Chemist Fresher Jobs in Hyderabad

Work Type: - Field Work Job Description:- The Quality Assurance (QA) & Quality Control vendor approval process involves evaluating a supplier's ability to consistently provide products or services that meet quality standards, including physical audits, sample analysis, and review of documentation. This process ensures that only reliable vendors are used to maintain product quality and safety, often a critical requirement in industries like pharmaceuticals. Here's a more detailed breakdown of the QA vendor approval process:1. Needs Assessment and Vendor Identification:Determine Needs: The organization identifies the need for a new vendor and the specific requirements for the product or service.Vendor Identification: Research and identify potential vendors who can meet the requirements. 2. Vendor Qualification:Vendor Questionnaire: Potential vendors are typically asked to complete a questionnaire that gathers information about their capabilities, quality systems, and compliance.Document Review: QA reviews the vendor's documentation, such as certificates of analysis (COAs), specifications, and method of analysis.Sample Analysis: The vendor provides samples, which are tested by Quality Control (QC) to ensure they meet the required standards.Site Audit: A physical audit of the vendor's manufacturing site is conducted to assess their quality control measures and overall compliance. 3. Vendor Evaluation and Approval:Compliance Assessment: A evaluates the results of sample analysis and the site audit to determine if the vendor meets the required standards. Risk Assessment: Vendors may be categorized by risk level, with those posing higher risks requiring more rigorous evaluation and monitoring. Approval Decision: Based on the evaluation, QA makes a decision to approve or reject the vendor. 4. Ongoing Monitoring and Re-evaluation:Performance Monitoring: Regularly monitor the vendor's performance on quality, timeliness.

Urgent Hiring for Lab Technicians with Attractive Salary + Food + Accommodation

After 45 days of free training (technical) followed by 15 days (non technical), candidates can be placed in pharma company. During training candidate need to take care of living expenses including food accomodation and local travel.

Job descriptionWe are looking for a Graduate Engineer Trainee Fresher for the CIVIL Domain.Role- Graduate Engineer Trainee-Civil Civil Engineer FresherQualifications: - B-Tech/B.E. CIVIL ENGINEERINGExperience- FresherJob Location: - Noida, Mumbai, Pune Hyderabad Bangalore.Note- Male & females both can apply.Skills-1. Problem-solving Skills2. Analytical Thinking3. Project Management skills4. Good Communication skills5. Good knowledge of Microsoft Office6. Excellent multi-tasking skills7. Ability to work independently8. Ability to work within a team.Responsibilities-Adhere to established design guidelines and procedures.Analyze design issues and recommend corrective actions.Perform civil design analysis and calculations according to project requirements.Manage design projects within allotted timelines and budgets.Perform design changes and improvements according to changing project demands.

Trainee chemist and chemist role for QC, R&D and QA departments in pharma company Provide the relevant training in handling and involve in QC wet analysis Responsible for documentation and Analysis part Assisting of R&D chemist to set up lab reactions Responsible for monitoring of lab reactions and QC analysis

Qualification: B.Sc (Chemistry) Experience : 0-5 Years1. Charging correct quantities of inputs as per batch manufacturing record.2. Maintain parameters as per batch manufacturing record.3. Following the instructions of shift in charge.4. Ensure safety practice being followed during manufacturing.5. Ensure equipment surroundings cleanness.6. Ensuring the yields and solvent recovery as per yield standards given in the BMR.7. Handle all packaging process stages (packaging and labelling).8. To check the utilities before batch charging.9. To maintain production area in clean & hygiene condition.10. To ensure proper allocation of works to the Helpers.11. To maintain status board and equipment usage log books in on line.12. To maintain the Batch Manufacturing Record (BMR) in on line.13. To ensure proper labeling for in-process sample label, Material status label, Quarantine label and Accessories status label.14. Report any deviations from standards to Shift in-charge Production Manager promptly.

We are looking for 04 Quality Control Chemist Posts in Nacharam, Hyderabad, Telangana,Experience in HPLC, with deep knowledge in Experience in HPLC and Required Educational Qualification is : B.Sc, M.Sc

Analytical Chemist - Analysis of Water, Fuels, Minerals, Soil, Food & Feed,

We have job opening for our organisation. Please find details enclosed: Gender Male Company Name Sri Krishna Pharma Department Production(API)Position Technical Trainee /Trainee / Jr. ChemistExperience FreshersQualification Intermediate (MPC) /B.Sc (Chemistry)Location UppalAge Not More than 28 YearsJob Role 1.Loading and Unloading of Material.2.Equipment Handling like Reactors ,ANFS ,Centrifuges, Pressure Reactions, Hydrogenations.3.Need to work in Drying Area.5.Need to work in shifts.6.Job Specific Training will be provided .

Job Description: Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis (Medical Problems) and Procedure (Treatments) Codes using ICD-10 CM and CPT code books.Requirement:knowledge in Anatomy and PhysiologyGood communication and interpersonal skillsBasic Computer SkillsNo of vacancy: 500Eligibility:NursingGNM/DGNMLife science graduatesPharmacyPhysician assistantBio medical EngineersBio chemistryBio technologyBio informaticsMicro biologyZoology and Advanced zoologyBiologyBotanyPlant biotechnologyGeneticsFood and NutritionParamedicalPhysiotherapyM.Sc. Clinical NutritionM.Sc. Human GeneticsM.Sc. Medical Laboratory TechnologyM.Sc. Medical SociologyM.Sc. EpidemiologyM.Sc. Molecular VirologyM.Sc. BiostatisticsM.Sc. Blood Banking TechnologyM.Sc. Regenerative MedicineM.Optom.M.Sc. Genetic CounselingM.Sc. Radiolog & Imaging TechnologyM.Sc. Medical BiochemistryM.Sc, Medical MicrobiologyM.Sc. Clinical Care TechnologyM.Sc. Clinical Care TechnologyM.Sc. Medical PhysicsB.Sc. - Accident & Emergency Care TechnologyB.Sc. - Audiology & speech Language PathologyB.Sc. - Cardiac TechnologyB.Sc. - Cardio Pulmonary Perfusion Care TechnologyB.Sc. - Critical Care TechnologyB.Sc. - Dialysis TechnologyB.Sc. - Neuro ElectrophysiologyB.Sc. - M.L.T.B.Sc. - Medical SociologyB.Sc. - Nuclear Medicine TechnologyB.Sc. - Operation Theatre & Anaesthesia TechnologyBachelor of Science in OptometryB.Sc. - Physician AssistantB.Sc. - Radiology Imaging TechnologyB.Sc. - Radiotherapy TechnologyB.Sc. - Medical Record ScienceB.Sc. - Respiratory TherapyB.Sc. - Fitness and Lifestyle ModificationsAccident & Emergency Care TechnologyCritical Care TechnologyNursing AideOperation Theatre & Anaesthesia TechnologyOphthalmic Nursing AssistantMedical Record ScienceOptometry TechnologyRadiology & Imaging TechnologyMedical

Research and development

Production:Handling of SSR,GLR, Pressure reacors,Solvent Distillation,Separation,centrifuge, Drier, willing to work shifts duties, follows as per BPR/BMR, production documentation,Team work, Clean rooms,Millers,HVD, Pulvariser, reportong to Incharge /HOD.Quality control:Wet analysis : Handling of (Titremetric analysis, water analysis, KF titrator, LOD,ROI,MR, SOR, TLC,FTIR,UV vis spectrophotometer, sampling of RM & FP ,stabilty studies, hardness,dissolution,disintegration,friability testInstrumentation: Operation and calibration of HPLC & GC (shimadzu, Waters,Agilent, perkin elmer,Thermo) with Lab solution,Empower 2&3, EZ chrome open lab softwares and server system) and Incidents,deviations,OOS,OOT,OOC,working standard , RS/OVI BY GCQuality Assurance: Preparation of SOPs, STPs,Change controls,Deviations, Issurence, document control, BPR review, OOS ,OOT, CAPA, ROOT CAUSE, APQR, complaints ,Trainings, IPQA.

Vacancy Production ChemistLoaction; hyderabadExp: 0-4 yearsEducation: Any degree.API Bulk Drugs

We have a job opening for the position of Trainee Scientific Relations/Program Coordinator. Number of Openings: 20 Office timings: 10 AM 7 PM (Morning shift) Essential Job Duties: Coordinates program related events such as workshops, symposium, national and international Scientific Events etc. with International Speakers and delegates. Designing scientific sessions for the conference. Invite professors, Assistant, Associate from Universities or Directors, Managers and Executive from Reputed companies throughout the world. Be a main point of contact for Program chairs, session chairs, scientific committee and invited speakers for Conference content/for all conference related communications. Forming an organizing committee and scientific squad with top quality scientists on the particular research. More intellectual in using scientific knowledge and footing on current scientific inventions. Desired Skills and qualification:Any Graduate with good communication skills can apply.Bachelors Degree in B Pharm, M Pharm, BSc, MSc. B.Tech( Biotechnology,) BME will be preferable.Working knowledge of Microsoft Office and strong computer skills.Ability to enter data into a computer quickly and accurately.Strong attention to detail and ability to think analytically.

Job DescriptionChemical Engineering:-Job descriptionInterpreting operating data of petroleum refineries and devising solutions based on the following:Computer Modeling and SimulationsProcess and Equipment Design PrinciplesStatistical AnalysisOptimization TechniquesReaction EngineeringPreparing reports and charts related to global refinery operations.Responsibilities and Duties- Setup desktop computers and peripherals and test network connections.

Job Description: Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis (Medical Problems) and Procedure (Treatments) Codes using ICD-10 CM and CPT code books.Requirement:knowledge in Anatomy and PhysiologyGood communication and interpersonal skillsBasic Computer SkillsNo of vacancy: 500Eligibility:NursingGNM/DGNMLife science graduatesPharmacyPhysician assistantBio medical EngineersBio chemistryBio technologyBio informaticsMicro biologyZoology and Advanced zoologyBiologyBotanyPlant biotechnologyGeneticsFood and NutritionParamedicalPhysiotherapyM.Sc. Clinical NutritionM.Sc. Human GeneticsM.Sc. Medical Laboratory TechnologyM.Sc. Medical SociologyM.Sc. EpidemiologyM.Sc. Molecular VirologyM.Sc. BiostatisticsM.Sc. Blood Banking TechnologyM.Sc. Rgnerative MedicineM.Optom.M.Sc. Genetic CounselingM.Sc. Radiolog & Imaging TechnologyM.Sc. Medical BiochemistryM.Sc, Medical MicrobiologyM.Sc. Clinical Care TechnologyM.Sc. Clinical Care TechnologyM.Sc. Medical PhysicsB.Sc. - Accident & Emergency Care TechnologyB.Sc. - Audiology & speech Language PathologyB.Sc. - Cardiac TechnologyB.Sc. - Cardio Pulmonary Perfusion Care TechnologyB.Sc. - Critical Care TechnologyB.Sc. - Dialysis TechnologyB.Sc. - Neuro ElectrophysiologyB.Sc. - M.L.T.B.Sc. - Medical SociologyB.Sc. - Nuclear Medicine TechnologyB.Sc. - Operation Theatre & Anaesthesia TechnologyBachelor of Science in OptometryB.Sc. - Physician AssistantB.Sc. - Radiology Imaging TechnologyB.Sc. - Radiotherapy TechnologyB.Sc. - Medical Record ScienceB.Sc. - Respiratory TherapyB.Sc. - Fitness and Lifestyle ModificationsAccident & Emergency Care TechnologyCritical Care TechnologyNursing AideOperation Theatre & Anaesthesia TechnologyOphthalmic Nursing AssistantMedical Record ScienceOptometry TechnologyRadiology & Imaging TechnologyMedical

Work Type: - Field Work Job Description:- The Quality Assurance (QA) & Quality Control vendor approval process involves evaluating a supplier's ability to consistently provide products or services that meet quality standards, including physical audits, sample analysis, and review of documentation. This process ensures that only reliable vendors are used to maintain product quality and safety, often a critical requirement in industries like pharmaceuticals. Here's a more detailed breakdown of the QA vendor approval process:1. Needs Assessment and Vendor Identification:Determine Needs: The organization identifies the need for a new vendor and the specific requirements for the product or service.Vendor Identification: Research and identify potential vendors who can meet the requirements. 2. Vendor Qualification:Vendor Questionnaire: Potential vendors are typically asked to complete a questionnaire that gathers information about their capabilities, quality systems, and compliance.Document Review: QA reviews the vendor's documentation, such as certificates of analysis (COAs), specifications, and method of analysis.Sample Analysis: The vendor provides samples, which are tested by Quality Control (QC) to ensure they meet the required standards.Site Audit: A physical audit of the vendor's manufacturing site is conducted to assess their quality control measures and overall compliance. 3. Vendor Evaluation and Approval:Compliance Assessment: A evaluates the results of sample analysis and the site audit to determine if the vendor meets the required standards. Risk Assessment: Vendors may be categorized by risk level, with those posing higher risks requiring more rigorous evaluation and monitoring. Approval Decision: Based on the evaluation, QA makes a decision to approve or reject the vendor.