6 Viscometer Jobs

Key Role & Responsibilities -To analysed & develop analytical method for the existing and new molecules. -To calibrate and validate the developed method as per the global standards. - To operates and maintains various analytical instruments -To document the developed process along with its calibration and validation data. -To transfer developed method to the quality control with the help of right technology transfer protocol. -To support organization in terms of achieving various quality accreditations. -Prepare COA (certificate of analysis) for finished goods lot as per specifications - Carry out standardization & calibration of LAB reagents and instruments & maintain records as per SOP - Carry out safe and standard operations of instruments/ Lab wares as per SOP - Maintain safe work practices by using applicable PPEs (Personnel protective equipment) w.r.t LAB - Maintain good housekeeping in the laboratory - Segregate the waste as per properties of the material/chemical - To maintain experimental data in ELN and LIMS. -To maintain instruments and equipments of the lab. - To support structural identification of impurities and by-products. -To support waste characterization. - To support synthesis lab, Kilo Lab, Pilot plant in terms of process development and scale up quality needs. - Provides Training and supervision to new executives on analytical methods - Actively searches literature in research publications, patents, etc - Follow BBS (Behavior based safety) to maintain safety culture at workplace - Prepares technical reports and presentations as required related to projects - Supports R&D projects at group level participating in meetings and sharing technical information and "best-practices - Encourages "best-practice" sharing through the participation and promotion of meetings, knowledge sharing tools and all other initiatives liaising on a world-wide basis - Implement Aarti Management System Job Requirements: 2 to 6 Years in industry as a team member. - Experience: a minimum of 2 years experience in analytical managerial roles in chemical companies is needed. - A previous experience in method development is highly appreciated - Knowledge: a good knowledge of analytical tools and organization in chemical companies is needed. - Extensive operation knowledge of GC, HPLC, IR, UV, KF, GCMS, Viscometer is highly recommended. - Knowledge of wet analysis is also required - ETP sample analysis, like COD, BOD, NH3-N, TSS,TDS etc is highly recommended. - Ensure calibration, inspection of measuring & test equipment used for analytical lab - Good knowledge of important IT tools: Scifinder, Chemdraw, and good computer proficiency is needed Qualification: M.Sc Analytical Chemistry or M.Sc (Chemistry with large industrial experience in analytical method development)

Job Objective - Maintain line continuity, productivity, quality of product, reduce wastages and adherence to cGMP, GDP and safety in-shift for the allocated line(s). Roles and Responsibilities - Check the allocated post production (ATS/Printing /camera)- line(s) in each shift as per the CTQ (critical to Quality) /CTP (Critical to Productivity) checklist Follow plan as per color change note by ensuring minimal change over time at each sub section Follow instructions from shift lead for timely change over by ensuring availability of roller(s)/ink etc Execute IPQC after every roller cleaning and checking of rejections of camera(s) after every hour for achieving zero defect Execute camera operations as per SOP to achieve productivity and quality Coordinate with contract associates to follow SOP at ATS /Camera/packing /Sealing and tumbling Execute preventive maintenance plan for line(s) to achieve zero downtime of the line(s) Execute troubleshooting activity for entire line(s) to achieve productivity. In certain cases, seek help from maintenance team for uptime of machine Reporting and controlling post production loss of printing and camera to achieve Targeted AFOE@Despatch Follow cGMP and GDP for allocated line (s) for ensuring regulatory compliances during the shift. Follow instructions from shift lead/team lead to implement CAPA for any customer complaint(s) Assist other line operator during colour change /Break down for timely start-up of line Making downtime and rejection entries on daily machine performance report Communicate attribute defects to Production /line lead on continuous basis Machine cleaning Shift handover and takeover Safety

Role & responsibilities Experience in operation and trouble shooting of process in plant. Isolation and purification of different organic compound using column chromatographic and crystallization techniques. Optimize the process parameters, what-if studies, holding studies etc. for scale up. Investigation of OOS/OOT and stability related issues. Analytical development In R&D department Reactions performed like Hydrogenation, Brominating, Oxidation, Reduction and condensation. Handling of Moisture sensitive reactions. Study and understand the project requirements, identifying and collection of suitable literature. Support lab manager to prepare weekly technical reports and other project related technical documents (impurity profile tables, Plant batch data, developmental reports) Executing assigned reactions of project. • Looking after the Safety equipment's management and maintaining it as per regulatory requirement in R&D lab. • Study the MSDS of each chemical using in every new project and make arrangement of Safety equipment's accordingly. Handled HPLC system of Agilent technologies Eriochrome (A.04.07) and version Open Lab cds2.4 • Good in Thin layer chromatography & Column chromatography. • Polymorph characterization with the aid of XRD, DSC, TGA and IR Techniques. • Having good ability to interpret analytical results like NMR, HPLC, GC, LCMS, MASS, IR & UV. Preferred candidate profile Perks and benefits

Inspect incoming raw and packing materials visually, as per set specifications. Monitor key process inputs and variables, and inform the production team for necessary adjustments. Operate equipment like Viscometer, Densimeter, and Refractometer. Required Candidate profile Check in-process products visually and dimensionally to ensure they meet specifications. Calibrate measuring and quality equipment regularly. Ensure cleanliness & discipline in the lab and shop floor. Perks and benefits Highest Monthly Salary, Bonuses, Canteen, Transp.

Job description Role & Responsibilities: Perform HPLC & GC analysis by adhering respective STPs as per the work allocated. On-time sampling and testing of Intermediates, Raw materials & finished products. The Quality Control has the authority to inform approve or reject of the Raw Materials, packing materials, intermediates and a finished Drug Substances based on analytical results and has the responsibility to control the non-conforming products. Responsible for calibration of equipment's in the laboratory. Responsible for implementation, improvement, and modification of analytical techniques for the existing products. Retention sample management. Verifications of daily calibrations for the standalone instruments. Execution of decontamination and product change over analysis. Ensuring of reagents and chemicals validity. To follow safety norms as per policy. Preferred candidate profile: Person Should Have M.Sc Analytical Chemistry / Organic Chemistry, With 1 to 7 Years Experience in Quality Control and Immediate Joiners are preferred. Positions: Chemist / Sr. Chemist / Executives For More Info Call to 8886311229 Share Your Resume To : tkamaleshkumar.hr@deccanchemicals.com Perks and benefits : PF, ESIC, Bonus, Mediclaim, Transport, Subsided Canteen, GPAP

Role & responsibilities Documentation is the key to GMP compliance and ensures traceability of all development, manufacturing, and testing activities. Documentation provides the route for auditors to assess the overall quality of operations within a company and the final product. Quality Management System (QMS) is ensuring that drugs are safe, effective, and of high quality is fundamental, as these factors directly impact patient health. Quality management systems are essential across the industry to uphold these stringent standards. • Officer - Documentation & QMS ensures that all documentation is clear and concise, and that it's followed by all personnel. This helps to ensure that the manufacturing process is consistent and safe. • Officer - Documentation & QMS play a critical role in ensuring that the pharmaceutical industry complies with a wide range of regulatory requirements and international standards. This involves preparing and submitting regulatory documents and conducting audits and inspections to ensure compliance with regulations. • He/she should have familiarity with guidelines such as GLP, FDA and cGMP regulation and principles of Quality Management. • Officer - Documentation & QMS will provide technical and general administrative support to this department and ensure that tasks are carried out in a timely manner, Preferred candidate profile Perks and benefits