Quality Documentation Specialist II — GMP & SOP Expert

Artech Information System LLC

Canton (MA)

On-site

USD 60,000 - 80,000

Full time

14 days+
Application generator

Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.

Get past ATS filters

Job summary

A leading IT staffing company in Canton, Massachusetts, is seeking a Documentation Specialist II. The role involves managing the documentation lifecycle for GMP documentation and ensuring compliance with regulatory requirements. Candidates should have 3 to 6 years of experience and exhibit strong interpersonal and critical thinking skills. Attention to detail and the ability to work in a fast-paced team environment are essential. This contract position offers the chance to work with a respected firm in the staffing industry.

Qualifications

  • 3 to 6 years of experience in documentation control.
  • Must possess sound interpersonal and information gathering skills.
  • Ability to work in a team environment and interact effectively with others.

Responsibilities

  • Manage the documentation lifecycle for GMP documentation.
  • Ensure compliance with regulatory requirements through formatting and editing.
  • Collaborate with teams for timely delivery of controlled documentation.

Skills

Expert word processing skills including Adobe Acrobat Professional
Attention to detail
Self‑managed critical thinker
Ability to learn quickly and acclimate to a fast‑paced dynamic culture

Education

Degree preferred – level of experience may be considered equivalent

Job description

A leading IT staffing company in Canton, Massachusetts, is seeking a Documentation Specialist II. The role involves managing the documentation lifecycle for GMP documentation and ensuring compliance with regulatory requirements. Candidates should have 3 to 6 years of experience and exhibit strong interpersonal and critical thinking skills. Attention to detail and the ability to work in a fast-paced team environment are essential. This contract position offers the chance to work with a respected firm in the staffing industry.
Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

GMP & QMS Documentation Specialist
GMP & QMS Documentation Specialist

Compunnel Inc. • West Sacramento (CA)

On-site
USD 65,000 - 85,000
GMP Documentation Specialist | Batch Records & Compliance
GMP Documentation Specialist | Batch Records & Compliance

Joulé • Illinois

On-site
USD 60,000 - 80,000
GMP Compliance Documentation Specialist
GMP Compliance Documentation Specialist

Planet Pharma • Illinois

On-site
USD 45,000 - 65,000
Quality Assurance Associate II
Quality Assurance Associate II

Scorpion Therapeutics • Fall River (MA)

On-site
USD 65,000 - 90,000
Quality Documentation Specialist II - Compliance & Editing
Quality Documentation Specialist II - Compliance & Editing

Artech Information System LLC • Rockville (MD)

On-site
USD 60,000 - 80,000
GMP Documentation & Records Specialist
GMP Documentation & Records Specialist

Integrated Resources Inc. • Richmond (VA)

On-site
USD 60,000 - 80,000
Sr. Documentation Technician
Sr. Documentation Technician

Unicon Pharma Inc • Austin (TX)

On-site
USD 52,000 - 68,000
GMP QA Documentation Specialist I
GMP QA Documentation Specialist I

VIVOS Professional Services, LLC • Bend (OR)

On-site
USD 60,000 - 80,000
Document Control Specialist - Confidential Clearance
Document Control Specialist - Confidential Clearance

Prolim • Newport News (VA)

On-site
USD 45,000 - 60,000
Document Control Specialist II | cGMP & Quality Systems
Document Control Specialist II | cGMP & Quality Systems

FUJIFILM Biotechnologies • Town of Texas (WI)

On-site
USD 50,000 - 70,000