0.0 years

0 Lacs

ahmedabad, gujarat, india

On-site

Job Description Job Description Prepare, Review and Approval of COA. Review and Approval of stability protocols, reports, and summary reports. Prepare justification for reduction of tests for Input material testing such as raw and packaging material; In-process testing; Finished product testing; Stability testing; Microbial testing. Prepare and review of specification/Method of analysis. Initiation, evaluation of Change control. Review of vendor qualification documents. Handling of item codification. Technical Skill Required Analytical documentation : Advanced ICH Guidelines : Advanced Stability Management : Advanced QMS Automation System : Intermediate US Guidelines : Advanced Qualification...

Posted 16 hours ago

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Executive, QMS Amneal Pharmaceuticals

5.0 - 9.0 years

0 Lacs

ahmedabad, gujarat

On-site

Role Overview: As a member of the team at Amneal, you will be responsible for preparing, reviewing, and approving Certificate of Analysis (COA) and stability protocols, reports, and summary reports. You will also play a key role in justifying the reduction of tests for various types of material and testing as well as handling item codification. Your expertise in analytical documentation, ICH Guidelines, Stability Management, QMS Automation System, and US Guidelines will be crucial for success in this role. Key Responsibilities: - Prepare, review, and approve Certificate of Analysis (COA) - Review and approve stability protocols, reports, and summary reports - Justify reduction of tests for v...

Posted 2 days ago

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Sr. Officer - ADL - Documentation with Globally CDMO Partner For Derma Best Fit Recruitment Rider

2.0 - 7.0 years

3 - 4 Lacs

mumbai

Work from Office

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top manag...

Posted 3 weeks ago

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Chemist II IFF

5.0 - 10.0 years

0 Lacs

rajasthan

On-site

Performs the analytical evaluation of raw material, intermediate and finished products, making pass/fail decisions. Conducts risk analysis and determines the usage of non-conformances. Offers technical support to both internal and external customers. Creates analytical documentation and reports to the Manager PIA. The ideal candidate should hold a Master's Degree in Chemistry and possess 5 to 10 years of experience in Quantitative Analysis using High-End Hyphenated Instruments. For further information on workplace diversity and inclusion, please visit IFF.com/careers/workplace-diversity-and-inclusion.,

Posted 3 months ago

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Scientist Analytical Aurigene Pharmaceutical Services Limited

0.0 years

0 Lacs

Bengaluru, Karnataka, India

On-site

Analytical method development Routine Analysis by HPLC, GC, LCMS, KF and FTIR Analytical documentation as like Protocols, specifications etc. Calibration of HPLC, GC instruments Aware about data integrity and ALCOA Chiral method development Show more Show less

Posted 4 months ago

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Executive or Sr Executive For Formulation -QA Biophore

2.0 - 7.0 years

2 - 7 Lacs

Hyderabad

Work from Office

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation DQA- Department . Position :Executive or Sr Executive Experience : 2 - 8 Yrs Job Description: 1) Handling of QMS documents like Incident, change control and LER. 2) Review of Formulation Analytical Development & Method Validation and Transfer Protocols and Reports. 3) Review of Product development with QbD approach. 4) Review of FRD Documents (LNBs, BDRs, PDRs, MFRs and MPR) 5) Preparation and Review and Approval of SOPs ,Guidelines. Responsible for conducting Internal Audits/External Audits for Cross functional Departments.Responsible for Review and Approval of Vendor Qualification Please S...

Posted 6 months ago

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