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QC Associate - qPCR, drug testing
Job in
Fremont, Alameda County, California, 94537, USA
Listed on 2026-01-27
Listing for:
Mindlance
Full Time
position Listed on 2026-01-27
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Data Scientist, Medical Science
Job Description & How to Apply Below
Mindlance is a national recruiting company which partners with many of the leading employers in the Life Sciences, IT, and Financial Services sectors, feel free to check us out at
Job DescriptionSkills:
- 3-5 years of industry expereince
- Experience with qPCR, UV-vis absorbance, gel electrophoresis, pH, Osmolality
- GMP experience is highly preferred
- Very smart with a great attitude and a willingness to work hard with the team
- Demonstrates strong interpersonal and communication skills (both written and oral), a strong customer focus, and an ability to interact with various departments and levels.
- Demonstrates ability to work independently and as part of a team, to meet departmental/facility goals; is also able to work across functions to achieve common goals.
- Demonstrates strong attention to detail, and an ability to focus on details of execution.
- Demonstrates good facilitation, organizational and problem solving skills, as well as demonstrated
- Education:
Bachelors degree in Biology or Life Sciences required
Analytical testing:
- Under supervision, performs testing, conducts lab investigations, problem-solves, and reports aberrant results to management.
- Performs biochemistry, qPCR, compendial testing, drug product device testing, CE, UV-vis absorbance, gel electrophoresis, pH, Osmolality.
- Ensures testing and release time lines are met. Follows well-defined and established procedures and best practices. Reviews QC test results Documentation.
- Generates, reviews and/or maintains records or documents in a detailed and consistent manner. Prepares sample reconciliation reports and other reports as needed. Assists with QC's data management, including data review and control charting.
Process improvement and compliance:
- Coordinates and manages continuous improvement projects.
- Revises standard operating procedures, training manuals, etc which are submitted to management for review and final approval.
- Maintains specific QC files and database records for process and/or quality improvement efforts. Manages and maintains deviation and change control records.
- 3-5 years of industry expereince
- Education:
Bachelors degree in Biology or Life Sciences required - Experience with qPCR, UV-vis absorbance, gel electrophoresis, pH, Osmolality
- GMP experience is highly preferred
- Very smart with a great attitude and a willingness to work hard with the team
- Demonstrates strong interpersonal and communication skills (both written and oral), a strong customer focus, and an ability to interact with various departments and levels.
- Demonstrates ability to work independently and as part of a team, to meet departmental/facility goals; is also able to work across functions to achieve common goals.
- Demonstrates strong attention to detail, and an ability to focus on details of execution.
- Demonstrates good facilitation, organizational and problem solving skills, as well as demonstrated
Position Requirements
10+ Years
work experience
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