Friday, 16 November 2018
Gland Pharma Limited - Walk-In Interviews for IPQA on 21st Nov' 2018
Greetings from Gland Pharma Limited!!
We have urgent requirement for IPQA (Injectable) department. If you are interested you can walk-in for an interaction on 21st November 2018 @ 10.00 AM.
1. Performing routine IPQA activities in optical testing, over printing (Track and Trace and aggregation activities) labeling and packing.
2. Carrying out the line clearance at all stages of operations as per SOP/BPCR.
3. Verification of batch packing records and cGMP records of packaging block.
4. Approval of stereo order form, storage, issuance and destruction control.
5. Sampling of control, stability and identification samples.
6. Monitoring of general hygiene of operators working in packaging block.
7. Implementation of systems and procedures as per written down standard operating procedures.
8. Conducting optical inspection validation for operators.
9. Coordination with Production, QC and Warehouse for smooth functioning of operations.
10. Reporting daily status to Incharge IPQA.
11. Reporting all the deviations to Incharge/Head IPQA.
NOTE: If you have already attended, Please share this mail for others to grab this opportunity.
Preferably Male Candidates
We have urgent requirement for IPQA (Injectable) department. If you are interested you can walk-in for an interaction on 21st November 2018 @ 10.00 AM.
1. Performing routine IPQA activities in optical testing, over printing (Track and Trace and aggregation activities) labeling and packing.
2. Carrying out the line clearance at all stages of operations as per SOP/BPCR.
3. Verification of batch packing records and cGMP records of packaging block.
4. Approval of stereo order form, storage, issuance and destruction control.
5. Sampling of control, stability and identification samples.
6. Monitoring of general hygiene of operators working in packaging block.
7. Implementation of systems and procedures as per written down standard operating procedures.
8. Conducting optical inspection validation for operators.
9. Coordination with Production, QC and Warehouse for smooth functioning of operations.
10. Reporting daily status to Incharge IPQA.
11. Reporting all the deviations to Incharge/Head IPQA.
NOTE: If you have already attended, Please share this mail for others to grab this opportunity.
Preferably Male Candidates
Openings: 25
Contact email: durgabhavani.ancha@glandpharma.com
Tuesday, 13 November 2018
MSN Labs - Walk-In Drive for Regulatory Affairs & FAR&D on 17th Nov' 2018
Walk- In Drive for Regulatory Affairs in API Division- R&D Center
Job Description: (API - Regulatory Affairs - API Division)
1. Should have minimum of 1 to 8 years of experience in API Regulatory Affairs
2. Thorough knowledge in US, EU and CA regions DMF submission procedures along with emerging markets such as Brazil, Taiwan, Japan, Russia, China etc
3. Should possess good response drafting skills to ensure that the responses to the regulatory queries are properly addressed
4. Should have knowledge and experience in eCTD submissions to US, CA and EU and troubleshooting the issues
5. Thorough review of regulatory submissions prepared by team members and to ensure the correctness of the documents or submissions.
6. Responsible for ensuring and sending response to all the technical queries received from various customers are properly responded as soon as possible.
7. Conducting meetings for the deficiency letters received from various regulatory authorities and tracking of deficiencies with respect to the target timelines and ensure that the response is sent to the authorities as per the stipulated timelines.
8. Participation in the Cross Functional Team (CFT) meetings and guidance to the product development team on regulatory issues.
9. Participation in the Technology Transfer Meetings and ensure that the product is meeting the regulatory requirements.
10. Responsible for ensuring that the regulatory database is properly maintained and updated.
11. Responsible for Review and approval of change control and should ensure that all the approved changes are reported to regulatory authorities.
Drug Regulatory Affairs API RA Dept.
Experience: 1 to 8 Years
Position: Executive / Sr. Executive / JM
Male Candidates Preferable .
Date of Interview: 17.11.2018 (Saturday)
Interview Time: 9.00 AM to 1.00 PM
Venue Details :
MSN Laboratories Pvt. Ltd.,
R&D Center, Pashamylaram
Ph No : +91-8452304799/4899
040-30438786
Work Location : Pashamylaram
Job Description: (API - Regulatory Affairs - API Division)
1. Should have minimum of 1 to 8 years of experience in API Regulatory Affairs
2. Thorough knowledge in US, EU and CA regions DMF submission procedures along with emerging markets such as Brazil, Taiwan, Japan, Russia, China etc
3. Should possess good response drafting skills to ensure that the responses to the regulatory queries are properly addressed
4. Should have knowledge and experience in eCTD submissions to US, CA and EU and troubleshooting the issues
5. Thorough review of regulatory submissions prepared by team members and to ensure the correctness of the documents or submissions.
6. Responsible for ensuring and sending response to all the technical queries received from various customers are properly responded as soon as possible.
7. Conducting meetings for the deficiency letters received from various regulatory authorities and tracking of deficiencies with respect to the target timelines and ensure that the response is sent to the authorities as per the stipulated timelines.
8. Participation in the Cross Functional Team (CFT) meetings and guidance to the product development team on regulatory issues.
9. Participation in the Technology Transfer Meetings and ensure that the product is meeting the regulatory requirements.
10. Responsible for ensuring that the regulatory database is properly maintained and updated.
11. Responsible for Review and approval of change control and should ensure that all the approved changes are reported to regulatory authorities.
Drug Regulatory Affairs API RA Dept.
Experience: 1 to 8 Years
Position: Executive / Sr. Executive / JM
Male Candidates Preferable .
Date of Interview: 17.11.2018 (Saturday)
Interview Time: 9.00 AM to 1.00 PM
Venue Details :
MSN Laboratories Pvt. Ltd.,
R&D Center, Pashamylaram
Ph No : +91-8452304799/4899
040-30438786
Work Location : Pashamylaram
Walk- In Drive for FAR&D - Formulation Division-R&D CENTER
Job Description: (Method Development / Method Validation AR&D - Formulation Division )1. Should have minimum of 1-8 years of experience in Formulation Analytical Research & Development (FAR&D).
Requirements:
FAR&D Method Development/ Analytical Method Validation.
Position: (FAR&D) Executive / Sr. Executive / JM
Formulation Analytical Research and Development ( FAR&D).
Experience: 1 to 8 Years
Date of Interview: 17.11.2018 (Saturday)
Interview Time : 9.00 AM to 1.00 PM
Venue Details :MSN House C-24,
Industrial Estate, Sanath Nagar ,
Hyderabad-500018
Ph No : 040-30438786
Work Location : Pashamylaram
Job Description: (Method Development / Method Validation AR&D - Formulation Division )1. Should have minimum of 1-8 years of experience in Formulation Analytical Research & Development (FAR&D).
Requirements:
FAR&D Method Development/ Analytical Method Validation.
Position: (FAR&D) Executive / Sr. Executive / JM
Formulation Analytical Research and Development ( FAR&D).
Experience: 1 to 8 Years
Date of Interview: 17.11.2018 (Saturday)
Interview Time : 9.00 AM to 1.00 PM
Venue Details :MSN House C-24,
Industrial Estate, Sanath Nagar ,
Hyderabad-500018
Ph No : 040-30438786
Work Location : Pashamylaram
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