Document Control Manager

Celcuity • Minneapolis, MN

34d • $85,000 - $125,000 • Remote

About The Position

We are seeking a Document Control Manager who will report to the Director, Quality Management Systems. You will focus on activities and tasks that support the control of policies and process standards, as well as the administration of the company's Content Management System for research records.

Requirements

• Bachelor's degree in the life sciences, chemistry, or related field; or relevant experience.
• Five plus (5+) years of experience in document control in a pharmaceutical company, or a related area.
• Proficiency and experience with electronic document management systems, Veeva strongly preferred.
• Knowledge of version control practices and document lifecycle workflows.
• Familiarity with industry standards such as FDA 21 CFR Part 11, ISO 9001, GMP.
• Strong attention to formatting, process, and metadata tagging.
• Document auditing and compliance tracking capabilities.
• Excellent written and verbal communication skills, with ability to influence and build credibility at all levels.
• Strong interpersonal skills for interacting with employees and leaders across various levels and functions.
• Attention to detail and ability to manage multiple processes and documentation requirements.
• Strong technical and analytical skills with advanced knowledge in MS Office including Word, Excel, and PowerPoint.
• Ability to work in a team or independently as required.
• Outstanding organizational skills with the ability to prioritize.
• Demonstrated independent and sound decision-making skills; ability to think critically and make decisions in a fast-paced environment.
• Continuous improvement mindset; seeking ways to drive innovation and efficiencies throughout the organization.
• Flexible and willing to learn; adapting to business and site needs in a dynamic environment.
• Maintain a positive, approachable, and professional attitude.

Responsibilities

• Facilitates the meticulous creation, revision, and retirement of controlled documents in the eDMS, including managing and tracking Document Change Control workflows and participants.
• Management and migration of legacy files into the eQMS.
• Coordinates with the Training Admin to create new or revisions to Training Requirements, learners, quizzes, and other training related to controlled documents.
• Helps eDMS users with the how-to of document creation and revision and works with the QMS Admin to keep relevant document control SOPs and Work Instructions up to date.
• Helps eDMS users find and use current effective documents.
• Facilitates meetings with the QMS Admin and document reviewers to complete content creation or revisions.
• Manages GxP record retention and destruction tasks.
• Facilitates Certified Copy creation and retention.
• Other duties as assigned.

Benefits

• medical
• dental
• vision insurance
• 401(k) match
• PTO
• paid holidays

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Industry: Miscellaneous Manufacturing
• Number of Employees: 51-100 employees