AdmissionNotice

Recruitment in Pfizer for Trainee Executive in Chennai

Full Time JOB SECTOR: Chemical Sector JOB SECTOR: Pharma Sector OWNERSHIP:-Private
  • Full Time
  • JOB SECTOR: Chemical Sector
  • JOB SECTOR: Pharma Sector
  • OWNERSHIP:-Private
  • CHENNAI
  • Applications have closed

Website pfizer PFIZER

LAST DATE TO APPLY: not disclosed

Job/Vacancy in Pfizer

Application’s are Invited by Pfizer, Which is Pfizer Inc. is an American global drug and biotechnology company settled on 42nd Street in Manhattan, New York City. Set up in 1849 in New York by two workers.

Interested and qualified applicants for the Trainee Executive post , in Chennai who fulfilling the criteria may submit or apply their application according to the prescribed format along with the details CV as per Norms.

And If you are a fresher/experienced remember always a well-written application/resume would be of great value. Before you start to writing you application letter, at first know what the company is looking for and whether you are a right fit to the company culture or norms in the given below:

DATE OF JOB POST:

10/8/2021

NAME OF THE POST:

Trainee Executive

LOCATION:

Chennai

QUALIFICATION & SKILLS:

Minimum – Postgraduate in Pharmacy or Science

Minimum 0 – 2 years of CMC experience within a regulatory function with  knowledge of INDs/IMPDs, NDAs, ANDAs, MAAs, CTDs and other regulatory components.

Sound understanding of drug development regulatory processes and requirements for defined market(s) and able to interpret and apply to projects.

Aware of external regulatory environment, including competitor intelligence and regulatory actions to assist regulatory strategy development.

Ability to identify inconsistencies and deficiencies in technical data and escalates to management for resolution.

RESPONSIBILITY:

Help with social occasion and deciphering worldwide clinical accommodation CMC prerequisites utilizing frameworks as well as in a joint effort with country administrative leads for the improvement of administrative methodology

May help with composing IND and IMPD CMC dossiers

Creator ROW IMPD CMC dossiers under management and in close joint effort with the CMC Lead and organize quality audit as indicated by inward techniques just as close down procedures(Reg-456/459 surveys).

Aid assortment of supporting documentation from Pharm Sci, PGS, and so forth Distinguish the necessary documentation and any substance, quality and additionally courses of events issues for worldwide entries and arrange the conveyance of supported specialized source reports as per project timetables.

 

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