What are the responsibilities and job description for the QA Specialist position at Actalent?
Description:
The QA Specialist will be responsible for reviewing paper batch records, coordinating and executing investigations, supporting the quality teams in the manufacturing departments, and completing deviations and CAPAs. This person will be spending 60-70% of their time in the office working on batch records and investigations and the other 30-40% on the production floor. When there is an error found in documentation this person must close the gap with other departments to figure out what needs to be updated in the records.
Additional Skills & Qualifications:
Bachelor's Degree in Sciences: Biology, Microbiology, Chemistry, Biochemistry, other life science degree
1-3 years of industry experience in QA/QC within a pharmaceutical environment - QA Associate
4 years of industry experience in QA/QC within a pharmaceutical environment - QA Specialist
Hours/Shift:
1st shift Monday-Friday
8am-4:30pm
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.