Pharmaceutical GMP QA Specialist

About the Role

Join synergy as a Pharmaceutical GMP QA Specialist in Dallas, Texas, United States.

Key Responsibilities

• cause internal audits and inspections of chemistry, microbiology, and molecular biology laboratories. Review and approve GMP

• related documentation, including test results, technical reports, investigation reports, and SOPs. Coordinate with cross

• functional teams to address non

Requirements

• cause internal audits and inspections of chemistry, microbiology, and molecular biology laboratories. Review and approve GMP

• related documentation, including test results, technical reports, investigation reports, and SOPs. Coordinate with cross

• functional teams to address non

• solving abilities. Excellent communication and interpersonal skills. Ability to work collaboratively in cross

Benefits & Compensation

• Health Care Plan (Medical, Dental & Vision) Paid Time Off (Vacation, Sick & Public Holidays) Training & Development.

Work Schedule

• Full-Time position.

• No explicit call, weekend, or night shift information provided.

Apply to join synergy as a Pharmaceutical GMP QA Specialist.