9 Polarimeter Jobs

Streamline the data review process across all GxP systems, including CDS, FTIR, UV, KF, LIMS, MES, and more. Pro CDS Hub Our Vision for Digital Manufacturing & Future Quality Control Pro ExtractEase Pro ExtractEase automates data extraction from Empower to facilitate insights from the data. Pro Das Is a versatile platform tailored to automate the Project Creation, Back-up/Restoration activities of Empower. Pro QMSuite Is a system that documents the policies, procedures, and controls necessary for an organization

Qualification - Msc Chemistry - 3- 6 Yrs Experience Experience of GC / HPLC Preferred . Experience in Zydus : Min.12 months Job Responsibilities o Handling of HPLC system /GC o Up-keep of all Instrument Usage Log,Inward Register, Training Records etc. o Usage of SOPs, Specifications and STPfor Inprocess, Intermediate, FiniAsh Product, Recovered Solvents, and CleaningSample. o Handling of LIMS for Receiving ofsample along with Intimation Slip for Inprocess, Intermediate, Finish Product,Recovered Solvents, Cleaning Sample and outside sample etc. and testing as pertheir Specification and STP. o To follow the GMP, Safety norms andadhere to companys policy. o Attending Training classes i.e.Internal and External program as per schedule. Usage of SOPs, Specificationsand STP for Inprocess, Intermediate, Finish Product, Recovered Solvents, andCleaning Sample. o Receiving of sample along withIntimation Slip for Inprocess, Intermediate, Finish Product, RecoveredSolvents, Cleaning Sample and outside sample etc. and testing as per theirSpecification and STP. o After analysing and writinganalytical data, hander over the raw data to senior person for review. o Timely reporting of results andinvestigation of any deviation, OOS, incident. Maintain house-keeping and GLPin working area. o Additional Job activities endorsed bySuperior.

To perform the environment monitoring of Aseptic area and supporting area. To perform the Microbiological test for Water system sample, SFG, RM, PM samples To prepare the trend data for the Microbiological monitoring of area and water system samples. To perform the Gowning qualification of other department personnel. To involve in media fill and Qualification of Micro lab and Mfg. area equipment.

Long Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Competencies Education Others Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs.

Roles and Responsibilities Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Desired Candidate Profile Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution or M.Sc. Strong understanding of analytical instruments such as HPLC/UPLC/GC/MS/ICP-MS/Wet Analysis etc.

Role & responsibilities Preferred candidate profile Perks and benefits

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

Role & responsibilities Responsible for microbiology lab activities & compliance Environmental Monitoring Risk Assessments/ rationales and area qualification Ensuring timely release of all microbiological tests thereby meeting company targets Handling of QMS activities like Change Controls, Incident, OOS and OOL investigations and impact assessments Review/ approval of protocols and reports of analytical method development, method suitability studies, process validations, Instruments/equipment qualifications and various miscellaneous microbiological validation/ activities and analytical documents Responsible for participation / evaluation of Risk Assessments/ impact assessments wherever applicable Review/approval of trends as applicable and to recommend any changes for the better control of the system Responsible to handle internal and external audits and coordinate with all cross functional teams for better productivity and quality Responsible to take the lab rounds on daily basis and correct the non-compliance if found any and to find out the opportunities for improvements Improvement of quality culture in the team and ensuring the safety in the lab Ensuring the compliance to Audit observations related to microbiology Regular updates to QC Head about incidents, OOS and CAPA's To ensure strict adherence to safety & cGMP all factory and maintain the data integrity in the microbiology lab Ability to work independently and as part of a team Preferred candidate profile Candidates with minimum 8 - 12 years experience from Pharmaceutical industry (formulation / topical background preferred)

Handling of HPLC Handling of GC Handling of UV.Vis Spectrophotometer