3433 Hplc Jobs - Page 27

Responsibilities: Process Improvement: Identify and implement continuous improvements for existing copper chemical manufacturing processes to boost efficiency, cut costs, enhance quality, and ensure safety. Troubleshoot production issues. New Product Development (NPD): Lead the entire NPD pipeline for new copper chemicals, from research and lab trials to pilot, manufacturing scale-up, and commercialization. Develop processes & specifications, and manage documentation. Cross-Functional Collaboration: Work closely with Production for technology transfer and scale-up. Partner with Quality Control (QC) on analytical methods and quality. Engage external experts to accelerate development. Complian...

Responsibilities: Synthetic Chemistry / Lab Work Perform multi-step organic synthesis of target molecules as per project requirements. Conduct reaction monitoring, work-up, purification, and isolation of intermediates and final products. Maintain accurate lab records and notebooks (ELN or manual) as per GLP standards. Process Development Assist in the optimization of reaction conditions to improve yield, purity, and scalability. Conduct literature searches and suggest alternative synthetic routes under supervision. Evaluate critical process parameters through small-scale experiments. Analytical Coordination Coordinate with the analytical team for sample submissions, impurity profiling, and m...

Role & responsibilities - Should be having sound knowledge & experience of Analysis of Packing Material/ Raw Material. - Preparation of Specification and STP. - Sampling of Packing Material/ Raw Material - Knowledge of all equipment and instruments Preferred candidate profile Bsc/Msc/B. Pharma with experience of QC (if Any) Good communication skills Interested candidates can share their updated resume at hr.ggn@stanlabs.com, along with the below mentioned details: 1.Total Experience- 2.Current company- 3.Current Designation- 4.CTC- 5.Expected CTC- 6.Notice Period- 7.Reason- 8.Current Location- 9.Belong- 10.Qualification- 11.OSD experience(Capsule & Tablet)- 12.Currently Working in which depa...

Responsibilities: To manage day to day activities of quality control. To distribute QC related work as per production planning Preparation & reviewing of QC SOPs. To monitoring of all the Q.C. testing & its complete follow up. To approve all the Raw materials, packing materials, inprocess & finished goods after proper testing with its online documents. To review SOP and STP. Checking out daily & monthly calibrations as per designed SOPs. To prepare and execute calibration calendar of QC instruments. Review out of Specification results and its documents for final conclusion. To participate in investigate of market complaint, product recall Sample. Coordinate training of workers and staff for ...

Responsibilities: Chemical Analysis & Testing Conduct regular chemical analysis of plating baths, rinse tanks, and process solutions. Prepare standard solutions and reagents for analysis. Perform titrations, pH, conductivity, and concentration checks. Process Monitoring & Control Monitor plating bath parameters (metal content, additives, pH, temperature). Maintain plating bath quality through timely replenishment of chemicals. Assist in troubleshooting process deviations and suggest corrective actions. Quality Assurance Test plated samples for thickness, adhesion, corrosion resistance, and appearance. Maintain accurate records of test results and share reports with supervisors. Ensure compli...

Responsibilities: Ensure timely and Accurately material testing (RAW/ In Process/Finish/ R&D). Accurate and On-time Reporting and documentation at all stages. Proper Calibration. Understanding of analytical chemistry. Hands-on experience in HPLC /GC Required Skills: Candidate must have good communication skill. Good leadership quality and time management. Ability to work independently and as part of a team. Required Qualification: - B.Sc/M.Sc - Chemistry

Responsibilities: Lead formulation development for OSD, external preparations, oral liquids, and injectables. Oversee pre-formulation studies, prototype development, and scale - up activities. Ensure compliance with regulatory guidelines (ICH, WHO, USFDA, etc.). Collaborate with cross-functional teams (QA, QC, RA, Production) for tech transfer. Mentor junior scientists and manage project timelines and documentation. Required skills: Strong knowledge of formulation science and process optimization. Experience in QbD, DoE, and stability studies. Excellent leadership and communication skills. Required Qualification: - B.Pharm/M.Pharm

Responsibilities: Effectively perform chemical analysis techniques specifically using HPLC, GC, Karl Fischer, Melting Point, IR, and UV-Vis instrumentation. Completes documentation relating to material analysis and enters data into database/software systems. Assist with production activities as required. Laboratory environment requiring the ability to carry out laboratory operating procedures in a safe manner, while maintaining a clean and orderly workspace. Carried out instructions from senior staff. Work effectively with computer software and hardware, including analytical instruments, spreadsheets, and word-processing applications. Maintain and perform regular Calibration and verification...

About The Role Project Role : VIS & BI Strategy Practitioner Project Role Description : Develop a VIS/BI vision, business case, and modernization strategy; discover and assess VIS/BI opportunities; identify industry- and function-centered VIS/BI use cases; guide clients on industry and function relevant measures and metrics; develop a VIS/BI roadmap and operating model; help drive adoption, decision making and behavior change; measure VIS/BI value. Must have skills : Kinaxis Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a VIS & BI Strategy Practitioner, you will engage in the development of a comprehe...

HOW YOU WILL CONTRIBUTE AND WHAT YOU WILL LEARN Your responsibilities will include:Designing, developing, and executing detailed functional test plans to verify product features and capabilities, ensuring comprehensive coverage of complex customer configurations and seamless system functionality Actively participating in and contributing to the System Development Lifecycle (SDLC) processes, including product/system requirement reviews, software design implementation discussions, and collaborating with the Product Management team to translate customer scenarios and use cases into detailed test plans Setting up complex test topologies based on feature requirements and optimizing equipment to b...

Roles and Responsibilities Conduct quality control tests on raw materials, in-process samples, and finished products using HPLC, GC, and other analytical techniques. Ensure compliance with cGMP guidelines during manufacturing processes by monitoring equipment maintenance schedules and conducting regular inspections. Collaborate with cross-functional teams to resolve issues related to product quality, stability testing, and documentation. Develop and implement effective warehousing procedures for storing biologics products under controlled conditions. Provide technical support to production staff on fermentation processes and troubleshoot problems as needed.

Walk-In Interview QC Department (1 to 9 Years Experience) Hyderabad 11th & 12th October On 11th October 2025 (Saturday) Time : 9:00 AM to 3:00 PM Location: 7-2-A2, Hetero Corporate , Industrial Estates, Sanathnagar,Hyderabad-500018 Location: Annora Pharma Private Limited, Sy No.261, Plot No13, Annaram (Village), Ginnaram (mandal), Hyderabad On 12th October 2025 (Sunday ) Time : 9:00 AM to 3:00 PM 3. Location: Hotel Krithunga Restaurant, 01st Floor, Above Reliance Smart, Opposite New Bus Stand, Jadcherla Hiring For: Quality Control (QC) API / Formulations / Injectables Experience Required : 1 to 9 Years Qualification : B.Sc / M.Sc / B.Pharm / M.Pharm Department : Quality Control HPLC, GC, Wet...

Role Overview: As a Research Associate / Executive in the API Research & Development (R&D) team, your main responsibilities will include chemical synthesis, process optimization, and scale-up of Active Pharmaceutical Ingredients (APIs). You will be tasked with designing and executing synthetic routes, improving process efficiency, and ensuring cost-effectiveness. Your role will also involve analyzing and characterizing products using advanced analytical techniques such as HPLC, GC, while maintaining regulatory and quality compliance throughout the development process. Collaborating with cross-functional teams to facilitate smooth technology transfer and troubleshooting will be a key aspect o...

As a Chemical Process Development Engineer, you will play a crucial role in leading the development and optimization of chemical processes using various flow reactors like microreactors, tubular reactors, and packed-bed reactors. Your responsibilities will include: - Collaborating with synthetic chemists and process engineers to transition batch processes to continuous flow - Developing and validating process parameters such as residence time, flow rates, mixing, pressure, and temperature - Integrating online/inline monitoring tools (PAT) including FTIR, UV-Vis, NMR, and HPLC - Ensuring robust data analysis, modeling, and documentation of experiments and findings Qualifications Required: - B...

As a Scientist I at the U.S. Pharmacopeial Convention (USP), you will play a crucial role in supporting the development of Reference materials. Your responsibilities will include: - Supporting reaction monitoring, scale up, and final analysis of samples as per monograph/in-house procedures, including method development if required. - Preparing development reports for Synthetic Support projects and being involved in project acceptance. Executing projects per approved test protocols when assigned. - Preparing, executing, and completing IQ/OQ/PQ of new instruments. Indenting the required glassware, chemicals, and columns for the ARD projects. Maintaining GLP and implementing safety procedures w...

Job Description Job Title: Assistant Manager - Research & Development About The Function Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo's 30,000+ people work in Supply Chain and Manufacturing. It's an intricate and sophisticated operation that's the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We're committed to realising our Society 2030: Spirit of Progress goals, to protect the environment an...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com. Job Summary Under the guidance of Manager-Instrumentation/R&D, responsible for installation...

Engineer should have on site installation, Qualification, repair and preventive maintenance experience on LPLC and HPLC products. Overall chromatography experience will get preference. The Services Technician will be responsible for delivering the desired customer service experience. The goal is to drive service success that improves customer satisfaction, maximizes customer retention and increases profitability. Main Responsibilities & Tasks Engineer should have experience on LPLC and HPLC product segments. Overall chromatography experience will get priority. Provide service and customer support during field and inhouse visits or dispatches. Manage all on site installation, repair, maintena...

Key Accountabilities And Responsibilities Analytical Method Development of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical Method Validation of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical Method Transfer of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. JOB SPECIFICATION Analytical method development and validation for pharmaceutical dosage forms. Literature search related to the drug substance, create analytical profiles. Execution of analytical method transfer for pharmaceutical dosage forms. Analysis of routine samples (product deve...

Job Description: You will be responsible for delivering lectures, practical classes, and tutorials in Pharmaceutical Chemistry / Cognosy to undergraduate and postgraduate students. Additionally, you will design and implement curriculum updates in line with current industry trends and regulatory standards. Supervising student projects, dissertations, and lab research work will be a key responsibility. You are expected to guide students in the use of analytical tools and drug design software. Furthermore, initiating and publishing research in recognized national and international journals is an essential aspect of the role. Ensuring adherence to PCI, AICTE, and NAAC documentation and academic ...

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...

Find what drives you on a team with a more than 70-year history of discovery, determination, and innovation. As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers protect people. Our products serve a wide range of markets, so if your interests lie along the spectrum of Life Sciences to Industrial, you'll find a rewarding role here. For the exponentially curious, Pall is a place you can thrive and amplify your impact on the world. Pall is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we're pioneering the future of science and medicine, developing products that enable researche...

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At Beckman Coulter Life Sciences, one of Danaher's 15+ operating companies, our work saves livesand we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact innovating at the speed of life. At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by au...

As a member of the o2h discovery team, your role involves: - Strong knowledge and hands-on experience in LC-MS/SFC/HPLC/Prep. method development for all types of chemistry molecules. - Strong understanding of various column chemistry. - Skilled in troubleshooting, instrument maintenance, and calibration. - Leading, training, coaching, and mentoring a team of motivated young scientists. To qualify for this role, you should: - Have a passion for HPLC/Prep./LCMS/SFC analysis and characterization techniques, along with a willingness for continuous learning and education. - Demonstrate creative thinking to identify new techniques and growth opportunities. - Be highly organized with the capability...

Job Title Executive API R&D Business Unit R&D1 Regulatory Affairs Job Grade G12A Location : Baroda At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you'll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other's journeys. Role To execute activities related to R&D impurity synthesis, along with a gro...