3439 Hplc Jobs - Page 45

DEAR CANDIDATE , WE ARE HIRING! LET'S JOIN OUR TEAM NOW! Department: R&D Position: Research Trainee / Research Associate Preferred Qualification: M.Sc. Biotechnology / M.Sc. Biochemistry Preferred candidate: Male Preferred Experience: 2 to 3 years of experience Should have good documentation skills and knowledge of GDP, GMP, GLP. Should have basic knowledge about proteins and protein purification. Should be a good team player with good interpersonal skills. Job description: Perform R&D related documentation like SOP preparation, data management and data analysis. Perform routine laboratory procedures, including buffer preparation, gel electrophoresis, western blot. Operation and maintenance ...

Main Accountabilities Routine analysis & Stability Analysis (assay, RS, dissolution, water content etc.) of R&D formulation projects (solid & liquid orals, injectables) Daily calibration of pH meters, balances etc. Stability sample management (loading & withdrawal as per stability plan) Preparation of Stability Reports & other protocol based study reports for assigned projects, as applicable Hands-on experience of analytical instrumental techniques (HPLC with chromatographic software etc.) Assisting analytical method development/validation/method transfer activities, as per need Supporting other assigned lab responsibilities for GLP compliance Performance Indicators: Timely execution of assi...

Walk-in Drive @ SEZ-Matoda|| Ahmedabad on 28th Sep '25 (Sunday) for Quality Control Department. We are having excellent job opportunities for Quality Control Department at Amneal Pharmaceuticals, SEZ Matoda Injectable. Interview Venue Details: Date: 28th Sep 25 (Sunday) Time: - 9:00 AM to 3:00 PM Venue : Amneal Pharmaceuticals Plot No 15, 16, 17 Pharmez | Village: Matoda | Sarkhej Bavla Road | Ahmedabad Gujarat - 382220. REQUIREMENT FOR INJECTABLE QUALITY CONTROL DEPARTMENT Designation: Officer/ Sr. Officer /Executive/ Sr. Executive Department: Quality Control Qualification: Diploma/ B.Sc./ M.Sc/ B. Pharm/ M. Pharm Total Experience: 02 to 07 years (Pharma experience only) Desired Profile: GL...

Roles and Responsibilities Responsible for Analytical Method Validation. Responsible for HPLC/GC instrument handling. Responsible for Daily review of Analytical balance and Daily Temperature monitoring. Responsible to follow analytical procedures and generate online raw data. Responsible for Stability Studies and Analysis. Responsible to operate and analyze of raw materials, In Process, cleaning samples, samples for vendor qualification, Stability samples, standard and Finish product Samples and instrumental method (HPLC / UPLC / GC) and to perform analysis of process validation. Responsible for Daily verification of analytical balance and daily temperature monitoring. Online entry in logboo...

Job Profile: Responsible for analysis of IP/FP/,PV, Semifinished products, hold time samples Responsible for maintaining compliance and to ensure GLP in lab. Responsible for analysis of samples on HPLC/GC etc. Responsible to provide request to section head for issuance of AWR and to record analysis related activities Responsible to receive samples of FP/IP/inprocess/,holdtime samples and maintain the record. Responsible for reconciliation and destruction of laboratory samples. Responsible to maintain records for FP/IP/PV/SFG/Holdtime samples Responsible for preparation of COAs Responsible to maintain individual training record Responsible for record details of OOS/OOT/OOC/Incidents and to pa...

Roles and Responsibilities Develop analytical methods for OSD products using techniques such as HPLC, GC, UV, etc. Conduct formulation research and development of injectable products. Prepare protocols, SOPs, and reports related to formulations and analysis. Collaborate with cross-functional teams to ensure successful product launches. Ensure compliance with regulatory requirements throughout the product lifecycle. Independently handling the Stability analysis of dosage forms. Has knowledge on Validation of the methods. Forced Degradation studies. Desired Candidate Profile Sound Knowledge about analytical method development and Stability analysis of dosage forms 2. Hands on experience in usi...

Job Location: Bangalore Department: Analytical Development Drug Product About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productiv...

We are seeking a detail-oriented and experienced Quality Control Engineer to ensure the quality and compliance of pharmaceutical products. Ensure compliance with GMP, GLP, and regulatory standards (FDA, WHO, ICH, etc.).

This Position reports to: TMC- (Trade and Transportation) Manager What we believe in At ABB, we are dedicated to addressing global challenges. Our core values: care, courage, curiosity, and collaboration - combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to empower everyone to create sustainable solutions. That's our story. Make it your story. Your role and responsibilities In this role, you will have the opportunity to manage Trade & Compliances processes, and look after the custom operation, Trade Advisory, Trade Compliance, Trade & Transport, follow with the Freight forwarders & shipping lines, ensure the material delivery. The work model...

Job Track Description: Performs tasks based on established procedures. Uses data organizing and coordination skills to perform business support or technical work. Requires vocational training, certifications, licensures, or equivalent experience. General Profile Requires limited prior training or licenses and training certifications. Has basic operational or analytical skills to perform tasks. Works within clearly defined standard operating procedures and adheres to quality guidelines. Work is completed with close supervision and under clearly defined procedures. Functional Knowledge Requires a basic understanding of theories, practices, and procedures. Business Expertise Understanding of ho...

As a member of the Analytical Development team at our clinical-stage vaccine innovation company, your primary responsibility will be to support the developmental activities in the laboratory. You will have the opportunity to assist in the design, execution, and interpretation of experiments to analyze drug substances and intermediates, including proteins and carbohydrates. Your key responsibilities will include: - Performing microplate assays, including enzymatic assays - Utilizing HPLC techniques, especially SEC and RP-HPLC with experience in Chemstation - Working with CE and iCIEF, especially with Protein Simple or PA-800 systems - Assisting in analytical method development of new assays -...

As a Quality Control professional at Medivisual Healthworld in the Pharmaceutical & Cosmetic Manufacturing industry, you will be responsible for: - Performing testing of raw materials, in-process, and finished products such as tablets, syrups, skin care products, etc. - Ensuring quality checks are conducted following laid Standard Operating Procedures (SOPs) and regulatory standards - Making independent quality decisions (accept/reject) based on control parameters - Maintaining and updating all test records, reports, and logbooks in compliance with regulatory norms - Ensuring compliance with legal, safety, and quality standards Key Skills Required: - Hands-on experience in HPLC / GLC - Profi...

As an Analytical Scientist C at BacAlt, you will play a crucial role in the Research and Development Department. Your primary responsibility will be to develop and validate analytical methods for various instruments such as HPLC, GC, GC-MS, IR, UV-Visible Spectroscopy, Particle Size Analyser, and more. Additionally, you will be responsible for conducting wet analysis in the lab, planning stability studies, and performing testing according to established protocols for formulations, APIs, and excipients. Key Responsibilities: - Develop and validate analytical methods for various instruments including HPLC, GC, GC-MS, IR, UV-Visible Spectroscopy, and more. - Conduct wet analysis in the lab and ...

We are looking for QC Chemist to join our QC. The role involves analysis of raw materials, in-process samples, and finished products in compliance with regulatory standards.Freshers candidates can apply.

We are looking for a skilled Control Tower Manager with 5 to 10 years of experience in a similar role, based in Bangalore. The ideal candidate will have strong analytical skills and the ability to collect, organize, analyze, and disseminate information with attention to detail and accuracy. Roles and Responsibility Manage and oversee the control tower operations for efficient and effective results. Analyze data and provide insights to improve operational efficiency. Develop and implement process improvements to increase productivity. Collaborate with cross-functional teams to achieve business objectives. Identify and mitigate risks to ensure compliance with regulatory requirements. Monitor a...

Responsible for management of QC/QA function of Chemical Manufacturing Plant including: Day to day operations of quality function from Raw Material testing till Finished Goods Dispatch Compliance of Quality Systems including IMS, GLP, CGMP, 5S, Kaizen Documentation and Audits (Internal & External) Customer Complaints and CAPA Team Management and its competency development Lead the continuous improvement projects for quality improvement Preferred candidate profile Ideal Candidate must be a Full Time M.Sc. in Chemistry/B.Tech -Chemical (Through out First Class) with 18 - 23 years of experience out of which minimum 5 years of leading QC/QA function in a large scale chemical manufacturing unit. ...

Job Description Synthesize and characterize novel NCEs as per client specifications, in an efficient and independent manner. Broad knowledge of modern organic chemistry and synthetic methods Heterocyclic chemistry, metal catalyzed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc. Work with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Up to date maintenance of Lab Note Books, as per client specifications and guidelines. Generation of final reports and other scientific documents, as...

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At Phenomenex, one of Danaher's 15+ operating companies, our work saves livesand we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact innovating at the speed of life. Phenomenex isn't your typical scientific company. Founded nearly 40 years ago, Phenomenex is a global technology leader committed to developing novel analytical chemistry solutions that solve t...

Job Description 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 p...

Operational experience of GC, HPLC, PH and other testing instruments of laboratory, Good communication, good command on chemistry, M.Sc. in chemistry, must have worked in quality control department. Halol, Vejalpur, Kalol and Godhra.

1. Amino acid validation. 2. In-Process and finished products analysis. 3. Product development product analysis. 4. Documentation. 5. Responsible for method process Share resume to hrd@stedmanpharma.com, Call 7904827192/9786920463 Perks and benefits Canteen and other welfare benefits.

Stedman Pharmaceuticals is looking for a dynamic and experienced candidate for the Quality Control (QC) department with hands-on experience in Analytical Method Validation for various dosage forms. Share your Resume to hrd@stedmanpharma.com

Role & responsibilities M.Sc.Organic Chemistry,B.Sc. Chemistry ,1 to 5 Year Experience in HPLC / GC /AMV Preferred candidate profile

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP S/4HANA Group Reporting Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application development aligns with business objectives, overseeing project timelines, and providing guidance to team members to...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP S/4HANA Group Reporting Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application requirements are met, overseeing the development process, and providing guidance to team members. You will also engage...