29 Sample Analysis Jobs

Job Overview: As a Microbiologist at our organization, you will be responsible for conducting research, experiments, and analysis within the fields of microbiology, water technology, and environmental science. Your role will involve collaborating on R&D projects, devising innovative solutions, analyzing data, and working closely with internal teams and external partners. It is essential to ensure compliance with scientific standards while contributing to the advancement of the organization's research objectives. Job Description: In this role, you will be expected to: - Execute scientific research and experiments in the microbiology field. - Develop new processes and technologies related to water, wastewater, and environmental applications. - Analyze and interpret data, and prepare comprehensive reports and presentations. - Collaborate effectively with cross-functional teams and external stakeholders. - Ensure that the laboratory complies with quality and safety standards such as NABL and ISO 17025. - Act as an authorized signatory for NABL reports. - Stay abreast of advancements in the field and integrate new technologies for continuous improvement. Key Qualifications: - Hold a Master's degree in microbiology, Environmental Science, or a related field. - Possess at least 5 years of experience in scientific research within the microbiology domain. - Demonstrate strong analytical, problem-solving, and data interpretation skills. - Proficient in the use of microbial lab equipment, research tools, and data analysis software. - Exhibit excellent communication and teamwork abilities. - Have knowledge of Microbial Test methods of APHA/BIS/BAM/ISO. - Skilled and experienced in testing water and wastewater samples. - Must be an NABL approved Authorized signatory for microbiology scope. - Capable of method development, validation, and evaluation of measurement uncertainty following International Standards. - Conduct sample analysis of water, wastewater, and sludge samples and coordinate with R&D projects. - Perform method verification and measurement uncertainty assessment. - Conduct critical consumables evaluation, media quality checks, and culture handling. - Monitor environmental parameters and instruments for calibration, breakdowns, and maintenance. - Handle ILC/PT raw data and calculations efficiently. - Develop documentation and systems in line with the Quality Management System per ISO/IEC 17025:2017.,

As a part of this role, you will be responsible for sample preparation, daily calibration, and the maintenance of equipment, including keeping a detailed log of all activities. You will also be involved in method development, method validation, and conducting sample analysis in accordance with ICH M10 guidelines. Operating, maintaining, and calibrating LCMS equipment will be a crucial part of your responsibilities. In addition, you will be required to adhere to documentation procedures as outlined in Bio analytical SOPs and ICH M10 guidelines. This will involve thorough record-keeping and ensuring all documentation is accurate and up to date. Furthermore, you will be expected to review data and reports to ensure quality and compliance with relevant standards. Your attention to detail, ability to follow guidelines meticulously, and commitment to maintaining accurate records will be essential for success in this role. If you are looking for a position that offers diverse responsibilities in a dynamic environment, this opportunity may be the perfect fit for you.,

As an Associate Quality Control at RADICI PLASTICS INDIA PVT LTD, you play a crucial role in ensuring the quality of production grades through meticulous online testing, sample analysis, and strict adherence to Quality Management System (QMS) protocols. Your responsibilities include maintaining and validating lab equipment, reducing QC setup time, minimizing production trials, and supporting continuous improvement initiatives. Additionally, you will oversee product audits, equipment calibration, and lab safety, while collaborating with cross-functional teams to enhance quality and streamline product development processes. Reporting directly to the Quality Control Manager, you will be responsible for various tasks, including but not limited to: - Ensuring the quality of grades/batches in the main production line - Performing online testing and coordinating in case of discrepancies in expected versus actual quality - Documenting testing and related activities in compliance with QMS - Conducting online sample analysis and composite sample analysis for all production grades - Contributing to reducing setup time and production trials through technical knowledge utilization - Minimizing B-grade generation in alignment with organizational targets - Validating laboratory equipment and ensuring equipment calibration - Conducting process and product audits as per the schedule - Ensuring compliance with safety regulations during all activities - Enhancing lab performance through safety improvements, Kaizen initiatives, and continuous improvement suggestions - Handling and maintaining lab equipment in optimal condition - Coordinating spare parts for lab equipment and validating equipment as per the schedule Your technical knowledge should encompass polymer compounding processes, materials, polymer testing methods, laboratory equipment, instrumentation, and understanding of Quality Management Systems. Effective communication skills, both written and verbal, are essential for this role. Job Requirements: - Diploma/B.Sc with CIPET/B-Tech/M.Sc in Polymer/Chemical - Previous experience in the plastics sector and compound - Minimum of 2 years of relevant experience This position is based in Halol, Gujarat. Join us at RADICI PLASTICS INDIA PVT LTD to make a significant impact on the quality control processes and contribute to the success of our high-performance polymers business.,

Senior Chemist with 4–5 yrs exp. in lab testing, QC of Ferro Vanadium, Moly Vanadium & CPC. Graduate/PG in Chemistry or B.E/B.Tech Metallurgy. Male/local candidates preferred. Location: Delari, Raigarh. Required Candidate profile Graduate/PG in Chemistry or B.E/B.Tech Metallurgy with 4–5 yrs exp. in lab testing, QC, and material analysis. Must know Ferro Vanadium, Moly Vanadium, CPC. Local male candidates preferred.

The Contract & Proposal (C&P) professional will be responsible for managing the end-to-end process of drafting, negotiating, and finalizing proposals and contracts related to bioanalytical services. This role bridges scientific understanding with commercial acumen, ensuring timely, compliant, and competitive proposals are delivered to clients and sponsors in alignment with business objectives. You will collaborate with Business Development, Project Management, and Scientific teams to understand client requirements and scope of work. Your responsibilities will include preparing detailed technical and commercial proposals for bioanalytical services such as PK/PD studies, method development & validation, and sample analysis. Additionally, you will coordinate internal costing exercises and build accurate pricing models based on resource and timeline inputs. In this role, you will draft, negotiate, and finalize various contract types (e.g., MSA, CDA, SOW, Work Orders) with clients. You will review RFPs and RFIs, and prepare responses ensuring compliance with client guidelines and internal standards. Maintaining a database of approved proposal templates, standard pricing modules, and contract clauses will also be part of your duties. Tracking proposal status, feedback, negotiations, and closure timelines in coordination with BD, as well as supporting audit and compliance documentation related to contracts and pricing, are crucial aspects of this role. Ensuring alignment with regulatory requirements (GLP/GCP), industry standards, and corporate policies in all documentation is essential. Building strong relationships with external sponsors and internal cross-functional teams is key to success in this role. Required Qualifications: - Bachelors or Masters degree in Life Sciences, Pharmacy, Chemistry, or related field. - 2-7 years of experience in C&P or Proposal Development roles in a Bioanalytical or Clinical CRO. - Strong understanding of bioanalytical lab services, GLP/GCP compliance, and clinical study structures. - Proficiency in MS Excel, Word, and PowerPoint; experience with CRM tools is a plus. - Excellent communication, negotiation, and writing skills. - Detail-oriented with strong analytical and time management skills. Preferred Attributes: - Experience dealing with international clients (US/EU/APAC) in a regulated environment. - Ability to manage multiple proposals simultaneously with tight deadlines. - Familiarity with regulatory frameworks (USFDA, EMA, DCGI) relevant to bioanalytical studies.,

Key areas: Perform microbiological testing of raw materials, in-process samples, and finished products Perform hygiene auditing of the Feed plants and suggest procedures to maintain hygienic conditions in the plant. Maintain accurate records of all tests and analyses Adhere to all safety and quality control procedures relevant to Feed and food production system. Provide a cost effective and quality Laboratory Service to GAVL Are you the one? This is a busy role with plenty of responsibility, so youll need to possess strong attention to detail and high levels of accuracy to succeed. We are looking for a strong team player who can multi-task with ease and will be comfortable managing high volumes of work. You’ll also be confident to speak up if something isn’t working or doesn’t seem right. Key areas: Qualification in Microbiology or related field desired Previous experience in laboratory is preferred. Excellent attention to detail and organizational skills. Ability to work effectively in a team environment Ability to work autonomously and manage your own workflow Passionate about promoting a culture of customer focus, empowerment, teamwork, open communication, safety, and quality within the laboratory department.

The job is based in Hyderabad and is suitable for freshers. Qualifications required are B.Pharm / M.Sc. / M.Pharm. Preferred skills include good communication and analytical skills, as well as the ability to work well in a team in order to complete tasks in a timely manner. The detailed responsibilities of the role include bioanalytical sample preparation using various extraction techniques, conducting method development, method validation, and sample analysis in accordance with regulatory requirements, operating laboratory equipment such as pipettes, centrifuges, evaporators, and extractors, as well as handling data generation, compilation, and reporting of results.,

Study Analyst Roles and Responsibilities:- General extraction procedures and instrument analysis of drugs in biological fluids. STUDY RELATED ACTIVITIES:- A. Perform the extraction of samples using wet chemistry. B. Centrifuges, evaporators, freeze specimens as required. C. Performs aliquots of samples for wet chemistry. D. Performs wet chemistry according to study protocol guidelines and/or SOPs. E. Completes QC sheets and makes log book entries as required by protocol and/or SOP. F. Operate HPLC, LC/MS/MS and ICP-OES; troubleshoots problems and performs minor repairs. GENERAL LAB DUTIES:- A. Prepares required reagents and solvents. B. Under direction of the project manager, may perform some method development. ADMINISTRATIVE DUTIES:- A. Confirm to training schedule for own position and maintains awareness of SOP content, according to company requirements. Skills & Abilities:- Demonstrate ability to pipette accurately. Knowledge of all basic wet chemistry instrumentation such as centrifuge, vortex, pH meter, evaporator, etc.

Unison Pharmaceuticals is urgently seeking talented Analytical Development Lab - Routine Analysts for OSD R&D team. Apply now to become a part of a growing team!! Experience: 2 to 5 years Job Role: ADL - Sample Analyst Markets: Domestic & Regulatory both Designation: Officer / Sr. Officer Location: Moraiya, Ahmedabad (Transportation is available from specific routes of Ahmedabad) No. of vacancies: 02 Roles and Responsibilities : Perform chemical, physicochemical and wet analysis as per product requirements. Routine In-process, Finished product (Initial & Stability samples) analysis. Data reporting with good documentation practice and presenting results in informative report format Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen Facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position. Interested one can share updated resume on career@unisonpharmaceuticals.com to be considered for this role. Join our team and take the first step towards a rewarding career!! Regards, Team HR Unison Pharmaceuticals Pvt Ltd

Job Title : Study Director - Pharmacokinetics and Immunogenicity Assays Job Location: Bangalore Department: Immunogenicity Research Laboratory - Translational & Clinical Research Job Purpose: The position holder is responsible for performing bioanalysis which includes performing ligand binding assays related to Pharmacokinetics and Immunogenicity. Key Responsibilities: Ensure activities conducted in the bioanalytical lab are in compliance with established SOPs, procedures, systems, regulatory guidance without deviating from established procedures. Regular interaction and participation with Study director, Quality Control (QC) and Quality Assurance (QA) during raw data and reports review, closure of observations and archival. Will be involved in strategic planning for project execution, documentation of data, data analysis, interpretation and presentation of the results • Ensure to complete the assigned tasks in timely manner. Actively involved in preparation of SOPs, protocols, method and reports Prepare reagents, buffers and maintain log book for assigned assays Interpret results - anticipate and understand the issues related to the assay. Participate in, and present data for discussions. Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Attend training on environment, health, and safety (EHS) measures imparted company Educational Qualification: Master's degree or Ph.D in Biological Sciences (Preferably Biochemistry background) or a related field Technical/functional Skills: Should have a strong background in immunoassay and bioanalytical Pharmacokinetics and Immunogenicity Assays with a good understanding as per regulatory guidance/ industry practices/internal Standard Operating Protocols. Should have hands-on experience in Ligand Binding Assay (LBA) development, validation and Sample analysis. Knowledge of ELISA and MSD assays are highly desirable. Knowledge and experience with regulatory requirements e.g. Organization for Economic Co-operation and Development (OECD), GXP, 21 CFR Part 11, European Medicines Agency (EMA) and Food and Drug Administration (FDA) guidelines. • Manuscript writing ability is preferable Proficiency in software like Laboratory Information Management System (LIMS), GraphPad, Adobe etc. Experience: 7+ years of experience in immunoassay laboratory. (CRO experience is preferable). Behavioral Skills: Ability to work independently as well as with team members A strong proactive and independent thinker • Excellent communication skills - written and oral in English Should have good interpersonal skills Large degree of flexibility and ability to work under strong time pressure 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.

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.

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.

Post:- Lab Technician Qualification- B.sc/M.Sc- Chemistry Experience:- 1-3 Years Job Location- Bahadurgarh(HR) No. of Vacancy:- 2 No Job Description:- Must have hands on experience on different type of analytical instruments like HPLC, GC, Titrator & Others, Maintaining Day to Day Testing Records & Must have working experience in Oil testing/Pharmaceutical Lab Receive, label and analyze samples, Design and execute laboratory testing according standard procedures, make observations and interpret findings, ,Organize and store all chemicals substances, fluids and compressed gases according to safety instructions, Record all data and results in specified forms (paper and electronic) with accuracy and responsibility Maintain equipment and assist in ordering laboratory supplies, Ensure that all safety guidelines are followed strictly at all times and maintain a clean and orderly environment ,Perform routine and non- routine tests and analyses using the appropriate technical equipment and instruments, Receive or collect, as well as process, samples Calculate test results, and log and report results using a computer/Manual calculations, Prepare and supervise experiments ,Perform quality control and calibrate equipment if necessary ,Maintain equipment in proper working order and maintain a clean work area ,Practice safe work habits, including complying with all safety, health, and environmental rules and regulations

We are seeking a skilled and detail-oriented Lab Technician to join our team. The successful candidate will be responsible for conducting tests, analyzing samples, and maintaining laboratory equipment. The ideal candidate will have a strong background in laboratory procedures and protocols, excellent analytical skills, and the ability to work accurately in a fast-paced environment. Conduct laboratory tests and analyses on samples - Maintain and calibrate laboratory equipment - Prepare and store samples for testing - Record and report test results accurately - Follow laboratory protocols and procedures - Maintain a clean and safe working environment - Collaborate with other lab staff to achieve goals.

Role & responsibilities Primary Responsibilities: 1. Performance of Method Development, Validation and Study Sample Analysis using LC-MS/MS systems. 2. Operation, Calibrations and Maintenance of Pipettes, pH meter, Balance, HPLC, Dispensers and Turbo-Evaporators, Centrifuge, Solid-Phase Extraction, and other Bioanalytical equipment. 3.Preparation of Method Validation Protocols, Method Validation Reports, Standard Test Procedures, SOPs, and Bioanalytical Reports. 4. Responsible for documentation as per in house SOPs and practices in raw data forms and logbooks. 5. Compilation of Calibration Data, Bio analytical raw data forms and logbooks. 6. Maintenance of Workplace. 7. Reporting to supervisor/HOD about progress of the jobs assigned. 8. Follow in-house procedures for safe disposal of waste generated in the lab. 9. Recording the temperature and humidity in the lab. 10. To ensure all applicable SOPs are complied with for the work being done. 11. To ensure that raw data and other documents are recorded appropriately reflecting the actual sequence of events. 12. To ensure that all the results are being transcribed, reported, and calculated appropriately matching with chromatographic data and raw data. 13. Maintain cleanliness and safety aspects in the Lab. 14. To ensure proper labeling for all the reagents, solutions, and chemicals in the laboratory. 15. Ensure the archival of all completed study and validated documents. Secondary Responsibilities: 1. Maintenance of Columns and Reference Standards in the lab. 2. Any other responsibilities assigned by HOD. Preferred candidate profile Qualification : M.Pharmacy / MSc Chemistry Experience : 1-6 Yrs in Clinical Research - Bioanalytical

Role & responsibilities- Conduct analysis of samples using HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Providing Technical support for internal and external stake holders Being the clear R&D player by working closely with cross-functional teams to drive execution across multiple projects while maintaining and achieving timelines to ensure speed to market. To conduct analysis of samples and provide inputs to R&D/QC teams Required Skill Sets: Hands on experience on HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Experience in analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Fair understanding of ISO/IEC 17025, ISO 9001, ISO14001, ISO 22000, ISO18001 Lab safety & GLP management

Role & responsibilities Development and validation of bioanalytical methods using LCMS and other sophisticated instruments. Routine calibration of the instruments. Strong basic knowledge about Analytical instruments of LCMS, HPLC, HPTLC, GC-MS and other instruments. Good understanding of GLP and documents thereof. Knowledge of USFDA guidelines. Excellent communication skills & co-ordination among all the team members. Should possess good interpersonal and management skills Accountable for the whole group productivity in terms of number of samples, analysis, quality, quantity timelines better Turn Around Time (TAT) improvement Preferred candidate profile The candidate should have 1-3 years of experience in Bioanalytical Lab.

Key Responsibilities: Develop and validate analytical methods using HPLC, UV, IR, and GC. Prepare protocols and reports for method development and validation. Perform stability studies and sample analysis for new products. Maintain instruments and lab notebooks as per SOPs and GMP guidelines. Coordinate with formulation development and QA teams. Requirements: M.Sc. / B.Pharm / M.Pharm in Chemistry/Pharmaceutical Sciences. Knowledge of ICH guidelines and regulatory documentation. Hands-on experience with chromatographic techniques and software. Analytical Method Development of Assay, Related Substances, Residual Solvents & Dissolution Test Methods with Literature Search & Report.

Role & responsibilities Company : RSPL Group is more than 6,000 Cr diversified conglomerate, which is committed to value for money propositions & credited with several innovations over last 3 decades. The sagacity to weave its business around consumer needs has conferred RSPL Group with a distinct value and identity. Efficient capital structure, cutting edge technology, operational discipline and a widespread distribution network, have together attributed to enhance RSPL Group and enabled the organization to deliver value to consumers. Diversified Group having product category in FMCG, Dairy Products, Hygiene Care, Foot wear, Real Estate, Renewable Energy. This position belongs to HCD Vertical Job Responsibilities: 1) Lead overall raw materials, lab process for the prototype lab. 2) Perform the validation tests for the SOPs for the prototype lab, for both Sannap and Diaper. 3) Regularly evaluate new technologies which can be inculcated in the current prototype lab setup. 4) Responsible for the preventive maintenance, calibration and proper functioning of the prototype lab machines. 5) Responsible for the production of prototype samples for both sannap and diaper as and when required. 6) Maintain expertise in the prototype lab function and train the new resources on the same. 7) Responsible for the product lab performance evaluation for the prototype samples and the commercial products for comparison. This position belongs to HCD vertical. Number of positions : 1 Job Location- Kasna Industrial Area, Greater Noida Office Timings- 09:30 am to 06:00 pm 2nd & 4th Saturday are off. Education : B.Sc.- Chemistry (Mandatory) Full Time Contact HR: Ms. Nancy Goyal Email- nancy.goyal@rsplgroup.com

Role & responsibilities Company : RSPL Group is more than 6,000 Cr diversified conglomerate, which is committed to value for money propositions & credited with several innovations over last 3 decades. The sagacity to weave its business around consumer needs has conferred RSPL Group with a distinct value and identity. Efficient capital structure, cutting edge technology, operational discipline and a widespread distribution network, have together attributed to enhance RSPL Group and enabled the organization to deliver value to consumers. Diversified Group having product category in FMCG, Dairy Products, Hygiene Care, Foot wear, Real Estate, Renewable Energy. This position belongs to HCD Vertical Job Responsibilities: 1) Lead overall raw materials, product lab tests process and the present the results in a right format and time. 2) Perform the validation tests for new test methods. 3) Regularly evaluate market samples and maintain proper records for the same. 4) Responsible for the preventive maintenance, calibration and proper functioning of the lab equipment. 5) Document knowledge, make the clear report and maintain the security of the result as required by RSPL policy. 6) Maintain expertise in at least one area of the company's technology as a Researcher for Feminine Care products. 7) Skillful handling of critical lab test equipment especially for those of Sanitary Napkin testing and evaluation. 8) Experience into pulp, paper & Non- woven. Number of positions : 1 Job Location- Kasna Industrial Area, Greater Noida Office Timings- 09:30 am to 06:00 pm 2nd & 4th Saturday are off. Contact HR: Ms. Nancy Goyal Email- nancy.goyal@rsplgroup.com

Strong Online Testing & Analysis knowledge Strong Sampling & Methodology knowledge Instrument Calibration & Validation Documentation & Label Method Development & Validation Strong SOP & QMS Compliance Candidates from Herbal/Phyto industry is required

Job Role: QC Assistant Job Location: Jaipur Education: BSC / MSC Experience: 1-2 Years About Brand: Minimalist (https://www.beminimalist.co) is a science-backed Indian skincare brand built on the core values of efficacy, transparency, and comprehensiveness. Known for its ingredient-first approach, the brand formulates high-performance skincare products using proven activities and clean formulations. The company believes in creating high-quality products using best-in-class ingredients at its own manufacturing facility. Minimalist empowers consumers with knowledgeclearly stating what goes into each product and whyso they can make informed choices. With a commitment to 'Hide Nothing,' the brand champions authenticity and honesty in skincare, creating solutions that work, without the fluff. With a robust portfolio of 60+ SKUs spanning Skincare, Haircare, and Bodycare, the brand is rapidly expanding its footprint. Focused on enhancing product availability, it is strategically deepening its penetration while strengthening both Modern Trade (MT) and General Trade (GT) channels in India. The brands global presence now extends across 15+ countries, including key markets such as the UK, USA, UAE, Malaysia, Indonesia, Germany, France & Italy. Roles and Responsibilities: Assist in the collection, labeling, and preparation of samples for analysis. Ensure proper storage and documentation of samples to maintain traceability. Perform regular cleaning and sterilization of laboratory equipment and workspaces. Dispose of waste materials following established safety protocols. Prepare reagents and solutions as per standard operating procedures (SOPs). Monitor inventory levels and assist in ordering laboratory supplies. Calibrate and maintain laboratory instruments to ensure accurate results. Maintain accurate records of all QC activities, including test results and equipment maintenance logs. Adhere to all laboratory safety guidelines and regulatory requirements. Qualifications: Bachelors degree in Microbiology, Chemistry, Biotechnology, or a related field. Minimum of 1-2 years of experience in a laboratory setting, preferably in quality control. Familiarity with laboratory equipment and basic analytical techniques. Strong organizational skills and attention to detail. Proficiency in using laboratory information management systems (LIMS) is a plus. Excellent communication skills and the ability to work collaboratively in a team environment.

We are seeking a skilled and detail-oriented Technician - Laboratory to join our team in India. The ideal candidate will have 1-7 years of experience in a laboratory environment and will be responsible for conducting experiments, analyzing samples, and maintaining laboratory equipment. RESPONSIBILITIES Prepare and analyze samples using laboratory equipment and techniques. Maintain laboratory equipment and ensure it is calibrated and functioning properly. Perform routine quality control checks on laboratory tests and results. Document and report laboratory findings in accordance with standard operating procedures. Assist in the development and validation of laboratory methods and procedures. Ensure compliance with safety regulations and maintain a clean laboratory environment. Collaborate with team members and other departments to support research and development activities. Skills and Qualifications Bachelor's degree in Biology, Chemistry, or a related field. 1-7 years of experience in a laboratory setting, preferably in a clinical or research laboratory. Proficient in laboratory techniques such as pipetting, centrifugation, and spectrophotometry. Familiarity with laboratory safety protocols and good laboratory practices (GLP). Strong analytical and problem-solving skills. Excellent attention to detail and ability to work independently or as part of a team. Effective communication skills, both written and verbal.

Responsible to prepare analytical method development, development validation, method transfer protocol and reports. Perform F&D Trial sample analysis, Wet analysis and stability sample analysis with proper data complication. Operation of machine and instrument like HPLC(Make = Shimadzu,Thermo Software =Chromeleon, Lab solution,LC Solution), UV spectrometer (Make = Shimadzu, Software = Lab Solution), IR (Make = Shimadzu, Software = Lab Solution) Dissolution apparatuses, Liquid partical counter and Karl fischer for water content. Perform instrument calibration as per respective SOP daily pH meter calibration and balance verification.

Role & responsibilities- Conduct analysis of samples using HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Providing Technical support for internal and external stake holders Being the clear R&D player by working closely with cross-functional teams to drive execution across multiple projects while maintaining and achieving timelines to ensure speed to market. To conduct analysis of samples and provide inputs to R&D/QC teams Required Skill Sets: Hands on experience on HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Experience in analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Fair understanding of ISO/IEC 17025, ISO 9001, ISO14001, ISO 22000, ISO18001 Lab safety & GLP management