Chemist Graduate Jobs in Hyderabad

We are seeking a dedicated Chemist to join our team in Hyderabad. The ideal candidate will have 3 to 5 years of experience in a laboratory setting and hold a relevant degree in Pharmacy or Science. **Key Responsibilities:**- **Conduct Experiments:** Perform chemical experiments to analyze substances and develop new products. This involves following protocols and ensuring safety measures are in place.- **Analyze Data:** Collect and interpret data obtained from experiments. Accurate analysis is crucial for understanding chemical properties and outcomes.- **Maintain Equipment:** Ensure that all laboratory equipment is properly maintained and calibrated. This is essential for reliable results and compliance with safety standards.- **Collaborate with Teams:** Work closely with other scientists and staff to share insights and enhance project outcomes. Team collaboration fosters innovation and efficiency.- **Document Findings:** Maintain detailed records of experiments, procedures, and results. Accurate documentation is vital for regulatory compliance and future reference.**Required Skills and Expectations:**The candidate should have strong analytical skills with a keen attention to detail. Proficiency in using laboratory equipment and software for data analysis is essential. A thorough understanding of chemical safety protocols and regulations is expected. The ability to work independently and as part of a team is important, along with effective communication skills to present findings clearly. A commitment to maintaining a clean and organized laboratory environment is also crucial. The successful candidate will be expected to contribute to a positive work culture while meeting project deadlines consistently.

process execution, equipment handling ,QA, Safety & Environment compliance, Documentation, shift management, Trouble shooting

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

looking for Research & Development Role : R & D Qualification : BSc chemistry [ mandatory ] Good communication skills Gender - males Salary : 21 k Experience: 6 months to 1 year location : Lb. Nagar Contact: 8328653177

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.

1. To make sure manufacturing operations are carried out in conformance with cGMP.2. To make sure all production records, BMRs, equipment performance, production employees attendance are recorded properly.3. To make sure all the production personnel who are directly involved in processing follow good hygienic practice and follow cGMP.4. To follow all activities in the plant, especially those that are carried out during non-General Shift.5. To report any irregular activities carried out during non-General Shift to his production manager.6. To make sure all equipments are in good condition before processing.7. To make sure that production areas clean and good house keeping.8. To make sure that all deviations occurred during in process is reported to production head immediately.9. To make sure that the status of the equipment is updated after each significant operation.10. To make sure that all the equipment used for the manufacturing are clean and dry as per the equipment cleaning procedure.

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.S.C food science and technology / B.Tech Food technology / B.S.C food science and nutrition.Assist in the development and documentation of new products and improvement of existing products from conceptualisation to product launch Run panel sessions and perform sensory tests for pre-launch products Work closely with cross-departments and various key stakeholders on product specifications, standards and procedures Review product artwork and creative materials to ensure compliance with customer, regulatory and/or export countrys requirements Performs physical and chemical analyses on Ingredients and/or food products.Develops product, process and/or packaging specifications for food products.Studies methods to improve quality of foods such as flavor, color, texture, nutritional value, or physical, chemical, and microbiological composition of foods.Lead key projects with R&D to support business goals. Develop research programs incorporating current developments to improve existing products and study the potential of new products. Understand customer expectations on to-be manufactured products.Plans and directs all aspects of an organization's research and development policies, objectives, and initiatives. Maintains an organization's competitive position and profitability by formulating research and development programs, policies, and procedures.Stay abreast with development of new products and technologies, trends and innovation, processing and equipment advance,Conduct research on current market trends, needs, as well as product and service gaps to identify product development opportunities Familiar with FSSAI food regulations and food management systems (HACCP, ISO and GMP certifications)Support any other duties assigned by the superior

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

Qualifications: M.Sc. (Organic Chemistry/Medicinal Chemistry)Experience: 2 6 years in CRO IndustryRoles and Responsibilities Execute the synthetic route for the target molecules under the supervision of Lab head or independently. Clear knowledge in setting up chemical reactions independently, different purification techniques and characterization of compounds by NMR, HPLC and LCMS. Handling of moisture sensitive and pyrophoric reagents and reactions. Perform troubleshooting in synthetic challenges. Should be capable of handling multiple reactions parallelly.Essential Requirements: Knowledge of literature search and retrieving experimental details from journals and patents Follow all laboratory safety protocol. Candidate should have a clear understanding of MSDS (Material Safety Data Sheet) of the chemicals. Knowledge of IP confidentiality and data integrity. Prior work experience in a CRO will be preferred.Immediate Joiners will be preferred.

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 .

Research and development

WE ARE LOOKING FOR QUALITY CONTROL EXECUTIVES FOR OUR LAB, WITH HPLC, GC, UV HANDLING EXPERIENCE, AND HERBAL EXTRACTION WORKING PERSONS WILL BE ADDED ADVANTAGE

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 vacant of 4 Production Chemist Jobs in Hyderabad, Visakhapatnam, Experience Required : 1 - 6 years Educational Qualification : B.Sc, B.E, M.Sc Skill Pharmaceutical Production etc.

we have vacancies for ITI,Diploma,msc chemistry,bsc chemistry,bpharm and mpharm in Hyderabad locationExperience : FreshersSalary : Negotiable

Required R&D Chemist/ ExecutiveExp:3-6 YearsLocation: HyderabadSalary: up to 3.6 lacksmale candidates only

Kreative Organics Private Limited is a manufacturer of Active Pharmaceutical Ingredients (APIs) for the world market. Kreative started operations in 1990.Kreative was established by Dr. S. Krishnamohan. Dr. Krishnamohan was formerly with TIFR, BARC, Caltech and NASA. He is a scientist of international repute and runs Kreative with professionalism and a focus on innovation.Kreative maintains strict quality standards and has developed a robust quality system around which all of our products are manufactured.Kreative invested in a state of the art cGMP facility in 2005 and expanded it to a US FDA class facility in 2013.Kreative, is WHO GMP certified and has successfully been audited by the US FDA in Feb 2020.

Maintaining Working Area Hygiene Documents, Floor cleaning, Daily calibration recordsas per standard operating Procedure2. Maintaining Proper Labelling System each product.3. Maintaining MSDS (Material Safety Data Sheet) Normal all lab chemicals.4. Maintaining Product Log Books, Patents and R&D Documents.5. Cleaning of the Glassware.6. Maintaining lab chemicals inward documents.7. Following the instructions of shift chemist.8. Before start the work persons should wear Apron, Nose masks, Gloves, Goggles and safetyshoe during process operations.9. Arrange several types of Set-ups in R&D Laboratory.10. To ensure proper allocation of works to the Lab assistant.11. Maintaining online documentation.12. Ensure the all standards; Reagents are within the valid period.

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.

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.