52 Autotitrator Jobs - Page 2

Posted On 04th Jun, 2025 : The candidate will be primarily responsible for laboratory testing and R&D activities both in the lab and on the plant floor. The role involves developing and implementing testing procedures for new products, ensuring compliance with ISO 9000 standards, and maintaining accurate records and documentation. Key Responsibilities: Conduct lab-based testing and support R&D activities within the lab and plant environment. Develop and implement testing protocols for new and existing products. Maintain and update all ISO 9000 documentation and records related to lab activities. Coordinate with the designated ISO representative (e.g., Mr. X) for documentation control and com...

Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA Calibration of the Analytical instruments as per the master calibration schedule Preparation and review of Specifications, Method of analysis procedures and Analytical development reports Experience 4 - 10 Years Industry Engineering Engineering Design R&D Quality Qualification M.Sc Key Skills QC Chemist Agrochemical Chemical QC QA Engineer Quality Control Engineer M.Sc Chemistry Chromatography UPLC HPLC SC

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials Required Candidate profile Experience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC.

Job description Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA Calibration of the Analytical instruments as per the master calibration schedule Required Candidate profile Preparation and review of Specifications, Method of analysis procedures and Analytical development reports

Department :- Quality Assurance & Quality Control Experience Required :- 06-08 years (Agrochemical or Chemical Industry Experience Must) JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) 1 Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. (qualitative and quantitative chemical and collect/physical analysis of raw materials, finished products and/or stability samples) 2 Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. 3 Using chromatography, spectroscopy, and spectrophotometry techniques. 4 Developing, improving, and customiz...

Greetings from Sri Krishna Pharma We are hiring Quality Control for our API , Formulation (OSD ) and Nutra .Biotech Units Roles and Responsibilities Conduct quality control tests on OSD (Oral Solid Dose) and API (Active Pharmaceutical Ingredient) products using various instruments such as HPLC, GC, UV-Vis Spectrophotometer, Polarimeter, Karl Fischer Titrator, pH Meter, Finished Products Analyzer, Melting Point apparatus, Auto titrator, IR Spectrometer, Potentiometer. Ensure compliance with cGMP guidelines during testing procedures. Maintain accurate records of test results and reports. Collaborate with cross-functional teams to resolve any issues related to product quality or manufacturing p...

Responsibilities: * Conduct analytical tests using HPLC, GC, Karl Fischer, spectrophotometer, pH meter, Karl Fischer titrator, viscometer, autotitrator & melting point apparatus.

We are seeking a skilled Analyst with hands-on experience in FTIR/Disso/UV/KF/HPLC/GC techniques(Multiple requirements). The candidate should be well versed with Method Development, Method Validation and routine analysis. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) If interested please share profiles on nilesh.kadam@geochem.net.in or any more information call on 9870476784

Position Executive / Sr. Executive- QC Grade : A3 A4 Business Unit / Function Department - Quality Control Location Bharuch; SEZ;;;; Reports to Lab In charge-QC; Summary of Job (Purpose/ objective of the job Department Organogram to be enclosed) candidate is required having complete experience in API/Bulk/ Intermediates industries as per global regulatory requirements and responsible for implementation and compliances of ICH-Q7A, cGMP, WHO-GMP, ISO9001, FSSC, HACCP / global QMS requirements at SEZ site. Key Responsibilities (Performance Indicators) Knowledge about IMS system (ISO 9001:2015, ISO 14001:2015 OHSAS 18001:2007, and cGMP, USFDA, FSSC - 22000, NABL. Analytical skill for QC instrume...

FERRING THERAPEUTICS PRIVATE LIMITED is looking for Analyst QC to join our dynamic team and embark on a rewarding career journey Analyze data, interpret trends, prepare reports, and support decision-making through insights Develop models, work with tools like Excel, SQL, or Python Ensure data accuracy, and contribute to business optimization and forecasting efforts

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

Company: Strides Pharma Science Limited Department: Quality Control Position: Executive Job Location: Alathur Qualification: M.Sc. (Chemistry), B-Pharm, M-Pharm 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 traceab...

KRA: To provide routine analytical support to the synthetic team for reaction monitoring by HPLC/GC, analysis of intermediates and API. Perform wet analysis as LOD, IR, Residue on Ignition, KF determination, Titrations etc. Calibration of instruments such as UV, IR, HPLC, GC, Autotitrator, polarimeter etc. LNB writing and all documentation as per 21 CFR compliance. Preparation of required documents for PDR. Skills required: Good communication skills, and effective team player with the ability to work on multiple projects. Robust knowledge of principles, working of applications techniques such as HPLC, GC, Autotitrator, UV spectrophotometer and other laboratory instruments. Responsibilities Q...

Streamline the data review process across all GxP systems, including CDS, FTIR, UV, KF, LIMS, MES, and more. Pro CDS Hub Our Vision for Digital Manufacturing & Future Quality Control Pro ExtractEase Pro ExtractEase automates data extraction from Empower to facilitate insights from the data. Pro Das Is a versatile platform tailored to automate the Project Creation, Back-up/Restoration activities of Empower. Pro QMSuite Is a system that documents the policies, procedures, and controls necessary for an organization

To perform the environment monitoring of Aseptic area and supporting area. To perform the Microbiological test for Water system sample, SFG, RM, PM samples To prepare the trend data for the Microbiological monitoring of area and water system samples. To perform the Gowning qualification of other department personnel. To involve in media fill and Qualification of Micro lab and Mfg. area equipment.

Responsible to develop, implement and be responsible for the production plan for their respective departments. To deliver timely and accurate analysis of samples to meet customer commitments. Be responsible for record control, measurement traceability and testing results review and approve the testing reports. Maintenance of Standard Reference Materials, Chemicals, Reagents, and Glassware used in the laboratory. To support the installation of additional analytical equipment, methods for the analysis of all kinds of food/feed/water matrices based on the transfer of existing methods and knowledge form the Eurofins Group Preparation of standard operating procedures. Validation of non-standard t...

Long Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Competencies Education Others Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs.

Dear Candidates, Greetings from KEYBIZ DASHBOARDS, We are looking for Quality Control Executive & Sr. Executive injectables &OSD for one of our reputed pharmaceutical client, based at Hyderabad & Vizag location. Please find below openings list. Quality Control 1.HPLC 2.GC 3.UV 4.FTIR 5.KF 6.Finished Products 7.Raw Materials 8.Packing Materials. The above positions we are looking for Hyderabad & Vizag locations, interested please share us updated cv to prasanthi@mydashboards.in or feel free to call on 6305391924 Thanks and Regards Prasanthi - Dashboards Team HR

Analytical QA Reviewer - Officer: Looking for a candidate with 2 to 4 years of work experience as QC analyst / AQA reviewer in reputed pharma companies. Should have Knowledge of handling/ analytical data review of HPLC , FTIR , UV spectrophotometer , KF Autotitrator , Dissolution apparatus. Have Basic knowledge of CGMP , GDP , Data integrity . Should have Basic knowledge of OOS (Out of specification), OOT, OOC

Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-8 Years Qualification: B.Pharma/M.sc/M. Pharma Location: Moriya, Ahmedabad Job Role : Physico Chemical (Analyst)- Friability / DT / Hardness / Thickness / UV Perform physical and chemical analysis for Raw material/ Inprocess / Finished Product based on the test requirements like UV, friability, DT, hardness, thickness, moisture, average weight, and uniformity weight. Prepare documents for each analysis performed and get those checked by the reviewer. Perks & Benefits Dynamic work environment Career development opportuniti...

Carry out bench scale lab reactions to deliver products in expected yields & quality Monitors progress of reactions and interprets analytical data Documents the actual results of all experiments/synthetic procedures/QC analyses in the right formats Required Candidate profile Maintain all laboratory / analytical equipment’s as per standards Ensure compliance to IMS /DMS wherever applicable Contact Mr Deep at 9867038868, Email Id: ops@empowerrecruitments.com

About the Job Join Our Mission for a Sustainable Plastic-to-Plastic Circular Economy! Are you excited to work at the forefront of innovative technologies and sustainability? PolyCycl invites a dedicated Research Assistant to contribute to groundbreaking advancements in chemical recycling at our R&D center in Chandigarh, India. We are developing cutting-edge methods to transform post-consumer plastic waste into reusable, high-purity resources, advancing the circular economy. What We Seek: We are looking for a skilled Research Assistant with a Bachelor's or Master's degree in Chemistry and Petroleum, with 0-5 years of hands-on experience in laboratory experiments and analytical equipment opera...

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

Responsibilities: Responsible for Documentation work in QC Department Candidate must have Experience of HPLC , GC & Wet Analysis. Shall maintained all records related to manufacturing Overall looking after the complete filling, packing activities and Procurement of the packing material. To ensure the compliance of safety Requirement Cleanliness Hygiene and Environment in Working Areas. Responsible for Domestic / Export/ batch production & their Documents for their smooth Dispatch Activity. Required Skills: Team player Good in communication Required Qualification: - B.Sc/M.Sc - Chemistry