This role will be on 100% Onsite.
Senior Quality Control Analysts have the following responsibilities:
Perform laboratory activities to support method validation.
Write method validation protocols and reports.
Generate and revise analytical test procedures.
Senior Quality Control Analysts should have the following skill set:
Familiar with current Good Manufacturing Practices and Good Lab Practices.
Familiar with current ICH and USP guidance for analytical method validation.
Familiar with analytical lab equipment and analytical lab techniques (e.g. HPLC, TLC, UV)
The ability to work independently following an approved protocol.
The ability to function in a team environment.
The flexibility to work overtime as required.
The ability to demonstrate creative and innovative thinking to solve analytical problems.
Good technical writing skills and the ability to communicate technical issues to project lead and team.
Minimum Qualifications:
Bachelors of Science degree in Chemistry or other science
5 years of analytical laboratory experience
3 years analytical method validation experience
Proficient in MS Word and Excel.
Preferred Qualifications:
3 years of experience in a Pharmaceutical manufacturing facility
7 years of analytical laboratory experience
5 years analytical method validation experience