3433 Hplc Jobs - Page 31

Sri Rajasree Educational Society is looking for Designation Professor / Associate to join our dynamic team and embark on a rewarding career journey Teaching and Instruction: Associate Professors are responsible for teaching undergraduate and/or graduate-level courses in their area of expertise They develop syllabi, prepare course materials, deliver lectures, facilitate discussions, and assess student performance They may also supervise student research projects, theses, and dissertations Research and Scholarship: Associate Professors engage in research activities, pursue scholarly publications, and contribute to the advancement of knowledge in their field They conduct research projects, secu...

Lead synthesis, purification, and characterization of agrochemical intermediates and actives. Optimize reactions, processes, and formulations for efficiency, yield, and cost-effectiveness. Support scale-up from lab to pilot plant and transfer processes to manufacturing. Mentor and guide junior chemists, review experimental plans, and ensure scientific rigor. Collaborate with analytical, quality, regulatory, and manufacturing teams. Contribute to product lifecycle management and IP documentation (patents, innovations). Ensure strict adherence to GLP, EHS, GMP, and laboratory safety protocols. Drive innovation by suggesting new synthetic routes, formulations, or process improvements. Key Skill...

Lead and oversee synthesis, process development, and formulation projects for agrochemical products. Mentor, train, and manage a team of Junior and Senior chemists, fostering a collaborative and high-performance environment. Drive technology transfer and scale-up from lab to pilot plant and support manufacturing integration. Collaborate with cross-functional teams including manufacturing, analytical, regulatory, and quality for successful product delivery. Define and execute R&D strategies and roadmaps , aligned with business objectives and market needs. Ensure compliance with GLP, EHS, GMP, and other applicable regulatory standards. Identify new opportunities for innovation, cost optimizati...

Conduct laboratory experiments related to synthesis, purification, and characterization of agrochemical intermediates and actives. Support formulation development (herbicides, pesticides, fungicides, insecticides). Perform reaction monitoring, analysis, and documentation of experimental results. Assist in scaling up lab processes to pilot level under senior supervision. Work with analytical teams to characterize compounds using NMR, HPLC, GC, LC-MS, etc. Ensure compliance with lab safety protocols, GLP, and EHS guidelines . Maintain accurate records of experiments, observations, and reports. Collaborate with cross-functional R&D and manufacturing teams to transfer learnings. Key Skills Quali...

Job Description: Will work in Analytical development Lab of BRL. Responsible for analytical deliverables of Biologics Projects for regulated markets. Deliverables involves but not limited to Method Development, Qualification, Technology transfer, Biosimilarity assessment, Forced degradation and Characterization activities. Responsible for Independent planning and execution of experiments. Techniques include but not limited to Chromatography, Electrophoresis, Spectrophotometry and Colorimetric assays for Biotherapeutics. Major responsibility will be planning and execution of HPLC, UPLC and CE based analysis Skill sets: Knowledge and hands-on experience of different chromatography modes like R...

The Opportunity: To Sell entire Biopharma product portfolio, with emphasis on Small Molecule Market. Close sales on more technical products, working in conjunction with internal functions, Identify and ensuring the process of converting sales opportunities for relevant products from Avantor Biopharma offerings. What we are looking for : Experience: 7-8 years of Biopharma / Pharma / Life science - Sales industry experience required. Education: BS degree in a life science area, or equivalent work experience required. Identify and close new biopharma business. Meeting the budgets for both top and bottom line, ensuring growth in sales figures along with market share by virtue of careful product ...

(Male Candidate Required) Role & responsibilities 1. Observation of Good Laboratory Practices as laid down in Quality Control Standard Operating procedures. 2. Sampling and analysis of In-process samples, Intermediates, Hold time samples, Process validation samples, Cleaning validation samples, Rinse samples, Swab samples, Raw materials, Particle size analysis and Finished products by HPLC. 3. Analysis of accelerated and long term stability studies of APIs. 4. Analysis for qualification of working standards and impurity standards as per requirement. 5. Initiation, completion and filing of Daily Analytical Reports. 6. Calibration of instruments as per calibration schedule. 7. To complete acti...

Role & responsibilities APLHC Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Control/Quality Assurance Experience Required: 1 - 6 years in USFDA Approved pharmaceutical manufacturing facility Quality Control and Quality Assurance Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: QC Routine & stability testing of RM / IP / FP samples on HPLC, GC, LCMS, UV, etc. Prepare/standardize analytical methods, calibration & instrument qualification (IQ/OQ/PQ) Adhere to GDP, ALCOA+ and cGMP guidelines; ensure timely LIMS/SAP data entry Investigate OOS/OOT results and implement effective CAPA Support regulatory, customer and internal audits...

Role & responsibilities Adequate knowledge of respective guidelines. i.e. ICH, USP,WHO, etc. Stability sample analysis by HPLC/GC/UV/Dissolution apparatus. Preparation of stability testing worksheets. Sample charge and withdrawal as per stability condition. Management of stability samples and stability chambers and maintain the schedule. Preparation of stability trend records and summarize the results Review the stability sample testing data. Review the stability analysis worksheet. Review the stability protocols, samples and stability chambers log records. Review of OOS/OOT and co-ordinate with respective concerns.

Role & responsibilities Use of HPLC/GC/UV/Dissolution apparatus. Integration for Assay and RS. Method development and force degradation study for FP and API. Preparation of method development protocol. Dissolution development and impurity profiling. Force degradation study for FP and API. Pharmacopeia method interpretation, Literature/references search. Listing the requirements for method development. Review and interpretation of development trial data. Preparation and review of method development protocol and report. Descriptive method right up.

Vibonum Technologies Private Limited, Mysore, (Althera Group), is conducting a Walk-in Interview on October 12th, 2025 to hire Quality Control professionals for its state-of-the-art OSD manufacturing facility in Nanjangud, Mysore . Department: Quality Control Work Location: OSD Plant, Nanjangud, Mysore Interview Date: Oct 12th, 2025 (Sunday) Time: 09.00 am to 05.00 pm Venue: Althera Laboratories India Pvt Ltd, Bangalore (https://maps.app.goo.gl/ozdZFQh9pN3YkYAb) Althera Laboratories India Pvt Ltd No S26, Yarandahalli, Bommasandra-Jigani link road, Hebbagodi post, Bengaluru 560099 Bengaluru, Karnataka 560099 Open Positions in Quality Control- 50 Nos Asst Manager - QC / Sr. Executive - QC / Ex...

Job Description Maintenance of GLP in the Laboratory Upkeep of Housekeeping in the Laboratory. Ensuring activity logs are maintained for all critical instruments /equipment’s. Timely preparation of Laboratory Documents. Timely review of analytical data generated in laboratory. Ensuring Analytical Technology transfer from transferring lab as per approved protocol. Review and approval of incident , out of specification ,out of trend report and approval of QC related activities. Involved in QAMS activities such as change control, CAPA , incidents, deviation etc. Approval of stability summery report. Timely review of Quality control procedures and initiation for up gradation of same. Compliance ...

About the role: This role is responsible for executing and managing analytical R&D projects related to alcoholic beverages. It includes conducting precise chemical and instrumental analysis of raw materials, intermediates, and finished liquids in alignment with defined test methods, Good Laboratory Practices (GLP), and ISO 17025 requirements. The position also supports senior analysts in innovation and research initiatives and contributes to technical capability building across stakeholders through training and knowledge sharing. Role Responsibilities: Key Technical Responsibilities: Conduct and support analytical R&D projects for product and process development Perform chemical analysis on ...

Job Objective: To enable establish QC efficient methods and processes for assigned products by performing analytical research activities while adhering to regulatory norms and established SOPs Job Responsibilities Analytical Method Development Assist the supervisor and team leader in conducting literature review by reviewing documents such aspharmacopeia, research available in public domain, etc. Conduct analytical procedures by following the trial and error methodology prescribed by Supervisor/ Team Leader to assess the workability of the proposed analytical method Analytical Method Validation and Method Transfer as per cGMP Check availability of required equipment and materials as per the ...

As a Peptides Production Trainee/Executive, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. **Key Responsibilities:** - Understand and follow standard operating procedures (SOPs) for peptide synthesis. - Assist in the preparation of reagents, solutions, and equipment for peptide production. - Execute peptide synthesis under the guidance of experienced personnel. - Learn and perform purification techniques such as HPLC, chromatography, and filtration. - Assist in maintaining accurate records...

You will be working at Cultivator Phyto Lab, India's top Testing, Inspection, and Certification Company, where your passion for positively impacting the environment is highly valued. The company culture prioritizes integrity, knowledge, respect, and trust, offering a fast-paced and rewarding work environment that focuses on both personal and professional growth. Your key responsibilities will include: - Conducting sample testing and analysis in compliance with ISO 17025:2017 and NABL standards - Developing and validating testing methods - Verifying testing methods - Efficiently managing a team of professionals - Handling internal and external audits effectively To qualify for this position, ...

Role Overview: As a Scientist II at USP, you will play a crucial role in supporting the development of reference materials, specifically focusing on analytical method development for in-process samples in the synthetic lab. Your responsibilities will include performing various analytical tests, ensuring a safe and GLP-compliant environment in the lab, evaluating reference standards, developing and validating official methods, conducting stability studies, and contributing to research projects within the analytical department. Key Responsibilities: - Support reaction monitoring, scale up, and final analysis of samples based on monograph/in-house procedures, including method development when n...

About Us Scimplify is a specialty chemicals manufacturing company offering a full-stack solutionfrom R&D and custom synthesis to large-scale manufacturing and doorstep delivery. Headquartered in Bengaluru, India, we serve multiple industries ranging from pharmaceuticals to agrochemicals and industrial chemicals to personal care and fragrances. We enable 500+ businesses across 20+ countries to develop and scale innovative chemicals from lab to commercial production. We have raised over $54 million from top tier investors such as Accel and Bertelsmann, We are a team of 250+ professionals with entities in India, Japan, USA, UAE, and Indonesia. Learn more about why Forbes thinks we are the top 1...

Roles and Responsibilities Conduct quality control analysis using HPLC, GC, UV, spectrophotometer, sterile techniques, and other relevant methods. Ensure compliance with USFDA, GMP, GLP regulations during regulatory audits. Develop and maintain SOPs for laboratory operations and testing procedures. Collaborate with cross-functional teams to resolve quality issues and improve processes. Perform stability studies on APIs and finished products as required. Desired Candidate Profile 2-7 years of experience in a pharmaceutical industry setting with expertise in QC analysis. MS/M.Sc(Science) degree in Chemistry or related field; Strong understanding of analytical instruments such as HPLC, GC, UV s...

Responsibilities: * Develop analytical methods, validate results. * Ensure compliance with GMP & WHO standards. * Conduct quality testing using HPLC & UV-VIS. * Manage QC processes, analyze data, report findings.

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 ...

Key Skills: Basic understanding of laboratory practices, analytical techniques, GMP/GLP concepts, and willingness to learn quality systems. Attention to detail, good communication, ability to follow SOPs. Willingness to learn, ability to work in a team, and flexibility to work in shifts . This is a walk-in post. Even then candidates are encouraged to share their resumes in advance at talenthire-unit4@metroapi.com with the subject line Profile for Quality Control . This will help our team connect with you beforehand and guide you about the position. We warmly welcome candidates who are currently working in Visakhapatnam and nearby areas.

Roles & 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 b...

Job Description Provides technical services & support to Agilent customers. This includes timely and cost-effective problem resolution with the objective to enhance our customer experience and meet Agilent contractual agreements. Leverage post sales interactions with customers to probe and qualify further revenue opportunities and provides highly qualified leads to sales. Performs a set of required admin tasks to ensure flawless customer service for contract and trade customers. Responsibilities of this position include but are not limited to; Responsible for providing technical support for Agilent analytical instruments to existing & new customers in markets of Biopharma/Proteomics/Pharma/F...

Job Description Provides technical & application services & support to Agilent customers. This includes timely and cost-effective problem resolution with the objective to enhance our customer experience and meet Agilent contractual agreements. Leverage post sales interactions with customers to probe and qualify further revenue opportunities and provides highly qualified leads to sales. Performs a set of required admin tasks to ensure flawless customer service for contract and trade customers. Responsibilities of this position include but are not limited to; Responsible for providing technical & application support for Agilent analytical instruments to existing & new customers in markets of P...