969 Chromatography Jobs

To own YBL Vision and Values. In depth knowledge and technical understanding of protein purification, protein analysis and its characterization. Hands on experience on Chromatographic purification, FPLC/AKTA system, UFDF, TFF. Completion of allotted projects in time bound manner. Solving the customer complaints of projects. Execution of policies and strategies implemented as and when for reducing the timeline for product/process development. On time calibration and validation of equipments. Documentation related of ISO, OHSAS, customer related or any other kind of audits. Interpretation and documentation of daily project activities in electronic lab notebook. Technology transfer document pre...

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:-1 to 5 Years Skills :- HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals Division :- Formulation Interview Date:-20-09-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur | MSNF-IV, Mekaguda | MSNF-V, RK Puram Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Car...

Field Service Engineer We are seeking a highly skilled and experienced Field Service Engineer to join our team on a contract basis. This role requires a minimum of 0 years and a maximum of 3 years of experience in the Pharma/Healthcare/Lifesciences industry, providing on-site technical support and maintenance in Bangalore, karnataka ,India.Tasks Provide on-site technical support and maintenance for gas chromatography and liquid chromatography equipment. Troubleshoot and resolve equipment malfunctions. Perform preventative maintenance and calibration procedures. Maintain accurate records of service activities and equipment performance. Collaborate with internal teams to ensure timely resoluti...

Description Brief Job Overview The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices. How will YOU create impact here at USP? In this role at USP, you cont...

Overview: This position will be responsible for: Direct sales ,customer support and satisfaction within the designated (Karnataka) territory in India. Managing and growing the business in the given territory and support other territories as needed. How You’ll Make an Impact: Achieve sales, marketing and financial objectives for relevant products Sales of product within approved price range Advise on maintenance of inventory levels so that the Company and customer expectations are met Develop new initiatives to grow sales and profit lines -Promote maximum usage of Bio-Rad products at all given customer sites- Responsible for coordinating between customers and other departments in the company ...

Company Overview : Foundation for Neglected Disease Research (FNDR) is a not-for-profit biotech R&D organization dedicated to discovering and developing novel therapeutics, diagnostics, and devices for diseases with a high socio-economic impact. Since its inception in 2014, FNDR has generated a portfolio of therapeutics in tuberculosis, nontuberculous mycobacteria, malaria, dengue, leishmania, serious bacterial infections, fungal infections, COVID-19 and RSV, spanning over early-stage discovery to late-stage clinical trials. FNDR&aposs R&D Centre, which includes state-of-the-art BSL2 and BSL3 laboratories for both in vitro and in vivo research, is in Bengaluru, India. For more information, p...

As a Process Development Scientist, you will be responsible for planning and executing microbial fermentation and purification processes for polysaccharides and proteins. This includes activities such as Tangential flow filtration (TFF), Chromatography, and sterile filtration. Your role will also involve preparing scale-up and scale-down study plans for tech-transfer and troubleshooting purposes. Key Responsibilities: - Plan and execute scale up and scale down experiments for Manufacturing Science & Technology. - Ensure timely completion of all assigned projects by designing, planning, and executing experiments effectively. - Coordinate with various departments such as DQA, DQC, Animal House...

Biological E. Limited invites experienced, dynamic and self-motivated candidates with 2 to 14 years of experience for the below positions at its Vaccine Business, Shamirpet, Hyderabad. RESEARCH AND DEVELOPMENT R&D Upstream Processing Designation: Sr. Executive/Executive Qualification: B. Pharm/ M. Pharm and B. Tech/ M. Tech/ M. Sc (Lifesciences) Preparation and maintenance of Research cell banks, Master cell banks, and working cell banks for different projects, Strong experience in day-to-day laboratory operation, e.g. using equipment, aseptic techniques, preparing media/solutions Knowledge of planning and executing the scale-up of fermentation processes, mathematical skills, specifically wi...

Description Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentors...

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Perform routine and non-routine analysis of raw materials, in-process samples, and ...

Operate and troubleshoot HPLC systems (e.g., Waters, Agilent, Shimadzu) including autosamplers, columns, and detectors (UV/Vis, PDA). - Prepare samples and standards: dilution, filtration, degassing, mobile phase preparation, buffer pH adjustment. - Develop or follow validated analytical methods; set up sequences, integration parameters, and system suitability tests. - Perform routine analyses for assay, related substances/impurities, dissolution, content uniformity, and stability studies. - Ensure data integrity: accurate chromatogram integration, audit trails, and metadata handling in CDS (e.g., Empower, Open Lab). - Maintain instruments: preventive maintenance, calibration checks, leak ch...

Job Description Business: Piramal Pharma Solutions Department: Quality Location: Kurla Travel: Low Job Overview: Remote support to PPL sites in reviewing analytical data remotely, preparing master build in LIMS (Lab Vantage / Labware), Document Preparation (specifications, test methods, protocols, etc.) and uploading for review in ensure, initiating QMS elements in Trackwise / eDMS. Key Stakeholders: Internal Site Quality Team (QC, QA), Corporate Functions Key Stakeholders: External Regulators (during inspection), Solution Providers Reporting Structure PPL Site Quality (Functionally) and CQA Document, Data Review & Creation (Administratively) Qualification B. Pharm / M. Pharm / M.Sc. Chemist...

This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that ...

Job Title: Business Development Manager Department: Gels Reporting To: VP - Gels Location: Vadodara Employment Type: Full-Time About Us: Sorbchem India Pvt. Ltd. is an established company in the chemical sector and part of the global Zeochem Group. We are involved in the supply and distribution of high-quality chemical products. As we continue to strengthen our presence and explore new business opportunities, we are looking for a motivated and business-oriented Business Development Manager (BDM) to support our growth. Website: www.sorbchemindia.com Job Summary: The Business Development Manager (BDM) is responsible for leading and motivating a team of Business Development Executives to achiev...

Company Description AnaZeal Analyticals & Research Pvt. Ltd. is a USFDA approved Contract Research Organization (CRO) with EU approved Analytical/Microbiological lab facilities. Located in Navi Mumbai, the company focuses on providing high-quality and reliable services in the pharmaceutical industry. Job Title: HPLC Operator Company: AnaZeal Analyticals & Research Pvt. Ltd. Location: Navi Mumbai, Maharashtra Industry: Research Services Employment Type: Full-time Key Responsibilities Operate High-Performance Liquid Chromatography (HPLC) equipment for analytical testing. Perform method validation and routine analysis of pharmaceutical samples. Ensure compliance with cGMP and regulatory guideli...

Designation: Executive/Senior Officer/ Officer Department: Manufacturing - Antigens (Production) Educational Qualification: M.Sc/ B.Sc/ B. Pharmacy/ B.Tech (Biotechnology)/ Diploma (Any Life Sciences background) Experience: 1-9 years Location: Biological E. Limited (Vaccine Division), Kolthur, Hyderabad Roles & Responsibilities: Execution of Upstream & Downstream production batches. Focus on timely execution, to ensure that the process is carried out as per GMP and batch timelines. To execute planned Upstream & Downstream activities to ensure high degree of confidence that the process is delivering a product that meets its target specifications. Routine monitoring of the equipment, Facility ...

This Position Will Be Responsible For Direct sales ,customer support and satisfaction within the designated (Karnataka) territory in India. Managing and growing the business in the given territory and support other territories as needed. How You’ll Make An Impact Achieve sales, marketing and financial objectives for relevant products Sales of product within approved price range Advise on maintenance of inventory levels so that the Company and customer expectations are met Develop new initiatives to grow sales and profit lines Promote maximum usage of Bio-Rad products at all given customer sites- Responsible for coordinating between customers and other departments in the company to ensure cus...

As a Senior Analyst in Bioanalytical Research at Veeda Lifesciences, your role involves conducting bioanalytical research activities including method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. You will be responsible for developing and validating methods for bioanalysis of biologics and biosimilars in compliance with regulatory requirements such as USFDA. Collaboration with cross-functional teams is key to ensuring the timely delivery of high-quality results. Additionally, you will perform stability testing of biological products under various conditions and troubleshoot issues related to...

Role & responsibilities 1. Execution of Batches in shift operation. 2. Maintains and documents proper records / log book / BPCRs / Reports as per GDP. 3. Error free online entries in BPCR as per GDP. 4. Timely completion and submission of BPCR 5. Execution of Performance Verification and PQ and commissioning of new equipments Understanding & execution of work in line with cGMP. 6. Coordination with other department VIZ. engineering, QA, QC and R&D for smoothly execution of production batches. 7. Coordination with QA for timely issuance, completion, filling of BPCR and other GMP documents. 8. In addition of above responsibilities, any responsibility assign by superior/HOD. Salary & Benefits: ...

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 for Oil & Gas Downstream Good to have skills : NAMinimum 12 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 day will involve overseeing the application development process and ensuring seamless communication within the team and stakeholders. Roles & Responsibilities:- Expected to be an SME- Collaborate and manage the team t...

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Perform routine and non-routine analysis of raw materials, in-process samples, and ...

Job Description ADL Skills Required: 1. Chromatographic skills like SEC, IEX, HIC, RP, etc with operation of HPLC, UPLC equipments. 2. N-Glycan analysis is preferred and higher order structure analysis experience will be advantage. 3. Electrophoresis skills like Capillary electrophoresis (cIEF, CE-SDS NR & R, CE-LIF) etc. 4. Work experience on analytical method development and validation for biotherapeutic products. 5. Experience on documentation preparations like SOPs, MOA, MDR, etc. Computer literacy in Microsoft office and softwares related to critical equipments. Roles and responsibilities: 1. Responsible for timely analytical deliverables of Biotherapeutic projects involving QTPP and Pr...

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolve...

Job Description: Planning & execution of microbial fermentation. Planning & execution of purification of polysaccharide and protein, including Tangential flow filtration (TFF), Chromatography & sterile filtration. Preparation of scale-up plan and scale-down study plan for tech-transfer and troubleshooting respectively. Execution (and oversight) of scale up & scale down experiment for Manufacturing Science & Technology. To ensure timely completion of all the projects assigned, experiment design, planning and execution of experiments. Interdepartmental co-ordination with DQA, DQC, Animal House, engineering & warehouse. Literature, research paper review and its implementation. Preparation of pr...

In this role at Foundation for Neglected Disease Research (FNDR), you will be responsible for designing and executing synthetic routes to prepare small molecules for drug discovery programs. Your key responsibilities will include tracking SAR, optimizing potency, selectivity, and properties of small molecules, as well as performing purification and structural characterization of compounds. You will also troubleshoot synthetic problems, optimize reaction conditions, and provide mentorship and guidance to junior colleagues. Additionally, you will maintain accurate lab records, contribute to technical reports, collaborate with analytical teams, and provide input on intellectual property activit...