Sr Associate Quality Control

Location: Thousand Oaks, CA
Date Posted: 02-13-2017
Individual should be able to perform moderately complex to complex laboratory activities under minimal supervision. The candidate should be experienced in the use of analytical tools used for pharmaceutical analysis, such as HPLC, GC, IR, KF and Dissolution testing. This work will be supporting process development for both Drug Substance and Drug Product. Working experience in a cGMP environment would be beneficial. The candidate should be familiar with chromatography data system such as Empower software.

We are looking for a person with an innate scientific curiosity and keen observation skills, knowing when to seek input and when to make independent judgments, being able to shift priorities quickly.


Education and Experience:
• Bachelor's degree in Chemistry, Biochemistry or related fields

Knowledge, Skills and Abilities:
• Proficient in the use of laboratory instruments, such as HPLC, GC, Dissolution Testing, Karl Fischer, UV-Vis and related software.
• Communicate effectively and follow detailed written and verbal instruction/methods/protocols.
• Maintain a laboratory notebook and complete all documentation with clear and accurate language and according to the SOP.
• Positive attitude and ability to work well with others in the team.
• Manage time effectively to complete assignments in expected time frame.

Possibility of extension
CW will be have to be onsite Full time.
CW will have a office space but majority time will be in the lab.

Performance will be measured based on the skill sets, how they are doing in lab and performing testing, documentation etc. 

"This posting is for Contingent Worker, not an FTE"
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