Associate Quality Control - Biotech Lab (JP4887)
Thousand Oaks, CA.
Clinical QC Technology Transfer
18 months with likely extension
3Key Consulting Inc. is recruiting for an Associate Quality
with 1+ years’ experience performing routine laboratory procedures, analytical testing, documenting and data analysis for a global, CA-based, bio-pharmaceutical company.
Under general supervision, this position will perform routine procedures and testing in support of the HPLC and CE (Capillary Electrophoresis) group. This position will be responsible for one or more of the following activities:
- Performing routine laboratory procedures
- Routine analytical testing - Documenting, computing, compiling, interpreting and entering data
- Maintaining and operating specialized equipment
- Initiating and / or implementing changes in controlled documents.
Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory log books. Skills: some lab experience is preferred.
Top Must-Have Skill Sets:
Science Degree (e.g. Biology, Chemistry, etc) Industry Experience' attention to detail
Day to Day Responsibilities
GMP analytical testing equipment and laboratory upkeep and maintenance attention to detail and adherence to written procedures and protocols
Employee Value Proposition:
Cross functional team and opportunity to learn different technologies. Opportunity to learn different techniques in the lab.
Lack of work experience.
Phone interview followed by in-person interview
We invite qualified candidates to send your resume to email@example.com
. If you decide that you’re not interested in pursuing this position, please feel free to take a look at the other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.