1425 Uv Jobs - Page 2

Maintaining GRNs Register updating. Raw material and Packing material receiving and ATRs raised to QC. Material issue updating in BIN cards. Raw materials Receipts, dispensing and updating Dispensing logbooks, Temperature Balance Calibration records, Housekeeping / Tools cleaning, records. Raw Material and solvents approved status updating. Hazardous material handling. Identification of the Re-test due materials and update details in logbook. Responsible for Raw Materials and Packing materials. To follow the cGMP And Safety Norms in the Warehouse. Responsible for Internal units materials transfers and dispatches. To Co-Ordinate our colleges and all over department. Re-test and Rejected logbo...

1. Sampling and routine monitoring of water systems. 2. Environmental Monitoring of Clean rooms. 3. Microbial Limit Test of Finished products, raw materials and water samples as applicable. 4. Bacterial Endotoxin Test of finished products and water samples, BET method validation of products. 5. Maintaining stock of Microbiological media and consumables. 6. Sub-culturing of Microbial Cultures. 7. Growth promotion test of media. 8. Calibration/ Qualification of Microbiology Lab equipment as per schedules. 9. Maintaining Microbiology lab in hygienic condition. 10. Microbiological method Development and validation for Finished products. 11. Preparation SOPs/ STPs, Protocols and other documentati...

Preparation of protocol, raw data sheets, reports, incident reports, excel validation sheets and SOPS. Review of Method validation activities Knowledge and handling of HPLC and GC instrument activities Qualification Groups Post Graduation M.Sc Graduation B.Pharma Graduation D Pharmacy Post Graduation M.Pharma

1. Sampling and routine monitoring of water systems. 2. Environmental Monitoring of Clean rooms. 3. Microbial Limit Test of Finished products, raw materials and water samples as applicable. 4. Bacterial Endotoxin Test of finished products and water samples, BET method validation of products. 5. Maintaining stock of Microbiological media and consumables. 6. Sub-culturing of Microbial Cultures. 7. Growth promotion test of media. 8. Calibration/ Qualification of Microbiology Lab equipment as per schedules. 9. Maintaining Microbiology lab in hygienic condition. 10. Microbiological method Development and validation for Finished products. 11. Preparation SOPs/ STPs, Protocols and other documentati...

Knowledge in Handling of HPLC and GC . Analysis results review and supported to team work. Competencies Result Orientation Breakthrough Achievement Speed Agility Exceptional Achievement Service Delivery Excellence Exceptional Achievement Teamwork Collaboration Breakthrough Achievement Business Knowledge Breakthrough Achievement Qualification Groups Graduation B.Sc Post Graduation M.Sc Post Graduation M.Pharma Graduation B.Pharma

Role & responsibilities Job Summary: We are seeking a detail-oriented and experienced Analytical R&D Chemist to join our synthesis lab. The ideal candidate will be responsible for developing, validating, and implementing analytical methods to support the research and development of new chemical entities and active pharmaceutical ingredients (APIs). This role requires a deep understanding of analytical chemistry, instrumental analysis, and method development. The Analytical R&D Chemist will collaborate with cross-functional teams to ensure the accuracy and reliability of analytical data. Key Responsibilities: Method Development and Validation: Develop and validate robust analytical methods fo...

Department: Quality Control &Production Division: API Location: Raichure Open Positions & Experience: Sr. Executive 06 to 08 years Executive 06 to 08 years Sr. Chemist 03 to 05 years Chemist 03 to 05 years Department: Production Open Positions & Experience: Executive – 05 to 07 years Sr. Chemist – 04 to 06 years Chemist – 02 to 04 years

Role & responsibilities Testing raw materials, in-process samples, and finished products against strict standards (GMP/GLP) to ensure drug safety, efficacy, and compliance, managing documentation (STPs, BPRs), handling deviations, investigating OOS/OOT, and providing batch release certification, requiring strong analytical skills, regulatory knowledge (FDA/ICH), and meticulous record-keeping. Handling Instruments like HPLC, GC.

Role Overview: As a Scientist at USP, you will play a crucial role in conducting analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods. Your expertise will enhance the laboratory's scientific proficiency and work ethic by providing technical support and knowledge. You will be proficient in various laboratory techniques and capable of offering valuable observations and insights into challenging projects. Your responsibilities will include executing analytical tests, preparing summary reports, and contributing to the Verification Program. Key Responsibilities: - Conduct verification projects on Dietary Supplements/Dietary Ingredients by perfo...

Role Overview: As a Scientist at USP, you will be responsible for conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods. Your role will involve enhancing the laboratory's scientific proficiency and work ethic by providing extensive technical support and knowledge. You will be proficient in various common laboratory techniques, offering valuable observations and insights into challenging projects. Your primary responsibility will be to provide technical aid to the Verification Program by executing analytical tests and preparing comprehensive summary reports. Key Responsibilities: - Conduct verification projects on Dietar...

Perform HPLC & GC testing for stability & finished products. Conduct HPLC analysis for cleaning samples. Support method validation, data compilation & reporting. Ensure Data Integrity, OOS, 21 CFR compliance, GMP documentation & lab incident handling

Department - Quality Control (Shift Duty) Section - HPLC Experience - 2 to 6 years Qualification - M.Sc chemistry (Full time) Job description 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 in...

As a member of Apotex Inc., a Canadian-based global health company, your role will involve planning and executing various analytical method development and validation for new products. You will be responsible for comprehensive testing of API and finished dosages while ensuring adherence to all established regulatory and compliance requirements. Your key responsibilities will include: - Preparing working plans and timelines for assigned projects - Developing stability indicative analytical methods for drug substance and finished product - Ensuring all activities in Analytical Development are in compliance with cGLP and departmental quality systems - Applying AQbD approach to analytical method...

Standard Reagents Pvt Ltd. an ISO 9001-2015 Chemical Manufacturing Company Head Quartered in Hyderabad, Manufacturing of Laboratoreis fine chemicals. QC Executives: Bsc /Msc with 2-3 year Experience. Only Male Candidates. Wet Analysis

Role: Quality Control Responsibilities : 1.Responsible for sampling and Instrumental/chemical analysis of RM, In-Process, Intermediate, Finished product, Cleaning samples, Validation samples, Market samples and Stability samples. 2.Responsible to perform the calibration of instrument/equipment available in Quality Control laboratory. 3.Maintain the laboratory as per GLP and GMP System. 4. Sampling, Analysis, and review of raw material/packing material, Wet analysis i.e., water content, IR, UV, LOD, Assay by potentiometry, Sulphated ash etc, finished goods sampling, working on HPLC & GC instrument. Other Conditions:- Manpower Required:- 3 Person for SSPL and ABPL Experience:- 2 to 4 Years Qua...

We are looking for skilled Chemists to join our team at Alvita Pharma, playing a crucial role in driving the development and implementation of new products and processes. The ideal candidate will have a strong background in chemistry and experience working with various chemical compounds. Roles and Responsibility Develop and optimize chemical synthesis routes for new products. Conduct experiments and analyze data to improve existing processes. Collaborate with cross-functional teams to design and implement new products. Troubleshoot issues related to chemical reactions and process optimization. Maintain accurate records of experiments, results, and procedures. Stay updated with industry tren...

Role & responsibilities Key Responsibilities Execution of experiments: Conduct experiments to evaluate water purifier-based components such as sediment, carbon blocks, RO membranes, etc. Also need to evaluate product performance as per specifications. He/She will be working under guidance of scientists/chemists. Documentation: Maintain comprehensive and accurate records of all experiments, results, and observations in lab computer. Reporting: Summarize experimental findings and project progress to seniors regularly. Safety and Compliance: Strictly adhere to all laboratory health, safety, and regulatory protocols, including Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GM...

Role & responsibilities Key Responsibilities Experimental Design: Plan and conduct experiments to evaluate water purifier based components such as sediment, carbon blocks, RO membranes, etc. Also need to evaluate product performance as per specifications. Analytical Testing: Perform chemical analyses using various basic instrumental techniques, including UV spectrophotometer, pH meter, TDS meter, turbidity meter and other basic instruments related to water analysis. Documentation: Maintain comprehensive and accurate records of all experiments, results, and observations in lab computer. Reporting: Summarize experimental findings and project progress in detailed technical reports and presentat...

Job Description Position Title: Manager Quality Control Department: Quality Control Location: Cadila Pharmaceuticals Ltd., Unit-II, Ankleshwar Reporting To: Quality Control Head Key Responsibilities: Plan and provide analytical support as per approved specifications, test procedures, and SOPs. Ensure all analyses are completed as per customer specifications and dispatch schedules , coordinating closely with planning and dispatch teams. Review and monitor daily QC activities and dispatch-related analysis , and report progress to the QC Head. Approve or reject raw materials, packing materials, intermediates, and finished products based on analytical data and established specifications. Review ...

Key Responsibilities : Good hands-on GC, HPLC, including troubleshoots Added advantages in selection process for operating knowledge. Instruments handle: - Dsc, Rheometers, Viscometer, auto titrator, spectrometer, Karl Fisher, FTNIR Basic Knowledge of LIMS & ERP Ready to work in shift 24X7 (All shifts)

QC Chemist role in a reputed specialty chemical company near Vadodara. Responsible for analytical testing, documentation, instrument handling, deviation analysis, and ensuring GMP/SOP compliance. Ideal for B.Sc Chemistry with 1–3 years’ experience. Perks and benefits Transportation + Canteen facility provided.

As a candidate with 2 to 7 years of experience in Analytical Chemistry, you have the opportunity to join a Chemical Manufacturing Company's Pharma Division in Ahmedabad. Your monthly salary will range from Rs. 35,000 to Rs. 40,000 based on your knowledge and expertise. Key Responsibilities: - Handle analytical instruments such as HPLC, GC, UV, IR - Perform instrument calibration - Analyze finished products and raw materials - Conduct wet lab analysis Qualifications Required: - 2 to 7 years of experience in Analytical Chemistry - Proficiency in handling analytical instruments - Strong knowledge of instrument calibration techniques - Ability to analyze finished products and raw materials - Exp...

Job Description: You should possess strong communication skills and be well-versed in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis. Key Responsibilities: - Demonstrate expertise in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis. - Communicate effectively within the team and with stakeholders. Qualifications Required: - Strong communication skills. - Proficiency in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis.,

Roles and Responsibilities Conduct analytical testing of finished products, including dissolution, UV-Vis, KF, FTIR, and GLP compliance. Develop and validate analytical methods for solid oral OSD products using techniques such as GC, HPLC, and UV spectroscopy. Perform method transfer and validation activities to ensure accuracy and reliability of test results. Collaborate with cross-functional teams to resolve OOS/OOT issues and implement corrective actions. Maintain accurate records of laboratory data, reports, and documentation in accordance with cGMP guidelines.

Division Department Employment Type Job Purpose Develop and finalize budget and monitor actual performance on key KPIs and support business by providing actionable insights to team to deliver long term sustainable & profitable growth To develop and implement systems for collecting, analysing, verifying, and accurate reporting financial information on a regular basis. To have an understanding of the business and prepare a rolling forecast to estimate the future performance of division. To create a robust MIS infrastructure to support decision making process. Accountabilities I. P&L Forecasting/ Budgeting ¢ Lead annual/quarterly forecasting/budgeting activity for business with help of marketin...