1128 Uv Jobs - Page 13

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP S/4HANA Group Reporting Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application requirements are met, overseeing the development process, and providing guidance to team members. You will also engage...

Analysis of routine samples (product development batches, stability study samples, raw materials etc.). Operation and Calibration of analytical instruments/equipment s. Analytical activities related to Quality control department. Qualification of working standards. Documentation of analytical activities as per good documentation practices. Work in laboratory as per good laboratory practices. To use PPEs and follow safe practices in lab. Any other task assigned by management. Sampling of raw materials from pilot plant dispensing area. Analysis of samples in quality control laboratory. Operation and Calibration of instruments in quality control laboratory

To ensure and carry out the analysis of sample and all other activities as per Standard Operating Procedure (SOP). To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside lab. To check, verify and review the calibration of all the analysis instruments whether performed as per the schedule. To ensure recording of all the data related to the testing online, on day-to-day basis and ensure traceability of the same. To work for lab readiness for audit and ensure compliance in Laboratory.

To ensure and carry out the analysis of stability sample and all other activities as per Standard Operating Procedure (SOP). To get involve and support in investigation of failure of any material or product in case of any out of specification (OOS) or Out of trend (OOT) or laboratory incident or non-conformity and take corrective and preventive actions. To raise and implement change control or document change request wherever necessary. To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside Stability lab. To ensure availability of the working & impurities standards as per various pharmacopoeia. To assist Supervis...

To ensure and carry out the analysis of stability sample and all other activities as per Standard Operating Procedure (SOP). To get involve and support in investigation of failure of any material or product in case of any out of specification (OOS) or Out of trend (OOT) or laboratory incident or non-conformity and take corrective and preventive actions. To raise and implement change control or document change request wherever necessary. To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside Stability lab. To ensure availability of the working & impurities standards as per various pharmacopoeia. To assist Supervis...

We are seeking a skilled Analyst with hands-on experience in FTIR/Disso/UV/KF/HPLC 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) Walk-in interview 22-Sept to 26-Sept 9.30am to 5pm on 27-Sept-25(Saturday) from 9.30am to 3pm

Conduct final inspection and testing of finished products to ensure compliance with quality standards and customer specifications. Hands-on experience in testing of Finished products Instruments must be handled like HPLC, GC, KF, IR, DT, and Dissolution. Hands-on experience like software like Empower and LIMS. Qualification M.SC/B.Pharma 3 to 6 years Additional Information

As an Analytical Chemist at the Pharma Division of a Chemical Manufacturing Company in Ahmedabad, you will be responsible for handling analytical instruments such as HPLC, GC, UV, IR. Your key responsibilities will include performing instrument calibration, analyzing finished products and raw materials, and conducting wet lab analysis. **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 - Knowledge of analytical instruments and techniques - Educational background in Chemistry ...

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: - Perform analytical testing using techniques such as HPLC, GC, IR, UV, and Wet analysis. - Communicate effectively with team members and stakeholders. - Maintain accurate records of all analytical tests conducted. Qualifications Required: - Proficiency in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis. - Strong communication skills. - Prior experience in a similar role would be an advantage.,

As a Process Design Engineer at our organization, you will be part of a transformative team working in the areas of water systems and treatment plant evaluation, modelling, design, master planning, and project delivery. It is essential to have 3-6 years of experience in the field. Your primary responsibilities will include: - Coordinating and adjusting the work effort within the project team to ensure project work is completed on schedule and within the allocated budget. - Working with various water treatment technologies such as Membranes, Ion Exchange, CDI, Filtration, Chemical Dosing Systems, and UV. - Executing project designs, managing resources within the constraints of project budget ...

Home The University Job Opportunities and Working At Swansea Current Vacancies Research Officer in Antihydrogen Physics Back to list Research Officer in Antihydrogen Physics Related pages Current Vacancies Benefits & Rewards Equality Diversity & Inclusion Information for Applicants Information for for colleagues from around the world Our reward and benefits, and ways of working enable those who join us to have enriching careers, matched by an excellent work-life balance, About The Role The group is a leading member of the ALPHA collaboration with responsibility for positrons, antihydrogen synthesis, laser-spectroscopy and frequency metrology Recent research highlights include the first laser...

quality control with experiance of hplc,gc,karlfisher,uv,spectometer

On-site assessment and selection of target trainees and hospitals to ensure the selections result in optimal quantity and quality of trainees and Phaco conversion rates for the Phaco Development Program. Onsite (Operating Room) and wet lab instruction and consultation of trainees in the entire process of converting from ECCE and SICS to Phaco. This includes working with designated outside-Alcon consultants (course instructors and on-site proctors) to ensure effective trainee Phaco conversion rates and high quality surgical results Demonstrate product and procedural excellence to best technical model and coach trainees and affiliated personnel how to achieve optimal surgical and patient resul...

About The Role : Job Title Transactional FX Specialist Corporate TitleAssociate LocationMumbai, India Role Description Transactional FX is a high-profile joint venture between the Corporate Bank (CB) and Investment Bank (IB). Transactional FX team is responsible for delivering one of the fastest growing revenue streams in CB & IB by providing market leading FX workflow solutions to clients. Transactional FX leverages the firms position as a market leader in CB and offers variety of standard and bespoke FX solutions to solve for clients FX workflow needs. What well offer you As part of our flexible scheme, here are just some of the benefits that youll enjoy, Best in class leave policy. Gender...

Job Purpose and Impact The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines. Key Accountabilities Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module. Provide ongoing technical support to stakeholders, investigate quality problems and deliver im...

i. Experienced in independent instrumental analysis of raw material, in process samples, finished product and stability samples of pharmaceutical products. ii. Well versed in analysis of Tablets, capsules, liquids samples, for common test as Assay, Related substances, Dissolution and preservative content analysis as per controlled specification and method of analysis. iii. Should able to operate, calibrate and maintain instruments like HPLC, GC, Dissolution apparatus, UV and FTIR etc. iv. Experience of Empower, Lab solution software shall be recommended. v. Exposure to perform AMV or development shall be preferred. vi. Aware about on line & good documentation practices. vii. Should have know...

Primary Function: Brief Job Description: Knowledge and use of concepts, practices, procedures. Applies basic knowledge of coatings, resins, and curing chemistries for certain segment, technology, or process to a business specific application. Panel preparation & testing as per product specification. Interprets and analyzes results, makes suggestions on path forward and contributes to formulating work plans and managing daily workflow {involves Preparing paint samples (including Pre-mixing, Grinding, Thinning) as per Formulation / Guidelines given by Supervisor; Panel preparation & testing as per product specification} Produces accurate and timely results with guidance from supervisor defined...

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:-1 to 5 Years Skills :- HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals Division :- Formulation Interview Date:-20-09-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur | MSNF-IV, Mekaguda | MSNF-V, RK Puram Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Car...

Good knowledge of QC processes and GMP compliance. Skills: MS Office proficiency and strong communication skills. Responsible for quality testing, documentation, and ensuring product compliance with industry standards. Required Candidate profile Experience: 5-6 years in Pharma/API Education: B.Sc / M.Sc in Chemistry Must have hands-on experience with HPLC.

Position Summary: Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs Gain a technical understanding of the techniques in which review is being performed Use MS Windows applications such as EXCEL, Word, Access, Outlook email Conducts all activities in a saf...

A QC Officer performs visual inspections, tests, and measurements on raw materials, in-process products, and finished goods. This is done to identify any defects or deviations from the quality standards and specifications. Required Candidate profile Previous experience in a quality control, quality assurance, or manufacturing environment is highly valued. A strong understanding of quality control principles, testing methods

GC, HPLC, UV, Malvern, LCMS | SOPs, MSDS, COA | 5S, NABL, GLP, IMS | Reports | Impurity Profiling Inventory, AMC, CMC & LIMS management. Monthly/Yearly report preparation. Audit exposure

QC Officer with strong expertise in HPLC, GC, UV-Vis, Karl Fischer, SAP, COA, Calibration, SOP preparation, and QMS compliance. Candidates with experience in pharma/chemical QC operations and knowledge of GMP, GLP, ICH & ISO/IEC 17025:2017 Required Candidate profile Skills: HPLC, GC, UV-Vis, Karl Fischer, SAP, COA, Calibration, SOP, QMS Preferred Industry: Chemical / Pharma API

Review overall QC documents, Prepare training modules as required and provide training to QC staff, Approve COAs for water analysis from the microbiology dpt, Required Candidate profile Propose new Standard Operating Procedures (SOPs) and analytical instruments, HPLC/UHPLC/GC/UV/FTIR, and stability data, Approve new equipment qualification (DQ/IQ/OQ/PQ).

Skills : Good Laboratory Practices, perform sampling and analysis of Finished product, analyze Raw material, KSM, In process, Intermediate and finished product on various instruments like HPLC/UV Visible spectrophotometer, IR, KF, Polari meter.