Senior QC Scientist - Validation & GMP Compliance

Astrix; Wilmington (OH); On-site; USD 61,992 - 75,768; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Job summary

A leading staffing solution firm in Wilmington, OH seeks a Quality Control Scientist to lead project coordination and ensure compliance with regulatory standards in pharmaceutical manufacturing. The ideal candidate holds a BSc in a science-related field with at least 10 years of experience or relevant advanced degrees. This role involves writing protocols, supporting audits, and managing multiple projects efficiently.

Qualifications

• 10+ years of experience in pharmaceutical manufacturing for BSc; 3-5+ for MS; 0-5 for PhD.
• Strong technical knowledge of test instrumentation and method validation.
• Excellent planning and organizational skills.

Responsibilities

• Lead project coordination and support.
• Write protocols and execute method verification and validation.
• Support regulatory audits and maintain laboratory operations.

Skills

Microbiological test instrumentation

Chemistry test instrumentation

Method development and validation

Project management

Communication skills

Education

BSc in a science-related field

MS degree

PhD

Tools

MS Office

Job description

A leading staffing solution firm in Wilmington, OH seeks a Quality Control Scientist to lead project coordination and ensure compliance with regulatory standards in pharmaceutical manufacturing. The ideal candidate holds a BSc in a science-related field with at least 10 years of experience or relevant advanced degrees. This role involves writing protocols, supporting audits, and managing multiple projects efficiently.