What are the responsibilities and job description for the Qc associate iii position at TalentZok?
Analytical QC Associate III- Simply Biotech OVERVIEW Are you looking for a new career opportunity with an exciting biotech company?
Then we've got the right team for you! In this role, you're responsible for the duties listed below. Immediate opening for an Analytical QC Associate III with a biotech company in San Diego, CA who possesses : -Method Development and Qualification experience-Experience in running ELISAs / HPLCs-At least 5 years of total QC experience Email resumes to tness@ FULL DESCRIPTION : The QC Associate III (Analytical) position performs routine and non-routine analytical testing to support Operations, and Process Development with minimal supervision.
This position may perform method transfers, method development, and method qualification with minimal supervision. This position will perform quality investigations (OOT, deviation, etc).
As part of the QC team, this position will be responsible for maintaining the QC laboratory, including cleaning the area, performing routine preventative maintenance, and ordering supplies.
This position requires hands-on laboratory work and close collaboration with the QC control team, Process Development Team, and the Operations team.
This position is expected to rigorously adhere to relevant cGMP guidelines, test methods, and SOP's. The selected candidate will be responsible for : -Perform routine and non-routine complex analytical testing with minimal supervision.
- Develop, qualify, and validate complex analytical testing following international guidance's, and client requirements with some supervision.
- Perform routine laboratory maintenance including, monthly routine cleaning procedures to ensure safety of laboratory personnel as well as monitor disposable equipment and reagent supplies to make certain materials are available for use.
- Prioritize daily tasks, related to operations, technology transfers, analytical testing and validation including equipment and procedures.
- Document and investigate any out of specification results, deviations, or investigations with minimal assistance. Assist in resolving any out of specification and out of trending results as well as performing and developing any corrective and preventative measures.
- Develop and revise SOPs under data integrity guidelines as well as perform periodic revisions to ensure the procedures are up to date to current standards.
- Trains new analysts and ensures personnel understand various analytical assays and standard operation procedures as well as conform to any departmental procedures.
- Assist Quality Assurance in ensuring compliance with applicable quality standards and regulatory requirements.-Capable of leading projects and adhering to timelines with supervision.
The selected candidate will also possess : -Bachelor or Masters of Science Degree in the Biological Sciences, Bioengineering or Chemistry with a combination of education and experience performing biochemistry, molecular biology, microbiology, and chemistry.
Last updated : 2024-11-16
Salary : $38 - $42
