CSVC Validation Lead - GxP & Data Integrity

Boehringer Ingelheim GmbH; United States; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive compensation

Health benefits

Work-life balance initiatives

Job summary

A leading pharmaceutical company in the United States is seeking a Principal Specialist to oversee computerized system validation. The ideal candidate will manage validation procedures, lead projects ensuring GxP compliance, and mentor team members. Candidates must have at least six years of experience in a cGMP organization and a relevant degree in Engineering or Information Technology. The position offers a competitive salary and a focus on employee well-being and development.

Qualifications

• Minimum of six years of relevant CSVC experience in a cGMP organization or similar manufacturing environment.
• Proven knowledge of GxP systems and related regulations.
• Demonstrated ability to work and lead in a team environment.

Responsibilities

• Oversee Computerized System Validation and Compliance procedures.
• Lead multiple CSVC projects and manage project budget.
• Mentor colleagues in problem resolution regarding GxP applications.

Skills

Computerized System Validation

Analytical Skills

Project Management

Team Leadership

Education

Bachelor of Science in Engineering, Information Technology, Chemistry, or related Science/Technology degree

Master’s degree in a related scientific/technology field

Tools

Relational Databases

Programming knowledge

Job description

A leading pharmaceutical company in the United States is seeking a Principal Specialist to oversee computerized system validation. The ideal candidate will manage validation procedures, lead projects ensuring GxP compliance, and mentor team members. Candidates must have at least six years of experience in a cGMP organization and a relevant degree in Engineering or Information Technology. The position offers a competitive salary and a focus on employee well-being and development.