341 Method Development Jobs - Page 2

Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc). isolation product and Optimize reaction conditions for improved yields and output.

R&D (Synthesis) -Agrochemical Industry-Saykha,Gujarat. Industry IT Software - Application Programming / Maintenance Qualification M.Sc Key Skills R&D Research & Development Executive UPLC HPLC GC Analytical Development

job description Monitor progress of the reactions by using standard methods & analytical techniques (TLC,GC,HPLC, LCMS etc).Plan, setup, monitor, and workup chemical reactions independently.Isolate product & Optimize reaction conditions for improved

R & D (Analytical Development) - Agrochemical Industry-Saykha,Gujarat. Capital Placement Services 3 - 8 years Industry Pharma / R&D / Biotech Qualification M.Sc Key Skills R & D Analytical Development LAB Agrochemical UPLC Green Field Projects HPL

Plan, setup, monitor, and workup chemical reactions independentlyMonitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc)<

Roles & Responsibilities : Perform Analysis: Collect samples for analysis from Custodian. Processing of samples by using various sample extraction technique (to determine the concentration of analyte). Batch sequence preparation and verification in coordination with LIMS Operator. Perform analysis via LCMS/ ICP-OES/ ICP-MS. Follow GxP. Mass Spectrometry operation and ESI, APCI conceptual clarity. Chiral chromatography, polar columns conceptual clarity. Sample extraction process using LLE, SPE, and PPT. Documentation and compliance: Receive controlled forms for various activities. Perform online documentation of development trial in Method Book (Laboratory Record Book), validation experiment documentations, entry in log books in control forms as per SOP, evaluate experiment outcome with pre-defined validation/ study protocol. Document all linked activities and forms as per SOP. Investigation approach in case of abnormality. Regulatory response and investigation writing skills. To check the documentation done by Jr. Analyst/ fresher. Solve the finding/ observation raised by the QC and QA in timely manner. Research & Development: Literature review i.e., published pharmacopeia guidelines/ research documents received from GL and SGL. Validation: Perform experiments as per protocol. Method development skills. Troubleshooting of method. Excel and MS-Word. Equipment Calibration : To calibrate lab equipments like micro-pipettes, analytical balance, pH meter, evaporators, roto spin extractor, centrifuge, Solid Phase Extraction (SPE) assembly and their performance check as and when required, to coordinate with engineer for any breakdown pertaining to lab equipment. Training : To coordinate assist/ support in on-the-job trainings for fresher. Regulatory guidelines and thorough training on SOPs. Presentation skill. Regulatory updates and latest guidance awareness. To understand GCP and GLP requirement and its awareness. General biosafety procedures, emergency procedures awareness. Knowledge of organization policies/ values. Desired Candidate Profile: Education: B.Pharm, M.Pharm, M.Sc Experience: 1-5 Years' experience in CRO.

We are seeking a dynamic and experienced Quality Control (QC) Manager to lead and manage QC operations, ensuring that products and processes meet stringent quality and regulatory requirements. The ideal candidate will possess deep technical expertise, a strong leadership background, and a commitment to data integrity and continuous improvement within the life sciences industry. A detail-oriented professional with expertise in Nitrosamines/NDSRI method development and validation by LC-MS focused on detecting and quantifying nitrosamine impurities in APIs and Finished Dosage Forms. You will contribute to method development, validation, instrument calibration, and document preparation while ensuring compliance with safety, regulatory, and cGLP standards. Preferred Manager profile: Design and implement robust QC procedures aligned with current Good Manufacturing Practices (cGMP) and industry standards. Ensure processes are optimized for efficiency, accuracy, and compliance. Regularly assess QC operations and procedures. Identify opportunities for improvement and implement enhancements to streamline workflow and ensure regulatory readiness. Ensure QC operations comply with global regulatory authorities including USFDA, EDQM, ANVISA, PMDA, and WHO. Maintain audit readiness and lead/support regulatory inspections. Team Leadership and Development Manage and mentor a team of QC professionals, ensuring high performance and ongoing professional development. Assign responsibilities, monitor progress, and promote a culture of accountability and collaboration. Data Integrity and Documentation Ensure accuracy, reliability, and confidentiality of all laboratory records and data. Enforce adherence to ALCOA+ principles for data integrity. Troubleshooting and CAPA Management Investigate quality-related issues, perform root cause analysis, and lead implementation of effective corrective and preventive actions (CAPAs). Cross-functional Collaboration Collaborate with AR&D, QA, and other departments to align quality strategies. Communicate quality metrics, performance, and issues to leadership and stakeholders. Quality System Contributions Support development and implementation of quality management systems (QMS). Review and approve analytical methods, validation protocols, and reports. Audit and Complaint Management Lead or support internal and external audits. Manage customer complaints and conduct trending analysis to drive quality improvements. Technical Skills: Hands-on experience and data interpretation of analytical instruments like LCMS, HPLC, GC,UV, KF, etc. Thorough understanding of cGMP, GLP, and regulatory requirements. Good documentation and analytical skills. Job Description: QC Data Review Specialist Job Summary We are seeking a meticulous and highly organized QC Data Review Specialist to join our Quality Control team. The successful candidate will be responsible for the comprehensive GMP (Good Manufacturing Practices) review of laboratory raw data, analytical reports, and related documentation. This role is critical to ensuring that all laboratory work is performed in compliance with established methods and protocols, that results are analytically sound and accurate, and that all documentation adheres to stringent GMP standards and regulatory requirements. Key Responsibilities Data and Document Review: Conduct detailed reviews of analytical data packages, including but not limited to raw data (e.g., chromatograms, spectra), laboratory notebooks, and summary reports for accuracy, completeness, and compliance with GMP. Compliance Verification : Ensure all testing was performed according to approved SOPs, analytical methods, and protocols. Verify that calculations and data transcriptions are correct and that any deviations or out-of-specification (OOS) results are properly documented, investigated, and reported. Method Validation Review : Review method validation/verification/transfer protocols and reports to ensure they meet regulatory and company standards. Stability Program Suppor t: Review stability testing data and reports, ensuring that data integrity is maintained throughout the stability study lifecycle. Audit Trail Review : Perform audit trail reviews of electronic data systems to ensure data integrity and identify any potential compliance risks. Documentation Management : Assist in the revision and approval of controlled documents such as SOPs, test methods, and specifications. Communication: Collaborate closely with laboratory analysts to resolve documentation errors, clarify discrepancies, and provide constructive feedback to prevent future issues. Act as a liaison between the QC laboratory and the Quality Assurance (QA) department. Continuous Improvement : Identify gaps in procedures and opportunities for improvement within the laboratory data review process to enhance efficiency and compliance. Qualifications Education: Bachelor of Science (B.S.) degree in Chemistry, Biology, Biochemistry, or a related life sciences field is required. Experience: A minimum of 3-8 years of hands-on experience in a GMP-regulated pharmaceutical or biotechnology laboratory environment. Direct experience in reviewing analytical data (e.g., HPLC, GC, UV-Vis, FTIR, wet chemistry) is essential. Prior experience in a dedicated data review or QA role is highly preferred. Knowledge: In-depth knowledge of GMP, GDP (Good Documentation Practices), and data integrity principles. Strong understanding of FDA, ICH, and other relevant regulatory guidelines. Familiarity with common laboratory software and electronic data systems (e.g., LIMS, Chromeleon, Empower). Required Skills and Competencies Attention to Detail: Exceptional ability to spot errors, inconsistencies, and deviations in complex technical documents. Analytical and Critical Thinking: Strong ability to interpret scientific data and assess its validity and compliance. Organizational Skills: Excellent time management skills with the ability to manage multiple review assignments and meet deadlines. Communication Skills: Clear and effective written and verbal communication skills are necessary to articulate findings and collaborate with team members. Problem-Solving: Proactive in identifying issues and working with the team to find compliant solutions. Integrity: Must uphold the highest standards of quality and ethical behavior. Teamwork: Ability to work effectively both independently and as part of a collaborative team. Behavioral & Leadership Skills: Strong analytical and problem-solving skills. Excellent communication and interpersonal abilities. Demonstrated ability to lead cross-functional teams and drive a culture of quality. Why JanSat? Our values and expectations are at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As JanSat focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities: Operating at pace and agile decision-making using evidence and applying judgement to balance pace, rigour and risk. Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution. Continuously looking for opportunities to learn, build skills and share learning. Sustaining energy and well-being. Building strong relationships and collaboration, honest and open conversations. Budgeting and cost-consciousness.

Role & responsibilities 1.Responsible for work planning and review of documents related to In process, DS, DP, stability testing, AMV and AMT activities within quality control laboratory. 2. To effectively plan and monitor shift duties of the QC analytical staff members to support 24*7 business operations. 3. Responsible for compliance to internal, external & statutory compliances as per quality policy of Enzene, pharmacopoeia guidelines and other regulated guidelines. 4. Responsible for periodic training management related to quality, GMP, regulatory aspects to quality control laboratory personnels and evaluation of effectiveness. 5. Responsible for the periodic assessments/audits to identify gaps / improvement opportunities for strengthening the quality & regulatory compliance. Prepare remediation/mitigation plan (CAPA) and execute it in a timely manner by coordinating cross functionally to uplift the level of compliance’s. 6. Responsible for review and approval of documentation such as SOP’s, Specifications, STP’s, TDS, reports for IRS analyst qualification, protocols, Qualifications and reports etc. 7. Responsible for investigations and approval of OOS, OOT and deviations. To recommend and approve CAPA, change controls. 8. To release or reject the samples handled in quality control laboratory.

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Job Title : LEAD SPECIALIST GOE CAL Location : Mumbai At dsm-firmenich we strive to achieve a world where you don't have to choose between taste, texture, or health - and can enjoy it all. Our innovative ingredients, expertise, and solutions bridge the gap between the delicious, the nutritious, and the sustainable. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Your key responsibilities: Analytical Support & Method Development Plan and conduct GC-MS, LC-MS, and other analytical techniques for flavors, perfumes, aroma chemicals, and natural products, while contributing to method development and technical growth of the team. Instrument & Lab Management Manage and maintain analytical instruments and lab operations, ensuring SOP compliance, accurate documentation, and inventory control. Cross-Functional Collaboration Work closely with Creation, Application, QA, and global/regional teams to ensure alignment and effective analytical support across functions. Volatile Compound Analysis Apply isolation and analytical techniques-particularly GC with various detectors and GC-MS-for in-depth volatile analysis. Reporting & Documentation Prepare, review, and manage analytical reports using in-house tools, and clearly communicate findings and recommendations to stakeholders. Scientific Expertise & External Coordination Serve as a subject matter expert in analytical/flavor chemistry, supporting global collaborations, literature research, and coordination with external resources. We bring: A team of diverse employees who aren't afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. A role that is crucial on projects and allows you to build your brand. A caring and supportive environment where you're empowered to grow and share your ideas. You bring: MSc. (with 5+ years experience) or Ph.D. (with 2+ years experience) in analytical chemistry or a related field. Proven expertise in gas chromatography and method development in commercial or research lab settings. Extensive hands-on experience with mass spectrometry for complex analytical applications. Knowledge of ISO 17025:2017 standards is a strong advantage. A curious, problem-solving mindset with a drive to explore new approaches and deliver innovative solutions. A strong sense of ownership and accountability , with the ability to deliver meaningful results and work collaboratively within diverse teams. The application process: Interested in thispositionPleaseapply on-line byuploadingyourresumein Englishvia ourcareer portal. For further information, please contact Shradha Tiwari , Talent AcquisitionPartner ( [HIDDEN TEXT] ). Equal Opportunities Commitment dsm-firmenich is fully dedicated to inclusion becausewhenpeople feelengagedand empowered,their creativityandinnovation drives unprecedented progress.We aimto buildaworkplace whereopportunity really is equal,soeveryonecanthrive.Wedonotdiscriminate: there'sa place for everyone at dsm-firmenich. Dsm-firmenich isanEqual Opportunityand Affirmative ActionEmployer. dsm-firmenich peopleareasdiverseas ourcustomers. For us that includesa commitmenttoensuring equal employmentopportunitiesfor alljob applicantsand employees.Employment decisions are baseduponjob-related reasons regardless ofan applicant'srace, color, religion,sex,sexualorientation,gender identity,age,nationalorigin,disability, maritalstatus, geneticinformation, protectedveteranstatus, oranyotherstatusprotected by law.Wearecommittedto providingreasonable supportfordisabledapplicants in our recruiting process.Shouldyouneedassistance, andarecomfortabletosharethis, please let us know. About dsm-firmenich As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the world's growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet dsm-firmenich is a Swiss-Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than 12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to life every day, everywhere, for billions of people.

Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R and D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services-from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)-in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology and In-vitro ADME Medicinal Chemistry Synthetic and Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world's leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com ;;;;; ; The Position Organization; : - Jubilant Biosys Designation and Level: - SRA Location: - Greater Noida Department: - Analytical Key Responsibilities Having exposure of 1-8y in analytical chemistry (SFC or purification) Interaction with synthetic team and problem solving skills. Should be able to handle the respective instrument Knowledge of instrumental technique with its application Should be able to handle routine analysis independently on respective instrument . SFC: Support analytical chiral method development, chiral purification in SFC/Normal Phase. Maintain TAT as per target. Periodic maintenance, calibration of SFC instruments, completing documentation on time, performing additional analysis (chiral screening) when required. Candidate requirements: . ;;;; Educational qualification: Post Graduate Degree in Chemical/Life Sciences - M. Pharm, M. Sc., . ;;;; Technical Knowledge: ; Person Profile Qualification: - M. Sc (Analytical Chemistry) Experience: - 2 years of relevant experience Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

Role & responsibilities Provide Support to routine analysis of API Synthesis R&D and Stability samples. Documentation of Daily analysis in corresponding product LNB. Development of analytical methods for drug substances, raw materials and intermediates. Perform AMV, AMDR, AMT activities. Preparation of Analytical method validation / AMT protocol & report. Preparation of Tentative STP/MOA during Development. Trouble shooting at the time instrument operation and analytical method related problem. Preparation of COA, MOA and provide to LIMS. HPLC and GC Calibration and Documentation and provide GLP for the same. Prepare method development report. Analytical method transfers and Documentary Methods Transferring new analytical techniques to Quality control. Development and validation of cleaning method for drug substance

Dear Applicants, Greetings from Biophore India !! We have opening for Formulation AR&D Department. Experience : 3 7 Years Qualification : B. Pharm /M. Pharm or M Sc Work Location: R&D Centre -Pashamylaram, Isnapur, Sanga Reddy. Job Description 1) Method Development and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity. 2) Responsible for Analytical Method Validation activities for solid orals and injectables. 3) Responsible for Routine and Stability analysis activities for solid orals and injectables. 4)Responsible for the Review of documents generated in Method development activity. 5)Responsible for the Preparation and Review of Tentative method of analysis and Method development Reports. Please Carry below documents: 1. Updated resume. 2. Last 3 months pay slips or bank statement 3. Offer letter or Increment letter from the present employer,4. Photocopies of all Education certificates Ref to Friends or colleagues. Contact Person- Prasad- HR Interview Date: 13 -09-2025 (Saturday) Time:9:30AM 2:00 PM

You will be responsible for ensuring the smooth operation of laboratory equipment and implementing the laboratory quality policy and objectives. This includes selecting, approving, and commissioning appropriate test methods based on customer requirements, as well as allocating samples to analysts/Microbiologists for analysis. You will also need to ensure that the laboratory has the necessary resources and capabilities to meet customer requirements. Your role will involve supervising the testing activities of analysts/Microbiologists, guiding them during testing, and verifying the results and calculations submitted by them. You will assist the Quality Manager in the QA program, ensuring the quality of results through various checks, including Proficiency Testing and Inter-laboratory testing programs. Additionally, you will be responsible for verifying in-house calibration and performance checks conducted by analysts/Microbiologists, reporting any discrepancies to the Quality Manager. You will review test reports, provide opinions and interpretations before signing off on them, and provide training to new analysts, Microbiologists, sampling persons, and attendants. Furthermore, you will identify training needs for analysts/Microbiologists, coordinate with the Quality Manager to arrange training, and authorize junior staff after successful training and demonstrated competence in specific types of testing. You will evaluate the competency of new analysts/Microbiologists, coordinate with the Quality Manager on external equipment calibration, and assist in risk analysis. You will also be responsible for coordinating with the Quality Department on any complaints, non-conforming work, and corrective actions. Additionally, you will review records of cultures and their intermediate checks, identify requirements for new cultures/equipment/media procurement, develop, modify, and validate methods, and provide statements of conformity or opinions in test reports. Moreover, you will review and authorize test results, prepare and update master STP for LIMS Software, calculate UM for parameters within the scope, and provide remarks on "additions to, deviations, or exclusions from the method" in the test report as applicable.,

Company Description Dravya Analytical Solution LLP specializes in providing comprehensive quality services to the pharmaceutical industry. Our lab is NABL Accrediated and FDCA Approved. Our experienced team of scientists employs the latest technologies to ensure the quality and safety of your products. From raw material testing to finished product testing, our laboratory is equipped to handle all your testing needs. We also offer analytical services to support method development and validation, regulatory filing, and stability studies. Our commitment to excellence ensures that you can trust the results of your products. Role Description This is a full-time on-site role for a QC Manager located in Ahmedabad. The QC Manager will be responsible for supervising and managing the quality control processes in the laboratory. Day-to-day tasks include overseeing raw material and finished product testing, ensuring compliance with regulatory standards, coordinating with the analytical team for method development and validation, and managing stability studies. The QC Manager will also be responsible for maintaining documentation, preparing reports, and ensuring the overall quality and safety of the products tested. Qualification Experience in managing quality control processes and laboratory operations Knowledge of raw material and finished product testing Familiarity with regulatory standards and compliance requirements Skills in method development, validation, and stability studies Excellent organizational and documentation skills Strong leadership and communication abilities Bachelor&aposs or Master&aposs degree in Pharmaceutical Sciences, Chemistry, or related field Experience in the pharmaceutical industry is a plus Show more Show less

Adobe Systems India Pvt. Ltd. is looking for Computer Scientist 1 (C++) to join our dynamic team and embark on a rewarding career journey Conduct research and development in computer science. Develop and implement computer algorithms and systems. Collaborate with computer science and engineering teams. Monitor and report on computer science performance. Ensure compliance with computer science standards and protocols. Provide support and guidance on computer science matters.

NOTE: Only Male & Candidates from AP & Telangana Preferred. Kindly Understand the JD It's not for the Clinical Trails Department 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Qualifications required: Bachelors / Masters (0-4 yrs. experience) degree level in biological/ life science, pharmacy qualification. Role and responsibility: In process quality control of ongoing studies. Review of raw data, chromatograms and reports of the method validations and studies. Checking of all the instruments and equipments for the calibration status and appropriate labeling. Checking and monitoring of the day-to-day activities in the lab for compliance to SOPs and GLP principles. Checking of the concentration data of subject samples before releasing to PK department. Generation, control and distribution of method SOPs. Logbook handling and archival of the completed logbooks. Performing the routine glassware validations and monitoring of the temperature and humidity in the Bio-analytical lab. Calibration of pipettes and multipedes. Coordinating for training programs on SOPs. Ensure cleanliness of laboratory and disposal of non-bio-waste & Bio-waste.

You should have a minimum of 2 years to a maximum of 6 years of experience in the field. Proficiency in working with Analytical instruments like HPLC and GC is required. Your responsibilities will include routine analysis and method development.,

You will be joining a company committed to delivering high-quality pharmaceutical products and services, with a mission to enhance the quality of life through innovative healthcare solutions. The culture at Zydus revolves around collaboration, integrity, and excellence. As the ADL - Analytical Development Laboratory Executive/Senior Executive, your primary responsibility will involve method development, verification, and validation to ensure compliance with Pharmacopeial standards. You will also support various analytical activities within the department. Your key responsibilities will include method development, verification, and validation for Pharmacopeial standards, DMF updations, and other requirements within the department. Additionally, you will be involved in calibration and other analytical activities such as Engineering Batch and F&D Batch. You may also provide on-site or off-site support to Site-QCs for investigations or analysis. Evaluation and analysis related to Elemental Impurities and Nitrosamine Impurities Compliance, stability sample management, and coordination for resolving IT, Electrical, Civil, and other lab instruments breakdown issues will be part of your duties. Qualifications required for this role include a degree in B. Pharm / M.Sc. / M. Pharm with a minimum of 3-5 years of experience. You should possess skills in Method Development, Method Validation, and Method Transfer for Drug Substances and Drug Products. Additionally, you should be proficient in evaluating, analyzing, and preparing reports for Elemental Impurities compliance in Excipients, Drug Substances, and Drug Products. Experience with advanced analytical techniques and regulatory compliance is a preferred skill for this position. Zydus is an equal opportunity employer that values diversity and is dedicated to fostering an inclusive environment for all employees.,

The job involves carrying out the complete maintenance of all instruments such as HPLC, pH meter, weighing balances, etc. It includes method development for non-pharmacopoeial and pharmacopoeial analysis of raw materials, formulations of pharmaceutical, ayurvedic, and food products. Regular analysis of raw materials, finished products, and intermediates of JP, JSRF, JIPL, and outsourced products is also part of the job description. Additionally, the analysis of stability samples of JP products, JSRF products, and outsourced products is required. The responsibilities also include maintaining spares required for the HVAC system and utility equipment, as well as carrying out validation and calibration for the instruments. Addressing complaints and troubleshooting problems related to product analysis, preparing standard operating and calibrating procedures for all equipment used in the instrument lab, and maintaining calibration records are essential tasks. Maintaining the cleanliness of the lab in coordination with the housekeeping department, controlling samples of received batches, and maintaining records are part of the job. Coordinating with the Quality Control department through the GM of R&D for timely analysis and report maintenance is also required. Any samples from any department and reports issued to other departments should go through the GM of R&D. Furthermore, the job involves respecting and following company policies and rules, undertaking cost reduction projects related to analysis, and preparing SOPs and other related documents. Other assigned tasks as needed by the department should also be undertaken. Interested candidates are requested to send their updated resume/CV with a photo to careers@jagdale.com.,

The job involves preparing and analyzing samples from various sources in order to provide information on compounds or quantities of compounds present. This includes using analytical techniques and instrumentation such as gas chromatography (GC), high performance liquid chromatography (HPLC), and spectroscopy (ultraviolet) to investigate chemical compositions. Additionally, wet analysis will be performed. The responsibilities also include interpreting data, reviewing and evaluating experiments and analyses, and presenting scientific results to relevant teams. The role requires the development of new HPLC and GC methods, as well as collaborating with cross-functional teams. Staying up to date with the latest scientific and technical trends is essential, as well as validating methods and equipment. This is a full-time position that offers a performance bonus and yearly bonus. The work location is in person.,

You will be responsible for performing microbiological analysis, media inventory, and culture maintenance. This includes executing microbiological method development, method validation, and method verification. In addition, you will be required to perform qualification and calibration of instruments and equipment. It is essential to ensure concurrent documentation of analysis to maintain accurate records. Furthermore, you will be responsible for water sampling and testing to ensure compliance with regulatory standards. Your attention to detail and precision in executing these tasks will be crucial for the successful completion of your responsibilities.,

Role & responsibilities Method development : HPLC/GC Stability study Wet chemistry analysis (UV, IR, SOR, Titration...etc) Reaction monitor Routine support GLP awareness

Job Summary: We are seeking a motivated and detail-oriented fresher to join our Analytical Chemistry team focused on small molecule analysis. The role involves working with advanced analytical instruments and supporting the development, validation, and quality testing of small molecule compounds in a pharmaceutical or chemical environment. Key Responsibilities: Assist in the analysis of small molecules using techniques such as NMR, HPLC, GC, UV, IR, and dissolution testing Prepare analytical test reports and maintain laboratory documentation in compliance with GLP/GMP guidelines Support method development and routine analysis under supervision Calibrate and maintain analytical instruments according to SOPs Follow safety protocols and ensure proper handling of chemicals and laboratory equipment Perform sample preparation, standardization, and solution preparations Assist in stability studies and impurity profiling of Compounds Participate in internal audits and regulatory inspections as needed Required Skills & Knowledge: Basic knowledge of analytical chemistry techniques such as NMR, HPLC, GC, UV-Vis, FTIR Understanding of small molecule behavior and common analytical challenges Familiarity with analytical documentation Good laboratory practices and attention to detail Willingness to learn and adapt in a fast-paced laboratory environment What We Offer: Hands-on training in modern analytical techniques and instrumentation Opportunity to work on real-time R&D and QC projects Exposure to regulatory and quality systems in a pharma/chemical setting A collaborative and learning-focused environment for career growth.

Job Summary: The Lab Technician is responsible for performing routine and specialized laboratory tests, preparing samples, maintaining lab equipment, and ensuring the accuracy and reliability of test results. This role supports research, development, quality control, or clinical analysis activities within the laboratory. Key Responsibilities: Collect, prepare, and analyze samples according to standard operating procedures (SOPs). Perform routine laboratory tests and record results accurately. Calibrate, maintain, and clean laboratory equipment and instruments. Maintain laboratory inventory, including reagents, supplies, and equipment. Ensure adherence to safety protocols and maintain a clean and organized workspace. Assist in documenting test procedures and results for reports. Troubleshoot and report any technical issues or discrepancies. Support research and development projects by providing technical assistance. Follow quality control and quality assurance procedures to maintain lab standards. Comply with all relevant regulatory and safety standards.