QC Associate I - qPCR, drug testing

Mindlance; Fremont (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

A national recruiting company is seeking a skilled professional in Fremont, California for analytical testing in Life Sciences. The ideal candidate has 3-5 years of industry experience with techniques such as qPCR and gel electrophoresis. Strong communication and problem-solving skills are essential, along with a Bachelor's degree in Biology or Life Sciences. The position offers opportunities for process improvement and collaborative work in a team-focused environment.

Responsibilities

• Perform testing under supervision and conduct lab investigations.
• Conduct biochemistry, qPCR testing, and ensure testing timelines are met.
• Generate and maintain records and documentation consistently.
• Coordinate and manage continuous improvement projects.

Skills

Industry experience

qPCR

UV-vis absorbance

gel electrophoresis

pH

Osmolality

GMP experience

Interpersonal skills

Communication skills

Attention to detail

Problem solving

Organizational skills

Education

Bachelor's degree in Biology or Life Sciences

Job 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 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