Global Quality Systems Lead – Document Control & Training

Kite Pharma; Frederick (MD); On-site; USD 153,935 - 199,210; Full time

Benefits offered by this job

Comprehensive medical, dental, and vision insurance

Discretionary annual bonus

Paid time off

Job summary

A leading biopharmaceutical company in Maryland is seeking a professional to manage their Global Document Control and Training Programs. This role will establish processes to ensure document integrity and compliance with regulatory standards. The ideal candidate holds a relevant PhD or equivalent experience in a biologics or pharma organization. They will drive continuous improvement, partner with cross-functional teams, and promote a quality-focused culture. Competitive salary and comprehensive benefits are offered.

Qualifications

• Experience in a biologics or pharma organization.
• Ability to manage Global Document Control processes.
• Experience leading training programs.

Responsibilities

• Develop and implement Document Control strategies.
• Ensure compliance with FDA and ISO regulations.
• Oversee selection and maintenance of electronic document systems.

Skills

Excellent communication and influencing skills

Creative problem-solving

Ability to work cross-functionally

Education

PhD in relevant field and 2+ years of experience

MS/MA with 8+ years of experience

BS/BA with 10+ years of experience

High School diploma with 14+ years of experience

Tools

Veeva eDMS

Job description

A leading biopharmaceutical company in Maryland is seeking a professional to manage their Global Document Control and Training Programs. This role will establish processes to ensure document integrity and compliance with regulatory standards. The ideal candidate holds a relevant PhD or equivalent experience in a biologics or pharma organization. They will drive continuous improvement, partner with cross-functional teams, and promote a quality-focused culture. Competitive salary and comprehensive benefits are offered.