Document Control Specialist II | cGMP & Quality Systems

FUJIFILM Biotechnologies; Town of Texas (WI); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Paid paternity leave

Paid maternity leave

Tuition assistance

Job summary

A leading biotechnology company in College Station, TX is seeking a Document Control Specialist II. This on-site role requires expertise in cGMP documentation and the ability to manage document control systems with minimal supervision. Ideal candidates will hold a related Bachelor's degree or equivalent experience in a regulated industry. Benefits include medical and vision insurance, 401(k), and tuition assistance.

Qualifications

• 2+ years of experience of cGMP supporting pharmaceutical or biotechnology products.
• 4+ years of experience in a regulated industry with an Associate's degree.
• 6+ years of experience in Pharmaceutical or Regulated Industry with a High School diploma.

Responsibilities

• Maintain official company training percentages.
• Ensure documents are routed to appropriate individuals.
• Verify and document staff training has been completed as required.

Skills

Excellent written and oral communication skills

Experience with Word

Experience with Excel

Experience with Adobe PDF

Education

Bachelor's degree in a related science concentration

Associate's degree in a related science concentration

High School or equivalent

Tools

Trackwise

Master Control

Job description

A leading biotechnology company in College Station, TX is seeking a Document Control Specialist II. This on-site role requires expertise in cGMP documentation and the ability to manage document control systems with minimal supervision. Ideal candidates will hold a related Bachelor's degree or equivalent experience in a regulated industry. Benefits include medical and vision insurance, 401(k), and tuition assistance.