Computerized System Validation (CSV) Specialist

Job highlights

• Computerized System Validation (CSV) Specialist Job Profile IVY Works has an opening for full time employee as a Computerized System Validation Specialist or Engineer
• Bachelors degree in engineering / science
• 3 years of work experience is a must
• Good communication and technical writing skills are a must
• Experience

Welcome to IVY Works : consulting and support services for compliance, validation, Computerized System Validation, IT Infrastructure Qualification and IT Solutions Pharma, Biotech, life sciences industry Call us at +91- 080- 41477219 E- mail: [email protected] IVY Works is currently hiring for following openings Senior Computerized System Validation (CSV) Specialist Job Profile IVY Works has an opening for full time employee as a Computerized System Validation Specialist or Engineer
Responsibilities
Developing validation documentation for pharmaceutical equipment, facilities and computerized systems used in GLP, GMP and GCP environments.
Project Deliverables will encompass validation plans, specifications, test protocols and standard operation procedures and systems may include Process Automation, Laboratory Automation, Enterprise IT Applications and Network Infrastructure. Experience
Bachelor's degree in engineering / science.
4- 6 years of work experience is a must.
3+ years of experience/ exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5.
Good communication and technical writing skills are a must.
Project Management experience Job Location Our Office is located in Bangalore and the job may involve travel to client locations.

Computerized System Validation (CSV) Specialist Job Profile IVY Works has an opening for full time employee as a Computerized System Validation Specialist or Engineer.
Responsibilities
Developing validation documentation for pharmaceutical equipment, facilities and computerized systems used in GLP, GMP and GCP environments.
Project Deliverables will encompass validation plans, specifications, test protocols and standard operation procedures and systems may include Process Automation, Laboratory Automation, Enterprise IT Applications and Network Infrastructure. Experience
Bachelor's degree in engineering / science.
2- 3 years of work experience is a must.
Experience/ exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5.
Good communication and technical writing skills are a must. Job Location Our Office is located in Bangalore and the job may involve travel to client locations.

Validation Specialist or Engineer Job Profile IVY Works has an opening for full time employee as a Validation Specialist or Engineer.
Responsibilities
Working on validation and compliance projects for clients. The projects will include developing validation documentation for pharmaceutical and biotechnology equipment, facilities and computerized systems used in GLP, GMP and GCP environments.
Project Deliverables will encompass validation plans, specifications, test protocols and standard operation procedures and systems may include Pharmaceutical and Biotech Manufacturing Equipment, Facilities, Utilities, and Process Automation. Experience
Bachelor's degree in engineering / science.
2- 4 years of work experience is a must.
Experience/ exposure to Equipment Validation, Facility Validation and GAMP 5
Good communication and technical writing skills are a must. Job Location Our Office is located in Bangalore and the job may involve travel to client locations.