26 Qc Analysis Jobs

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,

A dynamic and result-oriented Scientist R&D to lead the research and development activities of plant nutrition and bio stimulant products. The ideal candidate will be responsible for formulation development, innovation, process optimization, quality control, and regulatory compliance to bring next-generation products to market. Key Responsibilities: • Lead R&D projects on the development of bio stimulants, micronutrient formulations, specialty plant nutrition products and bio botanicals. • Identify and validate new active ingredients from natural sources. • Drive scientific innovation to improve product performance and process improvement of the existing products and new product development. Prioritize and manage multiple projects, ensuring timely progress, budgeting, and milestone achievements. • Prepare technical documentation including SOPs, and product dossiers. • Collaborate with agronomy, regulatory, and production teams for product concept, positioning, and scale-up. • Coordination with quality control department and production department to ensure product consistency and compliance. • Foster a culture of innovation, safety, and continuous learning. • Responsibility for patent drafting, scientific publications, and technical presentations. Job Specification: • Education: Ph.D. in Chemistry (Organic chemistry/ Analytical chemistry). • Experience: 1-3 years in Industrial R&D preferred. • Expertise in application of sophisticated analytical instruments like AAS, UV, IR, GC and HPLC for product characterisation and estimation of active molecules. Kindly drop your resume at hr@marisymbio.com / 8220342663

Role & responsibilities 1. Responsible for analysis of FG and Raw materials 2. Ensure adherence to GMP & cGMP 3. Maintain and calibrate GC instrument 4. Prepare and review analytical documents and reports Preferred candidate profile B.Sc./M.Sc/ or B.Pharm. Hands on experience in GC operation Familiarity with regulatory audits

The Quality Control Chemist is responsible for developing and implementing quality control procedures and standards, monitoring and inspecting product quality to ensure compliance with established standards, analyzing test results . Required Candidate profile 1. Must have experience in QC Lab / Validations. 2. Must have B.Sc. / M.Sc. Organic Chemistry. 3. Must have 01- 05 Years of experience in QC Labs. Perks and benefits Free Bus , ESI , PF , Subsidized Canteen Food .

Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-8 Years Qualification: B.Pharma/M.sc/M. Pharma Location: Moriya, Ahmedabad Job Role : Physico Chemical (Analyst)- Friability / DT / Hardness / Thickness / UV Perform physical and chemical analysis for Raw material/ Inprocess / Finished Product based on the test requirements like UV, friability, DT, hardness, thickness, moisture, average weight, and uniformity weight. Prepare documents for each analysis performed and get those checked by the reviewer. Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen Facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position. Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career!!! Regards Team HR Unison Pharmaceuticals Pvt. Ltd.

The Quality Control Chemist is responsible for developing and implementing quality control procedures and standards, monitoring and inspecting product quality to ensure compliance with established standards, analyzing test results . Required Candidate profile 1. Must have experience in QC Lab / Validations. 2. Must have B.Sc. / M.Sc. Organic Chemistry. 3. Must have 01- 05 Years of experience in QC Labs. Perks and benefits Free Bus , ESI , PF , Subsidized Canteen Food .

Preferred candidate profile Looking for a candidate with 2 to 4 years of work experience as QC analyst /AQA reviewer in reputed pharma companies. Should have Knowledge of handling/analytical data review of HPLC, FTIR, UV spectrophotometer, KF Autotitrator, Dissolution apparatus. Have Basic knowledge of CGMP, GDP, Data integrity. Should have Basic knowledge of OOS (Out of specification), OOT (Out of rend), OOC (Out of calibration).

Roles and Responsibilities: 1 . Analysis of In-process, Intermediates, Raw material, Packing material, Finished products, Stability study, Hold time study, Process validation, Cleaning samples, Vendor development and any analysis allocated by team leader and release with proper documentation.. 2. Ensuring analysis is performed compliance to GLP. 3. Ensuring analysis raw data is documented on-line. 4. Initiation, Completion and filing of Daily analysis reports. 5. Ensuring any abnormal results, incidents, deviations, discrepancies are reported immediately to the reporting Section Head. 6. Ensuring all relevant log entries are made for every activity wherever applicable. 7. Supervise compliance to all cGMP, GxP or any other regulatory requirements including EHS requirements. 8. Report any quality concerns or suggestions for improvements to Department Head. 9. Execute and supervise all tasks and activities as per the applicable SOPs and company policy. 10. To maintain the safety norms while working in lab. (e.g. Wear goggles, PPE, Disposal of sample/media as per procedure etc). 11. Ensuring analysis is performed as per valid procedures and by using calibrated instruments / Standards. 12. Ensuring self-discipline with respect to wearing aprons, attendance and personnel hygiene and inter relations. 13. To perform Labware LIMS related activities. 14. Any other assignment given by the Section Head or Department Head.

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

The Quality Control Chemist is responsible for developing and implementing quality control procedures and standards, monitoring and inspecting product quality to ensure compliance with established standards, analyzing test results . Required Candidate profile 1. Must have experience in QC Lab / Validations. 2. Must have B.Sc. / M.Sc. Organic Chemistry. 3. Must have 01- 05 Years of experience in QC Labs. Perks and benefits Free Bus , ESI , PF , Subsidized Canteen Food .

Roles and Responsibilities Ensure quality control processes are followed by production team. Conduct regular inspections to identify defects and implement corrective actions. Develop and maintain quality documentation, including SOPs, checklists, and reports. Collaborate with cross-functional teams to resolve quality issues and improve overall productivity. Analyze data from QC tools such as statistical process control charts (SPC) to optimize manufacturing processes. Inward, Outward QC Vendor development in QC requirement Documentations Instrument list and calibration report Desired Candidate Profile 3-6 years of experience in Quality Control or related field (Mechanical Engineering background preferred). Diploma/B.Tech/B.E. degree in Mechanical or relevant discipline. Strong understanding of QC engineering principles, methods, and techniques.

Technograph Consultancy Services is looking for Helper 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 The role is for QC Executive for an Australia-based Medical Device Company at Ahmedabad: Inspect Finished Goods, WIP and Raw materials for a Medical Device (Patient Warming Blankets) to ensure consistency and integrity. Maintain high-quality standards across all aspects, conduct testing according to protocol, and reduce rejection rates. Testing of Product, inspection of finished goods and details to information printing as per the requirement of Medical Device. Report problems or concerns to senior management and QA immediately. Provide training and guidance to the manufacturing staff for achieving high-quality products. Manage our quality control division and ensure all employees meet the training requirements. Inspection of finished goods before and after packaging to ensure conformity. Provide training and support to the QA team Create an effective, efficient testing protocol to be used across all product lines Preferred candidate profile 1. BTech in any specialisation. 2. Worked as a QC for 2 to 5 years. Perks and benefits 1. Group Health Insurance of Family (Employee, Spouse and 2 Children)

Freshers Can Apply Role & responsibilities Project Execution: Ensure adherence to project plans, schedules, and quality standards Site Management: Supervise the construction work at the site and monitor progress. Manage resources, including labor, materials, and equipment, efficiently. Identify potential delays or issues and report them to the Project Manager for timely resolution. Quality Control: Conduct regular quality checks to ensure compliance with design specifications and standard Safety Compliance: Implement and ensure compliance with safety protocols at the site. Conduct toolbox talks and enforce site safety regulations among workers Coordination: Liaise with clients, consultants, and other stakeholders for approvals and updates. Provide progress reports and updates to the Project Manager and other relevant departments. Preferred candidate profile Male Key Skills MEP Basics & Technical Knowledge Partition, Ceiling , Flooring execution Drawing Interpretation – Executions as per 2D/3D Drawings Vendor Coordination – Handling daily site-level vendors Quality & Safety – QC Checklist & Site Safety standards Adaptability – Workings under pressure Cultural Fit – Team player , Punctual

QC officer Perform chromatographic analyses and tests, including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and Thin-Layer Chromatography (TLC), on raw materials, in-process materials, and finished products. Required Candidate profile Urgent looking for Male candidate who is able to work in rotation shift.

QC Chemist Executive Min 2-3 Experience Salary: 15K-25K Location: Vadodara Gujrat

Handling of HPLC Handling of GC Handling of UV.Vis Spectrophotometer

Role & responsibilities Internal Business Process- To establish systems and procedures to ensure that the process, product and service quality leads to the satisfaction of the customer. To ensure towards making the department a system driven. To ensure availability of various materials in time to meet OTIF. To ensure that required resources in the department. Promote innovation and changes in dept. to improve business performance. Customer Satisfaction- Ensure Reduction in customer complaints Ensure OTIF Ensure fulfill the all customers requirements/query/documents Ensure customer satisfaction during plant visit/audit People Development- Ensure Training need identification (TNI) and provide training accordingly. Safety Compliance- Ensuring Zero Incidents and Lost Time Injury. Compliance to Job Safety Plan & SOPs. Ensuring Compliance to SOP by conducting Safety Observation Visits. Ensure Contractor Site Safety Audits. Ensure proper working conditions for safe working of own and contractor Preferred candidate profile Perks and benefits

Role & responsibilities : CORPORATE QUAKLITY ASSURANCE 1. Specification Preparation & Documentation Develop and maintain specifications for raw materials (APIs, excipients) and packing materials. Ensure specifications comply with pharmacopeial standards and in-house quality standards. Review and update specifications based on regulatory updates, stability studies, and supplier changes. Coordinate with purchase, packaging development, QC, and regulatory teams for finalizing specifications. 2. Raw Material (RM) Specification Management Maintain records of Material Safety Data Sheets (MSDS) and Certificates of Analysis (COA) from suppliers. 3. Packing Material (PM) Specification Management Develop specifications for primary, secondary, and tertiary packaging materials. Ensure packing materials comply with stability, compatibility, and regulatory requirements. Conduct compatibility studies to assess interaction with drug formulations. Define parameters like GSM, burst strength, WVTR, dimensions, artwork compliance. 4. Regulatory & Compliance Assurance Ensure regulatory compliance with global standards (USFDA, WHO-GMP) Assist in audit preparation and responses related to material specifications. Ensure proper documentation and version control of Master Specification Files. 5. Vendor & Cross-functional Coordination Collaborate with vendors for RM & PM specification approvals. Work with Quality Control (QC), Quality Assurance, and Procurement to resolve material specification issues. Participate in vendor qualification, site audits, and material evaluation. 6. Acting as SPOC Between Factory & Corporate Serve as the primary liaison between the corporate QA team and the factory team regarding RM & PM specifications. Ensure smooth communication and implementation of corporate quality standards at the factory level. Address and resolve factory concerns related to RM & PM specifications in coordination with corporate QA. 7.Addressing Factory Concerns & Quality Compliance Resolve factory-level issues related to raw and packing materials by aligning corporate directives. Support factory teams in implementing quality control procedures for RM & PM. Ensure material handling, storage, and testing compliance at factory sites. Coordinate and support regulatory inspections and customer audits at manufacturing sites. Ensure timely CAPA (Corrective and Preventive Action) implementation post-audits. Maintain audit readiness across manufacturing and distribution facilities Design and approve the corporate documents to meet highest levels of quality standards. Conduct vendor audits and qualification for raw materials, packing materials, and contract manufacturers (P2P). Collaborate with the Procurement Department to ensure suppliers meet the required quality standards. Establish quality agreements with vendors and monitor compliance. specifications in coordination with corporate QA. Knowledge Required 1. 8 10years of relevant experience in Pharma industry. 2. Strong knowledge of pharmacopeia standards (IP, USP, BP, EP). 3. Expertise in specification writing and document management. 4. Knowledge of analytical techniques (HPLC, GC, UV, Titration, etc.). 5. Familiarity with ICH Q3C, Q6A, GMP, and GDP guidelines. 6. Knowledge of Specification Preparation of Raw Material / Packing Material / Finished Product 7. Knowledge of Pharmacopeia Monograph - Indian Pharmacopoeia / British Pharmacopoeia / United States Pharmacopoeia 8. Must have knowledge of General Testing Procedures related to Raw Material / Packing Material / Finished Product testing. 9. Must have proficiency in computer operating ( Specially MS Word ) 10. Able to communicate effectively with Factory Site and Purchase / RA Dept.. 11. Shall be able to communicate with Purchase Dept. related to P2P products. 12. Ensure cross-functional teams (Production, Purchase, Regulatory Affairs) are aligned with quality expectations. 13. Should be able to travel to third party site/s. 14. Should possess good verbal and written communication skills. 15. Exposure to regulatory agencies audits such as Schedule - M, USFDA, MHRA, WHO, ISO etc. Please note: Female candidate is preferred provided she should be able to travel outstation once in week on monthly basis.

Experience in Quality Line Inspection- Injection Moulding Instrument Handling Incoming and Outgoing Inspections QCQA Documentation updation

Responsible perform/Report the analysis of Water and pure steam (Condensate) samples. Responsible for preparation of Standard operating procedures, Standard test procedures, specifications ,SOP, STP, Specification, ATDS CoA of the RM, PM, Consumable Required Candidate profile change control /deviation / OOS / OOT / OOC/CAPA. Analytical method transfer/Stability Protocols Report the analysis of Finished Product, In- IP, SFG, FP. Perform the analysis as or when required

Role: Proofreader & QC Specialist Full time Shift: General Shift (10 AM to 7 PM IST) Location: Bangalore Requirements: Minimum 3 to 5 YRs of exp, Review and proofread content and design of various technical documents, including ppts, RFPs, videos, infographics, newsletters and emailers to ensure accuracy, clarity and adherence to brand guidelines and stakeholder requirements. Need good communication skills.

Require a QC Executive with Micro Lab experience and having Gujarat FDA Certification