Job Description

Description:

The Quality Assurance Specialist is responsible for performing review of GMP documents/records and batch release as well as supporting the quality processes and maintaining quality assurance standards, processes, and controls. The Quality Assurance Specialist is also responsible for proving online support of manufacturing activities and will occasionally be required to work in a cleanroom environment. This person will be working across multiple departments to identify deviations, complete investigations, and perform CAPAs.

Skills:

quality assurance standards, gmp, quality control, fda, capa, audit, batch record review, document control, haccp, pharmaceutical, medical device, quality assurance, QA, batch record, sop, method validation

Additional Skills & Qualifications:

Bachelor\'s, or higher, degree in a scientific discipline, preferably biology or chemistry

1+ years of experience in a cGMP Quality Assurance/Compliance environment, open to someone from a QC role within a pharmaceutical environment

Experience Level:

Entry Level

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We\'re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Actalent