Chemist Job Vacancies in Bhiwadi

As a Quality Chemist, your primary focus will be to ensure that all products meet the required quality standards before they are released for distribution. Your responsibilities will include:- **Conducting Quality Tests**: Perform various chemical tests on raw materials and finished products to guarantee compliance with specifications and regulations.- **Analyzing Results**: Interpret test results and prepare detailed reports that summarize findings, including any deviations from expected quality standards.- **Maintaining Laboratory Equipment**: Ensure that all laboratory equipment is functioning properly and is calibrated regularly for accurate results.- **Documentation and Record Keeping**: Maintain accurate records of tests performed, results obtained, and any corrective actions taken to ensure traceability and compliance.- **Collaboration with Other Teams**: Work closely with production and safety teams to address any quality issues and to suggest improvements to processes and products.To excel in this role, you should possess the following skills and qualifications:- A Bachelors degree in Chemistry or a related field is required, providing a strong foundation in chemical principles and laboratory practices.- Strong attention to detail and analytical skills to effectively assess product quality and identify issues.- Basic understanding of laboratory safety protocols and procedures to ensure a safe working environment.- Ability to work independently and as part of a team, showing good communication skills to convey important findings and collaborate with colleagues.- A proactive attitude towards learning and adhering to quality standards in a fast-paced work environment.

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.

No.of Two Candidates Required lab chemist for QC department.

Male candidate with 1-3 years experience working in Q.A. or Q.C. Lab handling chemicals

As a Manufacturing Chemist, your primary role is to formulate, test, and producevarious chemical products following safety and quality standards.Responsibilities include operating equipment, conducting experiments, andanalyzing data to ensure product consistency and efficiency.You'll collaborate with teams to troubleshoot issues, optimize processes, andmaintain equipment. Attention to detail, adherence to protocols, and compliancewith regulatory requirements are vital.Additionally, you'll document procedures, maintain inventory, and uphold workplacesafety practices.Your contribution ensures the smooth operation of manufacturing processes andthe delivery of high-quality chemical products to meet customer demands.

Electroplating Chemicals Testing & Development activities

Analytical testing of materials. Develop and maintain quality management systemQualification : M.Sc Chemistry must

Pharmacy sale counter and billing

Note - We are looking for Assistant Manager R&D Formulation for Skin Care & Hair Care / Color Cosmetics company in Bawal , Rewari, Haryana.Job Details & Responsibilities Excellent knowledge of products Manufacturing of Colour Cosmetics / personal care, Skincare, Cream, Shampoo, Hair Oil, Conditioner, Face Wash, Body Wash, Body Lotion and Foot Care ,Lipstick, Nail Polish Etc. Lay down procedure to implement GMP & GLP norms and ensure documentation & compliance Define AQL for incoming raw material and components Develop vendor base to meet cost, quality (manufacturing and product), and innovation requirements Development of new formulation as per the business demand Preparation of documents & Registration of product, label compliance with regulatory authorities -local & overseas. Check & verify work orders by production & take action in case of discrepancy. Create methods of sampling, prepare format and forms to analyze, report & record information/data GRN clearance To be involved in all aspects of product formulation from the initial brief to final sign-off and overseeing the manufacture of pilot batches and full-scale production. Define product characteristics, technical concepts and ingredients composition. Match formulations of benchmark products to carry out the end to end development of product formulations. Reformulate or improve existing formulas through NPD trials / batch trials. Detail trials, test data and lab observations. Document basic information, creative ideas, and guidance to formulators. Implement robust testing procedures for toxicology assessments, accelerated stability and Preservative efficacy testing, microbial investigations. Support all documentation requirements for product registration in respective market zones. Validate Product information file, ingredients review, full for