About Krishnamurthi Rethinavel:
Hello,
Greetings!
Hope everything is fine at your end.
I am Krishnamurthi, i have done my Post-Graduate Diploma in Pharmaceutical Regulatory Affairs (May, 2020 – March 2021) in Toronto Institute of Pharmaceutical Technology (TIPT).
Currently working as a Regulatory Affairs and Quality Control Associate at Transpharm Canada Inc. (Toronto Institute of Pharmaceutical Technology).
And I have experience in preparation and compilation of CMC portions of eCTD and non-eCTD global regulatory submissions, Life cycle management and post approval submissions activities for Biosimilar (mAbs), write and peer review of the high quality CMC write ups for new submissions and query responses,
I am applying for Regulatory Affairs Associate position in your company. Please find attached my resume for your reference. I request you to kindly have a look at it & revert.
Looking forward to hearing from you.
Thanks and regards,
Krishnamurthi
Experience
Hello,
Greetings!
Hope everything is fine at your end.
I am Krishnamurthi, i have done my Post-Graduate Diploma in Pharmaceutical Regulatory Affairs (May, 2020 – March 2021) in Toronto Institute of Pharmaceutical Technology (TIPT).
Currently working as a Regulatory Affairs and Quality Control Associate at Transpharm Canada Inc. (Toronto Institute of Pharmaceutical Technology).
And I have experience in preparation and compilation of CMC portions of eCTD and non-eCTD global regulatory submissions, Life cycle management and post approval submissions activities for Biosimilar (mAbs), write and peer review of the high quality CMC write ups for new submissions and query responses.
Education
Pharmaceutical Regulatory Affairs
Professionals in the same Pharmaceutical / Bio-tech sector as Krishnamurthi Rethinavel
Professionals from different sectors near Brampton, Ontario
Jobs near Brampton, Ontario
-
Associate, Regulatory Affairs
3 weeks ago
SteriMax Inc. OakvilleThe Regulatory Affairs Associate will prepare regulatory submissions for complex injectable products · Cordinates the assembly of documents to support submissions including complex generics and biosimilars per established business processes · Fulfills lifecycle management activ ...
-
Associate, Regulatory Affairs
1 week ago
SUN PHARMA Brampton, OntarioPrepare and file drug product submissions to the US FDA · Prepare and/or review submissions to Health Canada and FDA for a variety of dosage forms. · ...
-
Associate, Regulatory Affairs
3 weeks ago
SteriMax Inc. Oakville, OntarioThe Associate Regulatory Affairs will prepare regulatory submissions for complex injectable products. · Coordinates the assembly of documents to support submissions including complex generics and biosimilars per established business processes. · ...
