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Address:
Business Village B, Deira, Dubai

Mayur Ramaiya
Manager
Vadodara

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Last seen: 25 December 2025 6:59 AM
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Profile Details
Experience More than 15 Years
U.A.E Experience Fresh
Industry Pharmaceutical
Nationality India
Visa Status Not Applicable
Qualification Master - Passes with 60% and Industrial chemistry as a main subject
Driving License NA
Industry Titles
Pharmaceutical

Pharmaceutical

Pharmaceutical
Summary of Career
  1. Effectively working with cross functional departments(FDD,ADD,QC,MSTG,QA,Production,Micro and Procurements) and presenting the topics

  2. Monitoring of Drug product and drug substances analysis and their seamless execution

  3. Compilation of results and discussion with team

  4. Drug substances and Drug product Analytical method transfer to GMP facilities

  5. Investigation of OOS and OOT results

  6. Stability design and protocol for filing batches

  7. Facilitate to completion of out sourced activities at CDMO's

  8. To provide support to QC during regulatory audits(USFDA ,EU and UK MHRA)

  9. Preparation and finalization of product specification for release and stability stage

  10. Align all stake at one platform for discussion of any OOS/OOT
Resume / CV

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Achievements
No achievements available.
Work Experience
Chemist
Indoco remedies Ltd
01 July 2005 — 01 July 2007
1)Performed In process analysis, FP analysis and stability analysis of Drug product for commercial batches.
2)Conducted IPQA activities (such as Line clearance, addition of active material during batch manufacturing, Material dispensing.) and performed raw material sampling

Chemist
Emcure Pharmaceuticals ltd
18 July 2007 — 25 November 2008
1)Performed In process analysis, FP analysis and stability analysis of Drug product for commercial batches and PV batches
2)Prepared stability data compilation and analysis for regulatory reporting.
.

Senior Technical officer-Quality control
Cadila Pharmaceuticals Ltd
30 November 2008 — 28 December 2010
1)Performed stability analysis of Drug product for Exhibit batches and commercial batches.
2)Prepared stability data compilation and analysis for regulatory reporting
3)Conducted stability samples pullout as per stability schedule withdrawal plan.

Executive
Zydus Lifesciences
30 December 2010 — 15 March 2016
1)Performed analysis of Drug product for Initial stability batches.
2) Handled troubleshooting of complex analytical challenges with effective problem-solving.
3)Conducted Analytical method transfer for site transfer projects.

Manger 1
SUN PHARMA ADVANCED RESEARCH COMAPNY
18 March 2016 — To date
1)Led AMT to QC and Contract manufacturing facilities
2)To ensure on handling of documents like ATP, specification, stability protocol, sampling directory from initiation till implementation
3)To ensure a timely and effective communication & escalation process exists to raise quality issues to appropriate levels of management
Academic Qualification
Matric
01 March 1999
Passed the matric with 72 % and English, Science, Maths ,History and Hindi as main subjects

Intermediate
01 March 2001
Passed in 12th standard with 52% marks and English, Physics, Maths, Chemistry and Biology as a main subject

Bachelor
30 April 2004
passed with 63% and Chemistry, Zoology and Analytical chemistry as a main subjects

Master
31 October 2006
Passes with 60% and Industrial chemistry as a main subject
Certifications
No certificates available.
Posts & Jobs Matching Titles / Positions
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Post Nov 12, 2024
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