18 Qc Executive Jobs

The Roles Responsibilities are: To arrange laboratory as per Good Laboratory practice (GLP). To prepare Standard operating procedures. To prepare Standard testing procedures To prepare Instrument Operating procedures. To calibrate all the instruments at specified regular intervals. Method development. To prepare and maintain QA/QC documents and registers. To maintain standard records and documents as per FAMI-QS. Inspect, test, or measure materials or products being produced Report inspection and test data. To carry out any work given by QC/Lab Incharge. To carry out the analysis work and report any abnormality to Seniors To do the analysis of RM / In-process / FP by chemicals instrumental methods of analysis. To prepare SOP for QC Instruments, and STP for RM / FP. To do the calibration of Instruments as and when required. Mandatory Skills: B.Sc or M.Sc with Chemistry. Should have working experience of 3-5 yrs. Knowledge of Wet Chemical analysis. Knowledge of Instrumental Analysis. Knowledge of Documentation SOPs and STPs. Knowledge of preparation of COA. To carry out daily calibration of instruments Desired Skills Well Versed with Titrimetric analysis. Well Versed with the handling of UV, GC, and HPLC. Should be able to prepare SOPs, STPs of RM, and FP when required. Should be able to prepare COA of FP when needed. To do daily calibration of Instruments like balance, PH meter, periodic calibration of GC, HPLC, UV. Designation: QC Executive / QC Officer. Job Location: Bhiwandi. Experience: Candidate with 3 to 5 years of experience. Qualification: B.Sc. or M.Sc. in Chemistry Qualifications Experience can be relaxed in the case of exceptionally talented candidates with the approval of Management

: Creation/Revision/ Review of Specifications and Methods for Site Transfers and ANDAs Method Validation Protocol knowledge. Creation/Revision/ Review of Validation Repot for Drug substance, Excipients and Drug products. Initiate Change controls as necessary for: Method and specification revisions and stability Protocol Modules preparation for Drug substance and Drug product. Batch Analysis - 32S/32P Reference Standards - 32S/32P Characterization of Impurities - 32S/32P Justification of Specification - 32S/32P Facility Templates Stability Summary Reports for ACC, CRT & RT 5313 Reports (Dissolution Comparative test) QOS & Stability Overview - 32S/32P (If ANDA) To prepare vendor qualification report based on the performance of material at test. To prepare justification reports towards reduction of tests in Input material testing such as raw and packaging material; In-process testing; Finished product testing; Stability testing. Preparation/Review of SOPs Required Skills: Analytical method Validation documentation : Advanced Laboratory Instrumentation Knowledge : Intermediate Data Integrity (ALCOA+ principles) : Advanced CTD / eCTD Module Preparation (Primarily Module 3.2.S & 3.2.P) : Advanced Impurity Profiling & Justification : Intermediate Stability Profiling Knowledge : Advanced

Job Description Shall follow the Good Laboratory Practices, Safety measures and good documentation practices while working. Follow the standard Operating Procedures and Standard Test Procedures while working. Responsible for analysis of RM PM samples, and compile the report as per ALCOA procedure, other miscellaneous samples, and compile their report. Regular participation in internal and external training programs. Maintain the instrument usage and maintenance of instruments like HPLC, Dissolution Test apparatus, UV Spectrophotometer, Balance, PH meter and Sonicator etc. Responsible for sampling and analysis of RM/PM/AVD samples as per approved protocols or spec & STP. Follow the organizational data integrity policy, GDP and its effectiveness up to compliance. Complies with the EHS Rules, Procedures, Guidelines, Policy, Practices, Requirements & Applicable Legal Compliances. Work Experience Education :- B.Pharm/ MSc. Experience :- 2 to 5 yrs. Education Others Competencies

Role & responsibilities 1. Candidate Should have a M.Sc in ( Analytical / Organic Chemistry). 2. Should have minimum work experience of 5 to 10 years in field. 3. Should have experience in working with chemical plant setup. 4. Must be willing to work during day/night shift. Preferred candidate profile 1. Ensure Safety at work place. 2. Should have expertise in handling & calibration of instruments like HPLC,GC,AAS, Moisture Analyzer, UV Spectrophometer etc. 3. Should have expertise in HPLC method Development & Validation. 4. Maintenance of Reference standard, working standards & their standardization 5. Should have expertise in all Wet Chemical analysis. 6. Assist in the training of new research associate/scientist. Provide technical & scientific leadership to other team members. 7. Should have some experience in Q/C & Q/A documentation & SOP preparation 8. Perform other duties as assigned by the Manager

Diploma / Graduate/ ITI with 1 to 3 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Incoming R M Inspection / In process Inspection / Final QC Inspection. Proper record keeping. Required Candidate profile To check the material as per the standard procedure and as per the time frequency. Detect non-conformities. Check the root cause of the non-conformity and take corrective and preventive action. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 1 to 3 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Incoming R M Inspection / In process Inspection / Final QC Inspection. Proper record keeping. Required Candidate profile To check the material as per the standard procedure and as per the time frequency. Detect non-conformities. Check the root cause of the non-conformity and take corrective and preventive action. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 1 to 3 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Incoming R M Inspection / In process Inspection / Final QC Inspection. Proper record keeping. Required Candidate profile To check the material as per the standard procedure and as per the time frequency. Detect non-conformities. Check the root cause of the non-conformity and take corrective and preventive action. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 1 to 3 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Incoming R M Inspection / In process Inspection / Final QC Inspection. Proper record keeping. Required Candidate profile To check the material as per the standard procedure and as per the time frequency. Detect non-conformities. Check the root cause of the non-conformity and take corrective and preventive action. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 1 to 3 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Incoming R M Inspection / In process Inspection / Final QC Inspection. Proper record keeping. Required Candidate profile To check the material as per the standard procedure and as per the time frequency. Detect non-conformities. Check the root cause of the non-conformity and take corrective and preventive action. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 1 to 3 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Incoming R M Inspection / In process Inspection / Final QC Inspection. Proper record keeping. Required Candidate profile To check the material as per the standard procedure and as per the time frequency. Detect non-conformities. Check the root cause of the non-conformity and take corrective and preventive action. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / B.Sc / B.Tech in Chemical or Civil Engineering Skills Required: Hands-on experience with Bitumen (VG) Knowledge of RS1, RS2, MS Familiarity with CRMB, PMB Understanding of BIS standards (IS 8887, IS 15462, IS 702) Experience with NABL procedures Job Description: The selected candidates will be responsible for conducting quality tests on various bitumen and emulsion products, ensuring compliance with BIS standards, and supporting R&D initiatives. The role demands strong technical expertise, attention to detail, and familiarity with laboratory protocols related to bitumen testing. Apply for this position Allowed Type(s): .pdf, .doc, .docx By using this form you agree with the storage and handling of your data by this website. * Your browser does not support the video tag.

Jr Officer / Officer / Executive QC Department: Project Qualification: BE / B. Tech Mechanical Experience: 13+ years Location: Saykha (Bharuch) Job Description: The candidate will be largely responsible for design review along with Site Construction. Should have minimum 10 years previous experience in greenfield pharma API projects.

Candidate should have adequate knowledge of HPLC,UV,FTIR, Dissolution test apparatus etc. Candidate should have experience in-process , Finish Goods , Stability samples testing and also require the knowledge of chemical analysis. Key Responsibilities: Conduct routine and non-routine testing of raw materials, in-process samples, and finished products as per standard operating procedures (SOPs). Perform physical, chemical, and microbiological analysis using appropriate instruments and techniques. Maintain accurate and detailed records of test results and laboratory activities. Ensure compliance with GMP, GLP, and regulatory guidelines. Report deviations, out-of-specification results, and investigate quality issues. Calibrate and maintain laboratory equipment to ensure accuracy and reliability. Assist in the preparation of quality documentation, batch records, and validation protocols. Coordinate with production and quality assurance teams to support quality initiatives. Participate in internal and external audits.

New product creation Existing product correction & duplication removal product channel mapping & correction Pharmarack (3rd party vendor) new product mapping, existing mapping correction & actionables B2C product QC B2c website images mobilization.

? Job Description: ? ? We are seeking for a motivated and detail-oriented QC Trainee / Executive to join our quality team. The ideal candidate will be responsible for supporting quality control operations in method development, routine analysis, and documentation for APIs and intermediates under development. ? ? Key Responsibilities: ? ? Perform sampling and testing of raw materials, intermediates, and finished products. ? ? Conduct instrumental analysis (HPLC, UV, IR, GC) as per approved methods. ? ? Prepare and maintain Certificates of Analysis (COAs), logbooks, and test records ? ? Maintain lab notebooks, data integrity, and QC documentation ? ? Support in creating analytical method to identify, quantify and monitor impurities and the quality of the product ? ? Work closely with R&D and QA teams ensure compliance ? ? Requirements: ? ? 0 1 years of relevant experience in QC role. ? ? Familiarity with laboratory instruments and quality systems. ? ? Basic understanding of analytical techniques and GLP/GMP concepts ? ? Basic understanding of data integrity and GLP practices and Willingness to work in shifts (if required). ? ? Strong attention to detail and documentation skills. ? ? Willingness to learn, good observation skills, and attention to detail ?

Role & responsibilities 1. Performing Stability analysis, Method transfer and Method Validation. 2. Preparation and review of Method Transfer Protocols, Validation protocols and all related protocols, procedures and reports. 3. To carry out analytical method development, method validation and testing of impurities in finished products on LCMS/MS and GCMS/MS 4. FG (HPLC) 5. Preparation, review of departmental SOPs and training of analysts. 6. Calibration and validation of instruments equipments. 7. Review and maintenance of all logbooks in the department. 8. Procurement of columns, chemicals/ reagents/ solvents and standards for Stability analysis, Method Transfer and Method Validation.

Conduct routine tests on raw and processed milk. Monitor product quality at each stage of production. Ensure compliance with quality norms and documentation. Handle customer complaints and implement corrective actions.

Conduct routine tests on raw and processed milk. Monitor product quality at each stage of production. Ensure compliance with quality norms and documentation. Handle customer complaints and implement corrective actions.