements. If you are passionate about pharmaceutical development, regulatory compliance, and analytical method validation, we encourage you to join our dynamic team at Rubicon Research Limited.,

You should possess a DMPK background with hands-on experience in DMPK-ADME assays and bioanalysis using LCMS/MS & HPLC techniques. Your strong scientific knowledge and excellent communication skills will be key in this role. As part of the team, you will work in the lab under supervision, ensuring the generation of quality data consistently and maintaining high individual productivity levels. Your responsibilities will include running ADME assays and taking charge of the archival of documents and data. Additionally, your ability to learn new techniques, experiments, and instruments will be crucial for success in this position.,

The pharmaceutical Quality Control (QC) professional ensures that drugs and related products meet quality standards throughout their lifecycle, from raw materials to finished goods. This involves a range of activities including testing, analysis, and documentation, all while adhering to regulatory guidelines and company procedures. Key Responsibilities: Testing and Analysis: Conducting various tests on raw materials, in-process samples, and finished products using analytical techniques like HPLC, GC, UV, and spectroscopy. Quality Standards Compliance: Ensuring products meet established quality standards, specifications, and regulatory requirements (e.g., GMP, ICH, USFDA, WHO). Documentation and Reporting: Maintaining detailed records of all testing, analysis, and investigations, including preparing certificates of analysis and other relevant reports. Equipment Management: Calibrating, maintaining, and troubleshooting analytical instruments and equipment. Deviation Investigations: Investigating and documenting any deviations from established quality standards or procedures (e.g., Out of Specification (OOS) results) and implementing corrective and preventive actions (CAPA). Stability Studies: Conducting and documenting stability studies to assess product shelf life and storage conditions. Method Validation: Validating analytical methods to ensure they are suitable for their intended use. Training and Supervision: Training and supervising QC technicians, ensuring they adhere to quality standards and procedures. Audits and Inspections: Participating in internal and external audits and inspections, addressing any findings, and ensuring compliance. Inventory Management: Managing the inventory of reagents, standards, and other materials needed for QC analysis. Process Improvement: Identifying opportunities to improve the efficiency and effectiveness of QC processes. Skills and Qualifications: Education: Typically requires a Bachelor's or Master's degree in Chemistry, Biochemistry, Microbiology, or a related field. Analytical Skills: Strong analytical and problem-solving skills, including the ability to interpret data, troubleshoot issues, and make informed decisions. Technical Skills: Hands-on experience with relevant analytical techniques and instrumentation. Regulatory Knowledge: Understanding of cGMP, ICH guidelines, and other relevant regulatory requirements. Attention to Detail: Meticulous attention to detail is crucial for accurate testing, documentation, and investigations. Communication and Interpersonal Skills: Ability to effectively communicate with team members, management, and other stakeholders. Problem-solving skills: Ability to identify the root cause of quality issues and implement effective corrective actions.,