Vishwas Parab Email & Phone Number | 25+ years of enriched experience in various functions like Regulatory Affairs, Quality Control and Quality Assurance of recongnised API and formulation manufacturing companies. Closely worked with the respective development (API & formulation) departments across the organisations for setting up the supporting systems for successful regulatory approvals. Expertize of QA / QC / compliance systems and Regulatory submissions for highly regulated and less regulated markets ( submissions in the regions (authorities) including US, EU, Japan, Australia, Canada, WHO, ASEAN, Middle east, Africa, APAC, CIS, SEE, LATAM, EDQM etc). Specialties: Manage regulatory activities of multiple (sterile / nonsterile) - API / Formulation manufacturing sites and development centres, Driving culture change and transformation, Creating synergies, leadership, developing new talents, creating opportunities and possibilities, customer service

Vishwas Parab

25+ years of enriched experience in various functions like Regulatory Affairs, Quality Control and...
Sandoz, Mumbai, India

*50 free lookup(s) per month.

Vishwas Parab’s Phone Numbers +1 609-627-****

Get VISHWAS’s Phone Number (For Free)

Social Media

Vishwas Parab’s Location Sandoz, Mumbai, India

Vishwas Parab’s Current Industry

Vishwas Parab’s Prior Industry Nicholas Piramal | Hexa Lab

Find accurate emails & phone numbers for over 700M professionals.

Head (GM), MRC Kalwe (API and Formulation Regulatory Team ) India

Present

Jr. Manager Qa/Qc

1996-09-01 00:00:00 - 2001-02-01 00:00:00

Analytical Chemist

1994-09-01 00:00:00 - 1996-08-01 00:00:00

No Skills Available

No Languages Available

Vishwas Parab is a 25+ years of enriched experience in various functions like Regulatory Affairs, Quality Control and Quality Assurance of recongnised API and formulation manufacturing companies. Closely worked with the respective development (API & formulation) departments across the organisations for setting up the supporting systems for successful regulatory approvals. Expertize of QA / QC / compliance systems and Regulatory submissions for highly regulated and less regulated markets ( submissions in the regions (authorities) including US, EU, Japan, Australia, Canada, WHO, ASEAN, Middle east, Africa, APAC, CIS, SEE, LATAM, EDQM etc). Specialties: Manage regulatory activities of multiple (sterile / nonsterile) - API / Formulation manufacturing sites and development centres, Driving culture change and transformation, Creating synergies, leadership, developing new talents, creating opportunities and possibilities, customer service