Quality Assurance Associate I - GMP/Pharma QA

Cedent; Cumberland (RI); On-site; USD 45,000 - 60,000; Full time

Job summary

A pharmaceutical company in Cumberland, RI is seeking a Quality Assurance Associate I to ensure compliance with FDA and GMP regulations. The role involves providing QA oversight, conducting audits, and reviewing documentation. Candidates should have strong problem-solving and communication skills, as well as the ability to train staff in quality assurance best practices. This full-time position requires a commitment of 40 or more hours per week, and the opportunity offers a chance to improve quality systems in a critical industry.

Qualifications

• Knowledge of pharmaceutical regulatory requirements such as FDA and GMP.
• Ability to conduct quality assurance audits and assessments.
• Experience in preparing and issuing audit reports.

Responsibilities

• Provide support to GMP investigations and validation reviews.
• Participate in internal/external audits and recommend actions.
• Review and approve all cGMP documents for compliance.
• Train staff in quality assurance processes and best practices.

Skills

Project Management

Problem Solving/Analysis

Communication Proficiency

Collaboration Skills

Job description

A pharmaceutical company in Cumberland, RI is seeking a Quality Assurance Associate I to ensure compliance with FDA and GMP regulations. The role involves providing QA oversight, conducting audits, and reviewing documentation. Candidates should have strong problem-solving and communication skills, as well as the ability to train staff in quality assurance best practices. This full-time position requires a commitment of 40 or more hours per week, and the opportunity offers a chance to improve quality systems in a critical industry.