16 Uv Spectroscopy Jobs

RESPONSIBILITIES: Complete technical/scientific understanding on purification/downstream process of biopharmaceutical products Expertise in downstream process lab scale/pilot scale/ manufacturing scale equipment handling e.g., chromatography system, TFF system, filtration process, centrifugation, etc. Knowledge of execution of small-scale purification process using scale down model. Handling and working knowledge of lab instruments e.g., UV spectroscopy, Solo VPE, pH and conductivity meter, turbidity meter. Knowledge of downstream process scale-up strategies Process data collection, basic data analysis skill. Effectively work and communicate with team, CFTs and partners for planning and exec...

As a member of our team, you will play a crucial role in the purification of synthetic compounds using chromatography techniques such as Preparative HPLC, Flash Chromatography, and LC-MS. Your primary responsibility will be to optimize purification methods to ensure the recovery of high-quality compounds. Additionally, you will need to perform routine analytical characterization of purified compounds using techniques like NMR, Mass Spectrometry, and UV Spectroscopy. Your duties will also include maintaining laboratory instruments by ensuring proper calibration and troubleshooting minor technical issues. It will be essential for you to keep detailed records of purification processes, observat...

What You'll Do: Contributing strategically to the overall success of Biotechnology R&D by driving innovation and enhancing team performance, aligning with departmental/organizational goals. Ensuring the security of intellectual property for R&D. Carrying out literature search by use of all available databases. Conduct research and develop microbial consortia for wastewater treatment Design and execute experiments for the purification of proteins using chromatography, filtration, and other downstream techniques. Develop, evaluate, and characterize purification processes from lab to pilot scale. Collaborate with upstream, analytical, and formulation teams to ensure end-to-end process integrati...

Exp: 2- 6 yrs • Knowledge in Method Development on Assay, RS, dissolution for formulation complex molecules. • understanding of Q1/Q2 evaluation • PEQ processes and characterization • Instruments: HPLC, GC, KF, UV, IR, etc. kiran.k@orbicular.co.in

Job Description: We are looking for a motivated and detail-oriented Research Associate to join our Analytical R&D team within the Peptide Synthesis division. The selected candidate will support the development and execution of analytical methods for peptide characterization, working closely with cross-functional teams in R&D and Quality. Key Responsibilities: Assist in developing and performing analytical methods (e.g., HPLC, UPLC, UV, FTIR, KF, LC-MS) for the characterization and quality assessment of peptides Conduct routine testing of raw materials, intermediates, and final peptide products Support method validation, transfer, and troubleshooting under the guidance of senior scientists Do...

HPLC -GC Analysis and Reporting, Perform and Monitoring Total Lab Activity, wet lab Analysis , Create and maintain documents for Routine Operation. work distribution and team work, Monitor calibration and preventive maintenance Required Candidate profile Must Efficient hand on HPLC- GC analysis. Problem solving in HPLC, GC and wet lab analysis, having exp. of wet analysis like Titration, gravimetry, UV, Polarimetry, water analysis

Department - Quality Control Experience - 2 to 5 years Qualification - M.Sc chemistry (Full time) Section - HPLC / GC / Wet lab To ensure that training is acquired for each activity/instrument prior to its execution/operation and that it is as per respective TNI. To perform Analysis (Chemical)of raw material/packaging material/in-process samples /intermediate /bulk & finished products/ process validation samples/ stability samples/ cleaning validation/method transfer sample, PD lab sample etc. To ensure that all tests carried out in the laboratory are documented contemporaneously in an appropriate authorized and controlled worksheet/ bound book. To make entries in the sample inward register ...

You will be part of the Formulation Development team, contributing your expertise in Biologic Formulations and pharmaceutical sciences. Your responsibilities will include conducting literature reviews, formulating biological products, designing and executing experiments, analyzing data using various techniques, calibrating instruments, performing proof-of-concept studies, conducting stability studies, writing scientific reports, and collaborating with cross-functional teams. To excel in this role, you should hold a minimum of a Postgraduate degree (MTech, MPharm) in Pharmaceutical Sciences, Chemistry, or a related field. Proficiency in analytical techniques like HPLC, GC, pH, Osmolality, KF,...

Perform analysis of raw, in-process & finished goods. Operate GC, HPLC, UV, KF, IR. Maintain records, follow GLP & SOPs. Support method validation. Ensure ISO/regulatory compliance & coordinate with QA/production for batch release.

Exp: 2- 6 yrs • Knowledge in Method Development on Assay, RS, dissolution for formulation complex molecules. • understanding of Q1/Q2 evaluation • PEQ processes and characterization • Instruments: HPLC, GC, KF, UV, IR, etc. pranathi.p@orbicular.co.in

- Raw Material Testing: Conduct qualitative and quantitative analysis of raw materials to ensure compliance with specifications. - Packaging Material Testing: Evaluate packaging materials for durability, compatibility, and regulatory compliance. - Finished Goods & In-Process Testing: Perform routine and non-routine tests to verify product quality at different stages of production. - Instrument Handling & Calibration: Operate and maintain laboratory instruments such as UV Spectroscopy, colorimeters, and audit trail calibration systems. - Chemical Analysis: Conduct titration, nitrogen determination, loss on drying (LOD), and other analytical techniques. - Herbal Material Analysis & Extraction:...

Role & responsibilities 1. He shall be responsible to undertake training from the Section in Charge and the senior Analyst to make independent to carry out analysis. 2. He shall report to the senior analyst or analyst if any chemical, reagents or reference material is not available as per the requirement to carry out the analysis. 3. He shall be responsible to analyse samples received as per the specifications and for reporting of the results under the supervision of the senior analyst. 4. He shall be responsible to follow the quality system as per the policies laid down in the quality manual. 5. He shall be responsible for the preparation and standardization of the chemicals under the guida...

Role & responsibilities Job responsibilities for a Senior Executive in Instrumentation lab at Hetero Plasma Sciences, with 5-6 years of experience in Quality Control department. Operate, maintain and troubleshooting of HPLC, Gas chromatography (GC), UV Spectroscopy and Kjeldahl system for various analytical applications. Good Laboratory Practices: Ensure all laboratory activities comply with GLP standards, maintaining high-quality and reliable results. Good Documentation Practices (GDP): Maintain accurate and thorough documentation of all analytical procedures, results, and maintenance activities Method validations: Execution of method validations as per protocols, documenting and ensuring c...

Role & responsibilities Preferred candidate profile

Job Title: Junior Analyst / Analyst Experience: 1 to 3 years Location: Hyderabad CTC: 2.5 3.5 LPA Qualification: M.Sc. in Chemistry / Analytical Chemistry Preferred profile: from a food testing laboratory background Job Description: We are seeking a dedicated and skilled chemist with 1 to 3 years of experience in HPLC impurity analysis handling within the food testing industry. The ideal candidate should have a strong foundation in analytical chemistry, method development, and instrument calibration. Key Responsibilities: Perform HPLC impurity analysis in accordance with regulatory and laboratory standards. Conduct routine calibration and maintenance of HPLC instruments. Ensure accurate docu...

Role & responsibilities Ensure All Biopharmaceutical Development Lab Equipment are in state of GLP and Safety Compliance by rectifying equipment breakdowns, maintaining critical spares & consumables and carrying out equipment installations as per approved protocols. Attend breakdown of S1, S2 & S20 Equipment/ Instrument in lab and get it operational with support from instrument vendor and E&M team. Responsible for IQ, OQ, PQ for new instrument installation, calibration and maintain the supporting documents in coordination with DQA and E&M team. Responsible for the equipment requalification and completion of documents coordination with DQA and E&M team. Ensure that the S1, S2 & S20 Equipment/...