13 Chromatographic Techniques Jobs

About the Company: Sea6 Energy Pvt. Ltd. is a pioneering Indian biotech company specializing in sustainable solutions in the areas of food, feed, and fuel research. Leveraging cultivated seaweed biomass as a raw material, we have developed automated technologies for large-scale seaweed cultivation. Our innovations include commercialized bio-stimulant products that enhance plant growth and yield. Applications are invited from candidates with expertise in biochemical engineering or bioprocess engineering for a Bioprocess engineer position at Sea6Energy Pvt Ltd., Bangalore. We, at Sea6 Energy, work with marine macroalgal biomass to develop novel sustainable solutions in the research areas of food, feed and fuel. The person will be responsible for the execution and analysis of research projects related to the improvement of seaweed processing and extraction. The candidate will be part of the interdisciplinary team between R&D and manufacturing teams. A working knowledge of process design of purification and the characterization of active ingredients from natural resources/microbes/seaweed sources towards the development of agro formulations / bio stimulants will be prioritized. The candidate should have an ability to independently execute, analyse, interpret experimental results to compile reports/presentations to discuss in the internal and external meetings. Education qualifications: MS degree (by research) / MTech degree (biochemical/bioprocess/chemical engineering) with at least 2 years of research experience or a BTech degree with about 3-4 years of work experience in the below mentioned area is desired. Responsibilities: Process development for new products and improving the process/formulation conditions for existing products. Planning and execution on unit operations like hydrolysis, extraction, evaporation and spray drying. Microbial fermentation, downstream processing operations. Focusing on process troubleshooting, cost optimization and alternate process conditions explorations. Data analysis and reporting. Coordinate analysis with third party laboratory providing services such as mass spectrometry, ICP-OES etc. Experience in carrying out experiments involving spectrophotometry and chromatographic techniques- HPLC, FTIR, estimation of chemical components of a complex mixture, liquid-liquid extractions, solid-liquid extractions etc. Show more Show less

The Quality Control (QC) Chemist position requires you to conduct routine and non-routine testing of raw materials, in-process samples, and finished products following relevant specifications and standards. You will need to work in rotational shifts to support 24x7 operations and ensure prompt release of batches. Your responsibilities will include performing chemical, physical, and performance tests on raw materials, intermediates, and finished products using standard test methods. It is crucial to ensure compliance with internal specifications, customer requirements, and regulatory standards. Maintaining accurate documentation of test results, observations, and deviations is essential. Additionally, you will be responsible for calibrating and maintaining laboratory equipment, collecting and preparing samples for analysis, investigating non-conforming results, and participating in root cause analysis. You will also assist in validation, stability studies, and method development, follow EHS and 5S practices, coordinate with production, R&D, and QA teams for sample processing and batch clearance, participate in shift handovers, and support internal and external audits by maintaining traceable records and ensuring data integrity. Ideally, you should have a B.Sc./M.Sc. in Chemistry or related field, with 1-3 years of experience in a chemical manufacturing or resin/paint/adhesive/polymer-based QC laboratory. Freshers with strong fundamentals and willingness to work in shifts may also be considered. Key skills required for this role include expertise in wet chemistry techniques, titration, viscosity, solids content, pH, and basic knowledge of spectroscopic and chromatographic techniques. Strong documentation, data interpretation, attention to detail, and adherence to quality standards are essential. Comfort with working in shifts and in a fast-paced manufacturing environment is crucial. This full-time position is located in Mahad MIDC, Maharashtra. Benefits include cell phone reimbursement and Provident Fund. Applicants must be willing to commute or relocate to Mahad, Maharashtra before starting work. Experience in QA/QC and quality control is preferred, and shift availability includes day, night, and overnight shifts. This role requires in-person work. Note: The above job description is a summarised version based on the provided details.,

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

Production: Execute production batches, ensure GMP, manage documentation QA: Ensure cGMP, Issuance and retrievals and manage records. QC: Analyze biopharma samples & maintain Documentation R&D: Prepare stocks and buffers, extract proteins & analyze.

should Independently be able to perform the development of analytical methods for injectable formulations like suspension, emulsion, peptides, and other simple & complex injectables. Should be able to work on handling chromatographic techniques- HPLC, TLC, SEC-HPLC, IC, GC and other physico-chemical techniques like UV-visible spectrophotometer, coulometer, FTIR, Raman, ATR, etc. Should be able to work on various dissolution techniques applicable for injectable formulations like USP type IV, Bottle rotating apparatus, Type II, selection and use of MWCO membranes, etc. Handling of UPLC, Plate- Assy techniques is desirable. Should be able to perform routine analytical activities independently. Should be conversant with cGLP and cGDP required for performing, documenting and review of routine development activities. Should be capable of transferring the analytical methods at QC Labs, CROs, etc. Should be able to perform validation & verification of analytical & compendial methods, cleaning validation, etc as and when required Should have understandings on Analytical Quality by design (QbD). Desirable to have multitasking capability along with ability to think out of the box. Required good interpersonal skills, effective verbal and written communication skills. Work Experience M.Sc. and M.Pharm candidates 6 years to 15 years. Ph.D. candiadtes- minimum 3 years of experience. Education Masters in Pharmacy Post Graduation in Science or Chemistry Competencies

Responsibilities: Chromatographic techniques & System Handling Column Packing(BPG & Chromoflow) TFF System Centrifuge System Filtration, Filter Integrity, Buffer Preparation Expertise in Documentation, GMP Compliance

Responsibilities: chromatographic techniques. TFF system. Filtration. Document processes accurately. maintain GMP standards Prepare buffers according to specifications

Responsibilities: * Ensure GMP compliance through documentation & filter integrity checks. * Prepare buffers according to SOPs using chromatography techniques.

Knowledge of Method Validation & verification as per Pharmacopiea requirement. To perform Method Validation & verification of Chromatographic GC / HPLC methods. Preparation of specification in DMS & SAP system. SOP preparation related to AMD work. Required Candidate profile Candidate Must be MSc Regular. AMD protocols & report preparation, non-chromatographic methods. Maintain require stds & Impurities stock, list etc. Operation of instruments like HPLC,GC,UV,IR etc.

Knowledge of Method Validation & verification as per Pharmacopiea requirement. To perform Method Validation & verification of Chromatographic GC / HPLC methods. Preparation of specification in DMS & SAP system. SOP preparation related to AMD work. Required Candidate profile Candidate Must be MSc Regular. AMD protocols & report preparation, non-chromatographic methods. Maintain require stds & Impurities stock, list etc. Operation of instruments like HPLC,GC,UV,IR etc.

Urgent Opening for QC Chemist Knowledge of HPLC, GC, Stability , KF, UV, validation, Documentation etc

Key Responsibilities: The successful candidate will become a member of a team with overall responsibility for purification and analysis of small compound libraries to support lead optimization in medicinal chemistry programs. Individual responsibilities will include analysis and purification of small molecule library compounds (primarily by analytical and preparative LCMS), HPLC and mass spectrometer instrument maintenance, training, and analytical data management. Optimization and/or troubleshooting of analysis conditions will be required to ensure on time delivery of high purity products. Educational Qualification: M.Sc. in Chemistry/Analytical chemistry with 1-3 years of experience in practical analytical chemistry, including both analysis and purification. Experience: 1-3 Years Required Skills: Knowledge and expertise in preparative HPLC, LCMS, and other chromatographic techniques is desirable. Strong computer skills and good communication skills, are preferable. Demonstrated ability to work in a highly team oriented, multitasking environment with experience in technology enabled analysis and purification will be highly appreciated. Behavioral Skills: Good communication skills, good presentation skills, hardworking, sincere and a team player. Must demonstrate integrity and take accountability of their work

Role & responsibilities : Knowledge in handling and troubleshooting purification chromatography systems & columns at small scale and large scale Various Chromatography techniques like Ion exchange, Affinity, HIC etc. TFF systems , Hollow Fiber/cassette Should be well versed with FPLC, AKTA- Process, AKTA- Pilot. Capabilities for linear scalability of R&D process to Mfg. scale. Batch planning, Resource management, Team Training. Shift Schedule Preparation, Audit readiness Handling QMS, Project management, Deviation, Change control, CAPA, OOS, GDP Plan daily downstream execution activities Drive the qualification activities for all downstream equipment. Execute, troubleshoot, and scale up of purification processes, aseptic Operation. Compliance to cGMP in all the manufacturing activity, and timely closure of executed documents and batch records. Active trouble shooting to minimize the various risks prior to execution and during execution. Preferred candidate profile: Should have good communication and presentation skills (verbal & written) Person with high self-motivation, go-getter, enthusiastic. Leadership skills, with steadfast resolve and personal integrity Should have minimum 7 + years of Experience.