792 Uv Jobs

Job Description Responsible for planning and execution of disinfectant preparation, equipment cleaning and laboratory cleaning activity. Responsible for Planning and execution of Microbial analysis of raw material, packing material, intermediate / in-process samples, Particulate matter testing, Bacterial Endotoxin testing, Antimicrobial effectiveness testing, Bio burden testing and swab testing. Responsible to perform the fogging activity in Microbiology area. Responsible to preparation, sterilization and maintenance of in-house / Ready to use culture media. Responsible to Dry heat sterilization of glassware’s. Responsible to maintain the equipment and instruments. Responsible for transfer, release and observation of microbiological analysis plates & tubes within timeline. Work Experience Education :-M.sc- Microbiology/Biotechnology Experience :- 2 to 6 yrs. Education Others Competencies

Effective operation and maintenance of equipment like autoclave, Garment cubicle, sealing machine, vessels CIP and SIP SKIDS To practice the c GMP activities and to follow the clean room discipline Cleaning and sterilization of the vessels and transfer lines using CIP & SIP equipment Preparation and filtration of disinfectant and cleaning of the area Monitoring of LAFU, AHU, Dynamic pass box, Garment cubicles and cold rooms Maintaining of all cGMP activities and housekeeping activities in the critical operations Maintenance and updating of equipment log books and GCRs Manual recording of the temperature and positive pressures Cleaning of equipment Blending of vaccines Preparation, Sanitization and sterilization of the items to be sent into Grade-B area Destruction of the rejected & unwanted materials and recording of the same Release of vaccine from blending to filling area To follow the usage of personnel protective equipment (PPE) during handing of corrosive liquids, WFI and steam Solution preparation Operation of Filter integrity machine Perform aseptic operations in Grade B area Any other tasks assigned by the supervisor.

Job Description :- Quality Control Officer / Sr. Officer Scicore Nutra Private Limited is a state-of-the-art facility, located in Sanand Gujarat, is dedicated to producing high-quality nutrition products that are safe, effective, and meet the highest standards of quality. Our team of experts is committed to ensuring that every product we manufacture is produced with the utmost care and attention to detail. At our manufacturing unit, we use only the best raw materials and employ advanced manufacturing processes to ensure that our products are of the highest quality. We also adhere to strict quality control measures to ensure that every product meets our rigorous standards. This starts with doing a rigorous vendor qualification as well as testing of all raw materials supplied by these vendors for every batch. We do in-house stability studies to make sure our products last the full shelf life and give the best results to our customers. Our goal is to provide our customers with nutraceutical products that promote health and wellness, and we are committed to using science-backed ingredients and formulations to achieve this goal. We are also committed to continuous innovation and improvement and are always looking for new ways to enhance our products and processes. Benefits Provided: 1 Free Air-Conditioned Transportation to the Factory 2 Paid Leave 3 Tea/Coffee & Canteen Facility 4 Accident Insurance 5 Provision for Bonus & Gratuity 6 Training programs for professional advancement 7 Progressive work environment conducive to personal and professional growth Job Title :- Quality Control Officer / Sr. Officer Role & Responsibility: - To follow and ensure Good Laboratory Practices. To perform the work according to work allotment. To follow good documentation practices while making entries in Documents and records. To support the investigation and learn from the senior. To perform the Calibration of Laboratory instruments as per PM scheduled. To enter the details in respective equipment logbook. To enter the details of intimation in respective register. To performed the Inventory control of chemicals and Glassware. To prepare the volumetric solutions, reagents and indicator. To perform the Standardization of volumetric solutions. To perform the analysis of raw material, packing material, semi-finished goods and finished goods. Handling of Reference standard and Working standard and qualification of working standard. To performed testing and release of incoming, in-process, finished and stability product as per the laid down specifications and method of analysis/STP. To perform the preparation of CoA of raw material, packing material, stability and finished product. To performed the rejection of raw material / Packing Material/Finished/ Stability Product. Make sure that materials are appropriately tested and results are reported. To perform the Initiation and review of any change related to the department. To perform the Preparation and review of all SOPs related to department, Specification and test procedures. Testing of raw material, packing material and water sample as per respective method of analysis/STP. To performed testing and release of incoming, in process, finished and stability product as per the laid down specifications and method of analysis/STP. To prepare SPEC,STP and TDS. Any additional job responsibilities as assigned by HOD. Department :- Quality Control Number Of Positions:- 01 Experience : 2 to 4yrs Employment Type: Full Time, Permanent Education UG: B.SC in Any Specialization PG: M.SC in Any Specialization Compensation :- As per Industry norms & experience Key Skills QC, UV, HPLC, ADL, Analytical, Method Development

We are seeking a highly skilled Executive / Sr. Executive Quality Assurance with 8 to 10 years of experience in API / Bulk Drug Manufacturing . The role involves overseeing laboratory incidents, OOS/OOT investigations, analytical method validations, data integrity compliance , and ensuring adherence to GMP and regulatory standards . Key Responsibilities: Handle and review laboratory incidents, OOS (Out of Specification), OOT (Out of Trend), deviations, and root cause investigations . Review and monitor calibration schedules and records for critical analytical instruments (HPLC, GC, UV, IR, AAS, ICP-MS). Oversee analytical method validation, method transfers, and specification reviews in alignment with regulatory requirements. Provide training to QC teams on laboratory procedures, data integrity , and documentation practices . Conduct surprise lab audits/visits and proactively identify compliance gaps to ensure readiness for inspections. Ensure compliance with cGMP, ICH, and regulatory guidelines throughout QA operations. Eligibility Criteria: Education: B.Sc / M.Sc in Chemistry or related field. Experience: Minimum 8 to 10 years in pharmaceutical Quality Assurance (API / Bulk Drug). Preferred Candidates: Male candidates available for immediate joining .

Responsibilities: (1) To conduct analysis such as GC, HPLC, Wet Chemistry, GC-MS, LC-MS, FTIR, UV-Vis, DSC, Particle Size Analyzer, Viscosity, Density etc.(2) To maintain Analytical Lab note books, procedures, documents and records(3) To maintain laboratory and work place as per norms(4) To maintain ISO 17025 and ISO 9001 management systems(5) To work safely and maintain housekeeping of the lab(6) To work in shifts as per requirement of the job(7) Implement SOP for the storage of analytical standards and reference samples at Thane under required conditions and maintain a database

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

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

Candidate must have strong knowledge in Core PHP, Laravel, MYSQL, jQuery, AJAX, HTML and CSS. Must have a work experience of 1-2 years on PHP & Laravel Framework. Web-based software application development and maintenance on PHP

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

1. Coordinate with Sales team and Plant from Order punching to despatch details 2. Regular Follow up for the Payments from clients 3. Support sales team for Quotes, Ledgers, PI, Debtor reports, monthly and weekly sales reports

Planned purchase to maintain stock. Having knowledge in IT Hardware & Software Procurement. Creating PO & Buying Activities. Having a good Knowledge in material Follow-up with Vendor & Supplier.

analytical lifecycle: specs with RA, method validation, testing of RM/PM/IP/FP, water & environmental monitoring, stability programs.data integrity (ALCOA+), LIMS audit trails chromatography governance (integration, SST, system suitability).

Responsibilities: * Manage post press operations from UV coating to packaging * Ensure quality control measures are implemented * Collaborate with printing team on monocartons and corrugated box production Assistive technologies Accessible workspace Flexi working

Officer Quality Control - API & Intermediates Education - M.SC - Analytical / Organic Experience 1 to 3 years experience in Quality Control from pharmaceutical industry. (This is a Fixed Term Contract role - On Company's Contract) Job Description - Sampling of raw, packing material, intermediate & finished product. Analysis of raw, packing material, intermediate, stability samples & finished product. Analysis of process & cleaning validation samples. Preparation of standard volumetric solution, reagent & standardization of volumetric solution and check for stability. Inventory of Instruments Spares, Chemicals & Glassware. To maintain cleanliness, personal and environmental safety & follow Good Laboratory Practices during work. Ensure environment protection by controlling Air / Water / Soil pollution from analytical activities. Accountable for the safe operation of the facility, their own safety and safety of other co- workers. Technical & Behavioral Competencies - • Instrumentation & Analysis in Quality Control • Aware of GXP requirement in Quality Control Laboratory, Data Integrity & ALCOA+ • Knowledge of laboratory investigation • Good Communication Skills, team player, collaboration. • Knowledge of MS Office - MS Word, Excel

About the Team At Nutanix Cloud Manager, we are trying to build the next generation platform to help enterprises model, develop and manage applications. We want to give them the ability to encapsulate not only infrastructure but even the application its architecture and deployment as code. You will be reporting to the Senior Manager Engineering, QA - NCM Team. Your Role As the gatekeeper of our product quality, you would be required to ensure that product releases adhere to the highest quality norms. You will design and develop a testing framework for our products and be part of a ruthless quality team. You will develop test tools, test cases, maintain test beds, and provide metrics and test/quality status. What You Will Bring: Be a self-starter who can flourish in a fast-paced technology company Be the owner of our automation and delivery systems Be actively participating in Coding & Code reviews Have expertise in languages like Python, JAVA Have expertise with automation and building tools such as Selenium, JMeter and Jenkins Strong systems background (Linux systems with exposure to Process, Memory and IO Management tools You will enable our engineers to generate known-quality releases with every commit, discover defects early and iterate fast. Thrive on working on open-source technologies. Excellent programming and scripting capabilities to develop code for automated tests. Should have an extremely good problem-solving approach with good hands-on knowledge of Algorithms & Data Structures.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC

Medcare Hospitals Medical Centres is looking for Senior Associate to join our dynamic team and embark on a rewarding career journey Gathers and collect all the financial data and information, to verify whether it has been accurately entered in the systemReview and post account payable ledger entries, manage and process invoices, to prepare and review account receivable, and other balance reconciliation Assists in tracking the journal entries by reviewing the source documentation and making relevant adjustments, assisting in the preparation of audit requirements, supporting in the preparation of statistical reports Provides support in budget preparation and drafting of relevant documents, perform miscellaneous filing, ad hoc reconciliation, etc Provide appropriate guidelines for improvising the process, and to identify opportunities for enhancement Prepares monthly and quarterly MIS required by the various stakeholders Monitoring and reconciling bank accounts and other financial accounts Uses financial modelling to predict the outcomes Review and upgrade the financial plans from time to time Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before

Job Description Handling of Potentiometer titration, Karl-Fisher , Calibration of Potentiometer titration , Karl Fischer , Handling of Polarimeter, Handling of UV Spectrophotometer, Handling & Calibration of PH meter, Show more Show less

Responsible for making Sales budgets for the corporate office Daily / Weekly / Monthly monitoring of the sales numbers and ensuring budgets are met Creative thinking / Brainstorming sessions with team members for improving sales numbers

We are seeking a talented and motivated R&D Executive specializing in synthesis to join our Agrochemical research and development team. The ideal candidate will be responsible for developing, optimizing

We are seeking a talented and motivated R&D Executive specializing in synthesis to join our Agrochemical research and development team. The ideal candidate will be responsible for developing, optimizing,

1.Understand the project requirements & deliverables from supervisor/manager 2.Carry out literature search by using SciFinder, Reaxys and other search engines 3.Comprehend and discuss the MSDS with supervisor/ team members.

Urgent Requirement in PHARMA Industry... Fresher's & Experience persons wanted in QUALITY CONTROL(Wet Analysis / HPLC / GC) AND RESEARCH & DEVELOPMENT (R&D) Department in Pharma Industry, Candidate should have good working experience in Pharma Manufacturing Units.. Roles and Responsibilities: FOR QC DEPARTMENT In the pharmaceutical industry, the Quality Control (QC) department is responsible for testing and analyzing raw materials, in-process materials, and finished drug products to ensure they meet safety, purity, and efficacy standards. QC Wet Analysis Department (or Wet Chemistry Lab) is responsible for performing traditional, bench-top chemical tests on raw materials, in-process samples, and finished products to ensure they meet quality specifications and regulatory standards. Gas Chromatography (GC) is a critical analytical technique used within the QC department to: analyze the chemical components of drugs, determine the purity of ingredients, and verify that the final product meets specifications for release. In the pharmaceutical industry, the Quality Control (QC) HPLC department uses High-Performance Liquid Chromatography (HPLC) to analyze raw materials, intermediate products, and final drug products, ensuring their identity, purity, potency, and stability. Roles and Responsibilities: For R&D DEPARTMENT The pharmaceutical R&D department is responsible for the entire lifecycle of new drugs, from discovering and developing them, through preclinical and clinical trials, to regulatory approval, manufacturing, and post-market surveillance. Key responsibilities include, conducting scientific research, designing experiments, analyzing data, managing clinical trials, ensuring regulatory compliance, and fostering innovation to bring safe and effective new treatments to patients. Qualification: B.SC(CHEMISTRY) / M.SC(CHEMISTRY) Experience: 0-5Years Salary: 15-30K Location : Jeedimetla ,Bollaram Hyderabad. Note : Only Male Persons Required. Contact: 8977333658.

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.

Responsible for making Sales budgets for the corporate office Daily / Weekly / Monthly monitoring of the sales numbers and ensuring budgets are met Creative thinking / Brainstorming sessions with team members for improving sales numbers