28 Qc Executive Jobs

HPLC & GC instrument knowledge required Fresher & QC Chemist Also apply Required Candidate profile Qualification :- B.sc / M.sc - Chemistry /B.Pharma / M.Pharma Experience :-2 + Years in pharmaceutical Company Exp required Salary - 2 to 4 lakhs note - Freher Can b apply Resume

The Senior QC Executive leads quality control activities, mentors junior staff, and ensures compliance with internal and external quality standards. Review and approve QC reports, ensuring accuracy, completeness, and compliance with SOPs

1. Daily work allocation planning of RM, PM, IP, FP, STB, Mic. 2. The Analysis and review of RM, PM, IP, FP, Stability sample and Data. 3. The analysis of Analytical method validation sample, Analytical method transfer sample and Analytical method verification sample as per procedure. 4. Perform the Calibration of Instrument as per procedure. 5. Preparation of Reagent and volumetric solution as per procedure. 6. To maintain and order sufficient Reagents, chemicals and Solvents. 7. Preparation of In-house working standard and maintenance of working standard in laboratory. 8. Review and reporting of Document as per Good Document practices. 9. To send sample and fallow up with public testing la...

We are expanding!! You are invited to join one of the fastest growing pharma companies in India!! About us : Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. Department: Quality Control Section: HPLC Analysis & Chemical Analysis/ QC QMS Experience: 2-7 ...

Walk-in Drive | TIL Healthcare | Multiple Openings in Production, QA, Engineering & QC TIL Healthcare is a part of "Jhaver Group of Companies" having a turnover of USD 450mn whose core activities include Manufacturing, Marketing, Engineering, Construction and Trading like diversified businesses. Our plants are accredited approvals like EUGMP, TGAAustralia, UK MHRAetc. TIL manufactures Tablets, Liquids, Powders in Sachets, and Capsules and with well-known partners for several European companies. We are considered as Pioneers in Amino Acids in India and few known brands include ApetaminT/AstyminT/Astyfer/Neutrosec/Urelog/Peglec/HappenzT. Walk-in Interview Details: Date: Sunday, 28th September ...

HPLC & GC instrument knowledge required Fresher & QC Chemist Also apply Required Candidate profile Qualification :- B.sc / M.sc - Chemistry Experience :-2 + Years in pharmaceutical Company Exp required Salary - 2 to 4 lakhs note - Freher Can b apply Resume

WALK IN Interview - SUNDAY 7th Sep 2025 - Quality Control - Unison Pharmaceuticals Pvt Ltd Ahmedabad About us : Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. We are expanding!! You are invited to join one of the fastest growing pharma companies in In...

Job Title: A. 1. QC Executive 2. Microbiologist 3. GC-MS Executive 4. QA Analytical Company: Pharma CRO Location: Moraiya , Ahmedabad Experience: 2-7 Yrs CTC: As per norms WP: 7383005000 Required Candidate profile Candidate having experience in Pharma or CRO in below department can apply. 1. QC Executive 2. Microbiologist 3. GC-MS Executive 4. QA Analytical

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

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 RD initiatives. The role demands strong technical expertise, attention to detail, and familiarity with laboratory protocols related to bitumen testing.

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 m...

: 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 ...

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 organizati...

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 rese...

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...

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 inves...

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 id...