Global GMP Documentation Specialist - Hybrid

Hlx Life Sciences; Gerona; Hybrid; EUR 40,000 - 60,000; Full time

Job summary

Hlx Life Sciences in Catalonia, Spain, is seeking a skilled professional to manage pharmaceutical documentation within GMP environments. This role blends on-site collaboration with flexible remote work, focusing on documentation integrity and lifecycle management.

The ideal candidate will have a strong understanding of GMP environments and relevant documentation experience, offering significant growth opportunities as the company expands internationally.

Qualifications

• Strong understanding of GMP environments.
• Experience with controlled quality documentation systems.
• Familiarity with analytical methods and regulatory documentation.

Responsibilities

• Managing and maintaining GMP-controlled documentation and records.
• Supporting product registrations across multiple countries.
• Ensuring compliance with GMP and pharmacopoeia requirements.

Skills

Understanding of GMP environments

Experience with controlled quality documentation systems

Familiarity with analytical methods and regulatory documentation

Strong Microsoft Office skills

Structured documentation skills

Education

Scientific or technical academic background

Job description

Hlx Life Sciences in Catalonia, Spain, is seeking a skilled professional to manage pharmaceutical documentation within GMP environments. This role blends on-site collaboration with flexible remote work, focusing on documentation integrity and lifecycle management.

The ideal candidate will have a strong understanding of GMP environments and relevant documentation experience, offering significant growth opportunities as the company expands internationally.