Pharma CQ/CSV Lead – Commissioning & Validation

Validation & Engineering Group; Windsor (CT); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading services supplier in the United States is seeking a professional to serve as the focal point for Commissioning & Qualification and Computer System Validation in assigned projects. Candidates should hold a Bachelor's Degree in Engineering or Science and have 3 to 5 years of experience in C&Q for Manufacturing Equipment or Facilities, with CSV experience as a plus. The role involves managing project goals and communicating with stakeholders in the pharmaceutical, biotechnology, or medical device sectors.

Qualifications

• 3 to 5 years of experience in C&Q for Manufacturing Equipment or Facilities.
• CSV experience is a plus.
• Must have at least 3 to 5 years of experience in the pharmaceutical, biotechnology or medical device industries.

Responsibilities

• Serve as focal point for Commissioning & Qualification and/or Computer System Validation (CSV).
• Work on multi-discipline engineering capital project teams.
• Manage assigned project goals within scope, on budget, and on schedule.
• Communicate proactively with stakeholders and senior management.
• Development and execution of C&Q/CSV Strategies and Validation Documents.

Skills

C&Q for Manufacturing Equipment

Computer System Validation (CSV)

Quality Systems

Education

Bachelor's Degree in Engineering or Science

Job description

• Full-time

Company Description

Validation & Engineering Group,Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical,and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, among other services.

Job Description

• Serve as focal point for Commissioning & Qualification and/or Computer System Validation (CSV) in assigned project.
• Work on multi-discipline engineering capital project teams, as well as other project-related, cross-functional teams with representatives from departments throughout the organization.
• Manage assigned project goals within scope, on budget, and on schedule.
• Communicate proactively with stakeholders and senior management regarding progress, issues, and plans for resolution.
• Development and execution of C&Q/CSV Strategies and Validation Documents.

Qualifications

• Bachelor Degree in Engineering or Science.
• 3 to 5 years of experience in C&Q for Manufacturing Equipment or Facilities
• CSV Experience is a plus
• Experiences in Quality Systems
• Must have at least 3 to 5 years of experience in the the pharmaceutical, biotechnology or medical device industries.

Additional Information

Positions availablefor Puerto Rico.

Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.

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