Validation Engineer

Validation Engineer – Life Sciences Group

Responsibilities:

• Support Client commissioning / validation for facility, utility, equipment and process validation projects
• Prepare and execute commissioning / validation documents
• Participate in any stage of clinical or commercial production including green field construction, facility renovation, new product development, product launch, or product/process upgrade
• Write summary reports for validation and qualification protocols
• Support project milestones, priorities and deadlines
• Write operating procedures for technical equipment and practices and procedures
• Schedule and coordinate protocol execution with other departments including manufacturing, facilities and project management
• Provide a practical approach to problem solving
• Individuals must represent GBA at client sites and interact confidently with clients, contractors, management and peers

Requirements:

• Bachelor’s degree in a related life sciences or engineering field
• 2 – 7 years GMP experience
• Aseptic process experience preferred
• Critical utility experience preferred
• Ability to converse about scientific matters
• Ability to work independently or in collaboration with others
• Excellent written communication skills with emphasis in technical writing
• Proficient in Microsoft Word, Excel, Power Point and Project
• Salary range is 75K-145K depending on experience level

On the job training will be provided by the validation team and manager, and through industry training and certification courses, both online and in person.

All candidates must be legally eligible to work in the United States.

Must be willing to travel regionally and / or nationally throughout the U.S.

We are an equal opportunity employer M/F/D/V

Full time and contract positions are available