15 Qc Analysis Jobs

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,

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.

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).