Quality Chemist Job Vacancies 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.

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.

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

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

Vacancy QC Chemist/ExecutiveInstrumentation Exp is MustExp; 2-5 yearsAPI/Bulk DrugsMale Candidate OnlyLocation: Hyderabad

Looking for Young Graduate in Physics or Chemistry to Work in Metal Alloy Manufacturing Company

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

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

Every Day 3 to 5 Hours Classes .if Online Can Be Taken Class from Your Own Place

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.

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.

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