GMP Doc Coordinator for Parenteral Manufacturing (Contract)

Randstad Enterprise; United States; On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Opportunity for training

Career counseling

Benefit options

Job summary

A leading staffing and consulting firm is seeking an experienced GMP Documentation Coordinator to join the Parenteral team in Durham, NC. This role involves coordinating with Quality Assurance and ensuring data accuracy in documentation. Ideal candidates will have strong attention to detail, relevant education, and experience in the pharmaceutical manufacturing industry. The position is 100% onsite, offering training and growth opportunities.

Qualifications

• 2 year or bachelor's degree preferred.
• Minimum: High School degree and 6+ months experience in a related role.
• Biowork certification and knowledge of cGMP practices are a plus.

Responsibilities

• Coordinate with Quality Assurance and Parenteral Manufacturing.
• Ensure data accuracy and compliance in documentation.
• Manage documentation and data processes.

Skills

Attention to detail

Time management

Documentation skills

Education

2 year or bachelor's degree

High School degree with 6+ months experience

Job description

A leading staffing and consulting firm is seeking an experienced GMP Documentation Coordinator to join the Parenteral team in Durham, NC. This role involves coordinating with Quality Assurance and ensuring data accuracy in documentation. Ideal candidates will have strong attention to detail, relevant education, and experience in the pharmaceutical manufacturing industry. The position is 100% onsite, offering training and growth opportunities.