The QA Associate I will provide support for the QA Systems team including Veeva DMS, Retention and Verification.

Key Duties:

• Document Management System Support
• Scanning Verification
• Retention and Destruction

Skills / Abilities:

• Experience in Pharmaceutical Quality Assurance, including the ability to identify and resolve compliance issues.  
• Ability to increase others knowledge of US end European GMP regulations and guidance.
• Strong written and oral communication skills.
• Experience in support of quality systems for drug product manufacturing and quality control operations.
• Strong written and oral communication skills.

Personal Attributes:

• Team Player committed to quality; motivated self-starter; detail and results oriented; Well organized, efficient worker with good communication skills; innovative thinker and problem solver; flexible and can embrace change; can manage multiple duties and tasks.
• Good computer skills.
• Good work ethic, dependable, punctual, and flexible.
• Good motivator of personnel.
• Good team player with a can-do attitude.
• Can get things done on the basis of influence.
• Can work in a fast-paced environment with multiple issues open simultaneously.
• Highly organized.
• Attention to detail.
• Identifies opportunities to improve and contributes to problem solving.
• Ability to utilize knowledge and interpersonal skills to provide leadership, direction and development of others.

Education/Experience: 

• Requires a Bachelor’s degree in a scientific discipline or equivalent.
• Minimum of 1 year experience in a Quality Assurance role in the pharmaceutical industry.