A pharma company in Massachusetts is actively seeking a new Document Control Specialist to support daily operations in Document Management and ensuring the proper maintenance of GxP documents.

About the Opportunity:
- Shift: Day
- Schedule: Full-time
- Hours: Standard business hours
Responsibilities:
- Adhering to Standard Operating Procedures and Work Instructions
- Managing activities associated with the Document Storage Room
- Organizing and managing a high volume of documentation
- Assisting with document filing and issuance
- Supporting document reconciliation and archival
- Performing other duties, as needed
Qualifications:
- 1+ years of relevant work experience
- Bachelor’s Degree in Engineering, Science, and/or related discipline
- Experience in Document Control and Electronic Document Management systems
- Knowledge of GDP and cGMP principles
- Proficiency in MS Excel, Word, and PowerPoint
- Effective teamwork and collaboration skills
- Strong attention to detail and organizational skills
- Ability to work independently and manage multiple tasks
Desired Skills:
- Knowledge of cGMP's and Pharmaceutical industry regulations
