Quality Control Operations & Documentation Specialist (GxP)

Planet Pharma; New York (NY); On-site; USD 70,000 - 80,000; Full time

Job summary

A leading pharmaceutical company in New York, NY, is seeking a Quality Control Associate responsible for coordinating QC sample shipment and testing activities. This role is crucial in maintaining quality documentation and supporting multiple internal teams. Candidates should have a Bachelor’s degree in Life Sciences and experience in a GxP-compliant environment. The role demands strong organizational skills and the ability to manage multiple tasks efficiently. A competitive salary of $70,000–$80,000 plus a 10% bonus is offered.

Qualifications

• Experience in a regulated GxP-compliant environment.
• Experience with quality systems in pharmaceutical or biotechnology.
• Comfortable in a fast-paced, results-driven environment.

Responsibilities

• Coordinate QC sample shipment and track testing submissions.
• Review QC data for accuracy and compliance.
• Prepare quality documentation to support QA review.

Skills

Strong written and verbal communication skills

Attention to detail

Ability to manage multiple activities

Proactive and self-motivated

Sound judgment and decision-making

Education

Bachelor’s degree in Life Sciences or related discipline

Job description

A leading pharmaceutical company in New York, NY, is seeking a Quality Control Associate responsible for coordinating QC sample shipment and testing activities. This role is crucial in maintaining quality documentation and supporting multiple internal teams. Candidates should have a Bachelor’s degree in Life Sciences and experience in a GxP-compliant environment. The role demands strong organizational skills and the ability to manage multiple tasks efficiently. A competitive salary of $70,000–$80,000 plus a 10% bonus is offered.