Clinical QC Inspector - cGMP & Lab Compliance

Clinigen Group; Malvern (Chester County); Sur place; USD 50 000 - 70 000; Plein temps

Résumé du poste

Clinigen Group is seeking a quality-focused professional to ensure compliance with established quality systems by inspecting incoming clinical supplies, labels, and in-process materials. This on-site role requires collaboration across departments and adherence to SOPs and GDP standards.

Strong attention to detail and confidentiality are essential. The successful candidate will perform routine cGMP inspections, prepare supporting documentation, and drive continuous improvement in quality

Qualifications

• High School Diploma or GED required.
• Associates Degree or 2 years equivalent work experience preferred.
• Experience with SOPs, cGMP, or GDP preferred.

Responsabilités

• Perform routine cGMP inspections and disposition of clinical trial labels and materials.
• Prepare documents for cGMP activities.
• Complete in-process inspections to ensure product quality and compliance.
• Collaborate with other departments to identify, investigate and resolve issues.

Connaissances

Attention to detail

Problem solving

Communication skills

Time management

Confidentiality

Team collaboration

Independent work

MS Office proficiency

Operations collaboration

Formation

High School Diploma or GED

Associates Degree or 2 years equivalent work experience

Description du poste

Clinigen Group is seeking a quality-focused professional to ensure compliance with established quality systems by inspecting incoming clinical supplies, labels, and in-process materials. This on-site role requires collaboration across departments and adherence to SOPs and GDP standards.

Strong attention to detail and confidentiality are essential. The successful candidate will perform routine cGMP inspections, prepare supporting documentation, and drive continuous improvement in quality