Technical Writer II — cGMP & Lab Compliance

Artech Information System LLC; Northborough (MA); On-site; USD 70,000 - 90,000; Full time

Job summary

A prominent IT staffing firm is seeking a candidate for a lab-focused role requiring a bachelor's degree in a related field and at least 5 years of experience in a cGMP laboratory environment. The ideal candidate will ensure the quality of QCRM documents and support regulatory inspections. Responsibilities include providing training and coordinating lab equipment tasks. This role is essential for maintaining safety and compliance in laboratory operations.

Qualifications

• Minimum of 5 years of experience in cGMP laboratory environment.
• Previous experience with lab control operations and quality systems.

Responsibilities

• Ensure timely and efficient creation/review of QCRM documents.
• Provide training and ensure proficiency of QCRM staff.
• Support readiness for regulatory inspections and compliance audits.
• Coordinate and conduct laboratory equipment tasks.

Skills

Analytical skills

Ability to manage lab equipment

Knowledge of cGMP regulations

Experience with quality systems

Education

Bachelor's degree in a related discipline

Job description

A prominent IT staffing firm is seeking a candidate for a lab-focused role requiring a bachelor's degree in a related field and at least 5 years of experience in a cGMP laboratory environment. The ideal candidate will ensure the quality of QCRM documents and support regulatory inspections. Responsibilities include providing training and coordinating lab equipment tasks. This role is essential for maintaining safety and compliance in laboratory operations.