14 Uv Spectrometer Jobs

Job Description: As a Lab Chemist / Scientist, you will be responsible for analyzing environmental (Water, Waste Water, Soil) and food samples. Your main duties will include maintaining documents in compliance with NABL & ISOI 7025 standards. Additionally, you will need to have knowledge about the uncertainty principle and hands-on experience in handling various equipment, especially UV spectrometers. Experience in handling an Instrumentation laboratory (GC-MS, ICP-OES) will be considered an added advantage. Your role will also involve analyzing results by calculating the quantity of elements in a sample and interpreting analytical data. Qualifications required for this position include a BSc / M.Sc / PhD in Chemistry or Biochemistry. The ideal candidate should have 0 to 5 years of relevant experience. This position is based in Chennai (Ayapakkam) and there are 3 vacancies available. The salary for this role is not a constraint for the right candidates, and bachelor accommodation will be provided for outstation individuals. If you meet the requirements for this role and are interested in joining our team, we encourage you to apply now. --- As an Oil & Gas professional, your responsibilities will include interpreting data to identify key performance indicators and trends, creating company reports and documentation that offer key data insights, and ensuring accuracy and consistency in reporting. Qualifications required for this position include Any Degree with 1 to 3 years of relevant experience. In addition to these responsibilities, you must be proficient in typing documents with a flexible typing speed and have knowledge of Excel, Word, and PPT. You will also be required to maintain documents as per NABL & ISO17025 standards. This role has 1 vacancy available and the salary is not a constraint for the right candidate. Bachelor accommodation will be provided for outstation individuals. If you believe you are the right fit for this role, we encourage you to apply now.,

You will be joining Credent Life Sciences Pvt Ltd, a company dedicated to the manufacturing and development of pharmaceutical formulations at its R&D and Manufacturing facility in Sehore, MP. In this full-time on-site role as a Quality Control Chemist Instrumentation, you will be responsible for handling instruments such as FTIR, UV Spectrometer, and HPLC. Your duties will include conducting quality control tests, analyzing samples, calibration and maintenance of laboratory equipment, documentation and interpretation of test results, and ensuring compliance with drug regulatory and safety requirements. To qualify for this position, you should hold a degree in M.Pharm/B.Pharm or MSc/BSc with 3-6 years of experience in a Pharmaceutical Quality Control laboratory. Proficiency in laboratory skills involving instruments like FTIR, UV spectrometer, and HPLC is essential. Your analytical skills will be crucial for interpreting and analyzing data and test results. Experience in calibration and maintenance of laboratory instruments is required, along with a keen eye for detail and strong organizational skills. Effective written and verbal communication skills are necessary, as well as the ability to work both independently and as part of a team.,

1. Analysis of Bulk/Granules/Intermediate/Stability & F.G 2.Sample analysis and reporting according to DCAD/DPAD 3. Raw data filling & online reporting 4.Analysis of raw material & finished product sample by HPLC & GC 5.Analysis of sample by UV-VIS Spectrophotometer & dissolution test. Preferred candidate from Pharma OSD Formulation experience only.

Responsibilities: * Conduct quality control tests using HPLC, UV spectrometer & Karl Fischer methods. * Ensure compliance with industry standards through regular inspections. Education: B.Sc/M.Sc in Chemistry, Food Science, Nutrition, Biochemistry Food allowance

QC Chemist

Key Responsibilities / Skills Required: We require a Q.C. Chemist for our chemical manufacturing plant located at Vatva, Ahmedabad . The ideal candidate should have hands-on experience with: Wet lab operations & basic titration UV Spectrophotometer Karl Fischer titration pH meter handling Moisture content, NV, and LOD analysis

Role & responsibilities Profile: QC Sr. Chemist/ QC Officer to Senior Officer for Active Pharma Ingredients Industry in Samba (Jammu). Distance from Pathankot(Punjab) to Samba (Jammu) Manufacturing Unit is 50Kms away. No. Of Positions - 8(QC Chemist/ QC Officer/ QC Executive/QC Sr. Executive) Mandate Qualification - B.Sc/ M.sc Chemistry Experience - 2-10years Knowledge of Instruments- HPLC, GC (Gas Chromatography), UV Spectrometer, Kal Fischer and Experience of Wet Lab Knowledge of GMP and cGMP and Safety of their concern area. Preferred candidate profile: Candidate required only from API Industry from Pharma Industry. Early Joiner will be preferred for this position

Role & responsibilities Monitoring the temperature & cleaning in QC area. Daily verifications of balance & pH meter. Preparation & Standardization of Volumetric solutions & there consumption records. Water sampling & analysis. Reagents & Buffer preparation & their records. Sampling & analysis of Raw Material, Packaging material, Semi Finished Products, Finished Products & retesting materials. Their documentation. Preparation & analysis of Working standards. Trace Sampling & analysis. ETP water analysis. Preparation of Specifications & raw data. Calibrations of instruments. Process validation & Hold time study of SFP. Updation of Raw Material, Packaging material, Semi Finished Products, Finished Products & retesting materials in SAP. Stability analysis.

Company: Strides Pharma Science Limited Department: Quality Control Profile: Executive Locations: Bangalore Qualification: B. Pharma/ M. Pharma/ M.Sc. Chemistry Experience: 2 to 6 years Key skills: Analysis of Material / Product by referring current version of specification STP with relevant material code. Responsible for initial set up of Instrument/Equipment before starting the analysis with relevant online entries in usage Log / LIMS. Perform the Assay and RS by LC/UV/Dissolution, content uniformity by LC analysis with simple and complex products Tests as per SOP/STP. Proper handling of chromatographic column used for analysis. Maintain data integrity and appropriate traceability

Company: Strides Pharma Science Limited Department: QA/QC Profile: Executive Locations: Alathur/Puducherry Qualification: B. Pharma/ M. Pharma/ M.Sc. Chemistry Experience: 2 to 6 years

Department: Quality Control Location: Tehsil Inodra, Kangra (HP). Near by Pathankot Reporting to: QC Manager / Head Quality Department Key Responsibilities: Conduct routine testing of raw materials, in-process materials, and finished products as per approved specifications and standard test procedures (STPs). Perform chemical and instrumental analysis using HPLC, UV, IR, GC, KF, etc. Maintain accurate and up-to-date laboratory records, worksheets, and logbooks. Ensure timely calibration and maintenance of laboratory instruments and equipment. Review and follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Assist in method development and method validation activities as required Conduct stability testing and prepare stability summary reports. Ensure compliance with company SOPs, quality standards, and regulatory requirements (such as USFDA, MHRA, WHO, etc.). Participate in internal and external audits and implement corrective and preventive actions (CAPA). Manage sampling, labeling, and storage of test samples as per SOPs. Handle out-of-specification (OOS), out-of-trend (OOT), and deviations according to quality procedures. Coordinate with production, QA, warehouse, and other departments for quality-related issues. Monitor environmental conditions of the lab as per the standard protocol. Desired Candidate Profile: Education: B.Pharm / M.Pharm / B.Sc / M.Sc Chemistry or related field Experience: 2–10 years in QC role within a pharmaceutical formulation plant Skills Required: Proficient in operating analytical instruments (HPLC, GC, etc.) Knowledge of GMP, GLP, ICH guidelines Strong documentation and communication skills Attention to detail and ability to work under pressure Good analytical and problem-solving skills

Role & responsibilities Knowledge of Polymer testing ,raw material testing ,in-process testing, utility samples -water, steam and ETP water testing and general chemical testing, instrument handling: GC,UV,KF,AUTO Titrator, Moisture balance, flame photometer and etc. Essential: above 2-3 years Desirable: Qc lab working experience of chemical industry

Hiring: Operators & Officers for OSD Production & Packing (Onco & Non-Onco) | Sterile Production | Quality Control | Microbiology Interview Location: Elite Hotel, Jadcherla Walk-in / Immediate Joiners Preferred 1. Operators & Officers for OSD Production & Packing (Onco & Non-Onco) Experience: 2 to 6 Years Qualifications: I.T.I / Diploma / D. Pharmacy / B. Pharmacy Job Responsibilities: Operation of equipment: Granulation, Compression, Coating, Capsule Filling, Blister & Bottle Packing Supervision of Granulation, Compression, Coating, and Packing lines (Blister/Bottle) 2. Officers & Operators for Sterile Production (Onco) Experience: 2 to 6 Years Qualifications: Diploma / B. Sc / D. Pharmacy / B. Pharmacy Job Responsibilities: Supervision of Manufacturing, Compounding, Filling, Filtration, and Packing areas Strong knowledge of QMS (minimum 5 years preferred) Hands-on experience in Manufacturing and Compounding Operation of equipment in Filling, Filtration, and Packing 3. Analyst for Quality Control Experience: 2 to 5 Years Qualifications: M.Sc / B. Pharmacy Job Responsibilities: Analytical testing of Finished Products, Stability Samples, and Packaging Materials Proficient in handling instruments HPLC, LIMS, Dissolution Apparatus, UV Spectrometer, KF Apparatus, IR Spectrometer, Metrohm Auto Titrator RM/PM/IP/FP analysis, Assay, and Dissolution using HPLC Strong understanding of GLP, GDP, cGMP, ALCOA & ALCOA+ principles 4. Microbiologist for QC Micro (OSD / Injectables) Experience: 0 to 6 Years Qualification: M. Sc (Microbiology) Job Responsibilities: MLT & BET Analysis, Sterility Testing Water Sampling and Analysis Environmental Monitoring Activities Note: Only Formulation experience with Regulatory exposure will be considered.

Perform sampling and testing of raw materials, packaging, and finished products. Maintain QC records and documentation as per SOPs. Ensure compliance with GMP, ISO, and regulatory standards. Report quality issues and support corrective actions. Required Candidate profile B.Sc./M.Sc. in Chemistry 2+ years in Quality Control, preferably in cosmetic or chemical ind Know of analytical instruments Strong attention to detail and understanding of quality standards.