EU Pharma Regulatory Specialist & Compliance Expert

Lachman Consultant Services, Inc; España; Hybrid; PHP 4,747,071 - 14,241,213; Part time

Job summary

A leading consulting firm is seeking per diem pharmaceutical consultants proficient in English and one other European language. Ideal candidates should have a B.S. in life sciences or engineering, with over 10 years of experience in regulatory compliance, quality assurance, and FDA regulations. Responsibilities include performing GMP audits, managing regulatory compliance evaluations, and contributing to the drug approval process. Strong communication and project management skills are essential.

Qualifications

• Must effectively communicate in English and one other European language.
• 10 years of related experience with detailed knowledge of FDA regulations.

Responsibilities

• Perform GMP/GLP audits covering laboratory procedures.
• Manage regulatory inspections and compliance evaluations.
• Lead projects and meet crucial timelines.

Skills

Regulatory compliance expertise

Quality Systems / Quality Assurance

Superb written and oral communication skills

Project management

Training

Education

B.S. in life sciences or engineering

Job description

A leading consulting firm is seeking per diem pharmaceutical consultants proficient in English and one other European language. Ideal candidates should have a B.S. in life sciences or engineering, with over 10 years of experience in regulatory compliance, quality assurance, and FDA regulations. Responsibilities include performing GMP audits, managing regulatory compliance evaluations, and contributing to the drug approval process. Strong communication and project management skills are essential.