Document Control Specialist

Overview 

Reporting to the Quality Assurance Supervisor, the Document Control Specialist is responsible for managing controlled document revision processes and supporting QA batch kit review activities within the Quality Management System (QMS). This role ensures all documentation is accurate, properly revised, compliant with regulatory requirements, and that batch records are complete and ready for QA disposition. 

About Us 

Founded in 2010 and based in the Austin area, Goodkind is a leading manufacturer of clean and green personal care and beauty products. Goodkind specializes in natural deodorant, skincare, and facial care products. The company has a wealth of experience in the formulation of these products and can develop according to a variety of guidelines from consumer organizations such as Ecocert to EWG, to retailers such as Credo or Sephora. 

Goodkind is a certified B Corporation. As such, we balance purpose and profit, considering the impact of decisions across associates, customers, suppliers, community, and the environment. Goodkind believes by following this central multi-stakeholder approach, we are creating optimal value for each stakeholder while leaving the world a better place. 

What You’ll Do 

Manage document revision control, including versioning, numbering, issuance, and lifecycle management of controlled documents 

Ensure only current, approved revisions of SOPs, Work Instructions (WIs), and Forms (FMs) are available for use 

Coordinate review, approval, and release of revised documents through established change control processes 

Maintain accurate revision history logs and audit trails within google suites/eQMS systems 

Support Change Control activities to ensure proper documentation updates and alignment with approved changes 

Archive obsolete documents and enforce document retention and retrieval procedures Support updates to validation documentation impacted by process or system changes Assist with internal and external audits by retrieving controlled documents and batch records 

Generate and track metrics related to document revisions and batch kit review status Perform additional duties as assigned.

Requirements

What We Require 

Bachelor’s degree in Life Sciences, Technical Writing, Business, or related field (or equivalent experience)

3+ years of experience in document control within a regulated industry (pharma, biotech, medical device, cosmetics or food manufacturing,) 

Knowledge of Good Manufacturing Practices (GMP) and documentation standards Experience with document management systems (e.g., eQMS, EDMS) Strong attention to detail and organizational skills 

Proficiency in google suit (Google Docs, Google Sheets, Google Slides) Preferred Qualitifications 

Experience with electronic Quality Management Systems (eQMS) 

Familiarity with regulatory standards from the U.S. Food and Drug Administration and International Organization for Standardization 

Experience supporting audits and inspections 

Key Skills and Competency 

Strong understanding of GMP and regulatory requirements 

Document accuracy and compliance mindset 

Strong written and verbal communication skills 

Strong organizational and time management skills 

Attention to detail and consistency 

Ability to manage multiple documents and deadlines 

Effective communication and cross-functional collaboration 

Understanding of data integrity and traceability principles 

Adaptability in a fast-paced, regulated environment

Benefits

11 Paid Holidays

PTO

401K

Benefits