CQV Engineer

Boston, NH - USA

Monthly Salary: Not Disclosed

Posted on: 20 hours ago

Vacancies: 1 Vacancy

Job Summary

Job Title : CQV

Location : Boston MA

General position summary:
The Engineer is actively involved in Commissioning Qualification Validation and Requalification activities for Cell and Gene Therapy facilities. The individual is responsible for executing qualification protocols facilities and collaborate with Global Engineering Facilities Operations GIS QA and PMO throughout the life cycle of the project.

Key Responsibilities:
The responsibilities of this position may include but are not limited to the following:

Develops and executes qualification and validation test plans and protocols.
Ensures that all validation documents align with the current client SOPs global standards and cGMP guidelines.
Coordinates with personnel onsite and other vendors to schedule and execute test plans.
If required coordinates with the construction team and Vertex operations teams to schedule execution of validation activities safely and effectively.
Effectively works with cross functional departmental stakeholders PMO GIS EH&S Global Security design teams EHS and QA.
Completes Vertex assigned training and ensures that they are 100% compliant 100% of the time.
Supports right-the-first time culture for all documents distributed across the organization.
Ensures the Global Engineering reputation and partnership is flourished with the cross-functional teams.

Minimum qualifications:

Receptive to change Adapts (quickly) to changing circumstances.
Minimum Bachelors degree in an Engineering (Chemical Biomedical Industrial Biotechnology) or related discipline with 2-4 years of CQV experience or equivalent professional experience.
Self-motivated and must be able to work independently with minimal supervision and direction.
Experience in developing and executing protocols in GMP industry.
Experience using Kaye Validator and Data loggers.
Understanding and application of technical principles theories and concepts in the field GMP ISO GAMP ANSI.
Ability to learn and demonstrate technical problem solving and troubleshooting skills

Job Title : CQV Location : Boston MA General position summary: The Engineer is actively involved in Commissioning Qualification Validation and Requalification activities for Cell and Gene Therapy facilities. The individual is responsible for executing qualification protocols facilities and colla...

Job Title : CQV

Location : Boston MA

Develops and executes qualification and validation test plans and protocols.
Ensures that all validation documents align with the current client SOPs global standards and cGMP guidelines.
Coordinates with personnel onsite and other vendors to schedule and execute test plans.
If required coordinates with the construction team and Vertex operations teams to schedule execution of validation activities safely and effectively.
Effectively works with cross functional departmental stakeholders PMO GIS EH&S Global Security design teams EHS and QA.
Completes Vertex assigned training and ensures that they are 100% compliant 100% of the time.
Supports right-the-first time culture for all documents distributed across the organization.
Ensures the Global Engineering reputation and partnership is flourished with the cross-functional teams.

Minimum qualifications:

Receptive to change Adapts (quickly) to changing circumstances.
Minimum Bachelors degree in an Engineering (Chemical Biomedical Industrial Biotechnology) or related discipline with 2-4 years of CQV experience or equivalent professional experience.
Self-motivated and must be able to work independently with minimal supervision and direction.
Experience in developing and executing protocols in GMP industry.
Experience using Kaye Validator and Data loggers.
Understanding and application of technical principles theories and concepts in the field GMP ISO GAMP ANSI.
Ability to learn and demonstrate technical problem solving and troubleshooting skills