QC Associate I - qPCR, drug testing

Company Description

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 http://www.mindlance.com.

Job Description

Skills:
•    3-5 years of industry expereince
•    Experience with qPCR, UV-vis absorbance, gel electrophoresis, pH, Osmolalilty
•    GMP experience is highly prefered
•    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, Osmolalilty
•    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 expereince

•    Education: Bachelors degree in Biology or Life Sciences required

•    Experience with qPCR, UV-vis absorbance, gel electrophoresis, pH, Osmolalilty
•    GMP experience is highly prefered
•    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

Additional Information