25 Uv Spectrometer Jobs

Responsible for conducting various chemical analyses, ensuring the safety and compliance of waste handling procedures, and contributing to the optimization of waste management processes. Exp: 2 to 5 years Salary : 5-7LPA Location : Baddi/Nalaghare

Date: 1 Aug 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Description Job Title: Junior Analytical Development Scientist Oral Solids Job Location: Bangalore Department: Analytical Development Drug Product About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SO...

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.

As a Chemist, you will be responsible for carrying out production and quality control activities in the pesticides industry. The role will be based in Raipur (Chhattisgarh) and Rawanbhata Industrial Area. Your primary duties will include operating laboratory equipment such as GLC, HPLC, UV spectrometer, and other related instruments. To excel in this role, you should have previous experience in handling production and quality control activities within the pesticides industry. If you have a strong background in chemistry and the capability to work with precision and attention to detail, we encourage you to apply for this position.,

Your key responsibilities: Chemical analysis of raw materials Instrument experience - Ultraviolet-Visible Spectroscopy (UV-Vis) , Infrared Spectroscopy (IR), Polarimeters , Potentiometers , total organic carbon (TOC) analysers, atomic absorption spectrophotometry (AAS) What you will bring to the team: Strong knowledge of analytical chemistry and instrumental techniques. Ability to work independently and as part of a cross-functional team. Problem-solving mindset and readiness to learn and adapt. B.Pharm / M.Sc. qualification with 23 years of experience in QC analysis of raw materials in the pharmaceutical industry.

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 BS...

Lab chemist required at pio manihari, sonipat for a spices company Qualification- Any graduate Exp- min 2 yrs Salary- upto 25k Timing - 9.30 to 7 pm

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 ...

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, Finis...

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...

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 ...

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.

Review SOPs, QMS, specs & test methods; follow cGMP & GDP; perform sampling/testing of raw, packaging, intermediate & finished products post-training; suggest QC improvements; complete tasks assigned by QC Manager accurately & on time.

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

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.

Role & responsibilities: 1 Preparation of standard operating procedure with its annexure. 2 Preparation of Specification, standard test procedure of Raw Material, Packing Material, Finished product as per pharmacopeia and in-house methods. 3 Performing instrument qualification and calibration as per schedule. 4Sampling , analysis and review of raw water, purified water, raw material, packing material, finished product and in process sample, stability sample as per Specification with ERP entries 5 Preparation of COA of raw material, packing material, finished product and in process sample and stability study summary sheet ,trend analysis. 6 Maintenance of reference standard, primary standard ...

Role & responsibilities Analysis of In-Process samples, Bulk and Stability Samples. Monitoring & recording of temperature and Humidity of quality control department. Operation and Calibration of Laboratory Instruments. Maintained Good Laboratory Practice in Laboratory. Perform verification of balance, conductivity & pH meter. Preparation of laboratory reagents & volumetric solution & standardization. Receiving of In-process samples, Bulk, finished product samples, stability samples for analysis from production in shift. Preparation and maintain his training records. Any other job assigned by section head and Head-QC.