Our client is seeking a Document Control Specialist at a new facility for commercial-scale manufacturing of sterile therapeutic radiopharmaceuticals! ***Must have some experience with electronic quality management systems (eQMS) to qualify!*** 

Why Us?

• Competitive wages and comprehensive health benefits
• Positive and safe work environments
• Opportunities for growth and development for all the stages of your career

Schedule: M-F 8a-5pm w/flexibility 

Pay: 55K-65K /yr


Responsibilities

• Manage the document control process, including the creation, review, approval, distribution, and archiving documents.
• Ensure that all documents comply with company policies and regulatory requirements.
• Maintain and update the document management system to ensure easy retrieval and reference.
• Collaborate with various departments to gather and prepare documentation for projects, audits, and inspections.
• Conduct regular audits of document control processes to identify areas for improvement.
• Provide training and support to staff on document control procedures and tools.
• Assist in the development and maintenance of document control procedures and best practices.
• Generate reports on document status and compliance for management review.

Experience/Education

• High School Diploma required
• 2-4 years of experience with QA in a GMP environment with Document Control
• eQMS experience is required (TrackWise, Master control, DOT compliance, etc) 
• Pharmaceutical experience preferred.

***This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!***

INDBH 
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