Quality 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.

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.

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,

Job descriptionWANTED Chemical, FMCG, Polymer, Plastic, Rubber, Petroleum Products & Pharma - Manufacturing Sectors hiring people for the following departments:- PRODUCTION / PROCESS / QC / LAB ANALYSTM / F, Fresh / Exp., Age : 18-35 Yrs.Eligibility :-Diploma's/ Engineers / Graduate's(B.Sc. / M.Sc) Graduates - Batches: 2017 - 2020.Desired Candidates are willing to work anywhere in India.Role Pharmacist/Chemist/Bio ChemistIndustry Type Pharma / Biotech / Clinical ResearchFunctional Area Medical, Healthcare, R&D, Pharmaceuticals, BiotechnologyEducationUG : B.Pharma - Pharmacy, B.Sc - General, Environmental science, Food Technology, Agriculture, Geology, Anthropology, Home science, Bio-Chemistry, Biology, Microbiology, Botany, Chemistry, Dairy Technology, Zoology, Diploma - Chemical, Vocational Course, B.Tech/B.E. - Petroleum, Environmental, Production/Industrial, Textile, Bio-Chemistry/Bio-Technology, Biomedical, Ceramics, Chemical, PG : M.Tech - Chemical, Petroleum, Agriculture, Environmental, Production/Industrial, Textile, Bio-Chemistry/Bio-Technology, Biomedical, Ceramics, MS/M.Sc(Science) - Botany, Chemistry, Dairy Technology, Zoology, Environmental science, Food Technology, Agriculture, Geology, Anthropology, Home science, Bio-Chemistry, Biology, Microbiology, M.Pharma - Pharmacy, PG Diploma - Chemical

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.