IT QC Analyst
Trail Blazer Trail Blazer Houston, TX Houston, TX Contract Contract Up to $35 an hour Up to $35 an hour 3 days ago 3 days ago 3 days ago VISAS:
NO H1B TITLE:
IT/QC Analyst LOCATION:
Houston, TX - ONSITE DURATION:
6
MONTHS CONTRACT TO HIRE INTERVIEW MODE:
Virtual
Job Description:
Qualification:
Certificate/ ASC/ BS in science-related discipline preferred and 5
years' experience in the biotech work environment.
Prior knowledge and experience of Automation/MES systems development and integration are preferred.
Excellent Communication Skills.
Ability to effectively communicate via writing and oral communication at all levels.
Express ideas effectively in individual and group situations (including non-verbal communication).
Ability to communicate with internal and external personnel.
Ability to secure relevant information and identify key issues and relationships from a base of information.
Relate and compare data from different sources, identify cause and effect relationships, and propose solutions.
Key
Responsibilities:
Lead the QC application implementation and integration projects for the Houston Site.
Procure, configure, and maintain any computers, instruments, and equipment's related to the QC labs.
Execute test scripts (design, execution, simulation, etc.
) with support and guidance from the supervisor.
Work together with customer, vendor, local and global teams to configure the application adapting to the local needs, and document any application deliverables.
Configure instruments and devices related to the implementation of QC systems and applications.
Author of Operational Handbook, User Management, Periodic Reviews/Maintenance and Disaster Recovery SOPs.
Responsible for the QC applications support (including system periodic reviews).
Assist the Quality department with deviation investigations.
Performs OIS review/approval of deviations.
Participate in RCAs as OIS representative.
Assist with the completion of CAPA actions.
Provide on-site support and training to system users.
Provide after-hours support as needed to resolve issues outside of normal business hours.
Review/revise OIS and manufacturing-related, SOPs, Functional Specifications, and work instructions, as a result of CAPA, equipment/process changes, error prevention activities, etc.
Utilize system documentation to solve complex problems.
Contribute to the design and implementation of new applications/ solutions related to the integration of QC instruments to QC applications/systems to enable data transfer.
Understand and comply with 21 CFR Part 11 regulations.
Job Type:
Contract Pay:
Up to $35.
00 per hour Schedule:
8 hour shift Application Question(s):
LinkedIn:
Experience:
Quality control:
5 years (Required) Automation:
1 year (Required) MES:
1 year (Required) Biotechnology:
5 years (Required) Work Location:
In person Qualification:
.
Estimated Salary: $20 to $28 per hour based on qualifications.
NO H1B TITLE:
IT/QC Analyst LOCATION:
Houston, TX - ONSITE DURATION:
6
MONTHS CONTRACT TO HIRE INTERVIEW MODE:
Virtual
Job Description:
Qualification:
Certificate/ ASC/ BS in science-related discipline preferred and 5
years' experience in the biotech work environment.
Prior knowledge and experience of Automation/MES systems development and integration are preferred.
Excellent Communication Skills.
Ability to effectively communicate via writing and oral communication at all levels.
Express ideas effectively in individual and group situations (including non-verbal communication).
Ability to communicate with internal and external personnel.
Ability to secure relevant information and identify key issues and relationships from a base of information.
Relate and compare data from different sources, identify cause and effect relationships, and propose solutions.
Key
Responsibilities:
Lead the QC application implementation and integration projects for the Houston Site.
Procure, configure, and maintain any computers, instruments, and equipment's related to the QC labs.
Execute test scripts (design, execution, simulation, etc.
) with support and guidance from the supervisor.
Work together with customer, vendor, local and global teams to configure the application adapting to the local needs, and document any application deliverables.
Configure instruments and devices related to the implementation of QC systems and applications.
Author of Operational Handbook, User Management, Periodic Reviews/Maintenance and Disaster Recovery SOPs.
Responsible for the QC applications support (including system periodic reviews).
Assist the Quality department with deviation investigations.
Performs OIS review/approval of deviations.
Participate in RCAs as OIS representative.
Assist with the completion of CAPA actions.
Provide on-site support and training to system users.
Provide after-hours support as needed to resolve issues outside of normal business hours.
Review/revise OIS and manufacturing-related, SOPs, Functional Specifications, and work instructions, as a result of CAPA, equipment/process changes, error prevention activities, etc.
Utilize system documentation to solve complex problems.
Contribute to the design and implementation of new applications/ solutions related to the integration of QC instruments to QC applications/systems to enable data transfer.
Understand and comply with 21 CFR Part 11 regulations.
Job Type:
Contract Pay:
Up to $35.
00 per hour Schedule:
8 hour shift Application Question(s):
LinkedIn:
Experience:
Quality control:
5 years (Required) Automation:
1 year (Required) MES:
1 year (Required) Biotechnology:
5 years (Required) Work Location:
In person Qualification:
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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