Junior Level Csv Professionals Job in Ivyworks
Junior Level Csv Professionals
Ivyworks
4+ weeks ago
- Pune, Pune Division, Maharashtra
- Not Disclosed
- Full-time
- Permanent
Job Summary
1) Computerized System Validation
The responsibilities will include developing validation documentation and support for computerized systems used in GLP, GMP and GCP environments. Validation documentation will encompass validation plans, specifications, test protocols and standard operation procedures. Systems may include Process Automation, Laboratory Automation, Enterprise IT Applications and Network Infrastructure.
Candidates are required to have at a minimum a bachelors degree in engineering / science.
Experience - 1 - 3 years
Candidate with at least 1 year experience in computerized system validation in pharmaceutical industry , should have done Validation Plan, IQ, OQ, PQ, RTM, summary report documentation for Manufacturing systems , PLC/SCADA . Should be able to execute and check system performance of manufacturing systems and PLC/SCADA. Should be able to independently handle and execute validation activity starting from documentation till completion of system validation summary. should have done Validation Plan, IQ, OQ, PQ, RTM, summary report documentation for QC lab system such as Tiamo, stability chambers etc.. ,and PLC/SCADA . Should be able to execute and check system performance of lab systems and PLC/SCADA. Should be able to independently handle and execute validation activity starting from documentation till completion of system validation summary .
Job Description
1) Computerized System Validation
The responsibilities will include developing validation documentation and support for computerized systems used in GLP, GMP and GCP environments. Validation documentation will encompass validation plans, specifications, test protocols and standard operation procedures. Systems may include Process Automation, Laboratory Automation, Enterprise IT Applications and Network Infrastructure.
Candidates are required to have at a minimum a bachelors degree in engineering / science.
Experience - 1 - 3 years
Candidate with at least 1 year experience in computerized system validation in pharmaceutical industry , should have done Validation Plan, IQ, OQ, PQ, RTM, summary report documentation for Manufacturing systems , PLC/SCADA . Should be able to execute and check system performance of manufacturing systems and PLC/SCADA. Should be able to independently handle and execute validation activity starting from documentation till completion of system validation summary. should have done Validation Plan, IQ, OQ, PQ, RTM, summary report documentation for QC lab system such as Tiamo, stability chambers etc.. ,and PLC/SCADA . Should be able to execute and check system performance of lab systems and PLC/SCADA. Should be able to independently handle and execute validation activity starting from documentation till completion of system validation summary .
Role:Healthcare & Life Sciences - Other
Salary: Not Disclosed by Recruiter
Industry:Pharmaceutical & Life Sciences
Functional Area:Healthcare & Life Sciences
Role Category:Healthcare & Life Sciences - Other
Employment Type:Full Time, Permanent
Key SkillsNetwork InfrastructureProcess AutomationNetworkingDocumentationGLPGMPComputer System ValidationEducation
UG:B.Pharma in Pharmacy,B.Tech/B.E. in Any Specialization
PG:Other Post Graduate
Doctorate:Other Doctorate
Company Profile
Ivy Works
IVYWORKS is a Compliance Consulting firm. We provide services to pharmaceutical and biotechnology industries. Visit http://www.ivyworks.net for more info.Company Info X View Contact Details+Contact Company:Ivy Works
Website:http:// www.ivyworks.net
Experience Required :
1 to 3 Year
Vacancy :
2 - 4 Hires
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