Manufacturing QA & Document Control Specialist

Harbor Clinical; United States; Hybrid; USD 41,328 - 61,992; Part time

Job summary

A certified clinical service firm is seeking a contract QA Specialist in the United States. This role requires a candidate with 2-6 years of experience in QA or manufacturing within life sciences. Responsibilities include supporting quality management systems, assisting with document control, and partnering with manufacturing teams to ensure compliance. The ideal candidate will be organized, adaptable, and possess a solid understanding of GMP. This position offers both part-time and full-time opportunities.

Qualifications

• 2-6 years in manufacturing, operations, or QA within life sciences or related fields.
• Experience with Document Control systems preferred.
• Understanding of GMP and quality fundamentals.

Responsibilities

• Maintain and support QMS activities, especially Document Control.
• Partner with manufacturing teams to ensure quality practices.
• Assist with SOP updates and quality documentation.

Skills

Manufacturing experience

Document Control

Quality Assurance

GMP understanding

Tools

Veeva

Job description

A certified clinical service firm is seeking a contract QA Specialist in the United States. This role requires a candidate with 2-6 years of experience in QA or manufacturing within life sciences. Responsibilities include supporting quality management systems, assisting with document control, and partnering with manufacturing teams to ensure compliance. The ideal candidate will be organized, adaptable, and possess a solid understanding of GMP. This position offers both part-time and full-time opportunities.