QA Chemist Jobs

As a Quality Assurance Chemist, your primary focus will be to ensure that all chemical products meet required standards of quality. You will play a critical role in maintaining compliance with regulations and ensuring safety in the lab environment.**Key Responsibilities:**- **Conduct Tests and Analysis:** Perform a series of laboratory tests to analyze the chemical composition and properties of products, ensuring they meet established quality standards.- **Document Findings:** Create detailed reports on test results, documenting any deviations from quality standards and recommending corrective actions.- **Maintain Laboratory Equipment:** Regularly check and calibrate lab equipment to ensure precise measurements and reliable results.- **Develop Quality Control Procedures:** Assist in developing and implementing quality control procedures to enhance product quality and uniformity.- **Collaborate with Team Members:** Work closely with other team members to discuss test results, share knowledge, and resolve quality issues promptly.- **Stay Informed on Regulations:** Keep updated on industry standards and regulations to ensure compliance and maintain laboratory accreditation.**Required Skills and Expectations:**Candidates should possess a Bachelor's degree in Chemistry or a related field. Strong attention to detail and analytical skills are crucial for spotting discrepancies and ensuring reliable outcomes. Effective communication skills are necessary for collaborating with team members and documenting findings accurately. Familiarity with laboratory safety protocols and a commitment to maintaining a safe work environment are essential. A proactive attitude and willingness to learn are beneficial for those with limited experience.

Designation :- QA Chemist Qualification:-BSC Or MSC & Any TradeExperience:- 2 Years To 4 YearsSalary:- As per interviewGender:- MaleJob Time:- 9:30 am to 6:00 pmVacancy:- 03Job Location:- Vasai, MaharashtraIndustry:- Chemical plant

Candidate should be aware about Analytical instruments, Chemical testing, Knowledge of GMP & ISO documentation.

Key Responsibilities:Implement and monitor QA systems (as per GMP/ISO/FDA guidelines).Conduct internal audits and support external audits (regulatory & client).Review and approve SOPs, batch records, and quality documents.Investigate and document deviations, CAPA, OOS, and change controls.Coordinate with production, QC, and regulatory teams for compliance.Ensure training and qualification of QA team members.Maintain records and documentation per regulatory standards.

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.

Q.A AND Q.C DEPARTMENT.AND PRODUCTION DEPARTMENT AND STORE

Newly Setup Coconut Products manufacturing Industry with highly automated machinery with 25+ products. candidate should possess a degree in micro biology, chemicals etc.,R & D Work

Designation: Sr. Executive - QA/QC Purely Lab Chemist with minimum 4 - 5 years of experienceQualification: M.Sc. Chemistry/ B.E. Chemical /Diploma in Chemical Engineering Location: Panvel 5+ years experience in QA/QC department in industrial chemicals manufacturing company. Operates, maintains, and tests laboratory equipment; identifies problems when equipment fails and conducts or recommends repairs. Perform in-process and finished product inspections to verify adherence to quality standards. Conduct testing and analysis of raw materials, intermediates, and finished products to ensure compliance with specifications. Managing activities such as product inspection, internal as well as external audits, regulatory agency inspections etc. Hands-on with quality management system like ISO 9001:2015, ZED etc. Responsible for preparing, updating and maintaining all QA related documents as per QMS in coordination with QC Manager. Maintain and update quality documentation, including specifications, standard operating procedures (SOPs), and quality manuals. Responsible of handling customer complaints and initiate Product Recall, if required. Take part in audit and surveillances. Maintain records of productions, inspections, quality training and safety. Coordinate all QA/QC activities with the QC manager

A. COORDINATION OF MANUFACTURING SITES FOR TABLETS, CAPSULES, OINTMENT AND INJECTIONS.. IPQC- VERIFICATION OF PARAMETERS ON SITE. B. FOR QUALITY ASSURANCE/QC- REGULATORY AFFARIS - FOR REGISTRATION OF PRODUCTS IN FOREIGN COUNTRY. PREPARATION OF ECTD AS PER FORMAT. VERFICATION OF QUALITY OF PRODUCTS, REPLYING TO QUERY FROM REGULATORY AUTHORITIES FROM FOREIGN AGENCY.

Must have knowledge of pH, Conductivity, titration.

Urgently Requirement for Qa Chemist. Quality Head, Lab Management, Quality Check, Documents Management, Quality Assurance,

Roles and Responsibilities Job B.pharma production QA/QC Pharma Companies for top pharmaceuticals at Baddi & Solan Available designation: - QA / QC and Production Department. Good Communication in hindi language of respective city. Eligibility -Bio Tech./B. Pharma & D.pharma Preference - Male / Female Applicants Can Apply. Industry / Company - Top Pharmaceuticals Companies based at Baddi HP. Experience Fresher / Experience. Salary Range -12000 to 30,000/m maximum for freshers and officers and experienced Job Location,Parwanoo Nalagarh Baddi solan nahan( Himachal Pradesh ) Functional :QC,QA and Production. Industry : Pharma Tha Saksham Success Enterprises near Central bank by pass solan 173212 himachal pradesh Contact us 9:30 AM to 5:30 pm visit saksham success enterprises solan

Job SummaryLooking for a Production Chemist with a minimum of 1-10 years experience in the pharmaceutical industry. Prior experience with the manufacturing of Active Pharmaceutical Ingredients preferredResponsibilities and DutiesManufacturing of Intermediates and Active Pharmaceutical Ingredients (APIs).Operation and Cleaning of Equipments.Execution of batches and Cleaning as per Batch Manufacturing Record.Calibration of Weighing scales and other measuring devicesMaintaining Equipment logs for each equipmentPerforming Process validationIn process samplingInvestigation of process related deviations.Salary range: 15,000/- to 45,000/- per monthJob location: Parawada, Vizag

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials.Experience in making lab SOPs and study reports6+ yrs of Agrochemicals/chemicals in Green field/brown field ProjectsExp in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD & DSC

Hiring for 4 QA QC Chemist Jobs in Pali, with a minimum three-Year Experience, The Required Educational Qualification is an M.Sc. with good knowledge in Analytical Chemistry, Documentation, QA-quality assurance Inspection, Quality Analysis, etc.

We have vacant of 1 analytical chemistry Job in Mumbai,Back Office Coordinator, for Freshers Educational Qualification : B.Sc, M.Sc Skill QA-Quality Assurance, Back Office Coordinator etc.

We have vacant of 1 QA QC Chemist Job in Karur, Experience Required : 1 Year Educational Qualification : B.Sc CHEMISTRY Skill Analytical Chemistry,Documentation,QA-Quality Assurance,QC Inspection,Quality Analysis etc.NOTE: Kindly apply the job from karur locality.

A. COORDINATION OF MANUFACTURING SITES FOR TABLETS, CAPSULES, OINTMENT AND INJECTIONS.. IPQC- VERIFICATION OF PARAMETERS ON SITE. B. FOR QUALITY ASSURANCE/QC- REGULATORY AFFARIS - FOR REGISTRATION OF PRODUCTS IN FOREIGN COUNTRY. PREPARATION OF ECTD AS PER FORMAT. VERFICATION OF QUALITY OF PRODUCTS, REPLYING TO QUERY FROM REGULATORY AUTHORITIES FROM FOREIGN AGENCY.

Pharma QA/QC Production Experienced Pharma Companies for top pharmaceuticals at Baddi & SolanAvailable designation: - QA / QC and Production Department.Good communication in local language of respective city.Eligibility - Bio Tech./ B OR D PharmaPreference - Male / Female Applicants Can Apply.Industry / Company - Top Pharmaceuticals Companies based at Baddi HP.Experience Fresher / Experience.Salary Range - 8000 to 18,000/m maximum for freshers and experiencedJob Location Baddi solan nahan ( Himachal Pradesh )Functional : QC,QA and Production.Industry : Pharma / Food TechnologyContact Person: sudarshna thakur

Roles and Responsibilities Job B.pharma production QA/QC Pharma Companies for top pharmaceuticals at Baddi & Solan Available designation: - QA / QC and Production Department. Good Communication in hindi language of respective city. Eligibility -Bio Tech./B. Pharma & D.pharma Preference - Male / Female Applicants Can Apply. Industry / Company - Top Pharmaceuticals Companies based at Baddi HP. Experience Fresher / Experience. Salary Range -8000 to 18,000/m maximum for freshers and officers and experienced Job Location,Parwanoo Nalagarh Baddi solan nahan( Himachal Pradesh ) Functional :QC,QAand Production. Industry : Pharma / Food Technology Tha Saksham Success Enterprises near Central bank by pass solan 173212 himachal pardesh Contact us 9:30 AM to 5:30 pm

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.

Job Title: Sr. Executive/ ExecutiveDepartment: QCExperience Required: 5 to 10 yearsJOB DUTIES and RESPONSIBILITIES (Please Mention In Below Table)1 Perform the testing of Raw Material/Finished goods/In process materials and report the results.2 Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSAetc3 Calibration of the Analytical instruments as per the master calibration schedule4 Investigate the analytical error/deviations during analysis and find out the root cause. propose appropriate correctiveand preventive action for the same5 Experience in making lab SOPs and study reports6 Execute method validation and prepare the necessary reports7 Reviews analytical chemistry testing records of raw materials, stability, and product for accuracy and adherence to test methods8 Preparation and review of Specifications, Method of analysis procedures and Analytical development reports9 Preparation and review of Specifications, Method of analysis procedures and Analytical development reports10 Discuss work plan on daily basis with supervisor/ manager and Mentor junior lab personnel11 Participate in project meetings and prepare weekly and monthly reports and submit to Manager12 Regular lab duties including equipment maintenance, chemical inventory and lab clean-up13 Maintain strict IP Confidentiality and adhere to all related data privacy policies

Job Title: Sr. Executive/ ExecutiveDepartment:QCExperience Required: 5 to 10 yearsJOB DUTIES and RESPONSIBILITIES (Please MentionInBelow Table)1 Perform the testing of Raw Material/Finished goods/Inprocess materials and report the results.2 Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSAetc3 Calibration of the Analytical instruments as per the master calibration schedule4 Investigate the analytical error/deviations during analysis and find out the root cause. propose appropriate correctiveand preventive actionforthe same5 Experienceinmaking lab SOPs and study reports6 Execute method validation and prepare the necessary reports7 Reviews analytical chemistry testing records of raw materials, stability, and productforaccuracy and adherence to test methods8 Preparation and review of Specifications, Method of analysis procedures and Analytical development reports9 Preparation and review of Specifications, Method of analysis procedures and Analytical development reports10 Discuss work plan on daily basis with supervisor/ manager and Mentor junior lab personnel11 Participateinproject meetings and prepare weekly and monthly reports and submit to Manager12 Regular lab duties including equipment maintenance,chemicalinventory and lab clean-up13 Maintain strict IP Confidentiality and adhere to all related data privacy policies

Job descriptionPreparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materialsRequired Candidate profileExperience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC.Role: QA / QC ExecutiveIndustry Type: Fertilizers / Pesticides / Agro chemicalsRole Category: Production & ManufacturingSheetal Tanwar

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