West Pharma Document Control 

United States, Nebraska 

185316857

Essential Duties and Responsibilities:

• Coordinate the site's document control program. Route procedures, protocols and other documents for approval.
• Publish and maintain controlled copies of documents.
• Ensure that all procedures, work instructions and forms are reviewed within a 3 year interval.
• Review new and revised corporate procedures, ensuring any lower-level document changes are implemented into site procedures where applicable.
• Assist QA Management in day-to-day operations.
• Perform internal audits to assess the adherence of the plant to approved and established procedures and requirements.
• Recommend, evaluate, and implement process changes that are designed to continually improve the quality management system including documentation.
• Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
• Performs other duties as assigned based on business/departmental needs.
• Exhibits regular, reliable, punctual and predictable attendance .

Basic Qualifications:

• High School or equivalent
• At least 3 years of experience
• Good leadership and organizational skills required

Preferred Knowledge, Skills and Abilities:

• QA experience preferred
• Good communication skills (oral and written)

Travel Requirements:

Physical & Mental Requirements:

• Perform job duties as required with limited physical demands