Pharma Validation Lead – GMP, BMS & Commissioning

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

Job summary

A leading IT staffing company in Zebulon, North Carolina, seeks an experienced validation specialist. This role involves ensuring compliance with regulatory requirements, overseeing the commissioning and validation of manufacturing processes in the Pharmaceutical industry, and collaborating with cross-functional teams. The ideal candidate should have a degree in a related field, extensive experience in validation, and strong project management skills. This position offers a unique opportunity to contribute to the improvement of critical systems in a dynamic environment.

Qualifications

• Expertise in regulatory compliance and validation.
• Minimum 3 years experience in Manufacturing validation.
• Knowledge of cGMP regulations.

Responsibilities

• Ensure compliance with regulatory requirements for commissioning.
• Develop and maintain Project Validation Master Plans.
• Collaborate with Engineering on validation protocols.

Skills

Regulatory compliance expertise

Project management

Documentation skills

Communication skills

Computer skills (MS Word, Excel, PowerPoint)

Education

BA/BS in a technical or scientific discipline + 5 years Pharmaceutical experience

MS + 3 years Pharmaceutical experience

2 years Pharmaceutical QA experience

Job description

A leading IT staffing company in Zebulon, North Carolina, seeks an experienced validation specialist. This role involves ensuring compliance with regulatory requirements, overseeing the commissioning and validation of manufacturing processes in the Pharmaceutical industry, and collaborating with cross-functional teams. The ideal candidate should have a degree in a related field, extensive experience in validation, and strong project management skills. This position offers a unique opportunity to contribute to the improvement of critical systems in a dynamic environment.