30 Qc Analysis Jobs

- Documentation of analysis, maintaining the raw data of observation & entries of required data into system. - Reporting on status of quality and raising appropriate defects. - Produce standard test scripts. Required Candidate profile - Excellent knowledge of MS Office. - Strong understanding of quality control standards and testing techniques.

We are looking for a highly skilled and experienced Analyst-QC to join our team at eClerx Services Ltd. The ideal candidate will have a strong background in IT Services & Consulting, with excellent analytical and quality control skills. Roles and Responsibility Collaborate with cross-functional teams to identify and prioritize testing requirements. Develop and implement comprehensive test plans and cases to ensure high-quality deliverables. Conduct thorough analysis of test results and identify areas for improvement. Work closely with the development team to resolve defects and enhance overall product quality. Participate in continuous improvement initiatives to optimize testing processes. Maintain accurate records of test cases, results, and defect reports. Job Requirements Strong understanding of software testing principles, methodologies, and tools. Excellent analytical, problem-solving, and communication skills. Ability to work effectively in a fast-paced environment and meet deadlines. Experience with quality control processes and procedures. Familiarity with industry standards and best practices for software testing. Strong attention to detail and ability to identify defects and errors.

Perform analysis of raw, in-process & finished goods. Operate GC, HPLC, UV, KF, IR. Maintain records, follow GLP & SOPs. Support method validation. Ensure ISO/regulatory compliance & coordinate with QA/production for batch release.

Responsible for day-to-day activities of Quality Control, prepare and maintain documentation as per cGMP norms. Working Experience on HPLC is must Coordinate with other depart for smooth running of plant Capable of handling external Audits Required Candidate profile Min Exp 2 to 10 years in Quality department of a reputed pharmaceutical Company Knowledge of working in GMP Co. MS Office (MS Word & MS Excel) / ERP software. and good time management skills Perks and benefits Performance linked incentive & annual bonus extra

Sodexo Food Solutions India Pvt. Ltd. ces is looking for Helper - FLS to join our dynamic team and embark on a rewarding career journey. Following instructions and procedures to perform assigned tasks. Complying with all safety procedures and guidelines. Maintaining a clean and organized work area. Ability to follow instructions and procedures. Communicating effectively to ensure a smooth and efficient work flow.

Role & responsibilities Key Responsibilities Develop maintain high level of relationship with all regulatory bodies specially Police, RTO and other regulatory bodies involving Transport at all operating Locations. Liaison with regularity authorities (RTO/ Police) Support development implementation of the Security procedures. Assesses the character professional integrity of employee and contractor staff incl. Drivers. Monitor and investigate the cases of the professional integrity perpetrated by employees or contractors or contractors employees. Report Enquiry report and results to Management. Monitor and reports on compliance with established Operating Procedures. Support and organize Security. Regulatory Compliance related Processes training through external regulatory agencies. Preferred candidate profile Understanding of Compliance. Experienced in handling Audits and Safety Checks. Handling of Drivers management and interaction. Responsible for driver training programs.

Role & responsibilities: 1. Raw Material Testing: Perform chemical and physical testing of ingredients such as flour, sugar, fats, oils, milk powder, and preservatives. Typical tests: moisture content, protein, ash, gluten content, acidity, pH, FFA, peroxide value, color and odor checks. Ensure that each lot of incoming raw material meets internal and regulatory specifications before approval. 2. In-Process Testing: Conduct tests during various stages of production (mixing, baking, cooling, packaging). Monitor parameters like dough temperature, consistency, pH, baking time, texture, and weight. Conduct rapid tests to ensure process control and product uniformity. 3. Finished Product Testing: Carry out final product analysis for quality release. Test parameters: moisture content, water activity (aW), shelf-life simulation, organoleptic testing (taste, texture, aroma). Compare results with product specifications. 4. Packaging Material Testing: Perform basic checks on films, packets, and cartons. Test for GSM, thickness, print quality, sealing strength, and compliance with labeling standards. 5. Lab Equipment Handling: Operate and calibrate lab instruments: hot air oven, pH meter, moisture analyzer, balance, water activity meter, etc. Maintain calibration records and ensure proper working condition of equipment. Documentation & Reporting: Record all test results accurately in both hard copy logbooks and soft copies Prepare COAs (Certificate of Analysis) for raw materials and finished products. Maintain proper sample retention records. Raise NCRs (Non-Conformance Reports) for any deviation observed during testing. Soft Copy Data Management: Maintain structured folders for test reports by date, batch, and product. Use Excel/Google Sheets for entering daily test data with formulas for spec validation. Ensure data is backed up and audit-ready at all times. Tag and link scanned COAs and test reports to batch records. Quality Systems Support: Assist in implementing and maintaining HACCP, ISO 22000, FSSAI, and BRC requirements. Support internal audits and external food safety inspections. Participate in periodic lab process validation and proficiency testing. Quality Control & Analysis: Perform chemical analysis of raw materials (flour, sugar, fats, etc.), additives, and final bakery products. Monitor parameters like moisture content, pH, fat content, ash content, acidity, water activity, etc. Conduct shelf-life studies and sensory evaluations. Data Maintenance in Soft Store scanned PDFs of supplier COAs with batch-wise tagging. Daily QA Summary -Materials tested, issues identified, corrective actions Non-Conformance Log -Rejections, reasons, corrective/preventive actions (CAPA) Inventory of Lab Chemicals reagents, expiry dates, stock levels Skills Required: Knowledge of food chemistry & analytical techniques Good lab hygiene and record-keeping practices Familiarity with FSSAI guidelines and food safety documentation Attention to detail and ability to work in a fast-paced environment Preferred candidate profile Candidates from bakery, confectionery, or FMCG will be preferred. Hands-on experience with chemical testing, wet lab techniques, and QA instrumentation.

Post : Maharashtra FDA Approved - QC Chemist Active Pharmaceutical Ingredients (APIs) and Pharmaceutical Intermediates Manufacturing Facility. Experience : Minimum 2-3 years’ experience in a Quality Control laboratory, preferably in the APIs Industry Willingness to work flexible hours or shift work if required. Location : MIDC Paithan, Chhatrapati Sambhaji Nagar. Educational Qualification : B.Sc. / M.Sc. (Analytical Chemistry) Job Description: Perform routine Quality Control testing on raw materials, in-process samples, and finished API products to ensure compliance with specifications. Utilize standard analytical techniques such as HPLC, GC, Spectroscopy, titration, IR, and dissolution testing. Conduct tests for purity, potency, identity, and impurities in accordance with official monographs (e.g., USP, EP) or internal specifications. Assist in the development, validation, and qualification of analytical methods, ensuring they are suitable for their intended purpose and meet regulatory standards. Participate in method transfer from development to manufacturing. Optimize existing methods to improve efficiency and accuracy. Maintain accurate, clear, and complete laboratory notebooks and test records following Good Laboratory Practices (GLP) and Good Documentation Practices (GDP). Prepare detailed test reports with data analysis and conclusions, highlighting any deviations or issues. Review and approve laboratory data, ensuring the correctness of the results and interpretation. Ensure compliance with SOPs (Standard Operating Procedures) and GMP (Good Manufacturing Practices) documentation Ensure all testing activities comply with FDA, EMA, ICH, USP, and other regulatory guidelines. Maintain awareness of industry trends, regulations, and changes in API quality control requirements. Support audits and inspections by regulatory bodies or internal teams to ensure adherence to compliance standards. Support stability studies for raw materials and API products by monitoring and testing products over time under various conditions. Analyse stability data to ensure product shelf life and quality. Prepare stability protocols and reports. Work closely with the Quality Assurance (QA) department to investigate deviations, out-of-specification (OOS) results, and corrective/preventive actions (CAPA). Assist in the investigation of non-conformities and participate in root cause analysis for issues related to product quality. Ensure proper maintenance, calibration, and performance verification of laboratory equipment. Monitor reagents and chemicals inventory to ensure availability for testing, and ensure proper storage and labelling. Adhere to safety protocols in the lab and ensure compliance with health and safety regulations. Participate in internal training on quality control procedures, new testing techniques, and regulatory updates. Assist in training junior QC chemists or new staff as required. Contribute to the ongoing improvement of Quality Control processes, laboratory procedures, and testing methods.

Role & responsibilities Monitor and control production processes. Maintain documentation and ensure adherence to SOPs. Ensure safety and compliance in all operational activities. Coordinate with QA/QC and other departments as required Preferred candidate profile Fresher with B.Sc. in Chemistry (20222025 pass-outs preferred) Willing to work in shifts and follow plant discipline Good communication and learning attitude

Experienced QC Inspector With Good Experience in Manufacturing Unit. Industrial background preferred Diploma or Graduate in Mechanical Engineering

Role & responsibilities Job Summary: We are seeking a diligent and experienced QA & QC & IPQA & HPLC Production . The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance (QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. Salary Range : 15,000 to 25,000 (negotiable based on experience & skills) Experience: Freshers & Experience Both Required in QA/QC/Production/ department of Tablet & Capsule or pharma manufacturing unit Role & responsibilities Quality control analyst Responsible for testing and analyzing pharmaceutical products to ensure they meet established quality standards. They work in laboratories, using analytical Techniques to test raw materials, in-process samples, and finished products. Quality assurance analyst Responsible for ensuring compliance with regulatory requirements by conducting audits, inspections, and assessments Preferred candidate profile Qualification: Relevant degree in any of the following fields, B.Pharma, M Pharma, D Pharma ,B.Sc or M.Sc, BBA, MBA, BA,ITI Any Tared Company - Top Pharmaceuticals Companies based at Baddi HP. Fresher & Experience. Job Location- Baddi Nalagarh Parwanno Solan ( Himachal Pradesh ) Functional : QC,QA & Production. Industry: Pharma manufacturing unit/ The Saksham Success Enterprises Near Sunder Ayan by pass solan 173212 Himachal Pradesh Contact us SHILPA 9129999003( 9:30 AM to 6:30 pm ) Preferred candidate profile The Saksham Success Enterprises Near Sunder Ayan by Pass Solan 173212 Himachal Pradesh Contact us SHILPA 9129999003( 9:30 am to 5:30 pm )

Roles and Responsibilities Only for male candidates Department requirements - Production, solvent recovery plant, Technical service dept, Warehouse, Quality assurance, Quality control, R&D, AR&D, DQA, RA and HR Ensure compliance with GMP guidelines and regulatory requirements for API manufacturing. Oversee bulk drug production, quality control, and warehousing operations. Develop and implement effective QA/QC procedures to ensure product quality and purity. Collaborate with cross-functional teams to resolve issues related to active pharmaceutical ingredients (APIs) and bulk drugs. Conduct regular audits and inspections to maintain high standards of quality assurance.

Instrument Analysis GC/HPLC for QC department Min 2-5 only API CO 1 to 3 year experiance HPLC/GC analysis like Assay, RS, Chiral, Purity, Residual solvent analysis Location- Nandesari, Vadodara, Gujarat, India.

We are hiring a QA/QC Engineer with experience in fabrication and engineering design. Must have knowledge of ISO standards, QAPs, and vendor documentation. Strong attention to detail and quality processes required.

Role & responsibilities 1.HPLC,UPLC and GC analysis of raw material, intermediate, finish product, stability sample, equipment cleaning and distilled solvent, Analytical Method development and validation 2.HPLC,GC, UPLC calibration HPLC and GC Analysis of all in-process,Intermediate, Finish Product,Stabiltity Analysis Equipment cleaning, Distilled Solvent and Raw materials. If required then sampling of finished product. Working Standard Qualification. Calibration of HPLC and GC. GCHS. R&D Analytical Metliod Development of new molecule. Analytical Method Validation. lnstnmrent Troubleshooting

To conduct research , develop innovative solutions and designing products or systems , while continuously striving to advance technology and contribute to the organizational goals.

* Ensure compliance with safety protocols & regulatory standards. * Oversee lab operations, testing & inspections. * Manage inventory & equipment maintenance. * quality control * supervision management * Trouble shooting * Documentation & Reporting Provident fund Annual bonus

QC Daily Analysis Conducted tests Assay and Dissolution KF ,PH Preparation of solutions for HPLC Analysis Documentation preparation like SOP,MOA,MSDS,STP

Coordinate to ensure minimum stoppage during shift Ensure manpower allocation as per planning. Regularly checking the Production Rate as per the quality standards Maintain all the register for process parameters Checking stage wise process samples Perks and benefits Medical, Canteen

- Analysis of finished goods & RM & maintain its documents - Analysis of all products as per inspection plan - Conduct the in- house calibration of instrument and equipment - Laboratory reagent preparation, its standardisation for daily use Perks and benefits Medical, Canteen

FERRING THERAPEUTICS PRIVATE LIMITED is looking for Analyst QC to join our dynamic team and embark on a rewarding career journey Analyze data, interpret trends, prepare reports, and support decision-making through insights Develop models, work with tools like Excel, SQL, or Python Ensure data accuracy, and contribute to business optimization and forecasting efforts

Experience: 2-4year experience in the clinical research in a quality control. Role & responsibilities 1) Review of clinical raw data as per predefined Quality Control Plan for completeness, accuracy, and for compliance with the Study Protocol, GCP, SOPs and applicable regulatory Guidelines. 2) Online Monitoring of study activities to ensure that studies are conducted in accordance with GCP, SOPs, Protocol and applicable regulatory guidelines. 3) Issuance, Reconciliation and Accountability of Controlled forms/ Documents as per applicable SOP. 4) Preparation of projects for QA audit and Archiving. 5) Review of Tabular listing appended to Clinical Study Report and Individual Subject CRF scan check (as applicable). 6) Assist QC in-charge in review of Quality Control- Clinic SOPs. 7) Any additional responsibility given by Head of the Department / Management 8) Perform source data verification (SDV) activity (as sponsor requirement) 9) Review the safety Lab data (as per Data Transfer Agreement) Job Location: Vadodara (Gujarat)

Aster Medcity is looking for Associate.Academics.Aster CMI Hospital Bangalore to join our dynamic team and embark on a rewarding career journey. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Preparation of operating budgets, financial statements, and reports. Reviewing existing financial policies and procedures to ensure regulatory compliance. Providing assistance with payroll administration. Keeping records and documenting financial processe

To perform the environment monitoring of Aseptic area and supporting area. To perform the Microbiological test for Water system sample, SFG, RM, PM samples To prepare the trend data for the Microbiological monitoring of area and water system samples. To perform the Gowning qualification of other department personnel. To involve in media fill and Qualification of Micro lab and Mfg. area equipment.

Applications are invited for the Post of, QC Analyst VIT Samsung Data Lab SCOPE at Vellore Institute of Technology (VIT), Vellore, T N, India, Job Title : QC Analyst VIT Samsung Data Lab SCOPE Qualification : Sc Mandatory Skills : Basic understanding of Microsoft Office tools (Excel, Word, etc ), Quality control and assurance knowledge with hands-on experience in data validation, of Vacancies : 2 Posts Experience : 1 to 2 Years experience Sponsoring Agency : Samsung R&D Institute India-Bangalore, Job Description : Analyse and validate annotated data to ensure accuracy, consistency, and compliance with project guidelines, Perform detailed quality checks on data (images, videos, text) to identify errors and suggest corrective actions, Develop and maintain quality standards by conducting regular audits and monitoring task outputs, Collaborate with annotators and provide constructive feedback to enhance data quality, Assist in defining quality control processes and updating guidelines as required, Ensure structured management of reviewed data, maintaining version control and secure storage, Participate in periodic training to stay aligned with evolving quality standards and annotation processes, Good communication and teamwork skills, ability to learn quickly and adapt to project-specific requirements, Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc through online http://careers vit ac in No TA and DA will be paid for appearing the interview, Shortlisted candidates will be called for an interview at a later date which will be intimated by email, The selected candidate will be expected to join at the earliest,