Walk-in on 22/03/14, Saturday Only for QC Chemist & QA in QC Reviewers - 20 Opening(s)
QC Chemist & QA in QC Reviewer
We have scheduled Walk-in interviews for QC Chemist & for QA in QC Reviewers on 22/03/14, Saturday from 09:30 hrs to 14:30 hrs at Formulation Manufacturing Plant, Cadila Healthcare Ltd, Sarkhej-Bavla N.H. No.8A, Moraiya, Tal: Sanand, Dist. Ahmedabad - 382 210.
For Chemist/Officer: Quality Control
Qualification: B.Sc / M.Sc
Experience: 02 to 04 years
Desired Profile
1. Must have experience of 01 to 02 years in performing HPLC Analysis
2. Must have experience in Pharma Company.
3. The candidate should have good experience in testing, documentation, validation and method development of pharmaceutical formulations/ injectables/ oral dosage/ ointment / Aerosol / Nasal etc.
4. Must have experience in handling sophisticated instruments such as HPLC, FTIR, TOC, GC etc.
5. Experience in handling HPLC instrument is essential
6. Must be willing to relocate to Ahmedabad
For QC preference will be given to those who matches with the following criteria:
1. Experience of handling HPLC analysis independently for minimum 01 to 02 year
2. Good knowledge of cGMP & cGLP
3. Candidates having experience of working in regulatory approved plants, exposure to GLP will be preferred.
For Executive/Sr. Executive: QA in QC
Qualification: B.Sc/M.Sc/B.Pharma
Experience: 05 to 07 years
Desired Profile:
1. Responsible for review of Analytical Reports / Work Sheets.
2. Review of chromatographic data audit trails and other software audit trails.
3. Responsible for review of Stability Protocols, data sheets and trend data.
4. Investigation, Review and disposition of OOS & OOT results.
5. Responsible for handling of Incidents, Deviations, and Change Controls in the Laboratory.
6. Review of all types of Qualification/Calibration documents.
7. Responsible for review of Good Laboratory Practices in the Laboratory.
8. Periodical review of SOPs and Formats as per current guidelines.
9. Review of Temperature & RH monitoring programme of Walk in chambers
10. Responsible for Audit Preparations and Compliance.
11. Conducing internal audits as a lead auditor.
12. Must be willing to relocate to Ahmedabad.
For QA in QC preference will be given to those who matches with the following criteria:
1. Handling of various Regulatory audits like USFDA, MHRA, TGA etc.
2. Good knowledge of cGMP and current industrial trends.
3. Candidates having experience of working in regulatory approved plants, exposure to GLP and LIMS Environment will be preferred.
Interested candidate may Walk-In for Interview along with their CVs and Salary Slip on 22/03/14, Saturday between 09:30 AM to 02:30 PM
Venue : Cadila Healthcare Ltd, Sarkhej-Bavla N.H. No.8A, Moraiya, Tal: Sanand, Dist. Ahmedabad - 382 210
Note : Fresher need not Walk-in for Personal Interview.
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QC Chemist & QA in QC Reviewer
We have scheduled Walk-in interviews for QC Chemist & for QA in QC Reviewers on 22/03/14, Saturday from 09:30 hrs to 14:30 hrs at Formulation Manufacturing Plant, Cadila Healthcare Ltd, Sarkhej-Bavla N.H. No.8A, Moraiya, Tal: Sanand, Dist. Ahmedabad - 382 210.
For Chemist/Officer: Quality Control
Qualification: B.Sc / M.Sc
Experience: 02 to 04 years
Desired Profile
1. Must have experience of 01 to 02 years in performing HPLC Analysis
2. Must have experience in Pharma Company.
3. The candidate should have good experience in testing, documentation, validation and method development of pharmaceutical formulations/ injectables/ oral dosage/ ointment / Aerosol / Nasal etc.
4. Must have experience in handling sophisticated instruments such as HPLC, FTIR, TOC, GC etc.
5. Experience in handling HPLC instrument is essential
6. Must be willing to relocate to Ahmedabad
For QC preference will be given to those who matches with the following criteria:
1. Experience of handling HPLC analysis independently for minimum 01 to 02 year
2. Good knowledge of cGMP & cGLP
3. Candidates having experience of working in regulatory approved plants, exposure to GLP will be preferred.
For Executive/Sr. Executive: QA in QC
Qualification: B.Sc/M.Sc/B.Pharma
Experience: 05 to 07 years
Desired Profile:
1. Responsible for review of Analytical Reports / Work Sheets.
2. Review of chromatographic data audit trails and other software audit trails.
3. Responsible for review of Stability Protocols, data sheets and trend data.
4. Investigation, Review and disposition of OOS & OOT results.
5. Responsible for handling of Incidents, Deviations, and Change Controls in the Laboratory.
6. Review of all types of Qualification/Calibration documents.
7. Responsible for review of Good Laboratory Practices in the Laboratory.
8. Periodical review of SOPs and Formats as per current guidelines.
9. Review of Temperature & RH monitoring programme of Walk in chambers
10. Responsible for Audit Preparations and Compliance.
11. Conducing internal audits as a lead auditor.
12. Must be willing to relocate to Ahmedabad.
For QA in QC preference will be given to those who matches with the following criteria:
1. Handling of various Regulatory audits like USFDA, MHRA, TGA etc.
2. Good knowledge of cGMP and current industrial trends.
3. Candidates having experience of working in regulatory approved plants, exposure to GLP and LIMS Environment will be preferred.
Interested candidate may Walk-In for Interview along with their CVs and Salary Slip on 22/03/14, Saturday between 09:30 AM to 02:30 PM
Venue : Cadila Healthcare Ltd, Sarkhej-Bavla N.H. No.8A, Moraiya, Tal: Sanand, Dist. Ahmedabad - 382 210
Note : Fresher need not Walk-in for Personal Interview.
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