GMP CQV Project Coordinator

Intone Networks - Holly Springs, NC

Full-time - Entry Level

Holly Springs, NC

Professional, Scientific, and Technical Services

About the position

The GMP CQV Project Coordinator will be responsible for coordinating and overseeing the Commissioning, Qualification, and Validation (CQV) processes within Good Manufacturing Practice (GMP) environments. This role is essential for ensuring compliance with regulatory standards and facilitating the successful execution of projects in the pharmaceutical or biotechnology sectors.

Responsibilities

• Coordinate and manage CQV activities for GMP projects.
• Ensure compliance with regulatory requirements and industry standards.
• Collaborate with cross-functional teams to support project execution.
• Assist in the preparation of validation documentation and reports.
• Monitor project timelines and deliverables to ensure timely completion.

Requirements

• Entry-level experience in GMP environments or related fields.
• Basic understanding of Commissioning, Qualification, and Validation processes.
• Strong organizational and communication skills.
• Ability to work collaboratively in a team environment.

Nice-to-haves

• Familiarity with pharmaceutical or biotechnology industry standards.
• Experience with project management tools and software.

Benefits

• Competitive salary based on experience and qualifications.
• Opportunity for professional development and training.