Associate Quality Control
3 Key Consulting
Job Title: Associate Quality Control - (JP9766)
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: ATO Quality Control Chemistry and Biochemistry
Duration: 1+ years (with likely extensions and/or conversion to permanent)
Posting Date: 2/2/2022
Notes: 3 Key Consulting is hiring an Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description:
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:
Day to Day Responsibilities:
Some lab experience is preferred. Employee Value Proposition:
Red Flags:
Lack of science background. Interview process:
Video Skype Panel Interview. We invite qualified candidates to send your resume to View email address on click.appcast.io you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: ATO Quality Control Chemistry and Biochemistry
Duration: 1+ years (with likely extensions and/or conversion to permanent)
Posting Date: 2/2/2022
Notes: 3 Key Consulting is hiring an Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description:
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.
- HPLC/CE.
- BS - Chemistry/Biology Background, preferred not required.
- Knowledge of GMP and Equipment Troubleshooting.
Day to Day Responsibilities:
- Performing routine laboratory procedures.
- Routine analytical testing.
- Documenting, computing, compiling, interpreting and entering data.
- Maintaining and operating specialized equipment.
Some lab experience is preferred. Employee Value Proposition:
- Training will available
- Great teammates and support
Red Flags:
Lack of science background. Interview process:
Video Skype Panel Interview. We invite qualified candidates to send your resume to View email address on click.appcast.io you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Vacancy posted 4 days ago
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