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QC Associate - qPCR, drug testing

Job in Fremont, Alameda County, California, 94537, USA
Listing for: Mindlance
Full Time position
Listed on 2026-02-28
Job specializations:
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: QC Associate I - qPCR, drug testing

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 Description

Skills:

  • 3-5 years of industry experience
  • 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

Duties:
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.
Qualifications
  • 3-5 years of industry experience
  • 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
  • Strong interpersonal and communication skills (written and oral), strong customer focus, and ability to interact with various departments and levels
  • Ability to work independently and as part of a team to meet departmental/facility goals; able to work across functions to achieve common goals
  • Strong attention to detail, and an ability to focus on details of execution
  • Good facilitation, organizational and problem solving skills
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Position Requirements
10+ Years work experience
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