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Prabu Rajan

Prabu Rajan

Pharmaceutical Quality Control professional

Talent
Milton KeynesMember since July 19, 2026
Routine releasesAnalytical method validationMethod transferTrackwise investigationsCAPA managementRegulatory complianceHPLCGCData integrityTrackwise
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Routine releasesAnalytical method validationMethod transferTrackwise investigationsCAPA management

About

Pharmaceutical Quality Control professional with around 11 years of experience in routine releases, analytical method validation, verification, and Method transfer. Strong expertise in LIMS/Trackwise investigations, CAPA management and regulatory compliance. Skilled in HPLC and GC techniques, with hands-on experience in audits by USFDA, MHRA, and CDSCO. Proven ability to lead team and ensure data integrity across global pharmaceutical operations.

Experience

Deputy Manager - Maiva Pharma Pvt. Ltd - Hosur, India

(2024-10)

USFDA Approved sterile injectable unit

Assistant Manager - CIPLA Ltd - Bangalore, India

(2021-04 - 2024-09)

USFDA Approved Oncology unit

Senior Officer - Oman Pharmaceutical products Co. LLC - Oman

(2018-12 - 2021-01)

USFDA Approved Formulation unit

Executive - Strides Pharma Science Ltd - Puducherry, India

(2016-06 - 2018-11)

USFDA Approved Formulation unit

Trainee - Piramal Enterprises Ltd - Chennai, India

(2015-03 - 2016-05)

WHO and CDSCO Approved unit

Education

M.Sc. - Chemistry - AVC College Mayiladuthurai (2014-04)

Skills

Pharmaceutical Quality Control professional

Reviews