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
SUN PHARMA LTD - Walk-In Interviews on 17th & 18th November, 2018
Walk-In Interviews at Sun Pharma, Mohali
Production (Technician / Officer /Executive)
Qualification Required-
12th / ITI / Diploma for Technician
B.Pharm / M.Pharm for Officer/Executive
Skill Set Required
Granulation (Wruster/ FBE/ RMG/ FBD)
Compression Fette/ Korsh/ Cadmach
Coating & Capsulation (AF 25/ 90/ KKE 1700)
Bottle Packing (CVC Line - Counting, Inline Capper, Labelling Literature Pasting, Shrink Bundler)
Minimum 2 years of Experience in regulatory environment.
Candidates must have exposure in regulatory audit: USFDA, MHRA, WHO
Date: 17th-18th November, 2018 (Saturday-Sunday)
Time: 10:00 A.M to 03:00 P.M
Venue:Sun Pharmaceutical Industries Ltd,
Production (Technician / Officer /Executive)
Qualification Required-
12th / ITI / Diploma for Technician
B.Pharm / M.Pharm for Officer/Executive
Skill Set Required
Granulation (Wruster/ FBE/ RMG/ FBD)
Compression Fette/ Korsh/ Cadmach
Coating & Capsulation (AF 25/ 90/ KKE 1700)
Bottle Packing (CVC Line - Counting, Inline Capper, Labelling Literature Pasting, Shrink Bundler)
Minimum 2 years of Experience in regulatory environment.
Candidates must have exposure in regulatory audit: USFDA, MHRA, WHO
Date: 17th-18th November, 2018 (Saturday-Sunday)
Time: 10:00 A.M to 03:00 P.M
Venue:Sun Pharmaceutical Industries Ltd,
SEZ Unit-1, Plot No. A-41,
Industrial Area, Phase VIII-A,
S.A.S. Nagar, Sector-75,
Mohali-160071 (Punjab) India
Interested candidates are requested to reach at Venue with their updated CVs along with latest Salary Supportings (Mandatory) and passport size photograph in given time. Candidates who are not able to attend interview may send their resumes atJyoti.gupta@sunpharma.com / TA.Mohali@sunpharma.com
For more information you may contact HR Mohali Talent Acquisition at : 0172-5218350
Interested candidates are requested to reach at Venue with their updated CVs along with latest Salary Supportings (Mandatory) and passport size photograph in given time. Candidates who are not able to attend interview may send their resumes atJyoti.gupta@sunpharma.com / TA.Mohali@sunpharma.com
For more information you may contact HR Mohali Talent Acquisition at : 0172-5218350
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