Document Control Specialist

redShift Recruiting, LLC

Pittsfield, MA

JOB DETAILS
SALARY
$20–$25 Per Hour
SKILLS
Cataloguing, Code of Federal Regulations, Communication Skills, Computer Skills, Current Good Manufacturing Practice (cGMP), Data Entry, Detail Oriented, Document Control, Document Management, Documentation, Establish Priorities, FDA (Food and Drug Administration), Federal Laws and Regulations, GMP (Good Manufacturing Practices), Microsoft Excel, Microsoft Office, OSHA, Organizational Skills, Physical Demands, Procedure Development, Recruiting/Staffing Agency, Regulatory Requirements, State Laws and Regulations
LOCATION
Pittsfield, MA
POSTED
3 days ago
Our well-established client located near Pittsfield, MA is seeking a Temporary Document Control Specialist to support the relocation and organization of their GMP archive room. This role will focus on cataloging, verifying, scanning, and properly filing controlled documentation in accordance with established procedures and compliance expectations. The ideal candidate is detail oriented, organized, and comfortable working with both physical and electronic records.
 
Duties: 
  1. Catalog GMP documentation within Excel spreadsheets, ensuring accuracy and completeness.
  2. Identify and verify scan status of records within designated shared drive pathways.
  3. Scan, upload, and file documents into appropriate electronic folders following established naming and storage conventions.
  4. Organize physical records into appropriate storage categories (e.g., binders, boxes, long term archive containers).
  5. Prepare, sort, label, and consolidate documents prior to relocation.
  6. Relocate large volumes of documentation from the existing archive room to the designated new storage area.
  7. Maintain good documentation practices (GDP) while handling all records.
  8. Assist with general archive room organization, inventorying, and cleanup as needed.
  9. Follow all safety, quality, and data integrity expectations during document handling.
 
Regulatory Responsibilities: 
  1. Understanding of cGMP, 21 CFR 210/211 and other regulatory agency requirements which apply to quality operations and compliance 
  2. Conduct business in a responsible manner that complies with all state, OSHA and Federal regulations
  3. Understanding of FDA, EU, and other regulatory agency requirements
 
Knowledge, Skills & Abilities:
 
  1. Experience handling and organizing GMP documentation.
  2. Knowledge of quality assurance (QA), GMP documentation, and basic compliance principles.
  3. Strong attention to detail and commitment to accuracy.
  4. Highly organized with the ability to prioritize and manage repetitive tasks.
  5. Proficiency in Microsoft Office, especially Excel, and overall computer literacy.
  6. Experience scanning and managing large volumes of documents.
  7. Ability to work independently and follow established procedures.
  8. Strong communication skills and ability to ask clarifying questions when needed.
 
Physical Requirements: 
  • Ability to sit for prolonged periods while cataloging or performing data entry.
  • Ability to stand for prolonged periods during scanning or document sorting.
  • Ability to lift, move, and carry boxes or stacks of documentation (up to 25 lbs).
  • Comfortable with repetitive motion tasks (e.g., sorting, scanning, filing).
 
Pay for this position is commensurate with experience and education, ranging roughly from $20-25/hr.
 
To see a full listing of all our open positions, please visit:
https://www.redshiftrecruiting.com/jobs-hiring-near-me

 
redShift Recruiting is the region's premier recruiting agency with over 100 years of combined experience in the recruiting field. We specialize in permanent, temporary, and temp-to-hire positions. Our superior service combined with our highly qualified and carefully selected bank of candidates sets us apart.
 
 
 

About the Company

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redShift Recruiting, LLC