Officer To Executive in QC Department (LOC: Mahad -EU GMP Approved) Titan Laboratories

2 - 7 years

2 - 5 Lacs

Mahad

Work from Office

Experience - 2 Years + In Formulation QC * QC - Finish Product - GC/HPLC/ Dissolution/AAS/UV * QC- In process- HPLC/UV/Dissolution/GC * QC - Validation- HPLC/UV/GC/Dissolution * RM - HPLC * Stability HPLC GC UV Dissolution * RM Reviewer

Posted 4 months ago

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ADL Manager- Otsuka Pharma, Ahmedabad Otsuka Pharmaceutical India Pvt Ltd

7.0 - 12.0 years

5 - 12 Lacs

ahmedabad

Work from Office

Role & responsibilities Timely develop and validate new analytical methods for formulations in line with the marketing requirements. Resolve issues related to analytical methods of existing products as and where they exist if any at the QC lab levels. Analytical method development and validation shall be in line with required documentation as per cGMP / GLP requirements following the laid down Quality management procedures by CQA. Review and approval of the analytical method validation protocol and report. Review and approval of final method development report as a part of the technology transfer document (TTD). Review and approve new Method of analysis (MOAs) or any changes as necessary thereafter in the existing MOAs in line with pharmacopeial or customer requirements. Facilitate analytical method transfer of new products to QC lab by providing physical presence of ADL personnel during the transfer. Face customer or regulatory audits and as and when required be available as auditee. Initiate any changes or upgradation in lab or equipment set up as necessary with time. Handle and guide team of ADL personnel for above activities. Preferred candidate profile Managerial skills Problem solving and decision making skills Guiding skills Team development skills System thinking Delegation Interested candidate can send their resume on Anee.Silas@otsukapharma.in

Posted Date not available

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ADL Officer/ Officer Icpa Health Products

1.0 - 3.0 years

2 - 3 Lacs

anklesvar, ankleshwar

Work from Office

To perform Analytical test method validation. To operate GC and HPLC To prepare working Standards To Maintain and calibrate R&D instruments and record it To prepare certificate analysis, routine protocols and related documents.

Posted Date not available

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Officer- Q.C ACUTAAS CHEMICALS LIMITED

3.0 - 6.0 years

3 - 5 Lacs

jhagadia

Work from Office

1) Working as per company / management policy & reporting to Quality Control Head. 2) To sample the incoming Raw materials and packing materials and also Finished Goods. 3) To conduct analysis and testing of Raw Material, Packing Material, In-Process sample, Finished goods, Stability samples etc. with the help of analytical instruments and techniques. 4) To calibrate / verifies analytical instruments like HPLC, GD, ICP-OES Wet lab and balances 5) To trouble shoot analytical instruments. 6) Preparation and standardization of Volumetric Solution. 7) Preparation and maintenance of records for stock / reagents. 8) Analysis of samples for qualitative and quantitative test parameters as per specification. 9) To maintain record of analysis and supporting logbooks as per GLP. 10) To have working experience in shift for supporting production activities by analysis of in-process samples. 11) To participate in laboratory investigation. 12) To checked by the In-Process analysis results.

Posted Date not available

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QC stability Officer People Link

4.0 - 8.0 years

2 - 3 Lacs

baddi

Work from Office

HPLC, Stability test ,

Posted Date not available

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