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Barry-Wehmiller

Capital equipment and engineering solutions provider

Validation Project Manager - CQV

Regulatory & Quality (Life Sciences)Updated on Nov 12
Full-timeIndianapolis, IN, USANo salary listed

About the Job

Requirements

  • A minimum of 7 years of experience with increasing responsibility in validation or quality service and project management of life sciences, biotechnology, or other FDA-regulated projects.
  • Experience with project management, good documentation practices, current Good Manufacturing Practices, and FDA validation methods and systems; ability to read engineering documents, set priorities, and work on multiple projects simultaneously.
  • Experience with financial systems, project administration, and client administration.
  • Strong leadership, verbal communication, technical writing, project management tool, and word processing skills.
  • Working knowledge of process automation and computer system validation concepts, GAMP methodologies, 21 CFR Part 11 compliance, and current industry expectations for data integrity.
  • Project management experience managing scope, cost, schedule, quality, and risk.
  • Experience in mentorship and multidisciplinary collaboration.
  • Demonstrated leadership in a consulting and service environment.
  • Willingness and ability to travel as necessary for project requirements, including project installation and start-up activities, client meetings, company-sponsored meetings, trainings, and industry-related seminars, forums, or conventions.
  • A Bachelor of Science degree in Engineering or a related technical degree.

Responsibilities

  • Interface with clients, lead teams of validation professionals, and provide subject matter expertise in validating utility, facility, and process equipment.
  • Help lead regional business development efforts by engaging new clients in the life sciences sector and expanding engagements with existing clients.
  • Develop project scope statements, estimates, and proposals.
  • Work on multiple projects simultaneously.
  • Contribute as a technical individual contributor to commissioning, qualification, and validation projects; work with clients and project teams to develop compliant validation approaches for FUE qualification, generate protocols, and lead execution efforts when necessary.

Desired Qualifications

  • A strong understanding of EPCMV, Quality by Design, and risk- and science-based compliance approaches.
  • Experience with system and process risk assessments, including Failure Mode and Effects Analysis, Hazard and Operability Analysis, and Fault Tree Analysis.
  • Diverse experience leading project teams related to commissioning and qualification of clean utilities, facility systems, process support systems, bioprocess manufacturing systems, and packaging equipment, as well as process and cleaning validation.

About the Company

Barry-Wehmiller

Capital equipment and engineering solutions provider

Barry-Wehmiller provides capital equipment and engineering solutions for manufacturing, helping clients improve operations through design, integration, and installation of machinery and systems. Their products and services cover the lifecycle of capital equipment for manufacturing, from concept through delivery and support. The company differentiates itself with a people-first culture called Truly Human Leadership, focusing on the growth and well-being of team members, which they say leads to better performance and better outcomes for customers and communities. Its goal is to build a better world by developing people and delivering reliable solutions that positively impact the lives of employees, customers, suppliers, and communities.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
St. Louis, MO
Founded
1885

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