1214 Hplc Jobs - Page 12

Job description - Research Associate (Protein Chemistry laboratory) 1. Process development, scale-up and transfer: (Downstream) Undertake on-going referencing and literature reviews and provide strategic inputs to projects at all stages Conduct lab experiments as per the shortlisted methodologies in order to develop & finalize purification processes for various recombinant therapeutic products. Provide own inputs and insights to optimize/improve process Provide samples to analytical labs for testing, collect and file reports of analysis, compile the data and do data analysis for conclusion of experiments Support plant activities as per need Present data in project review meetings Prepare process development report and technology transfer documents Participate in at-scale demo batches and handover as part of technology transfer Jointly monitor purification process at production facility and resolve any queries that may arise during production 2. Materials and equipment management: Oversee installation of new equipment and attend demos Maintain all IQ/OQ/PQ documents Ensure scheduled and breakdown maintenance by coordinating with maintenance team Create and maintain all maintenance/ repair logs Support management of chemical, consumables: o Transfer/store as per set norms o Engage in technical discussions with vendors in order to suggest suitable vendors o Maintain material logs and calculate shortfalls (for order placement) o Post materials required onto SAP 3. Regulatory and compliance: Accurately capture all lab experiments in laboratory notebooks in real-time Adhere to regulatory, SOPs and safety guidelines for all processes Modify SOPs in own area of work Ensure timely closure of regulatory queries by conducting and documenting lab experiments Ensure data integrity in all respects 4. Learning and improvement Attend all mandatory trainings Take initiative to provide inputs (based on expertise/interest) to other on-going projects Take initiatives for self-development and update self on recent developments in own area of work Take initiative to train fresh RAs upon induction or guide them with select lab processes (basis expertise) 5. Compliance management Ensuring GDP compliance Ensuring CC/ IQ/OQ/PQ/CSV of new instrument Ensuring calibration/PM/AMC of equipment Be audit ready and prepare audit responses as per audit points Lab cleanliness, lab maintenance

To work as per cGMP and ensure its compliance as per current guideline and SOPs. Responsible to align with organization goal and other responsibilities assigned by reporting authority. Responsible to perform the calibration of instrument and to maintain instrument/equipment as per SOPs. Responsible to follow safety precaution as per laboratory procedure. Responsible for method development studies of Drug Substance, Drug Product & In process Materials related to Peptides. Responsible for method Validation studies of Drug Substance, Drug Product & In process Materials related to Peptides. Responsible for analysis of routine samples and stability studies of Drug Product & In process Material Drug Substance, Drug Product & In process Materials related to Peptides. Responsible to prepare Study Protocol and Study Reports. Responsible for analysis of Oligonucleotides (DNA & RNA molecules) of single strand (Sense and Antisense) and Duplexes molecules. Responsible for Development of IEX and Ion Pair method for Sense and Antisense to separate charge variants in DNA and RNA molecules Responsible for Development of SEC method to separate size variants in DNA and RNA molecules. Responsible for Isolation of Peptide molecules from impurities by PREP HPLC.

JOB DESCRIPTION Designation: AQA Reviewer Job Location: Bangalore Department: Analytical Quality Assurance About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . 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 Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Job Purpose: To review the data & reports generated from GMP Laboratory (Stability) and to monitor the GMP Lab compliance. Key responsibilities: 1) Online Sequence & Document review in HPLC, GC, KF, PXRD, ICPMS, LCMS & other all analytical instruments. (CD & FC - Intermediate, FP & Stability) 2) Offline Raw Data review in ELN (CD & FC - IPQC, Intermediate, FP & Stability) and release of IPQC TI sheets in 24/7 3) Daily verification data review, PM reports and Lamp intensity report review in ELN. 4) Compiled Report review (CD & FC - IPQC, Intermediate, FP & Stability). 5) Calibration sequence, data review of HPLC (S17) and release of instrument. Raw material data review and release in LIMS & SAP. 6) Reconciliation of EDMS issued prints (formats). 7) Audit trial review of Standalone systems and chromeleon application. 8) Monthly Date & Time verification of approximately 20 standalone instruments. 9) Review of analytical raw data generated by analyst, protocols/ reports pertaining to the section as per the standard operating procedure and specification. 10) Ensuring, verifying and reviewing the instrument usage log periodically and accordingly checking the labels as per SOP. 11) Review of Outsourced analytical report. 12) Review of logbooks with respect to all activity performed in the lab. 13) Responsible for taking any other job allocated by Department Head / Department In charge. 14) Review of technical data in analytical document viz. Calculations, Chromatograms, method parameters, integration, logbook entries, WS/RS and Column usage records, method parameters, reconciliation, vendor COA and other technical data in analytical document. 15) Reviewer shall ensure the documents physically for availability of all the pages of ODS and supporting documents. 16) Review the documents for completeness, compliance to Good documentation practices, test results against specification limits or acceptance criteria as mentioned in protocol and reconciliation of forms issued as applicable 17) In case of any discrepancy, immediately notify to the reporting manager or his designee or Head or designee GMP Analytical Laboratory. 18) Ensuring of conducting regular GMP rounds at Quality Control Laboratory. Educational Qualification: M. Sc. Chemistry or Analytical or equivalent Technical/functional Skills: The candidate should possess good communication, leadership and technical skills in Laboratory instruments like HPLC, GC, GCMS, LCMS, PXRD, KF etc. , . He / she should have working knowledge in quality, conducting investigations and quality management systems. He / she should have experience in review of data generated from QC team of QA professional. Experience: 4 to 8 years Equal Opportunity Employer: .

Hands on skill and Knowledge of LCMS, HPLC, UHPLC, GC, GCMS, Wet chemical Understanding of analytical chemistry, discussion with synthesis, plant, PE laboratory analysis of samples in time., Ensure that laboratory work is carried out in a safe manner Required Candidate profile Analytical Research & analytical method development for organic molecules. Method validation. Method transfer. Stability studies. GLP. GDP, Building Problem Solving, Customer Centricity, Analysis

Conducting laboratory tests and experiments, following established procedures and protocols. Analyzing samples and interpreting data, and recording and reporting results. Maintaining laboratory equipment and ensuring it is in good working order. Developing and validating new laboratory methods and procedures. Collaborating with other scientists and technicians to conduct research and develop new products or processes. Conducting quality control tests to ensure compliance with established standards and specifications. Identifying and resolving technical problems, and proposing solutions to improve laboratory operations. Ensuring compliance with safety regulations and laboratory protocols. Writing technical reports and presenting findings to colleagues or clients. Good analytical and problem-solving skills. Strong attention to detail and ability to maintain accurate records.

Develop and implement business development strategies. Identify and engage potential clients. Collaborate with internal and external stakeholders. Monitor business development performance and suggest improvements. Prepare reports and documentation. Provide training and support to staff.

Responsibilities: * Develop analytical methods using HPLC, ELISA , colorimetry & spectrophotometry. * Validate methods according to GLP & GDP guidelines. * Conduct quality control testing on biologics products.

Role & responsibilities Familiar/experienced of HPLC/Dissolution apparatus breakdown/services Preferred candidate profile Male

Analysis of RM/PM, in process, finished product, stability samples by using HPLC, GC, UVFTIR, etc. & QC Instruments calibration, Maintain the GLP/GMP in laboratory, Compliance to regulatory requirement for MHRA, TGA, Health Canada, PDMA Japan .

Lab Experience for Analytical Method Development, regular and Stability sample analysis. Handling of HPLC for Assay, Dissolution, Related substances tests for solid orals. Lab Experience for Analytical Method Validation. Lab experience for Particles Size Distribution Analysis using Particle sizer and microscope.

Long Description 1 Coordination, Implementation, execution, and completion of projects in time within allocation budget. 2 Coordination with between different inter-departmental team, site project team, consultant, and vendors. 3 Project planning and preparing schedule and tacking work progress. 4 Check and track all long lead items for procurement of materials. 5 Preparation of techno commercial evaluation. 6 Ability to work multiple projects in various stages. 7 Hands of experience in handling Electrical, Instrumentation projects, Pharma Process equipment & utilities, Water system. Competencies Strategic Agility Innovation & Creativity Process Excellence Customer Centricity Collaboration Stakeholder Management Developing Talent Result Orientation Education B.Tech Graduation in Electrical Work Experience Year of Experience 5 to 6 Years in field of Pharma

About Us Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs. Job Roles & Responsibilities Analytical Method Development & Validation: Develop and optimize analytical methods for pharmaceutical compounds using HPLC, GC, UV-Vis, and other analytical techniques. Perform method validation studies including accuracy, precision, linearity, specificity, and robustness testing. Transfer analytical methods between laboratories and ensure successful implementation. Troubleshoot analytical methods and resolve technical issues. Sample Analysis & Testing: Conduct routine analysis of raw materials, intermediates, and finished pharmaceutical products. Perform quantitative and qualitative analysis following established protocols and regulatory guidelines. Execute stability studies and analyze samples at designated time points. Instrumentation & Maintenance: Operate and maintain analytical instruments including HPLC, GC, GC-MS, FTIR, UV-Vis spectrophotometers. Perform routine calibration. Troubleshoot instrument issues and coordinate with service technicians when needed. Ensure proper documentation of instrument performance and maintenance activities. Data Management & Reporting: Analyze and interpret analytical data using statistical methods and software. Prepare technical reports, certificates of analysis, and regulatory submissions. Maintain accurate laboratory records and electronic data systems. Knowledge & Experience Master's degree in Analytical Chemistry, Chemistry, or related field. 2 - 4 years of relevant experience in pharmaceutical, chemical, or analytical laboratory settings. Strong foundation in analytical chemistry principles and techniques. Preferred Qualifications Experience with advanced analytical techniques (DSC, TGA). Previous experience in pharmaceutical or biotech industry. Understanding of stability testing and forced degradation studies. Knowledge of cleaning validation by UV / HPLC. Why Join MPDRPL? Be part of an organization driving cost-effective global healthcare solutions . Work on end-to-end projects from concept to market. Collaborate with experts across departments in a quality-driven, innovation-centric environment . Access to modern formulation laboratories and pilot-scale facilities. Competitive compensation with performance-linked incentives . Professional development and career advancement opportunities . Comprehensive employee benefits including healthcare and retirement plans .

About Us Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) is a dynamic pharmaceutical R&D organization committed to developing high-quality, affordable generic and novel products for global markets. With a focus on innovation and regulatory compliance, we work in the area of ANDA, NCEs, 50b2, API development and novel polymorphs. Job Roles & Responsibilities Design and optimize Route of Synthesis (RoS) for novel medicinal drugs. Synthesize and purify medicinal compounds using advanced laboratory techniques. Conduct laboratory experiments to test the efficacy and safety of synthesized compounds. Analyse data from various analytical techniques to assess compound quality and properties. Improve the physicochemical properties of existing drugs to enhance performance and stability. Collaborate with other scientists and departments to advance drug development projects. Follow strict health and safety guidelines to ensure a safe working environment. Review and interpret the structure and purity of chemical compounds using modern analytical tools. Knowledge & Experience Bachelors in Medicinal Chemistry with Masters in Medicinal Chemistry, Organic Chemistry, or a related field. With M.Sc. (2 to 4 years of Experience) At least 2 years of hands-on experience in chemical synthesis within a pharmaceutical or biotech setting. Proficiency in modern synthetic techniques and analytical methods (e.g., NMR, HPLC, MS). strong problem-solving skills and the ability to design efficient synthetic routes. Excellent laboratory skills, including safe handling of chemicals and operation of laboratory equipment. Ability to work collaboratively in a team-oriented environment. Excellent written and verbal communication skills. Detail-oriented with strong organizational skills. Commitment to continuous learning and staying current with scientific advancements. Why Join MPDRPL? Be part of an organization driving cost-effective global healthcare solutions . Work on end-to-end projects from concept to market. Collaborate with experts across departments in a quality-driven, innovation-centric environment . Access to modern formulation laboratories and pilot-scale facilities. Competitive compensation with performance-linked incentives . Professional development and career advancement opportunities . Comprehensive employee benefits including healthcare and retirement plans .

Responsibilities: * Develop analytical methods using HPLC, ELISA , colorimetry & spectrophotometry. * Validate methods according to GLP & GDP guidelines. * Conduct quality control testing on biologics products.

Role & responsibilities Sent CV dipika@uppl.in Name Qualification Age Mobile No. Applied for Position Current Company Name Current Location Current Designation Current Company Experience (in years) Total Experience (in years) Brief of Current Profile Current Fixed CTC (Per Annum)+ Variable if any+ other benefits Expected CTC (Per Annum) Notice Period Are you ready to relocate to Bharuch ? (Yes/No) Reason for Job Change Please provide family details (dependents, etc.) Is your wife a Housewife/Working Is your family supportive of relocation? (Yes/No) If offered, can you assure us you will not negotiate with your current company? (Yes/No) Preferred candidate profile

Junior Scientist ?? Analytical Development (IP) Location: Hyderabad Experience: 2-5 years About the Role: Join our analytical development team to ensure high-quality analysis and method development for For . Ltd.. Get In Touch Page load link |pharmaceutical products. Key Responsibilities: Perform analysis using UV/HPLC, GC, and dissolution techniques. Validate test procedures (dissolution, assay, related substances, etc.). Maintain error-free documentation and calibrated instruments. Apply Now Location:Hyderabad Experience:2-5 years Phone: +91 040 2379 2190 Email: info@aizant.com |Business Inquiries: bd@aizant.com Development Pre-Formulation Formulation Development Analytical Development Regulatory Support & Dossier Compilation Manufacturing Clinical Trial Material Commercial Supplies Technology Transfer Clinical Research Bioanalytical BABE Clinical Trial Services Our Portfolio Co-Development Out-licensing About Us Quick Links Careers We are hiring Social responsibility Sustainability Environment, Health & Safety Knowledge Hub Contact Us Copyright 2025 All Rights Reserved | Aizant Drug Research Solutions Pvt

Akshara Consultancy - Laboratory Items Distribution Company Qualifications: Bachelors degree,or masters preferably Pharmaceutics, or Pharmacology 2-3 years of sales experience, preferably in pharmaceutical laboratory items. Key Responsibilities: Sell laboratory items, including microbiology and chromatography products (HPLC/GC vials and columns). Develop and expand client relationships. Conduct regular field visits to follow up with clients and secure orders. Maintain and enhance sales performance for both existing and new business. Travel across Telangana to meet clients and ensure customer satisfaction. Desired Skills and Attributes: Strong interpersonal and communication skills. Ability to work independently and manage time effectively. Self-motivated with a proactive sales approach. Willingness to travel extensively within the region.

Job Overview As a Peptides Production Executive, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. Roles & Responsibilities: Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunitie Experience 4 to 6 Yrs experience in Peptides Manufacturing Preferred candidate profile: Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes.

Job Overview As a Peptides Production Sr Executive, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. Key Responsibilities: Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunities. Experience 4 to 6 Yrs experience Peptides Production Preferred candidate profiles Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes. Qualifications Masters/Bachelors degree in Chemistry or a related field.

-Conducting experiments using proper lab equipment -Preparing and testing solutions -Analyzing and reporting on test results -Develop nonstandard tests for chemical products -Excellent analytical and research skills M Pharma & B Pharma Don't apply

B.Sc,M.Sc,B.pharm----Quality control exp of 1 to 5 yrs Analysis of Raw Material,Packing material Instrument handling HPLC,GC Required Candidate profile Candidate to note that Weekly off:-Friday Ready to work in shifts Job location Rabale(Navi Mumbai) Ready to join immediately with one week resume to sunil@flamingopharma.com hr@flamingopharma.com

Inspect products to ensure that they meet quality standards Create tests for QC of products Monitor PDN to ensure conformance to set standards Ensure products meet customer expectations Communicate the results of inspections Document deficiencies Required Candidate profile MSc Chemistry 3+yrs exp into QC / LAB QAULITY with PHARMA/AGRO/CHEMICAL major Strong exp in LAB QAULITY, QA TESTS, TEST EQUIPMENTS like GC, HPLC, AAS, ICP-MS, ICP-OES, XRD, XRF etc Work @ CUDDALORE Perks and benefits Excellent Perks. Must relocate near CUDDALORE

Job Description : Job Title: Senior Executive - Analytical (R&D) About the Function: Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo s 30,000+ people work in Supply Chain and Manufacturing. It s an intricate and sophisticated operation that s the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We re committed to realising our Society 2030: Spirit of Progress goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we ll help you to thrive in our inclusive culture. Role Responsibilities: Role Purpose: This role is responsible for supporting analytical R&D projects related to alcoholic beverages. It includes to support and conduct precise chemical and instrumental analysis of raw materials, intermediates, and finished liquids in alignment with defined test methods. The position also to supports senior analysts in innovation and research initiatives. Qualifications & Experience: Education : MSc in Analytical Science / Chemistry / Organic Chemistry Experience : Minimum 1-2 years of experience in chemical and instrumental analysis of food, beverage, alcoholic beverages. Key Technical Responsibilities: Perform chemical analysis on raw materials, intermediates, and finished liquids using validated methods Assist and support in method development, verification, and validation Core Technical Competencies: Instrumental Techniques: Basic understanding of the operation and data interpretation of: GC-FID / GC-ECD/GC-MS - For volatile compounds, congeners, fusel oils HPLC - For organic acids, polyphenols, flavor-active compounds UV-Vis Spectroscopy - For color, % transmittance, phenolic profiling Hands-on experience in general laboratory instrumentation: pH meter, Conductivity meter, Turbidity meter, etc. Classical Wet Chemistry Techniques: Titration for acidity, sulfur content, etc. Alcohol content analysis using pycnometer, hydrometer, or digital density meter Analytical Methodology: Sound knowledge of: Method verification and development Instrument qualification (IQ/OQ/PQ) Calibration and measurement uncertainty Basic application of statistical techniques (e.g., ANOVA, control charts) Data Handling & Reporting: Understanding of data analytics and statistical tools for research applications Clear, structured reporting and presentation of analytical findings Accurate and timely documentation of results as per regulatory and internal standards Leadership & Behavioral Expectations: Organizational Impact : Understands role priorities and delivers as per direction from manager. Supports team-level goals and process improvements. Decision-Making & Problem Solving: Anticipates analytical challenges and recommends practical, data-based solutions. Integrates technical knowledge with insights to improve outcomes. Communication & Collaboration : Clearly articulates scientific findings in verbal and written form. Engages cross-functional teams through knowledge sharing and training initiatives. Self-Management & Ownership : Independently plans workload and seeks guidance when needed. Demonstrates accountability, precision, and curiosity in laboratory work. Flexible Working Statement: Flexibility is key to our success. From part-time and compressed hours to different locations, our people work flexibly in ways to suit them. Talk to us about what flexibility means to you so that you re supported from day one. Diversity statement: Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this. We embrace diversity in the broadest possible sense. This means that you ll be welcomed and celebrated for who you are just by being you. You ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more. Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world. Feel inspired? Then this may be the opportunity for you. If you require a reasonable adjustment, please ensure that you capture this information when you submit your application. Worker Type : Regular Primary Location: Bangalore Technical Centre Additional Locations : 2025-07-01

Job Description : Job Title: Assistant Manager - Research & Development About the Function: Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo s 30,000+ people work in Supply Chain and Manufacturing. It s an intricate and sophisticated operation that s the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We re committed to realising our Society 2030: Spirit of Progress goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we ll help you to thrive in our inclusive culture. About the role: This role is responsible for executing and managing analytical R&D projects related to alcoholic beverages. It includes conducting precise chemical and instrumental analysis of raw materials, intermediates, and finished liquids in alignment with defined test methods, Good Laboratory Practices (GLP), and ISO 17025 requirements. The position also supports senior analysts in innovation and research initiatives and contributes to technical capability building across stakeholders through training and knowledge sharing. Role Responsibilities: Key Technical Responsibilities: Conduct and support analytical R&D projects for product and process development Perform chemical analysis on raw materials, intermediates, and finished liquids using validated methods Ensure compliance with GLP and ISO 17025 in all laboratory operations Assist in method development, verification, and validation Train internal teams and stakeholders on analytical techniques and data interpretation Core Technical Competencies: Instrumental Techniques: Proficient operation and data interpretation of: GC-FID / GC-ECD/GC-MS - For volatile compounds, congeners, fusel oils HPLC- For organic acids, polyphenols, flavor-active compounds UV-Vis Spectroscopy - For color, % transmittance, phenolic profiling Strong hands-on experience in general laboratory instrumentation: pH meter, Conductivity meter, Turbidity meter, etc. Classical Wet Chemistry Techniques: Titration for acidity, sulfur content, etc. Alcohol content analysis using pycnometer, hydrometer, or digital density meter Analytical Methodology & Validation: Sound knowledge of: Method development, verification, and validation Instrument qualification (IQ/OQ/PQ) Calibration and measurement uncertainty Determining LOD/LOQ Chemometric tools and application of statistical techniques (e.g., ANOVA, control charts) Data Handling & Reporting: Understanding of data analytics and statistical tools for research applications Clear, structured reporting and presentation of analytical findings Accurate and timely documentation of results as per regulatory and internal standards Leadership & Behavioral Expectations: Organizational Impact: Understands role priorities and delivers as per direction from manager. Supports team-level goals and process improvements. Decision-Making & Problem Solving: Anticipates analytical challenges and recommends practical, data-based solutions. Integrates technical knowledge with insights to improve outcomes. Communication & Collaboration: Clearly articulates scientific findings in verbal and written form. Engages cross-functional teams through knowledge sharing and training initiatives. Self-Management & Ownership: Independently plans workload and seeks guidance when needed. Demonstrates accountability, precision, and curiosity in laboratory work. Experience / skills required: Education: PhD or MSc in Analytical Science / Chemistry / Organic Chemistry Experience: Minimum 5 years of experience in chemical and instrumental analysis in the food and beverage or allied industries

Role & responsibilities 1. Ready to work in all shifts 2. Knowledge in Analytical chemistry, Spectroscopic technique and Titration 3. Safe handling of apparatus, equipments and glasswares as per SOP. 4. Ensuring cleanliness of apparatus. 5. Hands on GC, HPLC, KF and Wet analysis. Able to handle shift independently. 6. Hands on Biproduct analysis, Effluent analysis. 7. Calibration of Instruments GC, HPLC 8. Awareness to IMS / EHS system. 9. Good computer proficiency. 10. Daily analysis report. Preferred candidate profile QC Officer - Qualification: M.Sc. Analytical / Organic Chemistry with 1-3 years’ experience in agrochemicals, specialty/ fine chemicals, and pharma