Quality Assurance Associate

Ampcus, Inc; Winchester (KY); On-site; USD 60,000 - 75,000; Full time

Job summary

A leading consulting services provider in Winchester, KY, is looking for a Quality Assurance Associate to join their team. The right candidate will have a BS degree in Chemistry or Biochemistry, along with a minimum of 3 years of experience in GMP environments. Responsibilities include reviewing analytical release data and approving controlled documents, all while ensuring compliance with regulations. Strong critical thinking and communication skills are essential for success in this role.

Qualifications

• 3+ years of GMP industry experience, including analytical laboratory or QA experience.
• Familiarity with GMP regulations is essential.
• Ability to make independent decisions based on compliance requirements.

Responsibilities

• Review analytical release and stability data with minimal supervision.
• Review and approve controlled documents like protocols and test methods.

Skills

Critical thinking

Organizational skills

Effective communication

Education

BS science degree in Chemistry or Biochemistry

Job description

Ampcus Inc. is a certified global provider of a broad range of Technology and Business consulting services. We are in search of a highly motivated candidate to join our talented team.

Job Title: Quality Assurance Associate
Location: Winchester, KY.

A QA Associate must be familiar with applicable GMP regulations and systems and have the ability to make independent decisions based those requirements.

This individual will be responsible for evaluating the compliance of analytical documentation such as test methods, protocols, and stability and release data with minimal supervision.

This individual must demonstrate excellent critical thinking and organizational skills. Professional, effective, and proactive communication with peers, management, and interdepartmental colleagues is required.

Essential Duties and Responsibilities

Essential Duties and Responsibilities include the following. Other duties may be assigned.

• Review of analytical release and stability data, with minimal supervision.
• Review and approval of controlled documents such as protocols, test methods, and specifications.

Education and/or Experience

• Minimum of 3 years of applicable GMP industry experience. Analytical laboratory, QC laboratory, Manufacturing, QA experience may be considered applicable.
• BS science degree, preferably in Chemistry or Biochemistry.

Ampcus is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veterans or individuals with disabilities.