1376 Hplc Jobs - Page 4

Key Accountabilities Accountability Cluster Major Activities / Tasks Develop new analytical methods for analysis of routine as well as stability samples by following proper GLPs to provide results or information regarding products to formulators Perform part method validation, forced degradation studies, excipient compatibility studies, reverse engineering, add-mixture studies, in-use studies, hold-time study and analysis of routine & stability studies Conduct cleaning validation studies Perform analysis of API, excipients and secondary material (packaging material, ink, adhesive etc.) Develop cost effective & time saving analytical method for new or existing product Evaluate the pharmacopeia and verify the documents Perform maintenance and calibration of lab instruments / equipment to get accurate and reproducible analytical result for proper interpretation Maintain the lab instruments / equipment and troubleshoot the issues Perform calibration (schedule / breakdown) and calculate instrument utilisation Up-keep the HPLC/GC/IC columns as per cGLP Document and interpret the analytical data in a timely manner as per GLP / GMP requirements to maintain records and compliance of regulatory norms Record and document all analytical activities in timely manner in Lab note-book, instrument/equipment and column log book Provide base documents for MOA / COA preparation for better coordination in analytical studies Provide support to units or CFTs for transfer of analytical methods and techniques by visiting and demonstrating them with the relevant analysis to ensure successful and timely transfer of products Transfer methods and technologies to other units and departments Study the literature to resolve units and regulatory queries and conduct investigation studies in stipulated time period Analyse samples at pilot plant and unit for trace determination (Cleaning Validation) Maintain proper safety, GLP, and GMP environment in the work place to minimize accidents and incidents Follow safety guidelines by ensuring use of PPE & MSDS of chemicals at time of analysis Upkeep the samples given for analysis and ensure timely destruction after analysis as per SOP Dispose solvents and waste generated during the analysis Review the analytical requirements and recommend corrections in specifications by coordinating with units and CFTs to ensure smooth operations Arrange analytical requirements like column, impurities, standards, placebo and samples for units and other department like Validation Lab or Outsourced Lab Review and recommend corrections in the MOA, COA & Specifications Major Challenges Delay in developing analytical method due to unavailability of HPLC/ GC columns, reference impurities and specific instruments. Overcome by prior planning and by using alternate resources Additional or rework due to frequent changes in project priorities. Overcome by proper planning Key Interactions Internal External Formulation R&D for improving the quality of product (Daily) Loan Licence Team for analytical requirements which has to be provided (Weekly) Units for execution of project in unit (Twice a week) CRO for outsource analysis, validation, verification, release etc. (Twice a week) Service Engineers for breakdown of equipment and instruments (Fortnightly) Dimensions Average number of projects : 8 (FY2016-17) Average number of analytical method developed : 10 (FY2015-16) Average number of part method validation : 7 (FY2015-16) Average number of method transfers / unit queries : 2 Average number of additional projects: 4 (e.g. CIP, CHC, POC, etc.) Average number of Tec Mar studies completed : 10 per year Average number of new monographs evaluated : 10 per year Key Decisions: Decisions Recommendations Finalisation of analytical method or any change in existing method to Group/Sub-Group Leader - Formulation ADL Comments: Skills & Knowledge Educational qualifications: M. Sc. (Analytical Chemistry) / M. Pharm. Relevant experience: 2-4 years of experience in pharmaceutical organisation with knowledge of handling instruments like HPLC, GC, Dissolution tester and DPI related instruments Knowledge of current guidelines like ICH, EMEA, WHO

1. Educational Qualification & Work Experience Preferred Qualification M.Sc. Chemistry / M. Pharm Preferred Years of Experience 3 - 7 yrs. Experience profile required We are seeking a highly skilled Analytical Scientist to join our Analytical development team. The ideal candidate will possess advanced expertise in analytical chemistry, with demonstrated proficiency in HPLC/UPLC, GC, IC, UV, FTIR, and related techniques. The candidate should have a deep understanding of cGMP, GDP, and regulatory standards, along with strong analytical thinking, problem-solving, and decision-making skills. This role requires the ability to manage multiple projects, prioritize tasks, and lead scientific initiatives. The Senior Analytical Scientist will play a pivotal role in advancing scientific excellence and operational effectiveness, contributing directly to the organization s scientific goals. 2. Job Role (Describe the primary purpose, objective and/or function of this job) Key Responsibilities: Design and execute experiments. Operate various analytical instruments (HPLC/UPLC, GC, IC, UV, FTIR etc.). Contributes to scientific problem-solving, analytical thinking, and decision-making. Drives innovation and scientific excellence in laboratory operations and projects. Leads scientific initiatives, manages projects, and prioritizes tasks for project teams. Acts as a pivotal influence in strategic decisions impacting the direction and success of project teams. 3. Job Description - Responsibilities & Duties (The personnel must be able to perform all of the following duties and responsibilities)) Manage laboratory activities with in-depth knowledge of daily operations and verify assigned tasks for accuracy and compliance. Demonstrate significant hands-on experience with analytical equipment such as HPLC/UPLC, GC, IC, UV, FTIR, and other advanced instruments. Possess a strong background in analytical method development, validation and transfer. Carry out peer reviews of colleagues work, ensuring scientific rigor and data integrity. Act as a technical resource and provide expert consultation within the work group or project team. Develop and implement novel processes or hypotheses, frequently using new ideas and knowledge to solve complex problems. Manage projects, prioritizing activities, evaluating resource use, and making insightful, timely decisions that may impact the entire work group or project team. Propose mitigation and contingency plans in anticipation of potential changes or risks within projects. Receive instructions primarily for unusual or complex problems; otherwise, perform activities under limited supervision with periodic review. Identify and devise initiatives, align action plans, and drive scientific activities/projects to support group or project team goals. Understand and apply industry-specific standards and regulations, including cGMP, Environmental, Health, and Safety guidelines. Work Location Assignment: On Premise Research and Development #LI-PFE

Key Responsibilities Drive sales of laboratory products, particularly microbiology and chromatography items, including HPLC/GC vials and columns. Build and maintain strong relationships with clients across the assigned territory. Conduct regular client visits to follow up on leads and ensure order closures. Consistently improve sales performance by nurturing both existing accounts and identifying new business opportunities. Travel extensively within Telangana to engage with customers and ensure satisfaction. Lead and mentor a team of field sales executives, providing direction and support. Track team performance, coach team members, and help achieve set sales targets. Work closely with senior management to plan and execute region-specific sales strategies. Desired Skills & Attributes Demonstrated ability to lead and manage sales teams effectively Strong interpersonal and communication skills A proactive and self-driven sales approach Capability to plan strategically and execute sales initiatives Flexibility and readiness to travel as required within the region Preferred Background: Experience with distribution networks or laboratory product sales will be an added advantage. Educational Qualifications B.Sc / M.Sc in Life Sciences (Microbiology, Biochemistry, Biotechnology, Chemistry) B.Pharm / M.Pharm / Pharm.D

Compilation and Review of all types of data of the products analyzed at each stage (RM, PM, FG, Stability and GLP documents). Responsible for Review of Calibration and Audit Trials Verification. Responsible for assuring all Laboratory activity are carried out in compliance with existing SOP. Responsible for Integration of HPLC and GC data and new Method Creation. Verification of chemicals, volumetric solutions and reagents in LIMS. Preparation of LIMS protocols for testing of RM,PM and FG Testing and release.

Walk In Drive For Quality Control Department In Formulation Division @ Burgula Department :- Quality Control Qualification :- BSC | B Pharmacy | MSC | M Pharmacy Experience :- 5 to 6 Years Interview Date:- 30-07-2025 Interview Time:- 9AM TO 2.00PM Work Location: - MSNF-VI,Burgula Venue Address:- X59Q+P95, Mothighanapur, Burgula, Telangana 509202 Note:- Candidate should bring Update Resume , Offer Letter, Increment Letter,CTC,Payslips ,Bank Statement, Certificates,Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Key Responsibilities: Analytical Method Development & Validation Develop and validate robust HPLC methods for characterization and quantification of biological products (e.g., monoclonal antibodies, recombinant proteins). Perform method optimization, robustness studies, and transfer protocols as per ICH guidelines. Routine & Stability Testing Conduct analysis of in-process, release, and stability samples using: HPLC/UPLC Capillary and Gel Electrophoresis UV spectrophotometric methods Host Cell DNA quantification (e.g., qPCR-based methods) HCP ELISA and other immunoassays Instrument Operation & Maintenance Perform routine maintenance, calibration, and troubleshooting of analytical instruments including HPLC, electrophoresis systems, spectrophotometers, and ELISA readers. Ensure timely qualification and performance verification of instruments. Documentation & Compliance Prepare and review SOPs, STPs, protocols, reports, and analytical records in compliance with regulatory requirements. Maintain accurate and complete documentation in laboratory notebooks and electronic systems. Quality & Regulatory Compliance Participate in internal and external audits, and support regulatory submissions with analytical data. Cross-functional Collaboration Work closely with R&D, Quality Control, and Regulatory Affairs teams to support product development and lifecycle management. Provide technical support during investigations, deviations, and CAPAs. Training & Development Train junior analysts and new team members on analytical techniques and laboratory practices. Stay updated with advancements in analytical technologies and regulatory expectations. Qualifications & Experience: M.Sc. / M.Tech / M.Pharm in Biotechnology, Biochemistry, or related life sciences discipline. 4 8 years of relevant experience in analytical development or QC of biopharmaceuticals. Hands-on experience with HPLC method development and ELISA based techniques. Familiarity with regulatory guidelines (ICH, FDA, EMA) and quality systems. Key Skills: Strong analytical and problem-solving skills Attention to detail and data integrity Excellent documentation and communication abilities Proficiency in software tools like Empower, Chromeleon, SoftMax Pro, etc. Ability to manage multiple projects and meet deadlines

Roles and Responsibilities Ensure compliance with GLP guidelines, including investigation of OOS/OOT events and vendor qualification. Maintain accurate records of GLP documents, instruments, and equipment through preventive maintenance schedules. Conduct calibrations on instruments according to CGMP requirements and perform spares management tasks. Implement LIMS system for effective inventory control and HPLC analysis. Perform CAPA activities as needed to resolve quality issues. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Organic Chemistry from a recognized university. Minimum 10-15 years of experience in pharmaceutical industry with expertise in GLP practices. Strong understanding of instrument calibration procedures under cGMP regulations. Proficiency in maintaining IQ, OQ, PQ documentation for laboratory equipment.

Its involve developing, validating, and implementing analytical methods for pharmaceutical products, ensuring compliance with quality and regulatory standards and require expertise in various analytical techniques like HPLC, GC, and spectrophotometry

1. Educational Qualification & Work Experience Preferred Qualification M. Pharm / M. Sc. Preferred Years of Experience 0 to 2 years Experience profile required We are seeking a highly motivated scientist to join our dynamic research team. The ideal candidate will hold M. Pharm / M. Sc (Chemistry) and possess extensive basic knowledge on modern analytical techniques. The incumbent preferred to have proficiency in handling of analytical techniques such as Spectroscopy (UV-Vis, FT-IR), Chromatography (HPLC) and other instruments (Potentiometric titrator, KF), etc. and have adequate interpretation skills. 2. Job Role Key Responsibilities: Analysis of raw material, In-Process and finished products. Generation of analytical data with respect to accuracy and adequacy. Preparation of reference, working and Impurity standards. To ensure timely completion of assigned Training Modules and Skill Evaluation. Ensure the availability of all the consumables like chemicals, columns, Standards etc. before and during experimental activities. Maintain and adhere to safety and quality culture. Participate in Lab activities necessary to maintain compliance in the lab. 3. Job Description - Responsibilities & Duties Knowledge on Method development /Stability analysis Expertise in Handling Spectroscopy (UV-Vis, FT-IR), Chromatography (HPLC) and other instruments (Potentiometric titrator, KF) Basic knowledge of cGMP, GLP and GDP procedures etc. Understanding of development activities and processes in pharmaceutical industry. Actively listens, shares information in a clear, concise and impartial manner. Actively contributes to achieving team Goals Maintain accurate records of research activities and results. Safety: To follow appropriate safety practices in the workplace. Participate in routine safety training and maintain current knowledge on safety related corporate and site policies. Enforce safety requirements as they relate to job function. Work Location Assignment: On Premise Research and Development #LI-PFE

Approving all Specifications, Test Methods, and Batch Process and Control Records (BMRs). approving validation protocols and reports, and conducting the General Good Manufacturing Practices (GMP) training.

Proven Experience as QA/ QC manager in Chemical Manufacturing unit . Knowedlge of all lab insruments and have experience of handling internal and external audit.

To maintain hygiene and cleanliness for allotted areas. Key Responsibilities Clean and maintain all areas assigned Collection and disposable of garbage Work area cleaning and sanitization Refilling of all consumables Use of appropriate cleaning equipment and chemicals Duties as scheduled for each work area Maintain high level of Safety and hygiene Respond and close all calls with regards to immediate assistance for cleaning Daily rounds of allocated area Well-groomed at all times Complying with all HSE requirements Ensuring the cleanliness and hygiene of allocated area Usage of appropriate cleaning agents and equipment Completing work allotted within the defined time and frequency Being well groomed Using appropriate PPE

Inventory Management: Maintain accurate records of inventory levels, stock movements, and stock transactions using inventory management software/systems. Conduct regular physical stock counts and reconcile discrepancies between physical counts and system records. Receiving and Dispatch: Receive incoming goods, verify quality and quantity against purchase orders, and process goods receipt notes. Coordinate with suppliers and logistics providers for timely dispatch of goods to customers or internal departments. Storageand Warehousing: Organize and maintain storage areas to ensure efficient space utilization and accessibility of goods. Implement proper storage methods to preserve the quality and condition of stored items. Stock Control and Replenishment: Monitor stock levels and initiate replenishment orders as per reorder levels and inventory policies. Coordinate with procurement team for timely procurement of materials and supplies. Documentationand Reporting: Prepare and maintain accurate documentation related to inventory, including stock records, purchase orders, and delivery notes. Generate regular reports on inventory status, stock movements, and performance metrics for management review. Qualityand Compliance: Ensure compliance with company policies and procedures related to inventory management, storage, and stock control. Implement quality control measures to prevent stock damage, loss, or theft. TeamCollaboration: Collaborate with procurement, logistics, and other departments to optimize inventory management processes and resolve issues. Provide support and assistance to other teams as needed for inventory-related matters.

Dear All, Greetings from Vivo Bio Tech Limited! Job Title: Analytical Scientist, Phy-Chem Studies (Agrochemical & Pharma) Experience: 3+ years Location: Hyderabad MOI: - Virtual 6-day week Job Description: We are seeking a detail-oriented and skilled Analytical Scientist with hands-on experience in conducting Phy-Chem and validation studies for agrochemicals and pharmaceutical compounds. The ideal candidate will have strong knowledge of global regulatory guidelines and be capable of preparing study-related documentation while maintaining audit readiness at all times. Key Responsibilities: Conduct Physico-Chemical studies for agrochemical compounds in accordance with regulatory requirements. Perform method validation studies for agrochemical products as per SANTEE/SANCO guidelines. Execute validation studies for pharmaceutical compounds as per ICH guidelines. Carry out dose formulation analysis to support toxicological and regulatory studies. Prepare and maintain Standard Operating Procedures (SOPs) for newly initiated studies. Develop study plans and compile final study reports as per relevant regulatory guidelines. Ensure all studies are conducted in compliance with GLP, OECD, OPPTS, CIPAC, SANCO, and SANTEE guidelines. Maintain effective communication with Quality Assurance (QA) personnel throughout the study lifecycle. Utilize Microsoft Excel for accurate calculations, data analysis, and result interpretation. Remain audit-ready at all times for sponsor audits, NGCMA inspections, or other regulatory reviews. Desired Candidate Profile: Strong understanding of regulatory frameworks applicable to agrochemical and pharmaceutical studies. Prior experience working in a GLP-compliant environment. Excellent documentation and report writing skills. Detail-oriented with good communication and coordination skills. Flexible and proactive approach, especially regarding audit preparedness. Vivo Bio Tech Ltd Survey # 349/A, Pregnapur Village, Gajwel Mandal. Siddipet District, PIN 502311,Telangana, India. Regards, Chandra Kanth | HRD chandrakanth.k@virinchi.com

newmark is looking for Analyst 1 - Gerald Eve to join our dynamic team and embark on a rewarding career journeyCollect, analyze, and interpret data from various sources to support business decisions and strategy development.Prepare detailed reports, dashboards, and visualizations that highlight trends, patterns, and actionable insights.Collaborate with cross-functional teams to understand data requirements and deliver accurate analytical solutions.Use statistical methods and data modeling techniques to solve business problems and improve processes.Validate data integrity and ensure accuracy in all analyses and reports.Monitor key performance indicators (KPIs) and provide regular updates to management with recommendations.

Responsible to work as per cGMP and maintain the compliance requirement. Responsible to develop the method for Extractable and Leachable compounds. Responsible to perform method validation & verification on different technique for E&L related work. Responsible to perform extractable & leachable(s) study for different packaging materials by using different analytical techniques like GC/GC-MS, HPLC/LC-MS, ICP/ICP-MS, IR, UV and other relevant techniques. Responsible to perform Identification, Investigation and troubleshooting task. Responsible to perform chemical analysis like, Extraction, Refluxing, Residue on ignition, Centrifuging & Evaporation etc. Responsible to prepare the study template, extractable & leachable(s) reports, analytical method validation & verification reports & protocols.

Description: Responsible for ensuring the accuracy and reliability of laboratory instruments through regular calibration and preventive maintenance. This role involves the daily verification of key instruments, such as balances, pH meters, and Milli-Q water systems, as well as monitoring environmental conditions like temperature. The analyst will perform chemical and instrumental analyses (including Wet Chemistry, HPLC, GC, AAS, etc.) to support R&D and production processes, ensuring product quality at various stages of development and manufacturing. Ensuring data integrity in all laboratory activities. Essential Functions: Perform the calibration and preventive maintenance of the instruments as per the respective schedules. Perform the determination of KF factor, Daily verification of Balances, pH meter, Milli-Q water system, Hygro meters, Refrigerator temperature monitoring . Perform the in-process/ intermediate/ finished products analysis by Wet/ Chromatography techniques for R&D/ Plant support. Chemical/ instrument analysis (i.e. Wet/ HPLC/ GC/ AAS/ ICP-MS, etc.) Perform the Impurity standard/ working standard/ primary reference standards To maintain cGMP and Data integrity. Additional Responsibilities: Activities other than the defined in the Job Responsibility are to be done, as per the requirement of HOD

Associate / Senior Associate- Analytical Services Location: Pune Date posted: 23 Jul 2025 Apply until: 30 Aug 2025 Position: Regular Experience: 2-7 years Job function: Analytical Services Role: Full time Job Description We are seeking a skilled and motivated Senior Associate, Analytical Services to join our team. This role requires a robust theoretical understanding in instrumental analysis, coupled with extensive practical experience in operating and troubleshooting equipments such as HPLC, GC, FTIR, Elemental, and Thermal Analyzers. Independently executing complex analytical workflows. Actively undertake method development on various analytical equipments for a diverse range of molecules. Prepare and participate in laboratory expansion strategies through new service delivery. Participate in writing project proposals to seek various types of funding. Performing routine maintenance and calibration of laboratory instruments. Actively participating in laboratory inventory management and procurement of essential consumables and equipment. Designing and delivering impactful workshops on various analytical chemistry topics. Candidate Profile MSc in Analytical /Organic/Inorganic /Pharmaceutical Chemistry. The candidate should demonstrate good written and verbal communication skills, a proactive and enthusiastic approach to their work, and a strong desire to learn and a proactive attitude. Experience of 2-5 years in similar roles. General requirements and expectations from Venture Center employees: Venture Center is a non profit organization with aim to benefit society by promoting entrepreneurs and start ups. Thus, Venture Center seeks employees and consultants with a strong interest and passion in seeing technology innovators, entrepreneurs, and start ups succeed, and a strong "service" ethos. A strong feature of Venture Center jobs is the rich learning environment and opportunity provided to employees to experiment, take initiative and be creative. The work of most employees has visible impact which can be satisfying. All employees benefit from access to high quality facilities and work environments. Compensation packages can be flexible but are often conservative due to Venture Center s non profit status. General requirements include: a) strong ethical standards and work ethics, b) comfort with computers, computer applications and internet, c) strong communication skills spoken and written. Venture Center s working hours are 9 AM 6.00 PM (Monday to Saturday) and are designed to keep operations of Venture Center convenient for the start ups, entrepreneurs, inventors and others that the organization serves. Managers in certain functions are provided the opportunity to avail of flexible hours. All jobs are located at Pune, Maharashtra, India. Our Company is an equal-opportunity employer and does not discriminate against any employee or applicant based on age, color, disability, gender, national origin, race, religion, sexual orientation or parental status.

We are looking for a highly skilled and experienced Analyst-QC to join our team at eClerx Services Ltd. The ideal candidate will have a strong background in IT Services & Consulting, with excellent analytical and quality control skills. Roles and Responsibility Collaborate with cross-functional teams to identify and prioritize testing requirements. Develop and implement comprehensive test plans and cases to ensure high-quality deliverables. Conduct thorough analysis of test results and identify areas for improvement. Work closely with the development team to resolve defects and enhance overall product quality. Participate in continuous improvement initiatives to optimize testing processes. Maintain accurate records of test cases, results, and defect reports. Job Requirements Strong understanding of software testing principles, methodologies, and tools. Excellent analytical, problem-solving, and communication skills. Ability to work effectively in a fast-paced environment and meet deadlines. Experience with quality control processes and procedures. Familiarity with industry standards and best practices for software testing. Strong attention to detail and ability to identify defects and errors.

Applications are invited from interested and motivated candidates for the post of Junior Research Fellow (JRF) in a time bound research project for a temporary period, purely on contractual basis as per the following details. Position Junior Research Fellow (JRF) Number of Vacancy 01 Project Title High temperature corrosion and mechanical behavior of AM fabricated Haynes 282 alloy Department Mechanical Engineering Project Tenure 3 years Job Description The project aims to investigate the corrosion behavior and high temperature mechanical behavior of additively manufactured Haynes 282 alloy. Knowledge about Selective Laser Melting, corrosion, Fatigue, microstructural characterization is required. Strong communication and writing skills are desirable. Essential Qualification Minimum requirement: B.Tech in Mechanical Engineering/Materials Engineering/ Materials and Metallurgical Engineering with a valid GATE score. Desirable: M.Tech in Mechanical Engineering/ Materials Engineering/ Materials and Metallurgical Engineering with a valid GATE score. Age Limit JRF-28Yrs. Age relaxation The upper age limit is relax-able up-to 5 years in the case of candidates belonging to scheduled castes/tribes/OBC, women and physically handicapped candidates. Fellowship Junior Research Fellow (JRF)- Rs.37,000/-p.m. Principal investigator Dr. Devasri Fuloria Assistant Professor Senior (Grade I) School of Mechanical Engineering Vellore Institute of Technology Vellore, Tamil Nadu - 632014 Send your resume along with relevant documents pertaining to the details of qualifications, GATE/NET score card, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (5/08/2025) through online http://careers.vit.ac.in Please note that the CV should include contact details (address, mobile phone no., email ID), date of birth, qualifications mentioned clearly. Complete information regarding publications of research papers in SCI Journals should be mentioned in the CV. Incomplete applications will be rejected. No TA and DA will be paid for appearing in the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

You get to collaborate on: Work closely with discovery specialists, disease area scientists and in vivo team members. Handling of laboratory animals like rat, mice, Guniea Pig and Rabbits. Dose administration to experimental animals by different routes and small animals surgery (like cannulations, CSF fluid collection) and handling, followed by compound dose preparation, administration to experimental animals. Contributing to the ongoing drug discovery programs by conducting in vivo DMPK studies for NCEs with a good knowledge of in vivo animal models. Data generation, analysis, compilation, report preparation. Regular uploading of the data. Conduct statistically supported data (analysis using win online) and deliver results in a timely manner to enable informed decision-making Understanding systems, processes, and compliance. Prepare, review, and deliver scientific presentations for internal/external use. Participate in cross-functional team activities, add value to research projects through creative ideas. Learn from top-notch drug discovery scientists across the world and opportunity to get trained in people skills. PK-PD studies in rat and mice of NCE.

Qualification :- M.Sc Chemistry Experience :- 0 to 3 year in Pharma or Chemical Company Location :- Jarod ( Vadodara ) Related Experience in HPLC , GC , Wet Analysis

Interview for R&D Associate for Chemical Company in Dahej on 28-07-2025, Monday Qualification: MSC Chemistry Experience: 1 to 4 Years CTC: Up to 5 LPA Send CV on sdpbharuch@gmail.com with Subject: R&D Dahej & Call on 9727755967 Share with Friends Required Candidate profile No Job Placement Charges Share with your Friends & Colleagues Interview Venue: SDP HR SOLUTION, Sixth Floor, 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch Interview Time: 09:00 Perks and benefits Transportation Medical PF Bonus

HIRING FOR OSD - PRODUCTION & QC PRODUCTION(OSD) Experience: (01-07Years) Compression, Granulation, Coating, Capsule filling, Inspection QC Experience: (02-09Years) HPLC, GC, RM,PM, Stability, IP/FP, Method Development, Method Transfer QUALIFICATION : ITI/DIPLOMA/BSC/MSC/B PHARM/M PHARM With relevant Experience ITI/DIPLOMA/BSC/MSC/B PHARM Freshers can Apply DESIGNATIONS: Operator/Sr Operator/Jr Officer/Officer/Jr Executive/Executive INTERVIEW VENUE: SK Consultancy Services, H.No-1-77, 3rd Floor, Bachupally X Road, Opposite Sri Swastik Multi Specialty Hospital, Towards Nizampet Road DATE &TIME: 26th July 2025 ( Saturday); From 09.00 A.M. to 03.00 P.M NEED TO CARRY: Resume 3 Month Pay slips Increment letter Previous company relieving letters Education Documents and ID Proofs Help Us Spread the Word (Refer): Circulate it in your Social Networking sites and groups for better reach and Refer your friends and colleagues, it could be a great opportunity for someone in need! WORK LOCATION: Hetero Labs Limited, UNIT V Polleypally, Jadcherla, Mahabubnagar CONTACT INFO: E-mail: Ashok.ch@hetero.com & Contact:8555912639 for further info.

Crop Care Pesticides India Pvt. Ltd. is seeking a candidate with experience in working on HPLC & GLC, preferably from an Agricultural/Pesticides formulation background. The ideal candidate should be able to join immediately. This is a full-time position with a day shift schedule. The job location is in Derabassi, Mohali, Punjab. Candidates should be willing to reliably commute to the workplace or plan to relocate before starting work. Candidates with a Master's degree are preferred for this role. The ideal candidate should have a total of 4 years of relevant experience. The salary for this position will be as per company norms.,