Experience required: Min. 6 years or more

Brief Job Description:

• Comprehensive understanding of risk-based qualification methodology

• Experience in pharmaceutical OSD facility / Sterile facility or both is preferred

• Excellent knowledge of process equipment, utilities, HVAC and laboratory analytical instruments

• Experience in authoring and review of all Qualification documents as per GMP guidelines

• Excellent knowledge of cGMP standards and relevant EU/FDA regulations

• Complete ownership of full validation cycle process implementation and associated documentation

• Understanding of computer system validation as per GAMP 5 and CFR part 11 regulations

Competencies:

•  Must have good communication skills
•  Must have the ability to work independently while meeting the project schedules
•  Willing to travel to client sites

Please share your CV at:
joginder.mittal@glatt-india.com